Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
G |
A |
10: 78,924,147 (GRCm39) |
S103L |
possibly damaging |
Het |
Acvr2a |
G |
A |
2: 48,787,071 (GRCm39) |
A389T |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,784,001 (GRCm39) |
S1037P |
probably damaging |
Het |
Adcyap1 |
A |
G |
17: 93,511,446 (GRCm39) |
Y140C |
probably damaging |
Het |
Ampd3 |
A |
G |
7: 110,404,183 (GRCm39) |
N569S |
probably damaging |
Het |
Bin1 |
G |
T |
18: 32,510,511 (GRCm39) |
V18L |
probably benign |
Het |
Ccdc158 |
A |
G |
5: 92,814,620 (GRCm39) |
Y69H |
probably damaging |
Het |
Ccdc70 |
A |
G |
8: 22,463,611 (GRCm39) |
R134G |
possibly damaging |
Het |
Cmtm2a |
A |
G |
8: 105,019,286 (GRCm39) |
V101A |
probably damaging |
Het |
Edar |
T |
C |
10: 58,441,860 (GRCm39) |
|
probably benign |
Het |
Gcc2 |
T |
C |
10: 58,134,691 (GRCm39) |
|
probably benign |
Het |
Gm10961 |
A |
G |
3: 107,540,281 (GRCm39) |
|
probably benign |
Het |
Hsd3b3 |
T |
C |
3: 98,649,216 (GRCm39) |
D369G |
probably benign |
Het |
Khk |
C |
A |
5: 31,082,189 (GRCm39) |
H67N |
probably benign |
Het |
Kif7 |
T |
A |
7: 79,360,314 (GRCm39) |
|
probably null |
Het |
Mbd1 |
C |
T |
18: 74,402,614 (GRCm39) |
|
probably benign |
Het |
Mtor |
A |
G |
4: 148,556,494 (GRCm39) |
H968R |
probably damaging |
Het |
Nadk |
A |
G |
4: 155,673,157 (GRCm39) |
|
probably benign |
Het |
Or11g27 |
A |
G |
14: 50,771,618 (GRCm39) |
T250A |
probably benign |
Het |
Or2f1b |
A |
G |
6: 42,739,046 (GRCm39) |
D20G |
probably damaging |
Het |
Or5d40 |
A |
T |
2: 88,015,629 (GRCm39) |
H136L |
probably benign |
Het |
Otol1 |
T |
C |
3: 69,935,057 (GRCm39) |
F350L |
probably damaging |
Het |
Pramel22 |
T |
C |
4: 143,383,042 (GRCm39) |
N59S |
probably damaging |
Het |
Prkcg |
G |
A |
7: 3,352,342 (GRCm39) |
|
probably benign |
Het |
Rps6kc1 |
A |
T |
1: 190,505,837 (GRCm39) |
S1042T |
possibly damaging |
Het |
Rtn1 |
C |
T |
12: 72,263,709 (GRCm39) |
V741I |
possibly damaging |
Het |
Tor2a |
T |
A |
2: 32,650,595 (GRCm39) |
|
probably benign |
Het |
Vmn1r177 |
T |
C |
7: 23,565,688 (GRCm39) |
I63V |
probably benign |
Het |
Vmn2r58 |
T |
A |
7: 41,514,703 (GRCm39) |
I89F |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,343,849 (GRCm39) |
D2030G |
probably benign |
Het |
Zfp326 |
T |
C |
5: 106,036,451 (GRCm39) |
S121P |
probably damaging |
Het |
|
Other mutations in Ifi202b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02019:Ifi202b
|
APN |
1 |
173,802,550 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02466:Ifi202b
|
APN |
1 |
173,799,875 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02508:Ifi202b
|
APN |
1 |
173,802,338 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02567:Ifi202b
|
APN |
1 |
173,791,370 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02644:Ifi202b
|
APN |
1 |
173,799,280 (GRCm39) |
missense |
probably benign |
0.00 |
R0282:Ifi202b
|
UTSW |
1 |
173,804,926 (GRCm39) |
missense |
probably benign |
0.00 |
R1178:Ifi202b
|
UTSW |
1 |
173,799,788 (GRCm39) |
missense |
probably benign |
0.02 |
R3414:Ifi202b
|
UTSW |
1 |
173,791,479 (GRCm39) |
missense |
probably benign |
0.19 |
R5739:Ifi202b
|
UTSW |
1 |
173,798,918 (GRCm39) |
critical splice donor site |
probably null |
|
R5944:Ifi202b
|
UTSW |
1 |
173,791,365 (GRCm39) |
missense |
probably benign |
0.00 |
R6805:Ifi202b
|
UTSW |
1 |
173,802,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Ifi202b
|
UTSW |
1 |
173,791,524 (GRCm39) |
missense |
probably benign |
0.00 |
R7291:Ifi202b
|
UTSW |
1 |
173,802,381 (GRCm39) |
missense |
probably benign |
0.02 |
R7555:Ifi202b
|
UTSW |
1 |
173,799,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R7825:Ifi202b
|
UTSW |
1 |
173,802,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Ifi202b
|
UTSW |
1 |
173,804,923 (GRCm39) |
missense |
probably benign |
0.00 |
R8379:Ifi202b
|
UTSW |
1 |
173,802,298 (GRCm39) |
critical splice donor site |
probably null |
|
R8887:Ifi202b
|
UTSW |
1 |
173,802,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Ifi202b
|
UTSW |
1 |
173,804,949 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R9642:Ifi202b
|
UTSW |
1 |
173,799,850 (GRCm39) |
nonsense |
probably null |
|
|