Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
A |
11: 109,844,422 (GRCm39) |
R870C |
possibly damaging |
Het |
Abcf2 |
A |
T |
5: 24,779,210 (GRCm39) |
L113I |
probably damaging |
Het |
Abi1 |
C |
T |
2: 22,861,240 (GRCm39) |
R106Q |
probably damaging |
Het |
Arhgef28 |
A |
G |
13: 98,036,324 (GRCm39) |
V1645A |
probably benign |
Het |
Ceacam1 |
G |
A |
7: 25,175,912 (GRCm39) |
A94V |
possibly damaging |
Het |
Fat2 |
G |
A |
11: 55,173,168 (GRCm39) |
T2515I |
probably damaging |
Het |
Gm5800 |
T |
C |
14: 51,951,983 (GRCm39) |
Y93C |
probably benign |
Het |
Gnl1 |
A |
G |
17: 36,299,548 (GRCm39) |
D573G |
probably damaging |
Het |
Gosr1 |
A |
G |
11: 76,645,229 (GRCm39) |
M105T |
probably benign |
Het |
Gramd1c |
A |
T |
16: 43,825,868 (GRCm39) |
Y303N |
probably benign |
Het |
Heatr9 |
A |
G |
11: 83,404,085 (GRCm39) |
|
probably null |
Het |
Iigp1c |
T |
A |
18: 60,378,883 (GRCm39) |
Y139* |
probably null |
Het |
Itih2 |
T |
C |
2: 10,111,546 (GRCm39) |
D464G |
probably damaging |
Het |
Jcad |
T |
C |
18: 4,673,902 (GRCm39) |
Y555H |
probably benign |
Het |
Krtap19-3 |
A |
T |
16: 88,674,609 (GRCm39) |
*88R |
probably null |
Het |
Mrps11 |
T |
C |
7: 78,440,453 (GRCm39) |
F114S |
probably damaging |
Het |
Nat8 |
A |
T |
6: 85,807,875 (GRCm39) |
V86E |
possibly damaging |
Het |
Nek5 |
T |
C |
8: 22,569,158 (GRCm39) |
T555A |
probably benign |
Het |
Or6c3 |
A |
T |
10: 129,309,474 (GRCm39) |
K304N |
probably benign |
Het |
Pprc1 |
C |
T |
19: 46,049,948 (GRCm39) |
T10I |
possibly damaging |
Het |
Prss16 |
A |
G |
13: 22,187,417 (GRCm39) |
V409A |
possibly damaging |
Het |
Sema3d |
T |
A |
5: 12,513,189 (GRCm39) |
L53Q |
probably damaging |
Het |
Sfmbt2 |
T |
C |
2: 10,582,628 (GRCm39) |
Y696H |
probably damaging |
Het |
Sh2d3c |
C |
T |
2: 32,615,270 (GRCm39) |
A120V |
probably benign |
Het |
Smn1 |
A |
G |
13: 100,264,365 (GRCm39) |
Y32C |
probably damaging |
Het |
Sun2 |
C |
T |
15: 79,622,849 (GRCm39) |
R110Q |
probably benign |
Het |
Tcp11l2 |
T |
G |
10: 84,440,764 (GRCm39) |
D323E |
possibly damaging |
Het |
Tex55 |
A |
T |
16: 38,648,355 (GRCm39) |
S251R |
probably damaging |
Het |
Tnni3k |
A |
T |
3: 154,667,451 (GRCm39) |
S296R |
probably damaging |
Het |
Uck1 |
G |
A |
2: 32,148,334 (GRCm39) |
R161C |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,135,869 (GRCm39) |
S2435T |
probably damaging |
Het |
Vmn2r114 |
C |
A |
17: 23,510,652 (GRCm39) |
K609N |
probably damaging |
Het |
|
Other mutations in Ccdc198 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01433:Ccdc198
|
APN |
14 |
49,473,341 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02133:Ccdc198
|
APN |
14 |
49,470,424 (GRCm39) |
missense |
probably benign |
0.05 |
R1751:Ccdc198
|
UTSW |
14 |
49,473,341 (GRCm39) |
missense |
probably benign |
0.09 |
R1767:Ccdc198
|
UTSW |
14 |
49,473,341 (GRCm39) |
missense |
probably benign |
0.09 |
R1846:Ccdc198
|
UTSW |
14 |
49,473,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Ccdc198
|
UTSW |
14 |
49,464,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R4563:Ccdc198
|
UTSW |
14 |
49,471,955 (GRCm39) |
missense |
probably benign |
0.27 |
R4883:Ccdc198
|
UTSW |
14 |
49,482,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Ccdc198
|
UTSW |
14 |
49,470,351 (GRCm39) |
missense |
probably benign |
0.01 |
R5381:Ccdc198
|
UTSW |
14 |
49,470,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R5986:Ccdc198
|
UTSW |
14 |
49,470,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R6379:Ccdc198
|
UTSW |
14 |
49,481,191 (GRCm39) |
missense |
probably benign |
0.02 |
R6829:Ccdc198
|
UTSW |
14 |
49,464,025 (GRCm39) |
makesense |
probably null |
|
R6841:Ccdc198
|
UTSW |
14 |
49,481,270 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7337:Ccdc198
|
UTSW |
14 |
49,471,948 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8327:Ccdc198
|
UTSW |
14 |
49,470,356 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9154:Ccdc198
|
UTSW |
14 |
49,473,367 (GRCm39) |
missense |
probably benign |
0.00 |
|