Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accs |
T |
C |
2: 93,666,298 (GRCm39) |
D463G |
probably damaging |
Het |
Acsbg3 |
G |
T |
17: 57,183,221 (GRCm39) |
|
probably benign |
Het |
Adcy8 |
C |
T |
15: 64,588,001 (GRCm39) |
V929I |
probably benign |
Het |
Anp32a |
A |
T |
9: 62,249,275 (GRCm39) |
I16F |
possibly damaging |
Het |
Arpin |
T |
C |
7: 79,577,997 (GRCm39) |
E144G |
probably damaging |
Het |
Asb18 |
T |
C |
1: 89,942,110 (GRCm39) |
T64A |
probably benign |
Het |
Asxl2 |
A |
G |
12: 3,546,893 (GRCm39) |
N559S |
probably benign |
Het |
Brd7 |
G |
T |
8: 89,084,169 (GRCm39) |
Q148K |
probably damaging |
Het |
Brinp1 |
A |
G |
4: 68,711,201 (GRCm39) |
W336R |
probably benign |
Het |
Btnl9 |
A |
G |
11: 49,060,434 (GRCm39) |
V438A |
probably benign |
Het |
Cat |
T |
C |
2: 103,304,705 (GRCm39) |
T107A |
probably damaging |
Het |
Catsperg2 |
T |
C |
7: 29,397,263 (GRCm39) |
Y1080C |
possibly damaging |
Het |
Ccdc138 |
T |
A |
10: 58,411,527 (GRCm39) |
F632I |
possibly damaging |
Het |
Cd46 |
C |
T |
1: 194,744,719 (GRCm39) |
V340I |
possibly damaging |
Het |
Celf1 |
T |
C |
2: 90,839,552 (GRCm39) |
S326P |
possibly damaging |
Het |
Ces1e |
T |
G |
8: 93,935,240 (GRCm39) |
D404A |
probably benign |
Het |
Clhc1 |
A |
G |
11: 29,528,244 (GRCm39) |
|
probably benign |
Het |
Cops8 |
C |
T |
1: 90,534,342 (GRCm39) |
|
probably benign |
Het |
Cpox |
G |
A |
16: 58,495,649 (GRCm39) |
G322D |
probably damaging |
Het |
Csmd2 |
C |
T |
4: 128,380,677 (GRCm39) |
R2078C |
probably benign |
Het |
Dnm1l |
A |
C |
16: 16,151,732 (GRCm39) |
V240G |
probably damaging |
Het |
Fezf1 |
C |
T |
6: 23,248,010 (GRCm39) |
V22M |
probably benign |
Het |
Gm6818 |
T |
G |
7: 38,099,911 (GRCm39) |
|
noncoding transcript |
Het |
Hand2 |
C |
T |
8: 57,775,080 (GRCm39) |
L47F |
probably damaging |
Het |
Insyn2b |
A |
T |
11: 34,353,058 (GRCm39) |
T367S |
probably benign |
Het |
Itga7 |
C |
A |
10: 128,779,027 (GRCm39) |
R351S |
probably benign |
Het |
Mmp8 |
G |
T |
9: 7,567,507 (GRCm39) |
A456S |
probably benign |
Het |
Mroh5 |
TGGAG |
TG |
15: 73,654,923 (GRCm39) |
|
probably benign |
Het |
Opn4 |
T |
C |
14: 34,314,894 (GRCm39) |
T460A |
probably benign |
Het |
Or6b2 |
A |
T |
1: 92,408,019 (GRCm39) |
V108E |
possibly damaging |
Het |
Otog |
T |
C |
7: 45,918,753 (GRCm39) |
F943S |
probably damaging |
Het |
Pcnx1 |
A |
T |
12: 82,028,825 (GRCm39) |
Y1668F |
probably damaging |
Het |
Pheta1 |
A |
G |
5: 121,990,794 (GRCm39) |
E52G |
possibly damaging |
Het |
Phf24 |
A |
T |
4: 42,933,831 (GRCm39) |
|
probably null |
Het |
Phkg2 |
GCTGCCGGACGAGTGGCCT |
GCT |
7: 127,181,929 (GRCm39) |
|
probably null |
Het |
Ppargc1a |
G |
A |
5: 51,620,167 (GRCm39) |
|
probably benign |
Het |
Ptprd |
G |
A |
4: 75,872,405 (GRCm39) |
R1355* |
probably null |
Het |
Ptprn2 |
A |
T |
12: 117,175,482 (GRCm39) |
M721L |
probably damaging |
Het |
Sec23ip |
A |
G |
7: 128,367,860 (GRCm39) |
E624G |
probably benign |
Het |
Sfmbt1 |
G |
A |
14: 30,538,777 (GRCm39) |
V799M |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,073,607 (GRCm39) |
V1335A |
probably benign |
Het |
Sp140 |
G |
A |
1: 85,538,545 (GRCm39) |
|
probably null |
Het |
Spdye4c |
T |
C |
2: 128,434,560 (GRCm39) |
S46P |
possibly damaging |
Het |
Syde1 |
T |
C |
10: 78,425,871 (GRCm39) |
R99G |
probably benign |
Het |
T2 |
A |
T |
17: 8,636,835 (GRCm39) |
M57L |
probably benign |
Het |
Tasor2 |
G |
A |
13: 3,625,744 (GRCm39) |
S1402L |
probably benign |
Het |
Tfap2e |
T |
C |
4: 126,628,439 (GRCm39) |
I172M |
probably benign |
Het |
Tk1 |
A |
T |
11: 117,707,367 (GRCm39) |
V140E |
probably damaging |
Het |
Tln2 |
G |
A |
9: 67,149,641 (GRCm39) |
T1192M |
probably damaging |
Het |
Tmed8 |
C |
A |
12: 87,220,957 (GRCm39) |
A210S |
probably damaging |
Het |
Tnip2 |
A |
G |
5: 34,671,108 (GRCm39) |
L45P |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,260,703 (GRCm39) |
V1396A |
probably benign |
Het |
Ttn |
G |
T |
2: 76,562,436 (GRCm39) |
S28803Y |
probably damaging |
Het |
Wdr90 |
A |
T |
17: 26,080,441 (GRCm39) |
|
probably benign |
Het |
Zfp7 |
G |
A |
15: 76,775,422 (GRCm39) |
R488Q |
probably damaging |
Het |
|
Other mutations in Chd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00478:Chd3
|
APN |
11 |
69,247,888 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00551:Chd3
|
APN |
11 |
69,237,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00661:Chd3
|
APN |
11 |
69,248,209 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00698:Chd3
|
APN |
11 |
69,240,697 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01075:Chd3
|
APN |
11 |
69,250,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01309:Chd3
|
APN |
11 |
69,248,557 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01317:Chd3
|
APN |
11 |
69,244,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Chd3
|
APN |
11 |
69,250,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01444:Chd3
|
APN |
11 |
69,239,568 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01617:Chd3
|
APN |
11 |
69,249,060 (GRCm39) |
unclassified |
probably benign |
|
IGL01635:Chd3
|
APN |
11 |
69,252,076 (GRCm39) |
splice site |
probably benign |
|
IGL01942:Chd3
|
APN |
11 |
69,240,931 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01962:Chd3
|
APN |
11 |
69,248,319 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01981:Chd3
|
APN |
11 |
69,251,501 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02022:Chd3
|
APN |
11 |
69,251,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02098:Chd3
|
APN |
11 |
69,250,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Chd3
|
APN |
11 |
69,242,920 (GRCm39) |
unclassified |
probably benign |
|
IGL02415:Chd3
|
APN |
11 |
69,239,739 (GRCm39) |
splice site |
probably benign |
|
IGL02648:Chd3
|
APN |
11 |
69,242,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Chd3
|
APN |
11 |
69,251,874 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03030:Chd3
|
APN |
11 |
69,245,230 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03102:Chd3
|
APN |
11 |
69,252,022 (GRCm39) |
nonsense |
probably null |
|
IGL03168:Chd3
|
APN |
11 |
69,239,741 (GRCm39) |
splice site |
probably benign |
|
IGL03327:Chd3
|
APN |
11 |
69,241,012 (GRCm39) |
missense |
probably damaging |
1.00 |
burg
|
UTSW |
11 |
69,247,380 (GRCm39) |
missense |
probably damaging |
1.00 |
castello
|
UTSW |
11 |
69,246,648 (GRCm39) |
critical splice acceptor site |
probably benign |
|
feste
|
UTSW |
11 |
69,245,252 (GRCm39) |
nonsense |
probably null |
|
Fortress
|
UTSW |
11 |
69,254,876 (GRCm39) |
nonsense |
probably null |
|
moat
|
UTSW |
11 |
69,250,011 (GRCm39) |
missense |
probably damaging |
0.98 |
Redoubt
|
UTSW |
11 |
69,244,727 (GRCm39) |
unclassified |
probably benign |
|
schloss
|
UTSW |
11 |
69,252,886 (GRCm39) |
nonsense |
probably null |
|
siege
|
UTSW |
11 |
69,247,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Chd3
|
UTSW |
11 |
69,240,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R0009:Chd3
|
UTSW |
11 |
69,240,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R0056:Chd3
|
UTSW |
11 |
69,250,739 (GRCm39) |
unclassified |
probably benign |
|
R0129:Chd3
|
UTSW |
11 |
69,239,327 (GRCm39) |
nonsense |
probably null |
|
R0130:Chd3
|
UTSW |
11 |
69,250,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Chd3
|
UTSW |
11 |
69,247,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Chd3
|
UTSW |
11 |
69,247,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Chd3
|
UTSW |
11 |
69,248,367 (GRCm39) |
missense |
probably damaging |
0.98 |
R0502:Chd3
|
UTSW |
11 |
69,244,931 (GRCm39) |
missense |
probably damaging |
0.98 |
R0540:Chd3
|
UTSW |
11 |
69,235,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R0571:Chd3
|
UTSW |
11 |
69,252,495 (GRCm39) |
critical splice donor site |
probably null |
|
R0607:Chd3
|
UTSW |
11 |
69,235,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R0616:Chd3
|
UTSW |
11 |
69,236,313 (GRCm39) |
missense |
probably damaging |
0.96 |
R0630:Chd3
|
UTSW |
11 |
69,238,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Chd3
|
UTSW |
11 |
69,248,400 (GRCm39) |
splice site |
probably null |
|
R1484:Chd3
|
UTSW |
11 |
69,250,725 (GRCm39) |
missense |
probably benign |
0.17 |
R1741:Chd3
|
UTSW |
11 |
69,246,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R1748:Chd3
|
UTSW |
11 |
69,255,523 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1751:Chd3
|
UTSW |
11 |
69,244,727 (GRCm39) |
unclassified |
probably benign |
|
R1833:Chd3
|
UTSW |
11 |
69,244,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Chd3
|
UTSW |
11 |
69,239,878 (GRCm39) |
missense |
probably benign |
0.01 |
R2101:Chd3
|
UTSW |
11 |
69,239,877 (GRCm39) |
missense |
probably benign |
|
R2147:Chd3
|
UTSW |
11 |
69,239,854 (GRCm39) |
missense |
probably benign |
0.00 |
R2513:Chd3
|
UTSW |
11 |
69,251,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Chd3
|
UTSW |
11 |
69,251,998 (GRCm39) |
nonsense |
probably null |
|
R2879:Chd3
|
UTSW |
11 |
69,254,924 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2880:Chd3
|
UTSW |
11 |
69,242,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2881:Chd3
|
UTSW |
11 |
69,242,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2973:Chd3
|
UTSW |
11 |
69,251,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R3611:Chd3
|
UTSW |
11 |
69,252,973 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3743:Chd3
|
UTSW |
11 |
69,254,876 (GRCm39) |
nonsense |
probably null |
|
R3845:Chd3
|
UTSW |
11 |
69,237,585 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3889:Chd3
|
UTSW |
11 |
69,250,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R4007:Chd3
|
UTSW |
11 |
69,239,827 (GRCm39) |
missense |
probably benign |
|
R4115:Chd3
|
UTSW |
11 |
69,248,343 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4515:Chd3
|
UTSW |
11 |
69,240,703 (GRCm39) |
missense |
probably benign |
0.00 |
R4612:Chd3
|
UTSW |
11 |
69,244,035 (GRCm39) |
nonsense |
probably null |
|
R4622:Chd3
|
UTSW |
11 |
69,239,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R4634:Chd3
|
UTSW |
11 |
69,253,013 (GRCm39) |
unclassified |
probably benign |
|
R4635:Chd3
|
UTSW |
11 |
69,253,013 (GRCm39) |
unclassified |
probably benign |
|
R4859:Chd3
|
UTSW |
11 |
69,250,722 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4930:Chd3
|
UTSW |
11 |
69,245,034 (GRCm39) |
unclassified |
probably benign |
|
R5173:Chd3
|
UTSW |
11 |
69,260,069 (GRCm39) |
unclassified |
probably benign |
|
R5403:Chd3
|
UTSW |
11 |
69,239,895 (GRCm39) |
splice site |
probably null |
|
R5511:Chd3
|
UTSW |
11 |
69,252,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Chd3
|
UTSW |
11 |
69,244,177 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5702:Chd3
|
UTSW |
11 |
69,252,261 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6045:Chd3
|
UTSW |
11 |
69,242,944 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6063:Chd3
|
UTSW |
11 |
69,240,063 (GRCm39) |
missense |
probably benign |
|
R6211:Chd3
|
UTSW |
11 |
69,243,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6215:Chd3
|
UTSW |
11 |
69,247,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6217:Chd3
|
UTSW |
11 |
69,236,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Chd3
|
UTSW |
11 |
69,244,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R6329:Chd3
|
UTSW |
11 |
69,252,510 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6349:Chd3
|
UTSW |
11 |
69,254,857 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6414:Chd3
|
UTSW |
11 |
69,243,371 (GRCm39) |
critical splice donor site |
probably null |
|
R6453:Chd3
|
UTSW |
11 |
69,240,938 (GRCm39) |
nonsense |
probably null |
|
R6548:Chd3
|
UTSW |
11 |
69,252,886 (GRCm39) |
nonsense |
probably null |
|
R6582:Chd3
|
UTSW |
11 |
69,259,982 (GRCm39) |
unclassified |
probably benign |
|
R6721:Chd3
|
UTSW |
11 |
69,260,045 (GRCm39) |
unclassified |
probably benign |
|
R6776:Chd3
|
UTSW |
11 |
69,245,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Chd3
|
UTSW |
11 |
69,245,271 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7085:Chd3
|
UTSW |
11 |
69,260,027 (GRCm39) |
missense |
unknown |
|
R7136:Chd3
|
UTSW |
11 |
69,239,264 (GRCm39) |
missense |
probably null |
0.37 |
R7164:Chd3
|
UTSW |
11 |
69,253,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R7200:Chd3
|
UTSW |
11 |
69,254,921 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7226:Chd3
|
UTSW |
11 |
69,260,037 (GRCm39) |
missense |
unknown |
|
R7238:Chd3
|
UTSW |
11 |
69,254,873 (GRCm39) |
missense |
probably benign |
0.31 |
R7316:Chd3
|
UTSW |
11 |
69,236,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R7560:Chd3
|
UTSW |
11 |
69,247,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R7684:Chd3
|
UTSW |
11 |
69,248,692 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7748:Chd3
|
UTSW |
11 |
69,246,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7820:Chd3
|
UTSW |
11 |
69,244,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7885:Chd3
|
UTSW |
11 |
69,247,451 (GRCm39) |
missense |
probably benign |
0.13 |
R8150:Chd3
|
UTSW |
11 |
69,254,510 (GRCm39) |
missense |
probably benign |
0.02 |
R8161:Chd3
|
UTSW |
11 |
69,241,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Chd3
|
UTSW |
11 |
69,251,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Chd3
|
UTSW |
11 |
69,241,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Chd3
|
UTSW |
11 |
69,245,252 (GRCm39) |
nonsense |
probably null |
|
R8690:Chd3
|
UTSW |
11 |
69,246,648 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8828:Chd3
|
UTSW |
11 |
69,247,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Chd3
|
UTSW |
11 |
69,253,146 (GRCm39) |
missense |
probably benign |
0.22 |
R9124:Chd3
|
UTSW |
11 |
69,260,162 (GRCm39) |
missense |
unknown |
|
R9170:Chd3
|
UTSW |
11 |
69,241,648 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9213:Chd3
|
UTSW |
11 |
69,255,628 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9285:Chd3
|
UTSW |
11 |
69,249,954 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9293:Chd3
|
UTSW |
11 |
69,244,027 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9368:Chd3
|
UTSW |
11 |
69,251,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Chd3
|
UTSW |
11 |
69,249,133 (GRCm39) |
missense |
probably benign |
0.01 |
R9544:Chd3
|
UTSW |
11 |
69,241,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Chd3
|
UTSW |
11 |
69,251,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Chd3
|
UTSW |
11 |
69,241,046 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Chd3
|
UTSW |
11 |
69,247,084 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Chd3
|
UTSW |
11 |
69,245,271 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1186:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1186:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1187:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1188:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1189:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1190:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1191:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Chd3
|
UTSW |
11 |
69,252,277 (GRCm39) |
missense |
probably benign |
|
Z1192:Chd3
|
UTSW |
11 |
69,239,271 (GRCm39) |
missense |
probably benign |
0.00 |
|