Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Appl2 |
A |
G |
10: 83,438,762 (GRCm39) |
F556L |
probably damaging |
Het |
Atad2b |
T |
A |
12: 4,992,030 (GRCm39) |
S210T |
possibly damaging |
Het |
Aurka |
A |
G |
2: 172,201,673 (GRCm39) |
|
probably null |
Het |
Chid1 |
T |
A |
7: 141,076,339 (GRCm39) |
|
probably benign |
Het |
Dnase2b |
T |
A |
3: 146,288,244 (GRCm39) |
I284F |
probably damaging |
Het |
Dst |
C |
T |
1: 34,267,999 (GRCm39) |
T5325I |
probably benign |
Het |
Erbb3 |
A |
G |
10: 128,409,279 (GRCm39) |
|
probably null |
Het |
Fancl |
A |
G |
11: 26,419,695 (GRCm39) |
N316S |
possibly damaging |
Het |
Gabrd |
C |
A |
4: 155,473,058 (GRCm39) |
V72L |
probably damaging |
Het |
Hephl1 |
T |
A |
9: 14,988,060 (GRCm39) |
T683S |
probably benign |
Het |
Jazf1 |
A |
G |
6: 52,871,071 (GRCm39) |
|
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,927,201 (GRCm39) |
S1219T |
probably benign |
Het |
L3mbtl1 |
A |
T |
2: 162,806,489 (GRCm39) |
Y460F |
possibly damaging |
Het |
Map1b |
C |
T |
13: 99,571,810 (GRCm39) |
V304M |
probably damaging |
Het |
Msantd4 |
A |
G |
9: 4,384,099 (GRCm39) |
E140G |
probably damaging |
Het |
Myo16 |
A |
G |
8: 10,525,988 (GRCm39) |
K843E |
probably damaging |
Het |
Rap1gds1 |
G |
T |
3: 138,689,632 (GRCm39) |
|
probably null |
Het |
Rsph4a |
T |
C |
10: 33,785,144 (GRCm39) |
C148R |
probably damaging |
Het |
Slc7a9 |
A |
T |
7: 35,169,525 (GRCm39) |
|
probably benign |
Het |
Sptbn1 |
A |
G |
11: 30,073,855 (GRCm39) |
S1405P |
probably damaging |
Het |
Tex35 |
T |
C |
1: 156,927,314 (GRCm39) |
K154E |
possibly damaging |
Het |
Tpm3 |
T |
A |
3: 89,994,968 (GRCm39) |
|
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,158,960 (GRCm39) |
F2438L |
probably benign |
Het |
Wfdc8 |
T |
C |
2: 164,440,984 (GRCm39) |
D253G |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,841,861 (GRCm39) |
|
probably benign |
Het |
Zfp687 |
A |
G |
3: 94,918,767 (GRCm39) |
I335T |
probably damaging |
Het |
|
Other mutations in Chd8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00572:Chd8
|
APN |
14 |
52,463,595 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00694:Chd8
|
APN |
14 |
52,455,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Chd8
|
APN |
14 |
52,468,989 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01022:Chd8
|
APN |
14 |
52,474,450 (GRCm39) |
missense |
probably benign |
|
IGL01066:Chd8
|
APN |
14 |
52,455,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01083:Chd8
|
APN |
14 |
52,458,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01313:Chd8
|
APN |
14 |
52,448,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01396:Chd8
|
APN |
14 |
52,442,044 (GRCm39) |
unclassified |
probably benign |
|
IGL01476:Chd8
|
APN |
14 |
52,442,947 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01731:Chd8
|
APN |
14 |
52,450,111 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01895:Chd8
|
APN |
14 |
52,436,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02090:Chd8
|
APN |
14 |
52,464,691 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02344:Chd8
|
APN |
14 |
52,439,107 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02573:Chd8
|
APN |
14 |
52,457,191 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02601:Chd8
|
APN |
14 |
52,451,757 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02617:Chd8
|
APN |
14 |
52,472,648 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02873:Chd8
|
APN |
14 |
52,459,970 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02974:Chd8
|
APN |
14 |
52,439,158 (GRCm39) |
splice site |
probably null |
|
IGL03058:Chd8
|
APN |
14 |
52,455,730 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03076:Chd8
|
APN |
14 |
52,463,619 (GRCm39) |
splice site |
probably benign |
|
IGL03239:Chd8
|
APN |
14 |
52,465,005 (GRCm39) |
missense |
possibly damaging |
0.92 |
PIT4431001:Chd8
|
UTSW |
14 |
52,455,706 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4468001:Chd8
|
UTSW |
14 |
52,455,338 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4468001:Chd8
|
UTSW |
14 |
52,445,453 (GRCm39) |
missense |
probably benign |
|
R0006:Chd8
|
UTSW |
14 |
52,472,750 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0022:Chd8
|
UTSW |
14 |
52,470,312 (GRCm39) |
missense |
probably benign |
0.00 |
R0115:Chd8
|
UTSW |
14 |
52,474,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0131:Chd8
|
UTSW |
14 |
52,442,783 (GRCm39) |
missense |
probably benign |
0.15 |
R0131:Chd8
|
UTSW |
14 |
52,442,783 (GRCm39) |
missense |
probably benign |
0.15 |
R0132:Chd8
|
UTSW |
14 |
52,442,783 (GRCm39) |
missense |
probably benign |
0.15 |
R0419:Chd8
|
UTSW |
14 |
52,441,517 (GRCm39) |
missense |
probably benign |
0.24 |
R0440:Chd8
|
UTSW |
14 |
52,442,283 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0452:Chd8
|
UTSW |
14 |
52,452,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Chd8
|
UTSW |
14 |
52,474,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0624:Chd8
|
UTSW |
14 |
52,457,214 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0650:Chd8
|
UTSW |
14 |
52,439,761 (GRCm39) |
missense |
probably benign |
0.09 |
R0691:Chd8
|
UTSW |
14 |
52,450,890 (GRCm39) |
missense |
probably damaging |
0.96 |
R0790:Chd8
|
UTSW |
14 |
52,441,482 (GRCm39) |
missense |
probably benign |
0.07 |
R0835:Chd8
|
UTSW |
14 |
52,441,482 (GRCm39) |
missense |
probably benign |
0.07 |
R1180:Chd8
|
UTSW |
14 |
52,458,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R1411:Chd8
|
UTSW |
14 |
52,462,103 (GRCm39) |
missense |
probably benign |
|
R1725:Chd8
|
UTSW |
14 |
52,470,030 (GRCm39) |
missense |
probably benign |
0.08 |
R1838:Chd8
|
UTSW |
14 |
52,442,340 (GRCm39) |
missense |
probably benign |
0.11 |
R1839:Chd8
|
UTSW |
14 |
52,442,340 (GRCm39) |
missense |
probably benign |
0.11 |
R1968:Chd8
|
UTSW |
14 |
52,458,450 (GRCm39) |
missense |
probably damaging |
0.98 |
R2020:Chd8
|
UTSW |
14 |
52,452,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R2024:Chd8
|
UTSW |
14 |
52,468,950 (GRCm39) |
missense |
probably benign |
0.23 |
R2139:Chd8
|
UTSW |
14 |
52,474,428 (GRCm39) |
missense |
probably benign |
0.32 |
R2163:Chd8
|
UTSW |
14 |
52,436,275 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2342:Chd8
|
UTSW |
14 |
52,442,674 (GRCm39) |
missense |
probably benign |
0.25 |
R2844:Chd8
|
UTSW |
14 |
52,441,952 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3500:Chd8
|
UTSW |
14 |
52,443,110 (GRCm39) |
missense |
probably benign |
0.00 |
R3861:Chd8
|
UTSW |
14 |
52,474,578 (GRCm39) |
missense |
probably benign |
0.13 |
R4154:Chd8
|
UTSW |
14 |
52,444,668 (GRCm39) |
unclassified |
probably benign |
|
R4445:Chd8
|
UTSW |
14 |
52,441,984 (GRCm39) |
splice site |
probably null |
|
R4628:Chd8
|
UTSW |
14 |
52,444,372 (GRCm39) |
missense |
probably benign |
0.03 |
R4779:Chd8
|
UTSW |
14 |
52,468,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Chd8
|
UTSW |
14 |
52,442,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Chd8
|
UTSW |
14 |
52,442,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Chd8
|
UTSW |
14 |
52,441,372 (GRCm39) |
missense |
probably benign |
0.09 |
R5280:Chd8
|
UTSW |
14 |
52,442,582 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5331:Chd8
|
UTSW |
14 |
52,439,571 (GRCm39) |
intron |
probably benign |
|
R5348:Chd8
|
UTSW |
14 |
52,470,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Chd8
|
UTSW |
14 |
52,441,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R5470:Chd8
|
UTSW |
14 |
52,450,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Chd8
|
UTSW |
14 |
52,452,652 (GRCm39) |
missense |
probably benign |
0.15 |
R5488:Chd8
|
UTSW |
14 |
52,450,505 (GRCm39) |
intron |
probably benign |
|
R5489:Chd8
|
UTSW |
14 |
52,450,505 (GRCm39) |
intron |
probably benign |
|
R5499:Chd8
|
UTSW |
14 |
52,441,888 (GRCm39) |
critical splice donor site |
probably null |
|
R5988:Chd8
|
UTSW |
14 |
52,455,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Chd8
|
UTSW |
14 |
52,458,528 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6125:Chd8
|
UTSW |
14 |
52,444,491 (GRCm39) |
missense |
probably benign |
0.16 |
R6212:Chd8
|
UTSW |
14 |
52,439,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Chd8
|
UTSW |
14 |
52,441,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Chd8
|
UTSW |
14 |
52,440,042 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6576:Chd8
|
UTSW |
14 |
52,453,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6590:Chd8
|
UTSW |
14 |
52,464,694 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6690:Chd8
|
UTSW |
14 |
52,464,694 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6786:Chd8
|
UTSW |
14 |
52,464,125 (GRCm39) |
missense |
probably benign |
0.33 |
R6913:Chd8
|
UTSW |
14 |
52,451,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R7090:Chd8
|
UTSW |
14 |
52,452,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R7107:Chd8
|
UTSW |
14 |
52,450,129 (GRCm39) |
missense |
probably benign |
0.07 |
R7138:Chd8
|
UTSW |
14 |
52,451,955 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7383:Chd8
|
UTSW |
14 |
52,452,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Chd8
|
UTSW |
14 |
52,470,312 (GRCm39) |
missense |
probably benign |
|
R7471:Chd8
|
UTSW |
14 |
52,441,569 (GRCm39) |
missense |
probably benign |
|
R7625:Chd8
|
UTSW |
14 |
52,474,534 (GRCm39) |
missense |
probably benign |
0.04 |
R7790:Chd8
|
UTSW |
14 |
52,463,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Chd8
|
UTSW |
14 |
52,451,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R7937:Chd8
|
UTSW |
14 |
52,464,963 (GRCm39) |
missense |
probably benign |
0.02 |
R8092:Chd8
|
UTSW |
14 |
52,455,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Chd8
|
UTSW |
14 |
52,450,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R8321:Chd8
|
UTSW |
14 |
52,470,024 (GRCm39) |
missense |
probably benign |
0.01 |
R8371:Chd8
|
UTSW |
14 |
52,470,275 (GRCm39) |
missense |
probably benign |
|
R8425:Chd8
|
UTSW |
14 |
52,448,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8674:Chd8
|
UTSW |
14 |
52,450,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R8794:Chd8
|
UTSW |
14 |
52,441,904 (GRCm39) |
missense |
probably damaging |
0.98 |
R8828:Chd8
|
UTSW |
14 |
52,448,037 (GRCm39) |
frame shift |
probably null |
|
R8909:Chd8
|
UTSW |
14 |
52,450,389 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9194:Chd8
|
UTSW |
14 |
52,439,650 (GRCm39) |
missense |
probably benign |
0.01 |
R9278:Chd8
|
UTSW |
14 |
52,472,627 (GRCm39) |
missense |
probably benign |
0.01 |
R9489:Chd8
|
UTSW |
14 |
52,457,055 (GRCm39) |
missense |
probably damaging |
0.98 |
R9501:Chd8
|
UTSW |
14 |
52,452,045 (GRCm39) |
missense |
probably benign |
0.04 |
R9546:Chd8
|
UTSW |
14 |
52,453,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R9605:Chd8
|
UTSW |
14 |
52,457,055 (GRCm39) |
missense |
probably damaging |
0.98 |
R9694:Chd8
|
UTSW |
14 |
52,441,341 (GRCm39) |
missense |
possibly damaging |
0.86 |
|