Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
C |
A |
8: 24,667,604 (GRCm38) |
C110F |
probably damaging |
Het |
Adrb3 |
T |
C |
8: 27,228,181 (GRCm38) |
D80G |
probably damaging |
Het |
Akap6 |
A |
T |
12: 52,888,034 (GRCm38) |
N770Y |
probably damaging |
Het |
Ank3 |
A |
G |
10: 69,706,894 (GRCm38) |
H28R |
probably benign |
Het |
Atrn |
A |
G |
2: 131,020,956 (GRCm38) |
M1319V |
probably benign |
Het |
BC034090 |
T |
C |
1: 155,241,498 (GRCm38) |
I291M |
probably benign |
Het |
Cc2d2a |
T |
C |
5: 43,736,109 (GRCm38) |
S1416P |
probably benign |
Het |
Col9a2 |
C |
A |
4: 121,050,407 (GRCm38) |
A335E |
possibly damaging |
Het |
Epb42 |
A |
T |
2: 121,030,039 (GRCm38) |
L160M |
probably damaging |
Het |
Gkn3 |
C |
T |
6: 87,383,525 (GRCm38) |
A163T |
probably damaging |
Het |
Igtp |
G |
A |
11: 58,206,593 (GRCm38) |
V197I |
probably damaging |
Het |
Nup214 |
G |
A |
2: 32,033,403 (GRCm38) |
V1315M |
probably damaging |
Het |
Olfr1186 |
T |
A |
2: 88,525,864 (GRCm38) |
C94S |
probably damaging |
Het |
Plek |
T |
C |
11: 16,990,142 (GRCm38) |
Y166C |
probably damaging |
Het |
Prdm4 |
T |
C |
10: 85,910,289 (GRCm38) |
N85D |
probably damaging |
Het |
Prelid1 |
T |
G |
13: 55,322,194 (GRCm38) |
V2G |
probably benign |
Het |
Serac1 |
T |
C |
17: 6,066,778 (GRCm38) |
I168V |
probably benign |
Het |
Setx |
GTGGCT |
GT |
2: 29,154,061 (GRCm38) |
1814 |
probably null |
Het |
Slc22a5 |
A |
G |
11: 53,869,326 (GRCm38) |
V388A |
probably benign |
Het |
Tmem181a |
T |
A |
17: 6,295,786 (GRCm38) |
L185H |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,108,934 (GRCm38) |
R281C |
probably damaging |
Het |
Trpv3 |
A |
T |
11: 73,285,941 (GRCm38) |
Y382F |
probably damaging |
Het |
Ttyh1 |
T |
C |
7: 4,133,219 (GRCm38) |
|
probably null |
Het |
Ubr2 |
T |
C |
17: 46,968,439 (GRCm38) |
Y681C |
probably damaging |
Het |
Unc80 |
G |
A |
1: 66,639,305 (GRCm38) |
V2082I |
probably benign |
Het |
Utp14b |
T |
C |
1: 78,665,339 (GRCm38) |
M318T |
probably damaging |
Het |
Vars2 |
A |
T |
17: 35,661,974 (GRCm38) |
I442N |
probably damaging |
Het |
Vmn2r63 |
A |
G |
7: 42,926,982 (GRCm38) |
F469S |
probably benign |
Het |
Wtap |
C |
T |
17: 12,967,538 (GRCm38) |
R374Q |
possibly damaging |
Het |
Zfp606 |
T |
C |
7: 12,489,664 (GRCm38) |
M34T |
probably damaging |
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 |
|
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 |
R8388:Chd6
|
UTSW |
2 |
161,019,651 (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 |
|