Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
T |
6: 121,654,971 (GRCm39) |
M1432L |
probably benign |
Het |
Alg11 |
A |
G |
8: 22,551,999 (GRCm39) |
R48G |
probably benign |
Het |
Armc8 |
T |
C |
9: 99,409,122 (GRCm39) |
|
probably benign |
Het |
Bmp4 |
T |
A |
14: 46,621,938 (GRCm39) |
D202V |
probably damaging |
Het |
Car12 |
T |
G |
9: 66,669,706 (GRCm39) |
L300R |
probably damaging |
Het |
Cdc37l1 |
T |
A |
19: 28,993,502 (GRCm39) |
*336R |
probably null |
Het |
Cep89 |
A |
G |
7: 35,124,080 (GRCm39) |
|
probably null |
Het |
Ces3b |
T |
A |
8: 105,811,901 (GRCm39) |
D103E |
possibly damaging |
Het |
Chd5 |
A |
G |
4: 152,445,033 (GRCm39) |
D338G |
probably damaging |
Het |
Crot |
A |
G |
5: 9,019,945 (GRCm39) |
C466R |
probably damaging |
Het |
Dach2 |
T |
C |
X: 112,660,101 (GRCm39) |
M194T |
probably benign |
Het |
Dmrtc1b |
A |
G |
X: 101,756,873 (GRCm39) |
D100G |
probably benign |
Het |
Epm2a |
G |
A |
10: 11,332,980 (GRCm39) |
R271H |
probably damaging |
Het |
Fem1c |
G |
T |
18: 46,638,781 (GRCm39) |
T407K |
probably benign |
Het |
Fer1l4 |
T |
C |
2: 155,889,848 (GRCm39) |
Y273C |
probably damaging |
Het |
Foxc2 |
C |
A |
8: 121,844,576 (GRCm39) |
A408E |
probably benign |
Het |
Gbp10 |
A |
T |
5: 105,366,368 (GRCm39) |
M512K |
possibly damaging |
Het |
Gm5134 |
T |
C |
10: 75,828,323 (GRCm39) |
L301P |
probably damaging |
Het |
Grk3 |
A |
T |
5: 113,117,100 (GRCm39) |
D100E |
probably benign |
Het |
Gsdma3 |
T |
A |
11: 98,526,707 (GRCm39) |
D322E |
probably damaging |
Het |
Gucy1a2 |
C |
A |
9: 3,894,556 (GRCm39) |
L680I |
possibly damaging |
Het |
Ighv7-2 |
T |
C |
12: 113,875,766 (GRCm39) |
Y79C |
probably damaging |
Het |
Igkv4-50 |
T |
C |
6: 69,678,024 (GRCm39) |
T27A |
probably benign |
Het |
Ints2 |
T |
C |
11: 86,106,404 (GRCm39) |
D1002G |
probably damaging |
Het |
Map4k5 |
T |
A |
12: 69,896,358 (GRCm39) |
I169F |
possibly damaging |
Het |
Mink1 |
T |
C |
11: 70,488,052 (GRCm39) |
V39A |
probably damaging |
Het |
Mms22l |
T |
A |
4: 24,508,482 (GRCm39) |
H301Q |
probably benign |
Het |
Myh4 |
C |
T |
11: 67,147,305 (GRCm39) |
T1650I |
probably benign |
Het |
Or52n4 |
A |
T |
7: 104,293,870 (GRCm39) |
D234E |
probably benign |
Het |
Or8b37 |
T |
A |
9: 37,958,662 (GRCm39) |
L48Q |
probably damaging |
Het |
Or8b44 |
T |
C |
9: 38,410,769 (GRCm39) |
M268T |
probably benign |
Het |
Pate10 |
T |
C |
9: 35,653,460 (GRCm39) |
I88T |
possibly damaging |
Het |
Pbxip1 |
C |
T |
3: 89,350,988 (GRCm39) |
T117M |
probably damaging |
Het |
Pgghg |
C |
T |
7: 140,526,251 (GRCm39) |
T572M |
probably damaging |
Het |
Phactr2 |
G |
A |
10: 13,121,167 (GRCm39) |
T511I |
probably damaging |
Het |
Pip5k1a |
T |
C |
3: 94,974,724 (GRCm39) |
I385V |
probably benign |
Het |
Pwp2 |
A |
G |
10: 78,018,828 (GRCm39) |
C60R |
probably damaging |
Het |
Rgs11 |
G |
A |
17: 26,426,605 (GRCm39) |
V279I |
probably benign |
Het |
Rttn |
G |
T |
18: 88,991,750 (GRCm39) |
D110Y |
probably damaging |
Het |
Setbp1 |
G |
T |
18: 78,798,925 (GRCm39) |
H1418Q |
probably damaging |
Het |
Sf3b3 |
T |
C |
8: 111,569,608 (GRCm39) |
I37V |
probably benign |
Het |
Slc27a6 |
A |
T |
18: 58,689,977 (GRCm39) |
I148F |
probably benign |
Het |
Slmap |
A |
G |
14: 26,180,621 (GRCm39) |
|
probably benign |
Het |
Speer4a3 |
A |
C |
5: 26,156,614 (GRCm39) |
Y122D |
probably benign |
Het |
Stil |
A |
G |
4: 114,880,893 (GRCm39) |
Q479R |
possibly damaging |
Het |
Svop |
A |
G |
5: 114,166,321 (GRCm39) |
*549Q |
probably null |
Het |
Tnks |
C |
T |
8: 35,316,453 (GRCm39) |
V889I |
possibly damaging |
Het |
Tnrc6c |
T |
A |
11: 117,633,826 (GRCm39) |
V1308E |
possibly damaging |
Het |
Vmn1r208 |
C |
A |
13: 22,956,993 (GRCm39) |
C168F |
probably damaging |
Het |
Vmn2r117 |
A |
T |
17: 23,678,758 (GRCm39) |
M822K |
possibly damaging |
Het |
Vwde |
A |
T |
6: 13,187,148 (GRCm39) |
F780I |
probably damaging |
Het |
Washc2 |
T |
C |
6: 116,197,577 (GRCm39) |
I184T |
possibly damaging |
Het |
Wdr26 |
A |
T |
1: 181,005,361 (GRCm39) |
|
probably benign |
Het |
Zfp608 |
G |
A |
18: 55,031,273 (GRCm39) |
T889M |
probably damaging |
Het |
Zfp955a |
G |
T |
17: 33,463,039 (GRCm39) |
Q31K |
probably damaging |
Het |
Zpbp2 |
T |
C |
11: 98,446,343 (GRCm39) |
L145S |
probably benign |
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 |
|
IGL02476:Vwa8
|
APN |
14 |
79,162,781 (GRCm39) |
missense |
possibly damaging |
0.62 |
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 |
|