Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
G |
T |
4: 129,992,132 |
D22Y |
probably damaging |
Het |
Ak7 |
T |
C |
12: 105,734,924 |
V242A |
probably benign |
Het |
Cacna1b |
T |
C |
2: 24,661,757 |
N1127S |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,971,569 |
H267L |
probably benign |
Het |
Ces1b |
C |
T |
8: 93,079,431 |
G61R |
probably damaging |
Het |
Cgnl1 |
T |
A |
9: 71,725,004 |
D355V |
probably damaging |
Het |
Col24a1 |
T |
C |
3: 145,315,244 |
S459P |
probably damaging |
Het |
Crygd |
T |
C |
1: 65,062,026 |
T137A |
probably benign |
Het |
Dctn4 |
T |
A |
18: 60,544,130 |
M174K |
probably benign |
Het |
Evi5 |
A |
G |
5: 107,816,924 |
|
probably benign |
Het |
Fat2 |
T |
G |
11: 55,283,980 |
D1969A |
probably benign |
Het |
Fcrl5 |
A |
T |
3: 87,446,299 |
E317V |
probably damaging |
Het |
Foxf2 |
G |
T |
13: 31,626,714 |
S212I |
probably damaging |
Het |
Gm21759 |
T |
A |
5: 8,180,685 |
|
probably benign |
Het |
Gm5414 |
A |
G |
15: 101,625,670 |
|
probably benign |
Het |
Gm7275 |
T |
C |
16: 48,073,583 |
|
noncoding transcript |
Het |
Hspa9 |
T |
C |
18: 34,938,708 |
E613G |
possibly damaging |
Het |
Il1rl1 |
A |
G |
1: 40,462,008 |
I515V |
possibly damaging |
Het |
Ins1 |
G |
T |
19: 52,264,735 |
A38S |
probably damaging |
Het |
Klhl31 |
A |
G |
9: 77,655,206 |
N418D |
probably benign |
Het |
Magi3 |
T |
C |
3: 104,054,462 |
K417E |
probably damaging |
Het |
Msh4 |
A |
G |
3: 153,857,589 |
Y823H |
probably damaging |
Het |
Myo6 |
T |
A |
9: 80,260,818 |
D421E |
probably damaging |
Het |
Myom3 |
T |
C |
4: 135,765,589 |
S150P |
possibly damaging |
Het |
Nectin1 |
C |
T |
9: 43,792,574 |
|
probably benign |
Het |
Nkx1-2 |
A |
T |
7: 132,599,474 |
I18N |
probably damaging |
Het |
Olfr1006 |
T |
C |
2: 85,674,941 |
D70G |
probably damaging |
Het |
Olfr1193 |
A |
G |
2: 88,678,733 |
T286A |
probably damaging |
Het |
Olfr1467 |
A |
T |
19: 13,365,443 |
I272F |
probably benign |
Het |
Olfr952 |
A |
C |
9: 39,426,338 |
H244Q |
probably damaging |
Het |
Pde8b |
T |
C |
13: 95,095,724 |
R237G |
probably damaging |
Het |
Pp2d1 |
G |
A |
17: 53,515,139 |
L300F |
probably damaging |
Het |
Ptpn21 |
A |
T |
12: 98,689,161 |
Y516N |
probably damaging |
Het |
Ptprm |
T |
A |
17: 67,063,163 |
|
probably benign |
Het |
Rabggtb |
A |
G |
3: 153,912,013 |
V16A |
probably damaging |
Het |
Rangap1 |
A |
T |
15: 81,720,663 |
C82S |
probably damaging |
Het |
Rasal2 |
T |
C |
1: 157,175,910 |
E393G |
probably damaging |
Het |
Rasgrf1 |
A |
T |
9: 89,974,836 |
E449V |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,870,895 |
H1143Q |
probably damaging |
Het |
Scap |
T |
C |
9: 110,379,481 |
I530T |
probably benign |
Het |
Sel1l |
T |
A |
12: 91,816,247 |
Q482L |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,039,665 |
M280T |
probably damaging |
Het |
Slc39a10 |
T |
A |
1: 46,832,735 |
H348L |
probably benign |
Het |
Slc7a2 |
T |
C |
8: 40,914,083 |
L542P |
possibly damaging |
Het |
Tas1r2 |
A |
T |
4: 139,669,177 |
Q609L |
probably damaging |
Het |
Tbc1d14 |
A |
T |
5: 36,508,437 |
|
probably benign |
Het |
Tfb2m |
A |
G |
1: 179,537,697 |
|
probably null |
Het |
Tpo |
T |
C |
12: 30,084,647 |
T771A |
possibly damaging |
Het |
Tpr |
G |
A |
1: 150,413,745 |
R609H |
possibly damaging |
Het |
Vmn1r193 |
G |
T |
13: 22,219,723 |
S33* |
probably null |
Het |
Vmn2r104 |
A |
C |
17: 20,029,925 |
S695A |
probably damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,787,445 |
D427G |
probably benign |
Het |
Vmn2r-ps159 |
C |
T |
4: 156,338,254 |
|
noncoding transcript |
Het |
Zfp362 |
A |
G |
4: 128,787,053 |
S160P |
probably benign |
Het |
|