Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
A |
G |
7: 119,380,297 (GRCm39) |
|
probably benign |
Het |
Adcy7 |
A |
G |
8: 89,051,472 (GRCm39) |
N864S |
probably damaging |
Het |
Anapc7 |
A |
G |
5: 122,576,279 (GRCm39) |
D302G |
probably benign |
Het |
Atm |
A |
T |
9: 53,419,107 (GRCm39) |
C782S |
probably benign |
Het |
Bicdl1 |
G |
A |
5: 115,808,215 (GRCm39) |
Q37* |
probably null |
Het |
Cabin1 |
T |
C |
10: 75,561,420 (GRCm39) |
D1027G |
possibly damaging |
Het |
Cbl |
T |
C |
9: 44,075,503 (GRCm39) |
I364V |
probably damaging |
Het |
Ccer1 |
T |
C |
10: 97,529,459 (GRCm39) |
S41P |
unknown |
Het |
Cenpf |
G |
A |
1: 189,390,065 (GRCm39) |
Q1256* |
probably null |
Het |
Copa |
T |
A |
1: 171,947,128 (GRCm39) |
I1093N |
probably benign |
Het |
Cped1 |
C |
T |
6: 22,017,004 (GRCm39) |
L118F |
probably damaging |
Het |
Cplane2 |
T |
C |
4: 140,945,964 (GRCm39) |
V169A |
probably benign |
Het |
Cstdc4 |
T |
A |
16: 36,006,777 (GRCm39) |
V37E |
probably benign |
Het |
Dner |
T |
C |
1: 84,361,731 (GRCm39) |
H626R |
probably benign |
Het |
Ears2 |
G |
A |
7: 121,662,311 (GRCm39) |
|
probably benign |
Het |
Eif3c |
A |
G |
7: 126,155,582 (GRCm39) |
I562T |
probably damaging |
Het |
Eml6 |
T |
C |
11: 29,769,090 (GRCm39) |
Y685C |
probably damaging |
Het |
Garin1b |
T |
C |
6: 29,320,700 (GRCm39) |
V108A |
probably damaging |
Het |
Gpt |
A |
G |
15: 76,582,982 (GRCm39) |
K321E |
probably damaging |
Het |
Hspd1 |
C |
T |
1: 55,120,285 (GRCm39) |
G306R |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,614,306 (GRCm39) |
Y138C |
probably damaging |
Het |
Lhcgr |
A |
G |
17: 89,049,865 (GRCm39) |
Y554H |
probably damaging |
Het |
Nell1 |
A |
T |
7: 50,350,956 (GRCm39) |
K534N |
probably benign |
Het |
Nob1 |
A |
G |
8: 108,151,360 (GRCm39) |
|
probably benign |
Het |
Or13a17 |
G |
A |
7: 140,271,531 (GRCm39) |
A238T |
probably damaging |
Het |
Phf12 |
C |
T |
11: 77,914,385 (GRCm39) |
P60L |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,531,451 (GRCm39) |
E1358G |
probably benign |
Het |
Rimbp3 |
A |
G |
16: 17,029,566 (GRCm39) |
T997A |
probably benign |
Het |
Slc9a9 |
T |
A |
9: 94,901,247 (GRCm39) |
N393K |
possibly damaging |
Het |
Sohlh2 |
T |
C |
3: 55,102,582 (GRCm39) |
S206P |
probably damaging |
Het |
Stard10 |
G |
A |
7: 100,971,187 (GRCm39) |
V125M |
probably benign |
Het |
Tff2 |
G |
T |
17: 31,362,240 (GRCm39) |
|
probably null |
Het |
Tha1 |
T |
C |
11: 117,759,425 (GRCm39) |
T355A |
probably benign |
Het |
Tmem120a |
G |
T |
5: 135,765,864 (GRCm39) |
F127L |
possibly damaging |
Het |
Tmem41b |
A |
G |
7: 109,577,909 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tonsl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Tonsl
|
APN |
15 |
76,522,696 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00763:Tonsl
|
APN |
15 |
76,518,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00796:Tonsl
|
APN |
15 |
76,509,349 (GRCm39) |
missense |
probably benign |
|
IGL00965:Tonsl
|
APN |
15 |
76,516,080 (GRCm39) |
splice site |
probably benign |
|
IGL01859:Tonsl
|
APN |
15 |
76,518,980 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02112:Tonsl
|
APN |
15 |
76,517,602 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02189:Tonsl
|
APN |
15 |
76,507,378 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02281:Tonsl
|
APN |
15 |
76,518,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02627:Tonsl
|
APN |
15 |
76,518,295 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02750:Tonsl
|
APN |
15 |
76,517,589 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02977:Tonsl
|
APN |
15 |
76,517,073 (GRCm39) |
missense |
probably benign |
0.00 |
R0127:Tonsl
|
UTSW |
15 |
76,517,685 (GRCm39) |
missense |
probably benign |
0.01 |
R0316:Tonsl
|
UTSW |
15 |
76,513,500 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0443:Tonsl
|
UTSW |
15 |
76,523,884 (GRCm39) |
missense |
probably benign |
|
R0714:Tonsl
|
UTSW |
15 |
76,517,921 (GRCm39) |
splice site |
probably benign |
|
R0946:Tonsl
|
UTSW |
15 |
76,507,421 (GRCm39) |
missense |
probably benign |
0.03 |
R0975:Tonsl
|
UTSW |
15 |
76,523,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R1263:Tonsl
|
UTSW |
15 |
76,506,762 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1468:Tonsl
|
UTSW |
15 |
76,520,761 (GRCm39) |
critical splice donor site |
probably null |
|
R1468:Tonsl
|
UTSW |
15 |
76,520,761 (GRCm39) |
critical splice donor site |
probably null |
|
R1610:Tonsl
|
UTSW |
15 |
76,522,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Tonsl
|
UTSW |
15 |
76,522,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Tonsl
|
UTSW |
15 |
76,522,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R1882:Tonsl
|
UTSW |
15 |
76,508,350 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1898:Tonsl
|
UTSW |
15 |
76,523,053 (GRCm39) |
splice site |
probably null |
|
R1932:Tonsl
|
UTSW |
15 |
76,508,797 (GRCm39) |
missense |
probably damaging |
0.97 |
R2141:Tonsl
|
UTSW |
15 |
76,516,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R2166:Tonsl
|
UTSW |
15 |
76,521,513 (GRCm39) |
missense |
probably benign |
0.13 |
R2191:Tonsl
|
UTSW |
15 |
76,516,880 (GRCm39) |
missense |
probably damaging |
0.96 |
R2198:Tonsl
|
UTSW |
15 |
76,520,872 (GRCm39) |
missense |
probably benign |
0.00 |
R2219:Tonsl
|
UTSW |
15 |
76,518,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R2762:Tonsl
|
UTSW |
15 |
76,514,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R3156:Tonsl
|
UTSW |
15 |
76,523,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R3508:Tonsl
|
UTSW |
15 |
76,523,956 (GRCm39) |
missense |
probably benign |
|
R4012:Tonsl
|
UTSW |
15 |
76,521,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4179:Tonsl
|
UTSW |
15 |
76,508,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Tonsl
|
UTSW |
15 |
76,508,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R4327:Tonsl
|
UTSW |
15 |
76,523,916 (GRCm39) |
missense |
probably benign |
|
R4627:Tonsl
|
UTSW |
15 |
76,521,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Tonsl
|
UTSW |
15 |
76,507,610 (GRCm39) |
missense |
probably benign |
0.01 |
R4825:Tonsl
|
UTSW |
15 |
76,517,448 (GRCm39) |
missense |
probably benign |
0.34 |
R4840:Tonsl
|
UTSW |
15 |
76,517,409 (GRCm39) |
missense |
probably benign |
|
R5030:Tonsl
|
UTSW |
15 |
76,522,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5143:Tonsl
|
UTSW |
15 |
76,520,857 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6238:Tonsl
|
UTSW |
15 |
76,520,418 (GRCm39) |
splice site |
probably null |
|
R6379:Tonsl
|
UTSW |
15 |
76,513,942 (GRCm39) |
missense |
probably benign |
|
R6401:Tonsl
|
UTSW |
15 |
76,517,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6534:Tonsl
|
UTSW |
15 |
76,513,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Tonsl
|
UTSW |
15 |
76,514,018 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6701:Tonsl
|
UTSW |
15 |
76,513,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7138:Tonsl
|
UTSW |
15 |
76,518,976 (GRCm39) |
missense |
probably benign |
|
R7206:Tonsl
|
UTSW |
15 |
76,517,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Tonsl
|
UTSW |
15 |
76,517,925 (GRCm39) |
splice site |
probably null |
|
R7615:Tonsl
|
UTSW |
15 |
76,514,807 (GRCm39) |
missense |
probably benign |
0.44 |
R7626:Tonsl
|
UTSW |
15 |
76,518,136 (GRCm39) |
missense |
probably null |
1.00 |
R7641:Tonsl
|
UTSW |
15 |
76,517,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Tonsl
|
UTSW |
15 |
76,518,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R8245:Tonsl
|
UTSW |
15 |
76,521,022 (GRCm39) |
missense |
probably benign |
0.10 |
R8311:Tonsl
|
UTSW |
15 |
76,517,463 (GRCm39) |
missense |
probably benign |
|
R8679:Tonsl
|
UTSW |
15 |
76,518,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Tonsl
|
UTSW |
15 |
76,517,076 (GRCm39) |
missense |
probably benign |
0.19 |
R9093:Tonsl
|
UTSW |
15 |
76,515,270 (GRCm39) |
missense |
probably damaging |
0.97 |
R9143:Tonsl
|
UTSW |
15 |
76,514,824 (GRCm39) |
missense |
probably damaging |
0.96 |
R9278:Tonsl
|
UTSW |
15 |
76,520,971 (GRCm39) |
intron |
probably benign |
|
R9286:Tonsl
|
UTSW |
15 |
76,515,213 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tonsl
|
UTSW |
15 |
76,520,353 (GRCm39) |
missense |
possibly damaging |
0.50 |
|