Variant #0000574967 (NC_000023.10:g.153784529G>A, NM_000402.3:c.-9444C>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.153784529G>A
DNA change (hg38) g.154556314G>A
Published as IKBKG(NM_001099857.4):c.337G>A (p.D113N), IKBKG(NM_001099857.5):c.337G>A (p.D113N)
ISCN -
DB-ID IKBKG_000001 See all 4 reported entries
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) 0.00945 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Protein level     
G6PD NM_000402.3 -?/. - c.-9444C>T r.(?) p.(=) - -
G6PD NM_001042351.1 -?/. - c.-8855C>T r.(?) p.(=) - -
IKBKG NM_003639.3 -?/. - c.337G>A r.(?) p.(Asp113Asn) - -


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