Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
G |
A |
10: 14,343,119 (GRCm39) |
P276L |
probably benign |
Het |
Asap1 |
G |
A |
15: 63,991,803 (GRCm39) |
|
probably benign |
Het |
Axl |
T |
C |
7: 25,460,297 (GRCm39) |
T723A |
probably damaging |
Het |
Barhl2 |
C |
T |
5: 106,603,365 (GRCm39) |
A265T |
possibly damaging |
Het |
Bltp1 |
A |
G |
3: 37,065,876 (GRCm39) |
N3491S |
probably benign |
Het |
Capn7 |
A |
G |
14: 31,085,535 (GRCm39) |
K503E |
probably benign |
Het |
Cbln4 |
A |
G |
2: 171,880,970 (GRCm39) |
V108A |
probably benign |
Het |
Ccdc71 |
C |
T |
9: 108,341,354 (GRCm39) |
T389M |
probably damaging |
Het |
Ccdc91 |
A |
G |
6: 147,508,452 (GRCm39) |
T393A |
unknown |
Het |
Cdh20 |
A |
T |
1: 104,881,612 (GRCm39) |
H359L |
probably benign |
Het |
Cfap119 |
A |
T |
7: 127,184,210 (GRCm39) |
S229T |
probably damaging |
Het |
Coro7 |
C |
T |
16: 4,452,500 (GRCm39) |
V364M |
possibly damaging |
Het |
Ctsq |
A |
T |
13: 61,185,528 (GRCm39) |
N204K |
probably damaging |
Het |
Dnaja3 |
C |
T |
16: 4,512,309 (GRCm39) |
R238C |
probably damaging |
Het |
Dynlt1a |
C |
T |
17: 6,362,062 (GRCm39) |
V39I |
possibly damaging |
Het |
Gp1ba |
A |
G |
11: 70,531,478 (GRCm39) |
|
probably benign |
Het |
Gtf3c3 |
T |
C |
1: 54,455,114 (GRCm39) |
Y583C |
probably damaging |
Het |
Invs |
T |
C |
4: 48,402,909 (GRCm39) |
F514S |
probably damaging |
Het |
Kif23 |
A |
T |
9: 61,833,750 (GRCm39) |
C484S |
probably benign |
Het |
Masp1 |
A |
G |
16: 23,295,062 (GRCm39) |
Y400H |
probably damaging |
Het |
Olfml3 |
G |
A |
3: 103,644,298 (GRCm39) |
|
probably null |
Het |
Pard3b |
T |
C |
1: 62,200,357 (GRCm39) |
S299P |
probably damaging |
Het |
Pcdhb16 |
A |
T |
18: 37,611,623 (GRCm39) |
E194D |
possibly damaging |
Het |
Pip5k1c |
A |
T |
10: 81,141,545 (GRCm39) |
T78S |
probably benign |
Het |
Septin11 |
T |
C |
5: 93,304,877 (GRCm39) |
|
probably null |
Het |
Septin8 |
A |
G |
11: 53,422,823 (GRCm39) |
N11D |
probably benign |
Het |
Smim8 |
T |
C |
4: 34,769,006 (GRCm39) |
T93A |
probably benign |
Het |
Tg |
A |
G |
15: 66,645,273 (GRCm39) |
I774M |
probably benign |
Het |
Tulp4 |
A |
G |
17: 6,189,351 (GRCm39) |
T58A |
probably damaging |
Het |
Virma |
T |
C |
4: 11,519,424 (GRCm39) |
|
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,970,177 (GRCm39) |
D210G |
probably damaging |
Het |
Zfp984 |
C |
T |
4: 147,839,343 (GRCm39) |
G503S |
probably benign |
Het |
|
Other mutations in Slc10a6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Slc10a6
|
APN |
5 |
103,756,991 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02893:Slc10a6
|
APN |
5 |
103,776,739 (GRCm39) |
missense |
probably benign |
0.39 |
R0681:Slc10a6
|
UTSW |
5 |
103,760,315 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1300:Slc10a6
|
UTSW |
5 |
103,754,550 (GRCm39) |
missense |
probably benign |
0.28 |
R1636:Slc10a6
|
UTSW |
5 |
103,777,012 (GRCm39) |
missense |
probably benign |
0.00 |
R2127:Slc10a6
|
UTSW |
5 |
103,756,922 (GRCm39) |
missense |
probably benign |
0.00 |
R2129:Slc10a6
|
UTSW |
5 |
103,756,922 (GRCm39) |
missense |
probably benign |
0.00 |
R4789:Slc10a6
|
UTSW |
5 |
103,776,848 (GRCm39) |
missense |
probably benign |
0.03 |
R4908:Slc10a6
|
UTSW |
5 |
103,754,493 (GRCm39) |
missense |
probably benign |
0.00 |
R4976:Slc10a6
|
UTSW |
5 |
103,754,470 (GRCm39) |
missense |
probably benign |
0.04 |
R5309:Slc10a6
|
UTSW |
5 |
103,756,958 (GRCm39) |
missense |
probably damaging |
0.96 |
R6784:Slc10a6
|
UTSW |
5 |
103,776,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R7362:Slc10a6
|
UTSW |
5 |
103,776,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R7658:Slc10a6
|
UTSW |
5 |
103,777,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R7708:Slc10a6
|
UTSW |
5 |
103,777,128 (GRCm39) |
start gained |
probably benign |
|
R8084:Slc10a6
|
UTSW |
5 |
103,760,327 (GRCm39) |
missense |
probably benign |
|
R9145:Slc10a6
|
UTSW |
5 |
103,776,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Slc10a6
|
UTSW |
5 |
103,765,571 (GRCm39) |
missense |
probably damaging |
0.96 |
R9345:Slc10a6
|
UTSW |
5 |
103,754,521 (GRCm39) |
missense |
probably benign |
0.01 |
RF009:Slc10a6
|
UTSW |
5 |
103,756,858 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Slc10a6
|
UTSW |
5 |
103,760,291 (GRCm39) |
missense |
probably benign |
0.00 |
|