Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afdn |
A |
G |
17: 13,818,229 (GRCm38) |
E283G |
probably damaging |
Het |
Ahnak |
A |
G |
19: 9,004,933 (GRCm38) |
I1194V |
probably benign |
Het |
Aqr |
T |
A |
2: 114,112,646 (GRCm38) |
N1149Y |
probably damaging |
Het |
Bms1 |
T |
C |
6: 118,416,519 (GRCm38) |
I131V |
probably benign |
Het |
Cacna1s |
A |
C |
1: 136,118,380 (GRCm38) |
T1461P |
probably benign |
Het |
Chrnb3 |
T |
C |
8: 27,393,369 (GRCm38) |
S113P |
probably damaging |
Het |
Col1a2 |
C |
T |
6: 4,516,398 (GRCm38) |
R171C |
unknown |
Het |
Cramp1l |
A |
G |
17: 24,985,050 (GRCm38) |
V318A |
probably damaging |
Het |
Csf2ra |
A |
G |
19: 61,226,537 (GRCm38) |
V163A |
possibly damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,401,492 (GRCm38) |
G219V |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,669,562 (GRCm38) |
D439G |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,027,445 (GRCm38) |
|
probably null |
Het |
Dyrk4 |
C |
A |
6: 126,880,231 (GRCm38) |
C495F |
probably damaging |
Het |
Gabra6 |
A |
G |
11: 42,307,417 (GRCm38) |
V402A |
probably benign |
Het |
Gba2 |
T |
C |
4: 43,568,538 (GRCm38) |
M643V |
possibly damaging |
Het |
Gbp9 |
A |
T |
5: 105,094,567 (GRCm38) |
|
probably benign |
Het |
Ginm1 |
A |
G |
10: 7,777,768 (GRCm38) |
|
probably benign |
Het |
Git1 |
T |
A |
11: 77,503,391 (GRCm38) |
D282E |
probably damaging |
Het |
Gm5799 |
T |
C |
14: 43,544,629 (GRCm38) |
I86T |
probably damaging |
Het |
Gm9894 |
T |
C |
13: 67,765,094 (GRCm38) |
|
noncoding transcript |
Het |
Gng12 |
A |
G |
6: 67,015,761 (GRCm38) |
K4R |
probably benign |
Het |
Hnrnpul1 |
A |
T |
7: 25,726,757 (GRCm38) |
D556E |
probably benign |
Het |
Kat6b |
T |
A |
14: 21,669,039 (GRCm38) |
L1153Q |
possibly damaging |
Het |
Ly75 |
A |
T |
2: 60,383,182 (GRCm38) |
L17Q |
probably null |
Het |
Mc5r |
T |
C |
18: 68,338,839 (GRCm38) |
F90L |
probably damaging |
Het |
Olfr1356 |
A |
T |
10: 78,847,063 (GRCm38) |
M284K |
probably damaging |
Het |
Olfr175-ps1 |
A |
T |
16: 58,824,656 (GRCm38) |
S18T |
probably benign |
Het |
Olfr524 |
T |
C |
7: 140,202,587 (GRCm38) |
Y61C |
probably damaging |
Het |
Olfr54 |
C |
A |
11: 51,027,365 (GRCm38) |
A121D |
probably damaging |
Het |
Olfr877 |
A |
T |
9: 37,855,360 (GRCm38) |
I181L |
probably benign |
Het |
Pi4ka |
A |
T |
16: 17,325,429 (GRCm38) |
Y6N |
probably damaging |
Het |
Polr2g |
C |
A |
19: 8,798,456 (GRCm38) |
|
probably null |
Het |
Psme3 |
A |
G |
11: 101,317,654 (GRCm38) |
Q82R |
probably benign |
Het |
Rab11a |
G |
T |
9: 64,726,647 (GRCm38) |
T17K |
possibly damaging |
Het |
Rbm12 |
A |
T |
2: 156,098,097 (GRCm38) |
L85Q |
probably damaging |
Het |
Skap1 |
A |
T |
11: 96,708,686 (GRCm38) |
Y188F |
probably damaging |
Het |
Tmprss6 |
A |
T |
15: 78,442,336 (GRCm38) |
F34I |
probably damaging |
Het |
Trip12 |
A |
C |
1: 84,794,133 (GRCm38) |
I98S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,878,188 (GRCm38) |
|
probably benign |
Het |
Ube2t |
A |
T |
1: 134,971,341 (GRCm38) |
K21* |
probably null |
Het |
Vmn1r216 |
T |
C |
13: 23,099,477 (GRCm38) |
V110A |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,937,876 (GRCm38) |
T2081A |
probably benign |
Het |
Zfp13 |
C |
T |
17: 23,576,098 (GRCm38) |
A493T |
probably benign |
Het |
|
Other mutations in Vmn2r109 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01313:Vmn2r109
|
APN |
17 |
20,550,157 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01383:Vmn2r109
|
APN |
17 |
20,541,121 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01469:Vmn2r109
|
APN |
17 |
20,541,409 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01762:Vmn2r109
|
APN |
17 |
20,554,392 (GRCm38) |
missense |
probably benign |
|
IGL01864:Vmn2r109
|
APN |
17 |
20,541,134 (GRCm38) |
missense |
probably benign |
0.28 |
IGL02028:Vmn2r109
|
APN |
17 |
20,541,080 (GRCm38) |
missense |
probably benign |
0.28 |
IGL02074:Vmn2r109
|
APN |
17 |
20,554,341 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02162:Vmn2r109
|
APN |
17 |
20,554,160 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02490:Vmn2r109
|
APN |
17 |
20,540,984 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL02604:Vmn2r109
|
APN |
17 |
20,540,701 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02669:Vmn2r109
|
APN |
17 |
20,554,256 (GRCm38) |
missense |
possibly damaging |
0.64 |
IGL02705:Vmn2r109
|
APN |
17 |
20,553,800 (GRCm38) |
missense |
probably benign |
|
IGL02745:Vmn2r109
|
APN |
17 |
20,541,250 (GRCm38) |
missense |
probably damaging |
0.99 |
PIT4142001:Vmn2r109
|
UTSW |
17 |
20,554,577 (GRCm38) |
critical splice acceptor site |
probably null |
|
R0389:Vmn2r109
|
UTSW |
17 |
20,541,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R0470:Vmn2r109
|
UTSW |
17 |
20,552,886 (GRCm38) |
missense |
probably benign |
0.06 |
R0570:Vmn2r109
|
UTSW |
17 |
20,540,675 (GRCm38) |
missense |
probably damaging |
0.99 |
R0855:Vmn2r109
|
UTSW |
17 |
20,541,408 (GRCm38) |
nonsense |
probably null |
|
R0882:Vmn2r109
|
UTSW |
17 |
20,554,580 (GRCm38) |
splice site |
probably benign |
|
R1241:Vmn2r109
|
UTSW |
17 |
20,555,241 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1587:Vmn2r109
|
UTSW |
17 |
20,540,740 (GRCm38) |
missense |
probably damaging |
1.00 |
R1931:Vmn2r109
|
UTSW |
17 |
20,553,810 (GRCm38) |
nonsense |
probably null |
|
R1957:Vmn2r109
|
UTSW |
17 |
20,564,707 (GRCm38) |
missense |
probably benign |
0.11 |
R1962:Vmn2r109
|
UTSW |
17 |
20,553,923 (GRCm38) |
missense |
probably damaging |
0.99 |
R2020:Vmn2r109
|
UTSW |
17 |
20,541,186 (GRCm38) |
nonsense |
probably null |
|
R2073:Vmn2r109
|
UTSW |
17 |
20,564,712 (GRCm38) |
missense |
probably benign |
0.00 |
R2436:Vmn2r109
|
UTSW |
17 |
20,554,536 (GRCm38) |
missense |
probably damaging |
0.99 |
R3123:Vmn2r109
|
UTSW |
17 |
20,540,986 (GRCm38) |
missense |
probably damaging |
1.00 |
R3839:Vmn2r109
|
UTSW |
17 |
20,554,442 (GRCm38) |
missense |
probably damaging |
1.00 |
R4019:Vmn2r109
|
UTSW |
17 |
20,553,812 (GRCm38) |
missense |
probably benign |
|
R4428:Vmn2r109
|
UTSW |
17 |
20,553,024 (GRCm38) |
missense |
probably benign |
|
R4584:Vmn2r109
|
UTSW |
17 |
20,554,558 (GRCm38) |
nonsense |
probably null |
|
R4652:Vmn2r109
|
UTSW |
17 |
20,541,394 (GRCm38) |
missense |
probably damaging |
1.00 |
R4708:Vmn2r109
|
UTSW |
17 |
20,541,343 (GRCm38) |
missense |
probably damaging |
0.97 |
R4823:Vmn2r109
|
UTSW |
17 |
20,553,891 (GRCm38) |
missense |
probably damaging |
1.00 |
R4831:Vmn2r109
|
UTSW |
17 |
20,541,232 (GRCm38) |
missense |
probably benign |
0.01 |
R4907:Vmn2r109
|
UTSW |
17 |
20,550,086 (GRCm38) |
missense |
probably damaging |
1.00 |
R5011:Vmn2r109
|
UTSW |
17 |
20,555,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R5296:Vmn2r109
|
UTSW |
17 |
20,554,341 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5600:Vmn2r109
|
UTSW |
17 |
20,540,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R5602:Vmn2r109
|
UTSW |
17 |
20,540,671 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5652:Vmn2r109
|
UTSW |
17 |
20,540,519 (GRCm38) |
makesense |
probably null |
|
R5702:Vmn2r109
|
UTSW |
17 |
20,554,145 (GRCm38) |
missense |
probably benign |
0.42 |
R5706:Vmn2r109
|
UTSW |
17 |
20,554,305 (GRCm38) |
missense |
probably benign |
0.16 |
R5714:Vmn2r109
|
UTSW |
17 |
20,552,859 (GRCm38) |
missense |
probably damaging |
1.00 |
R5832:Vmn2r109
|
UTSW |
17 |
20,541,056 (GRCm38) |
missense |
probably benign |
0.10 |
R6008:Vmn2r109
|
UTSW |
17 |
20,540,719 (GRCm38) |
missense |
probably damaging |
1.00 |
R6334:Vmn2r109
|
UTSW |
17 |
20,541,178 (GRCm38) |
missense |
probably benign |
0.18 |
R6377:Vmn2r109
|
UTSW |
17 |
20,564,534 (GRCm38) |
critical splice donor site |
probably null |
|
R6738:Vmn2r109
|
UTSW |
17 |
20,554,523 (GRCm38) |
missense |
possibly damaging |
0.52 |
R6857:Vmn2r109
|
UTSW |
17 |
20,540,670 (GRCm38) |
missense |
probably benign |
0.45 |
R6953:Vmn2r109
|
UTSW |
17 |
20,540,711 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7108:Vmn2r109
|
UTSW |
17 |
20,564,744 (GRCm38) |
missense |
probably benign |
0.03 |
R7229:Vmn2r109
|
UTSW |
17 |
20,540,963 (GRCm38) |
missense |
possibly damaging |
0.80 |
R7238:Vmn2r109
|
UTSW |
17 |
20,541,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R7244:Vmn2r109
|
UTSW |
17 |
20,540,683 (GRCm38) |
missense |
possibly damaging |
0.70 |
R7292:Vmn2r109
|
UTSW |
17 |
20,541,438 (GRCm38) |
missense |
probably benign |
0.05 |
R7354:Vmn2r109
|
UTSW |
17 |
20,540,781 (GRCm38) |
missense |
probably damaging |
1.00 |
R7357:Vmn2r109
|
UTSW |
17 |
20,541,274 (GRCm38) |
missense |
probably damaging |
1.00 |
R7522:Vmn2r109
|
UTSW |
17 |
20,554,403 (GRCm38) |
missense |
probably benign |
0.11 |
R7596:Vmn2r109
|
UTSW |
17 |
20,540,680 (GRCm38) |
missense |
probably damaging |
0.98 |
R7728:Vmn2r109
|
UTSW |
17 |
20,552,855 (GRCm38) |
missense |
probably damaging |
0.99 |
R7859:Vmn2r109
|
UTSW |
17 |
20,541,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R7871:Vmn2r109
|
UTSW |
17 |
20,540,520 (GRCm38) |
missense |
probably benign |
0.08 |
R8113:Vmn2r109
|
UTSW |
17 |
20,554,467 (GRCm38) |
missense |
probably benign |
0.01 |
R8153:Vmn2r109
|
UTSW |
17 |
20,564,707 (GRCm38) |
missense |
probably benign |
0.11 |
R8977:Vmn2r109
|
UTSW |
17 |
20,554,269 (GRCm38) |
missense |
possibly damaging |
0.96 |
R9687:Vmn2r109
|
UTSW |
17 |
20,555,070 (GRCm38) |
missense |
|
|
Z1176:Vmn2r109
|
UTSW |
17 |
20,552,994 (GRCm38) |
missense |
probably benign |
0.00 |
|