Other mutations in this stock |
Total: 9 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Btn2a2 |
T |
C |
13: 23,662,655 (GRCm39) |
I423V |
probably benign |
Het |
Dmxl1 |
T |
G |
18: 50,050,735 (GRCm39) |
D2454E |
probably benign |
Het |
Hif3a |
A |
T |
7: 16,785,841 (GRCm39) |
|
probably null |
Het |
Muc5b |
C |
A |
7: 141,409,335 (GRCm39) |
Q1140K |
unknown |
Het |
Sfswap |
T |
A |
5: 129,590,297 (GRCm39) |
Y265N |
probably damaging |
Het |
Spata31e5 |
A |
G |
1: 28,817,732 (GRCm39) |
L100P |
possibly damaging |
Het |
Susd2 |
A |
T |
10: 75,473,882 (GRCm39) |
M571K |
probably benign |
Het |
Tmco1 |
C |
A |
1: 167,143,837 (GRCm39) |
N89K |
probably damaging |
Het |
Ttc7b |
G |
A |
12: 100,342,472 (GRCm39) |
A518V |
probably benign |
Het |
|
Other mutations in Cngb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01301:Cngb3
|
APN |
4 |
19,425,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01735:Cngb3
|
APN |
4 |
19,415,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01756:Cngb3
|
APN |
4 |
19,367,850 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01812:Cngb3
|
APN |
4 |
19,461,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02123:Cngb3
|
APN |
4 |
19,367,801 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02636:Cngb3
|
APN |
4 |
19,396,690 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02648:Cngb3
|
APN |
4 |
19,428,489 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02935:Cngb3
|
APN |
4 |
19,425,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03025:Cngb3
|
APN |
4 |
19,283,498 (GRCm39) |
splice site |
probably benign |
|
IGL03068:Cngb3
|
APN |
4 |
19,375,246 (GRCm39) |
missense |
possibly damaging |
0.92 |
braced
|
UTSW |
4 |
19,395,922 (GRCm39) |
splice site |
probably benign |
|
ANU18:Cngb3
|
UTSW |
4 |
19,425,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R0014:Cngb3
|
UTSW |
4 |
19,396,685 (GRCm39) |
missense |
probably benign |
0.33 |
R0014:Cngb3
|
UTSW |
4 |
19,396,685 (GRCm39) |
missense |
probably benign |
0.33 |
R0195:Cngb3
|
UTSW |
4 |
19,280,975 (GRCm39) |
missense |
probably benign |
0.00 |
R0361:Cngb3
|
UTSW |
4 |
19,366,467 (GRCm39) |
missense |
probably benign |
0.00 |
R0480:Cngb3
|
UTSW |
4 |
19,309,517 (GRCm39) |
splice site |
probably benign |
|
R1103:Cngb3
|
UTSW |
4 |
19,309,658 (GRCm39) |
critical splice donor site |
probably null |
|
R1450:Cngb3
|
UTSW |
4 |
19,395,922 (GRCm39) |
splice site |
probably benign |
|
R1618:Cngb3
|
UTSW |
4 |
19,364,260 (GRCm39) |
missense |
probably benign |
|
R1891:Cngb3
|
UTSW |
4 |
19,366,446 (GRCm39) |
missense |
probably benign |
0.00 |
R2196:Cngb3
|
UTSW |
4 |
19,415,690 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2850:Cngb3
|
UTSW |
4 |
19,415,690 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3909:Cngb3
|
UTSW |
4 |
19,461,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R3941:Cngb3
|
UTSW |
4 |
19,396,786 (GRCm39) |
missense |
probably benign |
0.00 |
R4348:Cngb3
|
UTSW |
4 |
19,396,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R4490:Cngb3
|
UTSW |
4 |
19,415,684 (GRCm39) |
missense |
probably benign |
0.41 |
R4493:Cngb3
|
UTSW |
4 |
19,367,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Cngb3
|
UTSW |
4 |
19,425,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Cngb3
|
UTSW |
4 |
19,309,562 (GRCm39) |
missense |
probably benign |
|
R4774:Cngb3
|
UTSW |
4 |
19,415,713 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4860:Cngb3
|
UTSW |
4 |
19,425,569 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4860:Cngb3
|
UTSW |
4 |
19,425,569 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4898:Cngb3
|
UTSW |
4 |
19,395,926 (GRCm39) |
missense |
probably benign |
0.08 |
R5216:Cngb3
|
UTSW |
4 |
19,415,729 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5647:Cngb3
|
UTSW |
4 |
19,364,266 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5945:Cngb3
|
UTSW |
4 |
19,283,579 (GRCm39) |
missense |
probably null |
0.00 |
R6586:Cngb3
|
UTSW |
4 |
19,280,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R6650:Cngb3
|
UTSW |
4 |
19,364,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R6651:Cngb3
|
UTSW |
4 |
19,375,231 (GRCm39) |
missense |
probably benign |
0.01 |
R7070:Cngb3
|
UTSW |
4 |
19,425,593 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7316:Cngb3
|
UTSW |
4 |
19,425,599 (GRCm39) |
missense |
probably benign |
0.16 |
R7371:Cngb3
|
UTSW |
4 |
19,425,575 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7554:Cngb3
|
UTSW |
4 |
19,461,753 (GRCm39) |
nonsense |
probably null |
|
R7755:Cngb3
|
UTSW |
4 |
19,461,684 (GRCm39) |
missense |
probably benign |
0.01 |
R8004:Cngb3
|
UTSW |
4 |
19,505,273 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8025:Cngb3
|
UTSW |
4 |
19,280,960 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9143:Cngb3
|
UTSW |
4 |
19,375,190 (GRCm39) |
splice site |
probably benign |
|
R9366:Cngb3
|
UTSW |
4 |
19,395,983 (GRCm39) |
missense |
probably benign |
0.03 |
R9489:Cngb3
|
UTSW |
4 |
19,505,187 (GRCm39) |
missense |
probably benign |
0.17 |
R9605:Cngb3
|
UTSW |
4 |
19,505,187 (GRCm39) |
missense |
probably benign |
0.17 |
X0062:Cngb3
|
UTSW |
4 |
19,364,189 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0067:Cngb3
|
UTSW |
4 |
19,367,753 (GRCm39) |
missense |
probably damaging |
0.99 |
|