Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
A |
1: 156,642,069 (GRCm38) |
S968T |
probably benign |
Het |
Adcy8 |
T |
C |
15: 64,783,806 (GRCm38) |
D608G |
probably benign |
Het |
Adgb |
C |
T |
10: 10,378,734 (GRCm38) |
V1162M |
probably benign |
Het |
Agrn |
A |
G |
4: 156,173,889 (GRCm38) |
V1040A |
probably benign |
Het |
Amer3 |
A |
T |
1: 34,587,660 (GRCm38) |
T327S |
possibly damaging |
Het |
Apaf1 |
C |
T |
10: 91,059,658 (GRCm38) |
C426Y |
probably benign |
Het |
Bsn |
T |
C |
9: 108,110,033 (GRCm38) |
D2840G |
unknown |
Het |
Camsap1 |
A |
T |
2: 25,944,428 (GRCm38) |
C406* |
probably null |
Het |
Cbr2 |
A |
T |
11: 120,730,297 (GRCm38) |
M158K |
probably damaging |
Het |
Clnk |
C |
A |
5: 38,794,911 (GRCm38) |
|
probably null |
Het |
Csad |
T |
C |
15: 102,177,762 (GRCm38) |
M445V |
probably damaging |
Het |
Dnajb7 |
T |
A |
15: 81,407,399 (GRCm38) |
N246Y |
probably damaging |
Het |
Dok6 |
T |
C |
18: 89,473,947 (GRCm38) |
I169V |
probably benign |
Het |
H2bc14 |
T |
C |
13: 21,722,461 (GRCm38) |
Y122H |
probably benign |
Het |
Il1f10 |
T |
G |
2: 24,291,255 (GRCm38) |
I11R |
possibly damaging |
Het |
Irs1 |
C |
T |
1: 82,289,533 (GRCm38) |
V321M |
probably damaging |
Het |
Itga9 |
T |
C |
9: 118,877,143 (GRCm38) |
F938L |
probably damaging |
Het |
Kif7 |
T |
C |
7: 79,704,694 (GRCm38) |
D781G |
probably damaging |
Het |
Klhl41 |
A |
T |
2: 69,671,161 (GRCm38) |
N322I |
probably damaging |
Het |
Krtap31-1 |
T |
G |
11: 99,908,075 (GRCm38) |
C35G |
possibly damaging |
Het |
Lsm11 |
A |
T |
11: 45,933,997 (GRCm38) |
D234E |
probably benign |
Het |
Med6 |
T |
C |
12: 81,573,903 (GRCm38) |
K223R |
probably benign |
Het |
Mfsd4b2 |
G |
A |
10: 39,922,068 (GRCm38) |
T97I |
probably benign |
Het |
Mrgpra1 |
A |
T |
7: 47,335,456 (GRCm38) |
C158* |
probably null |
Het |
Nr2e1 |
T |
C |
10: 42,582,885 (GRCm38) |
T8A |
probably benign |
Het |
Oas2 |
T |
C |
5: 120,749,773 (GRCm38) |
M1V |
probably null |
Het |
Or13a27 |
T |
C |
7: 140,345,249 (GRCm38) |
I247V |
probably benign |
Het |
Or14a260 |
T |
A |
7: 86,335,677 (GRCm38) |
I240F |
probably benign |
Het |
Or1e33 |
T |
A |
11: 73,847,871 (GRCm38) |
M85L |
probably benign |
Het |
Or8k17 |
T |
C |
2: 86,236,160 (GRCm38) |
Y218C |
probably damaging |
Het |
Or8w1 |
T |
A |
2: 87,634,889 (GRCm38) |
N286I |
probably damaging |
Het |
Otof |
C |
T |
5: 30,380,194 (GRCm38) |
G1257D |
probably benign |
Het |
Phf2 |
T |
C |
13: 48,817,760 (GRCm38) |
T479A |
probably benign |
Het |
Pik3c2a |
T |
C |
7: 116,342,997 (GRCm38) |
N1516S |
probably benign |
Het |
Qrich1 |
C |
A |
9: 108,556,037 (GRCm38) |
T622K |
probably damaging |
Het |
Rasip1 |
A |
G |
7: 45,632,519 (GRCm38) |
K482R |
probably damaging |
Het |
Rgl2 |
T |
C |
17: 33,936,944 (GRCm38) |
F698L |
probably benign |
Het |
Scarb1 |
T |
C |
5: 125,303,137 (GRCm38) |
D124G |
probably benign |
Het |
Sclt1 |
A |
G |
3: 41,671,482 (GRCm38) |
I350T |
probably benign |
Het |
Sec23ip |
T |
G |
7: 128,767,640 (GRCm38) |
V696G |
probably damaging |
Het |
Serpina1e |
G |
T |
12: 103,951,095 (GRCm38) |
T105K |
probably benign |
Het |
Sin3a |
A |
G |
9: 57,113,544 (GRCm38) |
|
probably null |
Het |
Slc34a2 |
A |
G |
5: 53,060,840 (GRCm38) |
T154A |
probably damaging |
Het |
Slc9a3 |
T |
C |
13: 74,155,122 (GRCm38) |
L178P |
probably damaging |
Het |
Smarca2 |
A |
C |
19: 26,682,048 (GRCm38) |
I913L |
probably benign |
Het |
Spaca7b |
T |
A |
8: 11,665,056 (GRCm38) |
D46V |
probably damaging |
Het |
Tcea3 |
G |
A |
4: 136,273,716 (GRCm38) |
|
probably null |
Het |
Tektl1 |
G |
C |
10: 78,748,675 (GRCm38) |
Q338E |
probably benign |
Het |
Tmcc1 |
T |
A |
6: 116,043,474 (GRCm38) |
H339L |
|
Het |
Trpm2 |
G |
T |
10: 77,947,897 (GRCm38) |
H247Q |
probably damaging |
Het |
Tyr |
T |
A |
7: 87,472,516 (GRCm38) |
D356V |
probably damaging |
Het |
Vmn2r54 |
A |
T |
7: 12,615,961 (GRCm38) |
C565S |
probably damaging |
Het |
Vmn2r82 |
A |
C |
10: 79,377,802 (GRCm38) |
N74T |
probably benign |
Het |
Zcchc4 |
T |
C |
5: 52,815,918 (GRCm38) |
Y375H |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 108,948,721 (GRCm38) |
D2134E |
possibly damaging |
Het |
Zfhx4 |
T |
A |
3: 5,398,950 (GRCm38) |
Y1414* |
probably null |
Het |
Zfp282 |
A |
T |
6: 47,890,692 (GRCm38) |
E267D |
possibly damaging |
Het |
Zfp442 |
A |
T |
2: 150,409,176 (GRCm38) |
C269S |
possibly damaging |
Het |
Zp3 |
T |
A |
5: 135,985,564 (GRCm38) |
S246T |
probably benign |
Het |
|
Other mutations in Cgrrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Cgrrf1
|
APN |
14 |
46,832,322 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02507:Cgrrf1
|
APN |
14 |
46,853,444 (GRCm38) |
nonsense |
probably null |
|
IGL03298:Cgrrf1
|
APN |
14 |
46,846,321 (GRCm38) |
missense |
probably benign |
0.08 |
R0152:Cgrrf1
|
UTSW |
14 |
46,853,913 (GRCm38) |
missense |
probably damaging |
1.00 |
R1477:Cgrrf1
|
UTSW |
14 |
46,853,438 (GRCm38) |
missense |
probably benign |
0.12 |
R2020:Cgrrf1
|
UTSW |
14 |
46,830,445 (GRCm38) |
unclassified |
probably benign |
|
R2107:Cgrrf1
|
UTSW |
14 |
46,853,376 (GRCm38) |
splice site |
probably benign |
|
R3010:Cgrrf1
|
UTSW |
14 |
46,853,766 (GRCm38) |
missense |
probably benign |
|
R3801:Cgrrf1
|
UTSW |
14 |
46,832,363 (GRCm38) |
missense |
probably damaging |
1.00 |
R4296:Cgrrf1
|
UTSW |
14 |
46,832,355 (GRCm38) |
missense |
probably damaging |
0.99 |
R4681:Cgrrf1
|
UTSW |
14 |
46,853,826 (GRCm38) |
missense |
probably benign |
0.00 |
R4884:Cgrrf1
|
UTSW |
14 |
46,853,455 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6010:Cgrrf1
|
UTSW |
14 |
46,853,701 (GRCm38) |
missense |
probably damaging |
0.99 |
R6299:Cgrrf1
|
UTSW |
14 |
46,840,190 (GRCm38) |
missense |
probably damaging |
1.00 |
R6861:Cgrrf1
|
UTSW |
14 |
46,832,328 (GRCm38) |
missense |
probably damaging |
1.00 |
R6932:Cgrrf1
|
UTSW |
14 |
46,853,722 (GRCm38) |
missense |
probably benign |
0.09 |
R6986:Cgrrf1
|
UTSW |
14 |
46,832,129 (GRCm38) |
unclassified |
probably benign |
|
R7132:Cgrrf1
|
UTSW |
14 |
46,853,864 (GRCm38) |
missense |
probably damaging |
1.00 |
R7152:Cgrrf1
|
UTSW |
14 |
46,853,477 (GRCm38) |
nonsense |
probably null |
|
R7694:Cgrrf1
|
UTSW |
14 |
46,853,958 (GRCm38) |
missense |
possibly damaging |
0.79 |
R8081:Cgrrf1
|
UTSW |
14 |
46,854,011 (GRCm38) |
missense |
probably benign |
0.03 |
R9028:Cgrrf1
|
UTSW |
14 |
46,853,743 (GRCm38) |
missense |
probably benign |
0.01 |
R9430:Cgrrf1
|
UTSW |
14 |
46,853,874 (GRCm38) |
missense |
probably damaging |
1.00 |
|