Variant #0000000511 (NC_000023.11:g.154532439A>G, NM_000402.4:c.1401T>C (G6PD))

Individual ID 00000092
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.154532439A>G
Published as G6PD RFLP
Reference F Amini et al. (2011), dbSNP, (OMIM 0018), ClinVar
DB-ID G6PD_000013 See all 3 reported entries
dbSNP ID rs2230037
Frequency 16/25
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 2020-10-27 09:21:15 +08:00 (CST)
Date last edited 2021-08-22 14:27:06 +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 ?/. 11 c.1401T>C G6PD RFLP r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000107 DNA PCRm G6PD 3 Nuur Athirah Binti Mohd Daud