Variant #0000574959 (NC_000023.10:g.153775027C>A, NM_000402.3:c.59G>T (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153775027C>A
DNA change (hg38) g.154546812C>A
Published as G6PD(NM_000402.4):c.59G>T (p.G20V)
ISCN -
DB-ID IKBKG_000089
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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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 -?/. 1 c.59G>T r.(?) p.(Gly20Val) - -
G6PD NM_001042351.1 -?/. 1 c.-8-649G>T r.(=) p.(=) - -
IKBKG NM_003639.3 -?/. - c.-1293C>A r.(?) p.(=) - -


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