Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace |
C |
T |
11: 105,872,664 (GRCm39) |
P942L |
possibly damaging |
Het |
Adam28 |
A |
G |
14: 68,848,443 (GRCm39) |
V671A |
probably benign |
Het |
Arfgef1 |
A |
G |
1: 10,279,859 (GRCm39) |
V236A |
probably benign |
Het |
B020004C17Rik |
G |
T |
14: 57,254,645 (GRCm39) |
M156I |
possibly damaging |
Het |
Bicral |
T |
A |
17: 47,141,917 (GRCm39) |
M1L |
unknown |
Het |
Brpf3 |
A |
G |
17: 29,026,016 (GRCm39) |
E363G |
possibly damaging |
Het |
Cln3 |
G |
A |
7: 126,179,308 (GRCm39) |
|
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,668,071 (GRCm39) |
I1526T |
possibly damaging |
Het |
Entr1 |
T |
A |
2: 26,274,805 (GRCm39) |
N364I |
probably damaging |
Het |
Fmo3 |
T |
G |
1: 162,786,147 (GRCm39) |
E281A |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,559,491 (GRCm39) |
I1672T |
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,309,470 (GRCm39) |
I194V |
probably benign |
Het |
Gprc6a |
C |
A |
10: 51,497,197 (GRCm39) |
V449L |
probably benign |
Het |
Hk1 |
A |
G |
10: 62,126,098 (GRCm39) |
V396A |
probably benign |
Het |
Hoxc13 |
T |
C |
15: 102,829,675 (GRCm39) |
V18A |
possibly damaging |
Het |
Hr |
A |
G |
14: 70,801,024 (GRCm39) |
T699A |
probably benign |
Het |
Il19 |
A |
T |
1: 130,863,770 (GRCm39) |
C74S |
probably damaging |
Het |
Krt1c |
T |
C |
15: 101,719,562 (GRCm39) |
T703A |
unknown |
Het |
Lrig2 |
A |
T |
3: 104,365,160 (GRCm39) |
V664E |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,348,430 (GRCm39) |
K2755R |
unknown |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mbtd1 |
A |
G |
11: 93,796,001 (GRCm39) |
N13D |
probably benign |
Het |
Mfsd4b5 |
T |
C |
10: 39,850,704 (GRCm39) |
|
probably benign |
Het |
Nras |
A |
G |
3: 102,967,541 (GRCm39) |
I46V |
probably benign |
Het |
Oasl1 |
C |
T |
5: 115,070,957 (GRCm39) |
T274I |
probably damaging |
Het |
Ogfod2 |
C |
A |
5: 124,251,272 (GRCm39) |
|
probably null |
Het |
Or10q3 |
C |
A |
19: 11,847,869 (GRCm39) |
R237L |
possibly damaging |
Het |
Or10v1 |
T |
A |
19: 11,873,880 (GRCm39) |
F165Y |
probably damaging |
Het |
Or11a4 |
T |
C |
17: 37,536,049 (GRCm39) |
V11A |
probably benign |
Het |
Or2w1b |
T |
A |
13: 21,300,031 (GRCm39) |
H56Q |
probably benign |
Het |
Or4c3 |
C |
A |
2: 89,852,089 (GRCm39) |
G107V |
probably damaging |
Het |
Or6c5 |
C |
T |
10: 129,074,377 (GRCm39) |
R120C |
probably damaging |
Het |
Pkmyt1 |
A |
G |
17: 23,954,305 (GRCm39) |
M362V |
probably benign |
Het |
Ppfia2 |
A |
G |
10: 106,666,490 (GRCm39) |
T399A |
possibly damaging |
Het |
Ppp1r12b |
A |
G |
1: 134,693,713 (GRCm39) |
S983P |
probably benign |
Het |
Ptpn22 |
A |
G |
3: 103,780,957 (GRCm39) |
|
probably benign |
Het |
Raph1 |
A |
T |
1: 60,537,682 (GRCm39) |
D491E |
probably benign |
Het |
Rc3h1 |
A |
G |
1: 160,786,969 (GRCm39) |
|
probably null |
Het |
Rtn4 |
T |
C |
11: 29,643,819 (GRCm39) |
L5P |
probably benign |
Het |
Slc23a4 |
C |
T |
6: 34,930,723 (GRCm39) |
V400I |
probably benign |
Het |
Slco1a5 |
A |
G |
6: 142,204,698 (GRCm39) |
|
probably benign |
Het |
Smpd1 |
T |
C |
7: 105,205,108 (GRCm39) |
F329S |
probably benign |
Het |
Sycp2l |
A |
G |
13: 41,295,440 (GRCm39) |
I334M |
probably damaging |
Het |
Tas2r103 |
A |
G |
6: 133,013,280 (GRCm39) |
L262P |
probably benign |
Het |
Ten1 |
G |
A |
11: 116,107,771 (GRCm39) |
|
probably null |
Het |
Tfap2d |
C |
G |
1: 19,174,718 (GRCm39) |
S57C |
possibly damaging |
Het |
Tnr |
A |
G |
1: 159,719,593 (GRCm39) |
M957V |
probably benign |
Het |
Trbv13-3 |
A |
G |
6: 41,107,079 (GRCm39) |
|
probably benign |
Het |
Trp53rkb |
C |
T |
2: 166,637,446 (GRCm39) |
A134V |
possibly damaging |
Het |
Trp63 |
A |
G |
16: 25,639,490 (GRCm39) |
|
probably benign |
Het |
Vmn2r112 |
T |
A |
17: 22,822,096 (GRCm39) |
V258E |
probably damaging |
Het |
Vmn2r74 |
T |
C |
7: 85,607,345 (GRCm39) |
Y126C |
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,817,941 (GRCm39) |
I698N |
probably damaging |
Het |
|
Other mutations in Ccdc96 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Ccdc96
|
APN |
5 |
36,642,424 (GRCm39) |
unclassified |
probably benign |
|
R0167:Ccdc96
|
UTSW |
5 |
36,642,497 (GRCm39) |
missense |
probably benign |
0.18 |
R0302:Ccdc96
|
UTSW |
5 |
36,643,445 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0423:Ccdc96
|
UTSW |
5 |
36,642,591 (GRCm39) |
missense |
probably benign |
0.41 |
R0532:Ccdc96
|
UTSW |
5 |
36,643,710 (GRCm39) |
missense |
probably benign |
0.18 |
R3800:Ccdc96
|
UTSW |
5 |
36,643,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Ccdc96
|
UTSW |
5 |
36,643,419 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4720:Ccdc96
|
UTSW |
5 |
36,642,219 (GRCm39) |
unclassified |
probably benign |
|
R5476:Ccdc96
|
UTSW |
5 |
36,642,981 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5945:Ccdc96
|
UTSW |
5 |
36,643,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Ccdc96
|
UTSW |
5 |
36,643,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R6434:Ccdc96
|
UTSW |
5 |
36,643,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6493:Ccdc96
|
UTSW |
5 |
36,643,596 (GRCm39) |
missense |
probably damaging |
0.99 |
R6632:Ccdc96
|
UTSW |
5 |
36,642,533 (GRCm39) |
missense |
probably benign |
0.07 |
R6633:Ccdc96
|
UTSW |
5 |
36,642,533 (GRCm39) |
missense |
probably benign |
0.07 |
R7395:Ccdc96
|
UTSW |
5 |
36,642,609 (GRCm39) |
missense |
probably benign |
0.29 |
R7819:Ccdc96
|
UTSW |
5 |
36,643,329 (GRCm39) |
missense |
probably damaging |
0.98 |
R8466:Ccdc96
|
UTSW |
5 |
36,642,252 (GRCm39) |
unclassified |
probably benign |
|
R9351:Ccdc96
|
UTSW |
5 |
36,642,069 (GRCm39) |
missense |
unknown |
|
X0022:Ccdc96
|
UTSW |
5 |
36,643,718 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ccdc96
|
UTSW |
5 |
36,642,938 (GRCm39) |
missense |
probably benign |
0.03 |
|