Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
G |
T |
2: 68,445,099 (GRCm39) |
|
probably null |
Het |
5730522E02Rik |
A |
T |
11: 25,719,014 (GRCm39) |
V44E |
unknown |
Het |
Adcy9 |
A |
G |
16: 4,236,673 (GRCm39) |
L246S |
possibly damaging |
Het |
Adk |
C |
T |
14: 21,284,997 (GRCm39) |
H123Y |
probably damaging |
Het |
Adra1b |
T |
A |
11: 43,726,794 (GRCm39) |
D41V |
probably benign |
Het |
Ankib1 |
T |
G |
5: 3,751,911 (GRCm39) |
K710Q |
probably damaging |
Het |
Aoc2 |
T |
A |
11: 101,219,203 (GRCm39) |
V542D |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,081,194 (GRCm39) |
N1221S |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGT |
CACTGGTTCTGTGGTTACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGT |
3: 95,795,450 (GRCm39) |
|
probably benign |
Het |
Bmal1 |
T |
C |
7: 112,898,631 (GRCm39) |
V353A |
probably benign |
Het |
Cacna1a |
C |
A |
8: 85,285,922 (GRCm39) |
R856S |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,590,304 (GRCm39) |
M1559V |
|
Het |
Cdh10 |
G |
C |
15: 19,013,445 (GRCm39) |
E682Q |
probably damaging |
Het |
Celsr1 |
T |
C |
15: 85,916,719 (GRCm39) |
D418G |
possibly damaging |
Het |
Cfap44 |
T |
C |
16: 44,291,111 (GRCm39) |
L1537P |
probably damaging |
Het |
Clca3a2 |
A |
G |
3: 144,519,340 (GRCm39) |
S279P |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,874,040 (GRCm39) |
V1449I |
not run |
Het |
Cpt2 |
A |
G |
4: 107,764,339 (GRCm39) |
F475S |
probably damaging |
Het |
Cpxm1 |
T |
C |
2: 130,235,487 (GRCm39) |
T502A |
probably benign |
Het |
Creb3l2 |
G |
T |
6: 37,356,794 (GRCm39) |
T91N |
probably benign |
Het |
D630045J12Rik |
A |
T |
6: 38,119,601 (GRCm39) |
S1714T |
possibly damaging |
Het |
Dennd1c |
C |
A |
17: 57,379,379 (GRCm39) |
V246F |
probably damaging |
Het |
Dse |
A |
G |
10: 34,028,561 (GRCm39) |
V843A |
probably benign |
Het |
Ern2 |
C |
A |
7: 121,769,756 (GRCm39) |
W810L |
probably damaging |
Het |
Fer1l6 |
G |
A |
15: 58,472,281 (GRCm39) |
D906N |
probably damaging |
Het |
Fry |
A |
G |
5: 150,389,791 (GRCm39) |
E140G |
|
Het |
Galnt7 |
A |
G |
8: 58,005,552 (GRCm39) |
V227A |
probably damaging |
Het |
Gas2l3 |
A |
G |
10: 89,249,763 (GRCm39) |
S452P |
probably benign |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
Gm826 |
A |
T |
2: 160,153,942 (GRCm39) |
S34T |
unknown |
Het |
Gzmk |
A |
T |
13: 113,308,535 (GRCm39) |
I222N |
probably benign |
Het |
Hivep3 |
A |
T |
4: 119,956,027 (GRCm39) |
T1448S |
probably benign |
Het |
Hk1 |
T |
C |
10: 62,131,524 (GRCm39) |
D278G |
probably damaging |
Het |
Ipo7 |
C |
A |
7: 109,638,401 (GRCm39) |
Q223K |
possibly damaging |
Het |
Itga9 |
T |
A |
9: 118,598,179 (GRCm39) |
I571N |
probably damaging |
Het |
Itgb6 |
T |
C |
2: 60,450,720 (GRCm39) |
Y573C |
probably damaging |
Het |
Kmt2c |
T |
A |
5: 25,489,562 (GRCm39) |
H4459L |
probably damaging |
Het |
Limch1 |
T |
G |
5: 67,211,580 (GRCm39) |
S894R |
probably damaging |
Het |
Lrit2 |
A |
T |
14: 36,790,867 (GRCm39) |
Q182L |
possibly damaging |
Het |
Mlph |
A |
T |
1: 90,867,100 (GRCm39) |
H374L |
possibly damaging |
Het |
Mmrn2 |
A |
G |
14: 34,121,374 (GRCm39) |
H748R |
probably damaging |
Het |
Mrpl58 |
T |
C |
11: 115,301,092 (GRCm39) |
V134A |
possibly damaging |
Het |
Nae1 |
A |
T |
8: 105,244,871 (GRCm39) |
D353E |
probably benign |
Het |
Naip5 |
A |
C |
13: 100,353,579 (GRCm39) |
F1227V |
probably benign |
Het |
Nln |
A |
T |
13: 104,205,831 (GRCm39) |
F108I |
probably damaging |
Het |
Nop16 |
C |
T |
13: 54,736,417 (GRCm39) |
V94I |
probably benign |
Het |
Nt5c1b |
A |
T |
12: 10,424,903 (GRCm39) |
T150S |
probably benign |
Het |
Or10d4b |
T |
G |
9: 39,535,268 (GRCm39) |
I281S |
possibly damaging |
Het |
Pcdha4 |
T |
C |
18: 37,087,689 (GRCm39) |
V624A |
probably damaging |
Het |
Pcdhga8 |
T |
C |
18: 37,860,483 (GRCm39) |
I513T |
probably benign |
Het |
Prc1 |
A |
T |
7: 79,959,239 (GRCm39) |
|
probably null |
Het |
Prpf4 |
T |
A |
4: 62,336,113 (GRCm39) |
F280Y |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,051,392 (GRCm39) |
E43G |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,446,485 (GRCm39) |
D181E |
probably benign |
Het |
Rab7 |
A |
G |
6: 87,990,624 (GRCm39) |
S17P |
probably damaging |
Het |
Rgs1 |
T |
C |
1: 144,121,134 (GRCm39) |
Y179C |
probably damaging |
Het |
Rrm1 |
T |
C |
7: 102,103,764 (GRCm39) |
C238R |
probably damaging |
Het |
Rusc2 |
T |
A |
4: 43,426,528 (GRCm39) |
L1484Q |
probably damaging |
Het |
Sall3 |
C |
T |
18: 81,015,920 (GRCm39) |
M669I |
probably benign |
Het |
Saxo1 |
A |
C |
4: 86,363,644 (GRCm39) |
F280V |
probably benign |
Het |
Scn2a |
T |
C |
2: 65,532,352 (GRCm39) |
S655P |
probably damaging |
Het |
Senp6 |
G |
T |
9: 80,031,010 (GRCm39) |
E571* |
probably null |
Het |
Sin3b |
C |
G |
8: 73,473,069 (GRCm39) |
T463S |
probably damaging |
Het |
Sirt7 |
C |
A |
11: 120,509,837 (GRCm39) |
R349L |
probably benign |
Het |
Skor1 |
T |
C |
9: 63,053,730 (GRCm39) |
T80A |
probably damaging |
Het |
Slc12a9 |
C |
A |
5: 137,321,082 (GRCm39) |
A478S |
probably damaging |
Het |
Slc25a23 |
T |
A |
17: 57,359,822 (GRCm39) |
R310* |
probably null |
Het |
Slco6c1 |
A |
T |
1: 97,055,579 (GRCm39) |
H107Q |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,377,336 (GRCm39) |
E455G |
probably benign |
Het |
Smo |
G |
C |
6: 29,736,119 (GRCm39) |
G37A |
probably damaging |
Het |
St6galnac1 |
T |
C |
11: 116,660,010 (GRCm39) |
K101R |
probably benign |
Het |
Stat1 |
C |
A |
1: 52,191,530 (GRCm39) |
N628K |
probably benign |
Het |
Syn2 |
A |
T |
6: 115,231,615 (GRCm39) |
Y302F |
probably benign |
Het |
Tapt1 |
T |
G |
5: 44,345,978 (GRCm39) |
Q324P |
probably damaging |
Het |
Tgoln1 |
C |
T |
6: 72,593,403 (GRCm39) |
A26T |
unknown |
Het |
Timm13 |
T |
A |
10: 80,736,378 (GRCm39) |
T43S |
probably benign |
Het |
Tnfrsf19 |
G |
A |
14: 61,242,654 (GRCm39) |
P77S |
possibly damaging |
Het |
Trem3 |
T |
G |
17: 48,564,969 (GRCm39) |
F157V |
probably benign |
Het |
Trgv3 |
T |
A |
13: 19,427,016 (GRCm39) |
M1K |
probably null |
Het |
Trim33 |
T |
A |
3: 103,233,464 (GRCm39) |
S420T |
probably benign |
Het |
Trip11 |
T |
C |
12: 101,851,694 (GRCm39) |
K790R |
probably damaging |
Het |
Trnt1 |
A |
G |
6: 106,755,865 (GRCm39) |
T307A |
probably benign |
Het |
Tshz1 |
T |
C |
18: 84,033,766 (GRCm39) |
Y214C |
probably damaging |
Het |
Vmn2r105 |
T |
A |
17: 20,448,827 (GRCm39) |
T117S |
probably benign |
Het |
Vmn2r45 |
A |
G |
7: 8,484,342 (GRCm39) |
Y488H |
probably benign |
Het |
Wdr35 |
T |
C |
12: 9,036,000 (GRCm39) |
V257A |
probably benign |
Het |
Zfp189 |
T |
A |
4: 49,521,569 (GRCm39) |
S3T |
probably benign |
Het |
Zscan22 |
G |
A |
7: 12,640,833 (GRCm39) |
C359Y |
probably damaging |
Het |
Zscan4-ps2 |
A |
T |
7: 11,251,812 (GRCm39) |
R283* |
probably null |
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 |
|
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 |
|
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 |
|