Variant #0000002289 (NC_000022.11:g.42128945C>T, NM_000106.6:c.1846G>A (CYP2D6))

Individual ID 00000501
Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.42128945C>T
Published as -
Reference Palden Wangyel Dorji et al.(2019)
DB-ID CYP2D6_000003 See all 2 reported entries
dbSNP ID rs3892097
Frequency 9/138
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-03-09 16:35:55 +08:00 (CST)
Date last edited 2021-08-01 13:19:36 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
CYP2D6 NM_000106.6 +/. - c.1846G>A - r.(=) p.(=) - drug response



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000547 DNA ? CYP2D6 6 Nur Aisyah Athirah