Other mutations in this stock |
Total: 215 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
G |
A |
1: 130,665,425 (GRCm39) |
|
probably null |
Het |
Abca7 |
T |
C |
10: 79,835,599 (GRCm39) |
L289P |
probably damaging |
Het |
Ache |
A |
G |
5: 137,288,837 (GRCm39) |
N181S |
possibly damaging |
Het |
Adgrf4 |
C |
T |
17: 42,977,789 (GRCm39) |
R518Q |
possibly damaging |
Het |
Adgrv1 |
T |
A |
13: 81,654,265 (GRCm39) |
H2922L |
probably benign |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Baz1a |
G |
A |
12: 54,955,805 (GRCm39) |
R1095C |
probably damaging |
Het |
Bcan |
T |
G |
3: 87,900,932 (GRCm39) |
I434L |
probably benign |
Het |
Brca1 |
A |
C |
11: 101,422,844 (GRCm39) |
|
probably null |
Het |
C4bp |
C |
G |
1: 130,570,725 (GRCm39) |
V284L |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,046,454 (GRCm39) |
F1761S |
probably benign |
Het |
Camsap2 |
C |
T |
1: 136,209,053 (GRCm39) |
R802Q |
probably benign |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cars1 |
C |
A |
7: 143,146,211 (GRCm39) |
R71M |
probably damaging |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
probably benign |
Het |
Cd55 |
C |
A |
1: 130,387,370 (GRCm39) |
A143S |
probably benign |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cd55b |
T |
A |
1: 130,316,392 (GRCm39) |
R273* |
probably null |
Het |
Cd74 |
T |
C |
18: 60,944,390 (GRCm39) |
V200A |
probably benign |
Het |
Cd82 |
C |
A |
2: 93,267,774 (GRCm39) |
V8F |
probably damaging |
Het |
Cdh19 |
C |
A |
1: 110,821,114 (GRCm39) |
E541D |
probably damaging |
Het |
Cdh20 |
C |
G |
1: 109,993,465 (GRCm39) |
L307V |
possibly damaging |
Het |
Cdh4 |
A |
G |
2: 179,439,273 (GRCm39) |
D140G |
probably benign |
Het |
Cfh |
C |
T |
1: 140,075,435 (GRCm39) |
V268I |
possibly damaging |
Het |
Cfh |
T |
C |
1: 140,064,526 (GRCm39) |
K374R |
probably benign |
Het |
Cfhr2 |
A |
G |
1: 139,741,180 (GRCm39) |
M265T |
probably benign |
Het |
Cfhr2 |
A |
C |
1: 139,741,197 (GRCm39) |
N259K |
probably benign |
Het |
Chd1l |
A |
G |
3: 97,495,615 (GRCm39) |
L361S |
probably damaging |
Het |
Chi3l1 |
C |
T |
1: 134,116,267 (GRCm39) |
A250V |
probably damaging |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Cntrl |
CAGAG |
CAG |
2: 35,012,818 (GRCm39) |
|
probably null |
Het |
Crb1 |
T |
C |
1: 139,165,269 (GRCm39) |
S952G |
probably damaging |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
probably benign |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Cxcr4 |
C |
T |
1: 128,517,014 (GRCm39) |
V216I |
probably benign |
Het |
Cyb5r1 |
C |
T |
1: 134,335,405 (GRCm39) |
R147W |
probably damaging |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dlc1 |
T |
A |
8: 37,404,739 (GRCm39) |
N350I |
probably benign |
Het |
Dpp9 |
A |
G |
17: 56,495,362 (GRCm39) |
I801T |
probably damaging |
Het |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,672,789 (GRCm39) |
D820G |
probably damaging |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Eme2 |
T |
C |
17: 25,112,367 (GRCm39) |
H186R |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,293,503 (GRCm39) |
G149W |
probably damaging |
Het |
Etnk2 |
C |
T |
1: 133,293,554 (GRCm39) |
R166* |
probably null |
Het |
Etnk2 |
G |
A |
1: 133,293,555 (GRCm39) |
R166Q |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,304,653 (GRCm39) |
V292E |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,304,784 (GRCm39) |
A336S |
probably benign |
Het |
Etnk2 |
C |
A |
1: 133,293,325 (GRCm39) |
D89E |
probably benign |
Het |
Fam72a |
C |
T |
1: 131,466,633 (GRCm39) |
T139M |
probably benign |
Het |
Fam72a |
T |
C |
1: 131,458,406 (GRCm39) |
I56T |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,739,317 (GRCm39) |
I206V |
probably benign |
Het |
Fcamr |
G |
A |
1: 130,740,366 (GRCm39) |
G262S |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,429 (GRCm39) |
I283V |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,740,475 (GRCm39) |
V298A |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,546 (GRCm39) |
M322V |
probably benign |
Het |
Fcamr |
C |
T |
1: 130,740,553 (GRCm39) |
P324L |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,742,334 (GRCm39) |
N574D |
probably benign |
Het |
Fcamr |
A |
C |
1: 130,732,364 (GRCm39) |
N117T |
probably benign |
Het |
Fcmr |
T |
C |
1: 130,806,006 (GRCm39) |
S321P |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,803,711 (GRCm39) |
T172A |
probably benign |
Het |
G6pc2 |
A |
T |
2: 69,051,186 (GRCm39) |
H93L |
possibly damaging |
Het |
Gdf3 |
T |
C |
6: 122,583,366 (GRCm39) |
T334A |
possibly damaging |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Gli2 |
C |
T |
1: 118,795,817 (GRCm39) |
A113T |
possibly damaging |
Het |
Gli2 |
G |
T |
1: 118,929,774 (GRCm39) |
H44Q |
probably benign |
Het |
Glrx2 |
C |
T |
1: 143,615,478 (GRCm39) |
A27V |
possibly damaging |
Het |
Gm10110 |
A |
G |
14: 90,134,825 (GRCm39) |
|
noncoding transcript |
Het |
Gm10563 |
C |
T |
4: 155,720,337 (GRCm39) |
|
probably benign |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gm9637 |
T |
C |
14: 19,402,408 (GRCm38) |
|
noncoding transcript |
Het |
Gpbp1 |
A |
T |
13: 111,577,308 (GRCm39) |
V194D |
probably benign |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Gpr39 |
G |
A |
1: 125,800,286 (GRCm39) |
V346M |
possibly damaging |
Het |
Gpr84 |
T |
A |
15: 103,217,754 (GRCm39) |
I108F |
probably damaging |
Het |
Grid2 |
G |
T |
6: 64,510,638 (GRCm39) |
C756F |
probably damaging |
Het |
Grm7 |
G |
C |
6: 111,335,256 (GRCm39) |
D556H |
probably damaging |
Het |
Has2 |
T |
C |
15: 56,545,006 (GRCm39) |
R199G |
probably benign |
Het |
Hivep1 |
C |
T |
13: 42,337,262 (GRCm39) |
A2447V |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Igf2bp2 |
A |
T |
16: 21,902,697 (GRCm39) |
Y59* |
probably null |
Het |
Igfn1 |
T |
C |
1: 135,926,421 (GRCm39) |
I10V |
unknown |
Het |
Igfn1 |
T |
C |
1: 135,926,363 (GRCm39) |
E29G |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,910,213 (GRCm39) |
R124W |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,907,653 (GRCm39) |
A231T |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,899,865 (GRCm39) |
R482Q |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,898,149 (GRCm39) |
S806G |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,895,937 (GRCm39) |
A1543V |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,887,666 (GRCm39) |
P2466L |
probably damaging |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Ikbke |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Irx5 |
T |
A |
8: 93,086,272 (GRCm39) |
N118K |
probably damaging |
Het |
Itk |
T |
C |
11: 46,227,309 (GRCm39) |
E438G |
probably damaging |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
probably benign |
Het |
Kdm5b |
T |
A |
1: 134,532,205 (GRCm39) |
L461* |
probably null |
Het |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,716 (GRCm39) |
R342G |
probably benign |
Het |
Lax1 |
G |
A |
1: 133,611,372 (GRCm39) |
P67S |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,931,214 (GRCm39) |
S3N |
probably benign |
Het |
Lgr6 |
G |
T |
1: 134,918,373 (GRCm39) |
H263N |
probably benign |
Het |
Lgr6 |
A |
T |
1: 134,915,747 (GRCm39) |
S334T |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Lrrtm1 |
T |
C |
6: 77,221,680 (GRCm39) |
V379A |
probably benign |
Het |
Mbd3l1 |
T |
G |
9: 18,396,435 (GRCm39) |
*187E |
probably null |
Het |
Micu1 |
T |
A |
10: 59,699,082 (GRCm39) |
M453K |
possibly damaging |
Het |
Mlh1 |
A |
T |
9: 111,058,997 (GRCm39) |
C676S |
probably damaging |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Myh7b |
G |
A |
2: 155,472,778 (GRCm39) |
E1391K |
probably damaging |
Het |
Myorg |
T |
A |
4: 41,498,553 (GRCm39) |
Y359F |
possibly damaging |
Het |
Myrfl |
A |
C |
10: 116,634,498 (GRCm39) |
M632R |
probably damaging |
Het |
Naif1 |
T |
C |
2: 32,344,902 (GRCm39) |
V202A |
possibly damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Ncor1 |
T |
C |
11: 62,275,610 (GRCm39) |
E525G |
possibly damaging |
Het |
Nlrx1 |
T |
C |
9: 44,174,937 (GRCm39) |
M280V |
possibly damaging |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Nrg1 |
T |
A |
8: 32,312,351 (GRCm39) |
H382L |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Or10w1 |
G |
A |
19: 13,631,868 (GRCm39) |
R25H |
probably benign |
Het |
Or12e13 |
G |
T |
2: 87,664,009 (GRCm39) |
V209F |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4g17 |
A |
G |
2: 111,209,918 (GRCm39) |
D191G |
probably damaging |
Het |
Or52e19 |
C |
T |
7: 102,959,428 (GRCm39) |
R167C |
probably damaging |
Het |
Or52n3 |
C |
T |
7: 104,530,447 (GRCm39) |
H178Y |
probably damaging |
Het |
Or52r1b |
C |
A |
7: 102,691,249 (GRCm39) |
H183N |
probably damaging |
Het |
Or5aq1b |
A |
T |
2: 86,902,265 (GRCm39) |
I71N |
probably damaging |
Het |
Or6aa1 |
T |
C |
7: 86,044,353 (GRCm39) |
M118V |
probably damaging |
Het |
Or8d2b |
A |
G |
9: 38,789,081 (GRCm39) |
N203S |
probably damaging |
Het |
Pah |
A |
G |
10: 87,403,330 (GRCm39) |
Q235R |
possibly damaging |
Het |
Pcdhb9 |
A |
G |
18: 37,536,136 (GRCm39) |
E710G |
probably benign |
Het |
Pcnt |
T |
A |
10: 76,190,971 (GRCm39) |
|
probably null |
Het |
Pdzk1 |
A |
T |
3: 96,758,889 (GRCm39) |
N98I |
probably benign |
Het |
Pigr |
C |
T |
1: 130,772,259 (GRCm39) |
A159V |
possibly damaging |
Het |
Pik3c2b |
C |
T |
1: 132,994,365 (GRCm39) |
P110S |
probably benign |
Het |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,455,825 (GRCm39) |
C25S |
probably benign |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
probably benign |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rasal2 |
T |
C |
1: 157,126,714 (GRCm39) |
E90G |
possibly damaging |
Het |
Ren1 |
C |
T |
1: 133,281,975 (GRCm39) |
T32I |
probably benign |
Het |
Ren1 |
T |
A |
1: 133,281,944 (GRCm39) |
W22R |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,287,745 (GRCm39) |
L360V |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,286,817 (GRCm39) |
E315D |
probably benign |
Het |
Ren1 |
C |
A |
1: 133,286,720 (GRCm39) |
|
probably null |
Het |
Rictor |
T |
C |
15: 6,786,054 (GRCm39) |
I190T |
probably benign |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Ro60 |
C |
T |
1: 143,635,752 (GRCm39) |
V465I |
probably benign |
Het |
Sbf2 |
T |
C |
7: 109,911,965 (GRCm39) |
T1694A |
probably benign |
Het |
Sbno2 |
C |
T |
10: 79,902,440 (GRCm39) |
E486K |
probably damaging |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
probably benign |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sctr |
G |
T |
1: 119,990,976 (GRCm39) |
E453D |
probably benign |
Het |
Semp2l2b |
A |
T |
10: 21,943,411 (GRCm39) |
C190S |
probably benign |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Serpinb10 |
C |
T |
1: 107,466,203 (GRCm39) |
S63F |
probably damaging |
Het |
Serpinb2 |
G |
A |
1: 107,443,365 (GRCm39) |
A55T |
probably damaging |
Het |
Serpinb2 |
A |
C |
1: 107,452,273 (GRCm39) |
S284R |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,624 (GRCm39) |
T259I |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,620 (GRCm39) |
H258Y |
probably benign |
Het |
Serpinb2 |
C |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Skint6 |
T |
C |
4: 113,093,678 (GRCm39) |
N155S |
probably damaging |
Het |
Slc26a9 |
C |
T |
1: 131,691,608 (GRCm39) |
A617V |
probably benign |
Het |
Slc26a9 |
C |
A |
1: 131,693,750 (GRCm39) |
R747S |
probably benign |
Het |
Slc30a5 |
T |
C |
13: 100,949,970 (GRCm39) |
T371A |
probably damaging |
Het |
Slit1 |
A |
T |
19: 41,591,774 (GRCm39) |
Y1283N |
probably damaging |
Het |
Steap3 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
probably benign |
Het |
Stx19 |
A |
T |
16: 62,642,343 (GRCm39) |
Q53L |
probably damaging |
Het |
Tbc1d4 |
T |
C |
14: 101,744,574 (GRCm39) |
S351G |
possibly damaging |
Het |
Tbx15 |
T |
A |
3: 99,259,260 (GRCm39) |
L377* |
probably null |
Het |
Tecta |
A |
T |
9: 42,286,605 (GRCm39) |
Y684N |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
Het |
Thsd7b |
T |
A |
1: 130,030,813 (GRCm39) |
H1049Q |
possibly damaging |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,556,628 (GRCm39) |
T328I |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 129,595,674 (GRCm39) |
F498Y |
probably benign |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Wnt5a |
T |
C |
14: 28,244,848 (GRCm39) |
V345A |
probably damaging |
Het |
Xylt1 |
A |
T |
7: 117,236,988 (GRCm39) |
H579L |
probably benign |
Het |
Zbtb4 |
A |
T |
11: 69,669,743 (GRCm39) |
Q822L |
probably benign |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zc3h12c |
A |
T |
9: 52,027,081 (GRCm39) |
S760R |
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
|
Other mutations in Ptprc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
lochy
|
APN |
1 |
138,011,528 (GRCm39) |
splice site |
probably benign |
|
IGL00486:Ptprc
|
APN |
1 |
138,043,359 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00771:Ptprc
|
APN |
1 |
138,041,415 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00833:Ptprc
|
APN |
1 |
138,006,230 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL00919:Ptprc
|
APN |
1 |
138,041,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Ptprc
|
APN |
1 |
138,047,911 (GRCm39) |
critical splice acceptor site |
probably null |
0.00 |
IGL01024:Ptprc
|
APN |
1 |
138,008,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01302:Ptprc
|
APN |
1 |
138,027,369 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01548:Ptprc
|
APN |
1 |
138,027,219 (GRCm39) |
critical splice donor site |
probably null |
0.00 |
IGL01620:Ptprc
|
APN |
1 |
137,996,148 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01775:Ptprc
|
APN |
1 |
137,992,497 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01820:Ptprc
|
APN |
1 |
137,993,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Ptprc
|
APN |
1 |
137,998,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Ptprc
|
APN |
1 |
138,027,251 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03169:Ptprc
|
APN |
1 |
138,041,357 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03308:Ptprc
|
APN |
1 |
138,054,058 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03404:Ptprc
|
APN |
1 |
138,020,739 (GRCm39) |
missense |
probably damaging |
1.00 |
belittle
|
UTSW |
1 |
138,137,493 (GRCm38) |
intron |
probably benign |
|
Benighted
|
UTSW |
1 |
138,054,039 (GRCm39) |
critical splice donor site |
probably null |
|
bletchley
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
Blush
|
UTSW |
1 |
138,045,458 (GRCm39) |
intron |
probably benign |
|
bruise
|
UTSW |
1 |
137,992,509 (GRCm39) |
missense |
probably damaging |
1.00 |
chor_muang
|
UTSW |
1 |
138,041,300 (GRCm39) |
critical splice donor site |
probably null |
|
crystal
|
UTSW |
1 |
137,999,993 (GRCm39) |
critical splice donor site |
probably null |
|
Dumpling
|
UTSW |
1 |
137,995,628 (GRCm39) |
missense |
probably damaging |
1.00 |
fluorescent
|
UTSW |
1 |
138,028,930 (GRCm39) |
missense |
probably damaging |
0.97 |
fuchsia
|
UTSW |
1 |
138,028,779 (GRCm39) |
critical splice donor site |
probably null |
|
Gentian
|
UTSW |
1 |
137,995,623 (GRCm39) |
critical splice donor site |
probably null |
|
guotie
|
UTSW |
1 |
137,996,139 (GRCm39) |
nonsense |
probably null |
|
guotie2
|
UTSW |
1 |
138,022,037 (GRCm39) |
missense |
probably damaging |
0.97 |
Guotie3
|
UTSW |
1 |
138,006,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
Gyoza
|
UTSW |
1 |
138,011,305 (GRCm39) |
missense |
probably damaging |
1.00 |
Half_measure
|
UTSW |
1 |
137,998,987 (GRCm39) |
missense |
probably damaging |
0.98 |
jirisan
|
UTSW |
1 |
138,041,416 (GRCm39) |
nonsense |
probably null |
|
mauve
|
UTSW |
1 |
138,027,423 (GRCm39) |
missense |
probably benign |
|
Perverse
|
UTSW |
1 |
138,028,782 (GRCm39) |
missense |
probably benign |
0.02 |
petechiae
|
UTSW |
1 |
138,041,446 (GRCm39) |
nonsense |
probably null |
|
ultra
|
UTSW |
1 |
138,006,183 (GRCm39) |
critical splice donor site |
probably null |
|
violaceous
|
UTSW |
1 |
138,011,377 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0013:Ptprc
|
UTSW |
1 |
138,041,297 (GRCm39) |
splice site |
probably null |
|
R0189:Ptprc
|
UTSW |
1 |
138,010,453 (GRCm39) |
missense |
probably benign |
0.10 |
R0390:Ptprc
|
UTSW |
1 |
138,050,313 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0504:Ptprc
|
UTSW |
1 |
138,016,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0602:Ptprc
|
UTSW |
1 |
138,017,223 (GRCm39) |
splice site |
probably benign |
|
R0627:Ptprc
|
UTSW |
1 |
137,996,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R0632:Ptprc
|
UTSW |
1 |
138,001,348 (GRCm39) |
missense |
probably benign |
0.01 |
R0751:Ptprc
|
UTSW |
1 |
138,020,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Ptprc
|
UTSW |
1 |
138,028,870 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0942:Ptprc
|
UTSW |
1 |
137,996,139 (GRCm39) |
nonsense |
probably null |
|
R0943:Ptprc
|
UTSW |
1 |
138,038,902 (GRCm39) |
missense |
probably damaging |
0.96 |
R1159:Ptprc
|
UTSW |
1 |
138,000,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Ptprc
|
UTSW |
1 |
138,000,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Ptprc
|
UTSW |
1 |
138,047,824 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1728:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1728:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1728:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1728:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1728:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1729:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1729:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1729:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1729:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1729:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1730:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1730:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1730:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1730:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1730:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1739:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1739:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1739:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1739:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1739:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1762:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1762:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1762:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1762:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1783:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1783:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1783:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1783:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1783:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1784:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1784:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1784:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1784:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1784:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1785:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1785:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1785:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1785:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1785:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1862:Ptprc
|
UTSW |
1 |
138,039,965 (GRCm39) |
missense |
probably benign |
0.13 |
R2145:Ptprc
|
UTSW |
1 |
138,001,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Ptprc
|
UTSW |
1 |
138,038,926 (GRCm39) |
missense |
probably benign |
0.00 |
R2403:Ptprc
|
UTSW |
1 |
138,016,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R2439:Ptprc
|
UTSW |
1 |
137,993,890 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2887:Ptprc
|
UTSW |
1 |
138,007,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R2906:Ptprc
|
UTSW |
1 |
137,992,272 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3774:Ptprc
|
UTSW |
1 |
137,992,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R3775:Ptprc
|
UTSW |
1 |
137,992,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R3776:Ptprc
|
UTSW |
1 |
137,992,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R3834:Ptprc
|
UTSW |
1 |
138,011,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Ptprc
|
UTSW |
1 |
138,006,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4377:Ptprc
|
UTSW |
1 |
137,995,663 (GRCm39) |
missense |
probably benign |
0.04 |
R4580:Ptprc
|
UTSW |
1 |
137,998,989 (GRCm39) |
missense |
probably benign |
0.09 |
R4923:Ptprc
|
UTSW |
1 |
138,006,236 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4925:Ptprc
|
UTSW |
1 |
138,027,235 (GRCm39) |
missense |
probably benign |
0.04 |
R4937:Ptprc
|
UTSW |
1 |
138,017,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Ptprc
|
UTSW |
1 |
138,022,037 (GRCm39) |
missense |
probably damaging |
0.97 |
R5112:Ptprc
|
UTSW |
1 |
138,022,037 (GRCm39) |
missense |
probably damaging |
0.97 |
R5145:Ptprc
|
UTSW |
1 |
138,017,304 (GRCm39) |
missense |
probably benign |
0.07 |
R5158:Ptprc
|
UTSW |
1 |
138,102,822 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5223:Ptprc
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
R5593:Ptprc
|
UTSW |
1 |
138,045,458 (GRCm39) |
intron |
probably benign |
|
R5689:Ptprc
|
UTSW |
1 |
138,045,515 (GRCm39) |
missense |
probably benign |
0.01 |
R5885:Ptprc
|
UTSW |
1 |
138,016,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Ptprc
|
UTSW |
1 |
138,028,794 (GRCm39) |
missense |
probably benign |
0.09 |
R6026:Ptprc
|
UTSW |
1 |
137,998,987 (GRCm39) |
missense |
probably damaging |
0.98 |
R6047:Ptprc
|
UTSW |
1 |
138,028,779 (GRCm39) |
critical splice donor site |
probably null |
|
R6173:Ptprc
|
UTSW |
1 |
137,995,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Ptprc
|
UTSW |
1 |
138,041,416 (GRCm39) |
nonsense |
probably null |
|
R6383:Ptprc
|
UTSW |
1 |
138,006,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6436:Ptprc
|
UTSW |
1 |
138,011,377 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6492:Ptprc
|
UTSW |
1 |
138,041,300 (GRCm39) |
critical splice donor site |
probably null |
|
R6520:Ptprc
|
UTSW |
1 |
138,007,881 (GRCm39) |
nonsense |
probably null |
|
R6805:Ptprc
|
UTSW |
1 |
137,995,623 (GRCm39) |
critical splice donor site |
probably null |
|
R6830:Ptprc
|
UTSW |
1 |
137,999,993 (GRCm39) |
critical splice donor site |
probably null |
|
R6847:Ptprc
|
UTSW |
1 |
138,016,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R6960:Ptprc
|
UTSW |
1 |
138,006,183 (GRCm39) |
critical splice donor site |
probably null |
|
R6995:Ptprc
|
UTSW |
1 |
138,016,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Ptprc
|
UTSW |
1 |
137,992,291 (GRCm39) |
missense |
probably damaging |
0.97 |
R7041:Ptprc
|
UTSW |
1 |
138,054,047 (GRCm39) |
missense |
probably benign |
0.04 |
R7055:Ptprc
|
UTSW |
1 |
138,017,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Ptprc
|
UTSW |
1 |
138,027,423 (GRCm39) |
missense |
probably benign |
|
R7164:Ptprc
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
R7188:Ptprc
|
UTSW |
1 |
137,998,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7191:Ptprc
|
UTSW |
1 |
138,028,782 (GRCm39) |
missense |
probably benign |
0.02 |
R7204:Ptprc
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
R7316:Ptprc
|
UTSW |
1 |
137,992,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Ptprc
|
UTSW |
1 |
137,995,645 (GRCm39) |
missense |
probably benign |
0.01 |
R7948:Ptprc
|
UTSW |
1 |
137,992,314 (GRCm39) |
missense |
probably benign |
0.45 |
R8029:Ptprc
|
UTSW |
1 |
138,006,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R8677:Ptprc
|
UTSW |
1 |
138,011,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R8704:Ptprc
|
UTSW |
1 |
138,043,362 (GRCm39) |
missense |
probably benign |
0.34 |
R8824:Ptprc
|
UTSW |
1 |
138,041,446 (GRCm39) |
nonsense |
probably null |
|
R8921:Ptprc
|
UTSW |
1 |
138,054,039 (GRCm39) |
critical splice donor site |
probably null |
|
R8998:Ptprc
|
UTSW |
1 |
138,028,930 (GRCm39) |
missense |
probably damaging |
0.97 |
R8999:Ptprc
|
UTSW |
1 |
138,028,930 (GRCm39) |
missense |
probably damaging |
0.97 |
R9154:Ptprc
|
UTSW |
1 |
138,016,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Ptprc
|
UTSW |
1 |
138,011,380 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9428:Ptprc
|
UTSW |
1 |
138,041,485 (GRCm39) |
missense |
probably benign |
0.01 |
R9467:Ptprc
|
UTSW |
1 |
137,993,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Ptprc
|
UTSW |
1 |
138,044,754 (GRCm39) |
missense |
probably benign |
0.01 |
R9479:Ptprc
|
UTSW |
1 |
138,001,388 (GRCm39) |
missense |
probably benign |
0.38 |
R9526:Ptprc
|
UTSW |
1 |
137,996,111 (GRCm39) |
missense |
probably benign |
0.02 |
R9632:Ptprc
|
UTSW |
1 |
138,008,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Ptprc
|
UTSW |
1 |
138,008,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9714:Ptprc
|
UTSW |
1 |
138,008,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Ptprc
|
UTSW |
1 |
138,047,901 (GRCm39) |
missense |
|
|
Z1177:Ptprc
|
UTSW |
1 |
137,995,645 (GRCm39) |
missense |
probably benign |
0.01 |
|