Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
T |
C |
5: 146,120,358 (GRCm39) |
Y160C |
probably damaging |
Het |
Abi3bp |
T |
C |
16: 56,412,999 (GRCm39) |
S314P |
probably damaging |
Het |
Abra |
T |
C |
15: 41,732,802 (GRCm39) |
H88R |
probably benign |
Het |
Bsn |
A |
G |
9: 107,987,617 (GRCm39) |
|
probably benign |
Het |
Clca3b |
A |
C |
3: 144,547,171 (GRCm39) |
|
probably null |
Het |
Cnot7 |
G |
T |
8: 40,952,386 (GRCm39) |
P190T |
probably damaging |
Het |
Cps1 |
A |
T |
1: 67,212,031 (GRCm39) |
|
probably benign |
Het |
Dennd2d |
A |
G |
3: 106,407,220 (GRCm39) |
T424A |
probably benign |
Het |
Dnhd1 |
C |
T |
7: 105,327,516 (GRCm39) |
R54C |
probably damaging |
Het |
Efhd1 |
G |
A |
1: 87,192,334 (GRCm39) |
E55K |
probably damaging |
Het |
Ep300 |
T |
C |
15: 81,495,638 (GRCm39) |
|
probably benign |
Het |
Ezh1 |
G |
T |
11: 101,090,166 (GRCm39) |
H529Q |
probably damaging |
Het |
Klhl3 |
A |
T |
13: 58,198,878 (GRCm39) |
S201T |
possibly damaging |
Het |
Krt1c |
A |
G |
15: 101,724,953 (GRCm39) |
F219S |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 41,172,172 (GRCm39) |
D751N |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,838,629 (GRCm39) |
C1848* |
probably null |
Het |
Macf1 |
A |
G |
4: 123,284,842 (GRCm39) |
|
probably null |
Het |
Med10 |
T |
C |
13: 69,961,819 (GRCm39) |
|
probably benign |
Het |
Msh4 |
T |
A |
3: 153,592,593 (GRCm39) |
T170S |
probably damaging |
Het |
Or52n3 |
T |
C |
7: 104,530,141 (GRCm39) |
C76R |
probably damaging |
Het |
Pelp1 |
T |
A |
11: 70,297,153 (GRCm39) |
|
probably benign |
Het |
Prex2 |
G |
A |
1: 11,367,963 (GRCm39) |
V1595I |
probably benign |
Het |
Prpf8 |
C |
T |
11: 75,392,660 (GRCm39) |
R1617* |
probably null |
Het |
Rabep1 |
T |
A |
11: 70,825,385 (GRCm39) |
L684Q |
probably damaging |
Het |
Slc22a4 |
G |
A |
11: 53,874,435 (GRCm39) |
|
probably benign |
Het |
Smox |
T |
C |
2: 131,362,037 (GRCm39) |
F153S |
probably damaging |
Het |
Tma16 |
A |
G |
8: 66,939,062 (GRCm39) |
|
probably null |
Het |
Unc80 |
G |
T |
1: 66,665,675 (GRCm39) |
R1814L |
possibly damaging |
Het |
Vmn2r108 |
C |
T |
17: 20,691,987 (GRCm39) |
D179N |
possibly damaging |
Het |
Washc2 |
A |
G |
6: 116,236,126 (GRCm39) |
E1199G |
probably benign |
Het |
Zic1 |
C |
A |
9: 91,244,525 (GRCm39) |
|
probably null |
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 |
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 |
|
R5287:Chd3
|
UTSW |
11 |
69,239,895 (GRCm39) |
splice site |
probably null |
|
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 |
|