Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
C |
A |
5: 121,640,788 (GRCm39) |
E86* |
probably null |
Het |
Ahnak |
T |
G |
19: 8,984,617 (GRCm39) |
I1967S |
possibly damaging |
Het |
Alox12e |
A |
G |
11: 70,212,600 (GRCm39) |
V83A |
possibly damaging |
Het |
Arhgap20 |
A |
T |
9: 51,754,977 (GRCm39) |
R439S |
probably damaging |
Het |
Arl1 |
A |
G |
10: 88,569,458 (GRCm39) |
I20V |
probably damaging |
Het |
Atad2 |
T |
C |
15: 57,995,628 (GRCm39) |
D93G |
probably benign |
Het |
Btbd7 |
T |
G |
12: 102,804,838 (GRCm39) |
K67N |
probably damaging |
Het |
C130050O18Rik |
A |
G |
5: 139,400,301 (GRCm39) |
N118S |
probably benign |
Het |
Ccz1 |
A |
C |
5: 143,946,120 (GRCm39) |
|
probably benign |
Het |
Cdk19 |
A |
G |
10: 40,355,728 (GRCm39) |
S479G |
unknown |
Het |
Chrd |
A |
G |
16: 20,555,737 (GRCm39) |
T503A |
probably damaging |
Het |
Clca4b |
G |
A |
3: 144,617,827 (GRCm39) |
R759* |
probably null |
Het |
Cpa5 |
G |
T |
6: 30,612,604 (GRCm39) |
M1I |
probably null |
Het |
Cr2 |
A |
T |
1: 194,834,029 (GRCm39) |
I920N |
probably benign |
Het |
Crmp1 |
C |
A |
5: 37,437,947 (GRCm39) |
Y430* |
probably null |
Het |
Dars1 |
A |
T |
1: 128,296,163 (GRCm39) |
V390D |
possibly damaging |
Het |
Dmtn |
A |
G |
14: 70,853,555 (GRCm39) |
S85P |
probably damaging |
Het |
Ermardl1 |
A |
G |
17: 15,242,364 (GRCm39) |
E416G |
unknown |
Het |
Fancm |
C |
A |
12: 65,122,605 (GRCm39) |
D42E |
probably damaging |
Het |
Gabrg3 |
T |
A |
7: 56,423,122 (GRCm39) |
Y192F |
possibly damaging |
Het |
Gpr3 |
A |
T |
4: 132,938,209 (GRCm39) |
Y154* |
probably null |
Het |
Huwe1 |
G |
A |
X: 150,716,084 (GRCm39) |
R4331Q |
unknown |
Het |
Ints5 |
C |
A |
19: 8,873,322 (GRCm39) |
P427Q |
possibly damaging |
Het |
Jhy |
A |
T |
9: 40,828,823 (GRCm39) |
V361D |
probably benign |
Het |
Klhl33 |
G |
A |
14: 51,130,322 (GRCm39) |
Q131* |
probably null |
Het |
Lama2 |
A |
T |
10: 27,080,881 (GRCm39) |
C981S |
probably damaging |
Het |
Mks1 |
C |
A |
11: 87,748,041 (GRCm39) |
L225I |
probably damaging |
Het |
Ms4a20 |
A |
T |
19: 11,083,055 (GRCm39) |
Y122N |
probably damaging |
Het |
Nfasc |
T |
A |
1: 132,539,343 (GRCm39) |
S402C |
probably damaging |
Het |
Or2a57 |
T |
C |
6: 43,213,358 (GRCm39) |
I272T |
possibly damaging |
Het |
Or4k50-ps1 |
A |
T |
2: 111,522,517 (GRCm39) |
Y218F |
unknown |
Het |
Or51g2 |
T |
C |
7: 102,622,560 (GRCm39) |
D213G |
probably damaging |
Het |
Pbx4 |
T |
A |
8: 70,316,999 (GRCm39) |
D85E |
possibly damaging |
Het |
Plcd1 |
T |
C |
9: 118,913,709 (GRCm39) |
T50A |
probably damaging |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Psen2 |
C |
A |
1: 180,056,972 (GRCm39) |
E351* |
probably null |
Het |
Rragd |
G |
A |
4: 32,996,083 (GRCm39) |
V143I |
probably damaging |
Het |
Rsph14 |
A |
T |
10: 74,795,423 (GRCm39) |
M254K |
probably damaging |
Het |
Selenoi |
C |
T |
5: 30,437,607 (GRCm39) |
|
probably benign |
Het |
Six6 |
T |
C |
12: 72,986,935 (GRCm39) |
S36P |
|
Het |
Slc12a8 |
T |
C |
16: 33,445,215 (GRCm39) |
S370P |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,716,432 (GRCm39) |
Y357H |
probably benign |
Het |
Socs2 |
A |
T |
10: 95,248,948 (GRCm39) |
V55D |
probably damaging |
Het |
Socs6 |
T |
C |
18: 88,888,852 (GRCm39) |
E21G |
probably benign |
Het |
Spata31e4 |
C |
T |
13: 50,857,007 (GRCm39) |
Q882* |
probably null |
Het |
Speg |
A |
T |
1: 75,365,076 (GRCm39) |
T486S |
possibly damaging |
Het |
Spryd3 |
A |
G |
15: 102,027,843 (GRCm39) |
Y235H |
probably damaging |
Het |
Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
Stxbp5l |
T |
C |
16: 37,165,473 (GRCm39) |
K82E |
probably damaging |
Het |
Sugt1 |
A |
G |
14: 79,825,155 (GRCm39) |
|
probably benign |
Het |
Synm |
T |
C |
7: 67,384,440 (GRCm39) |
Y1074C |
probably damaging |
Het |
Sytl2 |
A |
G |
7: 90,028,748 (GRCm39) |
T476A |
probably benign |
Het |
Tbc1d1 |
T |
C |
5: 64,414,349 (GRCm39) |
S237P |
probably benign |
Het |
Tbc1d5 |
C |
A |
17: 51,063,692 (GRCm39) |
M629I |
probably damaging |
Het |
Tlr11 |
G |
A |
14: 50,598,749 (GRCm39) |
G245D |
probably damaging |
Het |
Tspan4 |
T |
C |
7: 141,069,577 (GRCm39) |
V59A |
probably benign |
Het |
Tulp4 |
T |
A |
17: 6,283,472 (GRCm39) |
V1167E |
possibly damaging |
Het |
Usp42 |
G |
A |
5: 143,708,906 (GRCm39) |
T204M |
probably damaging |
Het |
Vapb |
A |
G |
2: 173,617,948 (GRCm39) |
K147R |
possibly damaging |
Het |
Vmn1r228 |
T |
C |
17: 20,997,422 (GRCm39) |
D32G |
probably benign |
Het |
Vmn2r33 |
A |
G |
7: 7,554,168 (GRCm39) |
F795S |
probably damaging |
Het |
Vmn2r34 |
A |
T |
7: 7,675,527 (GRCm39) |
N620K |
probably damaging |
Het |
Wdr81 |
T |
C |
11: 75,332,908 (GRCm39) |
E652G |
|
Het |
Wdr81 |
A |
T |
11: 75,343,207 (GRCm39) |
S687T |
probably benign |
Het |
Zcrb1 |
A |
G |
15: 93,285,456 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vwf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Vwf
|
APN |
6 |
125,635,835 (GRCm39) |
missense |
unknown |
|
IGL00561:Vwf
|
APN |
6 |
125,619,684 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01104:Vwf
|
APN |
6 |
125,660,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01404:Vwf
|
APN |
6 |
125,654,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01539:Vwf
|
APN |
6 |
125,567,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01550:Vwf
|
APN |
6 |
125,656,252 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01563:Vwf
|
APN |
6 |
125,568,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01637:Vwf
|
APN |
6 |
125,622,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01720:Vwf
|
APN |
6 |
125,619,798 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01834:Vwf
|
APN |
6 |
125,567,133 (GRCm39) |
splice site |
probably benign |
|
IGL02103:Vwf
|
APN |
6 |
125,623,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02120:Vwf
|
APN |
6 |
125,592,997 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02174:Vwf
|
APN |
6 |
125,532,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02203:Vwf
|
APN |
6 |
125,619,369 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02420:Vwf
|
APN |
6 |
125,654,879 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02723:Vwf
|
APN |
6 |
125,619,893 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02818:Vwf
|
APN |
6 |
125,640,511 (GRCm39) |
missense |
probably benign |
|
IGL02931:Vwf
|
APN |
6 |
125,592,931 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03015:Vwf
|
APN |
6 |
125,661,101 (GRCm39) |
splice site |
probably benign |
|
IGL03038:Vwf
|
APN |
6 |
125,581,120 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03060:Vwf
|
APN |
6 |
125,640,523 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Vwf
|
APN |
6 |
125,576,326 (GRCm39) |
nonsense |
probably null |
|
IGL03266:Vwf
|
APN |
6 |
125,655,040 (GRCm39) |
splice site |
probably benign |
|
gingerman
|
UTSW |
6 |
125,639,926 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0605_vwf_644
|
UTSW |
6 |
125,662,800 (GRCm39) |
missense |
probably benign |
0.02 |
R1575_Vwf_091
|
UTSW |
6 |
125,640,534 (GRCm39) |
nonsense |
probably null |
|
R1628_Vwf_608
|
UTSW |
6 |
125,624,701 (GRCm39) |
unclassified |
probably benign |
|
R1669_Vwf_448
|
UTSW |
6 |
125,624,869 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1833_Vwf_948
|
UTSW |
6 |
125,619,000 (GRCm39) |
missense |
probably benign |
0.14 |
R2130_vwf_946
|
UTSW |
6 |
125,634,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R6360_Vwf_065
|
UTSW |
6 |
125,660,489 (GRCm39) |
missense |
probably benign |
0.13 |
R7900_Vwf_938
|
UTSW |
6 |
125,605,439 (GRCm39) |
critical splice donor site |
probably null |
|
Russiahouse
|
UTSW |
6 |
125,616,304 (GRCm39) |
nonsense |
probably null |
|
B5639:Vwf
|
UTSW |
6 |
125,619,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Vwf
|
UTSW |
6 |
125,659,775 (GRCm39) |
missense |
probably benign |
0.05 |
R0025:Vwf
|
UTSW |
6 |
125,659,775 (GRCm39) |
missense |
probably benign |
0.05 |
R0087:Vwf
|
UTSW |
6 |
125,622,917 (GRCm39) |
missense |
probably benign |
0.03 |
R0194:Vwf
|
UTSW |
6 |
125,620,260 (GRCm39) |
missense |
probably benign |
|
R0206:Vwf
|
UTSW |
6 |
125,614,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Vwf
|
UTSW |
6 |
125,663,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0233:Vwf
|
UTSW |
6 |
125,663,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0390:Vwf
|
UTSW |
6 |
125,603,324 (GRCm39) |
nonsense |
probably null |
|
R0427:Vwf
|
UTSW |
6 |
125,650,902 (GRCm39) |
missense |
probably benign |
|
R0437:Vwf
|
UTSW |
6 |
125,543,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R0470:Vwf
|
UTSW |
6 |
125,605,391 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0499:Vwf
|
UTSW |
6 |
125,615,077 (GRCm39) |
missense |
probably benign |
0.10 |
R0554:Vwf
|
UTSW |
6 |
125,619,744 (GRCm39) |
missense |
probably benign |
0.13 |
R0605:Vwf
|
UTSW |
6 |
125,662,800 (GRCm39) |
missense |
probably benign |
0.02 |
R0711:Vwf
|
UTSW |
6 |
125,603,234 (GRCm39) |
missense |
probably benign |
0.01 |
R0723:Vwf
|
UTSW |
6 |
125,543,225 (GRCm39) |
missense |
probably benign |
0.01 |
R0973:Vwf
|
UTSW |
6 |
125,619,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Vwf
|
UTSW |
6 |
125,567,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1115:Vwf
|
UTSW |
6 |
125,632,028 (GRCm39) |
missense |
unknown |
|
R1156:Vwf
|
UTSW |
6 |
125,614,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1191:Vwf
|
UTSW |
6 |
125,576,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Vwf
|
UTSW |
6 |
125,580,271 (GRCm39) |
splice site |
probably null |
|
R1398:Vwf
|
UTSW |
6 |
125,580,420 (GRCm39) |
missense |
probably benign |
0.02 |
R1435:Vwf
|
UTSW |
6 |
125,619,212 (GRCm39) |
nonsense |
probably null |
|
R1528:Vwf
|
UTSW |
6 |
125,585,254 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1575:Vwf
|
UTSW |
6 |
125,640,534 (GRCm39) |
nonsense |
probably null |
|
R1575:Vwf
|
UTSW |
6 |
125,632,214 (GRCm39) |
missense |
unknown |
|
R1628:Vwf
|
UTSW |
6 |
125,624,701 (GRCm39) |
unclassified |
probably benign |
|
R1669:Vwf
|
UTSW |
6 |
125,624,869 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1699:Vwf
|
UTSW |
6 |
125,662,863 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1699:Vwf
|
UTSW |
6 |
125,620,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Vwf
|
UTSW |
6 |
125,623,245 (GRCm39) |
missense |
probably benign |
0.05 |
R1742:Vwf
|
UTSW |
6 |
125,644,513 (GRCm39) |
missense |
probably benign |
0.02 |
R1809:Vwf
|
UTSW |
6 |
125,567,138 (GRCm39) |
splice site |
probably benign |
|
R1833:Vwf
|
UTSW |
6 |
125,619,000 (GRCm39) |
missense |
probably benign |
0.14 |
R1866:Vwf
|
UTSW |
6 |
125,644,492 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1870:Vwf
|
UTSW |
6 |
125,619,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Vwf
|
UTSW |
6 |
125,605,335 (GRCm39) |
missense |
probably benign |
0.00 |
R1941:Vwf
|
UTSW |
6 |
125,616,242 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2061:Vwf
|
UTSW |
6 |
125,568,151 (GRCm39) |
missense |
probably damaging |
0.98 |
R2103:Vwf
|
UTSW |
6 |
125,623,293 (GRCm39) |
missense |
probably benign |
0.31 |
R2104:Vwf
|
UTSW |
6 |
125,623,293 (GRCm39) |
missense |
probably benign |
0.31 |
R2130:Vwf
|
UTSW |
6 |
125,634,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R2159:Vwf
|
UTSW |
6 |
125,603,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R2178:Vwf
|
UTSW |
6 |
125,619,095 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2656:Vwf
|
UTSW |
6 |
125,532,324 (GRCm39) |
missense |
probably benign |
0.00 |
R2913:Vwf
|
UTSW |
6 |
125,662,809 (GRCm39) |
missense |
probably benign |
0.08 |
R2917:Vwf
|
UTSW |
6 |
125,585,106 (GRCm39) |
missense |
probably benign |
0.07 |
R3726:Vwf
|
UTSW |
6 |
125,654,911 (GRCm39) |
utr 3 prime |
probably benign |
|
R3735:Vwf
|
UTSW |
6 |
125,565,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R3774:Vwf
|
UTSW |
6 |
125,626,062 (GRCm39) |
splice site |
probably null |
|
R3934:Vwf
|
UTSW |
6 |
125,532,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Vwf
|
UTSW |
6 |
125,619,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R4384:Vwf
|
UTSW |
6 |
125,632,079 (GRCm39) |
missense |
unknown |
|
R4743:Vwf
|
UTSW |
6 |
125,661,054 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4760:Vwf
|
UTSW |
6 |
125,547,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Vwf
|
UTSW |
6 |
125,543,268 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4791:Vwf
|
UTSW |
6 |
125,620,326 (GRCm39) |
missense |
|
|
R4871:Vwf
|
UTSW |
6 |
125,663,425 (GRCm39) |
missense |
probably benign |
0.25 |
R4894:Vwf
|
UTSW |
6 |
125,622,897 (GRCm39) |
nonsense |
probably null |
|
R4963:Vwf
|
UTSW |
6 |
125,644,446 (GRCm39) |
nonsense |
probably null |
|
R5010:Vwf
|
UTSW |
6 |
125,543,220 (GRCm39) |
missense |
probably benign |
0.15 |
R5289:Vwf
|
UTSW |
6 |
125,644,473 (GRCm39) |
utr 3 prime |
probably benign |
|
R5512:Vwf
|
UTSW |
6 |
125,650,850 (GRCm39) |
utr 3 prime |
probably benign |
|
R5523:Vwf
|
UTSW |
6 |
125,620,005 (GRCm39) |
missense |
|
|
R5642:Vwf
|
UTSW |
6 |
125,580,381 (GRCm39) |
missense |
|
|
R5860:Vwf
|
UTSW |
6 |
125,656,228 (GRCm39) |
utr 3 prime |
probably benign |
|
R5860:Vwf
|
UTSW |
6 |
125,620,053 (GRCm39) |
missense |
|
|
R5896:Vwf
|
UTSW |
6 |
125,655,725 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5926:Vwf
|
UTSW |
6 |
125,581,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Vwf
|
UTSW |
6 |
125,580,426 (GRCm39) |
missense |
|
|
R6053:Vwf
|
UTSW |
6 |
125,577,628 (GRCm39) |
missense |
probably benign |
0.21 |
R6151:Vwf
|
UTSW |
6 |
125,634,028 (GRCm39) |
missense |
unknown |
|
R6179:Vwf
|
UTSW |
6 |
125,626,252 (GRCm39) |
missense |
unknown |
|
R6181:Vwf
|
UTSW |
6 |
125,543,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R6234:Vwf
|
UTSW |
6 |
125,634,128 (GRCm39) |
missense |
unknown |
|
R6360:Vwf
|
UTSW |
6 |
125,660,489 (GRCm39) |
missense |
probably benign |
0.13 |
R6412:Vwf
|
UTSW |
6 |
125,656,279 (GRCm39) |
missense |
probably benign |
0.00 |
R6464:Vwf
|
UTSW |
6 |
125,616,363 (GRCm39) |
critical splice donor site |
probably null |
|
R6522:Vwf
|
UTSW |
6 |
125,639,926 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6766:Vwf
|
UTSW |
6 |
125,616,339 (GRCm39) |
missense |
unknown |
|
R6856:Vwf
|
UTSW |
6 |
125,619,113 (GRCm39) |
nonsense |
probably null |
|
R6877:Vwf
|
UTSW |
6 |
125,634,164 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6896:Vwf
|
UTSW |
6 |
125,543,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R7113:Vwf
|
UTSW |
6 |
125,632,007 (GRCm39) |
missense |
|
|
R7287:Vwf
|
UTSW |
6 |
125,614,430 (GRCm39) |
missense |
|
|
R7359:Vwf
|
UTSW |
6 |
125,543,220 (GRCm39) |
missense |
|
|
R7509:Vwf
|
UTSW |
6 |
125,619,132 (GRCm39) |
missense |
|
|
R7519:Vwf
|
UTSW |
6 |
125,644,506 (GRCm39) |
missense |
|
|
R7545:Vwf
|
UTSW |
6 |
125,591,060 (GRCm39) |
missense |
|
|
R7549:Vwf
|
UTSW |
6 |
125,603,230 (GRCm39) |
missense |
|
|
R7593:Vwf
|
UTSW |
6 |
125,624,731 (GRCm39) |
missense |
|
|
R7635:Vwf
|
UTSW |
6 |
125,659,697 (GRCm39) |
missense |
|
|
R7793:Vwf
|
UTSW |
6 |
125,663,483 (GRCm39) |
missense |
|
|
R7802:Vwf
|
UTSW |
6 |
125,643,640 (GRCm39) |
missense |
|
|
R7824:Vwf
|
UTSW |
6 |
125,635,778 (GRCm39) |
missense |
|
|
R7849:Vwf
|
UTSW |
6 |
125,633,766 (GRCm39) |
missense |
|
|
R7900:Vwf
|
UTSW |
6 |
125,605,439 (GRCm39) |
critical splice donor site |
probably null |
|
R7919:Vwf
|
UTSW |
6 |
125,624,822 (GRCm39) |
missense |
|
|
R7966:Vwf
|
UTSW |
6 |
125,616,304 (GRCm39) |
nonsense |
probably null |
|
R8101:Vwf
|
UTSW |
6 |
125,547,522 (GRCm39) |
nonsense |
probably null |
|
R8162:Vwf
|
UTSW |
6 |
125,622,799 (GRCm39) |
splice site |
probably null |
|
R8345:Vwf
|
UTSW |
6 |
125,656,265 (GRCm39) |
missense |
|
|
R8853:Vwf
|
UTSW |
6 |
125,634,227 (GRCm39) |
missense |
|
|
R9065:Vwf
|
UTSW |
6 |
125,623,262 (GRCm39) |
missense |
|
|
R9068:Vwf
|
UTSW |
6 |
125,625,792 (GRCm39) |
unclassified |
probably benign |
|
R9128:Vwf
|
UTSW |
6 |
125,619,693 (GRCm39) |
missense |
|
|
R9136:Vwf
|
UTSW |
6 |
125,576,356 (GRCm39) |
splice site |
probably benign |
|
R9164:Vwf
|
UTSW |
6 |
125,542,806 (GRCm39) |
missense |
|
|
R9177:Vwf
|
UTSW |
6 |
125,581,254 (GRCm39) |
missense |
|
|
R9334:Vwf
|
UTSW |
6 |
125,654,909 (GRCm39) |
missense |
|
|
R9508:Vwf
|
UTSW |
6 |
125,532,471 (GRCm39) |
missense |
|
|
R9553:Vwf
|
UTSW |
6 |
125,577,662 (GRCm39) |
missense |
|
|
R9660:Vwf
|
UTSW |
6 |
125,568,670 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9706:Vwf
|
UTSW |
6 |
125,601,536 (GRCm39) |
missense |
|
|
R9708:Vwf
|
UTSW |
6 |
125,634,053 (GRCm39) |
missense |
|
|
R9712:Vwf
|
UTSW |
6 |
125,601,536 (GRCm39) |
missense |
|
|
R9714:Vwf
|
UTSW |
6 |
125,601,536 (GRCm39) |
missense |
|
|
R9728:Vwf
|
UTSW |
6 |
125,568,670 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9758:Vwf
|
UTSW |
6 |
125,603,230 (GRCm39) |
missense |
|
|
X0021:Vwf
|
UTSW |
6 |
125,623,294 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Vwf
|
UTSW |
6 |
125,580,396 (GRCm39) |
missense |
probably null |
0.05 |
Z1176:Vwf
|
UTSW |
6 |
125,580,271 (GRCm39) |
splice site |
probably null |
|
Z1176:Vwf
|
UTSW |
6 |
125,568,194 (GRCm39) |
missense |
|
|
|