Variant #0000000084 (NC_000023.11:g.154532269C>A, NM_000402.4:c.1466G>T (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.154532269C>A
Published as -
Reference O. Ainoon et al.(2003), dbSNP, ClinVar
DB-ID G6PD_000004 See all 7 reported entries
dbSNP ID rs72554665
Frequency 86
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 14:52:13 +08:00 (CST)
Date last edited 2021-09-13 13:08:27 +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     
G6PD NM_000402.4 +/. 12 c.1466G>T - r.(?) p.(Arg489Leu) - ClinVar