Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
A |
16: 4,685,323 (GRCm39) |
S1142T |
possibly damaging |
Het |
Aadacl4fm5 |
T |
C |
4: 144,512,938 (GRCm39) |
I54V |
probably benign |
Het |
Actr3b |
T |
G |
5: 26,037,433 (GRCm39) |
V215G |
probably damaging |
Het |
Adam9 |
C |
T |
8: 25,460,634 (GRCm39) |
V617M |
probably damaging |
Het |
Adgrl2 |
G |
T |
3: 148,596,241 (GRCm39) |
P32T |
probably damaging |
Het |
Afg2a |
G |
T |
3: 37,518,694 (GRCm39) |
G743W |
probably damaging |
Het |
Ago3 |
A |
T |
4: 126,261,580 (GRCm39) |
|
probably benign |
Het |
Allc |
A |
C |
12: 28,623,206 (GRCm39) |
I20M |
probably benign |
Het |
Asic3 |
G |
A |
5: 24,621,972 (GRCm39) |
W361* |
probably null |
Het |
Atf7ip |
A |
G |
6: 136,583,577 (GRCm39) |
K1203E |
probably damaging |
Het |
Babam2 |
C |
A |
5: 32,162,116 (GRCm39) |
H272Q |
possibly damaging |
Het |
Baz2b |
G |
A |
2: 59,807,872 (GRCm39) |
T129I |
probably benign |
Het |
C130073F10Rik |
A |
T |
4: 101,747,590 (GRCm39) |
Y146* |
probably null |
Het |
Cd247 |
A |
G |
1: 165,684,986 (GRCm39) |
E74G |
probably damaging |
Het |
Cdh17 |
A |
T |
4: 11,814,908 (GRCm39) |
Q778L |
probably benign |
Het |
Ceacam1 |
T |
C |
7: 25,175,966 (GRCm39) |
D76G |
probably benign |
Het |
Cela3a |
T |
C |
4: 137,131,145 (GRCm39) |
K198E |
probably benign |
Het |
Cemip2 |
T |
A |
19: 21,789,241 (GRCm39) |
D558E |
probably damaging |
Het |
Ces2a |
T |
A |
8: 105,465,691 (GRCm39) |
D281E |
probably damaging |
Het |
Cetn2 |
A |
T |
X: 71,958,527 (GRCm39) |
D116E |
probably damaging |
Het |
Cracd |
A |
G |
5: 77,006,890 (GRCm39) |
K1084E |
unknown |
Het |
Ctu2 |
G |
T |
8: 123,205,530 (GRCm39) |
|
probably null |
Het |
Cybb |
T |
C |
X: 9,308,828 (GRCm39) |
N469D |
probably benign |
Het |
Cygb |
C |
T |
11: 116,540,749 (GRCm39) |
R79Q |
probably damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,288,069 (GRCm39) |
V186M |
possibly damaging |
Het |
Defb29 |
T |
A |
2: 152,380,942 (GRCm39) |
|
probably null |
Het |
Depdc7 |
T |
G |
2: 104,560,694 (GRCm39) |
Q100P |
probably damaging |
Het |
Dhx30 |
A |
C |
9: 109,926,251 (GRCm39) |
I91R |
probably damaging |
Het |
Dnm1l |
T |
A |
16: 16,159,288 (GRCm39) |
K105* |
probably null |
Het |
Eddm13 |
T |
C |
7: 6,272,898 (GRCm39) |
|
probably benign |
Het |
Efhc1 |
T |
C |
1: 21,037,567 (GRCm39) |
I248T |
probably damaging |
Het |
Elapor1 |
A |
G |
3: 108,380,182 (GRCm39) |
I309T |
probably benign |
Het |
Entpd2 |
A |
G |
2: 25,288,120 (GRCm39) |
T115A |
probably damaging |
Het |
Epb42 |
G |
T |
2: 120,856,227 (GRCm39) |
A439E |
probably benign |
Het |
Esm1 |
T |
G |
13: 113,346,618 (GRCm39) |
L81R |
probably damaging |
Het |
F8 |
T |
C |
X: 74,330,987 (GRCm39) |
S968G |
probably benign |
Het |
Fam234b |
T |
G |
6: 135,202,201 (GRCm39) |
Y308D |
probably damaging |
Het |
Fbxo46 |
T |
G |
7: 18,871,139 (GRCm39) |
V586G |
probably damaging |
Het |
Foxp1 |
C |
A |
6: 98,907,044 (GRCm39) |
|
probably benign |
Het |
Gm10754 |
A |
T |
10: 97,518,136 (GRCm39) |
|
probably benign |
Het |
Gm12695 |
A |
C |
4: 96,650,370 (GRCm39) |
|
probably benign |
Het |
Gm5468 |
T |
C |
15: 25,414,726 (GRCm39) |
|
probably benign |
Het |
Grhl1 |
T |
C |
12: 24,631,490 (GRCm39) |
S66P |
probably damaging |
Het |
Gstt3 |
A |
T |
10: 75,612,576 (GRCm39) |
|
probably null |
Het |
Gtf2i |
A |
G |
5: 134,308,281 (GRCm39) |
|
probably benign |
Het |
Gzmk |
C |
A |
13: 113,308,560 (GRCm39) |
G175C |
probably damaging |
Het |
Helz2 |
T |
C |
2: 180,872,939 (GRCm39) |
|
probably benign |
Het |
Ift20 |
T |
C |
11: 78,430,780 (GRCm39) |
|
probably benign |
Het |
Intu |
A |
G |
3: 40,642,216 (GRCm39) |
D491G |
probably damaging |
Het |
Itch |
G |
T |
2: 155,015,853 (GRCm39) |
|
probably null |
Het |
Itgb5 |
A |
G |
16: 33,665,362 (GRCm39) |
N26S |
possibly damaging |
Het |
Lama2 |
A |
T |
10: 26,891,534 (GRCm39) |
S2526R |
probably damaging |
Het |
Lat2 |
A |
G |
5: 134,637,027 (GRCm39) |
I40T |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,471,397 (GRCm39) |
M393L |
probably benign |
Het |
Lipa |
G |
T |
19: 34,471,371 (GRCm39) |
|
probably benign |
Het |
Lpcat1 |
T |
A |
13: 73,632,417 (GRCm39) |
L10H |
probably damaging |
Het |
Lpcat3 |
T |
C |
6: 124,679,970 (GRCm39) |
Y348H |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 40,591,842 (GRCm39) |
N50K |
unknown |
Het |
Lrrk2 |
T |
A |
15: 91,634,480 (GRCm39) |
Y1415N |
probably damaging |
Het |
Lsamp |
A |
T |
16: 41,965,078 (GRCm39) |
T312S |
probably benign |
Het |
Man2a2 |
T |
C |
7: 80,013,689 (GRCm39) |
E454G |
probably benign |
Het |
Mcm3 |
T |
C |
1: 20,879,063 (GRCm39) |
K570R |
probably damaging |
Het |
Mctp2 |
C |
A |
7: 71,878,219 (GRCm39) |
|
probably null |
Het |
Msantd2 |
T |
G |
9: 37,434,796 (GRCm39) |
C345W |
probably damaging |
Het |
Musk |
T |
C |
4: 58,354,078 (GRCm39) |
I362T |
probably benign |
Het |
Myh15 |
A |
T |
16: 48,965,767 (GRCm39) |
N1224I |
probably benign |
Het |
Myo18a |
A |
G |
11: 77,755,612 (GRCm39) |
Y1983C |
probably damaging |
Het |
Myo18a |
C |
T |
11: 77,720,699 (GRCm39) |
|
probably benign |
Het |
Myrfl |
G |
T |
10: 116,664,909 (GRCm39) |
Q374K |
probably damaging |
Het |
Ndrg1 |
T |
A |
15: 66,818,346 (GRCm39) |
Q87H |
probably benign |
Het |
Nol9 |
G |
A |
4: 152,131,030 (GRCm39) |
C351Y |
probably damaging |
Het |
Nr5a1 |
A |
G |
2: 38,598,141 (GRCm39) |
S219P |
probably benign |
Het |
Or8b43 |
T |
C |
9: 38,360,489 (GRCm39) |
F107S |
possibly damaging |
Het |
Or8g28 |
A |
T |
9: 39,169,520 (GRCm39) |
Y149* |
probably null |
Het |
Pcdhb19 |
A |
G |
18: 37,631,690 (GRCm39) |
D495G |
probably damaging |
Het |
Pfkm |
A |
G |
15: 98,026,123 (GRCm39) |
M573V |
probably damaging |
Het |
Plec |
A |
T |
15: 76,065,516 (GRCm39) |
L1586Q |
probably damaging |
Het |
Prelp |
C |
A |
1: 133,843,005 (GRCm39) |
E47* |
probably null |
Het |
Rbm33 |
T |
A |
5: 28,615,753 (GRCm39) |
I32N |
probably damaging |
Het |
Rgs12 |
A |
T |
5: 35,183,227 (GRCm39) |
D310V |
probably damaging |
Het |
Ripor2 |
A |
C |
13: 24,880,512 (GRCm39) |
H404P |
possibly damaging |
Het |
Sh3d21 |
T |
C |
4: 126,056,034 (GRCm39) |
E124G |
probably benign |
Het |
Shroom2 |
C |
T |
X: 151,442,549 (GRCm39) |
S872N |
probably benign |
Het |
Slc44a5 |
A |
G |
3: 153,956,651 (GRCm39) |
Y301C |
probably damaging |
Het |
Smap1 |
A |
T |
1: 23,930,995 (GRCm39) |
H66Q |
possibly damaging |
Het |
Smyd1 |
G |
T |
6: 71,198,007 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
T |
A |
7: 27,093,573 (GRCm39) |
|
probably benign |
Het |
Srsf3-ps |
T |
A |
11: 98,516,146 (GRCm39) |
R76* |
probably null |
Het |
Stag3 |
A |
G |
5: 138,280,955 (GRCm39) |
K49R |
probably damaging |
Het |
Stim1 |
C |
A |
7: 101,917,758 (GRCm39) |
A46E |
unknown |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tbc1d19 |
A |
G |
5: 53,992,559 (GRCm39) |
T114A |
probably benign |
Het |
Tln2 |
G |
A |
9: 67,128,807 (GRCm39) |
|
probably benign |
Het |
Trmt10a |
T |
A |
3: 137,857,945 (GRCm39) |
|
probably null |
Het |
Zfp773 |
T |
C |
7: 7,137,232 (GRCm39) |
T121A |
probably benign |
Het |
|
Other mutations in Vwde |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00725:Vwde
|
APN |
6 |
13,187,411 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01391:Vwde
|
APN |
6 |
13,190,526 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01432:Vwde
|
APN |
6 |
13,193,239 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01611:Vwde
|
APN |
6 |
13,219,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01835:Vwde
|
APN |
6 |
13,186,823 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01993:Vwde
|
APN |
6 |
13,219,977 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01997:Vwde
|
APN |
6 |
13,215,705 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02390:Vwde
|
APN |
6 |
13,190,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02612:Vwde
|
APN |
6 |
13,187,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02723:Vwde
|
APN |
6 |
13,205,759 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02731:Vwde
|
APN |
6 |
13,192,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02981:Vwde
|
APN |
6 |
13,193,112 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03031:Vwde
|
APN |
6 |
13,208,381 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03180:Vwde
|
APN |
6 |
13,205,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03182:Vwde
|
APN |
6 |
13,187,138 (GRCm39) |
missense |
probably damaging |
1.00 |
willy_brandt
|
UTSW |
6 |
13,208,404 (GRCm39) |
splice site |
probably null |
|
C9142:Vwde
|
UTSW |
6 |
13,168,053 (GRCm39) |
splice site |
probably benign |
|
R0089:Vwde
|
UTSW |
6 |
13,220,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Vwde
|
UTSW |
6 |
13,193,125 (GRCm39) |
missense |
probably benign |
0.16 |
R0355:Vwde
|
UTSW |
6 |
13,187,806 (GRCm39) |
splice site |
probably benign |
|
R0455:Vwde
|
UTSW |
6 |
13,187,528 (GRCm39) |
missense |
probably benign |
0.03 |
R0465:Vwde
|
UTSW |
6 |
13,215,805 (GRCm39) |
splice site |
probably benign |
|
R0946:Vwde
|
UTSW |
6 |
13,187,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R1087:Vwde
|
UTSW |
6 |
13,186,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R1236:Vwde
|
UTSW |
6 |
13,187,152 (GRCm39) |
nonsense |
probably null |
|
R1738:Vwde
|
UTSW |
6 |
13,190,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Vwde
|
UTSW |
6 |
13,187,454 (GRCm39) |
missense |
probably damaging |
0.98 |
R2014:Vwde
|
UTSW |
6 |
13,208,337 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2015:Vwde
|
UTSW |
6 |
13,208,337 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2303:Vwde
|
UTSW |
6 |
13,215,806 (GRCm39) |
splice site |
probably benign |
|
R3439:Vwde
|
UTSW |
6 |
13,208,374 (GRCm39) |
missense |
probably damaging |
0.98 |
R3688:Vwde
|
UTSW |
6 |
13,186,891 (GRCm39) |
missense |
probably damaging |
0.96 |
R4457:Vwde
|
UTSW |
6 |
13,196,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Vwde
|
UTSW |
6 |
13,205,851 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4849:Vwde
|
UTSW |
6 |
13,196,047 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4850:Vwde
|
UTSW |
6 |
13,196,047 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4851:Vwde
|
UTSW |
6 |
13,196,047 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4853:Vwde
|
UTSW |
6 |
13,215,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:Vwde
|
UTSW |
6 |
13,187,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Vwde
|
UTSW |
6 |
13,192,641 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5057:Vwde
|
UTSW |
6 |
13,192,641 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5060:Vwde
|
UTSW |
6 |
13,208,323 (GRCm39) |
splice site |
probably null |
|
R5126:Vwde
|
UTSW |
6 |
13,187,259 (GRCm39) |
missense |
probably benign |
0.04 |
R5154:Vwde
|
UTSW |
6 |
13,215,757 (GRCm39) |
missense |
probably benign |
0.01 |
R5277:Vwde
|
UTSW |
6 |
13,186,995 (GRCm39) |
missense |
probably benign |
0.03 |
R5432:Vwde
|
UTSW |
6 |
13,190,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Vwde
|
UTSW |
6 |
13,190,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R5472:Vwde
|
UTSW |
6 |
13,193,117 (GRCm39) |
missense |
probably benign |
0.00 |
R5518:Vwde
|
UTSW |
6 |
13,186,937 (GRCm39) |
missense |
probably benign |
0.00 |
R5791:Vwde
|
UTSW |
6 |
13,195,985 (GRCm39) |
nonsense |
probably null |
|
R6045:Vwde
|
UTSW |
6 |
13,219,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Vwde
|
UTSW |
6 |
13,205,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Vwde
|
UTSW |
6 |
13,205,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Vwde
|
UTSW |
6 |
13,208,404 (GRCm39) |
splice site |
probably null |
|
R6562:Vwde
|
UTSW |
6 |
13,193,122 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6905:Vwde
|
UTSW |
6 |
13,205,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R7021:Vwde
|
UTSW |
6 |
13,186,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Vwde
|
UTSW |
6 |
13,215,799 (GRCm39) |
missense |
probably benign |
0.03 |
R7356:Vwde
|
UTSW |
6 |
13,192,641 (GRCm39) |
missense |
probably damaging |
0.96 |
R7434:Vwde
|
UTSW |
6 |
13,187,639 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Vwde
|
UTSW |
6 |
13,204,980 (GRCm39) |
missense |
probably null |
1.00 |
R8026:Vwde
|
UTSW |
6 |
13,205,782 (GRCm39) |
missense |
probably benign |
0.16 |
R8544:Vwde
|
UTSW |
6 |
13,187,652 (GRCm39) |
missense |
probably benign |
0.00 |
R8557:Vwde
|
UTSW |
6 |
13,193,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Vwde
|
UTSW |
6 |
13,195,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9112:Vwde
|
UTSW |
6 |
13,205,051 (GRCm39) |
missense |
possibly damaging |
0.48 |
|