Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bmp3 |
A |
C |
5: 99,020,238 (GRCm39) |
R220S |
possibly damaging |
Het |
Bms1 |
A |
G |
6: 118,395,363 (GRCm39) |
|
probably benign |
Het |
Ccdc138 |
T |
A |
10: 58,411,537 (GRCm39) |
F635Y |
probably damaging |
Het |
Ccdc81 |
T |
C |
7: 89,518,823 (GRCm39) |
|
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,045,407 (GRCm39) |
I341T |
possibly damaging |
Het |
Cog5 |
C |
T |
12: 31,715,531 (GRCm39) |
|
probably benign |
Het |
Dcaf4 |
G |
A |
12: 83,586,107 (GRCm39) |
R358H |
probably damaging |
Het |
Ddx10 |
A |
C |
9: 53,071,326 (GRCm39) |
|
probably benign |
Het |
Fgf15 |
T |
A |
7: 144,453,629 (GRCm39) |
F201I |
probably damaging |
Het |
Galp |
A |
G |
7: 6,211,499 (GRCm39) |
Y40C |
probably damaging |
Het |
Ints6 |
A |
G |
14: 62,938,314 (GRCm39) |
|
probably benign |
Het |
Iqcb1 |
A |
T |
16: 36,676,649 (GRCm39) |
|
probably benign |
Het |
Kif19a |
G |
A |
11: 114,657,994 (GRCm39) |
V18I |
probably benign |
Het |
Lypd8l |
T |
G |
11: 58,503,707 (GRCm39) |
|
probably benign |
Het |
Morc1 |
A |
C |
16: 48,432,689 (GRCm39) |
Q719P |
probably damaging |
Het |
Pla2g4a |
T |
C |
1: 149,727,076 (GRCm39) |
D568G |
probably damaging |
Het |
Plscr4 |
A |
G |
9: 92,366,998 (GRCm39) |
E204G |
probably null |
Het |
Rasgrf1 |
A |
G |
9: 89,853,073 (GRCm39) |
T403A |
probably benign |
Het |
Sec16b |
A |
G |
1: 157,356,827 (GRCm39) |
T12A |
probably benign |
Het |
Slc12a7 |
A |
T |
13: 73,942,201 (GRCm39) |
N359I |
possibly damaging |
Het |
Slc14a2 |
G |
T |
18: 78,235,453 (GRCm39) |
D241E |
probably damaging |
Het |
Slc23a2 |
G |
T |
2: 131,943,420 (GRCm39) |
A27E |
probably benign |
Het |
Slc38a8 |
T |
C |
8: 120,220,958 (GRCm39) |
I200M |
probably benign |
Het |
Thrap3 |
C |
T |
4: 126,059,371 (GRCm39) |
G892S |
probably benign |
Het |
Tmc6 |
A |
G |
11: 117,669,872 (GRCm39) |
L20P |
probably damaging |
Het |
Tnfsfm13 |
T |
C |
11: 69,575,536 (GRCm39) |
D256G |
probably benign |
Het |
Usp28 |
A |
G |
9: 48,939,463 (GRCm39) |
T240A |
probably benign |
Het |
Zap70 |
A |
T |
1: 36,818,333 (GRCm39) |
D340V |
possibly damaging |
Het |
Zfp512b |
A |
T |
2: 181,231,944 (GRCm39) |
F100I |
probably damaging |
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 |
IGL00796:Tonsl
|
APN |
15 |
76,509,349 (GRCm39) |
missense |
probably benign |
|
IGL00965:Tonsl
|
APN |
15 |
76,516,080 (GRCm39) |
splice site |
probably benign |
|
IGL01434:Tonsl
|
APN |
15 |
76,515,302 (GRCm39) |
missense |
probably benign |
0.11 |
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 |
|