Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
A |
G |
9: 8,222,122 |
|
noncoding transcript |
Het |
AI182371 |
T |
C |
2: 35,085,206 |
N337S |
probably benign |
Het |
Aldh3b1 |
C |
T |
19: 3,914,024 |
R426H |
probably damaging |
Het |
Arap2 |
A |
G |
5: 62,706,659 |
F541L |
probably damaging |
Het |
Asap2 |
G |
T |
12: 21,213,185 |
R267L |
possibly damaging |
Het |
Ass1 |
A |
T |
2: 31,514,819 |
N371Y |
probably damaging |
Het |
Bmp8b |
T |
A |
4: 123,121,899 |
D226E |
probably benign |
Het |
C1ra |
T |
A |
6: 124,517,444 |
D283E |
possibly damaging |
Het |
Cacul1 |
G |
T |
19: 60,543,026 |
H268Q |
probably damaging |
Het |
Cd9 |
T |
C |
6: 125,472,433 |
N49D |
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 180,040,179 |
H193R |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,551,455 |
G1935E |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,914,723 |
I1362N |
probably damaging |
Het |
Chchd7 |
A |
T |
4: 3,943,416 |
N61I |
possibly damaging |
Het |
Clca1 |
A |
T |
3: 145,027,345 |
L134Q |
probably damaging |
Het |
Clec2j |
T |
C |
6: 128,656,602 |
|
noncoding transcript |
Het |
Clvs1 |
G |
A |
4: 9,281,801 |
A82T |
probably damaging |
Het |
Csn1s1 |
A |
T |
5: 87,677,627 |
Y231F |
possibly damaging |
Het |
Cyp2c55 |
A |
T |
19: 39,031,379 |
T254S |
probably benign |
Het |
D430042O09Rik |
A |
G |
7: 125,872,967 |
N1548S |
probably damaging |
Het |
Decr1 |
A |
G |
4: 15,919,849 |
S290P |
probably damaging |
Het |
Dnaic2 |
T |
A |
11: 114,745,189 |
|
probably benign |
Het |
Dock4 |
C |
A |
12: 40,838,438 |
|
probably benign |
Het |
Dst |
T |
C |
1: 34,266,960 |
|
probably null |
Het |
Elmo2 |
A |
G |
2: 165,298,330 |
I315T |
probably damaging |
Het |
Fam208b |
A |
G |
13: 3,588,364 |
S456P |
possibly damaging |
Het |
Fcho2 |
A |
G |
13: 98,748,267 |
F431L |
probably benign |
Het |
Fez2 |
A |
G |
17: 78,384,832 |
|
probably benign |
Het |
Gas2l3 |
C |
T |
10: 89,426,477 |
A128T |
probably damaging |
Het |
Hpse2 |
T |
C |
19: 43,013,163 |
I222M |
probably damaging |
Het |
Kcna2 |
A |
G |
3: 107,105,516 |
D471G |
probably benign |
Het |
Kcnj13 |
T |
A |
1: 87,386,846 |
Y218F |
probably benign |
Het |
Kif1a |
T |
C |
1: 93,018,997 |
H1763R |
probably damaging |
Het |
Krt2 |
C |
T |
15: 101,813,253 |
R451H |
probably damaging |
Het |
Lama2 |
A |
G |
10: 26,990,867 |
V2877A |
probably damaging |
Het |
Lrrc2 |
A |
T |
9: 110,962,617 |
M80L |
probably benign |
Het |
Naip6 |
A |
G |
13: 100,302,260 |
V343A |
probably benign |
Het |
Nedd4l |
T |
C |
18: 65,208,461 |
Y753H |
probably damaging |
Het |
Nif3l1 |
A |
C |
1: 58,447,828 |
S58R |
probably damaging |
Het |
Olfr1153 |
T |
A |
2: 87,896,493 |
V98E |
possibly damaging |
Het |
Olfr573-ps1 |
A |
T |
7: 102,942,051 |
C175* |
probably null |
Het |
Olfr823 |
G |
A |
10: 130,112,580 |
S70F |
probably damaging |
Het |
Osbpl11 |
C |
A |
16: 33,234,444 |
Y632* |
probably null |
Het |
Pask |
A |
T |
1: 93,320,917 |
D920E |
probably benign |
Het |
Pclo |
T |
C |
5: 14,681,594 |
V3370A |
unknown |
Het |
Ptpn21 |
G |
A |
12: 98,704,240 |
|
probably benign |
Het |
Rph3al |
T |
C |
11: 75,908,969 |
I55V |
probably benign |
Het |
Rsad2 |
T |
G |
12: 26,454,168 |
I121L |
possibly damaging |
Het |
Sergef |
T |
G |
7: 46,633,746 |
|
probably benign |
Het |
Sp110 |
C |
T |
1: 85,589,120 |
E219K |
possibly damaging |
Het |
Tas2r104 |
T |
C |
6: 131,685,471 |
I92V |
probably benign |
Het |
Tbc1d23 |
T |
A |
16: 57,173,106 |
I566F |
possibly damaging |
Het |
Tbc1d9b |
A |
G |
11: 50,168,228 |
|
probably null |
Het |
Tie1 |
T |
A |
4: 118,476,147 |
I841L |
possibly damaging |
Het |
Tpo |
A |
G |
12: 30,100,486 |
V465A |
probably benign |
Het |
Ttll3 |
A |
T |
6: 113,409,339 |
Q711L |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,953,041 |
R869H |
probably benign |
Het |
Uggt2 |
A |
G |
14: 119,095,336 |
V62A |
probably damaging |
Het |
Vmn1r17 |
C |
A |
6: 57,361,319 |
M20I |
probably benign |
Het |
Vmn1r71 |
G |
C |
7: 10,748,092 |
S223C |
possibly damaging |
Het |
Vmn2r120 |
C |
T |
17: 57,524,518 |
V424I |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,417,633 |
|
probably null |
Het |
Wdfy3 |
C |
A |
5: 101,957,443 |
A173S |
probably benign |
Het |
Wdr59 |
T |
C |
8: 111,486,997 |
|
probably null |
Het |
Ythdc2 |
A |
T |
18: 44,864,357 |
M994L |
probably benign |
Het |
Zfp808 |
T |
A |
13: 62,172,306 |
F450I |
probably damaging |
Het |
|