Variant #0000580802 (NC_000023.10:g.153760605G>A, NM_000402.3:c.1450C>T (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.153760605G>A
DNA change (hg38) g.154532390G>A
Published as G6PD-Maewo;Union
ISCN -
DB-ID G6PD_000018 See all 75 reported entries
Variant remarks WHO classification-Class II: severe enzyme deficiency with <0.10 normal activity
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-08-05 12:03:10 +02:00 (CEST)
Date last edited 2019-08-06 13:48:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Protein level     
G6PD NM_000402.3 +/. 11 c.1450C>T r.(?) p.(Arg484Cys) - -
G6PD NM_001042351.1 +/. 11 c.1360C>T r.(?) p.(Arg454Cys) - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.