Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34 |
T |
G |
8: 44,105,493 (GRCm39) |
T51P |
probably benign |
Het |
Alpk1 |
A |
T |
3: 127,464,720 (GRCm39) |
V1186E |
probably damaging |
Het |
Ankfn1 |
T |
C |
11: 89,296,423 (GRCm39) |
D102G |
probably damaging |
Het |
Armc2 |
A |
G |
10: 41,876,406 (GRCm39) |
I127T |
possibly damaging |
Het |
Atp6v1b2 |
T |
C |
8: 69,554,084 (GRCm39) |
L87P |
probably damaging |
Het |
Atp9a |
T |
A |
2: 168,482,617 (GRCm39) |
|
probably null |
Het |
BC048679 |
C |
G |
7: 81,144,993 (GRCm39) |
V123L |
probably benign |
Het |
Birc7 |
G |
A |
2: 180,571,307 (GRCm39) |
|
probably null |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
Cacna1d |
T |
A |
14: 30,068,774 (GRCm39) |
N155I |
probably damaging |
Het |
Cd300lg |
T |
C |
11: 101,933,852 (GRCm39) |
V33A |
probably damaging |
Het |
Cep290 |
A |
G |
10: 100,352,041 (GRCm39) |
D742G |
probably benign |
Het |
Cep95 |
A |
G |
11: 106,681,578 (GRCm39) |
N14S |
probably benign |
Het |
Cfap74 |
A |
T |
4: 155,525,734 (GRCm39) |
M728L |
probably benign |
Het |
Ctsll3 |
T |
A |
13: 60,949,205 (GRCm39) |
T9S |
probably benign |
Het |
Cyp3a44 |
A |
G |
5: 145,716,412 (GRCm39) |
S393P |
possibly damaging |
Het |
Dmbt1 |
T |
A |
7: 130,642,632 (GRCm39) |
L150* |
probably null |
Het |
Dnah2 |
A |
G |
11: 69,343,705 (GRCm39) |
I2868T |
probably damaging |
Het |
Dop1a |
A |
G |
9: 86,389,585 (GRCm39) |
H505R |
probably damaging |
Het |
Exo1 |
A |
G |
1: 175,733,519 (GRCm39) |
K781R |
probably damaging |
Het |
Fam184a |
A |
G |
10: 53,566,211 (GRCm39) |
Y459H |
probably damaging |
Het |
Foxp1 |
C |
T |
6: 98,907,164 (GRCm39) |
D540N |
probably damaging |
Het |
Fstl5 |
T |
A |
3: 76,615,034 (GRCm39) |
Y698* |
probably null |
Het |
Gm5141 |
T |
C |
13: 62,922,525 (GRCm39) |
K215E |
probably damaging |
Het |
Grik5 |
C |
A |
7: 24,757,923 (GRCm39) |
R386L |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,185,647 (GRCm39) |
S620R |
possibly damaging |
Het |
Kcnh3 |
A |
T |
15: 99,131,180 (GRCm39) |
M518L |
probably benign |
Het |
Lrrcc1 |
G |
T |
3: 14,623,416 (GRCm39) |
A748S |
probably damaging |
Het |
Mbd5 |
T |
G |
2: 49,169,091 (GRCm39) |
S1191A |
probably benign |
Het |
Med27 |
T |
C |
2: 29,390,283 (GRCm39) |
I70T |
probably damaging |
Het |
Mplkipl1 |
A |
G |
19: 61,163,908 (GRCm39) |
Y176H |
probably damaging |
Het |
Myh4 |
A |
G |
11: 67,149,479 (GRCm39) |
D1737G |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,081,478 (GRCm39) |
D1021G |
probably benign |
Het |
Ncor1 |
T |
C |
11: 62,301,746 (GRCm39) |
E212G |
probably damaging |
Het |
Neb |
A |
T |
2: 52,133,896 (GRCm39) |
N3362K |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,134,081 (GRCm39) |
S3301P |
probably damaging |
Het |
Neurod1 |
T |
G |
2: 79,284,526 (GRCm39) |
K286Q |
probably damaging |
Het |
Noc3l |
T |
C |
19: 38,778,095 (GRCm39) |
Q773R |
probably benign |
Het |
Nup205 |
T |
A |
6: 35,171,398 (GRCm39) |
N420K |
probably benign |
Het |
Olfml3 |
A |
T |
3: 103,644,330 (GRCm39) |
V113E |
probably benign |
Het |
Opa1 |
T |
C |
16: 29,430,279 (GRCm39) |
V439A |
probably damaging |
Het |
Or13c7 |
A |
G |
4: 43,854,417 (GRCm39) |
Y36C |
probably damaging |
Het |
Or14j7 |
A |
T |
17: 38,234,520 (GRCm39) |
H21L |
probably benign |
Het |
Or1j14 |
C |
T |
2: 36,417,994 (GRCm39) |
S190L |
probably damaging |
Het |
Or1o11 |
T |
A |
17: 37,756,593 (GRCm39) |
D60E |
probably damaging |
Het |
Pcdhb11 |
T |
C |
18: 37,555,818 (GRCm39) |
S383P |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,812,476 (GRCm39) |
V3803A |
probably damaging |
Het |
Plekhg1 |
A |
G |
10: 3,914,235 (GRCm39) |
D1319G |
probably benign |
Het |
Polq |
T |
A |
16: 36,882,355 (GRCm39) |
C1227* |
probably null |
Het |
Pramel22 |
A |
T |
4: 143,380,993 (GRCm39) |
N343K |
probably benign |
Het |
Psmc1 |
T |
C |
12: 100,085,487 (GRCm39) |
F283L |
probably damaging |
Het |
Psmd8 |
T |
C |
7: 28,875,552 (GRCm39) |
N189S |
probably damaging |
Het |
Ptger4 |
G |
A |
15: 5,272,382 (GRCm39) |
T104I |
probably benign |
Het |
Ptpro |
T |
G |
6: 137,345,294 (GRCm39) |
V100G |
possibly damaging |
Het |
Rab11fip1 |
T |
A |
8: 27,644,520 (GRCm39) |
T422S |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,570,891 (GRCm39) |
L1143P |
possibly damaging |
Het |
Rnf148 |
A |
G |
6: 23,654,072 (GRCm39) |
M308T |
probably damaging |
Het |
Sbsn |
T |
A |
7: 30,451,523 (GRCm39) |
|
probably benign |
Het |
Scube2 |
T |
A |
7: 109,424,044 (GRCm39) |
T487S |
probably benign |
Het |
Sema4c |
C |
A |
1: 36,592,892 (GRCm39) |
E109* |
probably null |
Het |
Sipa1l2 |
A |
T |
8: 126,207,071 (GRCm39) |
L544Q |
probably damaging |
Het |
Slc28a2 |
A |
G |
2: 122,288,702 (GRCm39) |
T603A |
probably benign |
Het |
Tbc1d7 |
T |
A |
13: 43,306,563 (GRCm39) |
T138S |
probably benign |
Het |
Timd4 |
A |
T |
11: 46,710,084 (GRCm39) |
T239S |
probably benign |
Het |
Trp53bp1 |
A |
G |
2: 121,066,498 (GRCm39) |
S743P |
probably damaging |
Het |
Tspan10 |
T |
A |
11: 120,335,120 (GRCm39) |
Y77N |
probably damaging |
Het |
Ttc14 |
T |
C |
3: 33,857,633 (GRCm39) |
S245P |
probably damaging |
Het |
Ttf1 |
T |
A |
2: 28,955,054 (GRCm39) |
S139R |
probably benign |
Het |
Tubd1 |
C |
A |
11: 86,448,616 (GRCm39) |
Q279K |
possibly damaging |
Het |
Twnk |
A |
G |
19: 44,996,026 (GRCm39) |
E153G |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,132,478 (GRCm39) |
D900G |
probably damaging |
Het |
Usp54 |
A |
G |
14: 20,620,432 (GRCm39) |
V691A |
probably benign |
Het |
Usp8 |
T |
C |
2: 126,559,952 (GRCm39) |
|
probably benign |
Het |
Vmn1r231 |
C |
T |
17: 21,110,490 (GRCm39) |
V142I |
probably benign |
Het |
Vmn2r15 |
C |
T |
5: 109,434,953 (GRCm39) |
A584T |
probably damaging |
Het |
Vmn2r6 |
A |
G |
3: 64,467,008 (GRCm39) |
S164P |
probably damaging |
Het |
Vps16 |
A |
G |
2: 130,280,770 (GRCm39) |
Y233C |
probably benign |
Het |
Wipf3 |
T |
G |
6: 54,460,882 (GRCm39) |
L110R |
possibly damaging |
Het |
Zfp945 |
T |
A |
17: 23,084,226 (GRCm39) |
N11I |
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 |
|
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 |
|
|
|