Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy10 |
T |
C |
1: 165,352,631 (GRCm39) |
|
probably null |
Het |
Anxa11 |
T |
C |
14: 25,874,652 (GRCm39) |
I221T |
probably damaging |
Het |
Arhgap33 |
C |
G |
7: 30,225,871 (GRCm39) |
R565P |
probably damaging |
Het |
Bmpr2 |
T |
C |
1: 59,880,584 (GRCm39) |
|
probably benign |
Het |
Btn2a2 |
T |
A |
13: 23,670,580 (GRCm39) |
H51L |
probably benign |
Het |
Casz1 |
T |
C |
4: 149,028,851 (GRCm39) |
S1099P |
probably benign |
Het |
Cnot4 |
A |
G |
6: 35,028,438 (GRCm39) |
S393P |
possibly damaging |
Het |
Cntnap5a |
T |
C |
1: 116,112,191 (GRCm39) |
|
probably benign |
Het |
Cobl |
T |
C |
11: 12,204,699 (GRCm39) |
T586A |
probably benign |
Het |
Crocc |
T |
C |
4: 140,747,224 (GRCm39) |
K1528R |
probably benign |
Het |
Crocc |
A |
G |
4: 140,744,382 (GRCm39) |
L1838P |
probably benign |
Het |
Dact2 |
A |
G |
17: 14,417,303 (GRCm39) |
V299A |
probably benign |
Het |
Dapk1 |
C |
A |
13: 60,909,198 (GRCm39) |
N1270K |
probably benign |
Het |
Ddx41 |
T |
C |
13: 55,680,819 (GRCm39) |
Y375C |
probably damaging |
Het |
Dock5 |
T |
A |
14: 68,022,383 (GRCm39) |
|
probably null |
Het |
Dyrk4 |
T |
G |
6: 126,863,612 (GRCm39) |
|
probably null |
Het |
Eno1b |
T |
C |
18: 48,180,806 (GRCm39) |
I328T |
probably benign |
Het |
Fam210b |
A |
G |
2: 172,187,773 (GRCm39) |
|
probably benign |
Het |
Fbxl13 |
A |
G |
5: 21,819,712 (GRCm39) |
I229T |
probably benign |
Het |
Fbxo39 |
A |
G |
11: 72,207,747 (GRCm39) |
D33G |
probably damaging |
Het |
Fbxw11 |
A |
G |
11: 32,670,496 (GRCm39) |
E120G |
probably damaging |
Het |
Fbxw2 |
A |
T |
2: 34,701,032 (GRCm39) |
L261Q |
probably damaging |
Het |
Gm5800 |
A |
C |
14: 51,953,461 (GRCm39) |
N51K |
probably benign |
Het |
Gm6899 |
A |
G |
11: 26,543,768 (GRCm39) |
|
probably benign |
Het |
Gpx8 |
T |
C |
13: 113,182,035 (GRCm39) |
T133A |
possibly damaging |
Het |
Grin3a |
C |
T |
4: 49,665,351 (GRCm39) |
V1095M |
probably damaging |
Het |
Grip2 |
T |
C |
6: 91,773,178 (GRCm39) |
|
probably benign |
Het |
Hacd4 |
A |
G |
4: 88,355,757 (GRCm39) |
F43L |
probably damaging |
Het |
Hif1a |
T |
G |
12: 73,989,049 (GRCm39) |
S645R |
probably benign |
Het |
Hipk3 |
A |
G |
2: 104,263,982 (GRCm39) |
S839P |
possibly damaging |
Het |
Idi2l |
C |
A |
13: 8,990,802 (GRCm39) |
|
probably benign |
Het |
Il16 |
A |
T |
7: 83,327,183 (GRCm39) |
|
probably benign |
Het |
Il3ra |
T |
A |
14: 14,351,166 (GRCm38) |
|
probably null |
Het |
Il5ra |
A |
G |
6: 106,721,296 (GRCm39) |
M1T |
probably null |
Het |
Klra2 |
G |
A |
6: 131,197,148 (GRCm39) |
R251C |
probably benign |
Het |
Lamc2 |
C |
T |
1: 153,009,367 (GRCm39) |
V813M |
probably benign |
Het |
Lbr |
A |
G |
1: 181,659,778 (GRCm39) |
V139A |
probably benign |
Het |
Lrp5 |
T |
C |
19: 3,650,777 (GRCm39) |
D1219G |
possibly damaging |
Het |
Map3k6 |
C |
T |
4: 132,972,863 (GRCm39) |
P341S |
possibly damaging |
Het |
Mcts2 |
A |
G |
2: 152,529,609 (GRCm39) |
E140G |
probably benign |
Het |
Med1 |
T |
C |
11: 98,060,264 (GRCm39) |
M222V |
probably benign |
Het |
Mef2a |
G |
T |
7: 66,884,896 (GRCm39) |
S406* |
probably null |
Het |
Muc19 |
A |
T |
15: 91,784,696 (GRCm39) |
|
noncoding transcript |
Het |
Nr1h2 |
A |
G |
7: 44,201,684 (GRCm39) |
|
probably benign |
Het |
Or13j1 |
A |
T |
4: 43,706,592 (GRCm39) |
|
probably null |
Het |
Or2w6 |
C |
A |
13: 21,843,316 (GRCm39) |
R59L |
probably damaging |
Het |
Or56a42-ps1 |
A |
G |
7: 104,777,425 (GRCm39) |
V73A |
possibly damaging |
Het |
Or5ac23 |
A |
T |
16: 59,149,123 (GRCm39) |
F250I |
probably damaging |
Het |
P4hb |
G |
A |
11: 120,459,070 (GRCm39) |
T141I |
possibly damaging |
Het |
Polr3a |
A |
G |
14: 24,534,202 (GRCm39) |
V101A |
probably benign |
Het |
Pou4f2 |
A |
G |
8: 79,161,869 (GRCm39) |
S245P |
probably benign |
Het |
Pramel26 |
G |
T |
4: 143,539,222 (GRCm39) |
N90K |
probably damaging |
Het |
Rnpep |
A |
G |
1: 135,200,157 (GRCm39) |
V266A |
probably damaging |
Het |
Scly |
G |
A |
1: 91,237,555 (GRCm39) |
G206R |
probably damaging |
Het |
Sec14l3 |
A |
T |
11: 4,024,814 (GRCm39) |
K254N |
probably damaging |
Het |
Sgpp1 |
A |
T |
12: 75,781,874 (GRCm39) |
I155N |
probably damaging |
Het |
Slc22a14 |
A |
G |
9: 119,001,190 (GRCm39) |
L468P |
probably damaging |
Het |
Slc22a27 |
A |
G |
19: 7,843,249 (GRCm39) |
F377L |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,253,719 (GRCm39) |
I625V |
probably benign |
Het |
Slc47a2 |
A |
T |
11: 61,200,802 (GRCm39) |
I373N |
probably damaging |
Het |
Slfn10-ps |
A |
T |
11: 82,926,479 (GRCm39) |
|
noncoding transcript |
Het |
Sort1 |
A |
G |
3: 108,246,226 (GRCm39) |
D401G |
probably damaging |
Het |
Sprr2a3 |
G |
T |
3: 92,195,897 (GRCm39) |
M1I |
probably null |
Het |
Sycp2 |
A |
C |
2: 177,998,373 (GRCm39) |
V1049G |
possibly damaging |
Het |
Tecrl |
T |
A |
5: 83,502,775 (GRCm39) |
K10* |
probably null |
Het |
Tnpo3 |
A |
T |
6: 29,578,564 (GRCm39) |
C303* |
probably null |
Het |
Vmn2r23 |
A |
G |
6: 123,706,680 (GRCm39) |
I503M |
probably benign |
Het |
Zbtb8os |
T |
A |
4: 129,240,670 (GRCm39) |
I164N |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,807,399 (GRCm39) |
N1882D |
probably benign |
Het |
Zfp91 |
T |
C |
19: 12,747,459 (GRCm39) |
I555V |
possibly damaging |
Het |
|
Other mutations in Smarcd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01516:Smarcd1
|
APN |
15 |
99,610,094 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01714:Smarcd1
|
APN |
15 |
99,610,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Smarcd1
|
APN |
15 |
99,609,082 (GRCm39) |
missense |
possibly damaging |
0.83 |
P0021:Smarcd1
|
UTSW |
15 |
99,610,242 (GRCm39) |
splice site |
probably benign |
|
R0645:Smarcd1
|
UTSW |
15 |
99,605,267 (GRCm39) |
splice site |
probably null |
|
R1531:Smarcd1
|
UTSW |
15 |
99,605,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Smarcd1
|
UTSW |
15 |
99,605,519 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1857:Smarcd1
|
UTSW |
15 |
99,607,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R3003:Smarcd1
|
UTSW |
15 |
99,610,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R4170:Smarcd1
|
UTSW |
15 |
99,605,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Smarcd1
|
UTSW |
15 |
99,605,862 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5116:Smarcd1
|
UTSW |
15 |
99,600,369 (GRCm39) |
missense |
probably benign |
0.00 |
R5358:Smarcd1
|
UTSW |
15 |
99,601,128 (GRCm39) |
nonsense |
probably null |
|
R5559:Smarcd1
|
UTSW |
15 |
99,601,176 (GRCm39) |
critical splice donor site |
probably null |
|
R6026:Smarcd1
|
UTSW |
15 |
99,603,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6424:Smarcd1
|
UTSW |
15 |
99,602,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Smarcd1
|
UTSW |
15 |
99,605,766 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7126:Smarcd1
|
UTSW |
15 |
99,607,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R8476:Smarcd1
|
UTSW |
15 |
99,600,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R8487:Smarcd1
|
UTSW |
15 |
99,605,657 (GRCm39) |
missense |
probably damaging |
0.96 |
R8872:Smarcd1
|
UTSW |
15 |
99,608,975 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Smarcd1
|
UTSW |
15 |
99,600,330 (GRCm39) |
missense |
probably benign |
0.13 |
|