Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
G |
T |
8: 24,715,119 |
|
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,472,899 |
N3911S |
probably benign |
Het |
Alox12b |
C |
T |
11: 69,168,876 |
Q585* |
probably null |
Het |
Amtn |
A |
G |
5: 88,378,085 |
Q36R |
probably benign |
Het |
Arg2 |
G |
A |
12: 79,149,891 |
G129S |
probably damaging |
Het |
Arhgef28 |
A |
C |
13: 97,957,793 |
Y948D |
probably damaging |
Het |
Atp10b |
T |
C |
11: 43,247,477 |
V1195A |
probably benign |
Het |
Bet1l |
G |
T |
7: 140,854,610 |
T42K |
probably benign |
Het |
Cabin1 |
G |
A |
10: 75,733,628 |
T875I |
probably benign |
Het |
Ccdc17 |
A |
G |
4: 116,596,836 |
|
probably null |
Het |
Crebrf |
A |
G |
17: 26,771,319 |
E612G |
probably damaging |
Het |
Dgkz |
A |
G |
2: 91,940,859 |
S414P |
probably damaging |
Het |
Dock10 |
G |
T |
1: 80,568,834 |
H411N |
probably damaging |
Het |
Dpyd |
A |
T |
3: 119,195,134 |
T749S |
probably benign |
Het |
Dsc1 |
C |
T |
18: 20,086,644 |
|
probably null |
Het |
Echdc1 |
A |
T |
10: 29,322,280 |
M74L |
probably damaging |
Het |
Edn1 |
C |
A |
13: 42,305,023 |
T104K |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,311,901 |
T116S |
probably benign |
Het |
Fcrl5 |
A |
T |
3: 87,435,883 |
|
probably null |
Het |
Fpgt |
C |
T |
3: 155,087,122 |
G423R |
probably damaging |
Het |
Gprc5b |
A |
T |
7: 118,984,193 |
V151E |
probably damaging |
Het |
Grm5 |
A |
G |
7: 88,036,070 |
Y465C |
probably damaging |
Het |
Idh3b |
T |
A |
2: 130,284,401 |
N6I |
probably benign |
Het |
Ighmbp2 |
T |
C |
19: 3,273,022 |
K308R |
possibly damaging |
Het |
Lrch1 |
A |
T |
14: 74,835,762 |
S146T |
possibly damaging |
Het |
Lyl1 |
C |
T |
8: 84,702,671 |
P3L |
possibly damaging |
Het |
Mterf3 |
T |
C |
13: 66,930,157 |
K16R |
probably damaging |
Het |
Ncapg |
T |
A |
5: 45,695,668 |
H825Q |
probably damaging |
Het |
Olfr1095 |
A |
C |
2: 86,851,614 |
L28R |
possibly damaging |
Het |
Olfr1138 |
A |
T |
2: 87,738,118 |
S69T |
probably benign |
Het |
Olfr1392 |
T |
A |
11: 49,294,161 |
I280N |
probably damaging |
Het |
Olfr1443 |
G |
A |
19: 12,680,923 |
V272M |
possibly damaging |
Het |
Olfr31 |
G |
A |
14: 14,328,851 |
V247I |
probably damaging |
Het |
Olfr984 |
A |
G |
9: 40,100,734 |
V252A |
probably damaging |
Het |
Pald1 |
A |
T |
10: 61,347,105 |
M355K |
probably benign |
Het |
Phc1 |
A |
G |
6: 122,323,469 |
|
probably benign |
Het |
Phkb |
T |
A |
8: 86,018,466 |
|
probably benign |
Het |
Pkn3 |
G |
T |
2: 30,085,245 |
R506L |
probably damaging |
Het |
Plod2 |
T |
C |
9: 92,573,567 |
Y100H |
probably damaging |
Het |
Prl7b1 |
G |
T |
13: 27,606,935 |
Q56K |
probably benign |
Het |
Rhot1 |
T |
A |
11: 80,242,581 |
C229* |
probably null |
Het |
Sema3a |
G |
A |
5: 13,599,488 |
R735Q |
probably damaging |
Het |
Slc18b1 |
A |
G |
10: 23,826,659 |
*460W |
probably null |
Het |
Slco6c1 |
T |
A |
1: 97,066,023 |
|
probably benign |
Het |
Slu7 |
T |
A |
11: 43,442,630 |
V359D |
possibly damaging |
Het |
Suco |
T |
C |
1: 161,834,480 |
Y794C |
possibly damaging |
Het |
Sult3a2 |
T |
C |
10: 33,779,773 |
N70S |
probably benign |
Het |
Taar2 |
A |
T |
10: 23,941,297 |
D245V |
probably damaging |
Het |
Taf1d |
A |
G |
9: 15,309,941 |
H181R |
possibly damaging |
Het |
Tmem33 |
T |
C |
5: 67,263,796 |
S38P |
probably damaging |
Het |
Traf3ip1 |
T |
C |
1: 91,522,887 |
S519P |
probably benign |
Het |
Ttc12 |
T |
C |
9: 49,458,062 |
K253E |
possibly damaging |
Het |
|