Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
T |
A |
4: 88,786,480 (GRCm39) |
D46V |
unknown |
Het |
Abcb9 |
A |
G |
5: 124,215,358 (GRCm39) |
V461A |
probably damaging |
Het |
Ackr4 |
T |
A |
9: 103,976,679 (GRCm39) |
L89F |
probably benign |
Het |
Acsf2 |
T |
C |
11: 94,452,196 (GRCm39) |
T449A |
probably benign |
Het |
Acsl4 |
C |
G |
X: 141,116,714 (GRCm39) |
G489R |
probably damaging |
Het |
Actl6a |
T |
A |
3: 32,779,469 (GRCm39) |
I399N |
probably damaging |
Het |
Adamts19 |
G |
A |
18: 59,144,220 (GRCm39) |
C934Y |
probably null |
Het |
Adsl |
A |
G |
15: 80,845,561 (GRCm39) |
E40G |
possibly damaging |
Het |
Alppl2 |
T |
G |
1: 87,016,465 (GRCm39) |
D203A |
probably damaging |
Het |
Asb10 |
C |
A |
5: 24,742,930 (GRCm39) |
A268S |
probably benign |
Het |
Atp9a |
T |
C |
2: 168,485,805 (GRCm39) |
S832G |
probably benign |
Het |
Bckdha |
A |
T |
7: 25,330,875 (GRCm39) |
I297N |
probably damaging |
Het |
Blm |
G |
A |
7: 80,114,694 (GRCm39) |
|
probably benign |
Het |
C9orf72 |
T |
A |
4: 35,197,207 (GRCm39) |
D122V |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,599,898 (GRCm39) |
|
probably benign |
Het |
Camsap2 |
G |
A |
1: 136,220,686 (GRCm39) |
Q298* |
probably null |
Het |
Ccdc38 |
A |
T |
10: 93,401,774 (GRCm39) |
K145* |
probably null |
Het |
Cfap45 |
C |
T |
1: 172,368,894 (GRCm39) |
T434M |
probably benign |
Het |
Cfap54 |
A |
T |
10: 92,870,524 (GRCm39) |
|
probably benign |
Het |
Clcn6 |
G |
A |
4: 148,097,213 (GRCm39) |
P618L |
probably damaging |
Het |
Copg1 |
T |
C |
6: 87,881,179 (GRCm39) |
|
probably benign |
Het |
Dctd |
T |
A |
8: 48,565,113 (GRCm39) |
N79K |
probably benign |
Het |
Dgkq |
A |
G |
5: 108,802,510 (GRCm39) |
|
probably benign |
Het |
Dntt |
A |
T |
19: 41,027,409 (GRCm39) |
T159S |
possibly damaging |
Het |
Doc2g |
G |
A |
19: 4,053,656 (GRCm39) |
R29Q |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,673,199 (GRCm39) |
T957A |
probably damaging |
Het |
Eif3c |
T |
A |
7: 126,157,795 (GRCm39) |
|
probably benign |
Het |
Ephb3 |
T |
A |
16: 21,036,859 (GRCm39) |
D107E |
probably benign |
Het |
Esrrb |
A |
T |
12: 86,517,255 (GRCm39) |
D108V |
probably damaging |
Het |
Exo1 |
A |
G |
1: 175,719,596 (GRCm39) |
K214E |
probably damaging |
Het |
Fam186a |
G |
A |
15: 99,839,644 (GRCm39) |
T2200I |
possibly damaging |
Het |
Fam227a |
C |
T |
15: 79,524,870 (GRCm39) |
W194* |
probably null |
Het |
Foxn4 |
A |
G |
5: 114,397,809 (GRCm39) |
|
probably null |
Het |
Gabbr2 |
T |
C |
4: 46,787,565 (GRCm39) |
K366R |
possibly damaging |
Het |
Garem2 |
T |
A |
5: 30,318,928 (GRCm39) |
V130E |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,756,303 (GRCm39) |
F474S |
probably damaging |
Het |
H2-M10.6 |
G |
T |
17: 37,124,934 (GRCm39) |
V284F |
probably damaging |
Het |
Helz2 |
C |
A |
2: 180,874,552 (GRCm39) |
G1981C |
probably damaging |
Het |
Hivep1 |
G |
T |
13: 42,308,911 (GRCm39) |
V384F |
probably damaging |
Het |
Hmox1 |
A |
G |
8: 75,823,736 (GRCm39) |
T135A |
probably damaging |
Het |
Hpse |
T |
C |
5: 100,867,378 (GRCm39) |
D28G |
probably benign |
Het |
Itm2b |
G |
T |
14: 73,602,058 (GRCm39) |
D213E |
probably benign |
Het |
Jakmip1 |
T |
A |
5: 37,291,627 (GRCm39) |
M692K |
possibly damaging |
Het |
Kdm3a |
T |
C |
6: 71,601,578 (GRCm39) |
Q151R |
probably null |
Het |
Limch1 |
C |
A |
5: 67,156,616 (GRCm39) |
A517E |
probably benign |
Het |
Lrit1 |
T |
A |
14: 36,783,677 (GRCm39) |
L335Q |
probably damaging |
Het |
Lrrc37a |
A |
G |
11: 103,390,616 (GRCm39) |
V1603A |
possibly damaging |
Het |
Mbtps1 |
T |
A |
8: 120,262,108 (GRCm39) |
N347I |
probably damaging |
Het |
Mier1 |
A |
T |
4: 102,996,716 (GRCm39) |
|
probably null |
Het |
Mt2 |
A |
T |
8: 94,899,476 (GRCm39) |
M1L |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,817,066 (GRCm39) |
E45V |
probably damaging |
Het |
Mybphl |
A |
G |
3: 108,281,484 (GRCm39) |
K67E |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,143,162 (GRCm39) |
K1030R |
probably damaging |
Het |
Myl3 |
T |
A |
9: 110,598,189 (GRCm39) |
D176E |
probably benign |
Het |
Ncapg2 |
A |
G |
12: 116,384,303 (GRCm39) |
|
probably null |
Het |
Ndor1 |
T |
C |
2: 25,138,718 (GRCm39) |
|
probably null |
Het |
Nedd4 |
T |
G |
9: 72,577,335 (GRCm39) |
N53K |
possibly damaging |
Het |
Nek11 |
C |
A |
9: 105,270,151 (GRCm39) |
A24S |
probably benign |
Het |
Nudt19 |
G |
T |
7: 35,250,939 (GRCm39) |
P267T |
probably benign |
Het |
Olfml2b |
T |
C |
1: 170,508,684 (GRCm39) |
M514T |
possibly damaging |
Het |
Or14a258 |
A |
T |
7: 86,035,582 (GRCm39) |
C95* |
probably null |
Het |
Or2ag17 |
C |
A |
7: 106,390,030 (GRCm39) |
M59I |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,406 (GRCm39) |
D93G |
probably benign |
Het |
Or6k4 |
A |
T |
1: 173,964,327 (GRCm39) |
T6S |
probably benign |
Het |
P3h1 |
T |
A |
4: 119,095,149 (GRCm39) |
F302Y |
probably damaging |
Het |
Pappa2 |
T |
A |
1: 158,592,671 (GRCm39) |
|
probably benign |
Het |
Pex2 |
A |
C |
3: 5,626,424 (GRCm39) |
H128Q |
probably benign |
Het |
Phf11d |
A |
C |
14: 59,590,180 (GRCm39) |
L214R |
probably damaging |
Het |
Plcg2 |
G |
A |
8: 118,300,136 (GRCm39) |
|
probably benign |
Het |
Ppargc1b |
A |
C |
18: 61,441,016 (GRCm39) |
L634R |
possibly damaging |
Het |
Prune1 |
A |
T |
3: 95,169,671 (GRCm39) |
I177N |
probably damaging |
Het |
Puf60 |
T |
C |
15: 75,942,334 (GRCm39) |
D496G |
probably damaging |
Het |
Rasl11b |
A |
G |
5: 74,356,824 (GRCm39) |
|
probably null |
Het |
Sdr42e1 |
A |
T |
8: 118,389,848 (GRCm39) |
F264L |
probably damaging |
Het |
Sec24b |
A |
T |
3: 129,777,814 (GRCm39) |
|
probably null |
Het |
Sgta |
G |
T |
10: 80,886,893 (GRCm39) |
P79T |
probably benign |
Het |
Shisa9 |
C |
T |
16: 11,802,818 (GRCm39) |
T125M |
probably damaging |
Het |
Shoc1 |
T |
A |
4: 59,066,534 (GRCm39) |
|
probably benign |
Het |
Slc12a2 |
A |
G |
18: 58,063,283 (GRCm39) |
D921G |
probably damaging |
Het |
Slc13a5 |
C |
T |
11: 72,136,059 (GRCm39) |
V494I |
probably benign |
Het |
Slc13a5 |
T |
A |
11: 72,152,956 (GRCm39) |
I42L |
possibly damaging |
Het |
Spire2 |
G |
A |
8: 124,089,750 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
G |
A |
7: 27,104,336 (GRCm39) |
R962C |
probably benign |
Het |
St8sia5 |
G |
A |
18: 77,342,420 (GRCm39) |
V377I |
probably benign |
Het |
Stag2 |
T |
G |
X: 41,295,014 (GRCm39) |
|
probably benign |
Het |
Syne1 |
C |
A |
10: 5,374,311 (GRCm39) |
M165I |
probably benign |
Het |
Synm |
C |
A |
7: 67,384,672 (GRCm39) |
V997L |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,392 (GRCm39) |
S279P |
probably benign |
Het |
Tbc1d10a |
T |
C |
11: 4,162,901 (GRCm39) |
|
probably null |
Het |
Tbc1d19 |
A |
G |
5: 54,017,498 (GRCm39) |
T302A |
probably damaging |
Het |
Tecpr1 |
A |
C |
5: 144,155,335 (GRCm39) |
N74K |
probably damaging |
Het |
Tmem120a |
T |
C |
5: 135,771,252 (GRCm39) |
E28G |
possibly damaging |
Het |
Tnfrsf1b |
A |
T |
4: 144,951,382 (GRCm39) |
I186N |
probably benign |
Het |
Trim55 |
A |
G |
3: 19,716,025 (GRCm39) |
D195G |
probably benign |
Het |
Trpm3 |
G |
T |
19: 22,692,720 (GRCm39) |
|
probably null |
Het |
Ttc39a |
T |
A |
4: 109,301,376 (GRCm39) |
S571T |
probably benign |
Het |
Wbp2nl |
T |
C |
15: 82,198,483 (GRCm39) |
F340S |
possibly damaging |
Het |
Yeats2 |
T |
C |
16: 19,971,719 (GRCm39) |
M1T |
probably null |
Het |
Zfp236 |
T |
A |
18: 82,675,112 (GRCm39) |
E460V |
probably damaging |
Het |
Zfp277 |
G |
A |
12: 40,428,876 (GRCm39) |
|
probably benign |
Het |
Zfp975 |
T |
A |
7: 42,311,916 (GRCm39) |
K232N |
probably benign |
Het |
Zxdc |
T |
C |
6: 90,349,519 (GRCm39) |
|
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 |
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 |
|
|
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 |
|
|
|