Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
G |
2: 25,337,363 (GRCm39) |
E2406G |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,454,205 (GRCm39) |
F341I |
probably benign |
Het |
Adam8 |
A |
T |
7: 139,563,224 (GRCm39) |
N767K |
possibly damaging |
Het |
Aig1 |
T |
C |
10: 13,744,366 (GRCm39) |
D46G |
possibly damaging |
Het |
Alms1 |
A |
G |
6: 85,599,862 (GRCm39) |
I2032V |
possibly damaging |
Het |
Ankrd16 |
A |
G |
2: 11,789,204 (GRCm39) |
I264V |
probably benign |
Het |
Areg |
T |
G |
5: 91,291,357 (GRCm39) |
V100G |
probably damaging |
Het |
Bcan |
A |
G |
3: 87,896,543 (GRCm39) |
Y718H |
probably damaging |
Het |
Brsk2 |
T |
A |
7: 141,539,200 (GRCm39) |
I188N |
probably damaging |
Het |
Cdt1 |
T |
C |
8: 123,296,722 (GRCm39) |
Y203H |
probably damaging |
Het |
Cfap119 |
A |
T |
7: 127,186,028 (GRCm39) |
|
probably null |
Het |
Chil3 |
A |
C |
3: 106,067,682 (GRCm39) |
|
probably null |
Het |
Ciao2b |
A |
G |
8: 105,366,718 (GRCm39) |
V132A |
probably damaging |
Het |
Cimip2c |
A |
G |
5: 30,641,210 (GRCm39) |
|
probably null |
Het |
Cth |
A |
G |
3: 157,613,073 (GRCm39) |
L253P |
probably damaging |
Het |
Cyp11b1 |
A |
G |
15: 74,712,666 (GRCm39) |
F132L |
possibly damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dnah11 |
A |
G |
12: 118,154,603 (GRCm39) |
S226P |
probably damaging |
Het |
Egfr |
A |
T |
11: 16,809,019 (GRCm39) |
Q71L |
probably benign |
Het |
Eml6 |
T |
A |
11: 29,696,282 (GRCm39) |
K1940* |
probably null |
Het |
Epn2 |
T |
A |
11: 61,414,014 (GRCm39) |
K391* |
probably null |
Het |
Erich1 |
A |
T |
8: 14,140,259 (GRCm39) |
S2T |
possibly damaging |
Het |
Evi5 |
A |
C |
5: 107,966,786 (GRCm39) |
L245R |
probably damaging |
Het |
Evpl |
T |
C |
11: 116,118,414 (GRCm39) |
Y731C |
probably damaging |
Het |
Exoc3l |
G |
A |
8: 106,021,645 (GRCm39) |
H128Y |
probably benign |
Het |
Extl1 |
G |
A |
4: 134,091,894 (GRCm39) |
Q320* |
probably null |
Het |
Fam91a1 |
T |
A |
15: 58,304,797 (GRCm39) |
S416T |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,849,694 (GRCm39) |
S3903T |
probably damaging |
Het |
Fer1l4 |
A |
G |
2: 155,871,605 (GRCm39) |
F1392L |
probably benign |
Het |
Fstl4 |
T |
C |
11: 53,059,005 (GRCm39) |
I488T |
possibly damaging |
Het |
Gak |
A |
T |
5: 108,752,243 (GRCm39) |
Y338* |
probably null |
Het |
Garin4 |
T |
A |
1: 190,896,018 (GRCm39) |
E208D |
probably benign |
Het |
Glp2r |
T |
C |
11: 67,648,367 (GRCm39) |
T112A |
probably benign |
Het |
Glrb |
G |
A |
3: 80,769,081 (GRCm39) |
T180I |
probably damaging |
Het |
Gm10118 |
C |
T |
10: 63,762,671 (GRCm39) |
|
probably benign |
Het |
Gpr19 |
A |
T |
6: 134,847,192 (GRCm39) |
F72I |
possibly damaging |
Het |
Grin3b |
C |
A |
10: 79,811,716 (GRCm39) |
N740K |
probably damaging |
Het |
Gstk1 |
A |
T |
6: 42,223,535 (GRCm39) |
T42S |
probably benign |
Het |
Hoxd1 |
G |
A |
2: 74,594,626 (GRCm39) |
A294T |
probably benign |
Het |
Hspg2 |
T |
A |
4: 137,275,323 (GRCm39) |
|
probably null |
Het |
Ift74 |
A |
T |
4: 94,573,940 (GRCm39) |
N472I |
probably benign |
Het |
Il1a |
C |
T |
2: 129,144,813 (GRCm39) |
D202N |
probably damaging |
Het |
Islr |
T |
C |
9: 58,064,778 (GRCm39) |
D243G |
probably damaging |
Het |
Kif21a |
C |
T |
15: 90,843,946 (GRCm39) |
E1098K |
probably damaging |
Het |
Krtap16-1 |
T |
C |
11: 99,876,852 (GRCm39) |
E184G |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 41,075,974 (GRCm39) |
I1889T |
possibly damaging |
Het |
Mcpt4 |
A |
G |
14: 56,297,416 (GRCm39) |
*247Q |
probably null |
Het |
Megf10 |
T |
C |
18: 57,410,802 (GRCm39) |
|
probably null |
Het |
Mettl2 |
T |
A |
11: 105,030,544 (GRCm39) |
H373Q |
probably benign |
Het |
Mocos |
A |
G |
18: 24,816,273 (GRCm39) |
K617E |
probably damaging |
Het |
Ms4a8a |
A |
G |
19: 11,053,761 (GRCm39) |
I115T |
probably damaging |
Het |
Ndst1 |
T |
C |
18: 60,828,580 (GRCm39) |
Y658C |
probably damaging |
Het |
Nin |
G |
A |
12: 70,077,712 (GRCm39) |
A1031V |
probably benign |
Het |
Nin |
C |
A |
12: 70,092,337 (GRCm39) |
K657N |
possibly damaging |
Het |
Noc4l |
G |
A |
5: 110,797,713 (GRCm39) |
R344* |
probably null |
Het |
Notch2 |
T |
C |
3: 98,052,443 (GRCm39) |
S1980P |
probably damaging |
Het |
Npat |
C |
T |
9: 53,473,960 (GRCm39) |
S584L |
probably benign |
Het |
Nphp4 |
A |
G |
4: 152,581,121 (GRCm39) |
T102A |
probably damaging |
Het |
Olfml2b |
A |
G |
1: 170,472,642 (GRCm39) |
N51S |
possibly damaging |
Het |
Or2n1e |
A |
G |
17: 38,585,932 (GRCm39) |
K90R |
probably benign |
Het |
Or2y16 |
T |
A |
11: 49,335,116 (GRCm39) |
I146N |
possibly damaging |
Het |
Or5al1 |
T |
C |
2: 85,990,280 (GRCm39) |
I145V |
probably benign |
Het |
Or5w22 |
A |
G |
2: 87,362,427 (GRCm39) |
T17A |
probably benign |
Het |
Pced1b |
T |
A |
15: 97,282,758 (GRCm39) |
W266R |
probably damaging |
Het |
Pdcd6ip |
A |
G |
9: 113,507,422 (GRCm39) |
V378A |
probably damaging |
Het |
Pde8b |
T |
A |
13: 95,169,374 (GRCm39) |
K683N |
probably damaging |
Het |
Pfas |
T |
G |
11: 68,888,872 (GRCm39) |
|
probably null |
Het |
Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
Plcd4 |
T |
G |
1: 74,587,394 (GRCm39) |
S51R |
probably benign |
Het |
Plekhh2 |
T |
A |
17: 84,884,612 (GRCm39) |
Y775* |
probably null |
Het |
Polr3a |
G |
A |
14: 24,534,232 (GRCm39) |
P91L |
probably damaging |
Het |
Ppp4r3b |
C |
T |
11: 29,163,765 (GRCm39) |
T47I |
possibly damaging |
Het |
Pter |
A |
T |
2: 12,999,572 (GRCm39) |
D169V |
probably damaging |
Het |
Ptpn12 |
A |
G |
5: 21,203,168 (GRCm39) |
S537P |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,506,361 (GRCm39) |
D1067V |
probably damaging |
Het |
Rcn1 |
A |
T |
2: 105,229,350 (GRCm39) |
D67E |
probably damaging |
Het |
Rfc4 |
T |
C |
16: 22,932,983 (GRCm39) |
E318G |
probably benign |
Het |
Samd13 |
C |
A |
3: 146,368,469 (GRCm39) |
R41L |
probably benign |
Het |
Shoc1 |
T |
C |
4: 59,113,926 (GRCm39) |
K13R |
unknown |
Het |
Slc6a2 |
T |
C |
8: 93,699,440 (GRCm39) |
I156T |
possibly damaging |
Het |
Spag16 |
T |
C |
1: 70,036,015 (GRCm39) |
F348L |
probably benign |
Het |
Spag4 |
T |
C |
2: 155,907,342 (GRCm39) |
Y21H |
probably damaging |
Het |
Stam2 |
G |
A |
2: 52,593,187 (GRCm39) |
A368V |
possibly damaging |
Het |
Stc1 |
A |
T |
14: 69,275,776 (GRCm39) |
M190L |
probably benign |
Het |
Stxbp1 |
A |
G |
2: 32,690,629 (GRCm39) |
L475P |
probably damaging |
Het |
Syn3 |
A |
T |
10: 85,916,075 (GRCm39) |
Y304N |
probably damaging |
Het |
Tbc1d15 |
G |
T |
10: 115,056,219 (GRCm39) |
T251K |
probably benign |
Het |
Tbpl2 |
A |
T |
2: 23,985,057 (GRCm39) |
M29K |
probably benign |
Het |
Tead3 |
T |
G |
17: 28,553,698 (GRCm39) |
Q170H |
possibly damaging |
Het |
Tpbpb |
T |
C |
13: 61,049,977 (GRCm39) |
N51D |
probably benign |
Het |
Tstd3 |
A |
G |
4: 21,759,400 (GRCm39) |
M124T |
probably benign |
Het |
Ttyh1 |
T |
A |
7: 4,122,695 (GRCm39) |
H14Q |
possibly damaging |
Het |
Tubgcp4 |
G |
A |
2: 121,020,374 (GRCm39) |
W449* |
probably null |
Het |
Txndc11 |
A |
G |
16: 10,905,639 (GRCm39) |
|
probably null |
Het |
Usp24 |
T |
A |
4: 106,296,024 (GRCm39) |
D2615E |
probably damaging |
Het |
Vars1 |
A |
G |
17: 35,233,734 (GRCm39) |
E1020G |
possibly damaging |
Het |
Vmn2r58 |
A |
G |
7: 41,509,951 (GRCm39) |
I542T |
probably benign |
Het |
Zfand1 |
A |
C |
3: 10,406,115 (GRCm39) |
V198G |
possibly damaging |
Het |
Zfp536 |
G |
A |
7: 37,268,879 (GRCm39) |
T179I |
probably damaging |
Het |
Zfp599 |
T |
C |
9: 22,161,700 (GRCm39) |
Y155C |
probably benign |
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 |
125,620,032 (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 |
|
|
|