Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
T |
C |
6: 124,333,380 (GRCm39) |
N72S |
possibly damaging |
Het |
A2m |
G |
A |
6: 121,653,862 (GRCm39) |
|
probably null |
Het |
Angptl3 |
A |
T |
4: 98,923,057 (GRCm39) |
|
probably benign |
Het |
Aox4 |
A |
G |
1: 58,301,746 (GRCm39) |
D1106G |
probably benign |
Het |
Capn13 |
G |
A |
17: 73,648,149 (GRCm39) |
|
probably benign |
Het |
Cep250 |
A |
G |
2: 155,832,191 (GRCm39) |
H1371R |
probably benign |
Het |
Col2a1 |
T |
C |
15: 97,879,923 (GRCm39) |
T813A |
unknown |
Het |
Dab2 |
T |
C |
15: 6,464,790 (GRCm39) |
V414A |
possibly damaging |
Het |
Dach2 |
T |
C |
X: 112,465,937 (GRCm39) |
|
probably benign |
Het |
Fap |
A |
G |
2: 62,333,699 (GRCm39) |
|
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,396 (GRCm39) |
V385D |
probably damaging |
Het |
Fmnl1 |
A |
G |
11: 103,088,008 (GRCm39) |
|
probably null |
Het |
Gorasp2 |
G |
A |
2: 70,513,336 (GRCm39) |
G201D |
probably damaging |
Het |
Gp2 |
T |
A |
7: 119,050,783 (GRCm39) |
Q316L |
probably damaging |
Het |
Gpx8 |
T |
C |
13: 113,179,696 (GRCm39) |
I202V |
probably damaging |
Het |
Gsta3 |
A |
G |
1: 21,335,173 (GRCm39) |
K218R |
probably benign |
Het |
Lama3 |
C |
T |
18: 12,686,340 (GRCm39) |
T1195I |
probably benign |
Het |
Map3k12 |
T |
C |
15: 102,410,514 (GRCm39) |
R488G |
possibly damaging |
Het |
Mapt |
A |
T |
11: 104,173,259 (GRCm39) |
Y18F |
probably damaging |
Het |
Med21 |
T |
C |
6: 146,544,143 (GRCm39) |
V12A |
probably benign |
Het |
Mgat4b |
A |
G |
11: 50,124,936 (GRCm39) |
E457G |
possibly damaging |
Het |
Mybl1 |
T |
A |
1: 9,742,780 (GRCm39) |
K609N |
probably damaging |
Het |
Ncaph2 |
T |
G |
15: 89,247,858 (GRCm39) |
V75G |
probably benign |
Het |
Neb |
A |
G |
2: 52,068,049 (GRCm39) |
Y5795H |
probably benign |
Het |
Nup153 |
A |
G |
13: 46,854,459 (GRCm39) |
|
probably null |
Het |
Or6c215 |
T |
C |
10: 129,638,340 (GRCm39) |
D18G |
probably damaging |
Het |
Or6y1 |
T |
A |
1: 174,276,435 (GRCm39) |
I82N |
probably damaging |
Het |
Plekhf2 |
G |
T |
4: 10,990,703 (GRCm39) |
T213K |
probably benign |
Het |
Plekho2 |
C |
A |
9: 65,466,776 (GRCm39) |
G105W |
probably damaging |
Het |
Polr3b |
G |
A |
10: 84,512,816 (GRCm39) |
G566D |
probably damaging |
Het |
Rasgrf1 |
T |
C |
9: 89,892,504 (GRCm39) |
I1068T |
probably damaging |
Het |
Rnf213 |
A |
T |
11: 119,312,294 (GRCm39) |
E907V |
probably benign |
Het |
Runx1t1 |
C |
T |
4: 13,881,107 (GRCm39) |
S469F |
probably damaging |
Het |
Spata31e4 |
G |
T |
13: 50,857,200 (GRCm39) |
C946F |
possibly damaging |
Het |
Top1 |
A |
T |
2: 160,535,647 (GRCm39) |
D182V |
unknown |
Het |
Uckl1 |
T |
C |
2: 181,211,982 (GRCm39) |
T375A |
probably benign |
Het |
Usp53 |
A |
T |
3: 122,727,370 (GRCm39) |
|
probably benign |
Het |
Vmn2r61 |
T |
A |
7: 41,909,517 (GRCm39) |
I14N |
probably benign |
Het |
Wbp4 |
A |
T |
14: 79,707,558 (GRCm39) |
N184K |
probably damaging |
Het |
|
Other mutations in Chrna1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Chrna1
|
APN |
2 |
73,400,986 (GRCm39) |
missense |
probably benign |
|
IGL02043:Chrna1
|
APN |
2 |
73,398,450 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02553:Chrna1
|
APN |
2 |
73,397,206 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02663:Chrna1
|
APN |
2 |
73,404,660 (GRCm39) |
splice site |
probably benign |
|
IGL02799:Chrna1
|
APN |
2 |
73,404,985 (GRCm39) |
splice site |
probably benign |
|
R0113:Chrna1
|
UTSW |
2 |
73,397,180 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0513:Chrna1
|
UTSW |
2 |
73,398,426 (GRCm39) |
splice site |
probably benign |
|
R0540:Chrna1
|
UTSW |
2 |
73,401,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Chrna1
|
UTSW |
2 |
73,396,596 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1922:Chrna1
|
UTSW |
2 |
73,398,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Chrna1
|
UTSW |
2 |
73,396,618 (GRCm39) |
missense |
probably benign |
|
R5481:Chrna1
|
UTSW |
2 |
73,397,270 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5598:Chrna1
|
UTSW |
2 |
73,397,075 (GRCm39) |
missense |
probably benign |
0.01 |
R5931:Chrna1
|
UTSW |
2 |
73,398,444 (GRCm39) |
missense |
probably benign |
0.39 |
R6153:Chrna1
|
UTSW |
2 |
73,403,653 (GRCm39) |
missense |
probably benign |
0.02 |
R6194:Chrna1
|
UTSW |
2 |
73,400,816 (GRCm39) |
missense |
probably benign |
0.17 |
R6301:Chrna1
|
UTSW |
2 |
73,400,828 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6455:Chrna1
|
UTSW |
2 |
73,397,180 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8293:Chrna1
|
UTSW |
2 |
73,400,850 (GRCm39) |
missense |
probably benign |
|
R8344:Chrna1
|
UTSW |
2 |
73,400,953 (GRCm39) |
missense |
probably benign |
0.12 |
X0026:Chrna1
|
UTSW |
2 |
73,400,955 (GRCm39) |
missense |
probably benign |
0.16 |
|