Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
G |
T |
1: 179,580,361 (GRCm39) |
T1947K |
probably benign |
Het |
Ak9 |
A |
C |
10: 41,303,234 (GRCm39) |
K1669T |
unknown |
Het |
Atp4b |
T |
C |
8: 13,439,700 (GRCm39) |
E174G |
probably benign |
Het |
Bcl6 |
A |
G |
16: 23,787,203 (GRCm39) |
|
probably benign |
Het |
Brca2 |
C |
G |
5: 150,475,863 (GRCm39) |
|
probably null |
Het |
Btnl4 |
A |
T |
17: 34,689,075 (GRCm39) |
|
probably null |
Het |
C4a |
G |
T |
17: 35,036,075 (GRCm39) |
|
noncoding transcript |
Het |
Cab39l |
A |
G |
14: 59,737,054 (GRCm39) |
D58G |
probably benign |
Het |
Cacna2d3 |
A |
T |
14: 29,015,092 (GRCm39) |
M100K |
probably damaging |
Het |
Car2 |
T |
A |
3: 14,960,624 (GRCm39) |
Y127* |
probably null |
Het |
Cdhr1 |
T |
C |
14: 36,818,194 (GRCm39) |
N86S |
probably benign |
Het |
Celsr3 |
A |
G |
9: 108,704,953 (GRCm39) |
I479V |
possibly damaging |
Het |
Cfhr1 |
A |
T |
1: 139,478,667 (GRCm39) |
Y53* |
probably null |
Het |
Cimap3 |
C |
A |
3: 105,905,701 (GRCm39) |
G148C |
probably damaging |
Het |
Clcn7 |
A |
T |
17: 25,376,935 (GRCm39) |
H636L |
probably damaging |
Het |
Cox10 |
T |
G |
11: 63,867,277 (GRCm39) |
T240P |
possibly damaging |
Het |
Crybg2 |
CTTCCAGAGCCATGGACCCATCTTTTCCA |
CTTCCA |
4: 133,800,029 (GRCm39) |
|
probably null |
Het |
Dbt |
A |
G |
3: 116,326,963 (GRCm39) |
D104G |
probably damaging |
Het |
F730035P03Rik |
T |
C |
7: 99,429,425 (GRCm39) |
|
noncoding transcript |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam186b |
T |
C |
15: 99,178,771 (GRCm39) |
K185R |
probably benign |
Het |
Fat4 |
T |
C |
3: 38,941,491 (GRCm39) |
L128P |
probably damaging |
Het |
Gbf1 |
A |
T |
19: 46,268,989 (GRCm39) |
Q1381L |
probably benign |
Het |
Glp2r |
C |
T |
11: 67,621,453 (GRCm39) |
|
probably null |
Het |
Gm18025 |
A |
G |
12: 34,340,884 (GRCm39) |
S70P |
probably benign |
Het |
Gpr45 |
A |
G |
1: 43,072,068 (GRCm39) |
D237G |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,441,678 (GRCm39) |
L1213F |
possibly damaging |
Het |
Hydin |
T |
C |
8: 111,233,103 (GRCm39) |
V1734A |
possibly damaging |
Het |
Kcnh5 |
A |
T |
12: 75,054,397 (GRCm39) |
S516T |
probably benign |
Het |
Liph |
A |
C |
16: 21,802,777 (GRCm39) |
S97R |
probably benign |
Het |
Mtcl1 |
T |
C |
17: 66,756,139 (GRCm39) |
T68A |
unknown |
Het |
Nsun7 |
T |
A |
5: 66,418,542 (GRCm39) |
S91T |
probably benign |
Het |
Or5an10 |
T |
C |
19: 12,276,413 (GRCm39) |
T28A |
probably benign |
Het |
Or6c75 |
A |
G |
10: 129,337,433 (GRCm39) |
I227V |
probably damaging |
Het |
Pcdh20 |
A |
T |
14: 88,705,052 (GRCm39) |
N749K |
probably damaging |
Het |
Pot1b |
A |
T |
17: 55,961,831 (GRCm39) |
D582E |
probably benign |
Het |
Pxdn |
T |
C |
12: 30,062,325 (GRCm39) |
I1212T |
probably benign |
Het |
Ramp1 |
T |
C |
1: 91,124,511 (GRCm39) |
V24A |
probably benign |
Het |
S100a8 |
T |
A |
3: 90,576,890 (GRCm39) |
D14E |
probably benign |
Het |
Stk31 |
A |
G |
6: 49,414,369 (GRCm39) |
D501G |
probably benign |
Het |
Tbc1d19 |
G |
A |
5: 54,029,595 (GRCm39) |
V319M |
probably damaging |
Het |
Tbcel |
G |
T |
9: 42,361,268 (GRCm39) |
H93Q |
probably damaging |
Het |
Traf3ip2 |
C |
T |
10: 39,515,256 (GRCm39) |
P345S |
possibly damaging |
Het |
Trpm8 |
A |
T |
1: 88,312,427 (GRCm39) |
I1103F |
possibly damaging |
Het |
Ttc19 |
T |
A |
11: 62,199,917 (GRCm39) |
C112* |
probably null |
Het |
Unc5c |
T |
G |
3: 141,474,374 (GRCm39) |
|
probably null |
Het |
Urb1 |
A |
T |
16: 90,601,425 (GRCm39) |
H115Q |
probably damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,434,488 (GRCm39) |
I739F |
probably damaging |
Het |
Zcchc14 |
G |
T |
8: 122,335,339 (GRCm39) |
|
probably benign |
Het |
Zfp408 |
G |
A |
2: 91,476,131 (GRCm39) |
P341L |
probably damaging |
Het |
Zfp638 |
G |
A |
6: 83,958,719 (GRCm39) |
V1166M |
possibly damaging |
Het |
|
Other mutations in Cgrrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Cgrrf1
|
APN |
14 |
47,069,779 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02507:Cgrrf1
|
APN |
14 |
47,090,901 (GRCm39) |
nonsense |
probably null |
|
IGL03298:Cgrrf1
|
APN |
14 |
47,083,778 (GRCm39) |
missense |
probably benign |
0.08 |
R0152:Cgrrf1
|
UTSW |
14 |
47,091,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1477:Cgrrf1
|
UTSW |
14 |
47,090,895 (GRCm39) |
missense |
probably benign |
0.12 |
R2020:Cgrrf1
|
UTSW |
14 |
47,067,902 (GRCm39) |
unclassified |
probably benign |
|
R2107:Cgrrf1
|
UTSW |
14 |
47,090,833 (GRCm39) |
splice site |
probably benign |
|
R3010:Cgrrf1
|
UTSW |
14 |
47,091,223 (GRCm39) |
missense |
probably benign |
|
R3801:Cgrrf1
|
UTSW |
14 |
47,069,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Cgrrf1
|
UTSW |
14 |
47,069,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R4884:Cgrrf1
|
UTSW |
14 |
47,090,912 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6010:Cgrrf1
|
UTSW |
14 |
47,091,158 (GRCm39) |
missense |
probably damaging |
0.99 |
R6299:Cgrrf1
|
UTSW |
14 |
47,077,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Cgrrf1
|
UTSW |
14 |
47,069,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R6932:Cgrrf1
|
UTSW |
14 |
47,091,179 (GRCm39) |
missense |
probably benign |
0.09 |
R6986:Cgrrf1
|
UTSW |
14 |
47,069,586 (GRCm39) |
unclassified |
probably benign |
|
R7132:Cgrrf1
|
UTSW |
14 |
47,091,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7152:Cgrrf1
|
UTSW |
14 |
47,090,934 (GRCm39) |
nonsense |
probably null |
|
R7694:Cgrrf1
|
UTSW |
14 |
47,091,415 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8081:Cgrrf1
|
UTSW |
14 |
47,091,468 (GRCm39) |
missense |
probably benign |
0.03 |
R8158:Cgrrf1
|
UTSW |
14 |
47,091,192 (GRCm39) |
missense |
probably benign |
0.00 |
R9028:Cgrrf1
|
UTSW |
14 |
47,091,200 (GRCm39) |
missense |
probably benign |
0.01 |
R9430:Cgrrf1
|
UTSW |
14 |
47,091,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|