Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
G |
T |
5: 64,056,182 (GRCm39) |
|
probably benign |
Het |
Acsbg2 |
A |
G |
17: 57,168,580 (GRCm39) |
Y180H |
probably damaging |
Het |
Adgrb3 |
G |
T |
1: 25,133,447 (GRCm39) |
T1213K |
probably damaging |
Het |
Atrn |
A |
G |
2: 130,802,388 (GRCm39) |
T510A |
probably benign |
Het |
Clasp1 |
C |
A |
1: 118,488,808 (GRCm39) |
T857N |
probably damaging |
Het |
Cldn8 |
A |
C |
16: 88,359,619 (GRCm39) |
M102R |
probably damaging |
Het |
Col12a1 |
C |
A |
9: 79,580,192 (GRCm39) |
V1562F |
possibly damaging |
Het |
Cyp4f40 |
T |
A |
17: 32,890,186 (GRCm39) |
D285E |
probably benign |
Het |
Dis3 |
G |
A |
14: 99,321,550 (GRCm39) |
S599L |
possibly damaging |
Het |
Dnah11 |
T |
C |
12: 117,951,186 (GRCm39) |
T3041A |
probably benign |
Het |
Erbin |
T |
C |
13: 103,981,393 (GRCm39) |
N511D |
probably benign |
Het |
F11 |
T |
A |
8: 45,694,511 (GRCm39) |
I617F |
probably damaging |
Het |
Gm11541 |
A |
T |
11: 94,595,048 (GRCm39) |
C7S |
unknown |
Het |
Klk12 |
A |
T |
7: 43,422,807 (GRCm39) |
R245W |
probably damaging |
Het |
Lao1 |
C |
A |
4: 118,822,504 (GRCm39) |
S141R |
probably benign |
Het |
Lrrk2 |
A |
G |
15: 91,632,023 (GRCm39) |
K1316E |
probably damaging |
Het |
Map3k6 |
A |
G |
4: 132,973,644 (GRCm39) |
Y445C |
possibly damaging |
Het |
Mup6 |
T |
C |
4: 60,004,000 (GRCm39) |
I31T |
probably damaging |
Het |
Ndnf |
T |
A |
6: 65,681,180 (GRCm39) |
D486E |
probably benign |
Het |
Or2a54 |
T |
C |
6: 43,092,852 (GRCm39) |
Y59H |
probably damaging |
Het |
Or8h7 |
A |
T |
2: 86,721,494 (GRCm39) |
N8K |
probably benign |
Het |
Or8k37 |
A |
T |
2: 86,469,478 (GRCm39) |
N191K |
probably benign |
Het |
Slc22a29 |
A |
T |
19: 8,140,088 (GRCm39) |
L439* |
probably null |
Het |
Slc5a1 |
A |
G |
5: 33,303,860 (GRCm39) |
E225G |
possibly damaging |
Het |
Slx4 |
A |
G |
16: 3,806,919 (GRCm39) |
V508A |
possibly damaging |
Het |
Snx25 |
A |
G |
8: 46,521,266 (GRCm39) |
S373P |
possibly damaging |
Het |
Stag2 |
A |
G |
X: 41,322,749 (GRCm39) |
S400G |
probably benign |
Homo |
Tas2r107 |
A |
G |
6: 131,636,972 (GRCm39) |
Y26H |
probably benign |
Het |
Tmem181a |
T |
A |
17: 6,346,061 (GRCm39) |
L185H |
probably damaging |
Het |
Zdhhc22 |
G |
A |
12: 87,034,997 (GRCm39) |
L152F |
probably benign |
Het |
Zfpm2 |
T |
G |
15: 40,959,557 (GRCm39) |
M80R |
probably benign |
Het |
|
Other mutations in Rab19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Rab19
|
APN |
6 |
39,365,132 (GRCm39) |
splice site |
probably benign |
|
IGL02188:Rab19
|
APN |
6 |
39,360,968 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02452:Rab19
|
APN |
6 |
39,366,732 (GRCm39) |
missense |
probably benign |
|
IGL03027:Rab19
|
APN |
6 |
39,360,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Rab19
|
UTSW |
6 |
39,366,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Rab19
|
UTSW |
6 |
39,361,023 (GRCm39) |
missense |
probably benign |
0.02 |
R0726:Rab19
|
UTSW |
6 |
39,360,893 (GRCm39) |
missense |
probably benign |
0.00 |
R1727:Rab19
|
UTSW |
6 |
39,365,095 (GRCm39) |
nonsense |
probably null |
|
R1954:Rab19
|
UTSW |
6 |
39,361,016 (GRCm39) |
missense |
probably benign |
0.06 |
R2169:Rab19
|
UTSW |
6 |
39,360,975 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3796:Rab19
|
UTSW |
6 |
39,360,975 (GRCm39) |
missense |
probably benign |
0.01 |
R5977:Rab19
|
UTSW |
6 |
39,360,860 (GRCm39) |
missense |
probably benign |
0.07 |
R6619:Rab19
|
UTSW |
6 |
39,365,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R7489:Rab19
|
UTSW |
6 |
39,365,039 (GRCm39) |
missense |
probably benign |
0.09 |
R8385:Rab19
|
UTSW |
6 |
39,360,892 (GRCm39) |
missense |
probably benign |
0.00 |
R9414:Rab19
|
UTSW |
6 |
39,360,855 (GRCm39) |
start codon destroyed |
probably null |
0.43 |
|