Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamp |
T |
A |
1: 74,320,683 (GRCm39) |
|
probably benign |
Het |
Birc6 |
A |
G |
17: 75,003,386 (GRCm39) |
E4752G |
possibly damaging |
Het |
Chd1 |
C |
T |
17: 15,954,535 (GRCm39) |
P468S |
probably damaging |
Het |
Cnot3 |
A |
G |
7: 3,661,067 (GRCm39) |
D556G |
probably benign |
Het |
Csnk1d |
A |
G |
11: 120,863,338 (GRCm39) |
Y201H |
probably damaging |
Het |
Dhtkd1 |
A |
G |
2: 5,935,717 (GRCm39) |
S132P |
possibly damaging |
Het |
Dhx58 |
G |
T |
11: 100,593,090 (GRCm39) |
Q206K |
probably benign |
Het |
Dio1 |
C |
A |
4: 107,149,574 (GRCm39) |
V195F |
probably damaging |
Het |
Dio3 |
T |
C |
12: 110,245,916 (GRCm39) |
V84A |
probably benign |
Het |
Dnai4 |
T |
A |
4: 102,944,545 (GRCm39) |
I3L |
possibly damaging |
Het |
Extl3 |
T |
C |
14: 65,314,693 (GRCm39) |
K163R |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,201,950 (GRCm39) |
S375T |
probably damaging |
Het |
Fbrs |
A |
G |
7: 127,086,841 (GRCm39) |
D73G |
probably damaging |
Het |
Fnip1 |
A |
G |
11: 54,390,393 (GRCm39) |
|
probably benign |
Het |
Frmpd4 |
A |
G |
X: 166,280,851 (GRCm39) |
V343A |
probably damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,468 (GRCm39) |
D283G |
probably benign |
Het |
Ghr |
T |
C |
15: 3,349,528 (GRCm39) |
D550G |
probably damaging |
Het |
Glycam1 |
G |
A |
15: 103,471,307 (GRCm39) |
|
probably benign |
Het |
Gpatch8 |
A |
G |
11: 102,369,417 (GRCm39) |
S1374P |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,565,197 (GRCm39) |
M1037K |
probably benign |
Het |
Gtpbp3 |
T |
C |
8: 71,945,242 (GRCm39) |
L438P |
probably damaging |
Het |
Ifi205 |
G |
T |
1: 173,842,627 (GRCm39) |
N356K |
probably damaging |
Het |
Ifi206 |
A |
G |
1: 173,309,132 (GRCm39) |
L288P |
probably benign |
Het |
Ift57 |
T |
C |
16: 49,584,252 (GRCm39) |
V291A |
probably benign |
Het |
Kif13a |
A |
C |
13: 46,938,772 (GRCm39) |
C166G |
probably damaging |
Het |
Lypd6 |
A |
G |
2: 50,080,740 (GRCm39) |
T143A |
possibly damaging |
Het |
Mtus2 |
G |
A |
5: 148,014,748 (GRCm39) |
A514T |
probably benign |
Het |
Neu2 |
T |
C |
1: 87,524,674 (GRCm39) |
W220R |
probably damaging |
Het |
Notch3 |
T |
C |
17: 32,377,612 (GRCm39) |
S155G |
possibly damaging |
Het |
Nrxn2 |
A |
G |
19: 6,505,015 (GRCm39) |
E286G |
probably damaging |
Het |
Onecut3 |
A |
G |
10: 80,349,724 (GRCm39) |
E406G |
probably benign |
Het |
Oog2 |
T |
A |
4: 143,921,799 (GRCm39) |
D236E |
probably benign |
Het |
Pck1 |
A |
G |
2: 173,000,075 (GRCm39) |
H502R |
probably benign |
Het |
Pld1 |
A |
G |
3: 28,102,188 (GRCm39) |
Y313C |
probably damaging |
Het |
Rhox3f |
A |
T |
X: 36,763,192 (GRCm39) |
|
probably benign |
Het |
Rpl34 |
A |
G |
3: 130,520,613 (GRCm39) |
|
probably benign |
Het |
Sema4c |
T |
C |
1: 36,595,031 (GRCm39) |
K31E |
probably damaging |
Het |
Septin11 |
T |
C |
5: 93,296,443 (GRCm39) |
|
probably null |
Het |
Slc4a9 |
T |
A |
18: 36,668,498 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
T |
A |
2: 127,059,408 (GRCm39) |
S434T |
probably benign |
Het |
Snx13 |
A |
T |
12: 35,136,940 (GRCm39) |
I134F |
probably damaging |
Het |
Syt2 |
T |
C |
1: 134,675,369 (GRCm39) |
S407P |
probably benign |
Het |
Tbc1d19 |
T |
C |
5: 54,046,755 (GRCm39) |
|
probably null |
Het |
Tbc1d32 |
G |
T |
10: 56,074,638 (GRCm39) |
Q192K |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,148,560 (GRCm39) |
C1681* |
probably null |
Het |
Vmn1r43 |
T |
A |
6: 89,847,043 (GRCm39) |
I148F |
possibly damaging |
Het |
|
Other mutations in Vwa8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00589:Vwa8
|
APN |
14 |
79,275,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01087:Vwa8
|
APN |
14 |
79,172,669 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01137:Vwa8
|
APN |
14 |
79,341,087 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01359:Vwa8
|
APN |
14 |
79,302,353 (GRCm39) |
nonsense |
probably null |
|
IGL01449:Vwa8
|
APN |
14 |
79,420,428 (GRCm39) |
nonsense |
probably null |
|
IGL01604:Vwa8
|
APN |
14 |
79,418,244 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01636:Vwa8
|
APN |
14 |
79,435,794 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01815:Vwa8
|
APN |
14 |
79,435,717 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02024:Vwa8
|
APN |
14 |
79,331,724 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02033:Vwa8
|
APN |
14 |
79,221,649 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02154:Vwa8
|
APN |
14 |
79,086,733 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02286:Vwa8
|
APN |
14 |
79,184,713 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02393:Vwa8
|
APN |
14 |
79,420,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02430:Vwa8
|
APN |
14 |
79,172,085 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02612:Vwa8
|
APN |
14 |
79,420,552 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02678:Vwa8
|
APN |
14 |
79,221,640 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02797:Vwa8
|
APN |
14 |
79,162,702 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02806:Vwa8
|
APN |
14 |
79,394,528 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02811:Vwa8
|
APN |
14 |
79,231,899 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02892:Vwa8
|
APN |
14 |
79,341,140 (GRCm39) |
splice site |
probably benign |
|
IGL03024:Vwa8
|
APN |
14 |
79,232,538 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03075:Vwa8
|
APN |
14 |
79,171,196 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03090:Vwa8
|
APN |
14 |
79,172,041 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03124:Vwa8
|
APN |
14 |
79,296,255 (GRCm39) |
splice site |
probably benign |
|
IGL03181:Vwa8
|
APN |
14 |
79,246,690 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03296:Vwa8
|
APN |
14 |
79,420,540 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03376:Vwa8
|
APN |
14 |
79,420,574 (GRCm39) |
splice site |
probably null |
|
R6812_Vwa8_870
|
UTSW |
14 |
79,434,859 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03052:Vwa8
|
UTSW |
14 |
79,302,361 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4468001:Vwa8
|
UTSW |
14 |
79,420,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Vwa8
|
UTSW |
14 |
79,331,179 (GRCm39) |
missense |
probably benign |
0.21 |
R0063:Vwa8
|
UTSW |
14 |
79,401,656 (GRCm39) |
splice site |
probably benign |
|
R0063:Vwa8
|
UTSW |
14 |
79,401,656 (GRCm39) |
splice site |
probably benign |
|
R0081:Vwa8
|
UTSW |
14 |
79,320,222 (GRCm39) |
missense |
probably benign |
0.02 |
R0305:Vwa8
|
UTSW |
14 |
79,246,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Vwa8
|
UTSW |
14 |
79,300,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Vwa8
|
UTSW |
14 |
79,184,629 (GRCm39) |
missense |
probably benign |
|
R0602:Vwa8
|
UTSW |
14 |
79,258,060 (GRCm39) |
missense |
probably benign |
0.00 |
R0615:Vwa8
|
UTSW |
14 |
79,145,590 (GRCm39) |
missense |
probably benign |
|
R0791:Vwa8
|
UTSW |
14 |
79,232,016 (GRCm39) |
splice site |
probably benign |
|
R1028:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1037:Vwa8
|
UTSW |
14 |
79,324,094 (GRCm39) |
nonsense |
probably null |
|
R1404:Vwa8
|
UTSW |
14 |
79,263,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R1404:Vwa8
|
UTSW |
14 |
79,263,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R1412:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Vwa8
|
UTSW |
14 |
79,341,134 (GRCm39) |
nonsense |
probably null |
|
R1467:Vwa8
|
UTSW |
14 |
79,341,134 (GRCm39) |
nonsense |
probably null |
|
R1539:Vwa8
|
UTSW |
14 |
79,300,002 (GRCm39) |
missense |
probably benign |
0.00 |
R1556:Vwa8
|
UTSW |
14 |
79,324,121 (GRCm39) |
missense |
probably benign |
|
R1589:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1591:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1645:Vwa8
|
UTSW |
14 |
79,420,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R1688:Vwa8
|
UTSW |
14 |
79,438,543 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1764:Vwa8
|
UTSW |
14 |
79,145,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Vwa8
|
UTSW |
14 |
79,318,576 (GRCm39) |
missense |
probably benign |
0.04 |
R1926:Vwa8
|
UTSW |
14 |
79,258,075 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Vwa8
|
UTSW |
14 |
79,219,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1971:Vwa8
|
UTSW |
14 |
79,162,694 (GRCm39) |
splice site |
probably benign |
|
R2078:Vwa8
|
UTSW |
14 |
79,145,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Vwa8
|
UTSW |
14 |
79,145,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R2230:Vwa8
|
UTSW |
14 |
79,329,843 (GRCm39) |
critical splice donor site |
probably null |
|
R2281:Vwa8
|
UTSW |
14 |
79,302,436 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2313:Vwa8
|
UTSW |
14 |
79,149,658 (GRCm39) |
missense |
probably damaging |
0.98 |
R2847:Vwa8
|
UTSW |
14 |
79,184,582 (GRCm39) |
missense |
probably benign |
0.00 |
R2848:Vwa8
|
UTSW |
14 |
79,184,582 (GRCm39) |
missense |
probably benign |
0.00 |
R2894:Vwa8
|
UTSW |
14 |
79,275,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R2991:Vwa8
|
UTSW |
14 |
79,232,589 (GRCm39) |
missense |
probably benign |
0.00 |
R3077:Vwa8
|
UTSW |
14 |
79,335,782 (GRCm39) |
missense |
probably benign |
0.03 |
R3405:Vwa8
|
UTSW |
14 |
79,401,660 (GRCm39) |
splice site |
probably benign |
|
R3406:Vwa8
|
UTSW |
14 |
79,401,660 (GRCm39) |
splice site |
probably benign |
|
R3708:Vwa8
|
UTSW |
14 |
79,300,136 (GRCm39) |
splice site |
probably benign |
|
R3779:Vwa8
|
UTSW |
14 |
79,339,762 (GRCm39) |
splice site |
probably benign |
|
R3799:Vwa8
|
UTSW |
14 |
79,302,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R4230:Vwa8
|
UTSW |
14 |
79,320,292 (GRCm39) |
missense |
probably benign |
0.00 |
R4425:Vwa8
|
UTSW |
14 |
79,320,246 (GRCm39) |
missense |
probably benign |
0.00 |
R4478:Vwa8
|
UTSW |
14 |
79,106,241 (GRCm39) |
missense |
probably benign |
0.00 |
R4627:Vwa8
|
UTSW |
14 |
79,341,137 (GRCm39) |
critical splice donor site |
probably null |
|
R4835:Vwa8
|
UTSW |
14 |
79,172,053 (GRCm39) |
missense |
probably benign |
0.11 |
R4868:Vwa8
|
UTSW |
14 |
79,420,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Vwa8
|
UTSW |
14 |
79,435,723 (GRCm39) |
missense |
probably benign |
0.05 |
R5137:Vwa8
|
UTSW |
14 |
79,302,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Vwa8
|
UTSW |
14 |
79,221,666 (GRCm39) |
missense |
probably benign |
0.00 |
R5658:Vwa8
|
UTSW |
14 |
79,219,838 (GRCm39) |
critical splice donor site |
probably null |
|
R5841:Vwa8
|
UTSW |
14 |
79,231,958 (GRCm39) |
missense |
probably benign |
|
R6057:Vwa8
|
UTSW |
14 |
79,320,313 (GRCm39) |
missense |
probably benign |
0.21 |
R6244:Vwa8
|
UTSW |
14 |
79,324,102 (GRCm39) |
missense |
probably benign |
|
R6264:Vwa8
|
UTSW |
14 |
79,324,252 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6290:Vwa8
|
UTSW |
14 |
79,331,772 (GRCm39) |
splice site |
probably null |
|
R6332:Vwa8
|
UTSW |
14 |
79,434,904 (GRCm39) |
missense |
probably benign |
|
R6395:Vwa8
|
UTSW |
14 |
79,331,184 (GRCm39) |
missense |
probably benign |
0.02 |
R6472:Vwa8
|
UTSW |
14 |
79,246,610 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6497:Vwa8
|
UTSW |
14 |
79,333,841 (GRCm39) |
missense |
probably benign |
0.00 |
R6527:Vwa8
|
UTSW |
14 |
79,184,653 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6552:Vwa8
|
UTSW |
14 |
79,435,662 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6812:Vwa8
|
UTSW |
14 |
79,434,859 (GRCm39) |
missense |
probably damaging |
0.99 |
R6994:Vwa8
|
UTSW |
14 |
79,145,596 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7040:Vwa8
|
UTSW |
14 |
79,149,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R7357:Vwa8
|
UTSW |
14 |
79,275,641 (GRCm39) |
missense |
probably null |
1.00 |
R7363:Vwa8
|
UTSW |
14 |
79,256,147 (GRCm39) |
missense |
probably benign |
0.05 |
R7381:Vwa8
|
UTSW |
14 |
79,333,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7406:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7408:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7409:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7410:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7483:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7484:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7491:Vwa8
|
UTSW |
14 |
79,320,254 (GRCm39) |
missense |
probably benign |
0.24 |
R7500:Vwa8
|
UTSW |
14 |
79,162,686 (GRCm39) |
splice site |
probably null |
|
R7514:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7582:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7584:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7585:Vwa8
|
UTSW |
14 |
79,219,674 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7647:Vwa8
|
UTSW |
14 |
79,172,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R7685:Vwa8
|
UTSW |
14 |
79,335,740 (GRCm39) |
missense |
probably benign |
|
R7703:Vwa8
|
UTSW |
14 |
79,263,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R7730:Vwa8
|
UTSW |
14 |
79,232,589 (GRCm39) |
missense |
probably benign |
0.00 |
R7775:Vwa8
|
UTSW |
14 |
79,275,587 (GRCm39) |
missense |
probably benign |
0.03 |
R7778:Vwa8
|
UTSW |
14 |
79,275,587 (GRCm39) |
missense |
probably benign |
0.03 |
R7824:Vwa8
|
UTSW |
14 |
79,275,587 (GRCm39) |
missense |
probably benign |
0.03 |
R7885:Vwa8
|
UTSW |
14 |
79,258,089 (GRCm39) |
missense |
probably benign |
0.00 |
R7902:Vwa8
|
UTSW |
14 |
79,329,731 (GRCm39) |
missense |
probably benign |
0.00 |
R8262:Vwa8
|
UTSW |
14 |
79,171,272 (GRCm39) |
critical splice donor site |
probably null |
|
R8458:Vwa8
|
UTSW |
14 |
79,302,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Vwa8
|
UTSW |
14 |
79,174,617 (GRCm39) |
nonsense |
probably null |
|
R8557:Vwa8
|
UTSW |
14 |
79,246,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Vwa8
|
UTSW |
14 |
79,184,702 (GRCm39) |
missense |
probably benign |
0.04 |
R8906:Vwa8
|
UTSW |
14 |
79,329,815 (GRCm39) |
missense |
probably benign |
0.00 |
R8947:Vwa8
|
UTSW |
14 |
79,438,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Vwa8
|
UTSW |
14 |
79,296,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Vwa8
|
UTSW |
14 |
79,324,150 (GRCm39) |
missense |
probably benign |
0.00 |
R9179:Vwa8
|
UTSW |
14 |
79,335,801 (GRCm39) |
missense |
probably benign |
|
R9433:Vwa8
|
UTSW |
14 |
79,335,871 (GRCm39) |
critical splice donor site |
probably null |
|
R9455:Vwa8
|
UTSW |
14 |
79,300,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9496:Vwa8
|
UTSW |
14 |
79,258,122 (GRCm39) |
missense |
probably benign |
|
R9530:Vwa8
|
UTSW |
14 |
79,172,639 (GRCm39) |
missense |
probably benign |
0.33 |
R9584:Vwa8
|
UTSW |
14 |
79,394,549 (GRCm39) |
missense |
probably benign |
|
R9763:Vwa8
|
UTSW |
14 |
79,186,988 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Vwa8
|
UTSW |
14 |
79,219,686 (GRCm39) |
missense |
probably benign |
0.38 |
Z1177:Vwa8
|
UTSW |
14 |
79,296,132 (GRCm39) |
missense |
probably damaging |
1.00 |
|