Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,899,113 (GRCm39) |
C698* |
probably null |
Het |
Acacb |
G |
A |
5: 114,345,387 (GRCm39) |
V947M |
probably benign |
Het |
Acadsb |
T |
G |
7: 131,042,968 (GRCm39) |
L343R |
probably damaging |
Het |
Adgrf2 |
C |
T |
17: 43,021,874 (GRCm39) |
E317K |
probably damaging |
Het |
Agap2 |
A |
G |
10: 126,923,154 (GRCm39) |
T663A |
unknown |
Het |
Akap8 |
A |
T |
17: 32,535,515 (GRCm39) |
F166L |
possibly damaging |
Het |
Ankrd17 |
A |
T |
5: 90,390,836 (GRCm39) |
M2278K |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,705,242 (GRCm39) |
S148P |
probably damaging |
Het |
Brf1 |
T |
C |
12: 112,933,835 (GRCm39) |
E266G |
probably damaging |
Het |
Cabin1 |
T |
C |
10: 75,581,187 (GRCm39) |
K380E |
probably damaging |
Het |
Catsper2 |
T |
C |
2: 121,227,544 (GRCm39) |
D542G |
possibly damaging |
Het |
Cbln4 |
C |
A |
2: 171,884,095 (GRCm39) |
D42Y |
probably damaging |
Het |
Ccn6 |
T |
A |
10: 39,034,473 (GRCm39) |
Q43L |
possibly damaging |
Het |
Cd5 |
C |
T |
19: 10,697,668 (GRCm39) |
R437Q |
probably damaging |
Het |
Ceacam18 |
G |
C |
7: 43,288,706 (GRCm39) |
E152D |
possibly damaging |
Het |
Chodl |
T |
G |
16: 78,738,335 (GRCm39) |
I101R |
probably damaging |
Het |
Clk4 |
T |
G |
11: 51,168,759 (GRCm39) |
F377L |
probably damaging |
Het |
Cntnap3 |
C |
T |
13: 64,929,539 (GRCm39) |
|
probably null |
Het |
Dab2 |
A |
G |
15: 6,458,780 (GRCm39) |
S231G |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,617,361 (GRCm39) |
H118Q |
probably benign |
Het |
Dnah10 |
T |
C |
5: 124,900,009 (GRCm39) |
F3869S |
probably damaging |
Het |
Edil3 |
C |
T |
13: 89,279,847 (GRCm39) |
T175I |
probably damaging |
Het |
Eif1ad18 |
T |
G |
12: 88,050,648 (GRCm39) |
I61R |
probably damaging |
Het |
Fap |
A |
G |
2: 62,372,522 (GRCm39) |
S319P |
probably benign |
Het |
Frmpd2 |
T |
A |
14: 33,293,761 (GRCm39) |
V1309E |
probably benign |
Het |
Galntl5 |
T |
A |
5: 25,394,842 (GRCm39) |
S70T |
probably benign |
Het |
Gm5622 |
G |
T |
14: 51,893,339 (GRCm39) |
E89* |
probably null |
Het |
Gna15 |
G |
A |
10: 81,343,881 (GRCm39) |
T260M |
probably damaging |
Het |
Gucy2c |
A |
G |
6: 136,705,342 (GRCm39) |
I531T |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,135,417 (GRCm39) |
V238A |
probably damaging |
Het |
Htr2a |
A |
G |
14: 74,943,182 (GRCm39) |
Y254C |
probably damaging |
Het |
Inpp5b |
A |
G |
4: 124,679,065 (GRCm39) |
R491G |
probably damaging |
Het |
Kcnt2 |
C |
T |
1: 140,523,778 (GRCm39) |
L1093F |
possibly damaging |
Het |
Kcp |
C |
A |
6: 29,491,861 (GRCm39) |
E922* |
probably null |
Het |
Lrp2 |
G |
A |
2: 69,296,089 (GRCm39) |
A3340V |
possibly damaging |
Het |
Lrrn1 |
T |
G |
6: 107,545,336 (GRCm39) |
V378G |
probably damaging |
Het |
Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
Net1 |
G |
A |
13: 3,938,510 (GRCm39) |
R126C |
probably damaging |
Het |
Nipsnap3a |
T |
C |
4: 52,993,978 (GRCm39) |
C20R |
probably benign |
Het |
Nxpe2 |
C |
T |
9: 48,232,006 (GRCm39) |
C317Y |
probably damaging |
Het |
Or10v9 |
T |
A |
19: 11,832,652 (GRCm39) |
I222F |
probably damaging |
Het |
Or52h1 |
T |
C |
7: 103,829,504 (GRCm39) |
Y37C |
probably damaging |
Het |
Or8b8 |
T |
C |
9: 37,809,360 (GRCm39) |
I220T |
probably damaging |
Het |
Or8g54 |
T |
G |
9: 39,707,086 (GRCm39) |
Y138* |
probably null |
Het |
Orm1 |
T |
A |
4: 63,262,949 (GRCm39) |
W39R |
probably damaging |
Het |
Pds5b |
A |
T |
5: 150,724,142 (GRCm39) |
K1240* |
probably null |
Het |
Pdss1 |
T |
A |
2: 22,802,681 (GRCm39) |
H173Q |
probably damaging |
Het |
Pebp1 |
A |
G |
5: 117,423,882 (GRCm39) |
W84R |
probably damaging |
Het |
Pla2g4e |
C |
T |
2: 120,001,759 (GRCm39) |
C630Y |
probably damaging |
Het |
Plaat3 |
T |
A |
19: 7,556,550 (GRCm39) |
V117E |
probably damaging |
Het |
Plekho2 |
G |
T |
9: 65,463,635 (GRCm39) |
Q405K |
probably benign |
Het |
Plppr2 |
T |
A |
9: 21,855,708 (GRCm39) |
V227E |
probably damaging |
Het |
Pphln1-ps1 |
T |
A |
16: 13,495,589 (GRCm39) |
D229E |
probably benign |
Het |
Rapgef4 |
T |
C |
2: 72,028,707 (GRCm39) |
S393P |
probably damaging |
Het |
Rapgefl1 |
A |
G |
11: 98,737,900 (GRCm39) |
|
probably null |
Het |
Ripk3 |
C |
A |
14: 56,025,803 (GRCm39) |
R19L |
probably benign |
Het |
Rnase10 |
G |
T |
14: 51,247,167 (GRCm39) |
V182F |
probably damaging |
Het |
Rsf1 |
T |
A |
7: 97,319,002 (GRCm39) |
S917R |
|
Het |
Sephs2 |
T |
C |
7: 126,872,187 (GRCm39) |
N302S |
possibly damaging |
Het |
Slc13a2 |
C |
T |
11: 78,289,950 (GRCm39) |
V455M |
possibly damaging |
Het |
Slc30a2 |
A |
T |
4: 134,071,429 (GRCm39) |
D54V |
probably benign |
Het |
Slco6c1 |
T |
C |
1: 97,047,706 (GRCm39) |
E199G |
possibly damaging |
Het |
Snx27 |
A |
T |
3: 94,436,247 (GRCm39) |
M256K |
probably benign |
Het |
Spag4 |
T |
A |
2: 155,908,519 (GRCm39) |
S150T |
probably benign |
Het |
Spon1 |
T |
A |
7: 113,635,945 (GRCm39) |
C720S |
probably damaging |
Het |
Tbc1d22a |
T |
C |
15: 86,123,356 (GRCm39) |
S166P |
probably benign |
Het |
Tbc1d9 |
T |
C |
8: 83,937,113 (GRCm39) |
I65T |
probably damaging |
Het |
Tmem176a |
T |
A |
6: 48,820,953 (GRCm39) |
V141D |
probably damaging |
Het |
Tmem268 |
G |
A |
4: 63,480,687 (GRCm39) |
|
probably benign |
Het |
Tonsl |
A |
G |
15: 76,518,976 (GRCm39) |
V519A |
probably benign |
Het |
Ttn |
G |
A |
2: 76,612,376 (GRCm39) |
P17204S |
possibly damaging |
Het |
Wrap53 |
T |
A |
11: 69,454,694 (GRCm39) |
D225V |
probably benign |
Het |
Zfhx4 |
G |
A |
3: 5,477,107 (GRCm39) |
A3241T |
possibly damaging |
Het |
Zfp1002 |
T |
C |
2: 150,097,372 (GRCm39) |
H47R |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,898,697 (GRCm39) |
R76G |
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 |
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 |
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 |
|