Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atxn7l1 |
A |
G |
12: 33,376,065 (GRCm39) |
N47D |
probably damaging |
Het |
Cer1 |
A |
T |
4: 82,803,062 (GRCm39) |
W87R |
probably damaging |
Het |
Chrna2 |
A |
G |
14: 66,388,415 (GRCm39) |
K477E |
probably damaging |
Het |
Chtf8 |
G |
A |
8: 107,612,904 (GRCm39) |
P12S |
probably damaging |
Het |
Cplane1 |
C |
A |
15: 8,216,942 (GRCm39) |
P720Q |
possibly damaging |
Het |
Deaf1 |
A |
T |
7: 140,877,461 (GRCm39) |
H555Q |
probably benign |
Het |
Dop1a |
T |
G |
9: 86,418,197 (GRCm39) |
I1975M |
probably damaging |
Het |
Ecpas |
A |
C |
4: 58,828,538 (GRCm39) |
V965G |
probably damaging |
Het |
Fsd2 |
C |
A |
7: 81,209,657 (GRCm39) |
V62L |
probably benign |
Het |
Fxyd6 |
T |
G |
9: 45,303,548 (GRCm39) |
L81R |
probably benign |
Het |
Htt |
T |
A |
5: 35,064,810 (GRCm39) |
S3008T |
probably benign |
Het |
Htt |
T |
A |
5: 35,037,172 (GRCm39) |
S2086T |
probably benign |
Het |
Mybbp1a |
G |
T |
11: 72,336,028 (GRCm39) |
R447L |
probably damaging |
Het |
Nup210 |
A |
G |
6: 90,998,411 (GRCm39) |
V792A |
possibly damaging |
Het |
Odad2 |
C |
A |
18: 7,129,434 (GRCm39) |
G915* |
probably null |
Het |
Odr4 |
T |
C |
1: 150,239,295 (GRCm39) |
E386G |
probably damaging |
Het |
Or1e32 |
T |
A |
11: 73,705,003 (GRCm39) |
I302L |
probably benign |
Het |
Or1j14 |
T |
C |
2: 36,418,140 (GRCm39) |
S239P |
probably damaging |
Het |
Prokr1 |
T |
C |
6: 87,565,482 (GRCm39) |
D121G |
possibly damaging |
Het |
Puf60 |
A |
G |
15: 75,942,229 (GRCm39) |
V548A |
possibly damaging |
Het |
Serpina3c |
T |
C |
12: 104,113,523 (GRCm39) |
I408V |
probably benign |
Het |
Ska2 |
A |
G |
11: 87,000,139 (GRCm39) |
|
probably benign |
Het |
Slc4a9 |
T |
A |
18: 36,668,654 (GRCm39) |
Y745N |
probably damaging |
Het |
Spart |
T |
C |
3: 55,029,106 (GRCm39) |
M299T |
probably benign |
Het |
Speer4f1 |
A |
G |
5: 17,685,332 (GRCm39) |
E209G |
possibly damaging |
Het |
Tmem202 |
T |
C |
9: 59,426,351 (GRCm39) |
T272A |
possibly damaging |
Het |
Vegfc |
T |
A |
8: 54,610,186 (GRCm39) |
I114N |
possibly damaging |
Het |
Vmn1r61 |
T |
A |
7: 5,613,493 (GRCm39) |
T274S |
possibly damaging |
Het |
Zfpm2 |
A |
G |
15: 40,966,170 (GRCm39) |
N753S |
probably benign |
Het |
Zmym6 |
A |
G |
4: 127,014,314 (GRCm39) |
T624A |
probably damaging |
Het |
|
Other mutations in 1700011L22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02969:1700011L22Rik
|
APN |
8 |
79,946,866 (GRCm39) |
splice site |
probably benign |
|
IGL02835:1700011L22Rik
|
UTSW |
8 |
79,937,284 (GRCm39) |
nonsense |
probably null |
|
R0331:1700011L22Rik
|
UTSW |
8 |
79,956,021 (GRCm39) |
missense |
probably benign |
0.08 |
R0904:1700011L22Rik
|
UTSW |
8 |
79,975,118 (GRCm39) |
start gained |
probably benign |
|
R3801:1700011L22Rik
|
UTSW |
8 |
79,974,922 (GRCm39) |
missense |
probably benign |
0.06 |
R3804:1700011L22Rik
|
UTSW |
8 |
79,974,922 (GRCm39) |
missense |
probably benign |
0.06 |
R4606:1700011L22Rik
|
UTSW |
8 |
79,937,374 (GRCm39) |
missense |
probably benign |
0.00 |
R6045:1700011L22Rik
|
UTSW |
8 |
79,955,996 (GRCm39) |
missense |
probably benign |
0.00 |
R6993:1700011L22Rik
|
UTSW |
8 |
79,975,053 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7249:1700011L22Rik
|
UTSW |
8 |
79,974,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7442:1700011L22Rik
|
UTSW |
8 |
79,946,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:1700011L22Rik
|
UTSW |
8 |
79,937,380 (GRCm39) |
nonsense |
probably null |
|
Z1177:1700011L22Rik
|
UTSW |
8 |
79,974,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|