Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429P17Rik |
A |
G |
13: 48,114,446 (GRCm39) |
|
noncoding transcript |
Het |
Agap2 |
T |
C |
10: 126,918,827 (GRCm39) |
|
probably benign |
Het |
Bicra |
G |
A |
7: 15,721,678 (GRCm39) |
T613I |
probably benign |
Het |
Cd163 |
T |
C |
6: 124,284,277 (GRCm39) |
S150P |
possibly damaging |
Het |
Cfap107 |
G |
A |
4: 144,165,098 (GRCm39) |
T26M |
probably damaging |
Het |
F830045P16Rik |
T |
G |
2: 129,314,614 (GRCm39) |
Q221P |
probably damaging |
Het |
Fam135b |
T |
A |
15: 71,328,784 (GRCm39) |
M1172L |
probably benign |
Het |
Fbxo2 |
G |
T |
4: 148,249,581 (GRCm39) |
|
probably null |
Het |
Frem1 |
C |
T |
4: 82,877,533 (GRCm39) |
|
probably benign |
Het |
Galnt17 |
C |
T |
5: 131,114,734 (GRCm39) |
|
probably null |
Het |
Gipc2 |
A |
G |
3: 151,833,771 (GRCm39) |
I170T |
probably damaging |
Het |
Gm2399 |
C |
T |
13: 12,717,417 (GRCm39) |
|
noncoding transcript |
Het |
Hdac10 |
T |
A |
15: 89,010,194 (GRCm39) |
M283L |
probably benign |
Het |
Icam5 |
A |
G |
9: 20,946,095 (GRCm39) |
E309G |
possibly damaging |
Het |
Ift70a1 |
A |
G |
2: 75,810,277 (GRCm39) |
V602A |
probably benign |
Het |
Igkv3-5 |
T |
A |
6: 70,640,865 (GRCm39) |
S115R |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,025,568 (GRCm39) |
R67G |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,840,232 (GRCm39) |
Y356C |
probably damaging |
Het |
Ly75 |
T |
C |
2: 60,168,655 (GRCm39) |
D751G |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,917,831 (GRCm39) |
D3297G |
probably damaging |
Het |
Mall |
A |
G |
2: 127,571,699 (GRCm39) |
F30L |
probably benign |
Het |
Map1b |
C |
T |
13: 99,571,512 (GRCm39) |
G403D |
probably damaging |
Het |
Mmp11 |
T |
C |
10: 75,762,730 (GRCm39) |
Y241C |
probably damaging |
Het |
Niban1 |
C |
A |
1: 151,579,555 (GRCm39) |
R425S |
probably damaging |
Het |
Or4a72 |
A |
G |
2: 89,405,557 (GRCm39) |
V171A |
probably benign |
Het |
Pcnt |
C |
T |
10: 76,228,609 (GRCm39) |
A1519T |
probably damaging |
Het |
Pcsk2 |
A |
G |
2: 143,529,490 (GRCm39) |
M96V |
probably benign |
Het |
Piwil4 |
T |
C |
9: 14,614,391 (GRCm39) |
D124G |
probably damaging |
Het |
Plb1 |
A |
T |
5: 32,471,041 (GRCm39) |
I538F |
probably damaging |
Het |
Polq |
A |
G |
16: 36,883,200 (GRCm39) |
D1788G |
probably damaging |
Het |
Pus7 |
A |
G |
5: 23,980,962 (GRCm39) |
S134P |
probably damaging |
Het |
Sec61a2 |
G |
A |
2: 5,891,363 (GRCm39) |
S56L |
possibly damaging |
Het |
Sel1l |
G |
T |
12: 91,810,033 (GRCm39) |
D26E |
probably benign |
Het |
Slc25a48 |
G |
A |
13: 56,612,758 (GRCm39) |
|
probably benign |
Het |
Tas2r126 |
T |
C |
6: 42,412,241 (GRCm39) |
F258S |
probably benign |
Het |
Tnfrsf13b |
G |
A |
11: 61,032,146 (GRCm39) |
V59I |
possibly damaging |
Het |
Usp6nl |
G |
A |
2: 6,445,879 (GRCm39) |
V619M |
probably benign |
Het |
Vmn2r71 |
A |
G |
7: 85,264,782 (GRCm39) |
D38G |
probably damaging |
Het |
|
Other mutations in Vmn1r67 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02812:Vmn1r67
|
APN |
7 |
10,180,945 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03121:Vmn1r67
|
APN |
7 |
10,181,394 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03208:Vmn1r67
|
APN |
7 |
10,181,025 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4142001:Vmn1r67
|
UTSW |
7 |
10,180,877 (GRCm39) |
missense |
probably benign |
0.13 |
R0048:Vmn1r67
|
UTSW |
7 |
10,180,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Vmn1r67
|
UTSW |
7 |
10,181,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Vmn1r67
|
UTSW |
7 |
10,181,597 (GRCm39) |
missense |
probably benign |
0.18 |
R1608:Vmn1r67
|
UTSW |
7 |
10,180,907 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2284:Vmn1r67
|
UTSW |
7 |
10,181,600 (GRCm39) |
missense |
probably damaging |
0.97 |
R3614:Vmn1r67
|
UTSW |
7 |
10,181,356 (GRCm39) |
missense |
probably damaging |
0.98 |
R4399:Vmn1r67
|
UTSW |
7 |
10,181,476 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4542:Vmn1r67
|
UTSW |
7 |
10,181,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R5216:Vmn1r67
|
UTSW |
7 |
10,181,090 (GRCm39) |
missense |
probably benign |
0.00 |
R5655:Vmn1r67
|
UTSW |
7 |
10,181,315 (GRCm39) |
missense |
probably benign |
0.43 |
R5837:Vmn1r67
|
UTSW |
7 |
10,180,949 (GRCm39) |
missense |
probably benign |
0.26 |
R6526:Vmn1r67
|
UTSW |
7 |
10,181,598 (GRCm39) |
missense |
probably benign |
0.05 |
R6735:Vmn1r67
|
UTSW |
7 |
10,181,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6846:Vmn1r67
|
UTSW |
7 |
10,180,840 (GRCm39) |
missense |
probably benign |
0.04 |
R7086:Vmn1r67
|
UTSW |
7 |
10,181,044 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7227:Vmn1r67
|
UTSW |
7 |
10,181,475 (GRCm39) |
nonsense |
probably null |
|
R7594:Vmn1r67
|
UTSW |
7 |
10,181,342 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7608:Vmn1r67
|
UTSW |
7 |
10,181,290 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7797:Vmn1r67
|
UTSW |
7 |
10,180,903 (GRCm39) |
missense |
probably benign |
0.30 |
R8681:Vmn1r67
|
UTSW |
7 |
10,181,128 (GRCm39) |
missense |
probably benign |
0.30 |
|