Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
T |
A |
8: 24,667,623 |
I104F |
probably benign |
Het |
Adgrg7 |
C |
T |
16: 56,770,311 |
V166I |
probably benign |
Het |
Agfg1 |
G |
T |
1: 82,882,245 |
V278L |
probably benign |
Het |
Alpk3 |
A |
G |
7: 81,092,580 |
E715G |
possibly damaging |
Het |
Ap2m1 |
A |
G |
16: 20,543,345 |
Y401C |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 97,965,452 |
S838N |
probably benign |
Het |
Ash2l |
A |
T |
8: 25,827,205 |
Y373* |
probably null |
Het |
Best2 |
C |
T |
8: 85,007,764 |
V442I |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,425,542 |
|
probably null |
Het |
Fat2 |
T |
A |
11: 55,285,030 |
D1619V |
probably damaging |
Het |
Fer1l6 |
A |
T |
15: 58,627,597 |
N1272I |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,417,996 |
*779C |
probably null |
Het |
Gm12216 |
G |
A |
11: 53,859,251 |
|
probably benign |
Het |
Gm17657 |
C |
A |
17: 29,519,373 |
V140L |
probably benign |
Het |
Gm7102 |
A |
G |
19: 61,175,535 |
V154A |
possibly damaging |
Het |
Grm2 |
C |
T |
9: 106,647,171 |
V311I |
|
Het |
Immt |
T |
A |
6: 71,874,705 |
D683E |
probably benign |
Het |
Itga8 |
T |
G |
2: 12,232,901 |
D336A |
probably damaging |
Het |
Jhy |
T |
C |
9: 40,961,157 |
T19A |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 181,135,092 |
M1V |
probably null |
Het |
Kctd17 |
A |
T |
15: 78,433,014 |
I117F |
probably damaging |
Het |
Lrp6 |
T |
C |
6: 134,507,401 |
T420A |
probably damaging |
Het |
Manba |
T |
C |
3: 135,517,912 |
S187P |
probably damaging |
Het |
Mef2b |
A |
T |
8: 70,164,288 |
D13V |
probably damaging |
Het |
Mical2 |
T |
C |
7: 112,303,756 |
F145L |
probably damaging |
Het |
Mphosph8 |
T |
A |
14: 56,685,040 |
D551E |
possibly damaging |
Het |
Myo10 |
C |
G |
15: 25,782,981 |
R1170G |
probably damaging |
Het |
Myo16 |
A |
C |
8: 10,272,687 |
Q39P |
unknown |
Het |
Myo1f |
A |
G |
17: 33,601,694 |
E837G |
probably benign |
Het |
Nell2 |
T |
A |
15: 95,435,393 |
I128F |
possibly damaging |
Het |
Olfr1357 |
A |
G |
10: 78,612,614 |
V9A |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,379,390 |
R659* |
probably null |
Het |
Pcdhga1 |
A |
G |
18: 37,839,975 |
Q881R |
possibly damaging |
Het |
Plekhm2 |
T |
G |
4: 141,642,459 |
E75A |
possibly damaging |
Het |
Prc1 |
A |
G |
7: 80,307,657 |
K357E |
possibly damaging |
Het |
Pxk |
T |
A |
14: 8,146,220 |
C377S |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,334,568 |
E1696G |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 123,001,367 |
S1532R |
unknown |
Het |
Scn5a |
G |
T |
9: 119,562,560 |
A22E |
probably benign |
Het |
Sctr |
G |
A |
1: 120,022,225 |
R48Q |
probably benign |
Het |
Siae |
T |
C |
9: 37,623,013 |
V115A |
probably damaging |
Het |
Slc16a6 |
A |
G |
11: 109,453,281 |
C563R |
probably benign |
Het |
Sntg1 |
A |
C |
1: 8,682,019 |
V58G |
possibly damaging |
Het |
Snx11 |
C |
T |
11: 96,773,159 |
V36M |
probably damaging |
Het |
Stk3 |
C |
A |
15: 34,959,036 |
S330I |
probably benign |
Het |
Synpo |
A |
G |
18: 60,629,559 |
F92S |
probably benign |
Het |
Tle1 |
A |
G |
4: 72,139,687 |
|
probably null |
Het |
Tmem117 |
A |
G |
15: 94,931,803 |
D173G |
possibly damaging |
Het |
Tmprss5 |
T |
C |
9: 49,114,541 |
W338R |
probably benign |
Het |
Tnfrsf19 |
T |
C |
14: 60,974,698 |
T168A |
possibly damaging |
Het |
Trhde |
C |
T |
10: 114,800,871 |
G144S |
possibly damaging |
Het |
Trim56 |
G |
T |
5: 137,114,243 |
Q140K |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,732,574 |
V28679M |
probably damaging |
Het |
Ubxn8 |
G |
A |
8: 33,623,203 |
R208C |
probably damaging |
Het |
Wdr38 |
T |
A |
2: 39,000,264 |
W137R |
probably damaging |
Het |
Zdhhc6 |
G |
T |
19: 55,304,500 |
N271K |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,718,547 |
S446P |
possibly damaging |
Het |
Zmynd8 |
T |
C |
2: 165,807,572 |
Q867R |
possibly damaging |
Het |
Zswim3 |
T |
C |
2: 164,820,482 |
I294T |
probably benign |
Het |
|