Variant #0000000777 (NC_000022.11:g.42127941G>A, CYP2D6(NM_000106.6):c.886C>T)

Individual ID 00000151
Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.42127941G>A
Published as 2850C>T
Reference Fee Wai Chin et al. (2016), dbSNP, (OMIM 0007), ClinVar
DB-ID CYP2D6_000004 See all 2 reported entries
dbSNP ID rs16947
Frequency 1/7
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
CYP2D6 NM_000106.6 -/. 6 c.886C>T - r.(?) p.(Arg296Cys) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000166 DNA PCRm CYP2D6 6 Nuur Athirah Binti Mohd Daud