Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,248,740 (GRCm39) |
V2829A |
probably benign |
Het |
Adk |
G |
T |
14: 21,142,496 (GRCm39) |
D26Y |
probably damaging |
Het |
Bpifb9a |
T |
C |
2: 154,106,145 (GRCm39) |
|
probably benign |
Het |
Dap |
G |
A |
15: 31,272,526 (GRCm39) |
|
probably benign |
Het |
Eqtn |
A |
T |
4: 94,795,892 (GRCm39) |
S270T |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,619,487 (GRCm39) |
D764G |
probably damaging |
Het |
Fbxl6 |
A |
T |
15: 76,421,283 (GRCm39) |
|
probably null |
Het |
Gtf3c1 |
A |
T |
7: 125,268,014 (GRCm39) |
|
probably benign |
Het |
H2-D1 |
G |
C |
17: 35,482,837 (GRCm39) |
M122I |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Map1s |
C |
A |
8: 71,366,832 (GRCm39) |
P579Q |
probably damaging |
Het |
Mapk10 |
A |
G |
5: 103,135,146 (GRCm39) |
|
probably benign |
Het |
Mllt6 |
C |
G |
11: 97,555,824 (GRCm39) |
C51W |
probably damaging |
Het |
Mzf1 |
C |
A |
7: 12,786,698 (GRCm39) |
R124L |
possibly damaging |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Neurod2 |
G |
T |
11: 98,218,147 (GRCm39) |
T339K |
probably benign |
Het |
Nfya |
G |
A |
17: 48,702,815 (GRCm39) |
Q29* |
probably null |
Het |
Nipbl |
A |
T |
15: 8,391,202 (GRCm39) |
D257E |
probably benign |
Het |
Pate5 |
T |
C |
9: 35,750,366 (GRCm39) |
D102G |
probably damaging |
Het |
Pex5 |
G |
A |
6: 124,376,896 (GRCm39) |
|
probably benign |
Het |
Pramel47 |
A |
C |
5: 95,489,186 (GRCm39) |
T210P |
probably damaging |
Het |
Prx |
T |
A |
7: 27,217,719 (GRCm39) |
F879Y |
probably damaging |
Het |
Resf1 |
G |
A |
6: 149,229,767 (GRCm39) |
A938T |
probably damaging |
Het |
Scai |
G |
A |
2: 38,965,164 (GRCm39) |
T560M |
possibly damaging |
Het |
Slfn10-ps |
T |
C |
11: 82,926,235 (GRCm39) |
|
noncoding transcript |
Het |
Spdye4b |
A |
G |
5: 143,181,423 (GRCm39) |
|
probably benign |
Het |
Ss18l1 |
A |
G |
2: 179,701,147 (GRCm39) |
Y287C |
probably damaging |
Het |
Tpbg |
C |
A |
9: 85,726,617 (GRCm39) |
F195L |
unknown |
Het |
Trbv16 |
T |
C |
6: 41,128,781 (GRCm39) |
|
probably benign |
Het |
Unc5c |
A |
G |
3: 141,509,601 (GRCm39) |
T620A |
probably benign |
Het |
Vangl1 |
A |
G |
3: 102,091,310 (GRCm39) |
S259P |
probably damaging |
Het |
Vmn1r52 |
T |
A |
6: 90,156,446 (GRCm39) |
M71K |
probably damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,719,094 (GRCm39) |
I816F |
probably damaging |
Het |
Zfp268 |
T |
C |
4: 145,348,745 (GRCm39) |
Y61H |
possibly damaging |
Het |
|
Other mutations in 1700011L22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02969:1700011L22Rik
|
APN |
8 |
79,946,866 (GRCm39) |
splice site |
probably benign |
|
IGL03344:1700011L22Rik
|
APN |
8 |
79,975,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:1700011L22Rik
|
UTSW |
8 |
79,937,284 (GRCm39) |
nonsense |
probably null |
|
R0331:1700011L22Rik
|
UTSW |
8 |
79,956,021 (GRCm39) |
missense |
probably benign |
0.08 |
R3801:1700011L22Rik
|
UTSW |
8 |
79,974,922 (GRCm39) |
missense |
probably benign |
0.06 |
R3804:1700011L22Rik
|
UTSW |
8 |
79,974,922 (GRCm39) |
missense |
probably benign |
0.06 |
R4606:1700011L22Rik
|
UTSW |
8 |
79,937,374 (GRCm39) |
missense |
probably benign |
0.00 |
R6045:1700011L22Rik
|
UTSW |
8 |
79,955,996 (GRCm39) |
missense |
probably benign |
0.00 |
R6993:1700011L22Rik
|
UTSW |
8 |
79,975,053 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7249:1700011L22Rik
|
UTSW |
8 |
79,974,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7442:1700011L22Rik
|
UTSW |
8 |
79,946,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:1700011L22Rik
|
UTSW |
8 |
79,937,380 (GRCm39) |
nonsense |
probably null |
|
Z1177:1700011L22Rik
|
UTSW |
8 |
79,974,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|