Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,665,856 (GRCm39) |
V255I |
probably benign |
Het |
Arfgef2 |
T |
C |
2: 166,701,702 (GRCm39) |
|
probably benign |
Het |
Bpifb2 |
A |
T |
2: 153,731,044 (GRCm39) |
Q205L |
probably damaging |
Het |
Ccdc30 |
C |
T |
4: 119,206,964 (GRCm39) |
R386Q |
possibly damaging |
Het |
Cdk5rap2 |
T |
A |
4: 70,273,114 (GRCm39) |
|
probably null |
Het |
Comtd1 |
A |
G |
14: 21,897,735 (GRCm39) |
|
probably null |
Het |
Dao |
T |
C |
5: 114,159,076 (GRCm39) |
C261R |
probably damaging |
Het |
Dner |
A |
G |
1: 84,563,059 (GRCm39) |
V187A |
possibly damaging |
Het |
Dsg3 |
T |
C |
18: 20,666,425 (GRCm39) |
|
probably benign |
Het |
Eif3j2 |
A |
G |
18: 43,610,444 (GRCm39) |
L123P |
possibly damaging |
Het |
Esf1 |
G |
A |
2: 139,996,706 (GRCm39) |
|
probably benign |
Het |
Exo5 |
G |
A |
4: 120,778,830 (GRCm39) |
T345I |
possibly damaging |
Het |
Fancl |
A |
T |
11: 26,337,299 (GRCm39) |
I29F |
probably damaging |
Het |
Gadl1 |
C |
T |
9: 115,795,335 (GRCm39) |
H313Y |
probably damaging |
Het |
Gm17190 |
G |
A |
13: 96,219,270 (GRCm39) |
|
probably benign |
Het |
Gtf3c1 |
G |
T |
7: 125,245,675 (GRCm39) |
T1580N |
possibly damaging |
Het |
Gtf3c6 |
T |
A |
10: 40,127,155 (GRCm39) |
I66L |
probably benign |
Het |
Hhla1 |
A |
G |
15: 65,813,639 (GRCm39) |
I231T |
probably damaging |
Het |
Hk2 |
A |
G |
6: 82,716,630 (GRCm39) |
Y273H |
probably damaging |
Het |
Hk2 |
A |
G |
6: 82,726,213 (GRCm39) |
I83T |
probably benign |
Het |
Igkv9-129 |
A |
T |
6: 67,817,172 (GRCm39) |
D92V |
probably damaging |
Het |
Lrrc1 |
A |
G |
9: 77,406,551 (GRCm39) |
F36S |
probably damaging |
Het |
Man1b1 |
A |
G |
2: 25,224,416 (GRCm39) |
E102G |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,179,031 (GRCm39) |
S475G |
probably benign |
Het |
Or52s1 |
T |
A |
7: 102,861,841 (GRCm39) |
V247D |
probably damaging |
Het |
Otud4 |
T |
A |
8: 80,390,419 (GRCm39) |
M343K |
probably benign |
Het |
Peg10 |
A |
T |
6: 4,756,647 (GRCm39) |
|
probably benign |
Het |
Plet1 |
T |
A |
9: 50,415,722 (GRCm39) |
N197K |
probably benign |
Het |
Ppp1r12a |
C |
T |
10: 108,097,115 (GRCm39) |
R243C |
probably damaging |
Het |
Serpinb10 |
A |
T |
1: 107,469,957 (GRCm39) |
K146N |
possibly damaging |
Het |
Sis |
A |
G |
3: 72,835,630 (GRCm39) |
F911L |
probably benign |
Het |
Spon1 |
G |
A |
7: 113,632,260 (GRCm39) |
V528M |
possibly damaging |
Het |
Tdrd9 |
T |
C |
12: 112,010,733 (GRCm39) |
V1100A |
probably benign |
Het |
Tmtc3 |
T |
C |
10: 100,283,468 (GRCm39) |
M696V |
probably benign |
Het |
Triobp |
A |
G |
15: 78,875,084 (GRCm39) |
E122G |
probably damaging |
Het |
Wt1 |
G |
A |
2: 105,000,368 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ifit1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Ifit1
|
APN |
19 |
34,625,533 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01484:Ifit1
|
APN |
19 |
34,626,243 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01505:Ifit1
|
APN |
19 |
34,625,854 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02663:Ifit1
|
APN |
19 |
34,618,380 (GRCm39) |
utr 5 prime |
probably benign |
|
R0655:Ifit1
|
UTSW |
19 |
34,625,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R1524:Ifit1
|
UTSW |
19 |
34,625,032 (GRCm39) |
missense |
probably damaging |
0.97 |
R1859:Ifit1
|
UTSW |
19 |
34,624,944 (GRCm39) |
missense |
probably benign |
0.00 |
R3805:Ifit1
|
UTSW |
19 |
34,625,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R4514:Ifit1
|
UTSW |
19 |
34,625,913 (GRCm39) |
nonsense |
probably null |
|
R4714:Ifit1
|
UTSW |
19 |
34,625,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R5310:Ifit1
|
UTSW |
19 |
34,626,204 (GRCm39) |
missense |
probably benign |
|
R5620:Ifit1
|
UTSW |
19 |
34,625,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R5787:Ifit1
|
UTSW |
19 |
34,624,975 (GRCm39) |
missense |
probably benign |
0.29 |
R5964:Ifit1
|
UTSW |
19 |
34,625,869 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8230:Ifit1
|
UTSW |
19 |
34,625,068 (GRCm39) |
missense |
probably benign |
0.00 |
R8249:Ifit1
|
UTSW |
19 |
34,618,389 (GRCm39) |
critical splice donor site |
probably null |
|
R8713:Ifit1
|
UTSW |
19 |
34,625,038 (GRCm39) |
missense |
probably benign |
0.01 |
R9054:Ifit1
|
UTSW |
19 |
34,625,887 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9227:Ifit1
|
UTSW |
19 |
34,625,236 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9230:Ifit1
|
UTSW |
19 |
34,625,236 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9723:Ifit1
|
UTSW |
19 |
34,626,257 (GRCm39) |
makesense |
probably null |
|
|