Variant #0000810169 (NC_000023.10:g.153780249G>A, NM_000402.3:c.-5164C>T (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.153780249G>A
DNA change (hg38) -
Published as IKBKG(NM_001099857.2):c.32G>A (p.C11Y)
ISCN -
DB-ID IKBKG_000146
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Protein level     
G6PD NM_000402.3 ?/. - c.-5164C>T r.(?) p.(=) - -
G6PD NM_001042351.1 ?/. - c.-4575C>T r.(?) p.(=) - -
IKBKG NM_003639.3 ?/. - c.32G>A r.(?) p.(Cys11Tyr) - -


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