Other mutations in this stock |
Total: 130 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930555F03Rik |
A |
T |
8: 49,953,527 (GRCm39) |
|
noncoding transcript |
Het |
A630073D07Rik |
T |
C |
6: 132,603,700 (GRCm39) |
|
probably benign |
Het |
Abca16 |
G |
A |
7: 120,032,834 (GRCm39) |
|
probably benign |
Het |
Abca5 |
A |
T |
11: 110,170,515 (GRCm39) |
D1265E |
probably damaging |
Het |
Abcf1 |
C |
T |
17: 36,272,079 (GRCm39) |
V312I |
probably benign |
Het |
Abhd12 |
T |
A |
2: 150,688,285 (GRCm39) |
|
probably null |
Het |
Adam23 |
A |
G |
1: 63,582,306 (GRCm39) |
H318R |
probably benign |
Het |
Adcy2 |
T |
A |
13: 68,826,725 (GRCm39) |
K660* |
probably null |
Het |
Adgrf3 |
T |
C |
5: 30,400,078 (GRCm39) |
T972A |
probably benign |
Het |
Adipoq |
T |
A |
16: 22,974,160 (GRCm39) |
D62E |
probably damaging |
Het |
Alk |
G |
T |
17: 72,910,578 (GRCm39) |
P43T |
probably damaging |
Het |
Arap2 |
AT |
ATT |
5: 62,807,250 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
G |
T |
13: 98,106,863 (GRCm39) |
T687K |
probably benign |
Het |
Arrb1 |
T |
C |
7: 99,243,884 (GRCm39) |
L278P |
probably damaging |
Het |
Atad2b |
C |
A |
12: 4,987,401 (GRCm39) |
D76E |
probably benign |
Het |
Atm |
A |
T |
9: 53,370,241 (GRCm39) |
Y2290* |
probably null |
Het |
Atrn |
T |
A |
2: 130,837,005 (GRCm39) |
|
probably null |
Het |
Bpifb1 |
A |
G |
2: 154,054,867 (GRCm39) |
D253G |
possibly damaging |
Het |
Bpifb9b |
C |
T |
2: 154,161,545 (GRCm39) |
T559M |
probably benign |
Het |
Bsn |
T |
C |
9: 107,984,439 (GRCm39) |
E3205G |
unknown |
Het |
Cacna1c |
T |
C |
6: 118,579,174 (GRCm39) |
Y1599C |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,133,630 (GRCm39) |
D590G |
probably damaging |
Het |
Ccdc68 |
A |
G |
18: 70,079,623 (GRCm39) |
|
probably null |
Het |
Ccdc97 |
G |
A |
7: 25,413,845 (GRCm39) |
R279C |
probably damaging |
Het |
Ccm2l |
A |
G |
2: 152,912,820 (GRCm39) |
T120A |
probably damaging |
Het |
Cfh |
A |
G |
1: 140,028,621 (GRCm39) |
S1043P |
probably benign |
Het |
Chil3 |
T |
C |
3: 106,063,072 (GRCm39) |
K173E |
probably benign |
Het |
Cib2 |
T |
C |
9: 54,461,780 (GRCm39) |
D26G |
possibly damaging |
Het |
Col24a1 |
T |
C |
3: 145,019,881 (GRCm39) |
V84A |
probably damaging |
Het |
Csn3 |
T |
C |
5: 88,077,730 (GRCm39) |
Y79H |
probably benign |
Het |
Ddx47 |
T |
A |
6: 134,994,085 (GRCm39) |
V149E |
probably damaging |
Het |
Dennd5b |
A |
T |
6: 148,934,760 (GRCm39) |
|
probably benign |
Het |
Desi1 |
T |
C |
15: 81,882,399 (GRCm39) |
N109D |
probably damaging |
Het |
Fam13c |
T |
C |
10: 70,372,182 (GRCm39) |
|
probably benign |
Het |
Fam234a |
A |
T |
17: 26,435,591 (GRCm39) |
D264E |
probably benign |
Het |
Fanca |
A |
G |
8: 124,014,809 (GRCm39) |
F831S |
probably damaging |
Het |
Fancm |
C |
T |
12: 65,144,091 (GRCm39) |
R518* |
probably null |
Het |
Fat2 |
A |
G |
11: 55,202,669 (GRCm39) |
V135A |
possibly damaging |
Het |
Fbxl17 |
A |
C |
17: 63,691,987 (GRCm39) |
F42V |
probably damaging |
Het |
Fgd3 |
A |
T |
13: 49,418,173 (GRCm39) |
V631E |
possibly damaging |
Het |
Fhod3 |
G |
A |
18: 25,245,736 (GRCm39) |
|
probably benign |
Het |
Focad |
T |
C |
4: 88,039,525 (GRCm39) |
|
probably benign |
Het |
Foxn4 |
C |
A |
5: 114,399,129 (GRCm39) |
|
probably benign |
Het |
Gm2381 |
A |
T |
7: 42,469,402 (GRCm39) |
C241S |
probably damaging |
Het |
Gm6483 |
T |
G |
8: 19,743,725 (GRCm39) |
F117V |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,481,295 (GRCm39) |
|
probably benign |
Het |
Hecw1 |
T |
A |
13: 14,455,027 (GRCm39) |
Q676L |
probably benign |
Het |
Hipk2 |
G |
A |
6: 38,724,420 (GRCm39) |
R437C |
possibly damaging |
Het |
Ifnar1 |
T |
C |
16: 91,298,570 (GRCm39) |
Y396H |
probably damaging |
Het |
Ints5 |
A |
T |
19: 8,873,383 (GRCm39) |
K447N |
probably damaging |
Het |
Iqsec1 |
T |
C |
6: 90,666,952 (GRCm39) |
Y495C |
probably damaging |
Het |
Itga5 |
C |
T |
15: 103,264,742 (GRCm39) |
|
probably null |
Het |
Kcnk4 |
T |
A |
19: 6,905,528 (GRCm39) |
|
probably benign |
Het |
Kmo |
A |
G |
1: 175,474,756 (GRCm39) |
T174A |
possibly damaging |
Het |
Krt36 |
T |
C |
11: 99,993,101 (GRCm39) |
D458G |
probably damaging |
Het |
Krtap16-1 |
G |
T |
11: 99,877,321 (GRCm39) |
P28T |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,552,315 (GRCm39) |
|
probably null |
Het |
Lrrc9 |
T |
C |
12: 72,529,788 (GRCm39) |
S920P |
probably damaging |
Het |
Lrrk2 |
A |
T |
15: 91,636,481 (GRCm39) |
Y1485F |
probably benign |
Het |
Mical1 |
C |
T |
10: 41,357,311 (GRCm39) |
A372V |
probably damaging |
Het |
Ms4a20 |
C |
A |
19: 11,089,764 (GRCm39) |
L40F |
probably damaging |
Het |
Mtr |
C |
T |
13: 12,236,318 (GRCm39) |
R636Q |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,570,925 (GRCm39) |
T662S |
possibly damaging |
Het |
Myo10 |
G |
A |
15: 25,738,091 (GRCm39) |
V546M |
probably damaging |
Het |
Nbeal1 |
G |
A |
1: 60,320,991 (GRCm39) |
W2034* |
probably null |
Het |
Nhlrc3 |
T |
C |
3: 53,366,044 (GRCm39) |
T150A |
probably damaging |
Het |
Nicol1 |
T |
C |
5: 34,140,896 (GRCm39) |
|
probably benign |
Het |
Nkx2-1 |
T |
C |
12: 56,581,640 (GRCm39) |
H69R |
possibly damaging |
Het |
Nlrp4g |
A |
T |
9: 124,349,540 (GRCm38) |
|
noncoding transcript |
Het |
Nod2 |
A |
G |
8: 89,379,859 (GRCm39) |
N120S |
probably benign |
Het |
Nol8 |
T |
C |
13: 49,807,921 (GRCm39) |
F46L |
possibly damaging |
Het |
Ntrk1 |
T |
C |
3: 87,691,240 (GRCm39) |
D308G |
possibly damaging |
Het |
Oog3 |
A |
T |
4: 143,886,784 (GRCm39) |
V112D |
probably benign |
Het |
Or10ag58 |
A |
G |
2: 87,265,005 (GRCm39) |
D58G |
probably damaging |
Het |
Or4a66 |
A |
G |
2: 88,531,040 (GRCm39) |
V211A |
probably damaging |
Het |
Or51i1 |
A |
T |
7: 103,671,196 (GRCm39) |
S110T |
probably damaging |
Het |
Or5af2 |
T |
C |
11: 58,707,975 (GRCm39) |
V47A |
probably damaging |
Het |
Or5b106 |
T |
C |
19: 13,123,727 (GRCm39) |
M99V |
probably benign |
Het |
Or5b120 |
C |
A |
19: 13,479,900 (GRCm39) |
N64K |
probably damaging |
Het |
Or5m9b |
A |
G |
2: 85,905,485 (GRCm39) |
M134V |
probably benign |
Het |
Or9s18 |
A |
T |
13: 65,300,692 (GRCm39) |
Y218F |
possibly damaging |
Het |
Pakap |
T |
C |
4: 57,829,434 (GRCm39) |
|
probably benign |
Het |
Pcdhb8 |
C |
T |
18: 37,490,100 (GRCm39) |
R593C |
probably benign |
Het |
Pgm3 |
A |
G |
9: 86,438,243 (GRCm39) |
|
probably null |
Het |
Pirt |
T |
A |
11: 66,816,998 (GRCm39) |
V103E |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,635,230 (GRCm39) |
D1332V |
probably damaging |
Het |
Ppfia4 |
A |
T |
1: 134,256,518 (GRCm39) |
V122E |
probably damaging |
Het |
Pramel14 |
A |
G |
4: 143,720,088 (GRCm39) |
|
probably benign |
Het |
Prmt2 |
C |
T |
10: 76,044,517 (GRCm39) |
|
probably benign |
Het |
Prrc2a |
G |
T |
17: 35,372,536 (GRCm39) |
P1702T |
probably damaging |
Het |
Prss39 |
A |
T |
1: 34,539,279 (GRCm39) |
H173L |
probably damaging |
Het |
Rabl6 |
A |
G |
2: 25,476,878 (GRCm39) |
|
probably null |
Het |
Rb1cc1 |
T |
A |
1: 6,319,014 (GRCm39) |
I794K |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,125,535 (GRCm39) |
D2716G |
probably damaging |
Het |
Sbf2 |
ACC |
AC |
7: 109,929,890 (GRCm39) |
|
probably null |
Het |
Sema6d |
T |
A |
2: 124,502,665 (GRCm39) |
F583L |
possibly damaging |
Het |
Setx |
T |
A |
2: 29,036,819 (GRCm39) |
H1101Q |
possibly damaging |
Het |
Sis |
A |
G |
3: 72,872,938 (GRCm39) |
C67R |
probably damaging |
Het |
Skint1 |
T |
A |
4: 111,886,596 (GRCm39) |
|
probably benign |
Het |
Smg6 |
C |
A |
11: 75,053,757 (GRCm39) |
T1413K |
probably benign |
Het |
Spata31d1a |
A |
T |
13: 59,850,073 (GRCm39) |
I685N |
possibly damaging |
Het |
Spef2 |
T |
A |
15: 9,592,844 (GRCm39) |
N1499I |
probably damaging |
Het |
Stk11ip |
T |
A |
1: 75,508,932 (GRCm39) |
|
probably null |
Het |
Stxbp1 |
A |
C |
2: 32,692,795 (GRCm39) |
I407S |
probably damaging |
Het |
Svil |
T |
C |
18: 5,117,002 (GRCm39) |
S2059P |
probably damaging |
Het |
Syne1 |
C |
T |
10: 5,300,933 (GRCm39) |
V932M |
probably damaging |
Het |
Tacc1 |
A |
C |
8: 25,668,020 (GRCm39) |
|
probably benign |
Het |
Tbc1d13 |
C |
A |
2: 30,025,576 (GRCm39) |
|
probably benign |
Het |
Tbc1d15 |
A |
C |
10: 115,075,204 (GRCm39) |
D59E |
probably damaging |
Het |
Tcaf2 |
A |
G |
6: 42,619,445 (GRCm39) |
F194S |
probably damaging |
Het |
Terf2ip |
T |
A |
8: 112,738,127 (GRCm39) |
M5K |
probably benign |
Het |
Tgfbr2 |
A |
T |
9: 115,987,388 (GRCm39) |
D40E |
probably benign |
Het |
Tm4sf5 |
T |
A |
11: 70,401,495 (GRCm39) |
S165T |
probably damaging |
Het |
Tmprss3 |
A |
T |
17: 31,412,886 (GRCm39) |
C129S |
probably damaging |
Het |
Tmx2 |
T |
C |
2: 84,502,740 (GRCm39) |
D256G |
probably benign |
Het |
Tnr |
A |
G |
1: 159,695,673 (GRCm39) |
D532G |
probably damaging |
Het |
Tnrc18 |
T |
A |
5: 142,762,494 (GRCm39) |
H465L |
unknown |
Het |
Togaram2 |
A |
T |
17: 72,007,504 (GRCm39) |
Q350L |
possibly damaging |
Het |
Topaz1 |
G |
A |
9: 122,578,971 (GRCm39) |
C627Y |
possibly damaging |
Het |
Tpx2 |
A |
T |
2: 152,715,058 (GRCm39) |
Q93L |
probably benign |
Het |
Trim54 |
T |
C |
5: 31,293,526 (GRCm39) |
|
probably null |
Het |
Troap |
T |
A |
15: 98,980,541 (GRCm39) |
C574S |
probably damaging |
Het |
Tut7 |
A |
T |
13: 59,964,669 (GRCm39) |
|
probably null |
Het |
Ubr4 |
T |
C |
4: 139,206,373 (GRCm39) |
|
probably null |
Het |
Vmn2r51 |
A |
G |
7: 9,834,396 (GRCm39) |
V214A |
possibly damaging |
Het |
Vmn2r66 |
A |
T |
7: 84,644,484 (GRCm39) |
M642K |
probably benign |
Het |
Vwa5a |
T |
A |
9: 38,635,191 (GRCm39) |
I232N |
probably damaging |
Het |
Zfp820 |
A |
T |
17: 22,038,685 (GRCm39) |
S214R |
probably damaging |
Het |
Zfp955b |
A |
T |
17: 33,524,437 (GRCm39) |
S43R |
probably damaging |
Het |
Zgrf1 |
C |
T |
3: 127,381,687 (GRCm39) |
T1162M |
probably benign |
Het |
|
Other mutations in Cfap54 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Cfap54
|
APN |
10 |
92,917,385 (GRCm39) |
missense |
unknown |
|
IGL02034:Cfap54
|
APN |
10 |
92,897,347 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02082:Cfap54
|
APN |
10 |
92,917,320 (GRCm39) |
missense |
unknown |
|
IGL02434:Cfap54
|
APN |
10 |
92,902,616 (GRCm39) |
missense |
probably benign |
0.20 |
R0011:Cfap54
|
UTSW |
10 |
92,901,087 (GRCm39) |
missense |
probably damaging |
0.97 |
R0011:Cfap54
|
UTSW |
10 |
92,901,087 (GRCm39) |
missense |
probably damaging |
0.97 |
R0032:Cfap54
|
UTSW |
10 |
92,768,559 (GRCm39) |
missense |
probably benign |
0.04 |
R0032:Cfap54
|
UTSW |
10 |
92,768,559 (GRCm39) |
missense |
probably benign |
0.04 |
R0040:Cfap54
|
UTSW |
10 |
92,812,901 (GRCm39) |
missense |
probably benign |
0.33 |
R0044:Cfap54
|
UTSW |
10 |
92,871,295 (GRCm39) |
missense |
probably null |
0.46 |
R0086:Cfap54
|
UTSW |
10 |
92,864,456 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0104:Cfap54
|
UTSW |
10 |
92,864,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Cfap54
|
UTSW |
10 |
92,870,524 (GRCm39) |
unclassified |
probably benign |
|
R0234:Cfap54
|
UTSW |
10 |
92,735,022 (GRCm39) |
nonsense |
probably null |
|
R0308:Cfap54
|
UTSW |
10 |
92,721,226 (GRCm39) |
missense |
unknown |
|
R0332:Cfap54
|
UTSW |
10 |
92,871,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0409:Cfap54
|
UTSW |
10 |
92,612,075 (GRCm39) |
missense |
probably benign |
0.00 |
R0433:Cfap54
|
UTSW |
10 |
92,814,942 (GRCm39) |
splice site |
probably benign |
|
R0436:Cfap54
|
UTSW |
10 |
92,874,837 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0463:Cfap54
|
UTSW |
10 |
92,710,805 (GRCm39) |
critical splice donor site |
probably null |
|
R0523:Cfap54
|
UTSW |
10 |
92,744,745 (GRCm39) |
utr 3 prime |
probably benign |
|
R0551:Cfap54
|
UTSW |
10 |
92,860,984 (GRCm39) |
missense |
probably benign |
0.35 |
R0595:Cfap54
|
UTSW |
10 |
92,720,598 (GRCm39) |
missense |
unknown |
|
R0632:Cfap54
|
UTSW |
10 |
92,720,958 (GRCm39) |
missense |
unknown |
|
R0730:Cfap54
|
UTSW |
10 |
92,870,599 (GRCm39) |
missense |
probably benign |
0.05 |
R0786:Cfap54
|
UTSW |
10 |
92,803,397 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0883:Cfap54
|
UTSW |
10 |
92,706,531 (GRCm39) |
missense |
unknown |
|
R1004:Cfap54
|
UTSW |
10 |
92,902,558 (GRCm39) |
splice site |
probably benign |
|
R1033:Cfap54
|
UTSW |
10 |
92,675,311 (GRCm39) |
missense |
probably benign |
0.07 |
R1168:Cfap54
|
UTSW |
10 |
92,773,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Cfap54
|
UTSW |
10 |
92,711,856 (GRCm39) |
missense |
unknown |
|
R1429:Cfap54
|
UTSW |
10 |
92,656,900 (GRCm39) |
missense |
probably benign |
0.01 |
R1443:Cfap54
|
UTSW |
10 |
92,768,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cfap54
|
UTSW |
10 |
92,805,625 (GRCm39) |
missense |
probably benign |
0.01 |
R1467:Cfap54
|
UTSW |
10 |
92,805,625 (GRCm39) |
missense |
probably benign |
0.01 |
R1557:Cfap54
|
UTSW |
10 |
92,820,089 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1687:Cfap54
|
UTSW |
10 |
92,768,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R1690:Cfap54
|
UTSW |
10 |
92,871,304 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1711:Cfap54
|
UTSW |
10 |
92,846,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Cfap54
|
UTSW |
10 |
92,883,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Cfap54
|
UTSW |
10 |
92,740,125 (GRCm39) |
critical splice donor site |
probably null |
|
R1835:Cfap54
|
UTSW |
10 |
92,798,237 (GRCm39) |
missense |
probably benign |
0.35 |
R1889:Cfap54
|
UTSW |
10 |
92,870,572 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1915:Cfap54
|
UTSW |
10 |
92,720,564 (GRCm39) |
missense |
unknown |
|
R1958:Cfap54
|
UTSW |
10 |
92,833,204 (GRCm39) |
missense |
probably benign |
0.18 |
R2005:Cfap54
|
UTSW |
10 |
92,720,630 (GRCm39) |
missense |
unknown |
|
R2018:Cfap54
|
UTSW |
10 |
92,852,466 (GRCm39) |
missense |
probably benign |
0.00 |
R2045:Cfap54
|
UTSW |
10 |
92,874,671 (GRCm39) |
splice site |
probably null |
|
R2059:Cfap54
|
UTSW |
10 |
92,778,841 (GRCm39) |
unclassified |
probably benign |
|
R2100:Cfap54
|
UTSW |
10 |
92,837,799 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2110:Cfap54
|
UTSW |
10 |
92,722,229 (GRCm39) |
missense |
unknown |
|
R2392:Cfap54
|
UTSW |
10 |
92,860,873 (GRCm39) |
critical splice donor site |
probably null |
|
R2508:Cfap54
|
UTSW |
10 |
92,833,236 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2852:Cfap54
|
UTSW |
10 |
92,776,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Cfap54
|
UTSW |
10 |
92,881,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R2871:Cfap54
|
UTSW |
10 |
92,757,281 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2871:Cfap54
|
UTSW |
10 |
92,757,281 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3107:Cfap54
|
UTSW |
10 |
92,830,545 (GRCm39) |
missense |
probably benign |
0.04 |
R3108:Cfap54
|
UTSW |
10 |
92,830,545 (GRCm39) |
missense |
probably benign |
0.04 |
R3157:Cfap54
|
UTSW |
10 |
92,834,918 (GRCm39) |
missense |
probably benign |
0.03 |
R3158:Cfap54
|
UTSW |
10 |
92,834,918 (GRCm39) |
missense |
probably benign |
0.03 |
R3159:Cfap54
|
UTSW |
10 |
92,834,918 (GRCm39) |
missense |
probably benign |
0.03 |
R3161:Cfap54
|
UTSW |
10 |
92,881,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Cfap54
|
UTSW |
10 |
92,881,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Cfap54
|
UTSW |
10 |
92,881,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R3508:Cfap54
|
UTSW |
10 |
92,721,286 (GRCm39) |
missense |
unknown |
|
R3730:Cfap54
|
UTSW |
10 |
92,847,335 (GRCm39) |
nonsense |
probably null |
|
R3770:Cfap54
|
UTSW |
10 |
92,714,398 (GRCm39) |
missense |
unknown |
|
R3776:Cfap54
|
UTSW |
10 |
92,880,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R3778:Cfap54
|
UTSW |
10 |
92,740,206 (GRCm39) |
utr 3 prime |
probably benign |
|
R3795:Cfap54
|
UTSW |
10 |
92,778,735 (GRCm39) |
unclassified |
probably benign |
|
R3834:Cfap54
|
UTSW |
10 |
92,636,985 (GRCm39) |
splice site |
probably benign |
|
R3891:Cfap54
|
UTSW |
10 |
92,874,708 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3932:Cfap54
|
UTSW |
10 |
92,665,619 (GRCm39) |
missense |
probably benign |
0.03 |
R3973:Cfap54
|
UTSW |
10 |
92,675,333 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3974:Cfap54
|
UTSW |
10 |
92,675,333 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3976:Cfap54
|
UTSW |
10 |
92,675,333 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3978:Cfap54
|
UTSW |
10 |
92,798,274 (GRCm39) |
missense |
probably benign |
0.01 |
R4190:Cfap54
|
UTSW |
10 |
92,720,885 (GRCm39) |
missense |
unknown |
|
R4389:Cfap54
|
UTSW |
10 |
92,803,362 (GRCm39) |
missense |
probably benign |
0.37 |
R4542:Cfap54
|
UTSW |
10 |
92,860,991 (GRCm39) |
missense |
probably benign |
0.12 |
R4564:Cfap54
|
UTSW |
10 |
92,675,402 (GRCm39) |
unclassified |
probably benign |
|
R4576:Cfap54
|
UTSW |
10 |
92,879,090 (GRCm39) |
critical splice donor site |
probably null |
|
R4620:Cfap54
|
UTSW |
10 |
92,805,619 (GRCm39) |
missense |
probably benign |
0.01 |
R4714:Cfap54
|
UTSW |
10 |
92,651,780 (GRCm39) |
missense |
probably benign |
0.01 |
R4762:Cfap54
|
UTSW |
10 |
92,897,315 (GRCm39) |
splice site |
probably null |
|
R4776:Cfap54
|
UTSW |
10 |
92,808,556 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4819:Cfap54
|
UTSW |
10 |
92,672,339 (GRCm39) |
nonsense |
probably null |
|
R4827:Cfap54
|
UTSW |
10 |
92,737,937 (GRCm39) |
utr 3 prime |
probably benign |
|
R4832:Cfap54
|
UTSW |
10 |
92,803,390 (GRCm39) |
missense |
probably benign |
0.01 |
R4965:Cfap54
|
UTSW |
10 |
92,902,661 (GRCm39) |
missense |
probably benign |
0.23 |
R5001:Cfap54
|
UTSW |
10 |
92,800,396 (GRCm39) |
missense |
probably benign |
0.01 |
R5060:Cfap54
|
UTSW |
10 |
92,875,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5067:Cfap54
|
UTSW |
10 |
92,902,628 (GRCm39) |
missense |
probably benign |
0.17 |
R5069:Cfap54
|
UTSW |
10 |
92,773,636 (GRCm39) |
missense |
probably benign |
|
R5094:Cfap54
|
UTSW |
10 |
92,734,861 (GRCm39) |
utr 3 prime |
probably benign |
|
R5109:Cfap54
|
UTSW |
10 |
92,773,753 (GRCm39) |
missense |
probably benign |
0.03 |
R5127:Cfap54
|
UTSW |
10 |
92,722,249 (GRCm39) |
splice site |
probably null |
|
R5143:Cfap54
|
UTSW |
10 |
92,865,020 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5147:Cfap54
|
UTSW |
10 |
92,773,700 (GRCm39) |
missense |
probably benign |
0.00 |
R5158:Cfap54
|
UTSW |
10 |
92,901,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Cfap54
|
UTSW |
10 |
92,880,885 (GRCm39) |
splice site |
probably null |
|
R5256:Cfap54
|
UTSW |
10 |
92,770,953 (GRCm39) |
nonsense |
probably null |
|
R5266:Cfap54
|
UTSW |
10 |
92,651,764 (GRCm39) |
missense |
probably benign |
0.16 |
R5304:Cfap54
|
UTSW |
10 |
92,656,968 (GRCm39) |
missense |
probably damaging |
0.97 |
R5369:Cfap54
|
UTSW |
10 |
92,897,119 (GRCm39) |
intron |
probably benign |
|
R5406:Cfap54
|
UTSW |
10 |
92,837,720 (GRCm39) |
missense |
probably benign |
0.33 |
R5471:Cfap54
|
UTSW |
10 |
92,864,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R5485:Cfap54
|
UTSW |
10 |
92,864,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5540:Cfap54
|
UTSW |
10 |
92,808,470 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5586:Cfap54
|
UTSW |
10 |
92,808,473 (GRCm39) |
nonsense |
probably null |
|
R5614:Cfap54
|
UTSW |
10 |
92,880,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Cfap54
|
UTSW |
10 |
92,740,125 (GRCm39) |
critical splice donor site |
probably benign |
|
R5680:Cfap54
|
UTSW |
10 |
92,814,879 (GRCm39) |
nonsense |
probably null |
|
R5797:Cfap54
|
UTSW |
10 |
92,803,438 (GRCm39) |
missense |
probably benign |
0.11 |
R5859:Cfap54
|
UTSW |
10 |
92,852,386 (GRCm39) |
nonsense |
probably null |
|
R5878:Cfap54
|
UTSW |
10 |
92,800,423 (GRCm39) |
missense |
probably benign |
0.01 |
R5910:Cfap54
|
UTSW |
10 |
92,901,043 (GRCm39) |
missense |
probably damaging |
0.99 |
R5936:Cfap54
|
UTSW |
10 |
92,798,274 (GRCm39) |
missense |
probably benign |
0.01 |
R5994:Cfap54
|
UTSW |
10 |
92,874,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R6080:Cfap54
|
UTSW |
10 |
92,881,197 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6268:Cfap54
|
UTSW |
10 |
92,874,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Cfap54
|
UTSW |
10 |
92,902,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R6409:Cfap54
|
UTSW |
10 |
92,803,354 (GRCm39) |
missense |
probably benign |
0.04 |
R6545:Cfap54
|
UTSW |
10 |
92,672,319 (GRCm39) |
missense |
probably benign |
0.31 |
R6570:Cfap54
|
UTSW |
10 |
92,651,820 (GRCm39) |
missense |
unknown |
|
R6597:Cfap54
|
UTSW |
10 |
92,834,902 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6702:Cfap54
|
UTSW |
10 |
92,704,596 (GRCm39) |
missense |
unknown |
|
R6703:Cfap54
|
UTSW |
10 |
92,704,596 (GRCm39) |
missense |
unknown |
|
R6720:Cfap54
|
UTSW |
10 |
92,656,981 (GRCm39) |
missense |
probably benign |
0.07 |
R6841:Cfap54
|
UTSW |
10 |
92,710,877 (GRCm39) |
missense |
unknown |
|
R6910:Cfap54
|
UTSW |
10 |
92,672,374 (GRCm39) |
missense |
probably benign |
0.29 |
R6953:Cfap54
|
UTSW |
10 |
92,830,540 (GRCm39) |
missense |
probably benign |
0.19 |
R7009:Cfap54
|
UTSW |
10 |
92,710,881 (GRCm39) |
missense |
unknown |
|
R7129:Cfap54
|
UTSW |
10 |
92,852,433 (GRCm39) |
missense |
probably benign |
0.06 |
R7131:Cfap54
|
UTSW |
10 |
92,656,966 (GRCm39) |
missense |
probably benign |
0.03 |
R7171:Cfap54
|
UTSW |
10 |
92,612,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R7189:Cfap54
|
UTSW |
10 |
92,773,590 (GRCm39) |
missense |
unknown |
|
R7225:Cfap54
|
UTSW |
10 |
92,740,236 (GRCm39) |
missense |
unknown |
|
R7270:Cfap54
|
UTSW |
10 |
92,675,320 (GRCm39) |
missense |
probably benign |
0.03 |
R7323:Cfap54
|
UTSW |
10 |
92,637,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7380:Cfap54
|
UTSW |
10 |
92,883,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Cfap54
|
UTSW |
10 |
92,720,565 (GRCm39) |
missense |
unknown |
|
R7411:Cfap54
|
UTSW |
10 |
92,704,617 (GRCm39) |
missense |
unknown |
|
R7503:Cfap54
|
UTSW |
10 |
92,723,298 (GRCm39) |
splice site |
probably null |
|
R7622:Cfap54
|
UTSW |
10 |
92,792,806 (GRCm39) |
missense |
unknown |
|
R7679:Cfap54
|
UTSW |
10 |
92,803,374 (GRCm39) |
missense |
probably benign |
0.01 |
R7776:Cfap54
|
UTSW |
10 |
92,704,603 (GRCm39) |
missense |
unknown |
|
R7844:Cfap54
|
UTSW |
10 |
92,737,920 (GRCm39) |
missense |
unknown |
|
R7980:Cfap54
|
UTSW |
10 |
92,817,922 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7988:Cfap54
|
UTSW |
10 |
92,737,941 (GRCm39) |
missense |
unknown |
|
R8101:Cfap54
|
UTSW |
10 |
92,720,658 (GRCm39) |
missense |
unknown |
|
R8119:Cfap54
|
UTSW |
10 |
92,704,672 (GRCm39) |
missense |
unknown |
|
R8134:Cfap54
|
UTSW |
10 |
92,714,378 (GRCm39) |
missense |
unknown |
|
R8168:Cfap54
|
UTSW |
10 |
92,744,739 (GRCm39) |
missense |
unknown |
|
R8179:Cfap54
|
UTSW |
10 |
92,833,178 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8392:Cfap54
|
UTSW |
10 |
92,798,279 (GRCm39) |
missense |
unknown |
|
R8436:Cfap54
|
UTSW |
10 |
92,800,398 (GRCm39) |
missense |
unknown |
|
R8505:Cfap54
|
UTSW |
10 |
92,814,855 (GRCm39) |
missense |
probably benign |
0.03 |
R8671:Cfap54
|
UTSW |
10 |
92,790,934 (GRCm39) |
missense |
unknown |
|
R8716:Cfap54
|
UTSW |
10 |
92,800,494 (GRCm39) |
missense |
probably benign |
0.00 |
R8816:Cfap54
|
UTSW |
10 |
92,714,454 (GRCm39) |
missense |
unknown |
|
R8822:Cfap54
|
UTSW |
10 |
92,875,003 (GRCm39) |
missense |
probably benign |
0.09 |
R8827:Cfap54
|
UTSW |
10 |
92,774,110 (GRCm39) |
missense |
unknown |
|
R8920:Cfap54
|
UTSW |
10 |
92,776,199 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8924:Cfap54
|
UTSW |
10 |
92,837,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R8954:Cfap54
|
UTSW |
10 |
92,879,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Cfap54
|
UTSW |
10 |
92,864,562 (GRCm39) |
nonsense |
probably null |
|
R9010:Cfap54
|
UTSW |
10 |
92,734,921 (GRCm39) |
missense |
unknown |
|
R9017:Cfap54
|
UTSW |
10 |
92,651,883 (GRCm39) |
missense |
probably benign |
0.07 |
R9093:Cfap54
|
UTSW |
10 |
92,651,770 (GRCm39) |
missense |
probably benign |
0.03 |
R9095:Cfap54
|
UTSW |
10 |
92,846,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9142:Cfap54
|
UTSW |
10 |
92,820,097 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9178:Cfap54
|
UTSW |
10 |
92,830,579 (GRCm39) |
missense |
probably benign |
0.10 |
R9196:Cfap54
|
UTSW |
10 |
92,873,753 (GRCm39) |
missense |
probably benign |
0.22 |
R9203:Cfap54
|
UTSW |
10 |
92,880,990 (GRCm39) |
missense |
probably benign |
0.30 |
R9258:Cfap54
|
UTSW |
10 |
92,770,960 (GRCm39) |
missense |
unknown |
|
R9275:Cfap54
|
UTSW |
10 |
92,875,048 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9287:Cfap54
|
UTSW |
10 |
92,805,565 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9289:Cfap54
|
UTSW |
10 |
92,656,936 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9310:Cfap54
|
UTSW |
10 |
92,798,177 (GRCm39) |
missense |
unknown |
|
R9397:Cfap54
|
UTSW |
10 |
92,833,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R9462:Cfap54
|
UTSW |
10 |
92,737,920 (GRCm39) |
missense |
unknown |
|
R9697:Cfap54
|
UTSW |
10 |
92,792,851 (GRCm39) |
missense |
unknown |
|
R9746:Cfap54
|
UTSW |
10 |
92,637,081 (GRCm39) |
missense |
probably benign |
0.03 |
R9755:Cfap54
|
UTSW |
10 |
92,757,230 (GRCm39) |
missense |
unknown |
|
X0022:Cfap54
|
UTSW |
10 |
92,768,476 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Cfap54
|
UTSW |
10 |
92,714,465 (GRCm39) |
missense |
unknown |
|
X0027:Cfap54
|
UTSW |
10 |
92,837,750 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0027:Cfap54
|
UTSW |
10 |
92,714,400 (GRCm39) |
missense |
unknown |
|
Z1177:Cfap54
|
UTSW |
10 |
92,814,888 (GRCm39) |
missense |
probably damaging |
1.00 |
|