Variant #0000000488 (NC_000023.11:g.154533122C>T, NM_000402.4:c.961G>A (G6PD))

Individual ID 00000089
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.154533122C>T
Published as G6PD Viangchan
Reference Narazah Mohd Yusoff et al. (2002)dbSNPClinVar
DB-ID G6PD_000001 See all 11 reported entries
dbSNP ID rs137852327
Frequency 4/20
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
Date created 2020-10-26 11:12:50 +08:00 (CST)
Date last edited 2021-08-22 11:51:12 +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 ./. - c.961G>A G6PD Viangchan r.(?) p.(Val321Met) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000104 DNA PCRm G6PD 5 Nuur Athirah Binti Mohd Daud