Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef11 |
T |
C |
3: 87,636,909 (GRCm39) |
F1023S |
probably damaging |
Het |
Atp1a1 |
G |
A |
3: 101,498,023 (GRCm39) |
R255C |
probably damaging |
Het |
Bbs12 |
A |
G |
3: 37,374,700 (GRCm39) |
I383V |
probably benign |
Het |
Cacna1h |
G |
A |
17: 25,604,668 (GRCm39) |
P1215L |
probably benign |
Het |
Calm5 |
A |
T |
13: 3,904,491 (GRCm39) |
K62* |
probably null |
Het |
Cspg4b |
A |
G |
13: 113,454,217 (GRCm39) |
T88A |
probably benign |
Het |
Dlgap2 |
A |
T |
8: 14,777,193 (GRCm39) |
H146L |
possibly damaging |
Het |
Dop1a |
G |
A |
9: 86,403,186 (GRCm39) |
R1462H |
probably damaging |
Het |
Dusp29 |
C |
A |
14: 21,736,758 (GRCm39) |
V115L |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,168,706 (GRCm39) |
N369S |
probably damaging |
Het |
Fer1l4 |
A |
C |
2: 155,888,907 (GRCm39) |
V422G |
probably damaging |
Het |
Fstl4 |
T |
C |
11: 53,077,130 (GRCm39) |
M629T |
probably benign |
Het |
Galnt18 |
A |
G |
7: 111,084,400 (GRCm39) |
Y507H |
probably damaging |
Het |
Gar1 |
C |
A |
3: 129,624,399 (GRCm39) |
|
probably benign |
Het |
Gm19402 |
T |
C |
10: 77,526,507 (GRCm39) |
T29A |
probably damaging |
Het |
Gm826 |
A |
G |
2: 160,169,034 (GRCm39) |
F92L |
unknown |
Het |
H1f0 |
T |
A |
15: 78,913,070 (GRCm39) |
I50N |
probably damaging |
Het |
H2-DMb1 |
A |
G |
17: 34,376,439 (GRCm39) |
Y186C |
probably damaging |
Het |
Hgf |
A |
G |
5: 16,803,159 (GRCm39) |
N357S |
probably damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hsf2 |
T |
C |
10: 57,388,101 (GRCm39) |
V415A |
probably benign |
Het |
Ins2 |
C |
A |
7: 142,233,430 (GRCm39) |
|
probably null |
Het |
Kel |
A |
T |
6: 41,667,720 (GRCm39) |
F89L |
probably damaging |
Het |
Lratd2 |
T |
C |
15: 60,695,146 (GRCm39) |
N200S |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,392,386 (GRCm39) |
D1013G |
probably benign |
Het |
Ltbp4 |
C |
A |
7: 27,027,180 (GRCm39) |
G397C |
probably damaging |
Het |
Madd |
A |
G |
2: 90,982,797 (GRCm39) |
|
probably null |
Het |
Map4k4 |
A |
G |
1: 40,043,125 (GRCm39) |
D660G |
possibly damaging |
Het |
Mdm4 |
G |
A |
1: 132,922,248 (GRCm39) |
T298I |
possibly damaging |
Het |
Mlip |
G |
A |
9: 77,137,764 (GRCm39) |
S381L |
probably damaging |
Het |
Mpdz |
A |
T |
4: 81,215,764 (GRCm39) |
C1487S |
probably benign |
Het |
Mtus1 |
A |
G |
8: 41,537,576 (GRCm39) |
S47P |
probably damaging |
Het |
Nek1 |
T |
C |
8: 61,481,735 (GRCm39) |
S217P |
probably damaging |
Het |
Or10ag59 |
T |
C |
2: 87,405,590 (GRCm39) |
I54T |
probably benign |
Het |
Or5b123 |
C |
T |
19: 13,597,249 (GRCm39) |
A241V |
probably benign |
Het |
Pcdhb10 |
T |
C |
18: 37,546,679 (GRCm39) |
V585A |
possibly damaging |
Het |
Perm1 |
A |
G |
4: 156,302,176 (GRCm39) |
E240G |
probably benign |
Het |
Pkdrej |
T |
C |
15: 85,700,585 (GRCm39) |
T1784A |
probably damaging |
Het |
Pnpla8 |
C |
T |
12: 44,354,772 (GRCm39) |
T644M |
possibly damaging |
Het |
Rgs2 |
T |
C |
1: 143,879,763 (GRCm39) |
K32E |
probably damaging |
Het |
Scyl3 |
A |
T |
1: 163,778,145 (GRCm39) |
M428L |
probably benign |
Het |
Slc30a8 |
A |
G |
15: 52,198,530 (GRCm39) |
D325G |
probably benign |
Het |
Slc5a9 |
G |
T |
4: 111,741,002 (GRCm39) |
T548K |
probably damaging |
Het |
Slc9b2 |
G |
A |
3: 135,036,457 (GRCm39) |
|
probably null |
Het |
Slco3a1 |
C |
T |
7: 73,968,254 (GRCm39) |
D489N |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,461,560 (GRCm39) |
|
probably null |
Het |
Stk39 |
C |
A |
2: 68,222,468 (GRCm39) |
G199C |
probably damaging |
Het |
Tbx1 |
A |
G |
16: 18,402,216 (GRCm39) |
F263L |
probably damaging |
Het |
Tcf21 |
G |
T |
10: 22,695,665 (GRCm39) |
N46K |
probably benign |
Het |
Tdrd9 |
T |
A |
12: 112,034,632 (GRCm39) |
M1357K |
possibly damaging |
Het |
Tll1 |
A |
G |
8: 64,504,521 (GRCm39) |
L625P |
probably damaging |
Het |
Tmem131 |
G |
A |
1: 36,847,387 (GRCm39) |
S1237L |
possibly damaging |
Het |
Trdv5 |
T |
C |
14: 54,386,298 (GRCm39) |
K56E |
possibly damaging |
Het |
Triml2 |
G |
A |
8: 43,640,659 (GRCm39) |
V172I |
probably benign |
Het |
Trmt44 |
C |
A |
5: 35,722,842 (GRCm39) |
D409Y |
probably damaging |
Het |
Ube2o |
C |
T |
11: 116,432,204 (GRCm39) |
A921T |
probably damaging |
Het |
Ube2o |
T |
C |
11: 116,435,576 (GRCm39) |
D404G |
possibly damaging |
Het |
Ube4b |
T |
C |
4: 149,483,203 (GRCm39) |
T22A |
probably benign |
Het |
Ugp2 |
A |
T |
11: 21,279,815 (GRCm39) |
F327L |
probably damaging |
Het |
Virma |
T |
C |
4: 11,521,172 (GRCm39) |
S910P |
probably damaging |
Het |
Vmn2r9 |
A |
G |
5: 108,990,836 (GRCm39) |
Y842H |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,463,871 (GRCm39) |
D1368G |
possibly damaging |
Het |
Zfp980 |
T |
A |
4: 145,429,208 (GRCm39) |
*646R |
probably null |
Het |
Zranb3 |
T |
A |
1: 127,887,482 (GRCm39) |
N982Y |
probably benign |
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 |
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 |
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 |
|