Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310030G06Rik |
A |
G |
9: 50,651,931 (GRCm39) |
L99P |
probably damaging |
Het |
Abcd2 |
A |
G |
15: 91,062,486 (GRCm39) |
V484A |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,588,185 (GRCm39) |
I4467T |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,892,622 (GRCm39) |
D1500E |
possibly damaging |
Het |
C1ql2 |
A |
T |
1: 120,269,409 (GRCm39) |
Y188F |
possibly damaging |
Het |
Cnga2 |
T |
A |
X: 71,049,733 (GRCm39) |
F133I |
possibly damaging |
Het |
Crybg2 |
T |
C |
4: 133,801,512 (GRCm39) |
S891P |
probably benign |
Het |
Hao2 |
T |
A |
3: 98,789,341 (GRCm39) |
I116F |
probably damaging |
Het |
Htr1b |
A |
T |
9: 81,513,592 (GRCm39) |
D338E |
probably benign |
Het |
Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
Kif9 |
A |
G |
9: 110,323,552 (GRCm39) |
E225G |
probably null |
Het |
Krt76 |
T |
C |
15: 101,798,917 (GRCm39) |
K256R |
possibly damaging |
Het |
Mapk4 |
T |
C |
18: 74,064,046 (GRCm39) |
D392G |
probably damaging |
Het |
Mthfr |
A |
G |
4: 148,135,884 (GRCm39) |
K278R |
probably benign |
Het |
Mup4 |
T |
A |
4: 59,960,547 (GRCm39) |
E18V |
probably damaging |
Het |
Nepro |
A |
G |
16: 44,556,089 (GRCm39) |
K416E |
probably damaging |
Het |
Ngf |
G |
A |
3: 102,428,015 (GRCm39) |
D255N |
probably damaging |
Het |
Nmu |
A |
G |
5: 76,491,909 (GRCm39) |
|
probably null |
Het |
Nt5m |
A |
G |
11: 59,739,173 (GRCm39) |
Y73C |
probably damaging |
Het |
Oaz3 |
A |
T |
3: 94,342,437 (GRCm39) |
|
probably null |
Het |
Pgap1 |
A |
G |
1: 54,567,751 (GRCm39) |
S365P |
probably benign |
Het |
Plxna2 |
C |
T |
1: 194,431,625 (GRCm39) |
S538F |
probably damaging |
Het |
Pus7l |
A |
G |
15: 94,429,498 (GRCm39) |
I440T |
possibly damaging |
Het |
Raph1 |
C |
T |
1: 60,542,028 (GRCm39) |
S362N |
possibly damaging |
Het |
Rftn2 |
A |
G |
1: 55,241,311 (GRCm39) |
Y330H |
possibly damaging |
Het |
Rhot2 |
G |
A |
17: 26,058,467 (GRCm39) |
H580Y |
probably benign |
Het |
Rusf1 |
T |
C |
7: 127,887,530 (GRCm39) |
D24G |
probably damaging |
Het |
Smchd1 |
T |
C |
17: 71,714,230 (GRCm39) |
T878A |
probably benign |
Het |
Snx1 |
A |
T |
9: 65,996,877 (GRCm39) |
V459E |
possibly damaging |
Het |
Suz12 |
A |
G |
11: 79,922,939 (GRCm39) |
T694A |
probably benign |
Het |
Tg |
G |
A |
15: 66,543,245 (GRCm39) |
C53Y |
probably damaging |
Het |
Tor1aip1 |
G |
T |
1: 155,882,870 (GRCm39) |
T326K |
probably damaging |
Het |
Vmn1r61 |
C |
A |
7: 5,613,924 (GRCm39) |
C130F |
possibly damaging |
Het |
Xlr5b |
T |
C |
X: 72,201,504 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rnase2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03390:Rnase2a
|
APN |
14 |
51,492,945 (GRCm39) |
missense |
probably damaging |
0.97 |
R2024:Rnase2a
|
UTSW |
14 |
51,493,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R4774:Rnase2a
|
UTSW |
14 |
51,493,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5431:Rnase2a
|
UTSW |
14 |
51,493,020 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6210:Rnase2a
|
UTSW |
14 |
51,493,131 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7104:Rnase2a
|
UTSW |
14 |
51,492,988 (GRCm39) |
missense |
probably benign |
|
R7699:Rnase2a
|
UTSW |
14 |
51,493,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Rnase2a
|
UTSW |
14 |
51,493,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8295:Rnase2a
|
UTSW |
14 |
51,493,096 (GRCm39) |
missense |
probably benign |
0.36 |
R8869:Rnase2a
|
UTSW |
14 |
51,493,101 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9640:Rnase2a
|
UTSW |
14 |
51,493,117 (GRCm39) |
missense |
probably damaging |
0.99 |
X0023:Rnase2a
|
UTSW |
14 |
51,493,161 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rnase2a
|
UTSW |
14 |
51,493,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|