Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
T |
C |
5: 114,342,767 (GRCm39) |
F878L |
possibly damaging |
Het |
Acr |
T |
A |
15: 89,458,146 (GRCm39) |
Y276N |
probably damaging |
Het |
AI987944 |
A |
T |
7: 41,023,814 (GRCm39) |
Y388* |
probably null |
Het |
Ankrd29 |
G |
A |
18: 12,412,835 (GRCm39) |
T114I |
probably damaging |
Het |
Ap5z1 |
T |
C |
5: 142,453,536 (GRCm39) |
M168T |
probably benign |
Het |
Bard1 |
A |
C |
1: 71,085,880 (GRCm39) |
C608W |
probably damaging |
Het |
Brd10 |
A |
G |
19: 29,731,072 (GRCm39) |
S647P |
possibly damaging |
Het |
Clspn |
A |
G |
4: 126,471,566 (GRCm39) |
R907G |
probably benign |
Het |
Cubn |
C |
T |
2: 13,355,743 (GRCm39) |
V1830I |
probably benign |
Het |
Cwc22 |
T |
C |
2: 77,754,913 (GRCm39) |
N221S |
probably damaging |
Het |
Dact3 |
A |
G |
7: 16,609,540 (GRCm39) |
E64G |
possibly damaging |
Het |
Dhx40 |
T |
C |
11: 86,680,330 (GRCm39) |
E381G |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,458,907 (GRCm39) |
S3744P |
possibly damaging |
Het |
Epha4 |
A |
G |
1: 77,351,513 (GRCm39) |
V914A |
probably benign |
Het |
Fbxw10 |
G |
A |
11: 62,753,482 (GRCm39) |
C492Y |
probably damaging |
Het |
G930045G22Rik |
C |
A |
6: 50,824,756 (GRCm39) |
|
noncoding transcript |
Het |
Gm21103 |
A |
T |
14: 17,484,855 (GRCm39) |
I63K |
probably damaging |
Het |
Gpr156 |
T |
C |
16: 37,825,619 (GRCm39) |
V612A |
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,229,572 (GRCm39) |
S33P |
probably benign |
Het |
Hibch |
A |
G |
1: 52,884,228 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,619,539 (GRCm39) |
C1192S |
probably damaging |
Het |
Hsd11b1 |
CGG |
CG |
1: 192,922,557 (GRCm39) |
|
probably null |
Het |
Igf2bp2 |
T |
G |
16: 21,907,835 (GRCm39) |
I89L |
probably damaging |
Het |
Il2ra |
A |
T |
2: 11,681,703 (GRCm39) |
T103S |
possibly damaging |
Het |
Ino80 |
T |
A |
2: 119,276,056 (GRCm39) |
M407L |
probably benign |
Het |
Jade1 |
A |
C |
3: 41,567,946 (GRCm39) |
K671N |
probably benign |
Het |
Lca5 |
C |
T |
9: 83,280,648 (GRCm39) |
S384N |
probably benign |
Het |
Lce1l |
G |
T |
3: 92,757,804 (GRCm39) |
P18H |
unknown |
Het |
Lrrc8d |
T |
C |
5: 105,945,536 (GRCm39) |
|
probably benign |
Het |
Ly75 |
T |
C |
2: 60,195,489 (GRCm39) |
N223S |
probably damaging |
Het |
Mcm3 |
A |
T |
1: 20,873,768 (GRCm39) |
F784Y |
possibly damaging |
Het |
Ncf4 |
T |
G |
15: 78,144,988 (GRCm39) |
|
probably benign |
Het |
Ncoa1 |
T |
A |
12: 4,303,746 (GRCm39) |
M1362L |
probably benign |
Het |
Or1e16 |
T |
C |
11: 73,286,003 (GRCm39) |
T282A |
probably benign |
Het |
Or5p5 |
A |
G |
7: 107,414,451 (GRCm39) |
Y220C |
probably benign |
Het |
Or6c8b |
G |
C |
10: 128,882,433 (GRCm39) |
F166L |
probably damaging |
Het |
Prkg2 |
T |
C |
5: 99,115,593 (GRCm39) |
R543G |
probably damaging |
Het |
Ptprd |
A |
C |
4: 75,977,904 (GRCm39) |
|
probably null |
Het |
Scap |
A |
G |
9: 110,210,497 (GRCm39) |
S969G |
possibly damaging |
Het |
Sgk2 |
T |
C |
2: 162,836,624 (GRCm39) |
F60S |
probably benign |
Het |
Sgpp1 |
G |
T |
12: 75,781,981 (GRCm39) |
Y119* |
probably null |
Het |
Siglech |
A |
T |
7: 55,418,413 (GRCm39) |
K31* |
probably null |
Het |
Slc40a1 |
A |
G |
1: 45,951,498 (GRCm39) |
Y220H |
probably damaging |
Het |
Smurf2 |
G |
A |
11: 106,743,389 (GRCm39) |
T219M |
possibly damaging |
Het |
Speer4f2 |
A |
G |
5: 17,581,526 (GRCm39) |
K156R |
possibly damaging |
Het |
Spp1 |
T |
G |
5: 104,588,424 (GRCm39) |
D276E |
probably benign |
Het |
Stk32b |
T |
C |
5: 37,617,078 (GRCm39) |
|
probably null |
Het |
Stxbp5 |
G |
A |
10: 9,638,668 (GRCm39) |
Q1044* |
probably null |
Het |
Sv2c |
T |
A |
13: 96,097,886 (GRCm39) |
T696S |
probably damaging |
Het |
Tubgcp2 |
A |
C |
7: 139,584,937 (GRCm39) |
|
probably null |
Het |
Ubap1l |
C |
T |
9: 65,278,973 (GRCm39) |
P91S |
probably damaging |
Het |
Vmn2r76 |
A |
T |
7: 85,874,657 (GRCm39) |
D773E |
probably damaging |
Het |
Xirp2 |
C |
G |
2: 67,345,646 (GRCm39) |
S2629C |
probably benign |
Het |
Zbtb20 |
C |
A |
16: 43,431,230 (GRCm39) |
C580* |
probably null |
Het |
Zfp957 |
T |
A |
14: 79,450,622 (GRCm39) |
Q392H |
unknown |
Het |
Zfyve19 |
C |
T |
2: 119,042,427 (GRCm39) |
T178M |
probably damaging |
Het |
Zswim6 |
T |
C |
13: 107,906,128 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Ifi214 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01413:Ifi214
|
APN |
1 |
173,356,995 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01418:Ifi214
|
APN |
1 |
173,356,995 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01821:Ifi214
|
APN |
1 |
173,356,891 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03341:Ifi214
|
APN |
1 |
173,354,082 (GRCm39) |
missense |
possibly damaging |
0.86 |
PIT4305001:Ifi214
|
UTSW |
1 |
173,355,485 (GRCm39) |
missense |
probably benign |
0.00 |
R1908:Ifi214
|
UTSW |
1 |
173,357,077 (GRCm39) |
missense |
probably benign |
0.44 |
R4239:Ifi214
|
UTSW |
1 |
173,352,509 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4731:Ifi214
|
UTSW |
1 |
173,354,157 (GRCm39) |
missense |
probably benign |
0.26 |
R4732:Ifi214
|
UTSW |
1 |
173,354,157 (GRCm39) |
missense |
probably benign |
0.26 |
R4733:Ifi214
|
UTSW |
1 |
173,354,157 (GRCm39) |
missense |
probably benign |
0.26 |
R5171:Ifi214
|
UTSW |
1 |
173,354,200 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6290:Ifi214
|
UTSW |
1 |
173,356,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R6499:Ifi214
|
UTSW |
1 |
173,352,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R7271:Ifi214
|
UTSW |
1 |
173,357,042 (GRCm39) |
missense |
probably damaging |
0.96 |
R7290:Ifi214
|
UTSW |
1 |
173,357,097 (GRCm39) |
missense |
probably benign |
0.03 |
R7765:Ifi214
|
UTSW |
1 |
173,352,402 (GRCm39) |
missense |
probably damaging |
0.96 |
R8712:Ifi214
|
UTSW |
1 |
173,355,486 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8807:Ifi214
|
UTSW |
1 |
173,354,133 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9144:Ifi214
|
UTSW |
1 |
173,355,434 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9452:Ifi214
|
UTSW |
1 |
173,356,894 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9534:Ifi214
|
UTSW |
1 |
173,354,092 (GRCm39) |
missense |
probably benign |
0.18 |
R9721:Ifi214
|
UTSW |
1 |
173,355,479 (GRCm39) |
missense |
possibly damaging |
0.95 |
|