Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
A |
G |
15: 11,258,182 (GRCm39) |
N498D |
possibly damaging |
Het |
Ap5s1 |
T |
C |
2: 131,053,293 (GRCm39) |
S26P |
probably damaging |
Het |
Apaf1 |
T |
C |
10: 90,894,216 (GRCm39) |
Y473C |
probably benign |
Het |
Cdc42ep4 |
C |
T |
11: 113,620,268 (GRCm39) |
G41D |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,115,101 (GRCm39) |
Y60N |
probably damaging |
Het |
Dpy19l1 |
C |
T |
9: 24,396,365 (GRCm39) |
R117Q |
probably damaging |
Het |
Drd3 |
T |
A |
16: 43,641,631 (GRCm39) |
L316M |
probably damaging |
Het |
Hadha |
C |
T |
5: 30,325,082 (GRCm39) |
G703R |
probably damaging |
Het |
Lrrc74a |
A |
C |
12: 86,801,189 (GRCm39) |
M347L |
probably benign |
Het |
Macf1 |
G |
T |
4: 123,284,879 (GRCm39) |
Q4208K |
probably damaging |
Het |
Myh15 |
C |
T |
16: 48,877,847 (GRCm39) |
|
probably benign |
Het |
Ndufa7 |
A |
T |
17: 34,057,122 (GRCm39) |
M101L |
probably benign |
Het |
Pla2g6 |
A |
G |
15: 79,202,057 (GRCm39) |
V38A |
probably benign |
Het |
Sar1a |
A |
G |
10: 61,521,406 (GRCm39) |
|
probably benign |
Het |
Sdc3 |
A |
G |
4: 130,546,378 (GRCm39) |
T246A |
probably damaging |
Het |
Sds |
C |
T |
5: 120,617,272 (GRCm39) |
R43* |
probably null |
Het |
Slc9a9 |
A |
G |
9: 94,842,499 (GRCm39) |
Y350C |
probably damaging |
Het |
Tln1 |
A |
G |
4: 43,555,890 (GRCm39) |
V108A |
probably damaging |
Het |
Vmn2r111 |
G |
T |
17: 22,788,054 (GRCm39) |
|
probably benign |
Het |
Wnk1 |
G |
A |
6: 119,925,358 (GRCm39) |
P1369S |
probably damaging |
Het |
Zfhx4 |
T |
A |
3: 5,307,105 (GRCm39) |
D110E |
probably benign |
Het |
Zfp462 |
A |
G |
4: 55,008,586 (GRCm39) |
Y184C |
probably benign |
Het |
|
Other mutations in Strc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01102:Strc
|
APN |
2 |
121,195,541 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01152:Strc
|
APN |
2 |
121,201,276 (GRCm39) |
missense |
probably benign |
|
IGL01608:Strc
|
APN |
2 |
121,206,075 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01695:Strc
|
APN |
2 |
121,205,779 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01906:Strc
|
APN |
2 |
121,208,115 (GRCm39) |
missense |
probably benign |
|
IGL02135:Strc
|
APN |
2 |
121,195,315 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Strc
|
APN |
2 |
121,199,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Strc
|
APN |
2 |
121,206,272 (GRCm39) |
unclassified |
probably benign |
|
IGL03029:Strc
|
APN |
2 |
121,194,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03176:Strc
|
APN |
2 |
121,202,661 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03272:Strc
|
APN |
2 |
121,202,232 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Strc
|
UTSW |
2 |
121,204,161 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02799:Strc
|
UTSW |
2 |
121,209,717 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Strc
|
UTSW |
2 |
121,205,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Strc
|
UTSW |
2 |
121,198,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Strc
|
UTSW |
2 |
121,210,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R1065:Strc
|
UTSW |
2 |
121,197,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Strc
|
UTSW |
2 |
121,202,558 (GRCm39) |
intron |
probably benign |
|
R1148:Strc
|
UTSW |
2 |
121,202,558 (GRCm39) |
intron |
probably benign |
|
R1203:Strc
|
UTSW |
2 |
121,202,604 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1343:Strc
|
UTSW |
2 |
121,195,596 (GRCm39) |
missense |
probably benign |
0.21 |
R1544:Strc
|
UTSW |
2 |
121,203,219 (GRCm39) |
splice site |
probably null |
|
R1650:Strc
|
UTSW |
2 |
121,211,366 (GRCm39) |
start gained |
probably benign |
|
R1840:Strc
|
UTSW |
2 |
121,209,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Strc
|
UTSW |
2 |
121,201,518 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2035:Strc
|
UTSW |
2 |
121,205,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Strc
|
UTSW |
2 |
121,209,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2158:Strc
|
UTSW |
2 |
121,196,343 (GRCm39) |
missense |
probably benign |
0.10 |
R2219:Strc
|
UTSW |
2 |
121,195,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Strc
|
UTSW |
2 |
121,195,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R4375:Strc
|
UTSW |
2 |
121,211,304 (GRCm39) |
missense |
unknown |
|
R4563:Strc
|
UTSW |
2 |
121,196,286 (GRCm39) |
missense |
probably benign |
0.02 |
R4578:Strc
|
UTSW |
2 |
121,208,484 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4607:Strc
|
UTSW |
2 |
121,203,426 (GRCm39) |
missense |
probably benign |
0.31 |
R4651:Strc
|
UTSW |
2 |
121,204,829 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4652:Strc
|
UTSW |
2 |
121,204,829 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4790:Strc
|
UTSW |
2 |
121,206,075 (GRCm39) |
missense |
probably benign |
0.05 |
R5480:Strc
|
UTSW |
2 |
121,195,300 (GRCm39) |
missense |
probably benign |
0.00 |
R5580:Strc
|
UTSW |
2 |
121,205,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R5679:Strc
|
UTSW |
2 |
121,198,581 (GRCm39) |
missense |
probably benign |
0.03 |
R5703:Strc
|
UTSW |
2 |
121,201,295 (GRCm39) |
missense |
probably benign |
|
R5841:Strc
|
UTSW |
2 |
121,196,358 (GRCm39) |
missense |
probably benign |
0.29 |
R5917:Strc
|
UTSW |
2 |
121,209,790 (GRCm39) |
missense |
probably benign |
|
R5958:Strc
|
UTSW |
2 |
121,207,403 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6320:Strc
|
UTSW |
2 |
121,205,439 (GRCm39) |
missense |
probably benign |
0.16 |
R6619:Strc
|
UTSW |
2 |
121,198,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R6695:Strc
|
UTSW |
2 |
121,207,705 (GRCm39) |
missense |
probably benign |
0.35 |
R6970:Strc
|
UTSW |
2 |
121,208,495 (GRCm39) |
missense |
probably benign |
0.41 |
R7018:Strc
|
UTSW |
2 |
121,199,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Strc
|
UTSW |
2 |
121,201,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Strc
|
UTSW |
2 |
121,199,507 (GRCm39) |
missense |
probably benign |
0.14 |
R7283:Strc
|
UTSW |
2 |
121,209,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R7694:Strc
|
UTSW |
2 |
121,207,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Strc
|
UTSW |
2 |
121,202,229 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7700:Strc
|
UTSW |
2 |
121,202,229 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7756:Strc
|
UTSW |
2 |
121,201,427 (GRCm39) |
missense |
probably benign |
|
R7758:Strc
|
UTSW |
2 |
121,201,427 (GRCm39) |
missense |
probably benign |
|
R7822:Strc
|
UTSW |
2 |
121,208,219 (GRCm39) |
missense |
probably benign |
0.01 |
R7830:Strc
|
UTSW |
2 |
121,205,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R7953:Strc
|
UTSW |
2 |
121,207,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R8137:Strc
|
UTSW |
2 |
121,197,219 (GRCm39) |
missense |
probably damaging |
0.98 |
R8394:Strc
|
UTSW |
2 |
121,209,490 (GRCm39) |
missense |
probably benign |
0.00 |
R8427:Strc
|
UTSW |
2 |
121,208,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Strc
|
UTSW |
2 |
121,208,286 (GRCm39) |
missense |
probably damaging |
0.99 |
R8874:Strc
|
UTSW |
2 |
121,205,353 (GRCm39) |
critical splice donor site |
probably null |
|
R8947:Strc
|
UTSW |
2 |
121,201,470 (GRCm39) |
missense |
probably benign |
0.09 |
R9285:Strc
|
UTSW |
2 |
121,195,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Strc
|
UTSW |
2 |
121,211,336 (GRCm39) |
missense |
unknown |
|
R9386:Strc
|
UTSW |
2 |
121,198,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R9438:Strc
|
UTSW |
2 |
121,198,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Strc
|
UTSW |
2 |
121,207,928 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Strc
|
UTSW |
2 |
121,209,525 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Strc
|
UTSW |
2 |
121,206,002 (GRCm39) |
missense |
probably damaging |
0.98 |
|