Variant #0000574961 (NC_000023.10:g.153780355C>T, NM_000402.3:c.-5270G>A (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.153780355C>T
DNA change (hg38) g.154552140C>T
Published as IKBKG(NM_001099857.2):c.138C>T (p.G46=)
ISCN -
DB-ID IKBKG_000091
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-22 09:16:36 +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.-5270G>A r.(?) p.(=) - -
G6PD NM_001042351.1 -?/. - c.-4681G>A r.(?) p.(=) - -
IKBKG NM_003639.3 -?/. - c.138C>T r.(?) p.(Gly46=) - -


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