Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot10 |
T |
C |
15: 20,666,262 |
N131S |
probably benign |
Het |
Agbl5 |
A |
G |
5: 30,891,833 |
Y220C |
probably damaging |
Het |
Ankdd1a |
C |
T |
9: 65,508,061 |
A227T |
possibly damaging |
Het |
Ap3b1 |
A |
T |
13: 94,528,295 |
Q914L |
unknown |
Het |
Arhgef25 |
T |
C |
10: 127,185,882 |
D216G |
possibly damaging |
Het |
Bcas2 |
T |
A |
3: 103,171,871 |
|
probably benign |
Het |
Bpifb5 |
A |
C |
2: 154,230,219 |
H282P |
possibly damaging |
Het |
Ccdc167 |
A |
G |
17: 29,705,582 |
I15T |
probably damaging |
Het |
Cd248 |
A |
G |
19: 5,069,981 |
N619S |
probably benign |
Het |
Chrna1 |
A |
G |
2: 73,570,484 |
F234S |
possibly damaging |
Het |
Clcc1 |
T |
G |
3: 108,673,366 |
M332R |
probably damaging |
Het |
Cmklr1 |
T |
A |
5: 113,614,938 |
M1L |
possibly damaging |
Het |
Cntnap5c |
A |
G |
17: 57,892,037 |
M109V |
probably benign |
Het |
Coq2 |
A |
G |
5: 100,661,863 |
I18T |
possibly damaging |
Het |
Crybg3 |
T |
C |
16: 59,530,338 |
S880G |
probably damaging |
Het |
Cubn |
A |
G |
2: 13,478,078 |
C286R |
probably damaging |
Het |
Defa24 |
T |
C |
8: 21,735,283 |
V63A |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,086,217 |
R2634H |
probably damaging |
Het |
Dusp8 |
T |
A |
7: 142,083,019 |
|
probably null |
Het |
Elac1 |
T |
C |
18: 73,738,868 |
D352G |
probably damaging |
Het |
Ermap |
A |
T |
4: 119,185,603 |
V241E |
probably damaging |
Het |
Fgf10 |
T |
A |
13: 118,715,511 |
M43K |
probably benign |
Het |
Gabrd |
A |
G |
4: 155,387,267 |
V193A |
probably damaging |
Het |
Gm13124 |
C |
T |
4: 144,558,654 |
A138T |
probably damaging |
Het |
Gm6588 |
A |
T |
5: 112,450,468 |
I294F |
possibly damaging |
Het |
Gm884 |
A |
T |
11: 103,618,930 |
|
probably benign |
Het |
Hook3 |
C |
T |
8: 26,034,940 |
W26* |
probably null |
Het |
Kif1a |
C |
A |
1: 93,054,941 |
E714* |
probably null |
Het |
Krt6b |
T |
C |
15: 101,678,951 |
E236G |
probably damaging |
Het |
Large2 |
A |
G |
2: 92,369,516 |
L209P |
probably damaging |
Het |
Lats1 |
A |
G |
10: 7,703,107 |
N665S |
probably benign |
Het |
Lrrtm3 |
T |
C |
10: 64,089,222 |
I55M |
probably benign |
Het |
Ltk |
A |
G |
2: 119,751,757 |
S838P |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,420,306 |
I348V |
probably benign |
Het |
Mag |
T |
A |
7: 30,900,679 |
S559C |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,612,294 |
H1072R |
possibly damaging |
Het |
Mycbp2 |
T |
A |
14: 103,155,426 |
Q833L |
probably damaging |
Het |
Myh4 |
G |
A |
11: 67,255,333 |
E1406K |
possibly damaging |
Het |
Npc1 |
C |
T |
18: 12,197,245 |
V950I |
probably benign |
Het |
Npl |
A |
G |
1: 153,518,881 |
|
probably null |
Het |
Olfr1493-ps1 |
A |
G |
19: 13,726,389 |
I43V |
probably benign |
Het |
Olfr165 |
A |
T |
16: 19,407,417 |
F200I |
possibly damaging |
Het |
Olfr743 |
T |
A |
14: 50,534,254 |
F281I |
probably benign |
Het |
Olfr883 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 38,026,540 |
|
probably null |
Het |
Oxsm |
A |
T |
14: 16,242,220 |
I183N |
probably damaging |
Het |
Pde7a |
T |
C |
3: 19,243,163 |
I108V |
probably benign |
Het |
Pgghg |
A |
T |
7: 140,946,376 |
T585S |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,589,525 |
D3949N |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,327,411 |
H1777Q |
possibly damaging |
Het |
Rela |
G |
A |
19: 5,645,410 |
|
probably null |
Het |
Rilpl1 |
C |
A |
5: 124,514,539 |
G41W |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,347,254 |
K1212E |
probably benign |
Het |
Sgca |
A |
C |
11: 94,972,567 |
L28V |
probably damaging |
Het |
Ssmem1 |
A |
G |
6: 30,519,759 |
R148G |
probably damaging |
Het |
St8sia5 |
A |
T |
18: 77,246,140 |
N165Y |
probably damaging |
Het |
Tbl2 |
A |
T |
5: 135,159,369 |
H339L |
probably benign |
Het |
Tcof1 |
G |
A |
18: 60,828,825 |
P718L |
probably damaging |
Het |
Trim72 |
A |
T |
7: 128,004,614 |
E44V |
possibly damaging |
Het |
Try10 |
T |
A |
6: 41,355,589 |
S60T |
probably benign |
Het |
Usp31 |
A |
T |
7: 121,648,276 |
S1315T |
possibly damaging |
Het |
Xrn2 |
A |
G |
2: 147,063,342 |
I856V |
probably benign |
Het |
|