Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
A |
T |
10: 76,293,346 (GRCm39) |
M156L |
probably benign |
Het |
4930470P17Rik |
C |
T |
2: 170,421,644 (GRCm39) |
A79T |
unknown |
Het |
4930522L14Rik |
A |
G |
5: 109,884,739 (GRCm39) |
I373T |
probably benign |
Het |
Amotl1 |
G |
A |
9: 14,504,669 (GRCm39) |
Q217* |
probably null |
Het |
Ankrd28 |
A |
T |
14: 31,454,011 (GRCm39) |
C254S |
probably damaging |
Het |
Ap2a1 |
A |
G |
7: 44,550,970 (GRCm39) |
|
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,529,995 (GRCm39) |
S245T |
probably benign |
Het |
Atp1b2 |
A |
T |
11: 69,492,387 (GRCm39) |
D224E |
probably damaging |
Het |
Bmal1 |
A |
T |
7: 112,884,244 (GRCm39) |
K94I |
probably damaging |
Het |
Boc |
G |
A |
16: 44,308,084 (GRCm39) |
R924W |
probably damaging |
Het |
Btbd8 |
C |
A |
5: 107,658,317 (GRCm39) |
A1117E |
probably damaging |
Het |
Car14 |
C |
T |
3: 95,806,185 (GRCm39) |
G292D |
probably benign |
Het |
Cenpb |
T |
C |
2: 131,020,103 (GRCm39) |
|
probably benign |
Het |
Ces1b |
A |
T |
8: 93,789,658 (GRCm39) |
D423E |
possibly damaging |
Het |
Cfap54 |
T |
A |
10: 92,808,556 (GRCm39) |
N1373I |
possibly damaging |
Het |
Chrdl2 |
T |
C |
7: 99,655,748 (GRCm39) |
|
probably benign |
Het |
Cic |
T |
G |
7: 24,982,308 (GRCm39) |
S12A |
possibly damaging |
Het |
Csmd2 |
A |
T |
4: 128,336,685 (GRCm39) |
Q1421L |
probably benign |
Het |
D630039A03Rik |
T |
C |
4: 57,910,452 (GRCm39) |
H120R |
possibly damaging |
Het |
Dicer1 |
T |
A |
12: 104,658,705 (GRCm39) |
D1779V |
probably damaging |
Het |
Dock9 |
G |
T |
14: 121,847,509 (GRCm39) |
H1016N |
possibly damaging |
Het |
Dxo |
T |
C |
17: 35,057,974 (GRCm39) |
L352P |
probably damaging |
Het |
Eif2b5 |
T |
A |
16: 20,318,983 (GRCm39) |
F78I |
probably damaging |
Het |
Eri2 |
A |
G |
7: 119,384,169 (GRCm39) |
|
probably benign |
Het |
Fbxw7 |
T |
G |
3: 84,832,996 (GRCm39) |
L13V |
possibly damaging |
Het |
Fgf7 |
T |
A |
2: 125,877,703 (GRCm39) |
C23* |
probably null |
Het |
Fubp1 |
T |
A |
3: 151,927,705 (GRCm39) |
|
probably null |
Het |
Gm2663 |
A |
T |
6: 40,972,887 (GRCm39) |
I240N |
probably damaging |
Het |
Gnb1l |
C |
T |
16: 18,366,846 (GRCm39) |
Q140* |
probably null |
Het |
Gnptab |
G |
A |
10: 88,272,390 (GRCm39) |
R1010Q |
probably damaging |
Het |
Gtf2h1 |
G |
A |
7: 46,472,302 (GRCm39) |
W544* |
probably null |
Het |
Gucy2c |
C |
T |
6: 136,699,512 (GRCm39) |
E586K |
probably damaging |
Het |
Hc |
T |
A |
2: 34,929,746 (GRCm39) |
E232V |
probably benign |
Het |
Ifi207 |
T |
A |
1: 173,557,622 (GRCm39) |
D372V |
unknown |
Het |
Igkv8-28 |
A |
T |
6: 70,121,102 (GRCm39) |
V15E |
probably benign |
Het |
Il1rap |
A |
G |
16: 26,511,549 (GRCm39) |
S198G |
possibly damaging |
Het |
Lct |
A |
G |
1: 128,228,124 (GRCm39) |
I1123T |
probably damaging |
Het |
Lhcgr |
T |
C |
17: 89,050,125 (GRCm39) |
E467G |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,369,808 (GRCm39) |
R86K |
probably benign |
Het |
Maml3 |
T |
A |
3: 51,763,953 (GRCm39) |
Q337L |
probably benign |
Het |
Marchf10 |
T |
A |
11: 105,280,863 (GRCm39) |
D474V |
probably benign |
Het |
Marchf2 |
G |
T |
17: 33,928,890 (GRCm39) |
T2K |
probably damaging |
Het |
Mast1 |
A |
G |
8: 85,663,822 (GRCm39) |
|
probably null |
Het |
Med12l |
T |
C |
3: 59,140,633 (GRCm39) |
I868T |
probably damaging |
Het |
Msrb1 |
T |
C |
17: 24,959,147 (GRCm39) |
S100P |
probably damaging |
Het |
Nlrp4c |
T |
C |
7: 6,069,125 (GRCm39) |
L342P |
probably benign |
Het |
Nrxn3 |
T |
A |
12: 90,298,730 (GRCm39) |
V417E |
possibly damaging |
Het |
Ntng1 |
T |
A |
3: 109,842,029 (GRCm39) |
D248V |
probably damaging |
Het |
Oaz3 |
T |
C |
3: 94,342,305 (GRCm39) |
Q117R |
probably benign |
Het |
Or2a56 |
A |
G |
6: 42,932,455 (GRCm39) |
I8V |
probably benign |
Het |
Or4f58 |
A |
G |
2: 111,851,276 (GRCm39) |
Y308H |
probably benign |
Het |
Or52e2 |
A |
G |
7: 102,804,621 (GRCm39) |
L111P |
probably benign |
Het |
Osbpl3 |
A |
C |
6: 50,277,953 (GRCm39) |
S767A |
probably benign |
Het |
Pafah1b1 |
A |
T |
11: 74,576,697 (GRCm39) |
|
probably benign |
Het |
Pard6b |
A |
G |
2: 167,940,708 (GRCm39) |
T232A |
probably damaging |
Het |
Paxip1 |
A |
T |
5: 27,970,204 (GRCm39) |
C596S |
probably damaging |
Het |
Pnpla6 |
T |
C |
8: 3,573,818 (GRCm39) |
V422A |
probably benign |
Het |
Psmd6 |
A |
T |
14: 14,120,932 (GRCm38) |
|
probably benign |
Het |
Relch |
T |
A |
1: 105,647,260 (GRCm39) |
Y683* |
probably null |
Het |
Rock2 |
T |
A |
12: 17,027,741 (GRCm39) |
C1353S |
probably damaging |
Het |
Rpl31-ps17 |
C |
T |
12: 54,748,397 (GRCm39) |
|
noncoding transcript |
Het |
Sel1l |
T |
A |
12: 91,780,667 (GRCm39) |
H658L |
probably damaging |
Het |
Sh3yl1 |
T |
A |
12: 30,990,313 (GRCm39) |
L105Q |
probably damaging |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Sirt1 |
T |
C |
10: 63,171,501 (GRCm39) |
K227E |
probably benign |
Het |
Slc25a34 |
A |
T |
4: 141,350,899 (GRCm39) |
F37I |
possibly damaging |
Het |
Slc39a5 |
T |
A |
10: 128,232,918 (GRCm39) |
I378F |
probably damaging |
Het |
Smarcad1 |
A |
T |
6: 65,075,808 (GRCm39) |
D731V |
probably null |
Het |
Sox6 |
T |
G |
7: 115,140,905 (GRCm39) |
K483N |
probably damaging |
Het |
Sp140 |
T |
A |
1: 85,538,549 (GRCm39) |
D95E |
possibly damaging |
Het |
Srgap1 |
G |
T |
10: 121,628,256 (GRCm39) |
D882E |
probably benign |
Het |
Syne4 |
T |
C |
7: 30,016,258 (GRCm39) |
|
probably benign |
Het |
Tasor2 |
A |
G |
13: 3,620,391 (GRCm39) |
F2170S |
probably damaging |
Het |
Tec |
T |
C |
5: 72,926,119 (GRCm39) |
Y289C |
probably benign |
Het |
Tmem102 |
A |
T |
11: 69,695,628 (GRCm39) |
Y115N |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trav17 |
T |
A |
14: 54,044,097 (GRCm39) |
M1K |
probably null |
Het |
Trdn |
T |
A |
10: 33,275,078 (GRCm39) |
|
probably null |
Het |
Trp53 |
A |
T |
11: 69,477,747 (GRCm39) |
I8F |
probably benign |
Het |
Ttn |
T |
A |
2: 76,585,006 (GRCm39) |
D22064V |
probably damaging |
Het |
Ube3c |
G |
A |
5: 29,837,836 (GRCm39) |
|
probably null |
Het |
Ulk1 |
C |
T |
5: 110,936,813 (GRCm39) |
|
probably null |
Het |
Upp1 |
T |
C |
11: 9,085,976 (GRCm39) |
V271A |
probably damaging |
Het |
Vmn2r4 |
T |
C |
3: 64,296,082 (GRCm39) |
E901G |
probably damaging |
Het |
Vmn2r96 |
G |
A |
17: 18,817,770 (GRCm39) |
G449D |
probably damaging |
Het |
Vps37b |
T |
C |
5: 124,144,675 (GRCm39) |
K165E |
probably damaging |
Het |
Wasf2 |
A |
G |
4: 132,912,315 (GRCm39) |
T56A |
probably benign |
Het |
Zdhhc23 |
C |
G |
16: 43,793,952 (GRCm39) |
D241H |
possibly damaging |
Het |
Zfp276 |
T |
C |
8: 123,981,623 (GRCm39) |
S57P |
probably benign |
Het |
Zxdc |
A |
G |
6: 90,347,500 (GRCm39) |
H287R |
probably damaging |
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 |
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 |
|
|
|