Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
C |
1: 159,902,994 (GRCm39) |
L88P |
probably damaging |
Het |
Adamtsl4 |
G |
A |
3: 95,590,684 (GRCm39) |
Q354* |
probably null |
Het |
Aox3 |
A |
C |
1: 58,222,645 (GRCm39) |
D1146A |
probably damaging |
Het |
Ap2a1 |
T |
A |
7: 44,555,850 (GRCm39) |
H340L |
probably damaging |
Het |
Ccni |
G |
T |
5: 93,335,636 (GRCm39) |
F167L |
probably benign |
Het |
Ctcf |
A |
G |
8: 106,391,013 (GRCm39) |
T207A |
probably benign |
Het |
D930020B18Rik |
A |
G |
10: 121,525,838 (GRCm39) |
H580R |
possibly damaging |
Het |
Dnaaf6rt |
A |
G |
1: 31,262,177 (GRCm39) |
D53G |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,939,271 (GRCm39) |
L159Q |
probably damaging |
Het |
Dync1i2 |
T |
C |
2: 71,093,095 (GRCm39) |
I630T |
possibly damaging |
Het |
Fchsd2 |
A |
G |
7: 100,847,715 (GRCm39) |
T202A |
probably benign |
Het |
Gdi2 |
A |
G |
13: 3,607,009 (GRCm39) |
Y214C |
probably damaging |
Het |
Gna14 |
T |
A |
19: 16,511,090 (GRCm39) |
S46R |
probably damaging |
Het |
Hfm1 |
A |
G |
5: 107,043,153 (GRCm39) |
I627T |
probably damaging |
Het |
Ighv1-19 |
G |
A |
12: 114,672,359 (GRCm39) |
A87V |
probably damaging |
Het |
Itch |
G |
A |
2: 155,014,506 (GRCm39) |
|
probably null |
Het |
Klrb1b |
T |
C |
6: 128,797,272 (GRCm39) |
Q72R |
possibly damaging |
Het |
Lrpprc |
A |
G |
17: 85,082,853 (GRCm39) |
F144L |
probably benign |
Het |
Lrrc7 |
A |
G |
3: 157,891,011 (GRCm39) |
|
probably benign |
Het |
Ndufa11 |
T |
A |
17: 57,028,338 (GRCm39) |
F72L |
probably damaging |
Het |
Neu1 |
T |
A |
17: 35,150,477 (GRCm39) |
V32E |
probably benign |
Het |
Or5k17 |
T |
A |
16: 58,746,833 (GRCm39) |
I34F |
possibly damaging |
Het |
Osmr |
T |
C |
15: 6,853,060 (GRCm39) |
K611E |
probably damaging |
Het |
Pcdh20 |
A |
G |
14: 88,706,280 (GRCm39) |
V340A |
possibly damaging |
Het |
Plxna2 |
T |
A |
1: 194,468,998 (GRCm39) |
|
probably benign |
Het |
Pou6f1 |
C |
T |
15: 100,481,306 (GRCm39) |
W210* |
probably null |
Het |
Ppat |
A |
G |
5: 77,063,079 (GRCm39) |
Y511H |
probably damaging |
Het |
Psme4 |
T |
G |
11: 30,791,586 (GRCm39) |
V1147G |
possibly damaging |
Het |
Scap |
C |
T |
9: 110,207,758 (GRCm39) |
T489I |
probably benign |
Het |
Sptb |
A |
G |
12: 76,654,754 (GRCm39) |
|
probably null |
Het |
Tcl1b5 |
T |
A |
12: 105,146,296 (GRCm39) |
|
probably benign |
Het |
Trim54 |
T |
A |
5: 31,289,509 (GRCm39) |
|
probably benign |
Het |
Unc13c |
C |
T |
9: 73,388,357 (GRCm39) |
R2143Q |
probably damaging |
Het |
Vmn2r66 |
A |
T |
7: 84,655,798 (GRCm39) |
M406K |
possibly damaging |
Het |
|
Other mutations in Vmn1r56 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02102:Vmn1r56
|
APN |
7 |
5,199,335 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02173:Vmn1r56
|
APN |
7 |
5,199,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Vmn1r56
|
UTSW |
7 |
5,199,372 (GRCm39) |
missense |
probably benign |
0.17 |
R0599:Vmn1r56
|
UTSW |
7 |
5,199,429 (GRCm39) |
missense |
probably benign |
|
R2110:Vmn1r56
|
UTSW |
7 |
5,199,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R3019:Vmn1r56
|
UTSW |
7 |
5,199,061 (GRCm39) |
missense |
probably benign |
|
R4883:Vmn1r56
|
UTSW |
7 |
5,199,443 (GRCm39) |
missense |
probably damaging |
0.98 |
R5655:Vmn1r56
|
UTSW |
7 |
5,198,700 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5728:Vmn1r56
|
UTSW |
7 |
5,199,122 (GRCm39) |
missense |
probably benign |
0.42 |
R6083:Vmn1r56
|
UTSW |
7 |
5,199,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:Vmn1r56
|
UTSW |
7 |
5,199,575 (GRCm39) |
missense |
probably benign |
0.02 |
R6786:Vmn1r56
|
UTSW |
7 |
5,198,961 (GRCm39) |
missense |
probably benign |
0.00 |
R7031:Vmn1r56
|
UTSW |
7 |
5,199,261 (GRCm39) |
nonsense |
probably null |
|
R7584:Vmn1r56
|
UTSW |
7 |
5,198,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Vmn1r56
|
UTSW |
7 |
5,199,516 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8472:Vmn1r56
|
UTSW |
7 |
5,198,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Vmn1r56
|
UTSW |
7 |
5,198,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R8813:Vmn1r56
|
UTSW |
7 |
5,198,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Vmn1r56
|
UTSW |
7 |
5,199,389 (GRCm39) |
missense |
probably damaging |
0.99 |
|