Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025G04Rik |
A |
T |
1: 151,856,266 (GRCm39) |
Y34N |
probably damaging |
Het |
A2m |
T |
C |
6: 121,618,966 (GRCm39) |
V237A |
probably damaging |
Het |
A2m |
A |
T |
6: 121,647,895 (GRCm39) |
D1129V |
possibly damaging |
Het |
Aadacl2fm3 |
T |
C |
3: 59,784,697 (GRCm39) |
I390T |
probably benign |
Het |
Abca7 |
A |
G |
10: 79,833,846 (GRCm39) |
|
probably null |
Het |
Adam34l |
C |
T |
8: 44,079,703 (GRCm39) |
G174R |
probably damaging |
Het |
Ap3m2 |
T |
C |
8: 23,282,770 (GRCm39) |
N256S |
probably benign |
Het |
Atr |
C |
T |
9: 95,789,436 (GRCm39) |
H1531Y |
possibly damaging |
Het |
Carmil3 |
C |
T |
14: 55,738,965 (GRCm39) |
A873V |
probably null |
Het |
Casp8 |
A |
C |
1: 58,872,898 (GRCm39) |
K258T |
probably benign |
Het |
Cast |
A |
G |
13: 74,885,084 (GRCm39) |
S222P |
probably benign |
Het |
Cpsf7 |
C |
T |
19: 10,512,737 (GRCm39) |
P274S |
probably damaging |
Het |
Ddx24 |
A |
T |
12: 103,382,519 (GRCm39) |
L688* |
probably null |
Het |
Ddx59 |
A |
G |
1: 136,361,559 (GRCm39) |
I475V |
probably benign |
Het |
Dhx29 |
T |
A |
13: 113,081,093 (GRCm39) |
S376T |
possibly damaging |
Het |
Dhx57 |
G |
T |
17: 80,582,290 (GRCm39) |
N438K |
probably benign |
Het |
Dlk1 |
T |
A |
12: 109,421,551 (GRCm39) |
|
probably null |
Het |
Efcab15 |
T |
C |
11: 103,091,004 (GRCm39) |
M114V |
probably benign |
Het |
Epha6 |
T |
C |
16: 59,595,931 (GRCm39) |
D920G |
probably damaging |
Het |
Exo5 |
A |
T |
4: 120,778,818 (GRCm39) |
V349E |
probably benign |
Het |
Fam234b |
T |
C |
6: 135,202,241 (GRCm39) |
V321A |
possibly damaging |
Het |
Gbp3 |
A |
G |
3: 142,274,822 (GRCm39) |
E383G |
probably benign |
Het |
Gga2 |
T |
C |
7: 121,596,553 (GRCm39) |
N408S |
probably benign |
Het |
Gse1 |
T |
C |
8: 121,296,043 (GRCm39) |
V532A |
unknown |
Het |
Hnrnpul2 |
T |
C |
19: 8,808,673 (GRCm39) |
Y712H |
probably damaging |
Het |
Hpca |
T |
C |
4: 129,014,019 (GRCm39) |
|
probably benign |
Het |
Ifitm3 |
A |
G |
7: 140,590,372 (GRCm39) |
F63L |
probably damaging |
Het |
Kank1 |
A |
T |
19: 25,399,525 (GRCm39) |
T940S |
probably benign |
Het |
Klhl9 |
C |
A |
4: 88,640,646 (GRCm39) |
|
probably benign |
Het |
Krt36 |
T |
C |
11: 99,993,786 (GRCm39) |
M351V |
probably benign |
Het |
Mthfd2 |
T |
C |
6: 83,288,830 (GRCm39) |
N125D |
probably benign |
Het |
Muc4 |
C |
G |
16: 32,575,221 (GRCm39) |
Q1269E |
probably benign |
Het |
Ncoa2 |
A |
G |
1: 13,247,350 (GRCm39) |
S358P |
possibly damaging |
Het |
Nmnat1 |
T |
C |
4: 149,557,808 (GRCm39) |
H78R |
probably benign |
Het |
Or10s1 |
T |
G |
9: 39,986,455 (GRCm39) |
L288R |
probably damaging |
Het |
Or5k1 |
T |
C |
16: 58,617,343 (GRCm39) |
I289V |
possibly damaging |
Het |
Or5m13b |
A |
T |
2: 85,754,146 (GRCm39) |
Y178F |
probably damaging |
Het |
Or9r3 |
A |
G |
10: 129,948,179 (GRCm39) |
M160T |
probably benign |
Het |
Pabpc4 |
A |
T |
4: 123,186,685 (GRCm39) |
D302V |
possibly damaging |
Het |
Pgap1 |
A |
T |
1: 54,582,345 (GRCm39) |
S167R |
probably damaging |
Het |
Phf12 |
T |
C |
11: 77,914,109 (GRCm39) |
L517P |
probably benign |
Het |
Rcan2 |
A |
G |
17: 44,328,689 (GRCm39) |
D86G |
probably benign |
Het |
Ryk |
T |
C |
9: 102,775,715 (GRCm39) |
Y442H |
probably damaging |
Het |
Scfd2 |
G |
T |
5: 74,623,271 (GRCm39) |
Q421K |
probably benign |
Het |
Sirpa |
G |
T |
2: 129,451,072 (GRCm39) |
V111F |
probably damaging |
Het |
Skint4 |
A |
T |
4: 111,975,468 (GRCm39) |
T143S |
possibly damaging |
Het |
Slc12a8 |
C |
A |
16: 33,445,494 (GRCm39) |
H463N |
probably benign |
Het |
Sp110 |
G |
A |
1: 85,506,813 (GRCm39) |
R417C |
probably benign |
Het |
Sptlc2 |
A |
G |
12: 87,388,463 (GRCm39) |
Y340H |
probably damaging |
Het |
Ssc5d |
T |
A |
7: 4,945,745 (GRCm39) |
W926R |
possibly damaging |
Het |
Tgfa |
A |
G |
6: 86,246,944 (GRCm39) |
E82G |
probably damaging |
Het |
Thrsp |
A |
G |
7: 97,066,514 (GRCm39) |
I66T |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,681,988 (GRCm39) |
E1003G |
unknown |
Het |
Tube1 |
A |
T |
10: 39,018,262 (GRCm39) |
H113L |
probably benign |
Het |
Uri1 |
A |
G |
7: 37,681,053 (GRCm39) |
V117A |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,380,606 (GRCm39) |
C2305Y |
probably damaging |
Het |
Zbtb7a |
T |
G |
10: 80,980,010 (GRCm39) |
V68G |
probably damaging |
Het |
Zfr |
T |
A |
15: 12,159,763 (GRCm39) |
D686E |
possibly damaging |
Het |
Zscan4f |
G |
A |
7: 11,135,308 (GRCm39) |
S238N |
possibly damaging |
Het |
|
Other mutations in Inava |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:Inava
|
APN |
1 |
136,147,513 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02466:Inava
|
APN |
1 |
136,144,173 (GRCm39) |
splice site |
probably null |
|
IGL03408:Inava
|
APN |
1 |
136,142,143 (GRCm39) |
missense |
probably benign |
|
R0053:Inava
|
UTSW |
1 |
136,155,288 (GRCm39) |
missense |
probably benign |
0.01 |
R0053:Inava
|
UTSW |
1 |
136,155,288 (GRCm39) |
missense |
probably benign |
0.01 |
R0632:Inava
|
UTSW |
1 |
136,155,356 (GRCm39) |
missense |
probably benign |
0.06 |
R1218:Inava
|
UTSW |
1 |
136,142,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R1611:Inava
|
UTSW |
1 |
136,143,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R3618:Inava
|
UTSW |
1 |
136,142,110 (GRCm39) |
missense |
probably benign |
0.11 |
R4256:Inava
|
UTSW |
1 |
136,142,088 (GRCm39) |
missense |
probably benign |
0.00 |
R4348:Inava
|
UTSW |
1 |
136,153,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Inava
|
UTSW |
1 |
136,153,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Inava
|
UTSW |
1 |
136,153,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R5343:Inava
|
UTSW |
1 |
136,153,180 (GRCm39) |
missense |
probably benign |
0.01 |
R6296:Inava
|
UTSW |
1 |
136,148,809 (GRCm39) |
critical splice donor site |
probably null |
|
R6597:Inava
|
UTSW |
1 |
136,153,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:Inava
|
UTSW |
1 |
136,147,894 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7060:Inava
|
UTSW |
1 |
136,147,935 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7503:Inava
|
UTSW |
1 |
136,143,675 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7527:Inava
|
UTSW |
1 |
136,142,122 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7675:Inava
|
UTSW |
1 |
136,143,741 (GRCm39) |
missense |
probably benign |
0.04 |
R7756:Inava
|
UTSW |
1 |
136,144,171 (GRCm39) |
missense |
probably benign |
0.01 |
R7912:Inava
|
UTSW |
1 |
136,155,279 (GRCm39) |
missense |
probably benign |
0.03 |
R8261:Inava
|
UTSW |
1 |
136,153,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Inava
|
UTSW |
1 |
136,155,348 (GRCm39) |
missense |
probably benign |
|
X0017:Inava
|
UTSW |
1 |
136,147,920 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Inava
|
UTSW |
1 |
136,147,521 (GRCm39) |
missense |
possibly damaging |
0.77 |
|