Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030619P08Rik |
T |
A |
15: 75,301,801 (GRCm39) |
|
noncoding transcript |
Het |
Aadat |
A |
G |
8: 60,979,656 (GRCm39) |
I173V |
probably benign |
Het |
Acsl6 |
G |
A |
11: 54,216,432 (GRCm39) |
V200I |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,633,353 (GRCm39) |
|
probably null |
Het |
Arhgef17 |
A |
T |
7: 100,530,576 (GRCm39) |
D1403E |
possibly damaging |
Het |
Atp10b |
A |
G |
11: 43,121,387 (GRCm39) |
T1017A |
probably benign |
Het |
Capg |
C |
T |
6: 72,532,509 (GRCm39) |
R25C |
probably damaging |
Het |
Cd22 |
A |
G |
7: 30,576,959 (GRCm39) |
I116T |
probably damaging |
Het |
Cep135 |
AGTCTGCCTTTGG |
A |
5: 76,739,690 (GRCm39) |
|
probably benign |
Het |
Ciita |
A |
T |
16: 10,327,265 (GRCm39) |
I277F |
possibly damaging |
Het |
Col15a1 |
T |
C |
4: 47,296,112 (GRCm39) |
V943A |
possibly damaging |
Het |
Coq2 |
G |
A |
5: 100,805,698 (GRCm39) |
H313Y |
possibly damaging |
Het |
Csn3 |
C |
T |
5: 88,077,694 (GRCm39) |
P67S |
probably benign |
Het |
Csrnp3 |
A |
G |
2: 65,852,684 (GRCm39) |
T359A |
possibly damaging |
Het |
Cttnbp2nl |
A |
G |
3: 104,912,357 (GRCm39) |
L509P |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,297,749 (GRCm39) |
D431G |
probably benign |
Het |
Dtx3l |
A |
T |
16: 35,753,608 (GRCm39) |
C333S |
possibly damaging |
Het |
Ear-ps2 |
G |
A |
14: 44,284,517 (GRCm39) |
|
noncoding transcript |
Het |
Fam171a1 |
G |
C |
2: 3,179,390 (GRCm39) |
G72A |
probably damaging |
Het |
Fbxw17 |
T |
C |
13: 50,586,390 (GRCm39) |
|
probably benign |
Het |
Fry |
A |
G |
5: 150,393,185 (GRCm39) |
D605G |
possibly damaging |
Het |
Fyn |
T |
C |
10: 39,405,936 (GRCm39) |
F240S |
probably benign |
Het |
Gcfc2 |
T |
C |
6: 81,930,271 (GRCm39) |
L646P |
probably damaging |
Het |
Gm5087 |
C |
T |
14: 13,158,788 (GRCm38) |
|
noncoding transcript |
Het |
Got2 |
T |
A |
8: 96,602,477 (GRCm39) |
N91I |
probably benign |
Het |
Hspa4 |
C |
T |
11: 53,177,802 (GRCm39) |
V103I |
possibly damaging |
Het |
Itgad |
A |
G |
7: 127,792,600 (GRCm39) |
|
probably null |
Het |
Krt33a |
A |
G |
11: 99,904,961 (GRCm39) |
S182P |
probably damaging |
Het |
Mcph1 |
T |
C |
8: 18,721,254 (GRCm39) |
I694T |
probably damaging |
Het |
Mmp15 |
T |
C |
8: 96,097,696 (GRCm39) |
V502A |
probably benign |
Het |
Mov10l1 |
T |
C |
15: 88,867,235 (GRCm39) |
V23A |
probably benign |
Het |
Myo9a |
T |
A |
9: 59,817,900 (GRCm39) |
N2322K |
probably damaging |
Het |
Ndst4 |
A |
G |
3: 125,503,766 (GRCm39) |
Y11C |
probably damaging |
Het |
Nell1 |
T |
C |
7: 49,826,062 (GRCm39) |
F199S |
probably damaging |
Het |
Nup210 |
C |
T |
6: 91,003,951 (GRCm39) |
V646M |
probably damaging |
Het |
Nup98 |
A |
T |
7: 101,845,029 (GRCm39) |
S13R |
unknown |
Het |
Nxf1 |
T |
C |
19: 8,741,293 (GRCm39) |
I54T |
possibly damaging |
Het |
Or8b38 |
A |
G |
9: 37,973,446 (GRCm39) |
T277A |
probably damaging |
Het |
Pcdh10 |
C |
A |
3: 45,338,626 (GRCm39) |
R928S |
probably damaging |
Het |
Pou3f3 |
A |
G |
1: 42,737,438 (GRCm39) |
N378S |
probably benign |
Het |
Rfx6 |
T |
A |
10: 51,588,187 (GRCm39) |
Y109* |
probably null |
Het |
Rorc |
T |
A |
3: 94,304,632 (GRCm39) |
V339D |
probably benign |
Het |
Scin |
T |
A |
12: 40,127,558 (GRCm39) |
I411F |
probably benign |
Het |
Serpind1 |
A |
G |
16: 17,154,758 (GRCm39) |
Y195C |
probably damaging |
Het |
Tas2r117 |
T |
C |
6: 132,780,585 (GRCm39) |
V241A |
possibly damaging |
Het |
Tet3 |
T |
A |
6: 83,363,045 (GRCm39) |
E709V |
probably damaging |
Het |
Trbc1 |
T |
A |
6: 41,515,383 (GRCm39) |
|
probably benign |
Het |
Vmn2r42 |
T |
A |
7: 8,197,837 (GRCm39) |
K261* |
probably null |
Het |
Xrcc5 |
T |
A |
1: 72,379,209 (GRCm39) |
L438Q |
probably damaging |
Het |
Zfp142 |
T |
C |
1: 74,624,608 (GRCm39) |
N72S |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,809,755 (GRCm39) |
S1096R |
probably damaging |
Het |
|
Other mutations in Vmn1r212 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01131:Vmn1r212
|
APN |
13 |
23,067,329 (GRCm39) |
missense |
unknown |
|
IGL01678:Vmn1r212
|
APN |
13 |
23,068,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R0798:Vmn1r212
|
UTSW |
13 |
23,067,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Vmn1r212
|
UTSW |
13 |
23,067,638 (GRCm39) |
nonsense |
probably null |
|
R1331:Vmn1r212
|
UTSW |
13 |
23,067,562 (GRCm39) |
missense |
probably benign |
0.33 |
R2064:Vmn1r212
|
UTSW |
13 |
23,068,285 (GRCm39) |
missense |
probably benign |
0.28 |
R2356:Vmn1r212
|
UTSW |
13 |
23,068,120 (GRCm39) |
nonsense |
probably null |
|
R2846:Vmn1r212
|
UTSW |
13 |
23,068,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R3896:Vmn1r212
|
UTSW |
13 |
23,068,067 (GRCm39) |
missense |
probably benign |
0.00 |
R3937:Vmn1r212
|
UTSW |
13 |
23,067,358 (GRCm39) |
missense |
unknown |
|
R4722:Vmn1r212
|
UTSW |
13 |
23,068,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Vmn1r212
|
UTSW |
13 |
23,068,258 (GRCm39) |
missense |
probably damaging |
0.98 |
R7199:Vmn1r212
|
UTSW |
13 |
23,067,731 (GRCm39) |
missense |
probably benign |
0.12 |
R7413:Vmn1r212
|
UTSW |
13 |
23,067,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Vmn1r212
|
UTSW |
13 |
23,067,323 (GRCm39) |
missense |
unknown |
|
R8054:Vmn1r212
|
UTSW |
13 |
23,067,935 (GRCm39) |
missense |
probably benign |
0.25 |
R8844:Vmn1r212
|
UTSW |
13 |
23,067,526 (GRCm39) |
missense |
probably benign |
0.00 |
R8929:Vmn1r212
|
UTSW |
13 |
23,067,494 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9538:Vmn1r212
|
UTSW |
13 |
23,067,451 (GRCm39) |
missense |
probably benign |
0.03 |
R9612:Vmn1r212
|
UTSW |
13 |
23,067,443 (GRCm39) |
missense |
possibly damaging |
0.96 |
Z1088:Vmn1r212
|
UTSW |
13 |
23,067,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|