Variant #0000002297 (NC_000022.11:g.42129033C>G, NM_000106.6:c.1758G>A (CYP2D6))

Individual ID 00000502
Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.42129033C>G
Published as -
Reference Palden Wangyel Dorji et al.(2019)
DB-ID CYP2D6_000007 See all 2 reported entries
dbSNP ID rs5030865
Frequency -
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 2021-03-10 13:08:38 +08:00 (CST)
Date last edited 2021-08-01 13:19:49 +08:00 (CST)
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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 +/. - c.1758G>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000548 DNA ? CYP2D6 3 Nur Aisyah Athirah