Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Aff3 |
T |
C |
1: 38,248,768 (GRCm39) |
I779V |
possibly damaging |
Het |
Asap1 |
T |
G |
15: 64,221,692 (GRCm39) |
D15A |
probably benign |
Het |
Bcl2a1d |
A |
T |
9: 88,613,753 (GRCm39) |
M7K |
probably benign |
Het |
Ccdc168 |
T |
C |
1: 44,095,276 (GRCm39) |
I1941V |
probably benign |
Het |
Ccdc85a |
T |
C |
11: 28,526,457 (GRCm39) |
T384A |
probably benign |
Het |
Cd86 |
T |
C |
16: 36,441,194 (GRCm39) |
N91S |
probably benign |
Het |
Cdk17 |
T |
A |
10: 93,047,758 (GRCm39) |
|
probably null |
Het |
Cemip |
T |
C |
7: 83,636,637 (GRCm39) |
D332G |
probably null |
Het |
Ces2f |
G |
A |
8: 105,679,788 (GRCm39) |
R427H |
probably benign |
Het |
Clec4a2 |
G |
A |
6: 123,105,013 (GRCm39) |
|
probably null |
Het |
Coa8 |
T |
A |
12: 111,717,642 (GRCm39) |
D167E |
probably benign |
Het |
Coq9 |
T |
C |
8: 95,579,743 (GRCm39) |
F198L |
probably benign |
Het |
Ddx24 |
C |
A |
12: 103,390,233 (GRCm39) |
A253S |
probably damaging |
Het |
Esyt3 |
A |
T |
9: 99,240,078 (GRCm39) |
|
probably benign |
Het |
Fat2 |
C |
A |
11: 55,187,024 (GRCm39) |
G1274V |
probably damaging |
Het |
Ggn |
A |
T |
7: 28,870,976 (GRCm39) |
T132S |
probably damaging |
Het |
Gm11568 |
T |
A |
11: 99,749,421 (GRCm39) |
C209S |
unknown |
Het |
Gm6931 |
T |
A |
16: 49,245,225 (GRCm39) |
|
noncoding transcript |
Het |
Gpr20 |
C |
T |
15: 73,567,649 (GRCm39) |
V247I |
probably benign |
Het |
Grm8 |
A |
T |
6: 27,761,237 (GRCm39) |
V329E |
possibly damaging |
Het |
Gtf2ird2 |
T |
C |
5: 134,223,808 (GRCm39) |
L114P |
possibly damaging |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hivep3 |
C |
T |
4: 119,953,120 (GRCm39) |
P479S |
probably benign |
Het |
Igkv6-20 |
A |
G |
6: 70,313,104 (GRCm39) |
V23A |
probably damaging |
Het |
Ikbip |
T |
A |
10: 90,937,751 (GRCm39) |
N141K |
probably damaging |
Het |
Irag1 |
T |
C |
7: 110,476,124 (GRCm39) |
E815G |
probably damaging |
Het |
Krt77 |
A |
T |
15: 101,773,904 (GRCm39) |
V250E |
probably damaging |
Het |
Ltn1 |
A |
T |
16: 87,202,502 (GRCm39) |
C1050S |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,421,135 (GRCm39) |
I40V |
probably benign |
Het |
Or2h2b-ps1 |
A |
G |
17: 37,480,727 (GRCm39) |
F271L |
probably benign |
Het |
Or4k15b |
T |
C |
14: 50,272,287 (GRCm39) |
D191G |
probably damaging |
Het |
Pi4ka |
T |
C |
16: 17,100,246 (GRCm39) |
M1885V |
probably damaging |
Het |
Plek |
A |
G |
11: 16,942,972 (GRCm39) |
Y107H |
probably damaging |
Het |
Ppp1r15a |
C |
T |
7: 45,174,203 (GRCm39) |
V202M |
probably damaging |
Het |
Ppp1r3e |
C |
A |
14: 55,114,007 (GRCm39) |
A222S |
probably benign |
Het |
Rac2 |
G |
T |
15: 78,454,943 (GRCm39) |
Y32* |
probably null |
Het |
Sdf4 |
T |
G |
4: 156,093,404 (GRCm39) |
|
probably null |
Het |
Siah1b |
G |
A |
X: 162,854,688 (GRCm39) |
P131S |
probably damaging |
Het |
Spic |
T |
A |
10: 88,512,817 (GRCm39) |
R111S |
probably benign |
Het |
Ssh3 |
A |
G |
19: 4,315,394 (GRCm39) |
F315L |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,595,253 (GRCm39) |
K11972R |
probably damaging |
Het |
Tubd1 |
C |
T |
11: 86,439,745 (GRCm39) |
S30F |
probably benign |
Het |
Vmn1r17 |
G |
C |
6: 57,337,719 (GRCm39) |
I166M |
possibly damaging |
Het |
Vmn2r94 |
T |
C |
17: 18,478,645 (GRCm39) |
Y34C |
probably damaging |
Het |
Xpo7 |
G |
A |
14: 70,906,869 (GRCm39) |
T945M |
probably damaging |
Het |
Zfp316 |
C |
A |
5: 143,239,803 (GRCm39) |
A739S |
probably damaging |
Het |
Zswim3 |
T |
A |
2: 164,662,563 (GRCm39) |
C348S |
probably benign |
Het |
|
Other mutations in Ascc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02749:Ascc2
|
APN |
11 |
4,590,481 (GRCm39) |
critical splice donor site |
probably null |
|
R0485:Ascc2
|
UTSW |
11 |
4,622,302 (GRCm39) |
missense |
probably benign |
0.01 |
R0632:Ascc2
|
UTSW |
11 |
4,599,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Ascc2
|
UTSW |
11 |
4,632,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R0942:Ascc2
|
UTSW |
11 |
4,618,380 (GRCm39) |
missense |
probably benign |
0.31 |
R1893:Ascc2
|
UTSW |
11 |
4,622,305 (GRCm39) |
missense |
probably benign |
0.01 |
R1991:Ascc2
|
UTSW |
11 |
4,629,257 (GRCm39) |
missense |
probably benign |
|
R2062:Ascc2
|
UTSW |
11 |
4,631,496 (GRCm39) |
missense |
probably benign |
|
R2063:Ascc2
|
UTSW |
11 |
4,631,496 (GRCm39) |
missense |
probably benign |
|
R2065:Ascc2
|
UTSW |
11 |
4,631,496 (GRCm39) |
missense |
probably benign |
|
R2067:Ascc2
|
UTSW |
11 |
4,631,496 (GRCm39) |
missense |
probably benign |
|
R2068:Ascc2
|
UTSW |
11 |
4,631,496 (GRCm39) |
missense |
probably benign |
|
R2292:Ascc2
|
UTSW |
11 |
4,629,352 (GRCm39) |
splice site |
probably benign |
|
R3076:Ascc2
|
UTSW |
11 |
4,622,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Ascc2
|
UTSW |
11 |
4,596,653 (GRCm39) |
missense |
probably benign |
0.01 |
R5211:Ascc2
|
UTSW |
11 |
4,623,399 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5395:Ascc2
|
UTSW |
11 |
4,609,273 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5859:Ascc2
|
UTSW |
11 |
4,608,284 (GRCm39) |
missense |
probably benign |
0.11 |
R5917:Ascc2
|
UTSW |
11 |
4,631,506 (GRCm39) |
missense |
probably benign |
0.03 |
R7569:Ascc2
|
UTSW |
11 |
4,629,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7875:Ascc2
|
UTSW |
11 |
4,618,389 (GRCm39) |
missense |
probably benign |
0.00 |
R8411:Ascc2
|
UTSW |
11 |
4,597,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R8431:Ascc2
|
UTSW |
11 |
4,614,227 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0011:Ascc2
|
UTSW |
11 |
4,608,297 (GRCm39) |
missense |
probably benign |
|
Z1088:Ascc2
|
UTSW |
11 |
4,596,656 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Ascc2
|
UTSW |
11 |
4,622,487 (GRCm39) |
missense |
probably benign |
|
Z1176:Ascc2
|
UTSW |
11 |
4,596,653 (GRCm39) |
missense |
probably benign |
0.01 |
|