Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
A |
T |
12: 84,655,578 (GRCm39) |
|
probably null |
Het |
Agrn |
A |
T |
4: 156,254,667 (GRCm39) |
M1548K |
probably benign |
Het |
Als2 |
A |
G |
1: 59,246,945 (GRCm39) |
S565P |
probably damaging |
Het |
Atm |
T |
C |
9: 53,438,537 (GRCm39) |
I126M |
probably damaging |
Het |
Btbd9 |
G |
A |
17: 30,493,910 (GRCm39) |
R494* |
probably null |
Het |
Coro1c |
G |
T |
5: 113,982,454 (GRCm39) |
R461S |
probably damaging |
Het |
Gtf2h1 |
A |
G |
7: 46,451,165 (GRCm39) |
K19E |
probably damaging |
Het |
Kcnc1 |
A |
G |
7: 46,077,397 (GRCm39) |
T400A |
probably damaging |
Het |
Kcnh5 |
T |
C |
12: 75,134,379 (GRCm39) |
Y390C |
probably benign |
Het |
Ly75 |
G |
T |
2: 60,182,700 (GRCm39) |
S534R |
probably damaging |
Het |
Mapk15 |
A |
G |
15: 75,866,737 (GRCm39) |
E38G |
probably benign |
Het |
Or9i2 |
T |
A |
19: 13,815,830 (GRCm39) |
T236S |
probably damaging |
Het |
Otof |
A |
T |
5: 30,528,070 (GRCm39) |
N1924K |
probably benign |
Het |
Plekhm2 |
T |
A |
4: 141,355,617 (GRCm39) |
H861L |
probably benign |
Het |
Pramel25 |
T |
A |
4: 143,521,602 (GRCm39) |
F406Y |
probably benign |
Het |
Rufy4 |
A |
T |
1: 74,168,518 (GRCm39) |
K100N |
probably damaging |
Het |
Sptbn1 |
T |
C |
11: 30,088,496 (GRCm39) |
E879G |
probably damaging |
Het |
Stab2 |
T |
C |
10: 86,803,514 (GRCm39) |
N345S |
possibly damaging |
Het |
Tacc2 |
C |
T |
7: 130,330,582 (GRCm39) |
P1996S |
probably benign |
Het |
Tfcp2 |
A |
G |
15: 100,411,061 (GRCm39) |
|
probably benign |
Het |
Trpm8 |
A |
G |
1: 88,253,210 (GRCm39) |
T100A |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,765,304 (GRCm39) |
T2507A |
probably benign |
Het |
Vmn2r118 |
T |
C |
17: 55,917,517 (GRCm39) |
T332A |
probably benign |
Het |
Zfp189 |
T |
A |
4: 49,522,445 (GRCm39) |
D27E |
probably damaging |
Het |
|
Other mutations in 4931429P17Rik |
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