Variant #0001044222 (NC_000023.10:g.153780318G>A, NM_000402.3:c.-5233C>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.153780318G>A
DNA change (hg38) -
Published as IKBKG(NM_001099857.5):c.101G>A (p.(Gly34Glu))
ISCN -
DB-ID IKBKG_000161
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.-5233C>T r.(?) p.(=) - -
G6PD NM_001042351.1 ?/. - c.-4644C>T r.(?) p.(=) - -
IKBKG NM_003639.3 ?/. - c.101G>A r.(?) p.(Gly34Glu) - -


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