Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
A |
T |
16: 20,214,853 (GRCm39) |
V439D |
probably damaging |
Het |
Abcf3 |
T |
C |
16: 20,379,125 (GRCm39) |
S664P |
probably damaging |
Het |
Anp32a |
A |
G |
9: 62,282,019 (GRCm39) |
S202G |
unknown |
Het |
Aste1 |
G |
A |
9: 105,273,880 (GRCm39) |
C40Y |
probably benign |
Het |
AU040320 |
A |
G |
4: 126,735,032 (GRCm39) |
K782R |
probably benign |
Het |
Bach1 |
A |
G |
16: 87,515,999 (GRCm39) |
Q180R |
probably benign |
Het |
Ccdc149 |
A |
G |
5: 52,542,477 (GRCm39) |
S372P |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,091,481 (GRCm39) |
S1587G |
possibly damaging |
Het |
Chd2 |
A |
T |
7: 73,130,294 (GRCm39) |
I787N |
probably damaging |
Het |
Clca3a2 |
C |
A |
3: 144,777,322 (GRCm39) |
E850* |
probably null |
Het |
Clpb |
G |
A |
7: 101,427,780 (GRCm39) |
G375D |
probably damaging |
Het |
Cobl |
T |
A |
11: 12,328,235 (GRCm39) |
I124F |
possibly damaging |
Het |
Cope |
A |
G |
8: 70,765,363 (GRCm39) |
N271S |
probably benign |
Het |
Cyp11b2 |
T |
C |
15: 74,722,961 (GRCm39) |
D479G |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,419,041 (GRCm39) |
C611S |
probably benign |
Het |
Drosha |
G |
T |
15: 12,928,992 (GRCm39) |
V1299L |
probably damaging |
Het |
Dst |
A |
G |
1: 34,227,849 (GRCm39) |
Y1814C |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,209,130 (GRCm39) |
C1082R |
probably damaging |
Het |
Fbxw22 |
A |
T |
9: 109,207,920 (GRCm39) |
N450K |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,470,990 (GRCm39) |
I4925F |
possibly damaging |
Het |
Iho1 |
A |
T |
9: 108,282,500 (GRCm39) |
V396E |
probably benign |
Het |
Kin |
G |
T |
2: 10,085,478 (GRCm39) |
A13S |
probably benign |
Het |
Lrp1b |
G |
A |
2: 41,172,247 (GRCm39) |
R1581C |
|
Het |
Myl2 |
T |
C |
5: 122,241,921 (GRCm39) |
I66T |
probably benign |
Het |
Npy5r |
A |
G |
8: 67,134,137 (GRCm39) |
C219R |
probably damaging |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Oosp1 |
A |
T |
19: 11,664,757 (GRCm39) |
Y100N |
probably damaging |
Het |
Pdk4 |
A |
G |
6: 5,491,084 (GRCm39) |
L227P |
probably damaging |
Het |
Perm1 |
A |
T |
4: 156,302,177 (GRCm39) |
E240D |
probably benign |
Het |
Pi4ka |
A |
G |
16: 17,204,156 (GRCm39) |
L46P |
|
Het |
Pik3ca |
A |
G |
3: 32,504,062 (GRCm39) |
Y584C |
probably damaging |
Het |
Prnp |
T |
C |
2: 131,779,037 (GRCm39) |
S230P |
probably benign |
Het |
Rftn2 |
A |
G |
1: 55,241,355 (GRCm39) |
F315S |
possibly damaging |
Het |
Rp1l1 |
A |
G |
14: 64,266,039 (GRCm39) |
R542G |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,582,579 (GRCm39) |
N106S |
probably benign |
Het |
Sec24a |
A |
T |
11: 51,603,122 (GRCm39) |
N775K |
probably damaging |
Het |
Slc13a2 |
G |
A |
11: 78,291,633 (GRCm39) |
T340M |
probably damaging |
Het |
Slc5a3 |
A |
G |
16: 91,875,257 (GRCm39) |
Y438C |
probably damaging |
Het |
Smarca2 |
A |
G |
19: 26,617,977 (GRCm39) |
Q336R |
probably benign |
Het |
Snx7 |
A |
G |
3: 117,632,611 (GRCm39) |
V160A |
possibly damaging |
Het |
Stim1 |
A |
T |
7: 102,060,506 (GRCm39) |
D183V |
possibly damaging |
Het |
Strn3 |
A |
T |
12: 51,696,956 (GRCm39) |
D258E |
probably damaging |
Het |
Stxbp1 |
G |
A |
2: 32,692,825 (GRCm39) |
A397V |
probably benign |
Het |
Tacr3 |
A |
G |
3: 134,535,092 (GRCm39) |
H20R |
probably benign |
Het |
Tg |
T |
A |
15: 66,718,923 (GRCm39) |
D2626E |
possibly damaging |
Het |
Tmem131 |
A |
G |
1: 36,858,265 (GRCm39) |
M694T |
possibly damaging |
Het |
Tpp1 |
G |
A |
7: 105,398,464 (GRCm39) |
A284V |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,176,943 (GRCm39) |
T327S |
probably benign |
Het |
Trim14 |
A |
G |
4: 46,510,404 (GRCm39) |
W274R |
unknown |
Het |
Tshz2 |
A |
T |
2: 169,725,759 (GRCm39) |
E118D |
probably benign |
Het |
Tshz3 |
A |
G |
7: 36,470,980 (GRCm39) |
T990A |
probably damaging |
Het |
Usp40 |
T |
C |
1: 87,925,557 (GRCm39) |
D224G |
probably benign |
Het |
Vmn2r130 |
A |
G |
17: 23,282,650 (GRCm39) |
Q110R |
probably benign |
Het |
Zscan2 |
A |
G |
7: 80,525,890 (GRCm39) |
K537R |
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 |
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 |
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 |
|