Variant #0000574962 (NC_000023.10:g.153780374C>A, NM_000402.3:c.-5289G>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.153780374C>A
DNA change (hg38) g.154552159C>A
Published as IKBKG(NM_001099856.3):c.361C>A (p.(Arg121Ser))
ISCN -
DB-ID IKBKG_000092
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 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 ?/. - c.-5289G>T r.(?) p.(=) - -
G6PD NM_001042351.1 ?/. - c.-4700G>T r.(?) p.(=) - -
IKBKG NM_003639.3 ?/. - c.157C>A r.(?) p.(Arg53Ser) - -


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