Variant #0000931671 (NC_000023.10:g.153761811C>G, NM_000402.3:c.934G>C (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153761811C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID G6PD_000054 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs137852318
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00073 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-08-01 23:45:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Protein level     
G6PD NM_000402.3 +/. - c.934G>C r.(?) p.(Asp312His) - -


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