Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
T |
C |
19: 55,268,924 (GRCm39) |
V195A |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,452,466 (GRCm39) |
M211V |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,994,098 (GRCm39) |
M5127I |
probably benign |
Het |
Akr1c13 |
T |
C |
13: 4,244,111 (GRCm39) |
Y55H |
probably damaging |
Het |
Ap3d1 |
A |
T |
10: 80,544,313 (GRCm39) |
H1161Q |
probably benign |
Het |
Armh3 |
A |
T |
19: 45,922,307 (GRCm39) |
|
probably null |
Het |
Atp2b2 |
C |
T |
6: 113,750,349 (GRCm39) |
R625H |
probably damaging |
Het |
Bdnf |
G |
A |
2: 109,554,463 (GRCm39) |
C239Y |
probably damaging |
Het |
Bpifa5 |
G |
T |
2: 154,007,539 (GRCm39) |
|
probably null |
Het |
C9 |
T |
A |
15: 6,516,243 (GRCm39) |
F349I |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,927,975 (GRCm39) |
V1170A |
possibly damaging |
Het |
Celsr1 |
A |
G |
15: 85,815,477 (GRCm39) |
V1846A |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,190,652 (GRCm39) |
L120H |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,045,291 (GRCm39) |
I781K |
possibly damaging |
Het |
Cpne1 |
G |
T |
2: 155,919,339 (GRCm39) |
Q343K |
probably benign |
Het |
Dlc1 |
A |
T |
8: 37,405,702 (GRCm39) |
I29K |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,786,827 (GRCm39) |
D3602G |
possibly damaging |
Het |
Dock1 |
A |
G |
7: 134,475,879 (GRCm39) |
S885G |
probably benign |
Het |
Evpl |
T |
A |
11: 116,118,549 (GRCm39) |
Q686L |
probably damaging |
Het |
Fmo6 |
C |
T |
1: 162,748,132 (GRCm39) |
A311T |
probably damaging |
Het |
Gli1 |
A |
T |
10: 127,168,446 (GRCm39) |
M469K |
probably damaging |
Het |
Grin2c |
G |
A |
11: 115,141,472 (GRCm39) |
P882L |
probably damaging |
Het |
H2-Ob |
C |
T |
17: 34,461,588 (GRCm39) |
T109I |
probably damaging |
Het |
Jpt2 |
C |
A |
17: 25,167,647 (GRCm39) |
A101S |
probably benign |
Het |
Krt1c |
A |
G |
15: 101,724,932 (GRCm39) |
V226A |
probably damaging |
Het |
Lamc1 |
T |
C |
1: 153,110,358 (GRCm39) |
S1106G |
probably benign |
Het |
Lamc1 |
C |
A |
1: 153,110,326 (GRCm39) |
Q1116H |
possibly damaging |
Het |
Lamc1 |
T |
G |
1: 153,110,341 (GRCm39) |
Q1111H |
probably damaging |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,411,155 (GRCm39) |
D1399E |
probably benign |
Het |
Ltbp4 |
G |
T |
7: 27,024,485 (GRCm39) |
P715Q |
probably damaging |
Het |
Mtor |
T |
C |
4: 148,547,367 (GRCm39) |
V450A |
probably benign |
Het |
Muc6 |
G |
A |
7: 141,223,981 (GRCm39) |
|
probably benign |
Het |
Myom1 |
A |
T |
17: 71,428,131 (GRCm39) |
I1450F |
probably damaging |
Het |
Naip6 |
A |
G |
13: 100,420,274 (GRCm39) |
I1332T |
possibly damaging |
Het |
Ncstn |
A |
G |
1: 171,899,072 (GRCm39) |
V353A |
possibly damaging |
Het |
Nt5c3 |
T |
C |
6: 56,863,734 (GRCm39) |
T149A |
probably benign |
Het |
Or5ac21 |
A |
T |
16: 59,124,352 (GRCm39) |
I280F |
probably damaging |
Het |
Or5p81 |
A |
G |
7: 108,267,364 (GRCm39) |
H247R |
probably damaging |
Het |
Paip1 |
T |
C |
13: 119,566,854 (GRCm39) |
S54P |
possibly damaging |
Het |
Prdm14 |
G |
T |
1: 13,195,968 (GRCm39) |
A31E |
probably benign |
Het |
Prr14l |
A |
G |
5: 32,985,767 (GRCm39) |
S1243P |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,435,878 (GRCm39) |
M1T |
probably null |
Het |
Scube1 |
T |
A |
15: 83,512,277 (GRCm39) |
|
probably null |
Het |
Serpina3c |
T |
A |
12: 104,117,805 (GRCm39) |
I178F |
probably damaging |
Het |
Slc16a13 |
A |
T |
11: 70,111,457 (GRCm39) |
V16E |
probably damaging |
Het |
Slc30a6 |
T |
C |
17: 74,722,640 (GRCm39) |
S236P |
possibly damaging |
Het |
Sobp |
A |
C |
10: 42,898,689 (GRCm39) |
S299A |
probably damaging |
Het |
Sorcs3 |
C |
A |
19: 48,694,448 (GRCm39) |
T574K |
possibly damaging |
Het |
Trak2 |
A |
T |
1: 58,942,820 (GRCm39) |
M862K |
probably benign |
Het |
Ubox5 |
A |
T |
2: 130,442,630 (GRCm39) |
V19E |
probably damaging |
Het |
Vmn1r173 |
A |
G |
7: 23,402,160 (GRCm39) |
T132A |
probably benign |
Het |
Zfp267 |
A |
G |
3: 36,218,711 (GRCm39) |
M244V |
probably benign |
Het |
Zfp820 |
T |
C |
17: 22,038,509 (GRCm39) |
D273G |
probably benign |
Het |
|
Other mutations in Raver2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Raver2
|
APN |
4 |
100,960,065 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00778:Raver2
|
APN |
4 |
100,953,468 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01363:Raver2
|
APN |
4 |
100,977,780 (GRCm39) |
splice site |
probably benign |
|
IGL02631:Raver2
|
APN |
4 |
100,953,499 (GRCm39) |
missense |
probably damaging |
0.96 |
R0071:Raver2
|
UTSW |
4 |
100,977,642 (GRCm39) |
splice site |
probably benign |
|
R0071:Raver2
|
UTSW |
4 |
100,977,642 (GRCm39) |
splice site |
probably benign |
|
R1450:Raver2
|
UTSW |
4 |
100,993,349 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2044:Raver2
|
UTSW |
4 |
100,960,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5127:Raver2
|
UTSW |
4 |
100,960,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Raver2
|
UTSW |
4 |
100,959,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R5342:Raver2
|
UTSW |
4 |
100,959,889 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5557:Raver2
|
UTSW |
4 |
100,993,336 (GRCm39) |
missense |
probably benign |
0.04 |
R6190:Raver2
|
UTSW |
4 |
100,990,814 (GRCm39) |
missense |
probably benign |
0.00 |
R6248:Raver2
|
UTSW |
4 |
100,991,320 (GRCm39) |
splice site |
probably null |
|
R6449:Raver2
|
UTSW |
4 |
100,990,869 (GRCm39) |
missense |
probably benign |
0.41 |
R6640:Raver2
|
UTSW |
4 |
100,988,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R6852:Raver2
|
UTSW |
4 |
100,990,787 (GRCm39) |
missense |
probably benign |
0.00 |
R7196:Raver2
|
UTSW |
4 |
100,960,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Raver2
|
UTSW |
4 |
100,959,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7459:Raver2
|
UTSW |
4 |
100,964,410 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8025:Raver2
|
UTSW |
4 |
100,960,162 (GRCm39) |
nonsense |
probably null |
|
R8843:Raver2
|
UTSW |
4 |
100,994,942 (GRCm39) |
missense |
probably damaging |
0.96 |
R8898:Raver2
|
UTSW |
4 |
100,964,399 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9290:Raver2
|
UTSW |
4 |
100,977,387 (GRCm39) |
intron |
probably benign |
|
RF017:Raver2
|
UTSW |
4 |
100,960,195 (GRCm39) |
missense |
probably damaging |
0.99 |
|