Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
T |
C |
1: 53,226,724 (GRCm39) |
T13A |
probably benign |
Het |
Aldh1l2 |
T |
A |
10: 83,342,469 (GRCm39) |
K447I |
probably damaging |
Het |
Ankrd17 |
A |
G |
5: 90,392,151 (GRCm39) |
S1840P |
possibly damaging |
Het |
Ash1l |
A |
G |
3: 88,930,344 (GRCm39) |
I1940M |
probably benign |
Het |
Bfar |
T |
G |
16: 13,506,791 (GRCm39) |
|
probably null |
Het |
Bicra |
G |
T |
7: 15,713,390 (GRCm39) |
H937Q |
possibly damaging |
Het |
Brip1 |
A |
T |
11: 86,043,562 (GRCm39) |
M334K |
probably benign |
Het |
Camsap2 |
T |
G |
1: 136,232,050 (GRCm39) |
M182L |
probably benign |
Het |
Chd6 |
A |
T |
2: 160,811,383 (GRCm39) |
C1407S |
probably damaging |
Het |
Cmya5 |
A |
G |
13: 93,234,753 (GRCm39) |
S112P |
possibly damaging |
Het |
Csmd1 |
A |
T |
8: 16,281,341 (GRCm39) |
V728E |
probably damaging |
Het |
Cyp2j6 |
T |
A |
4: 96,434,001 (GRCm39) |
Q103L |
probably benign |
Het |
Ddias |
A |
T |
7: 92,515,830 (GRCm39) |
I21K |
probably damaging |
Het |
Derl2 |
A |
C |
11: 70,904,036 (GRCm39) |
|
probably benign |
Het |
Dgka |
A |
T |
10: 128,558,317 (GRCm39) |
|
probably benign |
Het |
Dusp11 |
T |
C |
6: 85,938,474 (GRCm39) |
D15G |
probably damaging |
Het |
Enpp2 |
T |
C |
15: 54,773,577 (GRCm39) |
D110G |
probably damaging |
Het |
Fkbp11 |
A |
T |
15: 98,622,471 (GRCm39) |
V134E |
probably damaging |
Het |
Gm57858 |
T |
A |
3: 36,087,065 (GRCm39) |
R176S |
possibly damaging |
Het |
Irag2 |
T |
C |
6: 145,120,344 (GRCm39) |
S520P |
possibly damaging |
Het |
Luzp2 |
T |
C |
7: 54,821,939 (GRCm39) |
|
probably benign |
Het |
Manea |
C |
A |
4: 26,328,127 (GRCm39) |
E305* |
probably null |
Het |
Manea |
T |
A |
4: 26,328,126 (GRCm39) |
E305V |
probably damaging |
Het |
Megf6 |
A |
G |
4: 154,337,606 (GRCm39) |
|
probably null |
Het |
Mrpl3 |
G |
T |
9: 104,931,726 (GRCm39) |
D59Y |
probably damaging |
Het |
Myh9 |
T |
C |
15: 77,675,942 (GRCm39) |
Y248C |
probably benign |
Het |
Nbeal2 |
G |
A |
9: 110,468,353 (GRCm39) |
|
probably benign |
Het |
Or10a5 |
G |
T |
7: 106,635,902 (GRCm39) |
C180F |
probably damaging |
Het |
Or1f19 |
T |
A |
16: 3,411,190 (GRCm39) |
I310K |
probably benign |
Het |
Or2y1c |
G |
T |
11: 49,361,893 (GRCm39) |
G305V |
probably benign |
Het |
Or8b40 |
A |
G |
9: 38,027,808 (GRCm39) |
T239A |
probably damaging |
Het |
Pax8 |
C |
A |
2: 24,331,642 (GRCm39) |
C147F |
probably damaging |
Het |
Phf12 |
T |
C |
11: 77,914,493 (GRCm39) |
V96A |
possibly damaging |
Het |
Psg18 |
A |
T |
7: 18,079,875 (GRCm39) |
I442K |
probably damaging |
Het |
Pygl |
T |
A |
12: 70,254,442 (GRCm39) |
|
probably null |
Het |
Rassf2 |
C |
A |
2: 131,846,307 (GRCm39) |
R150L |
probably benign |
Het |
Rdh7 |
A |
T |
10: 127,723,487 (GRCm39) |
W123R |
probably damaging |
Het |
Saal1 |
T |
C |
7: 46,339,223 (GRCm39) |
|
probably null |
Het |
Sall1 |
T |
C |
8: 89,757,383 (GRCm39) |
D907G |
probably damaging |
Het |
Spag1 |
T |
A |
15: 36,234,964 (GRCm39) |
F876I |
probably damaging |
Het |
Syncrip |
G |
A |
9: 88,361,932 (GRCm39) |
A61V |
probably damaging |
Het |
Trbv3 |
A |
T |
6: 41,025,576 (GRCm39) |
K55N |
probably benign |
Het |
Vmn1r178 |
A |
G |
7: 23,593,871 (GRCm39) |
|
probably null |
Het |
Vmn2r84 |
T |
C |
10: 130,229,995 (GRCm39) |
D39G |
possibly damaging |
Het |
|
Other mutations in Gm3248 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:Gm3248
|
APN |
14 |
5,943,928 (GRCm38) |
missense |
probably benign |
0.14 |
IGL02302:Gm3248
|
APN |
14 |
5,943,011 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02817:Gm3248
|
APN |
14 |
5,945,825 (GRCm38) |
missense |
probably benign |
0.01 |
R3691:Gm3248
|
UTSW |
14 |
5,943,068 (GRCm38) |
missense |
probably damaging |
0.96 |
R4790:Gm3248
|
UTSW |
14 |
5,945,831 (GRCm38) |
missense |
probably damaging |
0.99 |
R7394:Gm3248
|
UTSW |
14 |
5,945,781 (GRCm38) |
critical splice donor site |
probably null |
|
R7806:Gm3248
|
UTSW |
14 |
5,943,883 (GRCm38) |
missense |
probably benign |
|
R8779:Gm3248
|
UTSW |
14 |
5,943,869 (GRCm38) |
missense |
probably benign |
0.19 |
R9670:Gm3248
|
UTSW |
14 |
5,944,993 (GRCm38) |
missense |
probably benign |
0.06 |
|