Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
A |
2: 68,566,904 (GRCm39) |
H434Q |
possibly damaging |
Het |
5430401F13Rik |
A |
T |
6: 131,529,555 (GRCm39) |
I50L |
probably benign |
Het |
Ahnak |
G |
A |
19: 8,981,957 (GRCm39) |
M1080I |
probably benign |
Het |
Aoc1 |
A |
G |
6: 48,884,577 (GRCm39) |
K540R |
probably benign |
Het |
Aplp2 |
T |
C |
9: 31,064,712 (GRCm39) |
M585V |
probably benign |
Het |
C3 |
A |
G |
17: 57,511,281 (GRCm39) |
L1607P |
probably benign |
Het |
C6 |
A |
G |
15: 4,826,396 (GRCm39) |
K660E |
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,549,419 (GRCm39) |
T1329A |
probably benign |
Het |
Ccdc141 |
T |
A |
2: 76,888,268 (GRCm39) |
N499I |
probably damaging |
Het |
Cdh5 |
A |
G |
8: 104,869,560 (GRCm39) |
D762G |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,428,394 (GRCm39) |
R746G |
possibly damaging |
Het |
Cps1 |
A |
T |
1: 67,187,933 (GRCm39) |
Q198L |
probably benign |
Het |
Eri3 |
T |
C |
4: 117,422,057 (GRCm39) |
F112L |
probably damaging |
Het |
Fam180a |
C |
A |
6: 35,290,488 (GRCm39) |
R165L |
probably benign |
Het |
Fkbp10 |
A |
C |
11: 100,313,481 (GRCm39) |
I252L |
probably benign |
Het |
Gtf2f1 |
G |
T |
17: 57,310,918 (GRCm39) |
Q410K |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,439,579 (GRCm39) |
Y5535C |
probably damaging |
Het |
Ifrd2 |
T |
A |
9: 107,469,369 (GRCm39) |
D372E |
probably benign |
Het |
Il3ra |
A |
G |
14: 14,350,760 (GRCm38) |
N165S |
probably benign |
Het |
Kntc1 |
A |
G |
5: 123,957,183 (GRCm39) |
N2164S |
probably benign |
Het |
Krtap19-9a |
A |
G |
16: 88,721,099 (GRCm39) |
|
noncoding transcript |
Het |
Nopchap1 |
T |
A |
10: 83,200,309 (GRCm39) |
M90K |
probably damaging |
Het |
Or12d13 |
T |
A |
17: 37,647,664 (GRCm39) |
H153L |
possibly damaging |
Het |
Pclo |
T |
C |
5: 14,764,177 (GRCm39) |
S4217P |
unknown |
Het |
Ppfibp1 |
G |
A |
6: 146,928,806 (GRCm39) |
V798I |
probably damaging |
Het |
Prune2 |
A |
T |
19: 17,170,775 (GRCm39) |
R165* |
probably null |
Het |
Ptges |
T |
C |
2: 30,782,698 (GRCm39) |
Y118C |
probably damaging |
Het |
Rab11fip5 |
C |
A |
6: 85,325,540 (GRCm39) |
G289W |
probably damaging |
Het |
Rfc1 |
T |
C |
5: 65,468,506 (GRCm39) |
D69G |
possibly damaging |
Het |
Scube1 |
A |
G |
15: 83,606,044 (GRCm39) |
|
probably benign |
Het |
Slc5a6 |
G |
A |
5: 31,194,511 (GRCm39) |
P565L |
probably benign |
Het |
Sncaip |
C |
A |
18: 53,040,128 (GRCm39) |
T774K |
probably benign |
Het |
Spata31f1a |
C |
A |
4: 42,849,431 (GRCm39) |
L908F |
possibly damaging |
Het |
Specc1l |
G |
A |
10: 75,082,158 (GRCm39) |
S535N |
probably damaging |
Het |
Tbk1 |
C |
T |
10: 121,395,767 (GRCm39) |
G442E |
probably null |
Het |
Thoc7 |
A |
T |
14: 13,953,443 (GRCm38) |
M78K |
possibly damaging |
Het |
Usp15 |
A |
G |
10: 122,966,937 (GRCm39) |
F461S |
probably damaging |
Het |
Vmn2r6 |
T |
A |
3: 64,463,911 (GRCm39) |
I308L |
possibly damaging |
Het |
Zhx2 |
C |
A |
15: 57,685,663 (GRCm39) |
T344N |
probably damaging |
Het |
|
Other mutations in Cstpp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6768_1110051M20Rik_026
|
UTSW |
2 |
91,252,303 (GRCm39) |
missense |
probably damaging |
0.97 |
BB004:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
BB014:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Cstpp1
|
UTSW |
2 |
91,112,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Cstpp1
|
UTSW |
2 |
91,252,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Cstpp1
|
UTSW |
2 |
91,135,109 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0846:Cstpp1
|
UTSW |
2 |
91,214,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R6768:Cstpp1
|
UTSW |
2 |
91,252,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R6888:Cstpp1
|
UTSW |
2 |
91,252,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Cstpp1
|
UTSW |
2 |
91,214,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R7754:Cstpp1
|
UTSW |
2 |
91,135,188 (GRCm39) |
splice site |
probably null |
|
R7808:Cstpp1
|
UTSW |
2 |
91,274,939 (GRCm39) |
start gained |
probably benign |
|
R7927:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Cstpp1
|
UTSW |
2 |
91,107,343 (GRCm39) |
missense |
probably benign |
0.39 |
R9610:Cstpp1
|
UTSW |
2 |
91,135,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Cstpp1
|
UTSW |
2 |
91,135,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Cstpp1
|
UTSW |
2 |
91,112,099 (GRCm39) |
missense |
probably benign |
0.00 |
|