Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,071,084 (GRCm39) |
K1536E |
possibly damaging |
Het |
Abhd16a |
T |
A |
17: 35,320,936 (GRCm39) |
|
probably null |
Het |
Actrt3 |
C |
T |
3: 30,652,696 (GRCm39) |
A133T |
probably benign |
Het |
Adcy10 |
C |
T |
1: 165,391,806 (GRCm39) |
R1329W |
probably damaging |
Het |
Apol7b |
T |
C |
15: 77,307,656 (GRCm39) |
M280V |
possibly damaging |
Het |
Canx |
A |
T |
11: 50,202,455 (GRCm39) |
D50E |
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,338,696 (GRCm39) |
D470E |
probably damaging |
Het |
Cyp2c23 |
C |
T |
19: 44,003,369 (GRCm39) |
D269N |
probably damaging |
Het |
Ddah1 |
T |
C |
3: 145,464,774 (GRCm39) |
V53A |
probably benign |
Het |
Epha7 |
C |
T |
4: 28,871,937 (GRCm39) |
S422L |
probably benign |
Het |
Fastkd5 |
A |
G |
2: 130,456,961 (GRCm39) |
V543A |
possibly damaging |
Het |
Fggy |
G |
A |
4: 95,657,743 (GRCm39) |
G295R |
probably damaging |
Het |
Glipr1 |
A |
T |
10: 111,824,737 (GRCm39) |
N156K |
probably benign |
Het |
Gnpnat1 |
C |
T |
14: 45,622,074 (GRCm39) |
V40I |
probably benign |
Het |
H2-Q7 |
T |
C |
17: 35,658,939 (GRCm39) |
L130P |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,358,665 (GRCm39) |
L86* |
probably null |
Het |
Hspg2 |
T |
C |
4: 137,275,679 (GRCm39) |
L2778P |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,284,503 (GRCm39) |
I3487N |
possibly damaging |
Het |
Htra4 |
T |
G |
8: 25,515,716 (GRCm39) |
I441L |
probably benign |
Het |
Ints7 |
A |
T |
1: 191,328,336 (GRCm39) |
H203L |
probably damaging |
Het |
Lama2 |
T |
C |
10: 27,142,676 (GRCm39) |
T601A |
possibly damaging |
Het |
Lin7b |
T |
C |
7: 45,017,856 (GRCm39) |
|
probably benign |
Het |
Lmbr1l |
G |
A |
15: 98,806,572 (GRCm39) |
Q280* |
probably null |
Het |
Lpin3 |
G |
T |
2: 160,745,674 (GRCm39) |
|
probably null |
Het |
Map1lc3b |
A |
T |
8: 122,320,268 (GRCm39) |
H27L |
possibly damaging |
Het |
Mfsd14a |
C |
A |
3: 116,427,532 (GRCm39) |
V369F |
probably damaging |
Het |
Ndufa12 |
C |
T |
10: 94,056,641 (GRCm39) |
A123V |
probably benign |
Het |
Nek9 |
A |
G |
12: 85,350,288 (GRCm39) |
F929L |
probably benign |
Het |
Nup210 |
A |
T |
6: 91,053,679 (GRCm39) |
D279E |
probably benign |
Het |
Or52m2 |
A |
G |
7: 102,264,145 (GRCm39) |
V17A |
probably benign |
Het |
Parp1 |
T |
C |
1: 180,427,777 (GRCm39) |
|
probably null |
Het |
Phc3 |
T |
C |
3: 30,961,601 (GRCm39) |
I944V |
probably damaging |
Het |
Phf20 |
C |
T |
2: 156,144,771 (GRCm39) |
A793V |
probably benign |
Het |
Phf21a |
A |
C |
2: 92,187,352 (GRCm39) |
R540S |
probably benign |
Het |
Pogk |
A |
G |
1: 166,229,480 (GRCm39) |
C124R |
probably benign |
Het |
Rif1 |
C |
T |
2: 51,966,187 (GRCm39) |
S93L |
probably damaging |
Het |
Sanbr |
T |
C |
11: 23,516,191 (GRCm39) |
T709A |
probably benign |
Het |
Sele |
A |
G |
1: 163,877,084 (GRCm39) |
E120G |
probably damaging |
Het |
Slc4a1ap |
T |
C |
5: 31,703,539 (GRCm39) |
L49P |
|
Het |
Snap47 |
T |
C |
11: 59,319,373 (GRCm39) |
D255G |
probably damaging |
Het |
Tcstv3 |
T |
C |
13: 120,779,146 (GRCm39) |
V15A |
probably damaging |
Het |
Tmcc1 |
A |
T |
6: 116,020,092 (GRCm39) |
Y453* |
probably null |
Het |
Tpsg1 |
G |
T |
17: 25,592,184 (GRCm39) |
G86V |
probably damaging |
Het |
Urb1 |
CACTTAC |
CAC |
16: 90,569,461 (GRCm39) |
|
probably benign |
Het |
Usp20 |
T |
A |
2: 30,901,486 (GRCm39) |
V459E |
probably damaging |
Het |
Vmn1r202 |
A |
T |
13: 22,685,790 (GRCm39) |
L209Q |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,576,585 (GRCm39) |
S998P |
probably damaging |
Het |
|
Other mutations in Frs2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00807:Frs2
|
APN |
10 |
116,910,791 (GRCm39) |
splice site |
probably benign |
|
IGL02300:Frs2
|
APN |
10 |
116,913,496 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03028:Frs2
|
APN |
10 |
116,909,838 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0001:Frs2
|
UTSW |
10 |
116,910,781 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0513:Frs2
|
UTSW |
10 |
116,910,570 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0708:Frs2
|
UTSW |
10 |
116,909,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R0735:Frs2
|
UTSW |
10 |
116,910,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Frs2
|
UTSW |
10 |
116,916,979 (GRCm39) |
missense |
probably benign |
0.30 |
R1934:Frs2
|
UTSW |
10 |
116,914,806 (GRCm39) |
missense |
probably damaging |
0.99 |
R1938:Frs2
|
UTSW |
10 |
116,917,011 (GRCm39) |
start gained |
probably benign |
|
R1992:Frs2
|
UTSW |
10 |
116,910,459 (GRCm39) |
missense |
probably benign |
|
R2095:Frs2
|
UTSW |
10 |
116,910,507 (GRCm39) |
missense |
probably benign |
0.00 |
R3878:Frs2
|
UTSW |
10 |
116,914,815 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:Frs2
|
UTSW |
10 |
116,909,998 (GRCm39) |
missense |
probably benign |
0.31 |
R4733:Frs2
|
UTSW |
10 |
116,909,998 (GRCm39) |
missense |
probably benign |
0.31 |
R5186:Frs2
|
UTSW |
10 |
116,914,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5326:Frs2
|
UTSW |
10 |
116,913,468 (GRCm39) |
missense |
probably benign |
0.00 |
R5894:Frs2
|
UTSW |
10 |
116,917,011 (GRCm39) |
start gained |
probably benign |
|
R6084:Frs2
|
UTSW |
10 |
116,912,714 (GRCm39) |
critical splice donor site |
probably null |
|
R7468:Frs2
|
UTSW |
10 |
116,910,007 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8179:Frs2
|
UTSW |
10 |
116,912,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Frs2
|
UTSW |
10 |
116,910,784 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8721:Frs2
|
UTSW |
10 |
116,909,935 (GRCm39) |
missense |
probably benign |
0.00 |
R9104:Frs2
|
UTSW |
10 |
116,910,070 (GRCm39) |
missense |
probably benign |
0.19 |
Z1177:Frs2
|
UTSW |
10 |
116,910,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|