Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
C |
T |
11: 119,900,445 (GRCm39) |
A1291T |
probably benign |
Het |
Anks1b |
G |
A |
10: 90,143,560 (GRCm39) |
R523Q |
probably damaging |
Het |
Arhgap12 |
T |
A |
18: 6,028,056 (GRCm39) |
I690F |
probably damaging |
Het |
Caln1 |
T |
C |
5: 130,868,124 (GRCm39) |
V220A |
possibly damaging |
Het |
Cep290 |
A |
T |
10: 100,379,220 (GRCm39) |
K67N |
probably damaging |
Het |
Col19a1 |
T |
C |
1: 24,377,017 (GRCm39) |
T443A |
possibly damaging |
Het |
Col25a1 |
A |
G |
3: 130,389,324 (GRCm39) |
I636V |
probably benign |
Het |
Col9a3 |
C |
T |
2: 180,245,590 (GRCm39) |
P154S |
unknown |
Het |
Cyp3a11 |
T |
A |
5: 145,795,593 (GRCm39) |
M453L |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Eno1b |
T |
C |
18: 48,180,560 (GRCm39) |
V246A |
possibly damaging |
Het |
Eogt |
T |
C |
6: 97,092,965 (GRCm39) |
Y404C |
probably damaging |
Het |
Ephx3 |
T |
A |
17: 32,404,006 (GRCm39) |
E380V |
possibly damaging |
Het |
Fancl |
T |
C |
11: 26,357,615 (GRCm39) |
L114P |
probably damaging |
Het |
Flad1 |
C |
T |
3: 89,314,837 (GRCm39) |
G287S |
probably benign |
Het |
Gcm1 |
G |
T |
9: 77,967,061 (GRCm39) |
K93N |
probably damaging |
Het |
Golga3 |
T |
A |
5: 110,350,578 (GRCm39) |
D704E |
probably benign |
Het |
Grb14 |
A |
C |
2: 64,747,197 (GRCm39) |
I451S |
probably damaging |
Het |
Gtf3c3 |
T |
C |
1: 54,462,666 (GRCm39) |
N366D |
probably benign |
Het |
Hecw1 |
A |
T |
13: 14,486,356 (GRCm39) |
H376Q |
probably benign |
Het |
Helb |
A |
T |
10: 119,941,161 (GRCm39) |
V509E |
probably benign |
Het |
Hephl1 |
C |
T |
9: 14,981,111 (GRCm39) |
E774K |
probably damaging |
Het |
Hkdc1 |
T |
C |
10: 62,229,622 (GRCm39) |
E685G |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,894,519 (GRCm39) |
T2016A |
probably benign |
Het |
Igkv5-43 |
T |
G |
6: 69,800,515 (GRCm39) |
Q57H |
probably damaging |
Het |
Lamc3 |
T |
A |
2: 31,820,657 (GRCm39) |
V1224E |
probably damaging |
Het |
Lgals3bp |
C |
T |
11: 118,284,309 (GRCm39) |
W423* |
probably null |
Het |
Mcm9 |
G |
A |
10: 53,414,669 (GRCm39) |
T137I |
possibly damaging |
Het |
Mdga1 |
C |
A |
17: 30,061,816 (GRCm39) |
|
probably null |
Het |
Mocos |
C |
T |
18: 24,799,572 (GRCm39) |
P269S |
probably damaging |
Het |
Naa40 |
A |
G |
19: 7,207,322 (GRCm39) |
V134A |
probably damaging |
Het |
Neb |
G |
A |
2: 52,082,571 (GRCm39) |
L5680F |
probably damaging |
Het |
Nedd9 |
A |
G |
13: 41,492,099 (GRCm39) |
V137A |
probably benign |
Het |
Nup133 |
T |
C |
8: 124,642,112 (GRCm39) |
I784V |
probably benign |
Het |
Nup214 |
T |
C |
2: 31,915,256 (GRCm39) |
S1147P |
possibly damaging |
Het |
Or10x4 |
A |
T |
1: 174,218,805 (GRCm39) |
M57L |
probably damaging |
Het |
Or8g28 |
G |
T |
9: 39,169,897 (GRCm39) |
Q24K |
possibly damaging |
Het |
Plcb4 |
T |
A |
2: 135,824,043 (GRCm39) |
|
probably null |
Het |
Pomt1 |
C |
T |
2: 32,143,848 (GRCm39) |
T671I |
probably benign |
Het |
Pomt2 |
G |
T |
12: 87,157,150 (GRCm39) |
P723H |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,394,181 (GRCm39) |
Y1741* |
probably null |
Het |
Ptprs |
C |
G |
17: 56,758,697 (GRCm39) |
V175L |
probably benign |
Het |
Slc36a4 |
T |
C |
9: 15,633,250 (GRCm39) |
F95L |
probably benign |
Het |
Smn1 |
C |
T |
13: 100,267,648 (GRCm39) |
P225S |
probably benign |
Het |
Snrpa |
A |
T |
7: 26,891,174 (GRCm39) |
I99N |
probably benign |
Het |
Tgm5 |
G |
T |
2: 120,878,977 (GRCm39) |
Y588* |
probably null |
Het |
Tmeff2 |
T |
A |
1: 51,224,404 (GRCm39) |
|
probably null |
Het |
Tmem120b |
T |
C |
5: 123,254,741 (GRCm39) |
F314S |
probably damaging |
Het |
Trim43b |
C |
T |
9: 88,967,661 (GRCm39) |
R325H |
probably benign |
Het |
Vmn1r26 |
C |
T |
6: 57,985,755 (GRCm39) |
A145T |
probably benign |
Het |
Wdfy4 |
T |
C |
14: 32,693,531 (GRCm39) |
|
probably null |
Het |
Wnt5a |
C |
A |
14: 28,244,713 (GRCm39) |
T320K |
probably damaging |
Het |
Wrn |
AGCAGGTAATACATACCG |
AG |
8: 33,775,149 (GRCm39) |
|
probably null |
Het |
Zfp398 |
T |
C |
6: 47,842,910 (GRCm39) |
S321P |
probably benign |
Het |
Zfp959 |
T |
A |
17: 56,205,501 (GRCm39) |
C513S |
possibly damaging |
Het |
Zfr2 |
A |
G |
10: 81,080,559 (GRCm39) |
D411G |
probably damaging |
Het |
Zkscan5 |
T |
A |
5: 145,147,988 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cd79b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
hallasan
|
UTSW |
11 |
106,203,267 (GRCm39) |
critical splice acceptor site |
probably null |
|
Jeju
|
UTSW |
11 |
106,203,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R0070:Cd79b
|
UTSW |
11 |
106,202,744 (GRCm39) |
splice site |
probably benign |
|
R0070:Cd79b
|
UTSW |
11 |
106,202,744 (GRCm39) |
splice site |
probably benign |
|
R0731:Cd79b
|
UTSW |
11 |
106,203,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R4400:Cd79b
|
UTSW |
11 |
106,202,836 (GRCm39) |
nonsense |
probably null |
|
R4591:Cd79b
|
UTSW |
11 |
106,202,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R4948:Cd79b
|
UTSW |
11 |
106,203,687 (GRCm39) |
missense |
probably benign |
0.01 |
R6214:Cd79b
|
UTSW |
11 |
106,203,267 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6215:Cd79b
|
UTSW |
11 |
106,203,267 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6605:Cd79b
|
UTSW |
11 |
106,203,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Cd79b
|
UTSW |
11 |
106,205,365 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7401:Cd79b
|
UTSW |
11 |
106,203,678 (GRCm39) |
missense |
probably benign |
0.02 |
R8052:Cd79b
|
UTSW |
11 |
106,204,526 (GRCm39) |
missense |
probably damaging |
0.97 |
R8790:Cd79b
|
UTSW |
11 |
106,202,873 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8921:Cd79b
|
UTSW |
11 |
106,203,632 (GRCm39) |
missense |
probably benign |
0.07 |
R9717:Cd79b
|
UTSW |
11 |
106,202,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9753:Cd79b
|
UTSW |
11 |
106,203,457 (GRCm39) |
critical splice donor site |
probably null |
|
|