Other mutations in this stock |
Total: 223 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447A16Rik |
G |
A |
15: 37,439,844 (GRCm39) |
|
probably benign |
Het |
Aadat |
A |
G |
8: 60,979,746 (GRCm39) |
T203A |
probably damaging |
Het |
Abca13 |
T |
A |
11: 9,199,680 (GRCm39) |
F104L |
probably benign |
Het |
Acox1 |
T |
A |
11: 116,089,109 (GRCm39) |
|
probably null |
Het |
Adam34l |
T |
C |
8: 44,078,620 (GRCm39) |
N535D |
probably damaging |
Het |
Adamts17 |
C |
T |
7: 66,799,704 (GRCm39) |
R1060* |
probably null |
Het |
Adgrg6 |
T |
C |
10: 14,315,526 (GRCm39) |
T593A |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,291,071 (GRCm39) |
P1454Q |
probably benign |
Het |
Ap2m1 |
T |
A |
16: 20,358,088 (GRCm39) |
N35K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Atr |
G |
A |
9: 95,779,634 (GRCm39) |
V1331I |
probably benign |
Het |
Bola1 |
C |
T |
3: 96,104,426 (GRCm39) |
G56D |
probably benign |
Het |
Brsk1 |
A |
G |
7: 4,707,218 (GRCm39) |
D257G |
probably damaging |
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 |
Cbs |
G |
T |
17: 31,839,923 (GRCm39) |
A337E |
probably benign |
Het |
Ccdc186 |
A |
C |
19: 56,797,652 (GRCm39) |
H306Q |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cd55 |
C |
A |
1: 130,387,370 (GRCm39) |
A143S |
probably benign |
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 |
Cfh |
C |
T |
1: 140,075,435 (GRCm39) |
V268I |
possibly damaging |
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 |
Chi3l1 |
C |
T |
1: 134,116,267 (GRCm39) |
A250V |
probably damaging |
Het |
Chrnb1 |
C |
A |
11: 69,676,588 (GRCm39) |
D388Y |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,276,448 (GRCm39) |
F360Y |
possibly damaging |
Het |
Clgn |
A |
G |
8: 84,149,659 (GRCm39) |
S387G |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Coil |
G |
A |
11: 88,864,802 (GRCm39) |
V10I |
probably damaging |
Het |
Col4a1 |
G |
A |
8: 11,262,712 (GRCm39) |
P1256S |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,939,554 (GRCm39) |
F597Y |
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 |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,880,015 (GRCm39) |
Q391L |
probably damaging |
Het |
Cspg4 |
G |
T |
9: 56,805,821 (GRCm39) |
V2211L |
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 |
Dhx30 |
T |
C |
9: 109,927,819 (GRCm39) |
H101R |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,880,666 (GRCm39) |
D3818V |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,960,345 (GRCm39) |
C2572Y |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Ehf |
T |
G |
2: 103,104,251 (GRCm39) |
T186P |
possibly damaging |
Het |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Etnk2 |
C |
A |
1: 133,293,325 (GRCm39) |
D89E |
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 |
Fam187b |
C |
T |
7: 30,688,445 (GRCm39) |
Q268* |
probably null |
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 |
Fat3 |
A |
C |
9: 15,907,611 (GRCm39) |
V2797G |
possibly damaging |
Het |
Fcamr |
A |
C |
1: 130,732,364 (GRCm39) |
N117T |
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 |
G |
1: 130,732,306 (GRCm39) |
R98G |
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 |
Fut10 |
T |
A |
8: 31,691,418 (GRCm39) |
S88T |
probably benign |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gli2 |
G |
T |
1: 118,929,774 (GRCm39) |
H44Q |
probably benign |
Het |
Gli2 |
C |
T |
1: 118,795,817 (GRCm39) |
A113T |
possibly damaging |
Het |
Glrx2 |
C |
T |
1: 143,615,478 (GRCm39) |
A27V |
possibly damaging |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Gse1 |
G |
A |
8: 121,294,992 (GRCm39) |
|
probably benign |
Het |
Heatr4 |
T |
C |
12: 84,014,346 (GRCm39) |
I630M |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,439,902 (GRCm39) |
Y1134F |
possibly damaging |
Het |
Igfn1 |
G |
A |
1: 135,887,666 (GRCm39) |
P2466L |
probably damaging |
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 |
C |
T |
1: 135,907,653 (GRCm39) |
A231T |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,910,213 (GRCm39) |
R124W |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,363 (GRCm39) |
E29G |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,421 (GRCm39) |
I10V |
unknown |
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 |
Ildr1 |
A |
T |
16: 36,528,698 (GRCm39) |
T48S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,945,526 (GRCm39) |
F749S |
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnh5 |
T |
C |
12: 75,184,465 (GRCm39) |
D86G |
probably benign |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif1b |
T |
C |
4: 149,272,179 (GRCm39) |
T1541A |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,087,859 (GRCm39) |
I983V |
possibly damaging |
Het |
Kif26a |
T |
C |
12: 112,143,219 (GRCm39) |
S1158P |
possibly damaging |
Het |
Kmt2d |
A |
G |
15: 98,763,013 (GRCm39) |
C279R |
probably damaging |
Het |
Kpna3 |
T |
A |
14: 61,605,150 (GRCm39) |
E499V |
probably benign |
Het |
Krt16 |
T |
C |
11: 100,138,533 (GRCm39) |
E205G |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
probably benign |
Het |
Lax1 |
G |
A |
1: 133,611,372 (GRCm39) |
P67S |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,716 (GRCm39) |
R342G |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
probably benign |
Het |
Lgr6 |
G |
T |
1: 134,918,373 (GRCm39) |
H263N |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,931,214 (GRCm39) |
S3N |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Mb21d2 |
A |
G |
16: 28,647,173 (GRCm39) |
V267A |
probably benign |
Het |
Mfrp |
A |
G |
9: 44,015,884 (GRCm39) |
T334A |
possibly damaging |
Het |
Morc1 |
T |
A |
16: 48,432,660 (GRCm39) |
D709E |
probably benign |
Het |
Mrgpra2b |
A |
G |
7: 47,114,627 (GRCm39) |
I35T |
probably benign |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,392,614 (GRCm39) |
C3206S |
probably damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Ndufaf7 |
A |
T |
17: 79,245,058 (GRCm39) |
K59M |
probably damaging |
Het |
Necab3 |
T |
C |
2: 154,388,795 (GRCm39) |
S208G |
probably benign |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
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 |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or3a1c |
A |
G |
11: 74,046,802 (GRCm39) |
D274G |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or5m13b |
T |
A |
2: 85,754,466 (GRCm39) |
L285I |
possibly damaging |
Het |
Or8b12i |
A |
T |
9: 20,082,209 (GRCm39) |
Y219* |
probably null |
Het |
Otoa |
T |
C |
7: 120,724,662 (GRCm39) |
V447A |
probably benign |
Het |
Papss1 |
A |
G |
3: 131,311,728 (GRCm39) |
N319D |
probably benign |
Het |
Patj |
G |
A |
4: 98,320,017 (GRCm39) |
G428D |
possibly damaging |
Het |
Pcdhb3 |
G |
A |
18: 37,434,931 (GRCm39) |
G299D |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,159,404 (GRCm39) |
D432G |
probably damaging |
Het |
Pde5a |
G |
T |
3: 122,541,889 (GRCm39) |
L126F |
probably damaging |
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 |
Pinx1 |
A |
G |
14: 64,115,559 (GRCm39) |
|
probably null |
Het |
Plec |
C |
A |
15: 76,061,892 (GRCm39) |
E2547* |
probably null |
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 |
Prrx1 |
T |
A |
1: 163,089,536 (GRCm39) |
N97I |
probably damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,575 (GRCm39) |
V400A |
probably benign |
Het |
Ptprc |
C |
A |
1: 138,035,562 (GRCm39) |
E402D |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,561 (GRCm39) |
S405P |
probably benign |
Het |
Ptprc |
T |
G |
1: 138,027,414 (GRCm39) |
N478T |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,039,992 (GRCm39) |
K212E |
possibly damaging |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rbsn |
A |
T |
6: 92,167,000 (GRCm39) |
L548Q |
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: 133,287,721 (GRCm39) |
N352Y |
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 |
Ren1 |
A |
C |
1: 133,284,195 (GRCm39) |
K187Q |
probably benign |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
Het |
Rnpep |
G |
C |
1: 135,211,715 (GRCm39) |
A11G |
probably benign |
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 |
Ryr2 |
C |
T |
13: 11,602,308 (GRCm39) |
V4525M |
possibly damaging |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
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 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
Het |
Slc13a5 |
C |
T |
11: 72,157,285 (GRCm39) |
|
probably null |
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 |
Slc9a8 |
T |
C |
2: 167,266,065 (GRCm39) |
F14S |
probably benign |
Het |
Spock3 |
T |
C |
8: 63,802,011 (GRCm39) |
L330P |
probably damaging |
Het |
Stab2 |
T |
G |
10: 86,773,903 (GRCm39) |
R809S |
probably benign |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
probably benign |
Het |
Steap3 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Tecta |
G |
A |
9: 42,303,218 (GRCm39) |
T138I |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
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 |
Traf7 |
A |
G |
17: 24,731,353 (GRCm39) |
F228L |
probably damaging |
Het |
Trhr |
A |
G |
15: 44,060,549 (GRCm39) |
E23G |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,577,968 (GRCm39) |
T779A |
probably benign |
Het |
Tusc2 |
A |
T |
9: 107,441,830 (GRCm39) |
I68F |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Upf2 |
A |
T |
2: 6,032,261 (GRCm39) |
S191C |
probably damaging |
Het |
Usp24 |
A |
G |
4: 106,217,618 (GRCm39) |
N447S |
possibly damaging |
Het |
Usp42 |
T |
C |
5: 143,700,381 (GRCm39) |
D1214G |
probably damaging |
Het |
Vcam1 |
T |
A |
3: 115,908,164 (GRCm39) |
I633L |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,507,086 (GRCm39) |
Y742C |
probably damaging |
Het |
Vmn2r81 |
C |
A |
10: 79,106,489 (GRCm39) |
T489K |
probably benign |
Het |
Ypel1 |
C |
G |
16: 16,907,283 (GRCm39) |
|
probably benign |
Het |
Zan |
C |
A |
5: 137,413,280 (GRCm39) |
|
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zfp616 |
A |
C |
11: 73,976,597 (GRCm39) |
K955N |
probably damaging |
Het |
Zfyve9 |
A |
C |
4: 108,575,698 (GRCm39) |
V461G |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
|
Other mutations in Sis |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00582:Sis
|
APN |
3 |
72,853,969 (GRCm39) |
missense |
probably benign |
|
IGL00715:Sis
|
APN |
3 |
72,841,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00721:Sis
|
APN |
3 |
72,850,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Sis
|
APN |
3 |
72,814,570 (GRCm39) |
splice site |
probably benign |
|
IGL00783:Sis
|
APN |
3 |
72,853,965 (GRCm39) |
missense |
probably benign |
|
IGL00805:Sis
|
APN |
3 |
72,841,532 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00932:Sis
|
APN |
3 |
72,848,289 (GRCm39) |
splice site |
probably benign |
|
IGL01020:Sis
|
APN |
3 |
72,874,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Sis
|
APN |
3 |
72,819,209 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01286:Sis
|
APN |
3 |
72,848,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Sis
|
APN |
3 |
72,868,354 (GRCm39) |
missense |
probably benign |
|
IGL01514:Sis
|
APN |
3 |
72,843,253 (GRCm39) |
splice site |
probably benign |
|
IGL01986:Sis
|
APN |
3 |
72,852,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Sis
|
APN |
3 |
72,836,032 (GRCm39) |
nonsense |
probably null |
|
IGL02132:Sis
|
APN |
3 |
72,854,804 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02152:Sis
|
APN |
3 |
72,796,319 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02200:Sis
|
APN |
3 |
72,850,937 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Sis
|
APN |
3 |
72,863,523 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02307:Sis
|
APN |
3 |
72,819,167 (GRCm39) |
splice site |
probably benign |
|
IGL02374:Sis
|
APN |
3 |
72,832,789 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02437:Sis
|
APN |
3 |
72,826,947 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02571:Sis
|
APN |
3 |
72,863,637 (GRCm39) |
splice site |
probably benign |
|
IGL02601:Sis
|
APN |
3 |
72,820,543 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03063:Sis
|
APN |
3 |
72,835,630 (GRCm39) |
missense |
probably benign |
|
IGL03382:Sis
|
APN |
3 |
72,836,052 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03397:Sis
|
APN |
3 |
72,843,212 (GRCm39) |
missense |
probably benign |
0.44 |
PIT1430001:Sis
|
UTSW |
3 |
72,830,162 (GRCm39) |
missense |
probably damaging |
0.97 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0046:Sis
|
UTSW |
3 |
72,839,427 (GRCm39) |
missense |
probably benign |
0.01 |
R0094:Sis
|
UTSW |
3 |
72,828,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sis
|
UTSW |
3 |
72,835,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Sis
|
UTSW |
3 |
72,867,629 (GRCm39) |
missense |
probably benign |
0.29 |
R0544:Sis
|
UTSW |
3 |
72,858,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Sis
|
UTSW |
3 |
72,832,740 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0617:Sis
|
UTSW |
3 |
72,872,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0698:Sis
|
UTSW |
3 |
72,817,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Sis
|
UTSW |
3 |
72,848,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Sis
|
UTSW |
3 |
72,857,155 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0706:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0710:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0752:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0753:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0754:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0767:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0769:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0772:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0774:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0776:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0818:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0885:Sis
|
UTSW |
3 |
72,819,282 (GRCm39) |
nonsense |
probably null |
|
R1076:Sis
|
UTSW |
3 |
72,841,431 (GRCm39) |
missense |
probably damaging |
0.97 |
R1140:Sis
|
UTSW |
3 |
72,858,949 (GRCm39) |
missense |
probably damaging |
0.98 |
R1175:Sis
|
UTSW |
3 |
72,865,437 (GRCm39) |
splice site |
probably benign |
|
R1301:Sis
|
UTSW |
3 |
72,853,915 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1437:Sis
|
UTSW |
3 |
72,841,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1472:Sis
|
UTSW |
3 |
72,796,360 (GRCm39) |
missense |
probably benign |
0.12 |
R1584:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1707:Sis
|
UTSW |
3 |
72,816,420 (GRCm39) |
splice site |
probably benign |
|
R1715:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1719:Sis
|
UTSW |
3 |
72,872,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1820:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R1973:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Sis
|
UTSW |
3 |
72,820,570 (GRCm39) |
missense |
probably benign |
0.01 |
R2233:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2235:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2276:Sis
|
UTSW |
3 |
72,821,934 (GRCm39) |
nonsense |
probably null |
|
R2435:Sis
|
UTSW |
3 |
72,819,237 (GRCm39) |
missense |
probably benign |
0.01 |
R2885:Sis
|
UTSW |
3 |
72,816,506 (GRCm39) |
missense |
probably benign |
0.01 |
R2966:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
probably benign |
0.30 |
R3708:Sis
|
UTSW |
3 |
72,850,856 (GRCm39) |
missense |
probably benign |
0.02 |
R3790:Sis
|
UTSW |
3 |
72,828,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Sis
|
UTSW |
3 |
72,832,929 (GRCm39) |
missense |
probably benign |
0.01 |
R3858:Sis
|
UTSW |
3 |
72,835,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R3974:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R3975:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R4037:Sis
|
UTSW |
3 |
72,835,935 (GRCm39) |
missense |
probably benign |
|
R4080:Sis
|
UTSW |
3 |
72,828,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Sis
|
UTSW |
3 |
72,868,415 (GRCm39) |
missense |
probably benign |
|
R4394:Sis
|
UTSW |
3 |
72,863,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Sis
|
UTSW |
3 |
72,835,492 (GRCm39) |
splice site |
probably null |
|
R4573:Sis
|
UTSW |
3 |
72,835,570 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4868:Sis
|
UTSW |
3 |
72,850,881 (GRCm39) |
missense |
probably benign |
0.09 |
R5023:Sis
|
UTSW |
3 |
72,841,455 (GRCm39) |
missense |
probably benign |
0.05 |
R5264:Sis
|
UTSW |
3 |
72,857,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R5414:Sis
|
UTSW |
3 |
72,859,826 (GRCm39) |
missense |
probably benign |
|
R5462:Sis
|
UTSW |
3 |
72,857,171 (GRCm39) |
missense |
probably damaging |
0.96 |
R5523:Sis
|
UTSW |
3 |
72,798,754 (GRCm39) |
missense |
probably benign |
0.00 |
R5584:Sis
|
UTSW |
3 |
72,817,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Sis
|
UTSW |
3 |
72,821,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5725:Sis
|
UTSW |
3 |
72,872,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Sis
|
UTSW |
3 |
72,835,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R5790:Sis
|
UTSW |
3 |
72,835,507 (GRCm39) |
missense |
probably benign |
|
R5864:Sis
|
UTSW |
3 |
72,857,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Sis
|
UTSW |
3 |
72,867,589 (GRCm39) |
critical splice donor site |
probably null |
|
R5925:Sis
|
UTSW |
3 |
72,828,713 (GRCm39) |
splice site |
probably null |
|
R6018:Sis
|
UTSW |
3 |
72,820,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6029:Sis
|
UTSW |
3 |
72,835,641 (GRCm39) |
missense |
probably benign |
0.30 |
R6124:Sis
|
UTSW |
3 |
72,860,544 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6171:Sis
|
UTSW |
3 |
72,868,360 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6182:Sis
|
UTSW |
3 |
72,811,626 (GRCm39) |
missense |
probably benign |
0.05 |
R6295:Sis
|
UTSW |
3 |
72,874,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R6416:Sis
|
UTSW |
3 |
72,819,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Sis
|
UTSW |
3 |
72,865,507 (GRCm39) |
missense |
probably benign |
0.00 |
R6472:Sis
|
UTSW |
3 |
72,846,067 (GRCm39) |
nonsense |
probably null |
|
R6517:Sis
|
UTSW |
3 |
72,814,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Sis
|
UTSW |
3 |
72,856,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Sis
|
UTSW |
3 |
72,872,951 (GRCm39) |
missense |
probably benign |
0.06 |
R6853:Sis
|
UTSW |
3 |
72,798,759 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6906:Sis
|
UTSW |
3 |
72,826,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Sis
|
UTSW |
3 |
72,810,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R7357:Sis
|
UTSW |
3 |
72,832,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Sis
|
UTSW |
3 |
72,820,625 (GRCm39) |
splice site |
probably null |
|
R7439:Sis
|
UTSW |
3 |
72,816,374 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7742:Sis
|
UTSW |
3 |
72,832,431 (GRCm39) |
missense |
probably benign |
0.19 |
R7813:Sis
|
UTSW |
3 |
72,832,801 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Sis
|
UTSW |
3 |
72,828,329 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7899:Sis
|
UTSW |
3 |
72,844,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7915:Sis
|
UTSW |
3 |
72,828,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7985:Sis
|
UTSW |
3 |
72,844,294 (GRCm39) |
splice site |
probably null |
|
R8020:Sis
|
UTSW |
3 |
72,816,298 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Sis
|
UTSW |
3 |
72,859,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R8029:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Sis
|
UTSW |
3 |
72,856,901 (GRCm39) |
nonsense |
probably null |
|
R8062:Sis
|
UTSW |
3 |
72,828,321 (GRCm39) |
nonsense |
probably null |
|
R8074:Sis
|
UTSW |
3 |
72,824,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Sis
|
UTSW |
3 |
72,814,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Sis
|
UTSW |
3 |
72,796,378 (GRCm39) |
missense |
probably benign |
0.22 |
R8349:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8366:Sis
|
UTSW |
3 |
72,865,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8449:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8474:Sis
|
UTSW |
3 |
72,836,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8515:Sis
|
UTSW |
3 |
72,836,742 (GRCm39) |
missense |
probably benign |
0.00 |
R8680:Sis
|
UTSW |
3 |
72,867,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Sis
|
UTSW |
3 |
72,867,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R9098:Sis
|
UTSW |
3 |
72,844,578 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9466:Sis
|
UTSW |
3 |
72,872,910 (GRCm39) |
critical splice donor site |
probably null |
|
R9574:Sis
|
UTSW |
3 |
72,828,490 (GRCm39) |
missense |
probably benign |
0.05 |
R9630:Sis
|
UTSW |
3 |
72,828,722 (GRCm39) |
missense |
probably benign |
0.11 |
R9680:Sis
|
UTSW |
3 |
72,863,621 (GRCm39) |
missense |
probably benign |
0.12 |
R9709:Sis
|
UTSW |
3 |
72,799,074 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9731:Sis
|
UTSW |
3 |
72,835,543 (GRCm39) |
missense |
probably benign |
0.01 |
X0009:Sis
|
UTSW |
3 |
72,796,355 (GRCm39) |
missense |
probably damaging |
0.99 |
X0024:Sis
|
UTSW |
3 |
72,836,003 (GRCm39) |
missense |
probably benign |
|
X0060:Sis
|
UTSW |
3 |
72,828,239 (GRCm39) |
intron |
probably benign |
|
Z1176:Sis
|
UTSW |
3 |
72,850,890 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Sis
|
UTSW |
3 |
72,811,606 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Sis
|
UTSW |
3 |
72,850,902 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,817,807 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,816,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
|