Other mutations in this stock |
Total: 1506 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012A03Rik |
T |
C |
6: 32,035,427 (GRCm39) |
W36R |
probably damaging |
Het |
1700016H13Rik |
G |
A |
5: 103,797,434 (GRCm39) |
P25L |
probably damaging |
Het |
1700017N19Rik |
A |
T |
10: 100,441,501 (GRCm39) |
K170M |
probably damaging |
Het |
1700020A23Rik |
C |
T |
2: 130,247,772 (GRCm39) |
P77L |
probably damaging |
Het |
1700020L24Rik |
A |
G |
11: 83,331,332 (GRCm39) |
Q81R |
probably damaging |
Het |
2210408I21Rik |
A |
C |
13: 77,323,010 (GRCm39) |
D13A |
probably damaging |
Het |
2310003L06Rik |
G |
T |
5: 88,120,165 (GRCm39) |
Q307H |
probably damaging |
Het |
2510039O18Rik |
G |
A |
4: 148,029,202 (GRCm39) |
E391K |
probably benign |
Het |
4930447C04Rik |
G |
C |
12: 72,986,169 (GRCm39) |
|
probably benign |
Het |
4932438H23Rik |
T |
A |
16: 90,852,701 (GRCm39) |
H145L |
probably benign |
Het |
4933405L10Rik |
G |
A |
8: 106,436,395 (GRCm39) |
G197E |
probably damaging |
Het |
A4gnt |
C |
T |
9: 99,495,894 (GRCm39) |
S110L |
probably damaging |
Het |
Aadacl4fm1 |
C |
A |
4: 144,255,239 (GRCm39) |
L220M |
probably damaging |
Het |
Aasdh |
T |
C |
5: 77,049,004 (GRCm39) |
|
probably null |
Het |
Abca13 |
A |
C |
11: 9,244,687 (GRCm39) |
Q2183H |
probably damaging |
Het |
Abca14 |
T |
A |
7: 119,815,358 (GRCm39) |
I202N |
probably benign |
Het |
Abca17 |
T |
A |
17: 24,498,053 (GRCm39) |
K1428M |
probably damaging |
Het |
Abca17 |
C |
G |
17: 24,565,193 (GRCm39) |
A80P |
probably damaging |
Het |
Abca17 |
G |
T |
17: 24,498,081 (GRCm39) |
P1419T |
probably benign |
Het |
Abca8b |
A |
T |
11: 109,867,308 (GRCm39) |
M250K |
probably benign |
Het |
Abcc1 |
C |
A |
16: 14,228,673 (GRCm39) |
H307N |
probably benign |
Het |
Abcc12 |
G |
A |
8: 87,286,908 (GRCm39) |
|
probably null |
Het |
Abcc8 |
A |
G |
7: 45,787,489 (GRCm39) |
F571L |
probably benign |
Het |
Abhd8 |
G |
A |
8: 71,914,445 (GRCm39) |
P61L |
probably benign |
Het |
Abtb3 |
C |
T |
10: 85,223,721 (GRCm39) |
H177Y |
probably benign |
Het |
Acan |
G |
T |
7: 78,737,948 (GRCm39) |
E218* |
probably null |
Het |
Acan |
A |
C |
7: 78,761,102 (GRCm39) |
H1938P |
probably benign |
Het |
Acan |
G |
C |
7: 78,749,858 (GRCm39) |
S1543T |
probably benign |
Het |
Accsl |
A |
C |
2: 93,696,293 (GRCm39) |
F106V |
probably benign |
Het |
Acnat1 |
T |
G |
4: 49,447,588 (GRCm39) |
K313T |
probably damaging |
Het |
Acot8 |
T |
C |
2: 164,641,733 (GRCm39) |
Q133R |
probably damaging |
Het |
Acox3 |
A |
T |
5: 35,745,566 (GRCm39) |
K18M |
probably damaging |
Het |
Acoxl |
A |
C |
2: 127,714,115 (GRCm39) |
D137A |
probably damaging |
Het |
Acsm5 |
A |
T |
7: 119,136,434 (GRCm39) |
K335M |
probably damaging |
Het |
Actn4 |
A |
C |
7: 28,594,003 (GRCm39) |
F855V |
probably damaging |
Het |
Acvr2a |
T |
C |
2: 48,760,385 (GRCm39) |
V47A |
probably benign |
Het |
Ada |
C |
G |
2: 163,570,036 (GRCm39) |
|
probably null |
Het |
Adam21 |
G |
A |
12: 81,607,460 (GRCm39) |
H101Y |
probably damaging |
Het |
Adam26a |
T |
A |
8: 44,022,735 (GRCm39) |
N252Y |
probably damaging |
Het |
Adam26b |
T |
C |
8: 43,973,634 (GRCm39) |
E456G |
probably damaging |
Het |
Adam3 |
C |
A |
8: 25,171,447 (GRCm39) |
|
probably benign |
Het |
Adamts14 |
A |
G |
10: 61,054,224 (GRCm39) |
F603L |
probably damaging |
Het |
Adamts18 |
T |
C |
8: 114,502,072 (GRCm39) |
K263R |
possibly damaging |
Het |
Adamts3 |
G |
A |
5: 89,832,308 (GRCm39) |
R932C |
probably damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,189,533 (GRCm39) |
S586P |
probably damaging |
Het |
Adamtsl3 |
T |
G |
7: 82,148,922 (GRCm39) |
F319V |
probably damaging |
Het |
Adcy1 |
G |
C |
11: 7,100,019 (GRCm39) |
A710P |
probably benign |
Het |
Adcy4 |
G |
A |
14: 56,018,413 (GRCm39) |
A178V |
probably benign |
Het |
Add1 |
T |
A |
5: 34,770,744 (GRCm39) |
L285* |
probably null |
Het |
Add2 |
G |
C |
6: 86,062,947 (GRCm39) |
R35P |
probably damaging |
Het |
Adgrb3 |
C |
T |
1: 25,170,352 (GRCm39) |
R982H |
probably damaging |
Het |
Adgrf3 |
T |
G |
5: 30,404,118 (GRCm39) |
K378T |
possibly damaging |
Het |
Adgrl3 |
A |
T |
5: 81,660,005 (GRCm39) |
D258V |
probably damaging |
Het |
Adgrl3 |
C |
A |
5: 81,477,729 (GRCm39) |
H61N |
probably benign |
Het |
Adgrl4 |
C |
A |
3: 151,205,812 (GRCm39) |
P175T |
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,624,791 (GRCm39) |
P3726L |
probably damaging |
Het |
Adra1a |
T |
G |
14: 66,964,945 (GRCm39) |
F312V |
probably damaging |
Het |
Adrm1b |
A |
G |
3: 92,336,397 (GRCm39) |
S102P |
probably damaging |
Het |
Aebp1 |
C |
T |
11: 5,821,460 (GRCm39) |
R620* |
probably null |
Het |
Afdn |
G |
A |
17: 14,104,042 (GRCm39) |
S1126N |
probably damaging |
Het |
Afg3l1 |
A |
C |
8: 124,214,981 (GRCm39) |
E216D |
possibly damaging |
Het |
Afp |
G |
C |
5: 90,652,874 (GRCm39) |
G448A |
possibly damaging |
Het |
Agap2 |
G |
T |
10: 126,924,111 (GRCm39) |
S775I |
unknown |
Het |
Agbl1 |
T |
G |
7: 76,069,652 (GRCm39) |
F143V |
probably benign |
Het |
Ahnak |
A |
T |
19: 8,993,446 (GRCm39) |
N4910I |
probably damaging |
Het |
Ak1 |
A |
T |
2: 32,520,283 (GRCm39) |
K27M |
probably damaging |
Het |
Aldh1b1 |
C |
T |
4: 45,802,540 (GRCm39) |
A26V |
probably benign |
Het |
Aldh1b1 |
G |
C |
4: 45,802,539 (GRCm39) |
A26P |
probably benign |
Het |
Alk |
C |
G |
17: 72,512,802 (GRCm39) |
G386R |
probably damaging |
Het |
Amn |
C |
T |
12: 111,242,117 (GRCm39) |
A368V |
probably benign |
Het |
Amotl2 |
TCC |
TC |
9: 102,600,897 (GRCm39) |
|
probably null |
Het |
Ampd3 |
T |
G |
7: 110,377,032 (GRCm39) |
L8V |
probably damaging |
Het |
Anapc2 |
G |
T |
2: 25,163,380 (GRCm39) |
G206* |
probably null |
Het |
Angel2 |
G |
A |
1: 190,669,751 (GRCm39) |
D144N |
probably damaging |
Het |
Angptl3 |
A |
G |
4: 98,922,757 (GRCm39) |
N266S |
probably benign |
Het |
Ank2 |
A |
G |
3: 126,823,158 (GRCm39) |
V397A |
possibly damaging |
Het |
Ankib1 |
C |
A |
5: 3,763,137 (GRCm39) |
E531* |
probably null |
Het |
Ankib1 |
T |
A |
5: 3,763,136 (GRCm39) |
E531V |
probably damaging |
Het |
Ankrd16 |
CCTCCGGTACTT |
C |
2: 11,784,629 (GRCm39) |
|
probably null |
Het |
Ankrd24 |
G |
A |
10: 81,474,490 (GRCm39) |
G74D |
probably damaging |
Het |
Ankrd44 |
A |
C |
1: 54,698,141 (GRCm39) |
L606R |
probably damaging |
Het |
Ankrd50 |
T |
G |
3: 38,511,314 (GRCm39) |
K351T |
probably damaging |
Het |
Anks4b |
G |
A |
7: 119,781,742 (GRCm39) |
D258N |
probably benign |
Het |
Anln |
T |
C |
9: 22,274,097 (GRCm39) |
E580G |
probably benign |
Het |
Ano3 |
G |
A |
2: 110,576,192 (GRCm39) |
L454F |
probably damaging |
Het |
Antxrl |
A |
T |
14: 33,789,928 (GRCm39) |
N340I |
probably damaging |
Het |
Anxa10 |
C |
T |
8: 62,545,540 (GRCm39) |
G64D |
probably damaging |
Het |
Aox1 |
G |
A |
1: 58,120,701 (GRCm39) |
V865M |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,555,071 (GRCm39) |
Y418C |
possibly damaging |
Het |
Ap5b1 |
A |
C |
19: 5,620,452 (GRCm39) |
K624T |
possibly damaging |
Het |
Apbb1 |
C |
T |
7: 105,208,343 (GRCm39) |
C654Y |
probably damaging |
Het |
Apbb2 |
T |
G |
5: 66,460,039 (GRCm39) |
K710T |
probably damaging |
Het |
Apc |
C |
T |
18: 34,446,220 (GRCm39) |
Q1021* |
probably null |
Het |
Apcdd1 |
T |
G |
18: 63,070,254 (GRCm39) |
F174V |
probably benign |
Het |
Apob |
A |
G |
12: 8,062,936 (GRCm39) |
N193S |
possibly damaging |
Het |
Apob |
C |
A |
12: 8,055,074 (GRCm39) |
L1358I |
possibly damaging |
Het |
Apob |
A |
T |
12: 8,055,945 (GRCm39) |
K1476* |
probably null |
Het |
Apobr |
G |
A |
7: 126,184,203 (GRCm39) |
R7H |
probably benign |
Het |
Apol11b |
A |
C |
15: 77,522,207 (GRCm39) |
I30R |
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,735,515 (GRCm39) |
T1727S |
possibly damaging |
Het |
Arfip2 |
G |
C |
7: 105,286,449 (GRCm39) |
L188V |
probably damaging |
Het |
Arhgap11a |
A |
G |
2: 113,673,239 (GRCm39) |
C115R |
probably damaging |
Het |
Arhgap18 |
A |
T |
10: 26,726,000 (GRCm39) |
|
probably null |
Het |
Arhgap26 |
G |
C |
18: 39,490,724 (GRCm39) |
|
probably benign |
Het |
Arhgap28 |
G |
A |
17: 68,168,272 (GRCm39) |
A465V |
possibly damaging |
Het |
Arhgdib |
C |
A |
6: 136,910,616 (GRCm39) |
K48N |
probably damaging |
Het |
Arhgef10 |
C |
G |
8: 15,014,191 (GRCm39) |
A364G |
probably benign |
Het |
Arhgef10l |
G |
C |
4: 140,309,046 (GRCm39) |
L17V |
possibly damaging |
Het |
Arhgef18 |
C |
T |
8: 3,489,628 (GRCm39) |
S320F |
probably damaging |
Het |
Arhgef28 |
G |
A |
13: 98,082,199 (GRCm39) |
R1203W |
probably damaging |
Het |
Arl5b |
G |
A |
2: 15,079,832 (GRCm39) |
M134I |
probably benign |
Het |
Armc1 |
C |
A |
3: 19,203,671 (GRCm39) |
S85I |
probably damaging |
Het |
Armc12 |
A |
G |
17: 28,751,033 (GRCm39) |
E83G |
probably benign |
Het |
Armh1 |
C |
T |
4: 117,070,992 (GRCm39) |
D378N |
probably benign |
Het |
Armh3 |
T |
C |
19: 45,807,344 (GRCm39) |
E684G |
probably damaging |
Het |
Arsj |
G |
T |
3: 126,232,781 (GRCm39) |
R509M |
possibly damaging |
Het |
Arvcf |
G |
A |
16: 18,221,391 (GRCm39) |
R602H |
probably damaging |
Het |
Asb14 |
A |
G |
14: 26,625,305 (GRCm39) |
K220R |
probably benign |
Het |
Ascc2 |
C |
G |
11: 4,596,656 (GRCm39) |
A59G |
probably benign |
Het |
Asf1b |
G |
C |
8: 84,695,781 (GRCm39) |
A141P |
possibly damaging |
Het |
Ash1l |
C |
A |
3: 88,890,016 (GRCm39) |
L632I |
probably benign |
Het |
Asph |
T |
A |
4: 9,630,715 (GRCm39) |
N211I |
possibly damaging |
Het |
Astn1 |
G |
A |
1: 158,424,776 (GRCm39) |
R646H |
possibly damaging |
Het |
Astn1 |
C |
A |
1: 158,511,666 (GRCm39) |
Y1169* |
probably null |
Het |
Astn1 |
C |
A |
1: 158,300,067 (GRCm39) |
P136T |
possibly damaging |
Het |
Asxl3 |
A |
C |
18: 22,649,829 (GRCm39) |
K606T |
probably benign |
Het |
Atf7 |
C |
G |
15: 102,455,617 (GRCm39) |
G249A |
probably benign |
Het |
Atg14 |
C |
G |
14: 47,805,749 (GRCm39) |
A39P |
probably damaging |
Het |
Atg7 |
T |
A |
6: 114,672,647 (GRCm39) |
F205I |
probably benign |
Het |
Atm |
T |
G |
9: 53,442,987 (GRCm39) |
K92T |
probably damaging |
Het |
Atp11b |
G |
T |
3: 35,866,362 (GRCm39) |
G387V |
probably damaging |
Het |
Atp12a |
G |
A |
14: 56,623,598 (GRCm39) |
V879I |
probably benign |
Het |
Atp13a5 |
T |
G |
16: 29,100,880 (GRCm39) |
K681N |
probably benign |
Het |
Atp2b2 |
A |
C |
6: 113,819,267 (GRCm39) |
F9V |
probably damaging |
Het |
Atp6v1h |
A |
C |
1: 5,168,271 (GRCm39) |
K147T |
probably damaging |
Het |
Atp8a2 |
T |
G |
14: 60,265,419 (GRCm39) |
S306R |
probably benign |
Het |
Atp8b2 |
T |
C |
3: 89,861,875 (GRCm39) |
K226R |
probably damaging |
Het |
Atr |
A |
G |
9: 95,767,373 (GRCm39) |
|
probably null |
Het |
Atrn |
G |
A |
2: 130,815,319 (GRCm39) |
S745N |
probably benign |
Het |
Auts2 |
T |
G |
5: 131,505,392 (GRCm39) |
|
probably benign |
Het |
Avpr1a |
G |
C |
10: 122,285,482 (GRCm39) |
S258T |
probably benign |
Het |
AW551984 |
C |
A |
9: 39,501,899 (GRCm39) |
E736* |
probably null |
Het |
B3galt6 |
C |
A |
4: 156,076,391 (GRCm39) |
R228L |
probably benign |
Het |
B3gnt3 |
G |
A |
8: 72,146,409 (GRCm39) |
S40F |
possibly damaging |
Het |
B3gnt8 |
C |
T |
7: 25,327,575 (GRCm39) |
R2C |
probably damaging |
Het |
Barx2 |
G |
A |
9: 31,758,162 (GRCm39) |
P259S |
possibly damaging |
Het |
Baz2b |
T |
A |
2: 59,790,359 (GRCm39) |
E618V |
probably damaging |
Het |
BC016579 |
C |
T |
16: 45,474,311 (GRCm39) |
D32N |
probably benign |
Het |
BC051665 |
T |
G |
13: 60,932,457 (GRCm39) |
E76A |
probably benign |
Het |
Bcl9 |
G |
T |
3: 97,117,957 (GRCm39) |
Q246K |
possibly damaging |
Het |
Best3 |
C |
T |
10: 116,860,075 (GRCm39) |
S445L |
probably benign |
Het |
Bfar |
C |
T |
16: 13,515,324 (GRCm39) |
P304L |
probably damaging |
Het |
Birc6 |
A |
C |
17: 74,918,537 (GRCm39) |
E1932D |
probably damaging |
Het |
Bltp1 |
A |
C |
3: 37,041,716 (GRCm39) |
E2698A |
probably damaging |
Het |
Bod1l |
C |
T |
5: 41,978,489 (GRCm39) |
E942K |
probably damaging |
Het |
Bod1l |
C |
G |
5: 41,966,107 (GRCm39) |
V2653L |
possibly damaging |
Het |
Bptf |
A |
C |
11: 106,965,408 (GRCm39) |
V1147G |
probably benign |
Het |
Braf |
A |
G |
6: 39,638,960 (GRCm39) |
C264R |
probably damaging |
Het |
Brca2 |
A |
T |
5: 150,466,228 (GRCm39) |
K1997N |
probably damaging |
Het |
Brf2 |
T |
G |
8: 27,614,019 (GRCm39) |
E389A |
probably damaging |
Het |
Brinp2 |
G |
A |
1: 158,074,559 (GRCm39) |
R521* |
probably null |
Het |
Brsk1 |
C |
T |
7: 4,710,371 (GRCm39) |
T460M |
possibly damaging |
Het |
Brwd3 |
A |
T |
X: 107,818,466 (GRCm39) |
V732E |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,964,018 (GRCm39) |
V863D |
probably damaging |
Het |
C1rl |
C |
A |
6: 124,485,701 (GRCm39) |
D357E |
probably benign |
Het |
Cacna1b |
T |
A |
2: 24,551,856 (GRCm39) |
K1096M |
probably damaging |
Het |
Cacna1b |
T |
A |
2: 24,623,957 (GRCm39) |
S208C |
probably damaging |
Het |
Cacna1f |
C |
G |
X: 7,476,490 (GRCm39) |
L144V |
probably damaging |
Het |
Cacna2d1 |
A |
C |
5: 16,399,761 (GRCm39) |
E121D |
probably benign |
Het |
Cacna2d3 |
G |
T |
14: 28,786,265 (GRCm39) |
A574D |
probably damaging |
Het |
Cadps |
C |
A |
14: 12,467,113 (GRCm38) |
D935Y |
probably damaging |
Het |
Camk2a |
T |
G |
18: 61,076,222 (GRCm39) |
|
probably benign |
Het |
Capn15 |
C |
T |
17: 26,182,321 (GRCm39) |
E530K |
probably damaging |
Het |
Carmil1 |
G |
A |
13: 24,228,165 (GRCm39) |
Q600* |
probably null |
Het |
Carmil3 |
C |
T |
14: 55,739,025 (GRCm39) |
T893M |
probably damaging |
Het |
Casp12 |
C |
T |
9: 5,354,582 (GRCm39) |
A317V |
possibly damaging |
Het |
Casp9 |
T |
G |
4: 141,532,772 (GRCm39) |
L223V |
probably benign |
Het |
Casz1 |
T |
C |
4: 149,028,816 (GRCm39) |
L1087P |
probably benign |
Het |
Catsper3 |
T |
G |
13: 55,955,917 (GRCm39) |
F328V |
probably damaging |
Het |
Cavin1 |
T |
C |
11: 100,849,484 (GRCm39) |
D382G |
probably damaging |
Het |
Ccdc116 |
C |
A |
16: 16,965,035 (GRCm39) |
|
probably benign |
Het |
Ccdc14 |
G |
A |
16: 34,511,174 (GRCm39) |
M1I |
probably null |
Het |
Ccdc141 |
T |
G |
2: 76,958,616 (GRCm39) |
E161D |
probably benign |
Het |
Ccdc175 |
G |
T |
12: 72,175,153 (GRCm39) |
H507N |
probably benign |
Het |
Ccdc24 |
C |
T |
4: 117,728,260 (GRCm39) |
|
probably null |
Het |
Ccdc83 |
T |
C |
7: 89,893,254 (GRCm39) |
K168E |
probably damaging |
Het |
Ccdc87 |
A |
G |
19: 4,890,750 (GRCm39) |
K414R |
probably benign |
Het |
Ccr1l1 |
T |
G |
9: 123,777,887 (GRCm39) |
I187L |
probably benign |
Het |
Cd209a |
G |
T |
8: 3,797,017 (GRCm39) |
S80Y |
probably damaging |
Het |
Cd2ap |
G |
A |
17: 43,118,884 (GRCm39) |
T518I |
probably benign |
Het |
Cd300lb |
A |
C |
11: 114,816,860 (GRCm39) |
L61V |
probably damaging |
Het |
Cd36 |
T |
A |
5: 18,000,573 (GRCm39) |
|
probably null |
Het |
Cd40 |
A |
T |
2: 164,904,960 (GRCm39) |
K92M |
probably damaging |
Het |
Cd48 |
A |
T |
1: 171,523,295 (GRCm39) |
D46V |
possibly damaging |
Het |
Cd55 |
T |
G |
1: 130,380,216 (GRCm39) |
D254A |
probably benign |
Het |
Cd59b |
G |
C |
2: 103,911,348 (GRCm39) |
S23T |
possibly damaging |
Het |
Cd8a |
T |
C |
6: 71,350,670 (GRCm39) |
L45P |
possibly damaging |
Het |
Cd93 |
T |
A |
2: 148,284,284 (GRCm39) |
D354V |
probably benign |
Het |
Cd99l2 |
G |
T |
X: 70,484,694 (GRCm39) |
P63Q |
probably damaging |
Het |
Cd99l2 |
C |
T |
X: 70,484,752 (GRCm39) |
|
probably null |
Het |
Cdan1 |
T |
C |
2: 120,560,817 (GRCm39) |
S251G |
probably damaging |
Het |
Cdca2 |
G |
C |
14: 67,937,747 (GRCm39) |
T302S |
probably benign |
Het |
Cdca7l |
A |
G |
12: 117,836,146 (GRCm39) |
M206V |
possibly damaging |
Het |
Cdcp3 |
T |
C |
7: 130,848,362 (GRCm39) |
C839R |
probably damaging |
Het |
Cdh20 |
C |
G |
1: 110,012,853 (GRCm39) |
I395M |
probably benign |
Het |
Cdh22 |
T |
C |
2: 164,954,350 (GRCm39) |
S724G |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,249,423 (GRCm39) |
T832A |
probably benign |
Het |
Cdh8 |
G |
T |
8: 100,006,134 (GRCm39) |
S151Y |
probably damaging |
Het |
Cdk11b |
G |
T |
4: 155,726,021 (GRCm39) |
|
probably benign |
Het |
Cdkal1 |
G |
C |
13: 29,961,219 (GRCm39) |
H117D |
probably damaging |
Het |
Cdr1 |
T |
G |
X: 60,227,710 (GRCm39) |
E485D |
possibly damaging |
Het |
Celf4 |
G |
C |
18: 25,629,306 (GRCm39) |
P406A |
probably benign |
Het |
Celf5 |
C |
T |
10: 81,302,783 (GRCm39) |
A301T |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,321,433 (GRCm39) |
S460C |
probably damaging |
Het |
Cenpf |
A |
C |
1: 189,385,128 (GRCm39) |
L2384R |
probably damaging |
Het |
Cenpp |
T |
C |
13: 49,801,134 (GRCm39) |
|
probably null |
Het |
Ces1a |
T |
G |
8: 93,752,235 (GRCm39) |
K374T |
probably benign |
Het |
Ces1b |
T |
C |
8: 93,791,594 (GRCm39) |
E335G |
probably damaging |
Het |
Ces1d |
T |
C |
8: 93,901,736 (GRCm39) |
K411R |
probably benign |
Het |
Ces1e |
T |
C |
8: 93,937,046 (GRCm39) |
T342A |
probably benign |
Het |
Ces2e |
A |
C |
8: 105,657,979 (GRCm39) |
K359T |
probably benign |
Het |
Ces2e |
A |
G |
8: 105,659,030 (GRCm39) |
|
probably null |
Het |
Cfap44 |
G |
T |
16: 44,221,829 (GRCm39) |
R14I |
probably damaging |
Het |
Cfap46 |
C |
T |
7: 139,214,980 (GRCm39) |
G1582R |
probably damaging |
Het |
Cfap47 |
C |
A |
X: 78,374,419 (GRCm39) |
L2544F |
probably damaging |
Het |
Cfap47 |
A |
T |
X: 78,374,420 (GRCm39) |
L2544* |
probably null |
Het |
Cfap57 |
C |
T |
4: 118,439,079 (GRCm39) |
D816N |
probably benign |
Het |
Cfap61 |
C |
T |
2: 145,971,147 (GRCm39) |
P919L |
probably benign |
Het |
Cfh |
A |
G |
1: 140,036,642 (GRCm39) |
L636P |
probably benign |
Het |
Cfh |
G |
A |
1: 140,075,456 (GRCm39) |
P243S |
possibly damaging |
Het |
Cfhr4 |
T |
A |
1: 139,681,999 (GRCm39) |
Q199L |
probably damaging |
Het |
Chd6 |
T |
C |
2: 160,808,408 (GRCm39) |
D1602G |
probably damaging |
Het |
Chi3l1 |
A |
G |
1: 134,117,238 (GRCm39) |
K345R |
probably benign |
Het |
Chrd |
T |
C |
16: 20,560,005 (GRCm39) |
F891L |
probably damaging |
Het |
Cilp |
TGGG |
TGG |
9: 65,187,412 (GRCm39) |
|
probably null |
Het |
Cilp2 |
C |
G |
8: 70,338,060 (GRCm39) |
K190N |
possibly damaging |
Het |
Cit |
A |
T |
5: 116,123,592 (GRCm39) |
S1421C |
possibly damaging |
Het |
Clca3a1 |
T |
G |
3: 144,452,714 (GRCm39) |
S590R |
probably damaging |
Het |
Clcn1 |
C |
A |
6: 42,277,294 (GRCm39) |
L462I |
probably benign |
Het |
Clcn1 |
A |
C |
6: 42,284,190 (GRCm39) |
K514T |
probably damaging |
Het |
Cldn4 |
G |
A |
5: 134,975,452 (GRCm39) |
L50F |
probably damaging |
Het |
Clec4g |
T |
G |
8: 3,766,548 (GRCm39) |
N251T |
probably damaging |
Het |
Clec4g |
A |
C |
8: 3,757,796 (GRCm39) |
|
probably benign |
Het |
Clu |
A |
C |
14: 66,214,362 (GRCm39) |
E278D |
probably benign |
Het |
Cmya5 |
C |
G |
13: 93,200,087 (GRCm39) |
A3414P |
probably benign |
Het |
CN725425 |
T |
G |
15: 91,129,965 (GRCm39) |
F276C |
possibly damaging |
Het |
Cnksr2 |
T |
G |
X: 156,636,216 (GRCm39) |
N854T |
probably benign |
Het |
Cnot7 |
ATTTATTTTTTA |
ATTTA |
8: 40,953,780 (GRCm39) |
|
probably benign |
Het |
Cnst |
G |
C |
1: 179,407,130 (GRCm39) |
G59A |
probably damaging |
Het |
Cntn3 |
A |
G |
6: 102,397,255 (GRCm39) |
L106P |
possibly damaging |
Het |
Cntnap4 |
C |
G |
8: 113,542,152 (GRCm39) |
P762A |
probably damaging |
Het |
Cntnap5a |
G |
A |
1: 115,987,981 (GRCm39) |
A171T |
probably benign |
Het |
Col17a1 |
A |
G |
19: 47,640,617 (GRCm39) |
S994P |
possibly damaging |
Het |
Col19a1 |
A |
C |
1: 24,319,021 (GRCm39) |
I1023S |
probably damaging |
Het |
Col4a1 |
T |
G |
8: 11,296,859 (GRCm39) |
|
probably benign |
Het |
Col4a4 |
A |
C |
1: 82,430,917 (GRCm39) |
L1662V |
unknown |
Het |
Col6a1 |
C |
G |
10: 76,545,393 (GRCm39) |
*1026Y |
probably null |
Het |
Col6a5 |
A |
C |
9: 105,803,266 (GRCm39) |
I1233S |
unknown |
Het |
Col7a1 |
C |
T |
9: 108,807,568 (GRCm39) |
|
silent |
Het |
Colec12 |
A |
G |
18: 9,848,727 (GRCm39) |
T302A |
probably benign |
Het |
Commd4 |
T |
C |
9: 57,063,540 (GRCm39) |
S73G |
probably benign |
Het |
Coro1c |
A |
G |
5: 113,988,710 (GRCm39) |
|
probably null |
Het |
Cpd |
C |
A |
11: 76,692,572 (GRCm39) |
C755F |
probably damaging |
Het |
Cpsf6 |
T |
C |
10: 117,191,946 (GRCm39) |
D518G |
unknown |
Het |
Creb3l4 |
C |
T |
3: 90,145,058 (GRCm39) |
V365M |
possibly damaging |
Het |
Crhr2 |
A |
G |
6: 55,080,201 (GRCm39) |
V126A |
possibly damaging |
Het |
Crim1 |
G |
T |
17: 78,675,264 (GRCm39) |
K824N |
probably benign |
Het |
Crispld1 |
A |
G |
1: 17,834,300 (GRCm39) |
T489A |
probably benign |
Het |
Crybg1 |
C |
T |
10: 43,873,307 (GRCm39) |
R1267H |
probably benign |
Het |
Cryzl2 |
G |
T |
1: 157,293,359 (GRCm39) |
L153F |
probably benign |
Het |
Csgalnact1 |
T |
C |
8: 68,853,982 (GRCm39) |
K273R |
probably damaging |
Het |
Csmd1 |
T |
G |
8: 16,239,992 (GRCm39) |
K1140T |
possibly damaging |
Het |
Csmd1 |
G |
T |
8: 16,250,072 (GRCm39) |
Q969K |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,396,631 (GRCm39) |
D433G |
probably damaging |
Het |
Csmd1 |
C |
T |
8: 16,142,272 (GRCm39) |
D1544N |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 15,971,875 (GRCm39) |
T2985N |
possibly damaging |
Het |
Csmd3 |
G |
A |
15: 47,499,789 (GRCm39) |
L3027F |
probably damaging |
Het |
Csmd3 |
G |
A |
15: 47,710,677 (GRCm39) |
P1637S |
probably damaging |
Het |
Csn2 |
T |
G |
5: 87,843,868 (GRCm39) |
|
probably benign |
Het |
Cspg4 |
C |
A |
9: 56,793,320 (GRCm39) |
L352M |
probably damaging |
Het |
Cspp1 |
C |
G |
1: 10,153,771 (GRCm39) |
D393E |
possibly damaging |
Het |
Ctcfl |
G |
A |
2: 172,960,137 (GRCm39) |
H149Y |
probably benign |
Het |
Ctnna3 |
C |
T |
10: 63,417,757 (GRCm39) |
S165F |
probably benign |
Het |
Ctnnd2 |
A |
C |
15: 30,966,959 (GRCm39) |
N970T |
probably benign |
Het |
Ctr9 |
T |
C |
7: 110,629,431 (GRCm39) |
L19P |
probably damaging |
Het |
Ctsd |
C |
T |
7: 141,930,334 (GRCm39) |
G403S |
probably damaging |
Het |
Cubn |
G |
A |
2: 13,299,040 (GRCm39) |
S3211L |
probably benign |
Het |
Cul3 |
A |
G |
1: 80,267,808 (GRCm39) |
V177A |
probably benign |
Het |
Cxcl16 |
C |
T |
11: 70,346,804 (GRCm39) |
G113E |
probably damaging |
Het |
Cyfip1 |
A |
C |
7: 55,524,800 (GRCm39) |
K144T |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,734,845 (GRCm39) |
K422R |
possibly damaging |
Het |
Cyp2a5 |
G |
T |
7: 26,540,532 (GRCm39) |
D69Y |
probably damaging |
Het |
Cyp2c50 |
C |
T |
19: 40,086,399 (GRCm39) |
A321V |
possibly damaging |
Homo |
Cyp2c68 |
C |
T |
19: 39,727,907 (GRCm39) |
A82T |
probably damaging |
Het |
Cyp2d11 |
C |
A |
15: 82,274,312 (GRCm39) |
M356I |
probably damaging |
Het |
Cyp2r1 |
C |
T |
7: 114,151,209 (GRCm39) |
R370K |
probably damaging |
Het |
Cyp2t4 |
G |
C |
7: 26,857,171 (GRCm39) |
G345R |
probably damaging |
Het |
Cyp3a59 |
A |
C |
5: 146,035,032 (GRCm39) |
N237H |
probably benign |
Het |
Cyp4a29 |
T |
G |
4: 115,105,693 (GRCm39) |
F132V |
probably benign |
Het |
Cyp4f15 |
G |
C |
17: 32,911,664 (GRCm39) |
|
probably null |
Het |
Cyp4f40 |
G |
A |
17: 32,892,976 (GRCm39) |
|
probably null |
Het |
D030056L22Rik |
A |
T |
19: 18,694,679 (GRCm39) |
S145C |
possibly damaging |
Het |
D7Ertd443e |
T |
G |
7: 133,896,711 (GRCm39) |
S154R |
probably benign |
Het |
Dab1 |
A |
C |
4: 104,336,429 (GRCm39) |
Q8H |
probably damaging |
Het |
Dag1 |
G |
C |
9: 108,085,867 (GRCm39) |
P425A |
possibly damaging |
Het |
Dapk2 |
T |
C |
9: 66,153,759 (GRCm39) |
F172L |
possibly damaging |
Het |
Daw1 |
A |
T |
1: 83,183,685 (GRCm39) |
K245M |
probably null |
Het |
Dbnl |
A |
T |
11: 5,746,797 (GRCm39) |
K176* |
probably null |
Het |
Dcaf13 |
C |
T |
15: 39,008,642 (GRCm39) |
R415C |
probably damaging |
Het |
Dcaf15 |
A |
C |
8: 84,829,410 (GRCm39) |
W111G |
probably damaging |
Het |
Dcaf8l |
A |
G |
X: 88,449,943 (GRCm39) |
V62A |
probably benign |
Het |
Dclk1 |
G |
T |
3: 55,407,526 (GRCm39) |
G235V |
probably damaging |
Het |
Dclre1c |
G |
T |
2: 3,439,117 (GRCm39) |
E92D |
possibly damaging |
Het |
Dda1 |
C |
G |
8: 71,927,139 (GRCm39) |
A4G |
probably damaging |
Het |
Ddb1 |
C |
A |
19: 10,596,594 (GRCm39) |
L438I |
probably damaging |
Het |
Ddit4l |
G |
C |
3: 137,332,123 (GRCm39) |
G163A |
probably benign |
Het |
Ddn |
T |
C |
15: 98,704,020 (GRCm39) |
E424G |
possibly damaging |
Het |
Ddx19b |
T |
G |
8: 111,742,207 (GRCm39) |
K176T |
probably benign |
Het |
Ddx23 |
A |
G |
15: 98,545,502 (GRCm39) |
V602A |
probably benign |
Het |
Ddx59 |
A |
C |
1: 136,360,189 (GRCm39) |
N401T |
possibly damaging |
Het |
Def8 |
A |
G |
8: 124,183,237 (GRCm39) |
R279G |
probably damaging |
Het |
Defb14 |
G |
T |
8: 19,245,200 (GRCm39) |
G59V |
probably damaging |
Het |
Defb8 |
A |
C |
8: 19,497,557 (GRCm39) |
L18R |
possibly damaging |
Het |
Defb9 |
A |
C |
8: 22,371,883 (GRCm39) |
F43L |
probably benign |
Het |
Dennd1a |
A |
G |
2: 37,690,704 (GRCm39) |
S799P |
probably benign |
Het |
Dennd2d |
C |
T |
3: 106,407,190 (GRCm39) |
R414* |
probably null |
Het |
Dennd4a |
G |
A |
9: 64,779,304 (GRCm39) |
A596T |
probably damaging |
Het |
Dennd5a |
T |
G |
7: 109,493,954 (GRCm39) |
D1250A |
possibly damaging |
Het |
Dennd5a |
T |
C |
7: 109,504,480 (GRCm39) |
K854E |
probably damaging |
Het |
Dera |
T |
G |
6: 137,814,116 (GRCm39) |
I99M |
possibly damaging |
Het |
Desi2 |
A |
G |
1: 178,015,510 (GRCm39) |
N10S |
probably benign |
Het |
Dgkg |
T |
G |
16: 22,288,078 (GRCm39) |
N763T |
probably damaging |
Het |
Dgkg |
A |
T |
16: 22,391,436 (GRCm39) |
S341T |
probably benign |
Het |
Dhh |
T |
C |
15: 98,792,790 (GRCm39) |
N157D |
probably benign |
Het |
Dhtkd1 |
C |
A |
2: 5,916,685 (GRCm39) |
A664S |
possibly damaging |
Het |
Dhx37 |
T |
C |
5: 125,493,655 (GRCm39) |
E968G |
possibly damaging |
Het |
Dhx57 |
A |
C |
17: 80,558,777 (GRCm39) |
L1061V |
probably damaging |
Het |
Dip2a |
T |
C |
10: 76,121,462 (GRCm39) |
K798R |
probably benign |
Het |
Disp3 |
G |
C |
4: 148,356,200 (GRCm39) |
A220G |
possibly damaging |
Het |
Dlg4 |
G |
A |
11: 69,921,956 (GRCm39) |
R66Q |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,208,162 (GRCm39) |
P992S |
probably damaging |
Het |
Dlgap2 |
C |
G |
8: 14,872,472 (GRCm39) |
A651G |
probably benign |
Het |
Dlx5 |
C |
A |
6: 6,879,607 (GRCm39) |
Q153H |
probably damaging |
Het |
Dmd |
A |
G |
X: 83,619,366 (GRCm39) |
T2614A |
probably benign |
Het |
Dmd |
C |
T |
X: 82,922,101 (GRCm39) |
S1457F |
possibly damaging |
Het |
Dmrt2 |
T |
G |
19: 25,656,006 (GRCm39) |
L535R |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,054,032 (GRCm39) |
N2546S |
probably benign |
Het |
Dnaaf3 |
G |
A |
7: 4,526,794 (GRCm39) |
R428W |
probably damaging |
Het |
Dnah1 |
T |
G |
14: 31,026,768 (GRCm39) |
K752T |
probably benign |
Het |
Dnah11 |
C |
A |
12: 117,946,704 (GRCm39) |
A3127S |
probably damaging |
Het |
Dnah11 |
G |
C |
12: 117,858,747 (GRCm39) |
T4121R |
probably damaging |
Het |
Dnah2 |
A |
C |
11: 69,321,619 (GRCm39) |
L3847R |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,685,520 (GRCm39) |
D164V |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,610,096 (GRCm39) |
K1769R |
probably null |
Het |
Dnah5 |
G |
A |
15: 28,366,503 (GRCm39) |
G2739S |
probably null |
Het |
Dnah5 |
A |
C |
15: 28,384,376 (GRCm39) |
D3040A |
probably damaging |
Het |
Dnah7a |
A |
C |
1: 53,507,802 (GRCm39) |
Y3090D |
probably damaging |
Het |
Dnajb12 |
C |
A |
10: 59,725,876 (GRCm39) |
P54T |
probably benign |
Het |
Dnajb8 |
G |
A |
6: 88,199,827 (GRCm39) |
G121D |
probably benign |
Het |
Dnajc6 |
G |
A |
4: 101,496,526 (GRCm39) |
V830M |
probably damaging |
Het |
Dnhd1 |
C |
G |
7: 105,361,934 (GRCm39) |
T3664S |
probably benign |
Het |
Dnmbp |
G |
A |
19: 43,863,423 (GRCm39) |
A453V |
probably benign |
Het |
Dnmbp |
G |
A |
19: 43,890,561 (GRCm39) |
P402L |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,406,276 (GRCm39) |
Y760C |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,510,064 (GRCm39) |
K1588R |
probably damaging |
Het |
Dock11 |
A |
G |
X: 35,266,186 (GRCm39) |
K718R |
probably benign |
Het |
Dock2 |
C |
A |
11: 34,586,039 (GRCm39) |
E548* |
probably null |
Het |
Dock2 |
A |
C |
11: 34,583,209 (GRCm39) |
L568R |
probably damaging |
Het |
Dock2 |
G |
A |
11: 34,388,300 (GRCm39) |
T211M |
probably benign |
Het |
Dock9 |
C |
T |
14: 121,792,687 (GRCm39) |
V1844M |
probably damaging |
Het |
Dop1b |
C |
T |
16: 93,560,214 (GRCm39) |
T720I |
probably benign |
Het |
Dpf2 |
A |
C |
19: 5,952,472 (GRCm39) |
F289V |
probably damaging |
Het |
Dpy19l2 |
C |
T |
9: 24,572,120 (GRCm39) |
|
probably null |
Het |
Dsc2 |
C |
T |
18: 20,179,361 (GRCm39) |
E236K |
probably damaging |
Het |
Dscam |
A |
C |
16: 96,573,761 (GRCm39) |
F734V |
probably benign |
Het |
Dscc1 |
A |
C |
15: 54,943,713 (GRCm39) |
S386A |
possibly damaging |
Het |
Duxf4 |
T |
G |
10: 58,071,733 (GRCm39) |
E160D |
probably damaging |
Het |
Dync1h1 |
GAAA |
GAA |
12: 110,596,351 (GRCm39) |
|
probably null |
Het |
Dyrk3 |
A |
G |
1: 131,056,970 (GRCm39) |
L401P |
probably damaging |
Het |
Ecm1 |
T |
C |
3: 95,642,188 (GRCm39) |
I466V |
probably benign |
Het |
Eef2 |
G |
C |
10: 81,017,723 (GRCm39) |
G795A |
probably damaging |
Het |
Efcab3 |
A |
C |
11: 104,642,728 (GRCm39) |
K1117T |
probably damaging |
Het |
Efcab6 |
A |
C |
15: 83,839,210 (GRCm39) |
L383R |
probably damaging |
Het |
Efl1 |
A |
C |
7: 82,342,058 (GRCm39) |
S489R |
probably benign |
Het |
Egfl8 |
C |
A |
17: 34,833,215 (GRCm39) |
G177V |
probably damaging |
Het |
Ehbp1l1 |
G |
C |
19: 5,766,315 (GRCm39) |
P399A |
possibly damaging |
Het |
Ehd2 |
G |
C |
7: 15,697,391 (GRCm39) |
A139G |
possibly damaging |
Het |
Eif1ad3 |
A |
C |
12: 87,843,704 (GRCm39) |
E117A |
possibly damaging |
Het |
Eif3j1 |
T |
G |
2: 121,881,094 (GRCm39) |
F182C |
probably damaging |
Het |
Eif3k |
T |
C |
7: 28,674,024 (GRCm39) |
|
probably null |
Het |
Eif3m |
A |
C |
2: 104,843,601 (GRCm39) |
L127R |
probably damaging |
Het |
Elac1 |
T |
G |
18: 73,872,161 (GRCm39) |
D278A |
probably benign |
Het |
Ell2 |
TCTAGGTGGCC |
TC |
13: 75,909,992 (GRCm39) |
|
probably benign |
Het |
Elmod1 |
A |
C |
9: 53,826,898 (GRCm39) |
S263A |
probably benign |
Het |
Eme2 |
T |
A |
17: 25,113,541 (GRCm39) |
|
probably null |
Het |
Eml1 |
T |
G |
12: 108,503,718 (GRCm39) |
F772V |
possibly damaging |
Het |
Emsy |
G |
A |
7: 98,249,929 (GRCm39) |
P786L |
probably damaging |
Het |
Epb41l3 |
T |
G |
17: 69,560,517 (GRCm39) |
F355V |
probably damaging |
Het |
Epg5 |
C |
G |
18: 78,002,354 (GRCm39) |
A591G |
probably benign |
Het |
Epha4 |
A |
C |
1: 77,483,299 (GRCm39) |
S237A |
possibly damaging |
Het |
Epha5 |
G |
C |
5: 84,385,381 (GRCm39) |
H317D |
probably benign |
Het |
Ephb1 |
C |
T |
9: 101,861,344 (GRCm39) |
V607I |
probably damaging |
Het |
Ephx2 |
A |
G |
14: 66,344,767 (GRCm39) |
F168L |
probably benign |
Het |
Eps15l1 |
T |
G |
8: 73,140,745 (GRCm39) |
N249T |
probably damaging |
Het |
Ercc6l2 |
A |
G |
13: 64,001,542 (GRCm39) |
E567G |
possibly damaging |
Het |
Ermp1 |
G |
C |
19: 29,590,325 (GRCm39) |
S792R |
probably damaging |
Het |
Esp8 |
A |
G |
17: 40,840,936 (GRCm39) |
T66A |
possibly damaging |
Het |
Esr1 |
C |
G |
10: 4,662,667 (GRCm39) |
A95G |
possibly damaging |
Het |
Esrrg |
A |
T |
1: 187,882,415 (GRCm39) |
E224V |
probably benign |
Het |
Etaa1 |
T |
C |
11: 17,896,465 (GRCm39) |
T551A |
possibly damaging |
Het |
Etv5 |
C |
T |
16: 22,202,339 (GRCm39) |
E472K |
probably benign |
Het |
Eva1a |
TGCAGCGACAGCAGCGACAGC |
TGCAGCGACAGCAGCGACAGCAGCGACAGC |
6: 82,068,918 (GRCm39) |
|
probably benign |
Het |
Exoc3l4 |
G |
A |
12: 111,395,921 (GRCm39) |
D645N |
probably benign |
Het |
Eya4 |
T |
C |
10: 22,989,887 (GRCm39) |
Q513R |
probably damaging |
Het |
F11 |
C |
T |
8: 45,698,809 (GRCm39) |
G445D |
possibly damaging |
Het |
F13a1 |
C |
T |
13: 37,172,986 (GRCm39) |
W131* |
probably null |
Het |
F13b |
A |
C |
1: 139,435,940 (GRCm39) |
S249R |
probably benign |
Het |
F5 |
A |
C |
1: 163,981,954 (GRCm39) |
K73T |
probably benign |
Het |
F8 |
C |
T |
X: 74,366,755 (GRCm39) |
|
probably null |
Het |
Fads2b |
T |
G |
2: 85,314,525 (GRCm39) |
K476T |
probably damaging |
Het |
Fads2b |
C |
A |
2: 85,332,421 (GRCm39) |
S201I |
probably benign |
Het |
Fam117a |
C |
G |
11: 95,262,350 (GRCm39) |
H151Q |
possibly damaging |
Het |
Fam186a |
T |
C |
15: 99,843,875 (GRCm39) |
S790G |
unknown |
Het |
Fam193a |
A |
T |
5: 34,578,239 (GRCm39) |
E244D |
probably benign |
Het |
Fancd2 |
C |
G |
6: 113,558,383 (GRCm39) |
H1167D |
probably benign |
Het |
Far2 |
A |
C |
6: 148,040,156 (GRCm39) |
K29T |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,476,844 (GRCm39) |
I1963M |
possibly damaging |
Het |
Fat4 |
C |
G |
3: 39,012,641 (GRCm39) |
A2312G |
probably benign |
Het |
Fat4 |
C |
G |
3: 38,941,199 (GRCm39) |
L31V |
possibly damaging |
Het |
Fbln2 |
G |
A |
6: 91,210,328 (GRCm39) |
D91N |
probably damaging |
Het |
Fbn1 |
C |
T |
2: 125,192,208 (GRCm39) |
D1434N |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,531,309 (GRCm39) |
K71M |
possibly damaging |
Het |
Fbxw21 |
T |
C |
9: 108,974,605 (GRCm39) |
H305R |
probably benign |
Het |
Fem1al |
C |
G |
11: 29,775,007 (GRCm39) |
G150A |
probably damaging |
Het |
Fgd4 |
T |
A |
16: 16,302,334 (GRCm39) |
K74* |
probably null |
Het |
Fgfr2 |
A |
T |
7: 129,771,529 (GRCm39) |
L596H |
probably damaging |
Het |
Fhl1 |
T |
A |
X: 55,824,851 (GRCm39) |
L10Q |
probably null |
Het |
Fig4 |
A |
C |
10: 41,129,727 (GRCm39) |
F498V |
probably damaging |
Het |
Fign |
A |
C |
2: 63,927,246 (GRCm39) |
S6R |
probably benign |
Het |
Filip1l |
G |
C |
16: 57,333,768 (GRCm39) |
S187T |
probably damaging |
Het |
Fitm2 |
C |
T |
2: 163,311,785 (GRCm39) |
E143K |
probably benign |
Het |
Flnb |
A |
C |
14: 7,905,871 (GRCm38) |
K1207T |
probably benign |
Het |
Flnc |
G |
A |
6: 29,457,150 (GRCm39) |
A2351T |
probably damaging |
Het |
Flt1 |
T |
C |
5: 147,618,459 (GRCm39) |
T261A |
possibly damaging |
Het |
Flt3 |
C |
G |
5: 147,286,374 (GRCm39) |
|
probably null |
Het |
Fmn1 |
A |
C |
2: 113,272,270 (GRCm39) |
|
probably benign |
Het |
Fmo9 |
A |
G |
1: 166,501,114 (GRCm39) |
|
probably null |
Het |
Fn1 |
A |
G |
1: 71,688,451 (GRCm39) |
I151T |
probably damaging |
Het |
Fndc1 |
T |
G |
17: 8,001,311 (GRCm39) |
E139A |
probably damaging |
Het |
Fndc3b |
G |
C |
3: 27,519,957 (GRCm39) |
C561W |
possibly damaging |
Het |
Fndc7 |
T |
C |
3: 108,790,816 (GRCm39) |
E70G |
probably damaging |
Het |
Folh1 |
T |
G |
7: 86,375,162 (GRCm39) |
K575T |
probably benign |
Het |
Foxc2 |
G |
C |
8: 121,843,698 (GRCm39) |
W115C |
possibly damaging |
Het |
Foxc2 |
G |
C |
8: 121,843,889 (GRCm39) |
R179P |
probably damaging |
Het |
Foxl1 |
G |
A |
8: 121,855,511 (GRCm39) |
E271K |
possibly damaging |
Het |
Foxred2 |
C |
T |
15: 77,836,203 (GRCm39) |
A385T |
probably damaging |
Het |
Fpr-rs4 |
T |
C |
17: 18,242,181 (GRCm39) |
S63P |
possibly damaging |
Het |
Fpr-rs4 |
G |
A |
17: 18,242,956 (GRCm39) |
R321K |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,906,001 (GRCm39) |
L3135P |
probably benign |
Het |
Fras1 |
A |
C |
5: 96,891,070 (GRCm39) |
Q2866H |
probably damaging |
Het |
Frem1 |
C |
T |
4: 82,890,504 (GRCm39) |
E974K |
probably damaging |
Het |
Frem3 |
A |
C |
8: 81,342,055 (GRCm39) |
Q1449H |
probably benign |
Het |
Frmd6 |
A |
G |
12: 70,927,452 (GRCm39) |
Q144R |
probably benign |
Het |
Frmd7 |
T |
G |
X: 49,985,024 (GRCm39) |
N382T |
possibly damaging |
Het |
Frmpd1 |
C |
T |
4: 45,284,080 (GRCm39) |
P967L |
possibly damaging |
Het |
Frmpd4 |
G |
A |
X: 166,280,836 (GRCm39) |
T348M |
probably damaging |
Het |
Fryl |
A |
C |
5: 73,248,052 (GRCm39) |
L1022V |
probably damaging |
Het |
Fryl |
A |
C |
5: 73,248,081 (GRCm39) |
L1012R |
probably damaging |
Het |
Fsd1 |
T |
A |
17: 56,298,203 (GRCm39) |
L176H |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,817,997 (GRCm39) |
S4577R |
possibly damaging |
Het |
Fsip2 |
G |
C |
2: 82,805,792 (GRCm39) |
E704Q |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,818,978 (GRCm39) |
K4904Q |
possibly damaging |
Het |
Fyb1 |
G |
A |
15: 6,688,021 (GRCm39) |
V794I |
probably benign |
Het |
Fzd10 |
T |
C |
5: 128,678,310 (GRCm39) |
L10P |
probably damaging |
Het |
Fzd7 |
G |
C |
1: 59,523,029 (GRCm39) |
G304A |
probably damaging |
Het |
Gadl1 |
A |
T |
9: 115,766,338 (GRCm39) |
I37L |
probably benign |
Het |
Gal3st1 |
C |
G |
11: 3,947,984 (GRCm39) |
P64A |
probably benign |
Het |
Gal3st2c |
A |
G |
1: 93,935,867 (GRCm39) |
H73R |
probably benign |
Het |
Galnt10 |
G |
A |
11: 57,612,157 (GRCm39) |
G66R |
possibly damaging |
Het |
Garin3 |
G |
A |
11: 46,298,550 (GRCm39) |
R618K |
possibly damaging |
Het |
Gbp2 |
G |
A |
3: 142,335,776 (GRCm39) |
D159N |
probably benign |
Het |
Gbp4 |
A |
T |
5: 105,268,863 (GRCm39) |
F430Y |
probably damaging |
Het |
Gbp9 |
C |
A |
5: 105,241,991 (GRCm39) |
G189W |
probably damaging |
Het |
Gclc |
G |
A |
9: 77,688,649 (GRCm39) |
|
probably null |
Het |
Gcm2 |
C |
A |
13: 41,256,268 (GRCm39) |
G494W |
probably damaging |
Het |
Gcnt2 |
C |
A |
13: 41,072,115 (GRCm39) |
P253T |
probably damaging |
Het |
Gdf10 |
C |
T |
14: 33,654,347 (GRCm39) |
R285C |
probably damaging |
Het |
Gdpd4 |
A |
G |
7: 97,615,516 (GRCm39) |
S114G |
probably damaging |
Het |
Gga1 |
C |
A |
15: 78,776,221 (GRCm39) |
D421E |
probably damaging |
Het |
Ggt5 |
T |
G |
10: 75,444,593 (GRCm39) |
F304V |
possibly damaging |
Het |
Gja3 |
A |
C |
14: 57,273,272 (GRCm39) |
L367V |
possibly damaging |
Het |
Gje1 |
A |
C |
10: 14,593,868 (GRCm39) |
F9V |
possibly damaging |
Het |
Glrb |
T |
G |
3: 80,752,541 (GRCm39) |
K407N |
possibly damaging |
Het |
Glyat |
A |
G |
19: 12,625,373 (GRCm39) |
T32A |
probably benign |
Het |
Gm10784 |
T |
G |
13: 50,099,179 (GRCm39) |
|
noncoding transcript |
Het |
Gm1110 |
A |
C |
9: 26,824,606 (GRCm39) |
L145V |
probably benign |
Het |
Gm11559 |
C |
A |
11: 99,755,775 (GRCm39) |
C141* |
probably null |
Het |
Gm13741 |
A |
T |
2: 87,486,765 (GRCm39) |
S167T |
probably damaging |
Het |
Gm13741 |
A |
C |
2: 87,487,221 (GRCm39) |
L15V |
probably benign |
Het |
Gm15127 |
A |
G |
X: 147,478,492 (GRCm39) |
T415A |
probably benign |
Het |
Gm15932 |
G |
C |
14: 55,813,297 (GRCm39) |
|
probably benign |
Het |
Gm1818 |
C |
A |
12: 48,602,907 (GRCm39) |
|
noncoding transcript |
Het |
Gm19965 |
T |
G |
1: 116,732,330 (GRCm39) |
F58V |
probably benign |
Het |
Gm20939 |
T |
C |
17: 95,184,861 (GRCm39) |
F503S |
probably damaging |
Het |
Gm21834 |
T |
G |
17: 58,049,116 (GRCm39) |
E33D |
possibly damaging |
Het |
Gm266 |
C |
G |
12: 111,451,606 (GRCm39) |
G200A |
probably damaging |
Het |
Gm266 |
T |
C |
12: 111,451,771 (GRCm39) |
E145G |
probably damaging |
Het |
Gm4775 |
C |
G |
14: 106,338,399 (GRCm39) |
|
noncoding transcript |
Het |
Gm4884 |
A |
G |
7: 40,692,300 (GRCm39) |
N90D |
possibly damaging |
Het |
Gm5114 |
T |
C |
7: 39,057,871 (GRCm39) |
K583E |
probably damaging |
Het |
Gm5565 |
G |
A |
5: 146,095,479 (GRCm39) |
T172I |
probably benign |
Het |
Gm8267 |
T |
C |
14: 44,962,322 (GRCm39) |
K33E |
probably benign |
Het |
Gm8674 |
T |
C |
13: 50,055,284 (GRCm39) |
|
noncoding transcript |
Het |
Gm8674 |
C |
A |
13: 50,054,830 (GRCm39) |
|
noncoding transcript |
Het |
Gm904 |
A |
C |
13: 50,799,298 (GRCm39) |
K86Q |
probably damaging |
Het |
Gm9637 |
A |
G |
14: 19,401,731 (GRCm38) |
|
noncoding transcript |
Het |
Gm9758 |
C |
G |
5: 14,963,553 (GRCm39) |
V92L |
probably benign |
Het |
Gm9805 |
A |
G |
17: 22,689,871 (GRCm38) |
Y34C |
probably benign |
Het |
Gm9964 |
T |
C |
11: 79,187,234 (GRCm39) |
E71G |
unknown |
Het |
Gnal |
G |
A |
18: 67,324,474 (GRCm39) |
D210N |
probably damaging |
Het |
Gnas |
A |
G |
2: 174,140,166 (GRCm39) |
S112G |
probably benign |
Het |
Gnat3 |
A |
C |
5: 18,220,321 (GRCm39) |
S228R |
probably damaging |
Het |
Golgb1 |
A |
C |
16: 36,740,104 (GRCm39) |
E2814D |
probably damaging |
Het |
Gorab |
C |
A |
1: 163,231,119 (GRCm39) |
E12* |
probably null |
Het |
Gorab |
C |
G |
1: 163,213,892 (GRCm39) |
S346T |
possibly damaging |
Het |
Gpaa1 |
A |
G |
15: 76,216,742 (GRCm39) |
E142G |
possibly damaging |
Het |
Gpatch8 |
T |
A |
11: 102,371,771 (GRCm39) |
K589I |
unknown |
Het |
Gphb5 |
A |
C |
12: 75,462,581 (GRCm39) |
L3V |
unknown |
Het |
Gpr141b |
C |
T |
13: 19,913,379 (GRCm39) |
|
noncoding transcript |
Het |
Gpr26 |
AC |
A |
7: 131,585,823 (GRCm39) |
|
probably null |
Het |
Gpr75 |
T |
G |
11: 30,841,139 (GRCm39) |
L15V |
probably benign |
Het |
Gprasp1 |
G |
T |
X: 134,700,190 (GRCm39) |
A128S |
possibly damaging |
Het |
Gpsm2 |
T |
C |
3: 108,608,076 (GRCm39) |
E234G |
probably damaging |
Het |
Grid1 |
G |
A |
14: 35,174,251 (GRCm39) |
R631H |
probably damaging |
Het |
Grm3 |
A |
C |
5: 9,620,183 (GRCm39) |
F354V |
probably damaging |
Het |
Grpel1 |
C |
T |
5: 36,627,958 (GRCm39) |
R80C |
probably damaging |
Het |
Gsdmd |
T |
G |
15: 75,735,323 (GRCm39) |
D22E |
probably benign |
Het |
Gtf2f2 |
C |
T |
14: 76,135,063 (GRCm39) |
G221S |
probably damaging |
Het |
Guca1a |
T |
C |
17: 47,711,335 (GRCm39) |
I4V |
probably benign |
Het |
Gucy2c |
G |
A |
6: 136,720,979 (GRCm39) |
P406L |
probably benign |
Het |
Gykl1 |
T |
A |
18: 52,827,237 (GRCm39) |
Y148* |
probably null |
Het |
H2-T22 |
G |
A |
17: 36,352,530 (GRCm39) |
R132W |
probably benign |
Het |
Hao2 |
A |
C |
3: 98,782,668 (GRCm39) |
V340G |
probably damaging |
Het |
Hapln1 |
A |
G |
13: 89,749,617 (GRCm39) |
H54R |
probably benign |
Het |
Haus6 |
A |
C |
4: 86,521,111 (GRCm39) |
L176V |
possibly damaging |
Het |
Hc |
T |
G |
2: 34,898,261 (GRCm39) |
T1145P |
possibly damaging |
Het |
Hc |
T |
A |
2: 34,919,482 (GRCm39) |
D668V |
probably benign |
Het |
Hccs |
C |
G |
X: 168,096,608 (GRCm39) |
R199T |
probably damaging |
Het |
Hdac9 |
T |
G |
12: 34,457,788 (GRCm39) |
K255T |
probably damaging |
Het |
Hdlbp |
G |
A |
1: 93,359,076 (GRCm39) |
|
probably benign |
Het |
Heatr5a |
G |
A |
12: 51,938,187 (GRCm39) |
A1497V |
probably damaging |
Het |
Heatr5a |
T |
C |
12: 51,997,859 (GRCm39) |
T347A |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,433,566 (GRCm39) |
|
probably null |
Het |
Heph |
T |
A |
X: 95,509,637 (GRCm39) |
V130D |
probably damaging |
Het |
Hephl1 |
A |
T |
9: 14,965,017 (GRCm39) |
L1126H |
probably damaging |
Het |
Herc2 |
T |
G |
7: 55,865,129 (GRCm39) |
V4202G |
possibly damaging |
Het |
Herc2 |
G |
A |
7: 55,781,040 (GRCm39) |
G1235D |
probably benign |
Het |
Herc2 |
G |
A |
7: 55,737,089 (GRCm39) |
A183T |
probably benign |
Het |
Herc2 |
G |
T |
7: 55,876,337 (GRCm39) |
C4450F |
probably damaging |
Het |
Herc2 |
C |
A |
7: 55,865,180 (GRCm39) |
A4219D |
probably damaging |
Het |
Heyl |
GGAAGAAG |
GGAAG |
4: 123,133,974 (GRCm39) |
|
probably benign |
Het |
Hgf |
C |
T |
5: 16,823,917 (GRCm39) |
R705C |
probably damaging |
Het |
Hip1r |
A |
T |
5: 124,137,195 (GRCm39) |
|
probably null |
Het |
Hipk1 |
T |
C |
3: 103,671,860 (GRCm39) |
E413G |
possibly damaging |
Het |
Hipk3 |
G |
A |
2: 104,264,974 (GRCm39) |
S702F |
probably damaging |
Het |
Hmcn1 |
G |
T |
1: 150,524,688 (GRCm39) |
A3414D |
probably damaging |
Het |
Hmcn2 |
C |
A |
2: 31,349,076 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
G |
T |
2: 31,271,079 (GRCm39) |
E1252D |
probably benign |
Het |
Hmg20b |
C |
G |
10: 81,182,407 (GRCm39) |
A310P |
probably damaging |
Het |
Hnrnpab |
T |
G |
11: 51,492,573 (GRCm39) |
|
probably benign |
Het |
Hoxa6 |
G |
C |
6: 52,183,525 (GRCm39) |
F173L |
possibly damaging |
Het |
Hoxc4 |
A |
T |
15: 102,943,189 (GRCm39) |
D14V |
probably damaging |
Het |
Hpdl |
G |
C |
4: 116,678,030 (GRCm39) |
P144A |
probably damaging |
Het |
Hsd3b6 |
T |
G |
3: 98,713,648 (GRCm39) |
K217T |
probably benign |
Het |
Hsf2 |
A |
T |
10: 57,372,264 (GRCm39) |
K72N |
probably damaging |
Het |
Hsf3 |
G |
T |
X: 95,363,922 (GRCm39) |
S193* |
probably null |
Het |
Hsf3 |
A |
T |
X: 95,363,923 (GRCm39) |
S250T |
possibly damaging |
Het |
Hspa13 |
C |
T |
16: 75,555,073 (GRCm39) |
G338S |
probably benign |
Het |
Hspa4l |
C |
G |
3: 40,721,425 (GRCm39) |
S282* |
probably null |
Het |
Hydin |
AGGG |
AGG |
8: 111,319,423 (GRCm39) |
|
probably null |
Het |
Hydin |
A |
G |
8: 111,026,605 (GRCm39) |
K108E |
probably benign |
Het |
Hydin |
G |
T |
8: 111,312,680 (GRCm39) |
K4140N |
probably benign |
Het |
I830077J02Rik |
C |
A |
3: 105,834,529 (GRCm39) |
A42S |
probably damaging |
Het |
Iars1 |
G |
A |
13: 49,874,564 (GRCm39) |
S746N |
probably benign |
Het |
Ifi203 |
A |
T |
1: 173,756,147 (GRCm39) |
|
probably benign |
Het |
Ifi206 |
T |
G |
1: 173,301,577 (GRCm39) |
E700D |
probably damaging |
Het |
Ifi209 |
A |
C |
1: 173,464,973 (GRCm39) |
K34N |
probably damaging |
Het |
Ifi209 |
A |
G |
1: 173,468,712 (GRCm39) |
K181E |
probably benign |
Het |
Ifi211 |
A |
T |
1: 173,735,226 (GRCm39) |
F68I |
possibly damaging |
Het |
Ifna16 |
C |
A |
4: 88,594,615 (GRCm39) |
S160I |
probably damaging |
Het |
Ift52 |
A |
C |
2: 162,865,278 (GRCm39) |
D43A |
possibly damaging |
Het |
Ift70b |
T |
G |
2: 75,768,326 (GRCm39) |
E142D |
probably benign |
Het |
Ighv13-2 |
G |
T |
12: 114,321,435 (GRCm39) |
Y82* |
probably null |
Het |
Ighv1-37 |
A |
T |
12: 114,860,244 (GRCm39) |
|
probably benign |
Het |
Ighv15-2 |
T |
G |
12: 114,528,424 (GRCm39) |
D43A |
probably damaging |
Het |
Ighv1-69 |
A |
C |
12: 115,586,873 (GRCm39) |
S87A |
probably benign |
Het |
Ighv5-9-1 |
C |
G |
12: 113,699,740 (GRCm39) |
C124S |
probably damaging |
Het |
Ighv7-4 |
A |
C |
12: 114,186,517 (GRCm39) |
V85G |
probably damaging |
Het |
Igkv12-98 |
C |
A |
6: 68,548,015 (GRCm39) |
T48N |
probably benign |
Het |
Igkv18-36 |
C |
A |
6: 69,969,483 (GRCm39) |
V104F |
probably damaging |
Het |
Igkv2-112 |
G |
A |
6: 68,197,631 (GRCm39) |
S101N |
possibly damaging |
Het |
Igkv5-48 |
C |
A |
6: 69,703,675 (GRCm39) |
G77W |
probably damaging |
Het |
Igsf10 |
C |
T |
3: 59,237,359 (GRCm39) |
V941I |
possibly damaging |
Het |
Ik |
C |
T |
18: 36,877,835 (GRCm39) |
R4* |
probably null |
Het |
Il11 |
G |
A |
7: 4,778,998 (GRCm39) |
S44F |
probably damaging |
Het |
Il18r1 |
C |
A |
1: 40,517,646 (GRCm39) |
S136Y |
probably damaging |
Het |
Il18r1 |
A |
C |
1: 40,513,911 (GRCm39) |
K39T |
probably damaging |
Het |
Il3ra |
G |
A |
14: 14,351,129 (GRCm38) |
R217Q |
probably benign |
Het |
Inpp4b |
G |
A |
8: 82,795,560 (GRCm39) |
|
probably null |
Het |
Inpp5f |
C |
G |
7: 128,296,673 (GRCm39) |
T381R |
probably benign |
Het |
Insm2 |
C |
G |
12: 55,646,582 (GRCm39) |
P109A |
probably damaging |
Het |
Ints11 |
G |
A |
4: 155,971,427 (GRCm39) |
D292N |
probably benign |
Het |
Ipo13 |
T |
C |
4: 117,761,877 (GRCm39) |
E441G |
probably benign |
Het |
Iqub |
C |
T |
6: 24,500,242 (GRCm39) |
|
probably null |
Het |
Itga2 |
G |
A |
13: 114,993,868 (GRCm39) |
P762S |
possibly damaging |
Het |
Itga7 |
T |
A |
10: 128,785,032 (GRCm39) |
I787N |
probably benign |
Het |
Itgb1 |
T |
G |
8: 129,439,850 (GRCm39) |
F180V |
probably damaging |
Het |
Itgb6 |
C |
T |
2: 60,450,555 (GRCm39) |
R628Q |
probably null |
Het |
Itk |
A |
C |
11: 46,244,689 (GRCm39) |
|
probably null |
Het |
Itpr3 |
C |
T |
17: 27,332,502 (GRCm39) |
S1782L |
possibly damaging |
Het |
Itsn2 |
A |
C |
12: 4,762,472 (GRCm39) |
S1578R |
probably damaging |
Het |
Izumo3 |
C |
T |
4: 92,035,170 (GRCm39) |
A16T |
probably damaging |
Het |
Jag1 |
C |
A |
2: 136,927,071 (GRCm39) |
W896L |
probably benign |
Het |
Jakmip1 |
A |
T |
5: 37,278,330 (GRCm39) |
I536F |
probably damaging |
Het |
Jmjd1c |
T |
C |
10: 67,073,953 (GRCm39) |
L1896P |
probably benign |
Het |
Jmy |
T |
A |
13: 93,577,589 (GRCm39) |
S860C |
probably damaging |
Het |
Jph2 |
G |
C |
2: 163,239,252 (GRCm39) |
S65R |
possibly damaging |
Het |
Jrk |
T |
C |
15: 74,579,243 (GRCm39) |
K14R |
unknown |
Het |
Kat6a |
C |
T |
8: 23,425,517 (GRCm39) |
R1021* |
probably null |
Het |
Kbtbd11 |
C |
G |
8: 15,077,839 (GRCm39) |
P146R |
probably damaging |
Het |
Kcna3 |
C |
A |
3: 106,944,269 (GRCm39) |
F177L |
probably damaging |
Het |
Kcna7 |
T |
G |
7: 45,056,383 (GRCm39) |
F200V |
probably benign |
Het |
Kcna7 |
A |
T |
7: 45,058,529 (GRCm39) |
K272M |
probably damaging |
Het |
Kcnb1 |
G |
C |
2: 167,029,981 (GRCm39) |
A188G |
probably benign |
Het |
Kcnb2 |
A |
C |
1: 15,780,315 (GRCm39) |
I396L |
probably benign |
Het |
Kcnb2 |
C |
T |
1: 15,781,252 (GRCm39) |
S708L |
probably benign |
Het |
Kcnh5 |
C |
T |
12: 74,944,535 (GRCm39) |
A905T |
probably benign |
Het |
Kcnh5 |
A |
C |
12: 75,012,069 (GRCm39) |
F617V |
possibly damaging |
Het |
Kcnh6 |
T |
G |
11: 105,899,874 (GRCm39) |
F48V |
probably damaging |
Het |
Kcnh7 |
G |
A |
2: 63,014,412 (GRCm39) |
R4C |
probably damaging |
Het |
Kcnh7 |
A |
C |
2: 62,566,447 (GRCm39) |
L828R |
probably damaging |
Het |
Kcnh8 |
A |
G |
17: 53,285,320 (GRCm39) |
S1097G |
probably benign |
Het |
Kcnh8 |
G |
C |
17: 53,032,918 (GRCm39) |
K68N |
probably damaging |
Het |
Kcnj15 |
A |
G |
16: 95,096,978 (GRCm39) |
K200R |
probably damaging |
Het |
Kcnk9 |
T |
A |
15: 72,417,864 (GRCm39) |
T89S |
possibly damaging |
Het |
Kcnn3 |
A |
T |
3: 89,574,437 (GRCm39) |
S650C |
probably damaging |
Het |
Kcnq5 |
G |
A |
1: 21,527,753 (GRCm39) |
P440L |
probably damaging |
Het |
Kcnt2 |
G |
T |
1: 140,501,384 (GRCm39) |
D917Y |
probably damaging |
Het |
Kcnt2 |
G |
A |
1: 140,511,896 (GRCm39) |
W1017* |
probably null |
Het |
Kctd19 |
A |
C |
8: 106,111,967 (GRCm39) |
L826R |
probably benign |
Het |
Kctd2 |
A |
G |
11: 115,312,813 (GRCm39) |
E115G |
possibly damaging |
Het |
Khdrbs2 |
T |
C |
1: 32,283,136 (GRCm39) |
|
probably benign |
Het |
Khsrp |
C |
T |
17: 57,331,249 (GRCm39) |
R443Q |
probably damaging |
Het |
Kif12 |
GGGGC |
GGGGCCTCCACCCGGCGGGC |
4: 63,089,660 (GRCm39) |
|
probably benign |
Het |
Kif18b |
T |
G |
11: 102,798,983 (GRCm39) |
K739N |
probably benign |
Het |
Kif20b |
G |
C |
19: 34,927,851 (GRCm39) |
E1038Q |
probably damaging |
Het |
Kif24 |
C |
A |
4: 41,395,091 (GRCm39) |
S594I |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,435,847 (GRCm39) |
Q1315H |
probably benign |
Het |
Klhl22 |
T |
G |
16: 17,594,407 (GRCm39) |
F179V |
possibly damaging |
Het |
Klhl26 |
T |
G |
8: 70,904,449 (GRCm39) |
E426A |
probably damaging |
Het |
Klhl41 |
A |
C |
2: 69,505,074 (GRCm39) |
K459T |
possibly damaging |
Het |
Klk1b1 |
A |
C |
7: 43,619,825 (GRCm39) |
K128T |
probably benign |
Het |
Klk1b26 |
A |
T |
7: 43,665,420 (GRCm39) |
Q109H |
probably benign |
Het |
Klk1b3 |
G |
A |
7: 43,849,729 (GRCm39) |
W38* |
probably null |
Het |
Klk1b9 |
G |
A |
7: 43,443,735 (GRCm39) |
G83D |
probably damaging |
Het |
Klk6 |
T |
C |
7: 43,477,912 (GRCm39) |
S95P |
probably benign |
Het |
Klra2 |
A |
C |
6: 131,205,253 (GRCm39) |
L196R |
probably damaging |
Het |
Klrh1 |
T |
C |
6: 129,749,426 (GRCm39) |
|
probably null |
Het |
Kmt2b |
G |
T |
7: 30,284,676 (GRCm39) |
Q739K |
probably benign |
Het |
Kprp |
G |
A |
3: 92,732,364 (GRCm39) |
Q229* |
probably null |
Het |
Kptn |
T |
C |
7: 15,856,995 (GRCm39) |
L161P |
probably damaging |
Het |
Kri1 |
C |
A |
9: 21,185,418 (GRCm39) |
E639D |
probably benign |
Het |
Krt32 |
C |
T |
11: 99,979,042 (GRCm39) |
S4N |
probably benign |
Het |
Krt36 |
A |
T |
11: 99,995,015 (GRCm39) |
L186M |
possibly damaging |
Het |
Krt75 |
C |
G |
15: 101,482,100 (GRCm39) |
G56A |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,798,986 (GRCm39) |
L233P |
probably damaging |
Het |
Krt78 |
C |
T |
15: 101,855,766 (GRCm39) |
E682K |
possibly damaging |
Het |
Krtap20-1 |
G |
A |
16: 88,881,053 (GRCm39) |
C28Y |
unknown |
Het |
Ksr1 |
G |
C |
11: 78,935,705 (GRCm39) |
|
probably null |
Het |
Ksr2 |
A |
C |
5: 117,885,467 (GRCm39) |
T764P |
probably damaging |
Het |
Lama1 |
G |
A |
17: 68,059,878 (GRCm39) |
D656N |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,078,077 (GRCm39) |
G1171S |
probably benign |
Het |
Lama1 |
G |
T |
17: 68,117,166 (GRCm39) |
G2487V |
probably damaging |
Het |
Large1 |
C |
T |
8: 73,638,731 (GRCm39) |
W282* |
probably null |
Het |
Lce1e |
A |
G |
3: 92,615,156 (GRCm39) |
C64R |
unknown |
Het |
Lce1f |
T |
C |
3: 92,626,561 (GRCm39) |
K32R |
unknown |
Het |
Lce1i |
C |
A |
3: 92,684,596 (GRCm39) |
|
probably null |
Het |
Lefty2 |
A |
T |
1: 180,725,280 (GRCm39) |
R337W |
probably damaging |
Het |
Lelp1 |
T |
A |
3: 92,042,905 (GRCm39) |
K48M |
unknown |
Het |
Lenep |
C |
G |
3: 89,309,876 (GRCm39) |
G24A |
probably damaging |
Het |
Lgr6 |
C |
T |
1: 134,915,809 (GRCm39) |
G313E |
possibly damaging |
Het |
Lhb |
A |
C |
7: 45,071,154 (GRCm39) |
|
probably null |
Het |
Lipo2 |
T |
C |
19: 33,699,085 (GRCm39) |
Y315C |
probably damaging |
Het |
Lmbr1 |
C |
A |
5: 29,528,814 (GRCm39) |
A110S |
probably damaging |
Het |
Lmtk2 |
A |
G |
5: 144,119,669 (GRCm39) |
S1377G |
probably benign |
Het |
Lpcat2b |
C |
T |
5: 107,581,177 (GRCm39) |
P169S |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,734,151 (GRCm39) |
F12S |
probably damaging |
Het |
Lrfn3 |
A |
C |
7: 30,059,626 (GRCm39) |
F200V |
probably damaging |
Het |
Lrif1 |
G |
A |
3: 106,639,886 (GRCm39) |
D324N |
probably benign |
Het |
Lrp1 |
G |
A |
10: 127,420,248 (GRCm39) |
R912C |
probably damaging |
Het |
Lrp10 |
A |
C |
14: 54,705,379 (GRCm39) |
T190P |
probably benign |
Het |
Lrpprc |
G |
A |
17: 85,039,212 (GRCm39) |
Q923* |
probably null |
Het |
Lrpprc |
C |
T |
17: 85,077,928 (GRCm39) |
|
probably null |
Het |
Lrrc18 |
C |
T |
14: 32,730,467 (GRCm39) |
A2V |
probably damaging |
Het |
Lrrc28 |
T |
G |
7: 67,179,379 (GRCm39) |
K329T |
possibly damaging |
Het |
Lrrc30 |
T |
C |
17: 67,938,690 (GRCm39) |
K297E |
possibly damaging |
Het |
Lrrc32 |
G |
A |
7: 98,148,267 (GRCm39) |
R349K |
probably benign |
Het |
Lrrc45 |
G |
T |
11: 120,611,057 (GRCm39) |
V572F |
probably damaging |
Het |
Lrrc52 |
C |
A |
1: 167,294,063 (GRCm39) |
G74V |
possibly damaging |
Het |
Lrrc63 |
C |
T |
14: 75,363,430 (GRCm39) |
E234K |
possibly damaging |
Het |
Lrrfip1 |
GAAGAACAAGAA |
GAAGAA |
1: 91,043,252 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
T |
A |
10: 103,038,307 (GRCm39) |
N832I |
probably damaging |
Het |
Lrrk2 |
T |
G |
15: 91,610,443 (GRCm39) |
V725G |
probably benign |
Het |
Ltbp4 |
C |
T |
7: 27,007,217 (GRCm39) |
A1364T |
probably damaging |
Het |
Luc7l |
T |
G |
17: 26,486,229 (GRCm39) |
L136R |
probably damaging |
Het |
Luc7l2 |
A |
C |
6: 38,580,304 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
A |
C |
11: 58,277,556 (GRCm39) |
T113P |
possibly damaging |
Het |
Lyst |
A |
T |
13: 13,918,018 (GRCm39) |
Q3359H |
probably benign |
Het |
Lyzl1 |
A |
C |
18: 4,181,156 (GRCm39) |
K114T |
probably damaging |
Het |
Magel2 |
G |
T |
7: 62,028,725 (GRCm39) |
R543L |
possibly damaging |
Het |
Mak16 |
A |
G |
8: 31,656,123 (GRCm39) |
L120P |
probably damaging |
Het |
Man2b2 |
C |
T |
5: 36,972,700 (GRCm39) |
D605N |
possibly damaging |
Het |
Map10 |
CGGG |
CGG |
8: 126,398,670 (GRCm39) |
|
probably null |
Het |
Map1b |
T |
G |
13: 99,644,623 (GRCm39) |
E93D |
probably benign |
Het |
Map1s |
T |
G |
8: 71,369,093 (GRCm39) |
F881V |
possibly damaging |
Het |
Map3k3 |
G |
A |
11: 106,041,179 (GRCm39) |
D383N |
possibly damaging |
Het |
Map3k6 |
C |
G |
4: 132,972,377 (GRCm39) |
H318D |
probably damaging |
Het |
Mapk13 |
A |
G |
17: 28,996,507 (GRCm39) |
E245G |
possibly damaging |
Het |
Mapkapk5 |
C |
T |
5: 121,669,654 (GRCm39) |
E115K |
probably benign |
Het |
Marchf10 |
C |
A |
11: 105,281,185 (GRCm39) |
G367W |
probably damaging |
Het |
Marveld3 |
G |
A |
8: 110,674,695 (GRCm39) |
R374C |
possibly damaging |
Het |
Mast4 |
T |
G |
13: 102,875,027 (GRCm39) |
K1255T |
probably damaging |
Het |
Maz |
GGCCCTG |
GG |
7: 126,623,646 (GRCm39) |
|
probably null |
Het |
Mcf2 |
T |
C |
X: 59,224,073 (GRCm39) |
H65R |
probably benign |
Het |
Mcm6 |
T |
G |
1: 128,272,035 (GRCm39) |
N454T |
probably damaging |
Het |
Mcpt4 |
T |
A |
14: 56,297,967 (GRCm39) |
R195* |
probably null |
Het |
Mdm1 |
A |
C |
10: 117,994,267 (GRCm39) |
K380N |
possibly damaging |
Het |
Mdm4 |
A |
G |
1: 132,922,285 (GRCm39) |
S286P |
probably benign |
Het |
Med13l |
C |
A |
5: 118,887,706 (GRCm39) |
T1660K |
probably damaging |
Het |
Med14 |
A |
C |
X: 12,543,845 (GRCm39) |
L1451R |
probably damaging |
Het |
Megf11 |
A |
T |
9: 64,567,758 (GRCm39) |
S416C |
probably damaging |
Het |
Megf8 |
G |
A |
7: 25,039,094 (GRCm39) |
E902K |
possibly damaging |
Het |
Mep1a |
C |
G |
17: 43,802,487 (GRCm39) |
W192C |
probably damaging |
Het |
Mfap3 |
T |
A |
11: 57,418,968 (GRCm39) |
F43I |
possibly damaging |
Het |
Mfhas1 |
C |
G |
8: 36,057,390 (GRCm39) |
P622A |
probably benign |
Het |
Mgam |
G |
C |
6: 40,619,994 (GRCm39) |
V28L |
probably benign |
Het |
Mgp |
T |
G |
6: 136,851,261 (GRCm39) |
|
probably null |
Het |
Micall2 |
A |
C |
5: 139,702,050 (GRCm39) |
L398V |
probably benign |
Het |
Micall2 |
T |
A |
5: 139,692,649 (GRCm39) |
K908M |
probably damaging |
Het |
Mill2 |
G |
A |
7: 18,590,324 (GRCm39) |
|
probably null |
Het |
Mir1966 |
C |
T |
8: 106,342,203 (GRCm39) |
R130* |
probably null |
Het |
Mkrn1 |
T |
A |
6: 39,377,390 (GRCm39) |
N282Y |
probably null |
Het |
Mkx |
C |
T |
18: 6,936,975 (GRCm39) |
A319T |
probably damaging |
Het |
Mn1 |
T |
A |
5: 111,566,146 (GRCm39) |
F39I |
possibly damaging |
Het |
Morc2b |
A |
T |
17: 33,355,060 (GRCm39) |
I904N |
possibly damaging |
Het |
Mpo |
T |
G |
11: 87,686,071 (GRCm39) |
F74V |
probably benign |
Het |
Mpv17l2 |
T |
G |
8: 71,212,056 (GRCm39) |
K139T |
probably damaging |
Het |
Mrgprb4 |
A |
G |
7: 47,848,430 (GRCm39) |
L166P |
possibly damaging |
Het |
Mrgprg |
C |
G |
7: 143,318,393 (GRCm39) |
A240P |
probably damaging |
Het |
Mrgprx1 |
T |
G |
7: 47,670,877 (GRCm39) |
K290T |
probably damaging |
Het |
Mroh5 |
G |
A |
15: 73,659,880 (GRCm39) |
A320V |
possibly damaging |
Het |
Mrpl1 |
T |
G |
5: 96,409,928 (GRCm39) |
M267R |
probably damaging |
Het |
Mrpl2 |
A |
G |
17: 46,958,404 (GRCm39) |
K62R |
probably null |
Het |
Mrps36 |
T |
G |
13: 100,875,641 (GRCm39) |
S58R |
possibly damaging |
Het |
Msantd3 |
A |
C |
4: 48,552,525 (GRCm39) |
D38A |
probably damaging |
Het |
Mta1 |
C |
T |
12: 113,096,820 (GRCm39) |
P547L |
probably benign |
Het |
Mta3 |
A |
G |
17: 84,070,343 (GRCm39) |
D16G |
probably benign |
Het |
Mtcl1 |
C |
T |
17: 66,650,723 (GRCm39) |
A1132T |
probably benign |
Het |
Mtf2 |
A |
G |
5: 108,235,195 (GRCm39) |
D139G |
probably damaging |
Het |
Mthfd1l |
T |
G |
10: 3,957,844 (GRCm39) |
F294V |
probably benign |
Het |
Mtus2 |
G |
A |
5: 148,240,073 (GRCm39) |
|
probably benign |
Het |
Muc4 |
A |
T |
16: 32,576,450 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
A |
C |
7: 141,365,429 (GRCm39) |
T1984P |
possibly damaging |
Het |
Muc5b |
A |
G |
7: 141,415,951 (GRCm39) |
S2966G |
probably benign |
Het |
Mup3 |
G |
C |
4: 62,005,426 (GRCm39) |
L15V |
unknown |
Het |
Mvd |
G |
C |
8: 123,166,469 (GRCm39) |
A56G |
probably benign |
Het |
Mvk |
G |
T |
5: 114,596,995 (GRCm39) |
G321W |
probably damaging |
Het |
Mxra7 |
G |
T |
11: 116,695,432 (GRCm39) |
N157K |
probably benign |
Het |
Mybpc2 |
T |
C |
7: 44,165,927 (GRCm39) |
K256R |
possibly damaging |
Het |
Mybpc3 |
A |
G |
2: 90,965,704 (GRCm39) |
E1172G |
probably benign |
Het |
Myh11 |
AGG |
AG |
16: 14,087,126 (GRCm39) |
|
probably null |
Het |
Myh2 |
C |
T |
11: 67,082,275 (GRCm39) |
L1326F |
probably damaging |
Het |
Myh2 |
GTATTTATTTA |
GTATTTA |
11: 67,071,589 (GRCm39) |
|
probably benign |
Het |
Myh6 |
C |
T |
14: 55,194,454 (GRCm39) |
R725H |
probably damaging |
Het |
Myh8 |
A |
C |
11: 67,189,418 (GRCm39) |
K1198T |
probably damaging |
Het |
Myh9 |
A |
G |
15: 77,659,458 (GRCm39) |
L96P |
probably damaging |
Het |
Myo18b |
C |
T |
5: 112,905,350 (GRCm39) |
E2083K |
probably benign |
Het |
Myo18b |
G |
A |
5: 112,840,809 (GRCm39) |
S2328L |
possibly damaging |
Het |
Myo1d |
T |
G |
11: 80,565,724 (GRCm39) |
N367T |
probably benign |
Het |
Myo5b |
G |
C |
18: 74,877,820 (GRCm39) |
E1606D |
probably benign |
Het |
Myo5c |
C |
G |
9: 75,152,341 (GRCm39) |
S76R |
probably damaging |
Het |
Myorg |
A |
C |
4: 41,497,557 (GRCm39) |
L691R |
probably benign |
Het |
Myrf |
C |
A |
19: 10,198,662 (GRCm39) |
Q195H |
probably damaging |
Het |
Nacc1 |
G |
C |
8: 85,399,915 (GRCm39) |
A434G |
probably damaging |
Het |
Naip2 |
A |
T |
13: 100,298,417 (GRCm39) |
Y540N |
probably benign |
Het |
Nap1l2 |
T |
G |
X: 102,228,802 (GRCm39) |
N372T |
probably damaging |
Het |
Nat8 |
G |
T |
6: 85,808,175 (GRCm39) |
|
probably benign |
Het |
Nav1 |
T |
C |
1: 135,398,462 (GRCm39) |
T707A |
probably benign |
Het |
Nbea |
G |
A |
3: 55,630,584 (GRCm39) |
T2251I |
probably benign |
Het |
Nbeal2 |
G |
C |
9: 110,461,440 (GRCm39) |
A1536G |
possibly damaging |
Het |
Ncapg |
T |
G |
5: 45,837,222 (GRCm39) |
L431R |
probably damaging |
Het |
Nck2 |
A |
C |
1: 43,593,543 (GRCm39) |
N250T |
possibly damaging |
Het |
Nckap5 |
G |
A |
1: 125,952,569 (GRCm39) |
R1264C |
possibly damaging |
Het |
Nckipsd |
G |
C |
9: 108,691,876 (GRCm39) |
K492N |
probably benign |
Het |
Ncor2 |
T |
A |
5: 125,144,852 (GRCm39) |
S597C |
unknown |
Het |
Ncor2 |
C |
T |
5: 125,163,904 (GRCm39) |
|
probably null |
Het |
Ndn |
T |
G |
7: 61,998,882 (GRCm39) |
F243V |
probably damaging |
Het |
Ndufs6 |
A |
G |
13: 73,476,555 (GRCm39) |
V4A |
probably benign |
Het |
Neb |
C |
T |
2: 52,059,884 (GRCm39) |
V2321I |
possibly damaging |
Het |
Neb |
T |
A |
2: 52,198,579 (GRCm39) |
K423M |
probably damaging |
Het |
Neb |
G |
C |
2: 52,113,164 (GRCm39) |
P7A |
probably benign |
Het |
Nedd4 |
G |
A |
9: 72,577,360 (GRCm39) |
V62M |
probably benign |
Het |
Nek7 |
C |
A |
1: 138,443,363 (GRCm39) |
V197L |
probably null |
Het |
Nelfcd |
GTT |
GT |
2: 174,268,287 (GRCm39) |
|
probably null |
Het |
Nell2 |
A |
T |
15: 95,332,978 (GRCm39) |
L194M |
probably damaging |
Het |
Neurod6 |
G |
A |
6: 55,656,347 (GRCm39) |
Q97* |
probably null |
Het |
Nfkbiz |
T |
C |
16: 55,638,599 (GRCm39) |
Y287C |
probably damaging |
Het |
Nfkbiz |
G |
C |
16: 55,636,801 (GRCm39) |
A500G |
probably damaging |
Het |
Nfrkb |
A |
C |
9: 31,322,629 (GRCm39) |
S900R |
possibly damaging |
Het |
Nhsl3 |
C |
T |
4: 129,116,091 (GRCm39) |
A903T |
probably damaging |
Het |
Nipbl |
T |
A |
15: 8,337,366 (GRCm39) |
E2065D |
probably damaging |
Het |
Nkapl |
C |
G |
13: 21,652,473 (GRCm39) |
G47R |
unknown |
Het |
Nlrc5 |
A |
G |
8: 95,231,092 (GRCm39) |
D1275G |
possibly damaging |
Het |
Nlrp12 |
T |
C |
7: 3,271,211 (GRCm39) |
K1034R |
probably benign |
Het |
Nlrp14 |
T |
G |
7: 106,785,829 (GRCm39) |
L635R |
probably damaging |
Het |
Nlrp3 |
G |
C |
11: 59,442,686 (GRCm39) |
S746T |
possibly damaging |
Het |
Nlrp4a |
T |
C |
7: 26,153,588 (GRCm39) |
V713A |
probably benign |
Het |
Nlrp4c |
A |
C |
7: 6,069,635 (GRCm39) |
K512T |
probably damaging |
Het |
Nlrp4f |
C |
T |
13: 65,342,116 (GRCm39) |
E510K |
probably benign |
Het |
Nlrp4g |
T |
G |
9: 124,349,201 (GRCm38) |
|
noncoding transcript |
Het |
Nlrp5 |
T |
C |
7: 23,117,011 (GRCm39) |
L245P |
probably damaging |
Het |
Nlrp5 |
G |
A |
7: 23,103,592 (GRCm39) |
E20K |
possibly damaging |
Het |
Nlrp9b |
T |
G |
7: 19,757,668 (GRCm39) |
F302V |
probably benign |
Het |
Nme8 |
T |
A |
13: 19,873,127 (GRCm39) |
E172D |
possibly damaging |
Het |
Nnt |
G |
A |
13: 119,474,982 (GRCm39) |
S649L |
probably damaging |
Het |
Nod2 |
G |
C |
8: 89,390,774 (GRCm39) |
Q345H |
probably damaging |
Het |
Nol4 |
C |
T |
18: 23,054,959 (GRCm39) |
S157N |
probably damaging |
Het |
Nolc1 |
G |
T |
19: 46,071,537 (GRCm39) |
|
probably benign |
Het |
Notch1 |
T |
G |
2: 26,367,127 (GRCm39) |
D680A |
probably damaging |
Het |
Notch3 |
C |
G |
17: 32,377,626 (GRCm39) |
G150A |
possibly damaging |
Het |
Notch4 |
C |
T |
17: 34,806,889 (GRCm39) |
P1942L |
probably damaging |
Het |
Nr3c2 |
C |
A |
8: 77,635,261 (GRCm39) |
Q121K |
possibly damaging |
Het |
Nr4a2 |
C |
T |
2: 57,001,626 (GRCm39) |
G213S |
probably damaging |
Het |
Nrg1 |
G |
C |
8: 32,408,033 (GRCm39) |
L67V |
possibly damaging |
Het |
Nrxn1 |
T |
A |
17: 90,366,933 (GRCm39) |
D31V |
probably damaging |
Het |
Nsd1 |
A |
C |
13: 55,361,661 (GRCm39) |
S210R |
possibly damaging |
Het |
Nsd2 |
T |
C |
5: 34,013,082 (GRCm39) |
|
probably null |
Het |
Nsd3 |
CCTTCT |
CCT |
8: 26,131,018 (GRCm39) |
|
probably benign |
Het |
Nsun2 |
A |
T |
13: 69,763,584 (GRCm39) |
K103M |
probably damaging |
Het |
Ntn5 |
G |
C |
7: 45,343,627 (GRCm39) |
G322A |
probably damaging |
Het |
Nudt4 |
C |
T |
10: 95,388,377 (GRCm39) |
G60S |
probably benign |
Het |
Numa1 |
C |
A |
7: 101,647,609 (GRCm39) |
Q447K |
probably benign |
Het |
Numa1 |
T |
G |
7: 101,647,538 (GRCm39) |
L423R |
probably damaging |
Het |
Nup214 |
T |
C |
2: 31,901,235 (GRCm39) |
F940L |
probably benign |
Het |
Nxpe5 |
G |
A |
5: 138,239,176 (GRCm39) |
|
probably null |
Het |
Nxph2 |
G |
T |
2: 23,290,229 (GRCm39) |
A194S |
probably benign |
Het |
Oaz1 |
C |
G |
10: 80,662,663 (GRCm39) |
R24G |
possibly damaging |
Het |
Obox2 |
A |
G |
7: 15,131,263 (GRCm39) |
K123R |
possibly damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Oca2 |
G |
T |
7: 55,980,123 (GRCm39) |
K609N |
probably null |
Het |
Ocln |
G |
A |
13: 100,671,560 (GRCm39) |
R266* |
probably null |
Het |
Ocstamp |
C |
A |
2: 165,237,838 (GRCm39) |
Q475H |
possibly damaging |
Het |
Odad2 |
G |
A |
18: 7,266,919 (GRCm39) |
S394L |
probably benign |
Het |
Odf1 |
A |
G |
15: 38,219,918 (GRCm39) |
Y82C |
probably benign |
Het |
Ogdh |
A |
C |
11: 6,305,427 (GRCm39) |
D978A |
probably benign |
Het |
Olfm3 |
G |
T |
3: 114,698,317 (GRCm39) |
|
probably benign |
Het |
Olfm5 |
T |
G |
7: 103,803,357 (GRCm39) |
S294R |
probably damaging |
Het |
Omg |
G |
C |
11: 79,393,146 (GRCm39) |
N237K |
possibly damaging |
Het |
Oog3 |
T |
A |
4: 143,884,877 (GRCm39) |
N353I |
probably benign |
Het |
Oog3 |
A |
G |
4: 143,886,206 (GRCm39) |
F131L |
probably benign |
Het |
Or10a2 |
C |
A |
7: 106,673,612 (GRCm39) |
D192E |
possibly damaging |
Het |
Or10a3m |
T |
G |
7: 108,312,745 (GRCm39) |
F50V |
probably benign |
Het |
Or10a3n |
G |
T |
7: 108,492,980 (GRCm39) |
F211L |
probably damaging |
Het |
Or10a48 |
A |
C |
7: 108,425,103 (GRCm39) |
Y34* |
probably null |
Het |
Or10ag52 |
T |
G |
2: 87,044,122 (GRCm39) |
I295M |
possibly damaging |
Het |
Or10ag54 |
G |
T |
2: 87,099,919 (GRCm39) |
G265* |
probably null |
Het |
Or10ag58 |
A |
G |
2: 87,265,503 (GRCm39) |
Y224C |
probably damaging |
Het |
Or10ag59 |
T |
C |
2: 87,406,024 (GRCm39) |
S199P |
possibly damaging |
Het |
Or10ak8 |
A |
C |
4: 118,773,785 (GRCm39) |
L293R |
probably damaging |
Het |
Or10al4 |
T |
A |
17: 38,036,983 (GRCm39) |
F23I |
probably damaging |
Het |
Or10g9b |
A |
G |
9: 39,917,892 (GRCm39) |
S118P |
probably damaging |
Het |
Or10j5 |
T |
A |
1: 172,784,891 (GRCm39) |
F176L |
probably damaging |
Het |
Or10q12 |
C |
A |
19: 13,745,780 (GRCm39) |
P25T |
probably benign |
Het |
Or10x1 |
G |
A |
1: 174,197,310 (GRCm39) |
V276I |
probably benign |
Het |
Or11g26 |
T |
C |
14: 50,752,984 (GRCm39) |
F108L |
possibly damaging |
Het |
Or12d13 |
A |
C |
17: 37,647,596 (GRCm39) |
F176V |
probably damaging |
Het |
Or12e10 |
C |
A |
2: 87,641,090 (GRCm39) |
L309I |
probably damaging |
Het |
Or12j5 |
A |
C |
7: 140,083,718 (GRCm39) |
V218G |
probably benign |
Het |
Or13a27 |
A |
G |
7: 139,925,717 (GRCm39) |
F62L |
probably benign |
Het |
Or13a28 |
A |
G |
7: 140,218,133 (GRCm39) |
K173R |
probably benign |
Het |
Or13p3 |
A |
G |
4: 118,567,423 (GRCm39) |
K273R |
probably benign |
Het |
Or14c43 |
T |
A |
7: 86,114,954 (GRCm39) |
F112I |
possibly damaging |
Het |
Or14j10 |
G |
T |
17: 37,935,320 (GRCm39) |
L69M |
probably damaging |
Het |
Or1e17 |
G |
A |
11: 73,831,964 (GRCm39) |
M297I |
probably benign |
Het |
Or1e19 |
T |
C |
11: 73,315,931 (GRCm39) |
S293G |
probably benign |
Het |
Or1j12 |
T |
G |
2: 36,342,918 (GRCm39) |
F107C |
possibly damaging |
Het |
Or1l4b |
T |
G |
2: 37,036,397 (GRCm39) |
F58V |
probably benign |
Het |
Or1p1 |
T |
C |
11: 74,179,661 (GRCm39) |
L63P |
probably damaging |
Het |
Or1q1 |
A |
C |
2: 36,887,717 (GRCm39) |
K298N |
possibly damaging |
Het |
Or2ag12 |
T |
G |
7: 106,277,664 (GRCm39) |
S10R |
probably benign |
Het |
Or2ag15 |
A |
T |
7: 106,340,350 (GRCm39) |
S264T |
probably benign |
Het |
Or2ag2 |
T |
A |
7: 106,485,503 (GRCm39) |
I174F |
probably damaging |
Het |
Or2d36 |
A |
C |
7: 106,747,419 (GRCm39) |
S299R |
probably benign |
Het |
Or2l13 |
T |
C |
16: 19,305,798 (GRCm39) |
L70P |
possibly damaging |
Het |
Or2y15 |
T |
G |
11: 49,351,283 (GRCm39) |
L259R |
probably damaging |
Het |
Or2z9 |
T |
G |
8: 72,854,361 (GRCm39) |
F252L |
probably benign |
Het |
Or3a1 |
A |
T |
11: 74,225,518 (GRCm39) |
F180I |
probably damaging |
Het |
Or4c110 |
C |
A |
2: 88,832,182 (GRCm39) |
G150V |
possibly damaging |
Het |
Or4c12 |
A |
G |
2: 89,774,114 (GRCm39) |
V115A |
probably benign |
Het |
Or4d10b |
T |
C |
19: 12,036,493 (GRCm39) |
T208A |
probably benign |
Het |
Or4e2 |
C |
A |
14: 52,688,666 (GRCm39) |
F265L |
probably benign |
Het |
Or4f53 |
T |
G |
2: 111,088,204 (GRCm39) |
V248G |
possibly damaging |
Het |
Or4k41 |
T |
C |
2: 111,279,802 (GRCm39) |
F106L |
probably benign |
Het |
Or4k44 |
A |
C |
2: 111,368,159 (GRCm39) |
I158M |
possibly damaging |
Het |
Or4p23 |
A |
C |
2: 88,576,922 (GRCm39) |
F103L |
probably damaging |
Het |
Or4s2b |
T |
G |
2: 88,509,008 (GRCm39) |
F263V |
probably damaging |
Het |
Or51a42 |
A |
C |
7: 103,708,523 (GRCm39) |
S95R |
possibly damaging |
Het |
Or51ah3 |
G |
C |
7: 103,210,597 (GRCm39) |
L304F |
probably damaging |
Het |
Or51ah3 |
A |
G |
7: 103,210,266 (GRCm39) |
K194R |
probably benign |
Het |
Or52e15 |
C |
A |
7: 104,645,661 (GRCm39) |
G150V |
probably benign |
Het |
Or52n2b |
G |
T |
7: 104,565,873 (GRCm39) |
A210E |
probably benign |
Het |
Or52s1b |
A |
G |
7: 102,822,013 (GRCm39) |
L277P |
possibly damaging |
Het |
Or52z1 |
T |
G |
7: 103,436,572 (GRCm39) |
K304T |
probably damaging |
Het |
Or52z15 |
T |
G |
7: 103,332,393 (GRCm39) |
I156S |
probably benign |
Het |
Or56b2j |
T |
C |
7: 104,353,700 (GRCm39) |
Y309H |
probably benign |
Het |
Or5an6 |
A |
C |
19: 12,371,663 (GRCm39) |
K12T |
probably benign |
Het |
Or5an9 |
A |
C |
19: 12,187,854 (GRCm39) |
K308T |
possibly damaging |
Het |
Or5b101 |
A |
C |
19: 13,005,391 (GRCm39) |
F101V |
probably benign |
Het |
Or5b116 |
T |
C |
19: 13,423,213 (GRCm39) |
V279A |
possibly damaging |
Het |
Or5b121 |
T |
G |
19: 13,507,216 (GRCm39) |
F104V |
possibly damaging |
Het |
Or5b124 |
C |
A |
19: 13,610,817 (GRCm39) |
A114E |
probably damaging |
Het |
Or5b21 |
T |
C |
19: 12,839,648 (GRCm39) |
C170R |
probably damaging |
Het |
Or5bb10 |
C |
A |
19: 12,206,588 (GRCm39) |
W107C |
probably damaging |
Het |
Or5d16 |
G |
A |
2: 87,773,792 (GRCm39) |
P60L |
probably damaging |
Het |
Or5e1 |
T |
G |
7: 108,354,311 (GRCm39) |
L83V |
probably benign |
Het |
Or5g26 |
C |
T |
2: 85,493,960 (GRCm39) |
V273I |
probably benign |
Het |
Or5i1 |
G |
T |
2: 87,612,972 (GRCm39) |
L29F |
probably damaging |
Het |
Or5j1 |
A |
C |
2: 86,878,777 (GRCm39) |
L268V |
probably benign |
Het |
Or5m13b |
T |
G |
2: 85,754,142 (GRCm39) |
F177V |
probably damaging |
Het |
Or5m3b |
T |
C |
2: 85,872,063 (GRCm39) |
S135P |
probably damaging |
Het |
Or5m9b |
G |
T |
2: 85,905,667 (GRCm39) |
E194D |
possibly damaging |
Het |
Or5p56 |
G |
A |
7: 107,589,938 (GRCm39) |
R122H |
probably benign |
Het |
Or5p57 |
C |
A |
7: 107,665,534 (GRCm39) |
C127F |
probably damaging |
Het |
Or5p73 |
T |
A |
7: 108,064,578 (GRCm39) |
F16I |
probably benign |
Het |
Or5p76 |
A |
C |
7: 108,122,605 (GRCm39) |
F184C |
probably damaging |
Het |
Or5t5 |
A |
G |
2: 86,616,817 (GRCm39) |
K248E |
probably damaging |
Het |
Or5w16 |
G |
T |
2: 87,576,833 (GRCm39) |
A98S |
probably damaging |
Het |
Or5w20 |
G |
A |
2: 87,726,977 (GRCm39) |
A145T |
probably benign |
Het |
Or6c201 |
T |
G |
10: 128,968,944 (GRCm39) |
K231T |
probably benign |
Het |
Or6c214 |
A |
C |
10: 129,591,208 (GRCm39) |
I37S |
possibly damaging |
Het |
Or6c217 |
T |
C |
10: 129,738,552 (GRCm39) |
E9G |
possibly damaging |
Het |
Or6c74 |
A |
C |
10: 129,869,657 (GRCm39) |
K54T |
probably damaging |
Het |
Or6k6 |
C |
T |
1: 173,944,881 (GRCm39) |
A234T |
probably benign |
Het |
Or6n2 |
C |
T |
1: 173,897,515 (GRCm39) |
S217F |
probably damaging |
Het |
Or7d10 |
T |
A |
9: 19,832,008 (GRCm39) |
F168I |
probably damaging |
Het |
Or7e173 |
A |
G |
9: 19,938,575 (GRCm39) |
S220P |
probably damaging |
Het |
Or7g19 |
G |
A |
9: 18,856,717 (GRCm39) |
V258I |
possibly damaging |
Het |
Or7g29 |
G |
A |
9: 19,286,980 (GRCm39) |
L66F |
probably damaging |
Het |
Or8b101 |
T |
C |
9: 38,020,882 (GRCm39) |
V295A |
probably damaging |
Het |
Or8b46 |
T |
C |
9: 38,450,445 (GRCm39) |
F85L |
probably damaging |
Het |
Or8b47 |
T |
G |
9: 38,435,155 (GRCm39) |
N42K |
probably damaging |
Het |
Or8b9 |
A |
C |
9: 37,766,614 (GRCm39) |
S167R |
probably benign |
Het |
Or8c17 |
T |
C |
9: 38,179,908 (GRCm39) |
L33S |
probably damaging |
Het |
Or8g17 |
A |
C |
9: 38,930,085 (GRCm39) |
F251V |
probably damaging |
Het |
Or8g28 |
G |
A |
9: 39,169,167 (GRCm39) |
S270L |
probably benign |
Het |
Or8h9 |
T |
G |
2: 86,789,010 (GRCm39) |
K264T |
probably benign |
Het |
Or8k23 |
A |
T |
2: 86,186,237 (GRCm39) |
I163N |
probably benign |
Het |
Or8k24 |
T |
G |
2: 86,216,523 (GRCm39) |
K80Q |
probably damaging |
Het |
Or8k24 |
T |
C |
2: 86,216,100 (GRCm39) |
I221V |
probably benign |
Het |
Or8k3 |
C |
A |
2: 86,058,566 (GRCm39) |
V250F |
probably damaging |
Het |
Or8k33 |
C |
T |
2: 86,384,310 (GRCm39) |
A53T |
probably benign |
Het |
Or8u10 |
C |
T |
2: 85,915,326 (GRCm39) |
S265N |
probably benign |
Het |
Or9g8 |
T |
G |
2: 85,607,466 (GRCm39) |
D179E |
probably damaging |
Het |
Or9i14 |
A |
C |
19: 13,792,912 (GRCm39) |
L14R |
probably damaging |
Het |
Or9m1 |
A |
C |
2: 87,733,928 (GRCm39) |
F31V |
possibly damaging |
Het |
Or9s27 |
T |
A |
1: 92,516,273 (GRCm39) |
S74T |
probably damaging |
Het |
Orc2 |
A |
C |
1: 58,515,675 (GRCm39) |
F230V |
probably benign |
Het |
Osbpl3 |
A |
G |
6: 50,274,077 (GRCm39) |
F846L |
probably damaging |
Het |
Pabpc1l |
G |
C |
2: 163,874,244 (GRCm39) |
|
probably null |
Het |
Pah |
C |
T |
10: 87,407,153 (GRCm39) |
S303F |
probably damaging |
Het |
Paip2b |
T |
G |
6: 83,785,864 (GRCm39) |
N122T |
probably benign |
Het |
Pak4 |
G |
T |
7: 28,264,653 (GRCm39) |
T83N |
probably damaging |
Het |
Pamr1 |
C |
A |
2: 102,464,791 (GRCm39) |
F313L |
possibly damaging |
Het |
Papln |
C |
G |
12: 83,823,150 (GRCm39) |
P396A |
probably benign |
Het |
Papss1 |
C |
G |
3: 131,348,728 (GRCm39) |
H559Q |
possibly damaging |
Het |
Parp14 |
C |
G |
16: 35,661,956 (GRCm39) |
D1360H |
probably damaging |
Het |
Pask |
C |
T |
1: 93,244,523 (GRCm39) |
S1166N |
probably damaging |
Het |
Pbk |
T |
A |
14: 66,051,397 (GRCm39) |
V145D |
probably damaging |
Het |
Pbrm1 |
G |
A |
14: 30,832,411 (GRCm39) |
R1443Q |
possibly damaging |
Het |
Pcbp3 |
C |
A |
10: 76,599,157 (GRCm39) |
Q326H |
probably benign |
Het |
Pcdh1 |
G |
C |
18: 38,331,120 (GRCm39) |
R767G |
probably damaging |
Het |
Pcdh17 |
A |
G |
14: 84,685,714 (GRCm39) |
K727R |
possibly damaging |
Het |
Pcdha2 |
G |
T |
18: 37,074,174 (GRCm39) |
G602C |
probably damaging |
Het |
Pcdha6 |
G |
A |
18: 37,102,270 (GRCm39) |
A488T |
probably damaging |
Het |
Pcdhac1 |
G |
T |
18: 37,225,243 (GRCm39) |
L685F |
probably damaging |
Het |
Pcdhac1 |
G |
T |
18: 37,225,619 (GRCm39) |
A811S |
probably damaging |
Het |
Pcdhb21 |
A |
G |
18: 37,647,594 (GRCm39) |
E241G |
probably benign |
Het |
Pcdhb22 |
A |
C |
18: 37,652,398 (GRCm39) |
T289P |
probably benign |
Het |
Pcdhb6 |
T |
A |
18: 37,468,199 (GRCm39) |
D373E |
probably damaging |
Het |
Pcdhga11 |
G |
C |
18: 37,889,237 (GRCm39) |
G82R |
probably damaging |
Het |
Pcmtd1 |
C |
T |
1: 7,233,554 (GRCm39) |
P222L |
possibly damaging |
Het |
Pcnx2 |
T |
G |
8: 126,592,757 (GRCm39) |
S736R |
probably damaging |
Het |
Pcnx2 |
C |
T |
8: 126,553,667 (GRCm39) |
E1151K |
probably damaging |
Het |
Pcsk5 |
A |
G |
19: 17,440,738 (GRCm39) |
L1284P |
probably damaging |
Het |
Pdgfra |
C |
T |
5: 75,327,238 (GRCm39) |
S145F |
probably benign |
Het |
Pdrg1 |
C |
T |
2: 152,855,957 (GRCm39) |
A46T |
probably damaging |
Het |
Pds5a |
A |
C |
5: 65,776,329 (GRCm39) |
I88M |
probably damaging |
Het |
Pdzk1 |
A |
G |
3: 96,761,873 (GRCm39) |
N162D |
probably benign |
Het |
Peds1 |
G |
C |
2: 167,486,784 (GRCm39) |
Y198* |
probably null |
Het |
Pelp1 |
A |
G |
11: 70,287,716 (GRCm39) |
L402P |
probably damaging |
Het |
Pex1 |
G |
A |
5: 3,656,075 (GRCm39) |
A301T |
probably benign |
Het |
Pex6 |
A |
T |
17: 47,023,148 (GRCm39) |
Q241H |
possibly damaging |
Het |
Pgap4 |
A |
G |
4: 49,587,135 (GRCm39) |
L11P |
probably damaging |
Het |
Pgm3 |
A |
G |
9: 86,446,760 (GRCm39) |
F253L |
probably damaging |
Het |
Phaf1 |
C |
T |
8: 105,957,804 (GRCm39) |
R37C |
probably damaging |
Het |
Pi4k2b |
G |
A |
5: 52,918,273 (GRCm39) |
R367Q |
possibly damaging |
Het |
Pi4kb |
T |
G |
3: 94,891,820 (GRCm39) |
F179V |
probably damaging |
Het |
Pid1 |
T |
G |
1: 84,093,735 (GRCm39) |
N51T |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,203,065 (GRCm39) |
G1525D |
probably damaging |
Het |
Piga |
A |
C |
X: 163,205,905 (GRCm39) |
K88N |
probably damaging |
Het |
Pigo |
G |
C |
4: 43,019,409 (GRCm39) |
P970A |
probably damaging |
Het |
Pik3r6 |
G |
A |
11: 68,416,428 (GRCm39) |
V6M |
probably damaging |
Het |
Piwil4 |
G |
A |
9: 14,645,813 (GRCm39) |
H142Y |
probably damaging |
Het |
Pkd1 |
T |
G |
17: 24,784,579 (GRCm39) |
L375R |
probably benign |
Het |
Pkd2 |
T |
G |
5: 104,646,727 (GRCm39) |
L780V |
probably damaging |
Het |
Pkdcc |
A |
G |
17: 83,529,579 (GRCm39) |
E380G |
probably damaging |
Het |
Pla2g12a |
C |
T |
3: 129,684,029 (GRCm39) |
S136F |
probably benign |
Het |
Pla2g2c |
T |
C |
4: 138,461,597 (GRCm39) |
F22S |
probably damaging |
Het |
Pla2g4c |
A |
T |
7: 13,063,678 (GRCm39) |
Q48H |
probably benign |
Het |
Plb1 |
T |
G |
5: 32,468,191 (GRCm39) |
F503V |
probably damaging |
Het |
Plb1 |
C |
T |
5: 32,468,261 (GRCm39) |
S526L |
probably benign |
Het |
Plcb1 |
A |
C |
2: 135,062,766 (GRCm39) |
E27D |
probably benign |
Het |
Plcl2 |
C |
A |
17: 50,914,020 (GRCm39) |
P343H |
probably damaging |
Het |
Pld1 |
A |
C |
3: 28,083,392 (GRCm39) |
I171L |
probably benign |
Het |
Plod2 |
T |
G |
9: 92,485,088 (GRCm39) |
F551V |
probably benign |
Het |
Plxna2 |
A |
G |
1: 194,446,847 (GRCm39) |
N786D |
probably benign |
Het |
Plxna2 |
A |
C |
1: 194,326,749 (GRCm39) |
I228L |
possibly damaging |
Het |
Plxnd1 |
C |
A |
6: 115,944,471 (GRCm39) |
S1033I |
probably benign |
Het |
Pmfbp1 |
A |
C |
8: 110,240,576 (GRCm39) |
E219D |
probably damaging |
Het |
Pml |
G |
T |
9: 58,141,873 (GRCm39) |
L320M |
probably damaging |
Het |
Pnisr |
C |
G |
4: 21,873,684 (GRCm39) |
R476G |
probably benign |
Het |
Pnliprp2 |
G |
A |
19: 58,750,757 (GRCm39) |
A149T |
probably damaging |
Het |
Pnp |
T |
G |
14: 51,188,952 (GRCm39) |
D248E |
probably benign |
Het |
Pnpla5 |
A |
G |
15: 84,007,272 (GRCm39) |
S15P |
probably damaging |
Het |
Pogz |
T |
A |
3: 94,786,387 (GRCm39) |
F992I |
probably damaging |
Het |
Pole |
C |
T |
5: 110,475,731 (GRCm39) |
L1847F |
possibly damaging |
Het |
Polr2b |
T |
G |
5: 77,490,569 (GRCm39) |
I903S |
possibly damaging |
Het |
Polr2b |
G |
A |
5: 77,493,248 (GRCm39) |
G1077S |
probably damaging |
Het |
Polr3a |
A |
C |
14: 24,529,792 (GRCm39) |
V266G |
probably damaging |
Het |
Pop1 |
C |
G |
15: 34,499,465 (GRCm39) |
A10G |
probably damaging |
Het |
Pop7 |
T |
C |
5: 137,500,273 (GRCm39) |
Y20C |
probably damaging |
Het |
Postn |
A |
T |
3: 54,282,548 (GRCm39) |
D503V |
probably benign |
Het |
Pou4f2 |
C |
G |
8: 79,162,230 (GRCm39) |
Q124H |
probably benign |
Het |
Ppl |
G |
A |
16: 4,907,371 (GRCm39) |
R975W |
probably damaging |
Het |
Ppp1cc |
C |
T |
5: 122,310,816 (GRCm39) |
S182F |
possibly damaging |
Het |
Ppp1r10 |
ACATGATGTCCCTAGCCAT |
ACAT |
17: 36,241,659 (GRCm39) |
|
probably benign |
Het |
Ppp1r7 |
T |
C |
1: 93,280,310 (GRCm39) |
L126P |
probably damaging |
Het |
Ppp2r1b |
A |
C |
9: 50,778,211 (GRCm39) |
E309D |
probably damaging |
Het |
Ppp4r3c1 |
T |
G |
X: 88,973,842 (GRCm39) |
D785A |
unknown |
Het |
Ppp4r3c1 |
C |
A |
X: 88,973,843 (GRCm39) |
D785Y |
unknown |
Het |
Pramel18 |
A |
G |
4: 101,766,315 (GRCm39) |
|
probably null |
Het |
Pramel18 |
A |
C |
4: 101,767,383 (GRCm39) |
I211L |
probably benign |
Het |
Pramel21 |
C |
A |
4: 143,341,802 (GRCm39) |
A77E |
possibly damaging |
Het |
Pramel23 |
T |
G |
4: 143,424,650 (GRCm39) |
Q264H |
probably benign |
Het |
Pramel24 |
T |
C |
4: 143,453,603 (GRCm39) |
L237P |
probably damaging |
Het |
Pramel28 |
C |
T |
4: 143,692,132 (GRCm39) |
E290K |
probably benign |
Het |
Pramel58 |
C |
A |
5: 94,831,692 (GRCm39) |
A233E |
probably benign |
Het |
Prdm1 |
G |
A |
10: 44,317,921 (GRCm39) |
R301W |
probably damaging |
Het |
Prg2 |
G |
T |
2: 84,812,609 (GRCm39) |
K106N |
possibly damaging |
Het |
Prkg2 |
A |
T |
5: 99,172,663 (GRCm39) |
H17Q |
probably benign |
Het |
Prob1 |
G |
C |
18: 35,785,822 (GRCm39) |
P811A |
possibly damaging |
Het |
Prox1 |
G |
C |
1: 189,894,196 (GRCm39) |
A83G |
probably damaging |
Het |
Prr23a1 |
G |
A |
9: 98,725,400 (GRCm39) |
R254Q |
possibly damaging |
Het |
Prr27 |
G |
A |
5: 87,990,505 (GRCm39) |
R31H |
probably damaging |
Het |
Prr30 |
G |
C |
14: 101,435,576 (GRCm39) |
Q329E |
probably benign |
Het |
Prrc2b |
G |
A |
2: 32,106,744 (GRCm39) |
R1582K |
probably damaging |
Het |
Prrc2b |
C |
A |
2: 32,104,441 (GRCm39) |
N1306K |
probably benign |
Het |
Prrx1 |
A |
C |
1: 163,089,446 (GRCm39) |
L127R |
probably damaging |
Het |
Prss36 |
G |
A |
7: 127,533,709 (GRCm39) |
R32* |
probably null |
Het |
Prss53 |
C |
T |
7: 127,486,570 (GRCm39) |
W352* |
probably null |
Het |
Psd3 |
T |
C |
8: 68,358,912 (GRCm39) |
|
silent |
Het |
Psg17 |
G |
A |
7: 18,550,835 (GRCm39) |
T340I |
probably benign |
Het |
Psg25 |
T |
A |
7: 18,263,516 (GRCm39) |
R102S |
probably benign |
Het |
Psmd11 |
A |
ATC |
11: 80,362,376 (GRCm39) |
|
probably null |
Het |
Ptcra |
G |
C |
17: 47,074,521 (GRCm39) |
A7G |
probably damaging |
Het |
Pten |
A |
C |
19: 32,777,398 (GRCm39) |
T131P |
probably damaging |
Het |
Pten |
C |
T |
19: 32,753,451 (GRCm39) |
A39V |
probably damaging |
Het |
Ptgfrn |
T |
G |
3: 100,963,753 (GRCm39) |
T620P |
probably damaging |
Het |
Ptgr3 |
G |
A |
18: 84,113,052 (GRCm39) |
V243I |
probably damaging |
Het |
Ptprn |
T |
A |
1: 75,237,264 (GRCm39) |
M20L |
possibly damaging |
Het |
Ptprq |
C |
T |
10: 107,535,533 (GRCm39) |
A411T |
possibly damaging |
Het |
Ptprt |
A |
G |
2: 162,080,041 (GRCm39) |
S253P |
possibly damaging |
Het |
Rab3gap2 |
A |
T |
1: 185,013,874 (GRCm39) |
L1173F |
probably damaging |
Het |
Rac1 |
C |
A |
5: 143,500,474 (GRCm39) |
A59S |
probably damaging |
Het |
Rad21 |
T |
G |
15: 51,846,022 (GRCm39) |
K16T |
probably damaging |
Het |
Rad21l |
C |
T |
2: 151,509,939 (GRCm39) |
R54Q |
probably damaging |
Het |
Rad9b |
A |
G |
5: 122,471,435 (GRCm39) |
F210L |
possibly damaging |
Het |
Raet1e |
A |
C |
10: 22,057,850 (GRCm39) |
T206P |
possibly damaging |
Het |
Ralgapa2 |
T |
G |
2: 146,276,825 (GRCm39) |
S472R |
probably benign |
Het |
Ranbp2 |
AGTTTGTGCTCGGT |
AGTTTGTGCTCGGTTTGTGCTCGGT |
10: 58,313,794 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
A |
T |
10: 58,328,715 (GRCm39) |
Q2871H |
probably benign |
Het |
Ranbp2 |
GGT |
GGTTTGTGCTCCGT |
10: 58,313,805 (GRCm39) |
|
probably null |
Het |
Rapgefl1 |
C |
G |
11: 98,736,721 (GRCm39) |
P285R |
probably damaging |
Het |
Rasgrp4 |
A |
C |
7: 28,849,961 (GRCm39) |
|
probably benign |
Het |
Rassf7 |
C |
G |
7: 140,797,058 (GRCm39) |
S90R |
probably damaging |
Het |
Rassf8 |
A |
C |
6: 145,762,342 (GRCm39) |
E371A |
probably benign |
Het |
Rassf8 |
A |
G |
6: 145,761,208 (GRCm39) |
Q178R |
probably benign |
Het |
Rb1cc1 |
AT |
ATT |
1: 6,319,242 (GRCm39) |
|
probably null |
Het |
Rbm12b1 |
G |
T |
4: 12,146,079 (GRCm39) |
V684L |
probably benign |
Het |
Rdh16f1 |
A |
C |
10: 127,624,702 (GRCm39) |
K180T |
probably damaging |
Het |
Rec8 |
A |
T |
14: 55,862,604 (GRCm39) |
K553M |
probably damaging |
Het |
Reg1 |
G |
T |
6: 78,403,901 (GRCm39) |
E23* |
probably null |
Het |
Rergl |
C |
A |
6: 139,470,424 (GRCm39) |
E135* |
probably null |
Het |
Resp18 |
T |
C |
1: 75,254,935 (GRCm39) |
K6R |
possibly damaging |
Het |
Rev3l |
C |
A |
10: 39,700,314 (GRCm39) |
Q1604K |
probably benign |
Het |
Rfc3 |
C |
T |
5: 151,568,327 (GRCm39) |
R213H |
probably benign |
Het |
Rfwd3 |
C |
A |
8: 112,024,238 (GRCm39) |
G28V |
probably benign |
Het |
Rfx3 |
G |
A |
19: 27,814,850 (GRCm39) |
S169F |
probably damaging |
Het |
Rfx8 |
T |
G |
1: 39,722,126 (GRCm39) |
E286D |
possibly damaging |
Het |
Rgl1 |
G |
A |
1: 152,550,771 (GRCm39) |
|
probably benign |
Het |
Rgs11 |
G |
C |
17: 26,424,746 (GRCm39) |
Q218H |
probably benign |
Het |
Rgs7 |
T |
C |
1: 174,911,586 (GRCm39) |
E345G |
possibly damaging |
Het |
Rims1 |
C |
G |
1: 22,358,810 (GRCm39) |
A1258P |
probably damaging |
Het |
Rint1 |
A |
G |
5: 24,010,312 (GRCm39) |
N174D |
probably benign |
Het |
Ripk3 |
T |
G |
14: 56,025,383 (GRCm39) |
E60D |
possibly damaging |
Het |
Rnf146 |
G |
A |
10: 29,223,568 (GRCm39) |
A106V |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,368,080 (GRCm39) |
K4705R |
possibly damaging |
Het |
Rnmt |
C |
T |
18: 68,440,745 (GRCm39) |
S136L |
probably benign |
Het |
Rp1l1 |
C |
T |
14: 64,266,207 (GRCm39) |
H598Y |
possibly damaging |
Het |
Rp1l1 |
T |
G |
14: 64,267,827 (GRCm39) |
F1138V |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 91,996,748 (GRCm39) |
F109I |
possibly damaging |
Het |
Rpgrip1l |
T |
G |
8: 91,987,603 (GRCm39) |
K818T |
possibly damaging |
Het |
Rpgrip1l |
A |
T |
8: 91,946,807 (GRCm39) |
*1265R |
probably null |
Het |
Rpl12 |
T |
A |
2: 32,853,031 (GRCm39) |
I82N |
possibly damaging |
Het |
Rpl13a |
G |
C |
7: 44,776,937 (GRCm39) |
A24G |
probably damaging |
Het |
Rpp14 |
A |
C |
14: 8,090,539 (GRCm38) |
E154D |
probably benign |
Het |
Rps19 |
G |
C |
7: 24,585,532 (GRCm39) |
|
probably benign |
Het |
Rptn |
C |
A |
3: 93,304,734 (GRCm39) |
P689H |
probably benign |
Het |
Rrbp1 |
C |
A |
2: 143,816,406 (GRCm39) |
G741V |
probably damaging |
Het |
Rreb1 |
G |
A |
13: 38,132,913 (GRCm39) |
R1696K |
probably benign |
Het |
Rsl1d1 |
C |
T |
16: 11,020,249 (GRCm39) |
G59R |
possibly damaging |
Het |
Rtl1 |
T |
A |
12: 109,558,753 (GRCm39) |
T1029S |
probably benign |
Het |
Runx1 |
C |
T |
16: 92,402,680 (GRCm39) |
A421T |
probably damaging |
Het |
Runx1t1 |
G |
A |
4: 13,865,892 (GRCm39) |
R380Q |
possibly damaging |
Het |
Rxfp1 |
C |
T |
3: 79,613,011 (GRCm39) |
G20R |
probably damaging |
Het |
Ryr3 |
C |
A |
2: 112,731,261 (GRCm39) |
G683V |
probably damaging |
Het |
S100a13 |
C |
G |
3: 90,423,249 (GRCm39) |
S80C |
probably damaging |
Het |
Samd1 |
CGAGGAGGAGGAGGAGGAGGA |
CGAGGAGGAGGAGGAGGA |
8: 84,725,625 (GRCm39) |
|
probably benign |
Het |
Satb1 |
C |
G |
17: 52,089,967 (GRCm39) |
Q293H |
probably damaging |
Het |
Satb1 |
G |
A |
17: 52,089,980 (GRCm39) |
S289F |
probably damaging |
Het |
Sbno1 |
T |
G |
5: 124,532,021 (GRCm39) |
K719N |
possibly damaging |
Het |
Sbno1 |
G |
T |
5: 124,542,367 (GRCm39) |
P308T |
probably damaging |
Het |
Sbpl |
A |
C |
17: 24,172,518 (GRCm39) |
F134V |
probably damaging |
Het |
Sbsn |
G |
T |
7: 30,451,176 (GRCm39) |
E64* |
probably null |
Het |
Scaf8 |
T |
G |
17: 3,213,258 (GRCm39) |
|
probably benign |
Het |
Scap |
A |
G |
9: 110,201,404 (GRCm39) |
N131S |
probably damaging |
Het |
Scarf1 |
C |
T |
11: 75,416,316 (GRCm39) |
A586V |
probably damaging |
Het |
Scd1 |
C |
A |
19: 44,386,362 (GRCm39) |
S355I |
probably benign |
Het |
Scgb2b26 |
A |
C |
7: 33,643,792 (GRCm39) |
F49L |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,584,308 (GRCm39) |
F1436L |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,544,295 (GRCm39) |
E399K |
probably damaging |
Het |
Scrib |
G |
A |
15: 75,920,080 (GRCm39) |
P1560S |
probably damaging |
Het |
Sctr |
GT |
G |
1: 119,964,136 (GRCm39) |
|
probably null |
Het |
Sec16a |
G |
A |
2: 26,329,105 (GRCm39) |
S970F |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,385,594 (GRCm39) |
|
probably null |
Het |
Sec23a |
A |
G |
12: 59,051,362 (GRCm39) |
F94L |
probably benign |
Het |
Sel1l3 |
C |
A |
5: 53,273,538 (GRCm39) |
A1081S |
probably damaging |
Het |
Selenok |
G |
A |
14: 29,695,401 (GRCm39) |
G93E |
probably damaging |
Het |
Selenov |
G |
A |
7: 27,990,093 (GRCm39) |
T137I |
possibly damaging |
Het |
Sema3b |
A |
C |
9: 107,476,233 (GRCm39) |
|
probably null |
Het |
Sema3e |
G |
A |
5: 14,276,470 (GRCm39) |
S285N |
probably damaging |
Het |
Sema5b |
T |
G |
16: 35,480,960 (GRCm39) |
F815V |
probably damaging |
Het |
Serac1 |
G |
A |
17: 6,099,193 (GRCm39) |
P533S |
probably damaging |
Het |
Serpina1a |
C |
A |
12: 103,820,926 (GRCm39) |
|
probably null |
Het |
Serpinb3b |
T |
G |
1: 107,085,481 (GRCm39) |
T87P |
probably damaging |
Het |
Serpinb6c |
A |
G |
13: 34,077,855 (GRCm39) |
F172L |
probably damaging |
Het |
Serpinb6c |
G |
A |
13: 34,077,906 (GRCm39) |
P155S |
probably benign |
Het |
Serpinb6d |
T |
C |
13: 33,855,237 (GRCm39) |
F304L |
possibly damaging |
Het |
Sertad4 |
G |
T |
1: 192,529,339 (GRCm39) |
T159N |
probably damaging |
Het |
Setbp1 |
G |
C |
18: 78,902,809 (GRCm39) |
P286R |
probably damaging |
Het |
Sez6 |
T |
G |
11: 77,864,023 (GRCm39) |
F502V |
possibly damaging |
Het |
Sez6l |
T |
G |
5: 112,588,781 (GRCm39) |
Q644P |
probably damaging |
Het |
Sfmbt2 |
A |
C |
2: 10,583,994 (GRCm39) |
T784P |
probably damaging |
Het |
Sgo2b |
T |
G |
8: 64,381,456 (GRCm39) |
T459P |
possibly damaging |
Het |
Sgo2b |
C |
A |
8: 64,380,039 (GRCm39) |
G931V |
probably damaging |
Het |
Sgtb |
T |
C |
13: 104,268,447 (GRCm39) |
L118P |
probably damaging |
Het |
Shank1 |
C |
T |
7: 44,001,590 (GRCm39) |
A1103V |
unknown |
Het |
Siglech |
A |
G |
7: 55,418,742 (GRCm39) |
I182V |
possibly damaging |
Het |
Sirpa |
C |
A |
2: 129,460,455 (GRCm39) |
A54D |
probably damaging |
Het |
Slamf1 |
T |
G |
1: 171,627,160 (GRCm39) |
V334G |
probably damaging |
Het |
Slc14a2 |
T |
G |
18: 78,238,995 (GRCm39) |
K208T |
probably damaging |
Het |
Slc15a1 |
C |
T |
14: 121,717,466 (GRCm39) |
R272Q |
probably benign |
Het |
Slc15a1 |
A |
G |
14: 121,728,456 (GRCm39) |
L65P |
probably damaging |
Het |
Slc15a2 |
A |
G |
16: 36,772,445 (GRCm38) |
M179T |
probably benign |
Het |
Slc1a5 |
C |
T |
7: 16,531,594 (GRCm39) |
P533L |
probably damaging |
Het |
Slc22a12 |
G |
A |
19: 6,588,493 (GRCm39) |
H342Y |
possibly damaging |
Het |
Slc22a2 |
G |
A |
17: 12,833,663 (GRCm39) |
E448K |
probably benign |
Het |
Slc22a28 |
A |
C |
19: 8,039,763 (GRCm39) |
S537A |
probably damaging |
Het |
Slc22a3 |
A |
T |
17: 12,644,568 (GRCm39) |
C472* |
probably null |
Het |
Slc22a30 |
C |
A |
19: 8,313,139 (GRCm39) |
V549F |
probably damaging |
Het |
Slc22a6 |
A |
G |
19: 8,599,197 (GRCm39) |
D276G |
probably benign |
Het |
Slc23a1 |
T |
C |
18: 35,757,561 (GRCm39) |
N237D |
probably benign |
Het |
Slc25a1 |
C |
G |
16: 17,745,070 (GRCm39) |
G130A |
probably benign |
Het |
Slc28a1 |
C |
G |
7: 80,787,916 (GRCm39) |
P268A |
probably damaging |
Het |
Slc2a6 |
G |
A |
2: 26,911,999 (GRCm39) |
P420L |
probably damaging |
Het |
Slc35a4 |
A |
C |
18: 36,816,146 (GRCm39) |
*325Y |
probably null |
Het |
Slc48a1 |
C |
A |
15: 97,688,562 (GRCm39) |
Y74* |
probably null |
Het |
Slc4a10 |
T |
G |
2: 62,058,915 (GRCm39) |
L141V |
probably damaging |
Het |
Slc4a8 |
C |
G |
15: 100,659,832 (GRCm39) |
P8A |
probably benign |
Het |
Slc6a19 |
C |
T |
13: 73,837,849 (GRCm39) |
E217K |
possibly damaging |
Het |
Slc6a5 |
C |
G |
7: 49,561,605 (GRCm39) |
P46A |
probably benign |
Het |
Slc7a14 |
G |
C |
3: 31,278,148 (GRCm39) |
L486V |
probably benign |
Het |
Slco2a1 |
C |
A |
9: 102,956,726 (GRCm39) |
L513M |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,459,695 (GRCm39) |
Y1308C |
probably damaging |
Het |
Slurp2 |
C |
A |
15: 74,614,950 (GRCm39) |
V64L |
probably damaging |
Het |
Slx9 |
C |
A |
10: 77,325,865 (GRCm39) |
S168I |
probably damaging |
Het |
Smad5 |
A |
T |
13: 56,876,441 (GRCm39) |
R258S |
probably benign |
Het |
Smarcc2 |
G |
C |
10: 128,297,303 (GRCm39) |
G65A |
probably damaging |
Het |
Smco1 |
A |
T |
16: 32,092,033 (GRCm39) |
D37V |
probably damaging |
Het |
Smg1 |
A |
C |
7: 117,753,858 (GRCm39) |
|
probably benign |
Het |
Smg1 |
A |
G |
7: 117,777,622 (GRCm39) |
L1358P |
possibly damaging |
Het |
Smg1 |
C |
A |
7: 117,767,884 (GRCm39) |
E1665* |
probably null |
Het |
Smim29 |
G |
A |
17: 27,783,215 (GRCm39) |
R51C |
possibly damaging |
Het |
Snx15 |
T |
C |
19: 6,171,441 (GRCm39) |
E211G |
probably damaging |
Het |
Snx5 |
C |
T |
2: 144,094,411 (GRCm39) |
R373Q |
probably benign |
Het |
Sod2 |
T |
A |
17: 13,232,425 (GRCm39) |
L150H |
probably damaging |
Het |
Sorcs1 |
C |
G |
19: 50,210,581 (GRCm39) |
Q761H |
probably benign |
Het |
Sox12 |
C |
G |
2: 152,239,385 (GRCm39) |
W78C |
probably damaging |
Het |
Sox17 |
G |
T |
1: 4,562,525 (GRCm39) |
S160Y |
probably damaging |
Het |
Sp9 |
G |
C |
2: 73,103,574 (GRCm39) |
A43P |
possibly damaging |
Het |
Spag17 |
A |
G |
3: 100,002,946 (GRCm39) |
K1890R |
probably benign |
Het |
Speer1c |
T |
C |
5: 10,293,097 (GRCm39) |
|
probably benign |
Het |
Speer4b |
C |
G |
5: 27,702,939 (GRCm39) |
E188D |
probably benign |
Het |
Speer4f1 |
A |
C |
5: 17,684,477 (GRCm39) |
E168D |
probably damaging |
Het |
Spen |
C |
A |
4: 141,205,287 (GRCm39) |
E1113D |
unknown |
Het |
Spen |
T |
C |
4: 141,205,288 (GRCm39) |
E1113G |
unknown |
Het |
Sphkap |
T |
G |
1: 83,256,325 (GRCm39) |
T475P |
probably damaging |
Het |
Sphkap |
T |
A |
1: 83,254,329 (GRCm39) |
N1140I |
probably damaging |
Het |
Spinkl |
G |
C |
18: 44,307,626 (GRCm39) |
L12V |
probably damaging |
Het |
Spire1 |
C |
A |
18: 67,628,222 (GRCm39) |
R509L |
possibly damaging |
Het |
Spon1 |
G |
A |
7: 113,365,623 (GRCm39) |
A20T |
possibly damaging |
Het |
Srd5a3 |
T |
C |
5: 76,297,668 (GRCm39) |
F33L |
possibly damaging |
Het |
Srebf2 |
T |
G |
15: 82,079,122 (GRCm39) |
F783L |
probably benign |
Het |
Srp68 |
TCCGCCGCCGCCGCCGC |
TCCGCCGCCGCCGCCGCCGCCGC |
11: 116,164,861 (GRCm39) |
|
probably benign |
Het |
Ssbp4 |
A |
C |
8: 71,052,485 (GRCm39) |
|
probably benign |
Het |
Ssc5d |
A |
C |
7: 4,931,433 (GRCm39) |
E213D |
probably damaging |
Het |
Ssh2 |
C |
A |
11: 77,340,321 (GRCm39) |
T491N |
probably damaging |
Het |
Ssrp1 |
G |
A |
2: 84,870,997 (GRCm39) |
R211H |
probably damaging |
Het |
Ssxb3 |
T |
G |
X: 8,455,427 (GRCm39) |
S5R |
probably benign |
Het |
Stam |
C |
A |
2: 14,143,901 (GRCm39) |
S397* |
probably null |
Het |
Stambpl1 |
A |
T |
19: 34,204,027 (GRCm39) |
N39I |
probably damaging |
Het |
Stap2 |
G |
C |
17: 56,306,748 (GRCm39) |
A275G |
probably benign |
Het |
Stard4 |
T |
C |
18: 33,336,773 (GRCm39) |
S181G |
probably benign |
Het |
Stard4 |
G |
T |
18: 33,336,770 (GRCm39) |
Q182K |
probably benign |
Het |
Stil |
T |
G |
4: 114,863,890 (GRCm39) |
L44R |
probably damaging |
Het |
Stk31 |
G |
T |
6: 49,394,122 (GRCm39) |
|
probably null |
Het |
Ston2 |
T |
G |
12: 91,615,841 (GRCm39) |
N189T |
possibly damaging |
Het |
Stxbp5l |
T |
G |
16: 37,024,851 (GRCm39) |
Q582H |
probably benign |
Het |
Styxl2 |
A |
G |
1: 165,926,852 (GRCm39) |
L920P |
probably damaging |
Het |
Sult2a1 |
T |
C |
7: 13,535,339 (GRCm39) |
Q238R |
probably benign |
Het |
Sult2a1 |
A |
T |
7: 13,535,360 (GRCm39) |
F231Y |
probably benign |
Het |
Sult2a1 |
T |
C |
7: 13,537,961 (GRCm39) |
I187M |
probably benign |
Het |
Sult2a6 |
T |
C |
7: 13,959,819 (GRCm39) |
Q238R |
probably benign |
Het |
Sycp2 |
C |
T |
2: 178,023,727 (GRCm39) |
V430I |
probably benign |
Het |
Sycp2 |
T |
G |
2: 178,016,160 (GRCm39) |
E767D |
probably benign |
Het |
Syna |
C |
T |
5: 134,587,383 (GRCm39) |
R522Q |
probably benign |
Het |
Syne4 |
C |
G |
7: 30,015,761 (GRCm39) |
S125C |
probably damaging |
Het |
Syngap1 |
A |
C |
17: 27,180,550 (GRCm39) |
D653A |
probably damaging |
Het |
Synm |
A |
C |
7: 67,401,634 (GRCm39) |
L285V |
probably damaging |
Het |
Synpo2l |
T |
G |
14: 20,716,035 (GRCm39) |
E183D |
probably damaging |
Het |
Syt10 |
C |
T |
15: 89,725,842 (GRCm39) |
G44D |
probably benign |
Het |
Szrd1 |
C |
A |
4: 140,845,898 (GRCm39) |
R99L |
probably damaging |
Het |
Taar9 |
G |
C |
10: 23,984,863 (GRCm39) |
C190W |
probably damaging |
Het |
Tab2 |
A |
T |
10: 7,796,030 (GRCm39) |
S77T |
possibly damaging |
Het |
Taf1a |
G |
T |
1: 183,185,614 (GRCm39) |
R291M |
possibly damaging |
Het |
Taf5l |
C |
A |
8: 124,724,077 (GRCm39) |
G581* |
probably null |
Het |
Tars1 |
G |
T |
15: 11,391,970 (GRCm39) |
P255H |
probably benign |
Het |
Tas1r2 |
C |
T |
4: 139,387,735 (GRCm39) |
A398V |
possibly damaging |
Het |
Tas2r109 |
T |
C |
6: 132,957,264 (GRCm39) |
Q222R |
probably benign |
Het |
Tas2r115 |
G |
T |
6: 132,714,044 (GRCm39) |
C302* |
probably null |
Het |
Tas2r116 |
A |
G |
6: 132,832,911 (GRCm39) |
N171D |
probably benign |
Het |
Tbc1d1 |
A |
G |
5: 64,432,736 (GRCm39) |
|
probably null |
Het |
Tbc1d13 |
T |
C |
2: 30,024,884 (GRCm39) |
|
probably null |
Het |
Tbc1d4 |
A |
C |
14: 101,689,859 (GRCm39) |
V1049G |
probably damaging |
Het |
Tbc1d5 |
C |
A |
17: 51,270,724 (GRCm39) |
R169I |
probably damaging |
Het |
Tbxa2r |
G |
C |
10: 81,169,049 (GRCm39) |
G246A |
probably damaging |
Het |
Tcaim |
A |
C |
9: 122,662,722 (GRCm39) |
K430T |
probably benign |
Het |
Tchh |
C |
T |
3: 93,352,989 (GRCm39) |
Q810* |
probably null |
Het |
Tcp10a |
G |
C |
17: 7,593,848 (GRCm39) |
A58P |
probably damaging |
Het |
Tctn1 |
C |
G |
5: 122,389,704 (GRCm39) |
A273P |
probably damaging |
Het |
Tctn3 |
A |
C |
19: 40,595,790 (GRCm39) |
F332V |
possibly damaging |
Het |
Tdrd6 |
T |
G |
17: 43,937,409 (GRCm39) |
E1213A |
probably benign |
Het |
Tead4 |
G |
C |
6: 128,247,867 (GRCm39) |
R57G |
probably damaging |
Het |
Teddm1a |
G |
A |
1: 153,767,772 (GRCm39) |
G79R |
probably benign |
Het |
Tekt5 |
G |
A |
16: 10,176,241 (GRCm39) |
R435W |
probably damaging |
Het |
Tenm1 |
G |
A |
X: 41,988,712 (GRCm39) |
P290S |
probably damaging |
Het |
Tenm2 |
C |
T |
11: 36,164,094 (GRCm39) |
A384T |
probably damaging |
Het |
Terf2 |
A |
G |
8: 107,807,855 (GRCm39) |
L240P |
probably damaging |
Het |
Tex13c2 |
A |
T |
X: 41,579,439 (GRCm39) |
S211C |
probably damaging |
Het |
Tex15 |
A |
C |
8: 34,061,343 (GRCm39) |
K532Q |
possibly damaging |
Het |
Tex15 |
A |
G |
8: 34,064,898 (GRCm39) |
N1443D |
probably benign |
Het |
Tex15 |
A |
G |
8: 34,061,838 (GRCm39) |
I697V |
possibly damaging |
Het |
Them6 |
G |
A |
15: 74,593,418 (GRCm39) |
R92H |
probably benign |
Het |
Thsd1 |
G |
A |
8: 22,742,235 (GRCm39) |
R301H |
probably damaging |
Het |
Thumpd3 |
C |
G |
6: 113,032,991 (GRCm39) |
T243S |
probably benign |
Het |
Tiam2 |
C |
T |
17: 3,465,294 (GRCm39) |
S341F |
probably benign |
Het |
Tie1 |
A |
G |
4: 118,341,626 (GRCm39) |
C229R |
probably damaging |
Het |
Timm44 |
C |
T |
8: 4,318,004 (GRCm39) |
E135K |
probably benign |
Het |
Tlr11 |
T |
G |
14: 50,599,795 (GRCm39) |
F594V |
possibly damaging |
Het |
Tlr4 |
G |
A |
4: 66,847,319 (GRCm39) |
D149N |
probably benign |
Het |
Tm9sf3 |
A |
G |
19: 41,220,817 (GRCm39) |
Y382H |
probably damaging |
Het |
Tm9sf5 |
A |
C |
X: 56,533,998 (GRCm39) |
I668L |
probably benign |
Het |
Tmc3 |
A |
C |
7: 83,252,676 (GRCm39) |
K359T |
probably damaging |
Het |
Tmem132a |
G |
A |
19: 10,836,299 (GRCm39) |
R744C |
probably damaging |
Het |
Tmem132c |
G |
A |
5: 127,581,985 (GRCm39) |
S400N |
probably benign |
Het |
Tmem198 |
C |
A |
1: 75,456,906 (GRCm39) |
Q11K |
probably benign |
Het |
Tmem219 |
G |
C |
7: 126,490,846 (GRCm39) |
P198A |
possibly damaging |
Het |
Tmem270 |
A |
C |
5: 134,935,510 (GRCm39) |
L15R |
probably damaging |
Het |
Tmem39a |
C |
A |
16: 38,396,140 (GRCm39) |
F124L |
possibly damaging |
Het |
Tmem39b |
C |
G |
4: 129,586,270 (GRCm39) |
A4P |
probably benign |
Het |
Tmem45b |
A |
G |
9: 31,339,323 (GRCm39) |
F131L |
probably damaging |
Het |
Tmppe |
G |
A |
9: 114,234,145 (GRCm39) |
R148H |
probably benign |
Het |
Tmprss4 |
T |
A |
9: 45,086,763 (GRCm39) |
N333Y |
probably damaging |
Het |
Tnni3k |
G |
C |
3: 154,645,307 (GRCm39) |
A526G |
probably damaging |
Het |
Tnpo1 |
C |
G |
13: 98,997,178 (GRCm39) |
G417A |
probably benign |
Het |
Tnpo3 |
C |
G |
6: 29,565,842 (GRCm39) |
G504A |
probably benign |
Het |
Tnr |
T |
C |
1: 159,722,665 (GRCm39) |
F1037L |
probably benign |
Het |
Tnrc6b |
C |
T |
15: 80,811,891 (GRCm39) |
R813* |
probably null |
Het |
Togaram2 |
A |
G |
17: 72,021,275 (GRCm39) |
K687R |
possibly damaging |
Het |
Tox |
C |
A |
4: 6,688,450 (GRCm39) |
R519M |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,144,781 (GRCm39) |
D656G |
probably damaging |
Het |
Trank1 |
G |
A |
9: 111,193,778 (GRCm39) |
D601N |
probably damaging |
Het |
Trav13d-4 |
C |
G |
14: 53,310,627 (GRCm39) |
T76S |
probably benign |
Het |
Trav16n |
C |
T |
14: 53,589,030 (GRCm39) |
A101V |
possibly damaging |
Het |
Trav5-4 |
A |
G |
14: 53,941,696 (GRCm39) |
E23G |
possibly damaging |
Het |
Trav8d-2 |
T |
G |
14: 53,280,265 (GRCm39) |
L85R |
probably damaging |
Het |
Tril |
G |
A |
6: 53,795,905 (GRCm39) |
T439M |
probably benign |
Het |
Trim30a |
C |
A |
7: 104,084,861 (GRCm39) |
W116C |
probably damaging |
Het |
Trim30b |
C |
A |
7: 104,015,307 (GRCm39) |
S27I |
probably damaging |
Het |
Trim42 |
T |
G |
9: 97,251,675 (GRCm39) |
N75H |
probably benign |
Het |
Trim43c |
A |
C |
9: 88,724,988 (GRCm39) |
|
probably null |
Het |
Trim45 |
A |
C |
3: 100,832,956 (GRCm39) |
E396D |
probably benign |
Het |
Trim5 |
C |
T |
7: 103,915,432 (GRCm39) |
A294T |
possibly damaging |
Het |
Trim67 |
A |
G |
8: 125,543,780 (GRCm39) |
Q380R |
probably damaging |
Het |
Triml1 |
T |
A |
8: 43,583,435 (GRCm39) |
I389F |
probably damaging |
Het |
Trip12 |
A |
C |
1: 84,743,889 (GRCm39) |
N500K |
probably damaging |
Het |
Trip4 |
G |
A |
9: 65,771,697 (GRCm39) |
R278* |
probably null |
Het |
Trp53bp1 |
T |
C |
2: 121,084,126 (GRCm39) |
K247E |
probably benign |
Het |
Trp63 |
G |
A |
16: 25,582,063 (GRCm39) |
R37K |
probably benign |
Het |
Trpm7 |
G |
T |
2: 126,639,201 (GRCm39) |
A1711E |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,771,007 (GRCm39) |
K2802R |
probably benign |
Het |
Tspan5 |
G |
C |
3: 138,604,087 (GRCm39) |
W228C |
possibly damaging |
Het |
Tssk4 |
A |
G |
14: 55,888,380 (GRCm39) |
K83R |
probably damaging |
Het |
Ttbk1 |
C |
A |
17: 46,757,251 (GRCm39) |
A1128S |
probably benign |
Het |
Ttc16 |
C |
A |
2: 32,659,345 (GRCm39) |
L251F |
probably damaging |
Het |
Ttc23l |
C |
A |
15: 10,533,753 (GRCm39) |
R263S |
probably damaging |
Het |
Ttc28 |
G |
C |
5: 111,434,181 (GRCm39) |
G2405A |
probably benign |
Het |
Ttc39c |
G |
T |
18: 12,820,020 (GRCm39) |
M15I |
possibly damaging |
Het |
Ttll1 |
C |
T |
15: 83,382,390 (GRCm39) |
V201I |
probably damaging |
Het |
Ttll12 |
T |
C |
15: 83,466,279 (GRCm39) |
Q394R |
probably damaging |
Het |
Ttll2 |
T |
G |
17: 7,618,925 (GRCm39) |
D334A |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,678,669 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
G |
2: 76,617,613 (GRCm39) |
K14540T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,582,863 (GRCm39) |
W20931R |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,582,574 (GRCm39) |
A14446E |
probably damaging |
Het |
Ttn |
C |
G |
2: 76,577,295 (GRCm39) |
E24533Q |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,569,031 (GRCm39) |
E25541D |
possibly damaging |
Het |
Tubal3 |
A |
C |
13: 3,983,511 (GRCm39) |
E430D |
probably benign |
Het |
Tubb3 |
G |
C |
8: 124,148,273 (GRCm39) |
G402A |
probably damaging |
Het |
Tubd1 |
A |
T |
11: 86,445,993 (GRCm39) |
K211M |
probably damaging |
Het |
Tubd1 |
G |
A |
11: 86,440,296 (GRCm39) |
G107S |
probably damaging |
Het |
Tubgcp5 |
G |
A |
7: 55,464,849 (GRCm39) |
G577S |
probably benign |
Het |
Tulp2 |
A |
C |
7: 45,171,410 (GRCm39) |
K404T |
probably damaging |
Het |
Tyro3 |
T |
G |
2: 119,639,948 (GRCm39) |
I377S |
probably benign |
Het |
Ube4b |
A |
G |
4: 149,419,582 (GRCm39) |
I1042T |
possibly damaging |
Het |
Ubl4b |
T |
G |
3: 107,461,719 (GRCm39) |
E180D |
unknown |
Het |
Ubqln5 |
T |
A |
7: 103,778,178 (GRCm39) |
K215N |
possibly damaging |
Het |
Ubqlnl |
A |
G |
7: 103,799,200 (GRCm39) |
V99A |
probably damaging |
Het |
Ubr3 |
A |
G |
2: 69,752,711 (GRCm39) |
T322A |
probably benign |
Het |
Uggt1 |
A |
C |
1: 36,213,272 (GRCm39) |
F861C |
probably damaging |
Het |
Ugt1a10 |
T |
C |
1: 87,983,564 (GRCm39) |
F121L |
probably benign |
Het |
Umps |
CCTGACTGA |
CCTGA |
16: 33,787,195 (GRCm39) |
|
probably null |
Het |
Unc13a |
C |
A |
8: 72,107,447 (GRCm39) |
|
probably null |
Het |
Unc5c |
T |
G |
3: 141,439,661 (GRCm39) |
L111V |
probably damaging |
Het |
Unc79 |
C |
A |
12: 102,987,271 (GRCm39) |
H187N |
probably damaging |
Het |
Unc80 |
C |
G |
1: 66,685,610 (GRCm39) |
P2245A |
possibly damaging |
Het |
Ush2a |
T |
C |
1: 188,644,180 (GRCm39) |
L4514P |
probably benign |
Het |
Ush2a |
A |
C |
1: 188,679,201 (GRCm39) |
N4803T |
probably benign |
Het |
Usp17lb |
G |
A |
7: 104,490,336 (GRCm39) |
P197L |
probably benign |
Het |
Usp43 |
C |
A |
11: 67,746,866 (GRCm39) |
R942L |
probably benign |
Het |
Usp51 |
C |
T |
X: 151,791,218 (GRCm39) |
P271S |
probably benign |
Het |
Usp51 |
C |
T |
X: 151,791,219 (GRCm39) |
P271L |
probably benign |
Het |
Vmn1r12 |
T |
G |
6: 57,135,966 (GRCm39) |
L21R |
probably damaging |
Het |
Vmn1r176 |
C |
T |
7: 23,534,598 (GRCm39) |
R185H |
probably benign |
Het |
Vmn1r179 |
A |
G |
7: 23,627,907 (GRCm39) |
I33V |
probably benign |
Het |
Vmn1r188 |
T |
C |
13: 22,272,450 (GRCm39) |
W135R |
probably damaging |
Het |
Vmn1r212 |
A |
C |
13: 23,067,932 (GRCm39) |
F134V |
probably damaging |
Het |
Vmn1r229 |
C |
A |
17: 21,035,327 (GRCm39) |
L191M |
probably damaging |
Het |
Vmn1r232 |
C |
A |
17: 21,134,100 (GRCm39) |
V167F |
probably benign |
Het |
Vmn1r4 |
G |
A |
6: 56,934,050 (GRCm39) |
V185M |
possibly damaging |
Het |
Vmn1r46 |
A |
G |
6: 89,953,723 (GRCm39) |
R191G |
probably damaging |
Het |
Vmn1r72 |
T |
G |
7: 11,404,100 (GRCm39) |
N116T |
probably benign |
Het |
Vmn1r78 |
A |
C |
7: 11,886,641 (GRCm39) |
K84T |
probably damaging |
Het |
Vmn2r10 |
A |
G |
5: 109,143,979 (GRCm39) |
F657S |
probably damaging |
Het |
Vmn2r101 |
C |
A |
17: 19,809,237 (GRCm39) |
A122D |
possibly damaging |
Het |
Vmn2r103 |
C |
A |
17: 20,015,309 (GRCm39) |
S483Y |
probably benign |
Het |
Vmn2r108 |
C |
T |
17: 20,691,375 (GRCm39) |
V383M |
probably benign |
Het |
Vmn2r110 |
T |
G |
17: 20,803,942 (GRCm39) |
H211P |
probably damaging |
Het |
Vmn2r112 |
C |
G |
17: 22,824,059 (GRCm39) |
S438C |
possibly damaging |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Vmn2r12 |
G |
T |
5: 109,240,646 (GRCm39) |
H156N |
probably benign |
Het |
Vmn2r16 |
TA |
T |
5: 109,511,779 (GRCm39) |
|
probably null |
Het |
Vmn2r16 |
A |
C |
5: 109,488,381 (GRCm39) |
Q418P |
probably benign |
Het |
Vmn2r19 |
T |
G |
6: 123,285,298 (GRCm39) |
L3V |
probably benign |
Het |
Vmn2r23 |
A |
C |
6: 123,719,067 (GRCm39) |
T807P |
probably damaging |
Het |
Vmn2r24 |
A |
C |
6: 123,781,155 (GRCm39) |
S454R |
probably benign |
Het |
Vmn2r45 |
T |
A |
7: 8,474,484 (GRCm39) |
E848V |
probably benign |
Het |
Vmn2r5 |
T |
G |
3: 64,416,963 (GRCm39) |
N65T |
probably benign |
Het |
Vmn2r50 |
G |
C |
7: 9,771,427 (GRCm39) |
T758R |
possibly damaging |
Het |
Vmn2r50 |
G |
T |
7: 9,780,086 (GRCm39) |
L432I |
probably benign |
Het |
Vmn2r59 |
G |
T |
7: 41,661,838 (GRCm39) |
A659E |
possibly damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,949,388 (GRCm39) |
T603A |
possibly damaging |
Het |
Vmn2r63 |
G |
A |
7: 42,577,983 (GRCm39) |
T185I |
probably benign |
Het |
Vmn2r65 |
C |
A |
7: 84,592,473 (GRCm39) |
|
probably null |
Het |
Vmn2r70 |
A |
C |
7: 85,213,968 (GRCm39) |
L395V |
possibly damaging |
Het |
Vmn2r79 |
T |
G |
7: 86,651,549 (GRCm39) |
F316C |
probably damaging |
Het |
Vmn2r8 |
A |
C |
5: 108,949,864 (GRCm39) |
F328V |
probably damaging |
Het |
Vmn2r82 |
T |
G |
10: 79,192,456 (GRCm39) |
F11C |
probably damaging |
Het |
Vmn2r87 |
C |
A |
10: 130,308,183 (GRCm39) |
R685M |
probably damaging |
Het |
Vmn2r90 |
C |
A |
17: 17,953,879 (GRCm39) |
A681E |
probably damaging |
Het |
Vmn2r93 |
A |
C |
17: 18,546,665 (GRCm39) |
K846Q |
probably damaging |
Het |
Vmn2r95 |
C |
A |
17: 18,660,663 (GRCm39) |
F358L |
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,817,628 (GRCm39) |
L594I |
possibly damaging |
Het |
Vmn2r99 |
C |
A |
17: 19,599,563 (GRCm39) |
Q416K |
probably benign |
Het |
Vmo1 |
T |
A |
11: 70,404,643 (GRCm39) |
L119F |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,821,257 (GRCm39) |
S1256P |
probably damaging |
Het |
Vwa8 |
C |
T |
14: 79,219,686 (GRCm39) |
A478V |
probably benign |
Het |
Washc4 |
C |
G |
10: 83,412,605 (GRCm39) |
A749G |
probably benign |
Het |
Wbp2 |
T |
A |
11: 115,977,739 (GRCm39) |
K5* |
probably null |
Het |
Wdcp |
A |
C |
12: 4,900,825 (GRCm39) |
K227T |
probably damaging |
Het |
Wdr13 |
A |
C |
X: 7,991,861 (GRCm39) |
F369V |
probably damaging |
Het |
Wdr13 |
C |
A |
X: 7,991,863 (GRCm39) |
S460I |
probably damaging |
Het |
Wdr3 |
T |
G |
3: 100,051,660 (GRCm39) |
K663T |
probably benign |
Het |
Wdr36 |
T |
G |
18: 32,999,065 (GRCm39) |
|
probably null |
Het |
Wdr53 |
T |
A |
16: 32,071,116 (GRCm39) |
S154T |
probably damaging |
Het |
Wdr5b |
G |
A |
16: 35,862,813 (GRCm39) |
A311T |
probably damaging |
Het |
Wdr64 |
A |
T |
1: 175,533,551 (GRCm39) |
Q62H |
possibly damaging |
Het |
Wdr82 |
A |
C |
9: 106,061,999 (GRCm39) |
I221L |
probably benign |
Het |
Wnt5a |
C |
T |
14: 28,244,685 (GRCm39) |
R311C |
probably damaging |
Het |
Wrap53 |
G |
A |
11: 69,469,324 (GRCm39) |
S144F |
probably damaging |
Het |
Wsb2 |
C |
A |
5: 117,515,571 (GRCm39) |
P392Q |
probably damaging |
Het |
Wwc1 |
T |
G |
11: 35,774,309 (GRCm39) |
N317T |
possibly damaging |
Het |
Wwp2 |
G |
A |
8: 108,281,719 (GRCm39) |
E303K |
probably damaging |
Het |
Xdh |
C |
T |
17: 74,193,423 (GRCm39) |
S1291N |
probably benign |
Het |
Xirp1 |
T |
G |
9: 120,016,907 (GRCm38) |
Q970P |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,343,665 (GRCm39) |
T1969A |
probably benign |
Het |
Xpot |
A |
C |
10: 121,437,228 (GRCm39) |
I830S |
probably damaging |
Het |
Xylb |
T |
A |
9: 119,210,680 (GRCm39) |
L388M |
probably benign |
Het |
Yju2b |
G |
A |
8: 84,985,538 (GRCm39) |
R244* |
probably null |
Het |
Ylpm1 |
G |
A |
12: 85,076,929 (GRCm39) |
R760K |
possibly damaging |
Het |
Zbtb34 |
C |
G |
2: 33,301,120 (GRCm39) |
E474Q |
probably damaging |
Het |
Zc3h12b |
A |
C |
X: 94,943,048 (GRCm39) |
K116T |
probably damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,781,327 (GRCm39) |
|
probably null |
Het |
Zfat |
G |
A |
15: 68,058,950 (GRCm39) |
A195V |
probably benign |
Het |
Zfhx2 |
T |
G |
14: 55,311,637 (GRCm39) |
Q352H |
possibly damaging |
Het |
Zfhx3 |
A |
C |
8: 109,677,989 (GRCm39) |
K3013T |
possibly damaging |
Het |
Zfp106 |
G |
T |
2: 120,360,971 (GRCm39) |
L1047I |
probably damaging |
Het |
Zfp109 |
A |
G |
7: 23,928,360 (GRCm39) |
F358L |
probably benign |
Het |
Zfp157 |
T |
C |
5: 138,455,461 (GRCm39) |
L553P |
probably damaging |
Het |
Zfp273 |
A |
T |
13: 67,973,513 (GRCm39) |
I214F |
possibly damaging |
Het |
Zfp326 |
T |
A |
5: 106,036,496 (GRCm39) |
Y136N |
probably damaging |
Het |
Zfp386 |
G |
A |
12: 116,018,393 (GRCm39) |
E21K |
possibly damaging |
Het |
Zfp42 |
C |
G |
8: 43,748,842 (GRCm39) |
V220L |
probably benign |
Het |
Zfp507 |
C |
G |
7: 35,493,702 (GRCm39) |
S447T |
possibly damaging |
Het |
Zfp518b |
C |
A |
5: 38,831,636 (GRCm39) |
S123I |
probably damaging |
Het |
Zfp541 |
A |
C |
7: 15,813,720 (GRCm39) |
K791T |
probably benign |
Het |
Zfp553 |
G |
T |
7: 126,834,670 (GRCm39) |
G75V |
probably damaging |
Het |
Zfp57 |
T |
C |
17: 37,321,030 (GRCm39) |
F295L |
probably damaging |
Het |
Zfp593 |
G |
C |
4: 133,972,753 (GRCm39) |
A21G |
probably benign |
Het |
Zfp598 |
CCAT |
CCATCAT |
17: 24,899,184 (GRCm39) |
|
probably benign |
Het |
Zfp638 |
A |
C |
6: 83,921,793 (GRCm39) |
K640T |
probably damaging |
Het |
Zfp648 |
T |
C |
1: 154,080,266 (GRCm39) |
F142L |
probably benign |
Het |
Zfp729b |
C |
T |
13: 67,741,189 (GRCm39) |
E359K |
possibly damaging |
Het |
Zfp775 |
G |
A |
6: 48,597,622 (GRCm39) |
E499K |
probably damaging |
Het |
Zfp868 |
TTAT |
TT |
8: 70,064,561 (GRCm39) |
|
probably null |
Het |
Zfp959 |
A |
G |
17: 56,205,135 (GRCm39) |
R391G |
probably damaging |
Het |
Zfp976 |
T |
G |
7: 42,262,184 (GRCm39) |
E551A |
possibly damaging |
Het |
Zfp997 |
A |
G |
13: 66,270,208 (GRCm39) |
K458R |
probably damaging |
Het |
Zfp998 |
A |
C |
13: 66,579,245 (GRCm39) |
C413G |
probably damaging |
Het |
Zfp998 |
C |
T |
13: 66,579,800 (GRCm39) |
G228S |
probably benign |
Het |
Zfp999 |
C |
A |
13: 66,375,170 (GRCm39) |
S73I |
probably benign |
Het |
Zfx |
A |
C |
X: 93,123,049 (GRCm39) |
L585V |
probably damaging |
Het |
Zglp1 |
C |
T |
9: 20,978,296 (GRCm39) |
R27Q |
possibly damaging |
Het |
Zhx3 |
GGAAG |
GG |
2: 160,621,675 (GRCm39) |
|
probably benign |
Het |
Zic2 |
A |
T |
14: 122,716,087 (GRCm39) |
H403L |
probably damaging |
Het |
Zim1 |
T |
G |
7: 6,680,658 (GRCm39) |
N335T |
possibly damaging |
Het |
Zkscan3 |
T |
C |
13: 21,572,735 (GRCm39) |
K299R |
possibly damaging |
Het |
Zkscan4 |
T |
G |
13: 21,668,067 (GRCm39) |
L173V |
probably damaging |
Het |
Zmiz2 |
A |
T |
11: 6,349,603 (GRCm39) |
H421L |
probably damaging |
Het |
Zmynd15 |
A |
C |
11: 70,351,961 (GRCm39) |
K60T |
possibly damaging |
Het |
Zmynd8 |
A |
C |
2: 165,670,091 (GRCm39) |
L481R |
probably benign |
Het |
Zpbp |
C |
A |
11: 11,358,568 (GRCm39) |
R233L |
probably damaging |
Het |
Zscan18 |
G |
T |
7: 12,508,994 (GRCm39) |
Q169K |
probably benign |
Het |
Zscan18 |
G |
A |
7: 12,509,020 (GRCm39) |
|
probably benign |
Het |
Zscan26 |
T |
G |
13: 21,629,633 (GRCm39) |
K290T |
probably damaging |
Het |
|