Here you could input region, variant, rsid or refgene you are interested again.

Example-Region:22:42126499-42130810, Y:9460000-9480000, Variant:10-94780653-G-A, 22-42128945-C-T, Y-9467257-G-A, Rsid:rs4986893, rs3892097, Gene ID:CYP2D6

Search: 22:42126499-42130810

Result

items per page

Total page: 23   Total amount: 229

Variant ID
dbSNP
Region
Gene ID
Exonic
function
Consequence
Allele
Count
Allele
Number
Allele
Frequency
rs28371702
ncRNA_intronic
LOC101929829
-
-
4223
5968
0.7076
rs1058164
exonic
CYP2D6;CYP2D7
synonymous SNV
CYP2D6:NM_000106:exon3:c.G408C:p.V136V
4207
5976
0.7040
rs1135840
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon8:c.G1304C:p.S435T,CYP2D6:NM_000106:exon9:c.G1457C:p.S486T
4193
5972
0.7021
rs28371699
ncRNA_intronic
LOC101929829
-
-
4187
5976
0.7006
rs2267447
ncRNA_intronic
LOC101929829
-
-
3167
5976
0.5300
rs1065852
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.C100T:p.P34S,CYP2D6:NM_001025161:exon1:c.C100T:p.P34S
3147
5976
0.5266
rs1081003
exonic
CYP2D6;CYP2D7
synonymous SNV
CYP2D6:NM_000106:exon2:c.C336T:p.F112F,CYP2D6:NM_001025161:exon2:c.C336T:p.F112F
3132
5976
0.5241
rs16947
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon5:c.C733T:p.R245C,CYP2D6:NM_000106:exon6:c.C886T:p.R296C
1063
5976
0.1779
rs28371730
ncRNA_intronic
LOC101929829
-
-
1061
5980
0.1774
rs28371701
ncRNA_intronic
LOC101929829
-
-
1059
5956
0.1778
Total page: 23   Total amount: 229