Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
T |
G |
14: 29,700,538 (GRCm39) |
L39R |
possibly damaging |
Het |
Amer3 |
T |
C |
1: 34,626,771 (GRCm39) |
S337P |
probably damaging |
Het |
Arhgef10l |
A |
T |
4: 140,344,226 (GRCm39) |
I12K |
probably damaging |
Het |
Atp2b4 |
A |
G |
1: 133,657,618 (GRCm39) |
V624A |
possibly damaging |
Het |
Bod1l |
A |
G |
5: 41,978,425 (GRCm39) |
V963A |
probably benign |
Het |
Bpifa6 |
T |
C |
2: 153,832,354 (GRCm39) |
L287S |
probably benign |
Het |
Bsnd |
A |
T |
4: 106,345,212 (GRCm39) |
L78Q |
probably damaging |
Het |
C1qtnf3 |
T |
C |
15: 10,958,156 (GRCm39) |
|
probably null |
Het |
Ccdc180 |
T |
G |
4: 45,921,950 (GRCm39) |
V1008G |
probably benign |
Het |
Ccl1 |
T |
G |
11: 82,068,860 (GRCm39) |
D59A |
possibly damaging |
Het |
Cfap58 |
T |
C |
19: 47,971,891 (GRCm39) |
I607T |
probably benign |
Het |
Chd1l |
G |
A |
3: 97,494,483 (GRCm39) |
A399V |
probably damaging |
Het |
Cntnap4 |
C |
T |
8: 113,484,105 (GRCm39) |
P386L |
possibly damaging |
Het |
Col1a1 |
G |
A |
11: 94,833,444 (GRCm39) |
|
probably null |
Het |
Dnajc13 |
A |
T |
9: 104,085,003 (GRCm39) |
D798E |
probably damaging |
Het |
Eml6 |
T |
G |
11: 29,699,875 (GRCm39) |
I1754L |
probably benign |
Het |
Ercc8 |
T |
A |
13: 108,320,344 (GRCm39) |
V310D |
probably damaging |
Het |
Fat2 |
G |
A |
11: 55,187,171 (GRCm39) |
T1225I |
probably damaging |
Het |
Gba1 |
A |
G |
3: 89,115,910 (GRCm39) |
Y510C |
probably damaging |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Gm43302 |
T |
A |
5: 105,423,726 (GRCm39) |
M416L |
probably benign |
Het |
Grxcr2 |
A |
T |
18: 42,124,955 (GRCm39) |
V151E |
probably benign |
Het |
Gtf2ird2 |
A |
G |
5: 134,240,066 (GRCm39) |
N296S |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,355,811 (GRCm39) |
I2354N |
possibly damaging |
Het |
Inhbc |
G |
A |
10: 127,193,309 (GRCm39) |
R236* |
probably null |
Het |
Itpr2 |
T |
C |
6: 146,013,975 (GRCm39) |
D2607G |
possibly damaging |
Het |
Kcnh7 |
T |
A |
2: 62,676,118 (GRCm39) |
D298V |
probably benign |
Het |
Klrb1c |
A |
G |
6: 128,761,148 (GRCm39) |
S160P |
probably benign |
Het |
Mrgpra2a |
C |
G |
7: 47,076,437 (GRCm39) |
E274Q |
probably benign |
Het |
Muc5ac |
T |
A |
7: 141,356,591 (GRCm39) |
F1059L |
probably benign |
Het |
Naglu |
T |
C |
11: 100,962,007 (GRCm39) |
I160T |
probably damaging |
Het |
Nasp |
A |
T |
4: 116,476,145 (GRCm39) |
L47Q |
probably damaging |
Het |
Opa1 |
C |
T |
16: 29,447,525 (GRCm39) |
T873I |
possibly damaging |
Het |
Or10a3n |
C |
T |
7: 108,493,318 (GRCm39) |
V99M |
possibly damaging |
Het |
Or52x1 |
T |
C |
7: 104,853,500 (GRCm39) |
T17A |
probably benign |
Het |
Or8u10 |
C |
A |
2: 85,915,784 (GRCm39) |
M112I |
probably benign |
Het |
Pttg1 |
A |
G |
11: 43,315,671 (GRCm39) |
F48L |
probably damaging |
Het |
Rho |
T |
C |
6: 115,909,218 (GRCm39) |
F85L |
possibly damaging |
Het |
Rnasel |
T |
C |
1: 153,630,432 (GRCm39) |
V316A |
probably benign |
Het |
Slc36a3 |
A |
G |
11: 55,026,089 (GRCm39) |
I243T |
probably benign |
Het |
Tada2b |
G |
A |
5: 36,634,029 (GRCm39) |
T183M |
possibly damaging |
Het |
Tbc1d22a |
A |
G |
15: 86,185,768 (GRCm39) |
M286V |
possibly damaging |
Het |
Trim69 |
G |
T |
2: 121,998,081 (GRCm39) |
E18* |
probably null |
Het |
Ttn |
T |
C |
2: 76,772,394 (GRCm39) |
T2503A |
possibly damaging |
Het |
Uox |
C |
T |
3: 146,330,332 (GRCm39) |
R163* |
probably null |
Het |
Zfp654 |
T |
A |
16: 64,612,310 (GRCm39) |
N192I |
possibly damaging |
Het |
Zfp809 |
G |
A |
9: 22,147,540 (GRCm39) |
R58H |
probably benign |
Het |
|
Other mutations in BB014433 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:BB014433
|
APN |
8 |
15,092,510 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01595:BB014433
|
APN |
8 |
15,092,499 (GRCm39) |
splice site |
probably null |
|
IGL02056:BB014433
|
APN |
8 |
15,092,435 (GRCm39) |
nonsense |
probably null |
|
IGL02470:BB014433
|
APN |
8 |
15,092,803 (GRCm39) |
missense |
unknown |
|
R0359:BB014433
|
UTSW |
8 |
15,092,540 (GRCm39) |
nonsense |
probably null |
|
R1066:BB014433
|
UTSW |
8 |
15,092,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R1837:BB014433
|
UTSW |
8 |
15,092,629 (GRCm39) |
missense |
unknown |
|
R1838:BB014433
|
UTSW |
8 |
15,092,629 (GRCm39) |
missense |
unknown |
|
R2227:BB014433
|
UTSW |
8 |
15,091,717 (GRCm39) |
missense |
probably benign |
0.34 |
R4508:BB014433
|
UTSW |
8 |
15,092,095 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4882:BB014433
|
UTSW |
8 |
15,092,016 (GRCm39) |
missense |
probably benign |
0.05 |
R4996:BB014433
|
UTSW |
8 |
15,092,166 (GRCm39) |
missense |
probably benign |
0.10 |
R5988:BB014433
|
UTSW |
8 |
15,091,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:BB014433
|
UTSW |
8 |
15,092,179 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6505:BB014433
|
UTSW |
8 |
15,092,304 (GRCm39) |
missense |
probably benign |
0.10 |
R7237:BB014433
|
UTSW |
8 |
15,091,765 (GRCm39) |
missense |
probably benign |
0.13 |
R7771:BB014433
|
UTSW |
8 |
15,092,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7847:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R7859:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R8377:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R8560:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R8993:BB014433
|
UTSW |
8 |
15,092,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:BB014433
|
UTSW |
8 |
15,092,623 (GRCm39) |
missense |
unknown |
|
R9446:BB014433
|
UTSW |
8 |
15,091,810 (GRCm39) |
small deletion |
probably benign |
|
R9542:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
X0066:BB014433
|
UTSW |
8 |
15,092,833 (GRCm39) |
missense |
unknown |
|
|