Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
T |
A |
2: 152,282,790 (GRCm39) |
V215D |
probably damaging |
Het |
Ablim1 |
A |
G |
19: 57,119,284 (GRCm39) |
S267P |
probably benign |
Het |
Adcy2 |
C |
T |
13: 68,768,945 (GRCm39) |
C1061Y |
probably damaging |
Het |
Aip |
C |
A |
19: 4,165,149 (GRCm39) |
C240F |
probably damaging |
Het |
Aldh1a2 |
A |
T |
9: 71,160,268 (GRCm39) |
D98V |
probably damaging |
Het |
Arhgef40 |
T |
C |
14: 52,228,419 (GRCm39) |
|
probably benign |
Het |
Cplx2 |
G |
T |
13: 54,526,736 (GRCm39) |
R48L |
probably damaging |
Het |
Ctrl |
C |
T |
8: 106,659,451 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
A |
G |
7: 105,353,006 (GRCm39) |
T2720A |
probably benign |
Het |
Fzd1 |
A |
G |
5: 4,805,696 (GRCm39) |
Y629H |
probably damaging |
Het |
Gins1 |
T |
C |
2: 150,770,038 (GRCm39) |
|
probably null |
Het |
Gpr149 |
C |
T |
3: 62,437,995 (GRCm39) |
A721T |
probably damaging |
Het |
Helb |
A |
T |
10: 119,920,835 (GRCm39) |
M1036K |
probably benign |
Het |
Il16 |
A |
G |
7: 83,337,335 (GRCm39) |
F127L |
probably benign |
Het |
Kctd20 |
A |
T |
17: 29,180,640 (GRCm39) |
H138L |
probably damaging |
Het |
Kctd9 |
T |
A |
14: 67,962,122 (GRCm39) |
L55* |
probably null |
Het |
Marf1 |
C |
T |
16: 13,950,611 (GRCm39) |
R925H |
probably benign |
Het |
Mbip |
A |
T |
12: 56,389,191 (GRCm39) |
|
probably benign |
Het |
Myo1c |
C |
T |
11: 75,562,461 (GRCm39) |
P918S |
probably benign |
Het |
Nod1 |
T |
G |
6: 54,925,014 (GRCm39) |
D99A |
probably damaging |
Het |
Olfm4 |
A |
G |
14: 80,259,107 (GRCm39) |
K419E |
probably damaging |
Het |
Or6c214 |
A |
T |
10: 129,591,232 (GRCm39) |
L29Q |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,521,845 (GRCm39) |
D137G |
probably benign |
Het |
Prdm4 |
T |
C |
10: 85,743,682 (GRCm39) |
E191G |
probably benign |
Het |
Rundc3b |
A |
T |
5: 8,629,071 (GRCm39) |
I110N |
probably damaging |
Het |
Sgsm3 |
C |
T |
15: 80,893,901 (GRCm39) |
R479C |
probably damaging |
Het |
Tmc7 |
A |
T |
7: 118,144,834 (GRCm39) |
Y575* |
probably null |
Het |
Trim33 |
T |
C |
3: 103,244,830 (GRCm39) |
L310S |
probably damaging |
Het |
Trpm2 |
C |
T |
10: 77,773,660 (GRCm39) |
R585Q |
probably benign |
Het |
Ttn |
T |
C |
2: 76,565,740 (GRCm39) |
E28204G |
probably damaging |
Het |
Vmn1r233 |
A |
T |
17: 21,214,002 (GRCm39) |
L316Q |
probably damaging |
Het |
Vmn2r110 |
A |
T |
17: 20,803,779 (GRCm39) |
N265K |
possibly damaging |
Het |
Xylb |
A |
G |
9: 119,196,559 (GRCm39) |
H114R |
probably damaging |
Het |
Ywhaz |
T |
C |
15: 36,791,166 (GRCm39) |
Y19C |
probably damaging |
Het |
|
Other mutations in Rassf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0905:Rassf10
|
UTSW |
7 |
112,554,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2903:Rassf10
|
UTSW |
7 |
112,553,756 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2904:Rassf10
|
UTSW |
7 |
112,553,756 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4559:Rassf10
|
UTSW |
7 |
112,554,338 (GRCm39) |
missense |
probably benign |
|
R4796:Rassf10
|
UTSW |
7 |
112,553,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R5063:Rassf10
|
UTSW |
7 |
112,553,631 (GRCm39) |
missense |
probably benign |
|
R5166:Rassf10
|
UTSW |
7 |
112,553,627 (GRCm39) |
missense |
probably benign |
0.00 |
R6478:Rassf10
|
UTSW |
7 |
112,554,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6769:Rassf10
|
UTSW |
7 |
112,553,635 (GRCm39) |
missense |
probably benign |
|
R6771:Rassf10
|
UTSW |
7 |
112,553,635 (GRCm39) |
missense |
probably benign |
|
R7161:Rassf10
|
UTSW |
7 |
112,553,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Rassf10
|
UTSW |
7 |
112,554,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R8787:Rassf10
|
UTSW |
7 |
112,554,738 (GRCm39) |
missense |
probably benign |
0.00 |
R9064:Rassf10
|
UTSW |
7 |
112,554,315 (GRCm39) |
missense |
probably benign |
0.08 |
R9652:Rassf10
|
UTSW |
7 |
112,554,784 (GRCm39) |
missense |
probably benign |
|
Z1177:Rassf10
|
UTSW |
7 |
112,554,364 (GRCm39) |
missense |
probably damaging |
0.99 |
|