Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apol7a |
T |
C |
15: 77,273,886 (GRCm39) |
|
probably null |
Het |
Asb2 |
C |
T |
12: 103,302,164 (GRCm39) |
G128E |
possibly damaging |
Het |
Atp11c |
A |
T |
X: 59,315,263 (GRCm39) |
S683T |
probably damaging |
Het |
Brinp3 |
A |
G |
1: 146,627,735 (GRCm39) |
|
probably benign |
Het |
Cpeb3 |
A |
T |
19: 37,103,782 (GRCm39) |
M369K |
possibly damaging |
Het |
Exoc5 |
A |
T |
14: 49,253,072 (GRCm39) |
C580* |
probably null |
Het |
Gzmk |
C |
T |
13: 113,317,084 (GRCm39) |
V32I |
probably damaging |
Het |
Hsf4 |
T |
C |
8: 105,998,221 (GRCm39) |
I129T |
probably damaging |
Het |
Igkv1-115 |
T |
A |
6: 68,138,516 (GRCm39) |
W40R |
probably damaging |
Het |
Iqub |
A |
T |
6: 24,500,312 (GRCm39) |
M314K |
probably benign |
Het |
Krt87 |
T |
C |
15: 101,389,099 (GRCm39) |
T78A |
probably benign |
Het |
Med28 |
T |
C |
5: 45,682,633 (GRCm39) |
S100P |
probably benign |
Het |
Prx |
G |
A |
7: 27,219,212 (GRCm39) |
V1238I |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,353,727 (GRCm39) |
N2263S |
probably benign |
Het |
Rab12 |
A |
G |
17: 66,826,384 (GRCm39) |
F61S |
probably damaging |
Het |
Serpinb9d |
T |
C |
13: 33,387,006 (GRCm39) |
F358S |
probably damaging |
Het |
Slc25a3 |
A |
T |
10: 90,953,987 (GRCm39) |
Y242N |
probably damaging |
Het |
Smtnl1 |
T |
C |
2: 84,649,034 (GRCm39) |
I73M |
possibly damaging |
Het |
Tnp1 |
C |
A |
1: 73,054,877 (GRCm39) |
|
probably benign |
Het |
Trim5 |
T |
C |
7: 103,928,638 (GRCm39) |
E101G |
probably damaging |
Het |
|
Other mutations in Gm9956 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02411:Gm9956
|
APN |
10 |
56,621,388 (GRCm39) |
missense |
unknown |
|
IGL02898:Gm9956
|
APN |
10 |
56,621,350 (GRCm39) |
missense |
unknown |
|
R0513:Gm9956
|
UTSW |
10 |
56,621,291 (GRCm39) |
start gained |
|
|
R0731:Gm9956
|
UTSW |
10 |
56,621,639 (GRCm39) |
nonsense |
probably null |
|
R0841:Gm9956
|
UTSW |
10 |
56,621,425 (GRCm39) |
missense |
unknown |
|
R0841:Gm9956
|
UTSW |
10 |
56,621,424 (GRCm39) |
missense |
unknown |
|
R1289:Gm9956
|
UTSW |
10 |
56,621,676 (GRCm39) |
missense |
probably damaging |
0.99 |
|