Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asb4 |
T |
C |
6: 5,423,416 (GRCm39) |
S188P |
probably benign |
Het |
Bbs5 |
A |
G |
2: 69,497,315 (GRCm39) |
|
probably benign |
Het |
Cdh13 |
G |
T |
8: 120,040,873 (GRCm39) |
G693W |
probably damaging |
Het |
Cdh20 |
T |
A |
1: 110,036,498 (GRCm39) |
Y559* |
probably null |
Het |
Cemip |
G |
A |
7: 83,636,538 (GRCm39) |
|
probably benign |
Het |
Crem |
A |
G |
18: 3,273,415 (GRCm39) |
|
probably benign |
Het |
Crygf |
A |
G |
1: 65,967,329 (GRCm39) |
Y151C |
probably damaging |
Het |
Dcp1b |
T |
C |
6: 119,157,019 (GRCm39) |
|
probably benign |
Het |
Fanca |
A |
G |
8: 124,043,198 (GRCm39) |
|
probably benign |
Het |
Fkbp15 |
A |
C |
4: 62,221,504 (GRCm39) |
|
probably benign |
Het |
Gabrp |
C |
T |
11: 33,502,616 (GRCm39) |
R416Q |
probably benign |
Het |
Iho1 |
T |
C |
9: 108,282,099 (GRCm39) |
S530G |
possibly damaging |
Het |
Impg2 |
T |
A |
16: 56,088,631 (GRCm39) |
Y1052* |
probably null |
Het |
Isg15 |
T |
C |
4: 156,284,319 (GRCm39) |
M70V |
probably benign |
Het |
Krit1 |
T |
A |
5: 3,861,248 (GRCm39) |
|
probably benign |
Het |
Lrrn3 |
T |
C |
12: 41,504,146 (GRCm39) |
D57G |
probably damaging |
Het |
Macrod1 |
A |
G |
19: 7,174,937 (GRCm39) |
E309G |
possibly damaging |
Het |
Notch1 |
A |
T |
2: 26,367,886 (GRCm39) |
|
probably benign |
Het |
Nptx1 |
T |
C |
11: 119,435,555 (GRCm39) |
T254A |
probably damaging |
Het |
Or12e9 |
A |
T |
2: 87,202,467 (GRCm39) |
D197V |
probably damaging |
Het |
Pigm |
A |
G |
1: 172,204,420 (GRCm39) |
Y52C |
probably damaging |
Het |
Pramel27 |
A |
T |
4: 143,578,489 (GRCm39) |
T250S |
possibly damaging |
Het |
Rif1 |
A |
G |
2: 52,002,611 (GRCm39) |
T2022A |
probably benign |
Het |
Rint1 |
T |
A |
5: 24,022,076 (GRCm39) |
L646Q |
probably damaging |
Het |
Rpe65 |
A |
T |
3: 159,309,978 (GRCm39) |
I84F |
probably damaging |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Scnn1a |
T |
C |
6: 125,319,744 (GRCm39) |
|
probably benign |
Het |
Selenop |
T |
C |
15: 3,310,104 (GRCm39) |
|
probably benign |
Het |
Siglecf |
T |
G |
7: 43,005,354 (GRCm39) |
V438G |
probably benign |
Het |
St8sia4 |
T |
A |
1: 95,581,499 (GRCm39) |
|
probably benign |
Het |
Tfeb |
T |
C |
17: 48,096,862 (GRCm39) |
F43S |
probably benign |
Het |
Tgm6 |
A |
G |
2: 129,980,851 (GRCm39) |
Y216C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,728,811 (GRCm39) |
C1234* |
probably null |
Het |
Ugt2a3 |
G |
A |
5: 87,484,439 (GRCm39) |
P195L |
probably damaging |
Het |
Usp24 |
T |
G |
4: 106,237,627 (GRCm39) |
I1095R |
probably damaging |
Het |
Usp34 |
C |
T |
11: 23,304,897 (GRCm39) |
H377Y |
probably damaging |
Het |
|
Other mutations in Try10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02001:Try10
|
APN |
6 |
41,333,523 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02608:Try10
|
APN |
6 |
41,332,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R0332:Try10
|
UTSW |
6 |
41,331,154 (GRCm39) |
missense |
probably benign |
0.18 |
R1628:Try10
|
UTSW |
6 |
41,334,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Try10
|
UTSW |
6 |
41,333,495 (GRCm39) |
missense |
probably benign |
0.02 |
R2471:Try10
|
UTSW |
6 |
41,333,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R3764:Try10
|
UTSW |
6 |
41,333,458 (GRCm39) |
missense |
probably benign |
0.07 |
R4008:Try10
|
UTSW |
6 |
41,333,608 (GRCm39) |
missense |
probably benign |
0.00 |
R4660:Try10
|
UTSW |
6 |
41,334,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Try10
|
UTSW |
6 |
41,332,386 (GRCm39) |
missense |
probably benign |
0.33 |
R5185:Try10
|
UTSW |
6 |
41,333,483 (GRCm39) |
missense |
probably damaging |
0.96 |
R6103:Try10
|
UTSW |
6 |
41,333,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R6301:Try10
|
UTSW |
6 |
41,332,523 (GRCm39) |
missense |
probably benign |
0.30 |
R6692:Try10
|
UTSW |
6 |
41,334,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R7786:Try10
|
UTSW |
6 |
41,332,463 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8391:Try10
|
UTSW |
6 |
41,334,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R9309:Try10
|
UTSW |
6 |
41,333,559 (GRCm39) |
missense |
probably benign |
|
R9636:Try10
|
UTSW |
6 |
41,332,505 (GRCm39) |
missense |
probably benign |
0.00 |
R9697:Try10
|
UTSW |
6 |
41,331,041 (GRCm39) |
start gained |
probably benign |
|
|