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
-
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon8:c.G1337A:p.R446H,CYP2D6:NM_000106:exon9:c.G1490A:p.R497H
1
5982
1.6717e-4
rs370580423
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon8:c.C1336T:p.R446C,CYP2D6:NM_000106:exon9:c.C1489T:p.R497C
1
5982
1.6717e-4
-
exonic
CYP2D6;CYP2D7
synonymous SNV
CYP2D6:NM_001025161:exon8:c.G1203A:p.E401E,CYP2D6:NM_000106:exon9:c.G1356A:p.E452E
1
5982
1.6717e-4
-
ncRNA_intronic
LOC101929829
-
-
1
5982
1.6717e-4
-
ncRNA_intronic
LOC101929829
-
-
1
5982
1.6717e-4
rs59421388
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon6:c.G859A:p.V287M,CYP2D6:NM_000106:exon7:c.G1012A:p.V338M
1
5982
1.6717e-4
rs761795361
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon6:c.C835T:p.R279C,CYP2D6:NM_000106:exon7:c.C988T:p.R330C
1
5982
1.6717e-4
rs549957019
exonic
CYP2D7
unknown
UNKNOWN
1
5982
1.6717e-4
rs747089665
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon7:c.C1087T:p.R363C,CYP2D6:NM_000106:exon8:c.C1240T:p.R414C
1
5980
1.6722e-4
rs769157652
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_001025161:exon7:c.G1075A:p.E359K,CYP2D6:NM_000106:exon8:c.G1228A:p.E410K
1
5980
1.6722e-4
Total page: 23   Total amount: 229