Variant #0000580820 (NC_000023.10:g.153764217C>T, NM_000402.3:c.292G>A (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.153764217C>T
DNA change (hg38) g.154536002C>T
Published as G6PD-Alabama;Betica;Castilla;Distrito Federal;Ferrara;Kabyle;Laghout;Matera;Tepic
ISCN -
DB-ID G6PD_000002 See all 15 reported entries
Variant remarks WHO classification-Class III: mild to moderate enzyme deficiency (0.10-0.60 normal activity)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00869 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)
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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 +/. 4 c.292G>A r.(?) p.(Val98Met) - -
G6PD NM_001042351.1 +/. 4 c.202G>A r.(?) p.(Val68Met) - -


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