Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt1 |
T |
C |
12: 112,657,084 |
E314G |
probably damaging |
Het |
Amtn |
C |
A |
5: 88,381,622 |
Q106K |
probably benign |
Het |
Birc6 |
T |
C |
17: 74,609,189 |
F1700S |
probably damaging |
Het |
Brdt |
T |
C |
5: 107,377,995 |
S905P |
possibly damaging |
Het |
Ccdc68 |
C |
T |
18: 69,947,165 |
Q194* |
probably null |
Het |
Cdc27 |
A |
G |
11: 104,526,981 |
|
probably benign |
Het |
Cdh13 |
A |
G |
8: 118,675,158 |
T100A |
probably benign |
Het |
Cdsn |
A |
G |
17: 35,555,894 |
H440R |
possibly damaging |
Het |
Cenpf |
C |
A |
1: 189,658,030 |
D1202Y |
probably damaging |
Het |
Chat |
C |
A |
14: 32,458,613 |
V21L |
probably benign |
Het |
Clca4c-ps |
T |
A |
3: 144,879,732 |
|
noncoding transcript |
Het |
Cst9 |
A |
G |
2: 148,835,283 |
I25V |
probably benign |
Het |
Dennd1b |
C |
A |
1: 139,168,967 |
|
probably benign |
Het |
Dpp3 |
T |
G |
19: 4,923,131 |
Q145P |
probably benign |
Het |
Elovl5 |
C |
T |
9: 77,981,502 |
T217M |
probably damaging |
Het |
Etl4 |
T |
C |
2: 20,808,029 |
V906A |
possibly damaging |
Het |
Gm10647 |
C |
T |
9: 66,798,261 |
|
probably benign |
Het |
Gm6614 |
C |
T |
6: 142,003,471 |
G60R |
probably damaging |
Het |
Grm5 |
A |
G |
7: 88,074,710 |
N736S |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,767,640 |
S1638P |
possibly damaging |
Het |
Hsd3b2 |
T |
G |
3: 98,716,424 |
E46A |
possibly damaging |
Het |
Igkv15-103 |
A |
G |
6: 68,437,690 |
T38A |
probably benign |
Het |
Itpr2 |
C |
A |
6: 146,385,979 |
V450L |
probably damaging |
Het |
Kbtbd12 |
T |
C |
6: 88,618,329 |
H173R |
probably benign |
Het |
Man1a |
G |
A |
10: 53,919,244 |
R638W |
probably damaging |
Het |
Mterf2 |
A |
T |
10: 85,120,014 |
S249T |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,648,361 |
D700G |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,348,916 |
H764R |
possibly damaging |
Het |
Myh7b |
A |
G |
2: 155,628,827 |
D1065G |
probably damaging |
Het |
Naip1 |
C |
A |
13: 100,433,262 |
W288L |
probably damaging |
Het |
Naip6 |
C |
A |
13: 100,300,660 |
A452S |
probably benign |
Het |
Nop2 |
A |
C |
6: 125,144,085 |
K610T |
possibly damaging |
Het |
Nop2 |
G |
T |
6: 125,144,070 |
G605V |
probably benign |
Het |
Npvf |
G |
A |
6: 50,652,690 |
R107W |
probably benign |
Het |
Olfr63 |
T |
A |
17: 33,269,354 |
I210K |
probably benign |
Het |
Olfr90 |
T |
C |
17: 37,086,156 |
|
probably null |
Het |
Os9 |
G |
A |
10: 127,099,393 |
|
probably benign |
Het |
Parp4 |
T |
C |
14: 56,648,869 |
S1802P |
unknown |
Het |
Piezo2 |
G |
A |
18: 63,020,633 |
S2547F |
probably benign |
Het |
Plekha7 |
G |
T |
7: 116,135,178 |
A1024E |
probably damaging |
Het |
R3hdm1 |
T |
C |
1: 128,174,940 |
|
probably benign |
Het |
Robo4 |
T |
C |
9: 37,413,382 |
S1022P |
probably damaging |
Het |
Sc5d |
T |
C |
9: 42,255,394 |
N283S |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,671,608 |
V202M |
probably damaging |
Het |
Spag16 |
T |
C |
1: 70,264,908 |
I366T |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,426,833 |
R222C |
possibly damaging |
Het |
Tlr9 |
C |
T |
9: 106,224,730 |
Q407* |
probably null |
Het |
Trappc12 |
G |
A |
12: 28,691,406 |
S768L |
probably damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,383,051 |
L63Q |
probably damaging |
Het |
Zfy2 |
C |
T |
Y: 2,106,894 |
G580D |
probably benign |
Het |
Zfy2 |
T |
A |
Y: 2,117,188 |
H213L |
probably benign |
Het |
|