Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J11Rik |
A |
G |
9: 39,962,338 (GRCm39) |
|
noncoding transcript |
Het |
1700025H01Rik |
G |
T |
16: 30,018,801 (GRCm39) |
|
noncoding transcript |
Het |
9330159F19Rik |
T |
C |
10: 29,101,136 (GRCm39) |
V503A |
probably benign |
Het |
Acacb |
A |
G |
5: 114,347,914 (GRCm39) |
N995S |
possibly damaging |
Het |
Anapc4 |
A |
G |
5: 53,020,991 (GRCm39) |
K630R |
probably benign |
Het |
Ankrd13a |
A |
C |
5: 114,930,234 (GRCm39) |
Q206H |
probably damaging |
Het |
Ano10 |
A |
T |
9: 122,090,356 (GRCm39) |
L319Q |
probably damaging |
Het |
Camkk2 |
T |
A |
5: 122,884,398 (GRCm39) |
D341V |
probably damaging |
Het |
Ccdc88a |
A |
G |
11: 29,413,279 (GRCm39) |
I606V |
probably benign |
Het |
Cdv3 |
G |
T |
9: 103,242,316 (GRCm39) |
|
probably benign |
Het |
Cep97 |
A |
G |
16: 55,745,315 (GRCm39) |
V155A |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,228,476 (GRCm39) |
E2204G |
probably damaging |
Het |
Cracr2b |
A |
G |
7: 141,046,136 (GRCm39) |
*395W |
probably null |
Het |
Defa27 |
A |
G |
8: 21,805,710 (GRCm39) |
E50G |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,670,812 (GRCm39) |
I480T |
probably benign |
Het |
Ep400 |
C |
A |
5: 110,831,037 (GRCm39) |
D2210Y |
unknown |
Het |
Fam170a |
T |
A |
18: 50,413,618 (GRCm39) |
S28T |
probably benign |
Het |
Fancc |
C |
A |
13: 63,550,767 (GRCm39) |
K18N |
probably damaging |
Het |
Flt4 |
AC |
ACC |
11: 49,541,861 (GRCm39) |
|
probably null |
Het |
Fndc8 |
T |
G |
11: 82,788,676 (GRCm39) |
S169A |
possibly damaging |
Het |
Get3 |
A |
T |
8: 85,745,173 (GRCm39) |
I298N |
possibly damaging |
Het |
Herc1 |
T |
C |
9: 66,409,338 (GRCm39) |
Y4688H |
probably damaging |
Het |
Ighv11-2 |
A |
T |
12: 114,011,959 (GRCm39) |
D85E |
possibly damaging |
Het |
Kat14 |
T |
C |
2: 144,231,180 (GRCm39) |
F196L |
possibly damaging |
Het |
Kctd19 |
C |
T |
8: 106,109,617 (GRCm39) |
V942I |
probably benign |
Het |
Llgl1 |
A |
G |
11: 60,597,297 (GRCm39) |
S249G |
probably benign |
Het |
Map1a |
T |
C |
2: 121,130,153 (GRCm39) |
V323A |
probably damaging |
Het |
Or4m1 |
C |
A |
14: 50,557,566 (GRCm39) |
C242F |
probably damaging |
Het |
Phf21a |
C |
A |
2: 92,182,097 (GRCm39) |
T342K |
possibly damaging |
Het |
Piezo2 |
T |
A |
18: 63,217,811 (GRCm39) |
D1122V |
possibly damaging |
Het |
Pklr |
A |
G |
3: 89,049,173 (GRCm39) |
Y173C |
probably damaging |
Het |
Plcz1 |
G |
T |
6: 139,938,778 (GRCm39) |
|
probably null |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Prom1 |
A |
T |
5: 44,158,147 (GRCm39) |
Y845N |
probably damaging |
Het |
Ret |
A |
T |
6: 118,158,936 (GRCm39) |
S159T |
probably benign |
Het |
Rfx1 |
C |
A |
8: 84,793,005 (GRCm39) |
|
probably null |
Het |
Scp2 |
A |
T |
4: 108,001,976 (GRCm39) |
|
probably null |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Smad5 |
T |
C |
13: 56,875,282 (GRCm39) |
F157L |
probably benign |
Het |
Smarcc2 |
C |
A |
10: 128,301,373 (GRCm39) |
D210E |
probably damaging |
Het |
Sptlc3 |
T |
C |
2: 139,478,643 (GRCm39) |
L534P |
possibly damaging |
Het |
Srrm1 |
A |
G |
4: 135,051,380 (GRCm39) |
|
probably benign |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Het |
Sugct |
T |
A |
13: 17,032,455 (GRCm39) |
Q432H |
probably damaging |
Het |
Tex9 |
A |
T |
9: 72,394,060 (GRCm39) |
|
probably null |
Het |
Tsc1 |
C |
A |
2: 28,576,920 (GRCm39) |
S1073* |
probably null |
Het |
Vmn1r72 |
T |
C |
7: 11,403,843 (GRCm39) |
S202G |
probably damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,385,871 (GRCm39) |
V703A |
probably benign |
Het |
Vmn2r67 |
A |
T |
7: 84,785,765 (GRCm39) |
Y747N |
probably damaging |
Het |
Zcchc4 |
A |
G |
5: 52,964,419 (GRCm39) |
I292V |
probably benign |
Het |
Zfp998 |
T |
C |
13: 66,579,722 (GRCm39) |
R254G |
probably benign |
Het |
Zswim2 |
C |
T |
2: 83,755,589 (GRCm39) |
G104E |
possibly damaging |
Het |
|
Other mutations in Qng1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Qng1
|
APN |
13 |
58,529,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02302:Qng1
|
APN |
13 |
58,529,749 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Qng1
|
UTSW |
13 |
58,532,827 (GRCm39) |
nonsense |
probably null |
|
R0055:Qng1
|
UTSW |
13 |
58,531,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Qng1
|
UTSW |
13 |
58,531,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R2874:Qng1
|
UTSW |
13 |
58,530,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R3954:Qng1
|
UTSW |
13 |
58,532,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R3956:Qng1
|
UTSW |
13 |
58,532,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R4012:Qng1
|
UTSW |
13 |
58,529,800 (GRCm39) |
nonsense |
probably null |
|
R4212:Qng1
|
UTSW |
13 |
58,529,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Qng1
|
UTSW |
13 |
58,530,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R4712:Qng1
|
UTSW |
13 |
58,529,617 (GRCm39) |
missense |
probably benign |
0.06 |
R6876:Qng1
|
UTSW |
13 |
58,532,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R6957:Qng1
|
UTSW |
13 |
58,529,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7285:Qng1
|
UTSW |
13 |
58,532,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R7599:Qng1
|
UTSW |
13 |
58,529,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R8553:Qng1
|
UTSW |
13 |
58,532,694 (GRCm39) |
missense |
probably damaging |
0.96 |
R8939:Qng1
|
UTSW |
13 |
58,532,875 (GRCm39) |
missense |
probably damaging |
1.00 |
|