Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730596B20Rik |
A |
G |
6: 52,156,500 (GRCm39) |
|
probably benign |
Het |
Acan |
A |
G |
7: 78,749,530 (GRCm39) |
S11G |
probably null |
Het |
Ankrd13d |
A |
C |
19: 4,332,256 (GRCm39) |
V56G |
probably damaging |
Het |
Arl15 |
A |
G |
13: 114,104,151 (GRCm39) |
Y76C |
probably damaging |
Het |
Aspg |
G |
A |
12: 112,087,432 (GRCm39) |
C296Y |
probably damaging |
Het |
Astl |
T |
A |
2: 127,187,889 (GRCm39) |
D101E |
probably benign |
Het |
Bmpr2 |
A |
G |
1: 59,881,977 (GRCm39) |
N202S |
probably benign |
Het |
Borcs7 |
T |
C |
19: 46,690,003 (GRCm39) |
*106Q |
probably null |
Het |
Brip1 |
A |
G |
11: 85,955,865 (GRCm39) |
S883P |
possibly damaging |
Het |
Cacng2 |
A |
T |
15: 78,002,991 (GRCm39) |
L34Q |
probably damaging |
Het |
Catip |
A |
C |
1: 74,402,077 (GRCm39) |
D84A |
probably damaging |
Het |
Ccdc162 |
A |
G |
10: 41,510,037 (GRCm39) |
L856S |
possibly damaging |
Het |
Ccdc38 |
A |
G |
10: 93,417,608 (GRCm39) |
K500E |
probably damaging |
Het |
Ccser2 |
T |
C |
14: 36,663,122 (GRCm39) |
K21E |
probably damaging |
Het |
Cd93 |
A |
T |
2: 148,283,439 (GRCm39) |
Y636N |
probably damaging |
Het |
Cep128 |
A |
T |
12: 91,262,998 (GRCm39) |
N300K |
possibly damaging |
Het |
Cfap44 |
A |
G |
16: 44,269,460 (GRCm39) |
T1155A |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,447,951 (GRCm39) |
L550P |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,618,787 (GRCm39) |
Y1867C |
probably damaging |
Het |
Cul3 |
A |
T |
1: 80,249,249 (GRCm39) |
I674N |
probably damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Cyp2d34 |
T |
C |
15: 82,500,552 (GRCm39) |
H429R |
probably benign |
Het |
Dab2ip |
T |
A |
2: 35,582,267 (GRCm39) |
C4* |
probably null |
Het |
Dcaf1 |
A |
G |
9: 106,731,446 (GRCm39) |
E641G |
probably damaging |
Het |
Dda1 |
T |
A |
8: 71,927,276 (GRCm39) |
|
probably benign |
Het |
Dmgdh |
C |
T |
13: 93,888,960 (GRCm39) |
T866I |
probably benign |
Het |
Ect2l |
T |
C |
10: 18,037,250 (GRCm39) |
T383A |
probably benign |
Het |
Ets2 |
A |
G |
16: 95,515,416 (GRCm39) |
N181D |
probably benign |
Het |
Ezh2 |
A |
G |
6: 47,529,357 (GRCm39) |
F222L |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,342,216 (GRCm39) |
L1503P |
probably damaging |
Het |
Fsip2 |
C |
A |
2: 82,809,777 (GRCm39) |
A2032E |
probably damaging |
Het |
Gm1818 |
C |
T |
12: 48,602,346 (GRCm39) |
|
noncoding transcript |
Het |
Gm9493 |
A |
G |
19: 23,597,106 (GRCm39) |
S1G |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,710,942 (GRCm39) |
I868T |
possibly damaging |
Het |
Ift22 |
A |
T |
5: 136,939,987 (GRCm39) |
T17S |
possibly damaging |
Het |
Il4ra |
T |
C |
7: 125,170,735 (GRCm39) |
W216R |
probably damaging |
Het |
Kcnj6 |
A |
T |
16: 94,633,236 (GRCm39) |
W274R |
probably damaging |
Het |
Kctd19 |
G |
A |
8: 106,123,082 (GRCm39) |
H111Y |
probably damaging |
Het |
Kremen2 |
A |
G |
17: 23,961,679 (GRCm39) |
V276A |
probably benign |
Het |
Lig1 |
C |
A |
7: 13,022,598 (GRCm39) |
Q143K |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,403,359 (GRCm39) |
D2071E |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,404,536 (GRCm39) |
M475I |
probably damaging |
Het |
Mbtd1 |
G |
A |
11: 93,820,485 (GRCm39) |
A427T |
probably damaging |
Het |
Myof |
A |
G |
19: 37,915,429 (GRCm39) |
|
probably null |
Het |
Nbeal2 |
T |
C |
9: 110,470,945 (GRCm39) |
D308G |
possibly damaging |
Het |
Ncdn |
T |
C |
4: 126,638,824 (GRCm39) |
Q665R |
probably benign |
Het |
Nkd1 |
T |
C |
8: 89,316,442 (GRCm39) |
|
probably null |
Het |
Nktr |
G |
A |
9: 121,577,455 (GRCm39) |
|
probably benign |
Het |
Npc1l1 |
A |
T |
11: 6,167,806 (GRCm39) |
M995K |
possibly damaging |
Het |
Or10ag59 |
C |
A |
2: 87,406,363 (GRCm39) |
R312S |
probably benign |
Het |
Or11g7 |
A |
T |
14: 50,691,201 (GRCm39) |
R231* |
probably null |
Het |
Or14n1-ps1 |
T |
A |
7: 86,092,397 (GRCm39) |
C69* |
probably null |
Het |
Padi4 |
T |
C |
4: 140,487,351 (GRCm39) |
T184A |
probably damaging |
Het |
Pgm2l1 |
C |
T |
7: 99,915,881 (GRCm39) |
P409S |
probably benign |
Het |
Pgpep1 |
G |
A |
8: 71,105,101 (GRCm39) |
T53M |
probably damaging |
Het |
Pgr |
T |
C |
9: 8,902,006 (GRCm39) |
L513P |
probably damaging |
Het |
Pikfyve |
T |
A |
1: 65,311,730 (GRCm39) |
I1989N |
probably damaging |
Het |
Prrc2a |
T |
C |
17: 35,371,716 (GRCm39) |
T1806A |
probably benign |
Het |
Psd |
T |
C |
19: 46,311,753 (GRCm39) |
E309G |
possibly damaging |
Het |
Qtrt1 |
C |
T |
9: 21,323,299 (GRCm39) |
T50I |
probably damaging |
Het |
Rims2 |
A |
C |
15: 39,538,416 (GRCm39) |
T1320P |
probably damaging |
Het |
Scn11a |
T |
G |
9: 119,594,514 (GRCm39) |
N1293T |
probably damaging |
Het |
Scn8a |
T |
C |
15: 100,872,548 (GRCm39) |
F529S |
possibly damaging |
Het |
Sec14l4 |
A |
T |
11: 3,985,142 (GRCm39) |
D25V |
possibly damaging |
Het |
Sema3a |
C |
T |
5: 13,615,832 (GRCm39) |
R419C |
probably damaging |
Het |
Slc12a1 |
T |
C |
2: 125,032,133 (GRCm39) |
Y595H |
probably damaging |
Het |
Slc25a28 |
A |
T |
19: 43,655,364 (GRCm39) |
H170Q |
possibly damaging |
Het |
Slc26a1 |
T |
A |
5: 108,821,631 (GRCm39) |
Q86L |
probably damaging |
Het |
Slc48a1 |
T |
A |
15: 97,687,798 (GRCm39) |
W51R |
probably damaging |
Het |
Sptlc3 |
T |
A |
2: 139,423,533 (GRCm39) |
V309D |
probably damaging |
Het |
Srcap |
G |
A |
7: 127,140,528 (GRCm39) |
S1375N |
probably damaging |
Het |
Tanc1 |
C |
A |
2: 59,647,837 (GRCm39) |
H986Q |
possibly damaging |
Het |
Tbc1d4 |
A |
G |
14: 101,727,353 (GRCm39) |
V486A |
probably damaging |
Het |
Tceanc2 |
T |
C |
4: 107,004,776 (GRCm39) |
D124G |
probably damaging |
Het |
Tdrd9 |
A |
G |
12: 111,979,720 (GRCm39) |
M402V |
possibly damaging |
Het |
Tmem132d |
T |
C |
5: 127,861,934 (GRCm39) |
D729G |
probably damaging |
Het |
Tmem62 |
T |
A |
2: 120,807,943 (GRCm39) |
I55N |
probably damaging |
Het |
Tnfrsf21 |
A |
T |
17: 43,350,606 (GRCm39) |
N257Y |
possibly damaging |
Het |
Trappc3 |
T |
C |
4: 126,167,834 (GRCm39) |
L131P |
probably damaging |
Het |
Vmn2r25 |
A |
T |
6: 123,799,900 (GRCm39) |
M814K |
possibly damaging |
Het |
Vmn2r87 |
T |
C |
10: 130,308,226 (GRCm39) |
I671V |
probably benign |
Het |
Xrcc4 |
C |
G |
13: 90,139,198 (GRCm39) |
A241P |
possibly damaging |
Het |
Xylt1 |
T |
A |
7: 117,191,135 (GRCm39) |
D310E |
probably benign |
Het |
Zfp27 |
T |
G |
7: 29,594,444 (GRCm39) |
H507P |
possibly damaging |
Het |
Zfp341 |
C |
T |
2: 154,466,954 (GRCm39) |
P108S |
probably benign |
Het |
Zfp641 |
T |
C |
15: 98,190,816 (GRCm39) |
N76S |
probably benign |
Het |
Zfp936 |
T |
C |
7: 42,839,787 (GRCm39) |
V418A |
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 |
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 |
|
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 |
|