Variant #0000000081 (NC_000023.11:g.154533122C>T, NM_000402.4:c.961G>A (G6PD))

Individual ID 00000015
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.154533122C>T
Published as -
Reference O. Ainoon et al.(2003)
DB-ID G6PD_000001 See all 11 reported entries
dbSNP ID rs149457059
Frequency 32/86
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 14:41:48 +08:00 (CST)
Date last edited 2021-09-13 13:13:55 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
G6PD NM_000402.4 ?/. 9 c.961G>A - r.(?) p.(Val321Met) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000014 DNA PCR G6PD 1 MyHVP