Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430015G10Rik |
T |
A |
4: 156,125,431 (GRCm38) |
Y173N |
probably damaging |
Het |
A2ml1 |
T |
C |
6: 128,571,974 (GRCm38) |
T282A |
probably benign |
Het |
Adamdec1 |
A |
T |
14: 68,573,235 (GRCm38) |
Y157* |
probably null |
Het |
Adgre5 |
A |
G |
8: 83,730,186 (GRCm38) |
Y189H |
probably damaging |
Het |
Alg11 |
G |
A |
8: 22,062,034 (GRCm38) |
V65I |
probably benign |
Het |
Bach1 |
G |
A |
16: 87,719,291 (GRCm38) |
R240Q |
probably benign |
Het |
Camk2b |
C |
T |
11: 5,989,026 (GRCm38) |
V278M |
probably damaging |
Het |
Ccdc57 |
G |
A |
11: 120,826,918 (GRCm38) |
P950L |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,230,582 (GRCm38) |
V683D |
probably damaging |
Het |
Cyfip1 |
A |
G |
7: 55,872,125 (GRCm38) |
Y59C |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,482,745 (GRCm38) |
E685G |
probably damaging |
Het |
Edaradd |
A |
T |
13: 12,483,603 (GRCm38) |
S78T |
probably benign |
Het |
Edc4 |
T |
C |
8: 105,887,507 (GRCm38) |
V430A |
probably damaging |
Het |
Efr3a |
T |
C |
15: 65,866,822 (GRCm38) |
S767P |
probably benign |
Het |
Enkd1 |
T |
C |
8: 105,704,393 (GRCm38) |
Q234R |
probably damaging |
Het |
Ercc6 |
ACGGTACCG |
ACGGTACCGGTACCG |
14: 32,570,340 (GRCm38) |
|
probably benign |
Het |
Hipk2 |
T |
A |
6: 38,745,695 (GRCm38) |
Y468F |
probably damaging |
Het |
Ifi207 |
GTT |
GT |
1: 173,729,450 (GRCm38) |
|
probably null |
Het |
Kcna5 |
A |
G |
6: 126,534,625 (GRCm38) |
V180A |
probably benign |
Het |
Kcnb1 |
T |
C |
2: 167,105,297 (GRCm38) |
I544V |
probably benign |
Het |
Kif21a |
A |
G |
15: 90,959,124 (GRCm38) |
S1119P |
possibly damaging |
Het |
Klk13 |
T |
C |
7: 43,723,811 (GRCm38) |
C190R |
probably damaging |
Het |
Mga |
T |
C |
2: 119,964,081 (GRCm38) |
S2749P |
probably benign |
Het |
Mpeg1 |
T |
C |
19: 12,462,914 (GRCm38) |
S579P |
probably damaging |
Het |
Msh3 |
A |
T |
13: 92,223,276 (GRCm38) |
I903K |
probably damaging |
Het |
Olfr1191-ps1 |
T |
A |
2: 88,642,961 (GRCm38) |
S65T |
probably damaging |
Het |
Ptx4 |
T |
C |
17: 25,120,923 (GRCm38) |
S25P |
probably damaging |
Het |
Sipa1l1 |
G |
T |
12: 82,169,485 (GRCm38) |
|
probably benign |
Het |
Slfn9 |
G |
C |
11: 82,987,286 (GRCm38) |
T339R |
probably benign |
Het |
Srsf12 |
C |
G |
4: 33,226,070 (GRCm38) |
P111R |
probably damaging |
Het |
Tex15 |
A |
G |
8: 33,575,209 (GRCm38) |
I1556V |
probably benign |
Het |
Ttc14 |
A |
G |
3: 33,800,586 (GRCm38) |
N21D |
probably benign |
Het |
|
Other mutations in Chd6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00837:Chd6
|
APN |
2 |
161,042,079 (GRCm38) |
missense |
probably benign |
0.01 |
IGL00899:Chd6
|
APN |
2 |
161,029,298 (GRCm38) |
splice site |
probably benign |
|
IGL01104:Chd6
|
APN |
2 |
160,961,927 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01295:Chd6
|
APN |
2 |
160,988,370 (GRCm38) |
splice site |
probably benign |
|
IGL01717:Chd6
|
APN |
2 |
160,965,259 (GRCm38) |
missense |
possibly damaging |
0.96 |
IGL01795:Chd6
|
APN |
2 |
160,961,374 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01814:Chd6
|
APN |
2 |
161,059,929 (GRCm38) |
missense |
probably benign |
0.25 |
IGL02016:Chd6
|
APN |
2 |
160,983,678 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02104:Chd6
|
APN |
2 |
160,977,512 (GRCm38) |
missense |
probably benign |
|
IGL02158:Chd6
|
APN |
2 |
161,026,292 (GRCm38) |
missense |
possibly damaging |
0.73 |
IGL02313:Chd6
|
APN |
2 |
160,965,675 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02472:Chd6
|
APN |
2 |
160,984,452 (GRCm38) |
splice site |
probably benign |
|
IGL02522:Chd6
|
APN |
2 |
160,965,796 (GRCm38) |
missense |
probably benign |
0.30 |
IGL02626:Chd6
|
APN |
2 |
161,039,350 (GRCm38) |
splice site |
probably benign |
|
IGL02727:Chd6
|
APN |
2 |
160,969,463 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02738:Chd6
|
APN |
2 |
160,965,698 (GRCm38) |
missense |
probably benign |
0.45 |
IGL02743:Chd6
|
APN |
2 |
160,960,263 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02800:Chd6
|
APN |
2 |
160,984,632 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02811:Chd6
|
APN |
2 |
160,990,301 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02850:Chd6
|
APN |
2 |
161,019,616 (GRCm38) |
nonsense |
probably null |
|
IGL02979:Chd6
|
APN |
2 |
160,966,170 (GRCm38) |
missense |
possibly damaging |
0.48 |
IGL02993:Chd6
|
APN |
2 |
161,052,384 (GRCm38) |
splice site |
probably benign |
|
IGL03277:Chd6
|
APN |
2 |
160,983,061 (GRCm38) |
missense |
probably null |
1.00 |
IGL03346:Chd6
|
APN |
2 |
160,960,362 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03357:Chd6
|
APN |
2 |
161,018,016 (GRCm38) |
splice site |
probably benign |
|
IGL03134:Chd6
|
UTSW |
2 |
160,965,483 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0106:Chd6
|
UTSW |
2 |
160,967,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R0106:Chd6
|
UTSW |
2 |
160,967,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R0212:Chd6
|
UTSW |
2 |
161,052,847 (GRCm38) |
missense |
probably damaging |
0.99 |
R0363:Chd6
|
UTSW |
2 |
161,014,324 (GRCm38) |
missense |
probably damaging |
1.00 |
R0399:Chd6
|
UTSW |
2 |
161,052,688 (GRCm38) |
missense |
probably damaging |
1.00 |
R0511:Chd6
|
UTSW |
2 |
160,992,191 (GRCm38) |
missense |
probably damaging |
0.99 |
R0771:Chd6
|
UTSW |
2 |
161,019,580 (GRCm38) |
missense |
probably damaging |
1.00 |
R1147:Chd6
|
UTSW |
2 |
160,990,271 (GRCm38) |
missense |
probably damaging |
1.00 |
R1147:Chd6
|
UTSW |
2 |
160,990,271 (GRCm38) |
missense |
probably damaging |
1.00 |
R1184:Chd6
|
UTSW |
2 |
161,030,802 (GRCm38) |
missense |
probably damaging |
1.00 |
R1277:Chd6
|
UTSW |
2 |
160,967,815 (GRCm38) |
missense |
probably damaging |
1.00 |
R1396:Chd6
|
UTSW |
2 |
160,983,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R1647:Chd6
|
UTSW |
2 |
161,042,058 (GRCm38) |
missense |
probably damaging |
1.00 |
R1648:Chd6
|
UTSW |
2 |
161,042,058 (GRCm38) |
missense |
probably damaging |
1.00 |
R1745:Chd6
|
UTSW |
2 |
160,981,667 (GRCm38) |
missense |
probably damaging |
0.96 |
R1766:Chd6
|
UTSW |
2 |
160,966,639 (GRCm38) |
missense |
probably damaging |
1.00 |
R1871:Chd6
|
UTSW |
2 |
160,990,256 (GRCm38) |
missense |
probably damaging |
1.00 |
R1928:Chd6
|
UTSW |
2 |
160,968,000 (GRCm38) |
splice site |
probably benign |
|
R1973:Chd6
|
UTSW |
2 |
160,966,387 (GRCm38) |
missense |
probably damaging |
0.99 |
R2200:Chd6
|
UTSW |
2 |
160,983,753 (GRCm38) |
missense |
probably damaging |
1.00 |
R2340:Chd6
|
UTSW |
2 |
160,965,759 (GRCm38) |
frame shift |
probably null |
|
R2341:Chd6
|
UTSW |
2 |
160,965,759 (GRCm38) |
frame shift |
probably null |
|
R2519:Chd6
|
UTSW |
2 |
161,029,876 (GRCm38) |
missense |
possibly damaging |
0.66 |
R2919:Chd6
|
UTSW |
2 |
160,967,880 (GRCm38) |
missense |
possibly damaging |
0.89 |
R3025:Chd6
|
UTSW |
2 |
160,966,552 (GRCm38) |
small deletion |
probably benign |
|
R3426:Chd6
|
UTSW |
2 |
160,990,255 (GRCm38) |
missense |
probably damaging |
1.00 |
R3427:Chd6
|
UTSW |
2 |
160,990,255 (GRCm38) |
missense |
probably damaging |
1.00 |
R4042:Chd6
|
UTSW |
2 |
160,988,333 (GRCm38) |
missense |
probably damaging |
1.00 |
R4273:Chd6
|
UTSW |
2 |
160,961,291 (GRCm38) |
missense |
probably benign |
0.04 |
R4360:Chd6
|
UTSW |
2 |
160,949,856 (GRCm38) |
missense |
possibly damaging |
0.48 |
R4399:Chd6
|
UTSW |
2 |
160,965,318 (GRCm38) |
missense |
probably benign |
|
R4458:Chd6
|
UTSW |
2 |
161,029,876 (GRCm38) |
missense |
possibly damaging |
0.66 |
R4583:Chd6
|
UTSW |
2 |
161,014,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R4625:Chd6
|
UTSW |
2 |
160,969,492 (GRCm38) |
missense |
probably damaging |
1.00 |
R4740:Chd6
|
UTSW |
2 |
160,970,183 (GRCm38) |
missense |
probably benign |
|
R4765:Chd6
|
UTSW |
2 |
160,966,244 (GRCm38) |
nonsense |
probably null |
|
R4779:Chd6
|
UTSW |
2 |
160,949,557 (GRCm38) |
missense |
probably damaging |
1.00 |
R4877:Chd6
|
UTSW |
2 |
161,029,299 (GRCm38) |
splice site |
probably benign |
|
R5068:Chd6
|
UTSW |
2 |
160,966,369 (GRCm38) |
missense |
possibly damaging |
0.54 |
R5215:Chd6
|
UTSW |
2 |
160,949,953 (GRCm38) |
missense |
probably damaging |
1.00 |
R5275:Chd6
|
UTSW |
2 |
160,969,363 (GRCm38) |
missense |
probably benign |
|
R5405:Chd6
|
UTSW |
2 |
160,965,390 (GRCm38) |
missense |
probably benign |
|
R5598:Chd6
|
UTSW |
2 |
161,014,112 (GRCm38) |
missense |
probably damaging |
1.00 |
R5693:Chd6
|
UTSW |
2 |
160,965,265 (GRCm38) |
missense |
probably benign |
|
R5697:Chd6
|
UTSW |
2 |
161,018,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R5715:Chd6
|
UTSW |
2 |
160,949,878 (GRCm38) |
missense |
probably benign |
0.00 |
R5759:Chd6
|
UTSW |
2 |
160,983,762 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5761:Chd6
|
UTSW |
2 |
160,957,079 (GRCm38) |
missense |
probably damaging |
1.00 |
R5761:Chd6
|
UTSW |
2 |
160,957,078 (GRCm38) |
missense |
probably damaging |
1.00 |
R5954:Chd6
|
UTSW |
2 |
160,965,827 (GRCm38) |
missense |
probably benign |
0.00 |
R6025:Chd6
|
UTSW |
2 |
160,965,582 (GRCm38) |
missense |
probably benign |
|
R6104:Chd6
|
UTSW |
2 |
161,014,132 (GRCm38) |
missense |
probably damaging |
1.00 |
R6247:Chd6
|
UTSW |
2 |
160,950,048 (GRCm38) |
missense |
probably damaging |
1.00 |
R6393:Chd6
|
UTSW |
2 |
160,979,487 (GRCm38) |
missense |
probably damaging |
1.00 |
R6452:Chd6
|
UTSW |
2 |
160,965,498 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6468:Chd6
|
UTSW |
2 |
161,013,067 (GRCm38) |
missense |
probably damaging |
1.00 |
R6784:Chd6
|
UTSW |
2 |
160,966,254 (GRCm38) |
missense |
probably damaging |
1.00 |
R6803:Chd6
|
UTSW |
2 |
160,960,359 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6869:Chd6
|
UTSW |
2 |
160,965,730 (GRCm38) |
missense |
probably benign |
|
R6895:Chd6
|
UTSW |
2 |
160,988,340 (GRCm38) |
missense |
probably damaging |
1.00 |
R6925:Chd6
|
UTSW |
2 |
161,013,127 (GRCm38) |
missense |
probably damaging |
0.98 |
R7061:Chd6
|
UTSW |
2 |
161,025,965 (GRCm38) |
nonsense |
probably null |
|
R7064:Chd6
|
UTSW |
2 |
160,950,063 (GRCm38) |
missense |
probably damaging |
1.00 |
R7248:Chd6
|
UTSW |
2 |
160,961,279 (GRCm38) |
nonsense |
probably null |
|
R7287:Chd6
|
UTSW |
2 |
161,008,392 (GRCm38) |
missense |
probably benign |
0.07 |
R7431:Chd6
|
UTSW |
2 |
161,026,328 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7486:Chd6
|
UTSW |
2 |
160,950,003 (GRCm38) |
missense |
probably damaging |
1.00 |
R7509:Chd6
|
UTSW |
2 |
161,013,154 (GRCm38) |
missense |
probably damaging |
1.00 |
R7699:Chd6
|
UTSW |
2 |
161,025,943 (GRCm38) |
missense |
probably benign |
0.13 |
R7748:Chd6
|
UTSW |
2 |
160,966,619 (GRCm38) |
missense |
probably benign |
0.37 |
R7785:Chd6
|
UTSW |
2 |
160,970,175 (GRCm38) |
missense |
possibly damaging |
0.51 |
R8002:Chd6
|
UTSW |
2 |
160,990,321 (GRCm38) |
missense |
probably damaging |
1.00 |
R8261:Chd6
|
UTSW |
2 |
160,957,082 (GRCm38) |
missense |
probably damaging |
1.00 |
R8317:Chd6
|
UTSW |
2 |
160,990,321 (GRCm38) |
missense |
probably damaging |
1.00 |
R8865:Chd6
|
UTSW |
2 |
161,021,069 (GRCm38) |
missense |
probably benign |
0.10 |
R8867:Chd6
|
UTSW |
2 |
161,021,069 (GRCm38) |
missense |
probably benign |
0.10 |
R8996:Chd6
|
UTSW |
2 |
160,981,623 (GRCm38) |
missense |
probably damaging |
1.00 |
R9091:Chd6
|
UTSW |
2 |
161,029,873 (GRCm38) |
nonsense |
probably null |
|
R9270:Chd6
|
UTSW |
2 |
161,029,873 (GRCm38) |
nonsense |
probably null |
|
R9310:Chd6
|
UTSW |
2 |
161,039,261 (GRCm38) |
missense |
probably damaging |
1.00 |
R9367:Chd6
|
UTSW |
2 |
161,029,864 (GRCm38) |
missense |
possibly damaging |
0.83 |
R9438:Chd6
|
UTSW |
2 |
160,957,158 (GRCm38) |
missense |
probably benign |
0.01 |
R9756:Chd6
|
UTSW |
2 |
160,960,339 (GRCm38) |
missense |
probably benign |
|
Z1088:Chd6
|
UTSW |
2 |
160,966,488 (GRCm38) |
missense |
probably damaging |
1.00 |
|