Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts19 |
A |
G |
18: 59,103,013 (GRCm39) |
N685D |
probably damaging |
Het |
Adh4 |
A |
T |
3: 138,129,860 (GRCm39) |
I229F |
probably damaging |
Het |
Ajm1 |
T |
C |
2: 25,467,172 (GRCm39) |
H913R |
possibly damaging |
Het |
Aldh3b1 |
T |
A |
19: 3,965,315 (GRCm39) |
S399C |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 98,124,779 (GRCm39) |
G501D |
probably benign |
Het |
Asb1 |
C |
A |
1: 91,468,551 (GRCm39) |
T6N |
unknown |
Het |
Asb18 |
C |
T |
1: 89,882,185 (GRCm39) |
V382I |
probably benign |
Het |
AU041133 |
T |
C |
10: 81,987,220 (GRCm39) |
I291T |
probably benign |
Het |
B4galnt2 |
C |
T |
11: 95,759,176 (GRCm39) |
|
silent |
Het |
Bcl7c |
T |
C |
7: 127,306,403 (GRCm39) |
|
probably benign |
Het |
Brinp1 |
T |
C |
4: 68,711,083 (GRCm39) |
N375S |
possibly damaging |
Het |
C6 |
A |
G |
15: 4,764,679 (GRCm39) |
Q125R |
probably benign |
Het |
Clec4a2 |
C |
A |
6: 123,100,608 (GRCm39) |
T21N |
probably damaging |
Het |
Cntnap2 |
C |
T |
6: 45,978,112 (GRCm39) |
L256F |
probably benign |
Het |
Cobll1 |
G |
A |
2: 64,981,503 (GRCm39) |
T29I |
probably benign |
Het |
Coq4 |
A |
T |
2: 29,685,433 (GRCm39) |
D149V |
probably damaging |
Het |
Dync1i1 |
T |
C |
6: 5,769,698 (GRCm39) |
L91S |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,201,397 (GRCm39) |
D559V |
probably damaging |
Het |
Gm4779 |
TGGCAGAGGCAGAGGCAGAGGCAGAGGCAGAGGCAG |
TGGCAGAGGCAGAGGCAGAGGCAGAGGCAGAGGCAGAGGCAG |
X: 100,836,917 (GRCm39) |
|
probably benign |
Het |
Gsdmc |
A |
T |
15: 63,676,407 (GRCm39) |
V12E |
probably damaging |
Het |
H2-Ab1 |
T |
C |
17: 34,486,378 (GRCm39) |
S146P |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,135,423 (GRCm39) |
V236A |
probably benign |
Het |
Hjv |
T |
C |
3: 96,435,710 (GRCm39) |
S323P |
probably benign |
Het |
Hmgcr |
C |
T |
13: 96,796,645 (GRCm39) |
C215Y |
probably damaging |
Het |
L3mbtl1 |
G |
T |
2: 162,789,632 (GRCm39) |
A57S |
probably benign |
Het |
Lilrb4b |
G |
A |
10: 51,357,863 (GRCm39) |
V186I |
probably damaging |
Het |
Map1a |
T |
C |
2: 121,132,823 (GRCm39) |
V1213A |
probably benign |
Het |
Marf1 |
T |
C |
16: 13,935,172 (GRCm39) |
E1532G |
probably damaging |
Het |
Mcm6 |
T |
C |
1: 128,279,264 (GRCm39) |
Y174C |
probably damaging |
Het |
Miga2 |
T |
A |
2: 30,261,239 (GRCm39) |
V178E |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,074,359 (GRCm39) |
I174F |
|
Het |
Ndufv1 |
G |
T |
19: 4,059,412 (GRCm39) |
A211E |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nlgn3 |
T |
C |
X: 100,352,390 (GRCm39) |
V179A |
probably damaging |
Het |
Nrp1 |
T |
C |
8: 129,229,144 (GRCm39) |
V874A |
possibly damaging |
Het |
Nsf |
C |
T |
11: 103,804,142 (GRCm39) |
G197S |
probably null |
Het |
Or10al2 |
A |
T |
17: 37,983,637 (GRCm39) |
H241L |
probably benign |
Het |
Or2t26 |
T |
C |
11: 49,039,822 (GRCm39) |
M246T |
probably damaging |
Het |
Pacs2 |
A |
G |
12: 113,014,137 (GRCm39) |
D196G |
probably benign |
Het |
Pbxip1 |
A |
G |
3: 89,351,012 (GRCm39) |
D118G |
probably benign |
Het |
Pcdhb11 |
A |
T |
18: 37,554,529 (GRCm39) |
|
probably benign |
Het |
Pgk2 |
C |
T |
17: 40,519,233 (GRCm39) |
G65D |
probably damaging |
Het |
Plcd3 |
T |
C |
11: 102,970,460 (GRCm39) |
D193G |
probably benign |
Het |
Plcl2 |
T |
G |
17: 50,915,127 (GRCm39) |
M712R |
probably damaging |
Het |
Plxna1 |
G |
A |
6: 89,334,522 (GRCm39) |
Q36* |
probably null |
Het |
Plxnb2 |
A |
G |
15: 89,052,015 (GRCm39) |
V68A |
probably benign |
Het |
Polr2b |
A |
G |
5: 77,493,224 (GRCm39) |
I1069V |
probably benign |
Het |
Rbfox1 |
A |
G |
16: 7,111,973 (GRCm39) |
T200A |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,349,621 (GRCm39) |
V3D |
probably damaging |
Het |
Serpinb6d |
T |
C |
13: 33,855,205 (GRCm39) |
M293T |
probably damaging |
Het |
Slc4a8 |
A |
G |
15: 100,680,913 (GRCm39) |
R72G |
probably benign |
Het |
Smarca5 |
A |
C |
8: 81,446,344 (GRCm39) |
L452W |
probably damaging |
Het |
Srcin1 |
T |
C |
11: 97,416,377 (GRCm39) |
K952E |
probably damaging |
Het |
Synpo2l |
G |
T |
14: 20,716,738 (GRCm39) |
Q79K |
possibly damaging |
Het |
Tmem174 |
T |
C |
13: 98,773,803 (GRCm39) |
E9G |
possibly damaging |
Het |
Tmem270 |
T |
C |
5: 134,930,644 (GRCm39) |
T206A |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,562,951 (GRCm39) |
T28668S |
possibly damaging |
Het |
Vmn1r118 |
A |
T |
7: 20,645,817 (GRCm39) |
S152R |
possibly damaging |
Het |
Vmn2r25 |
T |
A |
6: 123,816,960 (GRCm39) |
Q207L |
probably damaging |
Het |
Vmn2r81 |
T |
A |
10: 79,129,582 (GRCm39) |
S824R |
probably damaging |
Het |
Vps54 |
G |
A |
11: 21,258,771 (GRCm39) |
V733I |
probably benign |
Het |
Zfp518b |
G |
T |
5: 38,829,601 (GRCm39) |
D801E |
probably benign |
Het |
Zgrf1 |
C |
A |
3: 127,392,428 (GRCm39) |
P1316Q |
probably damaging |
Het |
Zzef1 |
C |
A |
11: 72,739,463 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Card14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01916:Card14
|
APN |
11 |
119,233,971 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02070:Card14
|
APN |
11 |
119,235,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02632:Card14
|
APN |
11 |
119,229,730 (GRCm39) |
missense |
probably benign |
0.02 |
R0183:Card14
|
UTSW |
11 |
119,217,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Card14
|
UTSW |
11 |
119,213,653 (GRCm39) |
missense |
probably benign |
|
R0766:Card14
|
UTSW |
11 |
119,215,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R1033:Card14
|
UTSW |
11 |
119,229,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:Card14
|
UTSW |
11 |
119,229,232 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1907:Card14
|
UTSW |
11 |
119,222,085 (GRCm39) |
missense |
probably benign |
0.00 |
R1992:Card14
|
UTSW |
11 |
119,212,647 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3729:Card14
|
UTSW |
11 |
119,224,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Card14
|
UTSW |
11 |
119,224,784 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4578:Card14
|
UTSW |
11 |
119,217,567 (GRCm39) |
missense |
probably benign |
0.20 |
R4763:Card14
|
UTSW |
11 |
119,234,001 (GRCm39) |
missense |
probably damaging |
0.99 |
R5117:Card14
|
UTSW |
11 |
119,229,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R5386:Card14
|
UTSW |
11 |
119,208,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R6457:Card14
|
UTSW |
11 |
119,230,428 (GRCm39) |
nonsense |
probably null |
|
R6622:Card14
|
UTSW |
11 |
119,224,814 (GRCm39) |
missense |
probably benign |
0.06 |
R6998:Card14
|
UTSW |
11 |
119,213,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7269:Card14
|
UTSW |
11 |
119,228,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R7304:Card14
|
UTSW |
11 |
119,228,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R7310:Card14
|
UTSW |
11 |
119,217,005 (GRCm39) |
missense |
probably null |
1.00 |
R7612:Card14
|
UTSW |
11 |
119,224,405 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7689:Card14
|
UTSW |
11 |
119,216,328 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8181:Card14
|
UTSW |
11 |
119,212,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R8188:Card14
|
UTSW |
11 |
119,228,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R8493:Card14
|
UTSW |
11 |
119,224,435 (GRCm39) |
critical splice donor site |
probably null |
|
R8499:Card14
|
UTSW |
11 |
119,222,070 (GRCm39) |
missense |
probably benign |
0.10 |
R8924:Card14
|
UTSW |
11 |
119,216,930 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9133:Card14
|
UTSW |
11 |
119,231,835 (GRCm39) |
missense |
probably damaging |
0.98 |
R9464:Card14
|
UTSW |
11 |
119,208,031 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Card14
|
UTSW |
11 |
119,231,887 (GRCm39) |
missense |
probably damaging |
0.98 |
|