Variant #0000574964 (NC_000023.10:g.153780386G>A, NM_000402.3:c.-5301C>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.153780386G>A
DNA change (hg38) g.154552171G>A
Published as IKBKG(NM_001099856.3):c.373G>A (p.(Glu125Lys)), IKBKG(NM_001099857.2):c.169G>A (p.E57K), IKBKG(NM_001099857.4):c.169G>A (p.E57K), IKBKG(NM_0010998...)
ISCN -
DB-ID IKBKG_000008 See all 5 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) 0.00115 View details
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 2024-08-28 13:16:32 +02:00 (CEST)
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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.-5301C>T r.(?) p.(=) - -
G6PD NM_001042351.1 ?/. - c.-4712C>T r.(?) p.(=) - -
IKBKG NM_003639.3 ?/. - c.169G>A r.(?) p.(Glu57Lys) - -


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