Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
G |
A |
13: 119,606,631 (GRCm39) |
R291K |
probably benign |
Het |
Abca2 |
T |
C |
2: 25,332,857 (GRCm39) |
S1519P |
probably damaging |
Het |
Abcb11 |
G |
A |
2: 69,087,639 (GRCm39) |
A1042V |
probably damaging |
Het |
Abcc10 |
A |
T |
17: 46,623,845 (GRCm39) |
|
probably null |
Het |
Abcc10 |
G |
T |
17: 46,623,846 (GRCm39) |
|
probably benign |
Het |
Alkbh3 |
A |
C |
2: 93,811,914 (GRCm39) |
L240V |
probably damaging |
Het |
Apol10b |
T |
C |
15: 77,469,608 (GRCm39) |
S190G |
probably benign |
Het |
Atp1a3 |
C |
A |
7: 24,698,392 (GRCm39) |
C135F |
probably benign |
Het |
Atp4a |
C |
G |
7: 30,419,526 (GRCm39) |
R659G |
probably benign |
Het |
Bicra |
A |
G |
7: 15,722,687 (GRCm39) |
S277P |
possibly damaging |
Het |
Bltp1 |
A |
T |
3: 37,043,953 (GRCm39) |
H2820L |
possibly damaging |
Het |
Bmp8a |
T |
C |
4: 123,210,690 (GRCm39) |
E275G |
probably benign |
Het |
Ccdc102a |
T |
C |
8: 95,640,054 (GRCm39) |
E80G |
probably damaging |
Het |
Cdh23 |
T |
C |
10: 60,246,576 (GRCm39) |
D954G |
probably damaging |
Het |
Chrm4 |
A |
G |
2: 91,758,788 (GRCm39) |
T399A |
possibly damaging |
Het |
Clcn3 |
A |
G |
8: 61,387,571 (GRCm39) |
V199A |
possibly damaging |
Het |
Crlf1 |
T |
C |
8: 70,952,164 (GRCm39) |
|
probably null |
Het |
Crx |
G |
T |
7: 15,605,071 (GRCm39) |
S57* |
probably null |
Het |
Cstpp1 |
A |
G |
2: 91,252,298 (GRCm39) |
L21P |
probably damaging |
Het |
Cyp4f16 |
A |
G |
17: 32,756,072 (GRCm39) |
I34V |
possibly damaging |
Het |
Daxx |
T |
C |
17: 34,132,598 (GRCm39) |
V576A |
probably benign |
Het |
Ddx17 |
C |
T |
15: 79,421,672 (GRCm39) |
R351H |
probably damaging |
Het |
Dhx38 |
T |
C |
8: 110,285,261 (GRCm39) |
|
probably benign |
Het |
Dnd1 |
T |
C |
18: 36,897,552 (GRCm39) |
|
probably benign |
Het |
Dync1i2 |
A |
T |
2: 71,058,169 (GRCm39) |
|
probably null |
Het |
E2f6 |
T |
C |
12: 16,866,446 (GRCm39) |
S52P |
probably benign |
Het |
Epb41l4a |
A |
G |
18: 34,013,326 (GRCm39) |
F116S |
probably damaging |
Het |
Ext1 |
T |
C |
15: 52,969,502 (GRCm39) |
N362S |
probably damaging |
Het |
Fam227a |
C |
A |
15: 79,528,189 (GRCm39) |
K79N |
possibly damaging |
Het |
Fam228a |
T |
A |
12: 4,782,759 (GRCm39) |
L111F |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,173,625 (GRCm39) |
T2363A |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,908,228 (GRCm39) |
N2591K |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,560,436 (GRCm39) |
M1357T |
possibly damaging |
Het |
Frmd4b |
A |
T |
6: 97,400,424 (GRCm39) |
V29D |
probably damaging |
Het |
G930045G22Rik |
A |
G |
6: 50,823,918 (GRCm39) |
|
noncoding transcript |
Het |
Galnt3 |
A |
G |
2: 65,937,573 (GRCm39) |
S46P |
possibly damaging |
Het |
Gmeb2 |
A |
G |
2: 180,895,766 (GRCm39) |
V468A |
possibly damaging |
Het |
Herc2 |
C |
T |
7: 55,869,563 (GRCm39) |
R4271* |
probably null |
Het |
Il5 |
C |
A |
11: 53,614,733 (GRCm39) |
|
probably benign |
Het |
Ints9 |
G |
A |
14: 65,223,818 (GRCm39) |
|
probably benign |
Het |
Itga10 |
T |
C |
3: 96,556,453 (GRCm39) |
F196S |
probably damaging |
Het |
Itgb3bp |
T |
C |
4: 99,670,126 (GRCm39) |
T138A |
probably damaging |
Het |
Kcnd1 |
G |
A |
X: 7,690,922 (GRCm39) |
V281M |
probably benign |
Het |
Lcp2 |
T |
C |
11: 34,037,229 (GRCm39) |
L391P |
probably benign |
Het |
Lrrc66 |
T |
C |
5: 73,765,030 (GRCm39) |
Y671C |
probably benign |
Het |
Mettl23 |
T |
C |
11: 116,740,120 (GRCm39) |
V197A |
possibly damaging |
Het |
Mmp15 |
C |
A |
8: 96,097,400 (GRCm39) |
D456E |
probably benign |
Het |
Mospd4 |
T |
C |
18: 46,598,848 (GRCm39) |
|
noncoding transcript |
Het |
Mov10l1 |
C |
A |
15: 88,889,515 (GRCm39) |
H484N |
probably damaging |
Het |
Mphosph9 |
T |
C |
5: 124,453,631 (GRCm39) |
Q197R |
probably benign |
Het |
Ms4a1 |
T |
A |
19: 11,233,933 (GRCm39) |
|
probably null |
Het |
Mybbp1a |
T |
C |
11: 72,339,674 (GRCm39) |
V919A |
possibly damaging |
Het |
Mycbpap |
A |
T |
11: 94,404,338 (GRCm39) |
|
probably benign |
Het |
Naip6 |
G |
A |
13: 100,433,432 (GRCm39) |
S1135F |
possibly damaging |
Het |
Ndufc2 |
T |
A |
7: 97,049,544 (GRCm39) |
M50K |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,648,082 (GRCm39) |
V842A |
probably damaging |
Het |
Ntsr2 |
G |
T |
12: 16,703,696 (GRCm39) |
G66W |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,885,914 (GRCm39) |
|
probably benign |
Het |
Optn |
C |
T |
2: 5,028,926 (GRCm39) |
G526R |
probably damaging |
Het |
Or4c11 |
T |
A |
2: 88,695,229 (GRCm39) |
N93K |
probably benign |
Het |
Or4c114 |
T |
A |
2: 88,904,956 (GRCm39) |
I160F |
probably benign |
Het |
Or6c33 |
T |
C |
10: 129,853,965 (GRCm39) |
V245A |
probably damaging |
Het |
Or6k14 |
G |
A |
1: 173,927,965 (GRCm39) |
G314R |
probably benign |
Het |
Otud4 |
T |
A |
8: 80,396,626 (GRCm39) |
H628Q |
probably benign |
Het |
Padi6 |
T |
C |
4: 140,456,240 (GRCm39) |
T585A |
probably benign |
Het |
Pex16 |
G |
T |
2: 92,205,937 (GRCm39) |
R10L |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,269,152 (GRCm39) |
|
probably benign |
Het |
Pom121l2 |
A |
G |
13: 22,167,375 (GRCm39) |
T549A |
possibly damaging |
Het |
Prdm15 |
A |
T |
16: 97,613,759 (GRCm39) |
M470K |
probably benign |
Het |
Prkag2 |
T |
A |
5: 25,233,503 (GRCm39) |
D49V |
possibly damaging |
Het |
Prl3c1 |
A |
G |
13: 27,383,447 (GRCm39) |
M38V |
probably benign |
Het |
Prpf18 |
T |
A |
2: 4,648,572 (GRCm39) |
I85F |
possibly damaging |
Het |
Psg27 |
A |
G |
7: 18,294,636 (GRCm39) |
|
probably benign |
Het |
Relt |
A |
G |
7: 100,497,991 (GRCm39) |
|
probably benign |
Het |
Rskr |
T |
C |
11: 78,182,362 (GRCm39) |
L57P |
probably benign |
Het |
Serpina3b |
A |
T |
12: 104,096,929 (GRCm39) |
N70I |
probably damaging |
Het |
Slc19a3 |
T |
C |
1: 83,000,286 (GRCm39) |
S244G |
probably benign |
Het |
Slc39a5 |
T |
C |
10: 128,235,716 (GRCm39) |
T81A |
possibly damaging |
Het |
Slc7a2 |
G |
A |
8: 41,357,563 (GRCm39) |
G277D |
probably damaging |
Het |
Slc9c1 |
C |
T |
16: 45,420,250 (GRCm39) |
|
probably benign |
Het |
Slx1b |
A |
G |
7: 126,291,753 (GRCm39) |
F104L |
probably benign |
Het |
Smg6 |
G |
A |
11: 74,820,527 (GRCm39) |
S266N |
probably damaging |
Het |
Spata9 |
T |
C |
13: 76,146,614 (GRCm39) |
V162A |
possibly damaging |
Het |
Szrd1 |
T |
C |
4: 140,846,055 (GRCm39) |
I47V |
probably benign |
Het |
Tha1 |
G |
T |
11: 117,759,401 (GRCm39) |
L363M |
probably benign |
Het |
Tmc6 |
G |
A |
11: 117,669,087 (GRCm39) |
T89I |
possibly damaging |
Het |
Tmem132d |
C |
T |
5: 127,866,849 (GRCm39) |
G684R |
probably damaging |
Het |
Trim55 |
G |
A |
3: 19,725,142 (GRCm39) |
G220S |
probably benign |
Het |
Ttn |
A |
G |
2: 76,600,874 (GRCm39) |
L18836P |
probably damaging |
Het |
Ubn1 |
G |
T |
16: 4,890,048 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
G |
1: 188,643,228 (GRCm39) |
W4197G |
probably benign |
Het |
Vmn1r189 |
A |
T |
13: 22,286,231 (GRCm39) |
V202E |
probably damaging |
Het |
Vmn1r209 |
T |
C |
13: 22,990,526 (GRCm39) |
I55V |
probably benign |
Het |
Vmn2r86 |
A |
T |
10: 130,282,412 (GRCm39) |
C735S |
probably damaging |
Het |
Zfp438 |
T |
C |
18: 5,214,910 (GRCm39) |
N16S |
probably damaging |
Het |
Zfp444 |
C |
T |
7: 6,192,408 (GRCm39) |
T142I |
probably benign |
Het |
Zfp804a |
A |
G |
2: 81,884,135 (GRCm39) |
M1V |
probably null |
Het |
Zfp936 |
T |
G |
7: 42,838,734 (GRCm39) |
I67S |
probably benign |
Het |
Zfp948 |
A |
T |
17: 21,807,260 (GRCm39) |
N151Y |
unknown |
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 |
|
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 |
|
|
R9027:Vwf
|
UTSW |
6 |
125,643,626 (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 |
|
|
|