Variant #0001027469 (NC_000023.10:g.153770651C>T, NC_000023.10(NM_000402.3):c.210+3600G>A (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.153770651C>T
DNA change (hg38) -
Published as IKBKG(NM_001099856.4):c.173C>T (p.A58V)
ISCN -
DB-ID IKBKG_000160
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) 3.0E-5 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 2025-02-07 18:57:27 +01:00 (CET)
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.210+3600G>A r.(=) p.(=) - -
G6PD NM_001042351.1 ?/. - c.120+3600G>A r.(=) p.(=) - -
IKBKG NM_003639.3 ?/. - c.-5669C>T r.(?) p.(=) - -


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