Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
T |
C |
13: 81,559,195 |
|
probably null |
Het |
Bmi1 |
T |
A |
2: 18,684,458 |
S318T |
probably benign |
Het |
Cntnap5c |
G |
A |
17: 58,034,853 |
V180I |
probably benign |
Het |
Cyp2b10 |
A |
G |
7: 25,913,937 |
E186G |
probably damaging |
Het |
Ddx25 |
G |
T |
9: 35,554,412 |
|
probably benign |
Het |
Dis3 |
A |
G |
14: 99,078,354 |
F901L |
probably benign |
Het |
Dnah7a |
T |
A |
1: 53,472,893 |
N3003I |
possibly damaging |
Het |
Ebf2 |
A |
G |
14: 67,238,953 |
D124G |
probably damaging |
Het |
Efcab5 |
A |
T |
11: 77,104,313 |
I1144N |
probably damaging |
Het |
Exoc4 |
G |
A |
6: 33,580,026 |
V489I |
possibly damaging |
Het |
Garem1 |
A |
G |
18: 21,148,450 |
V283A |
probably damaging |
Het |
Gfra2 |
G |
A |
14: 70,925,907 |
R210H |
possibly damaging |
Het |
Gli3 |
T |
C |
13: 15,726,786 |
|
probably benign |
Het |
Gm7247 |
A |
T |
14: 51,521,884 |
M107L |
probably benign |
Het |
Mki67 |
C |
T |
7: 135,698,632 |
D1558N |
probably damaging |
Het |
Mylk4 |
A |
G |
13: 32,729,066 |
|
probably benign |
Het |
Olfr1 |
A |
G |
11: 73,395,365 |
V219A |
probably benign |
Het |
Olfr112 |
G |
T |
17: 37,563,580 |
H244N |
possibly damaging |
Het |
Olfr2 |
A |
T |
7: 107,001,423 |
C146S |
probably damaging |
Het |
Olfr669 |
A |
G |
7: 104,939,369 |
N281S |
possibly damaging |
Het |
Plcd1 |
T |
C |
9: 119,084,641 |
T50A |
probably damaging |
Het |
Rasgrp3 |
A |
G |
17: 75,516,373 |
R480G |
probably benign |
Het |
Ripor3 |
T |
C |
2: 167,993,496 |
E185G |
probably damaging |
Het |
S1pr3 |
T |
C |
13: 51,419,056 |
I91T |
probably benign |
Het |
Slc26a4 |
C |
T |
12: 31,528,854 |
|
probably benign |
Het |
Slc28a3 |
T |
C |
13: 58,580,584 |
T104A |
probably benign |
Het |
Slc6a11 |
A |
G |
6: 114,238,396 |
D419G |
probably damaging |
Het |
St3gal2 |
A |
G |
8: 110,957,766 |
I19V |
probably benign |
Het |
Sycp1 |
C |
A |
3: 102,895,943 |
C517F |
probably benign |
Het |
Trav15-1-dv6-1 |
G |
A |
14: 53,559,998 |
E35K |
possibly damaging |
Het |
Vmn1r121 |
T |
C |
7: 21,098,476 |
E13G |
probably damaging |
Het |
Vmn1r199 |
T |
A |
13: 22,383,006 |
S114T |
probably damaging |
Het |
Vmn2r-ps159 |
T |
C |
4: 156,334,655 |
|
noncoding transcript |
Het |
|