Variant #0000336268 (NC_000023.10:g.153770663G>C, NC_000023.10(NM_000402.3):c.210+3588C>G (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.153770663G>C
DNA change (hg38) g.154542448G>C
Published as IKBKG(NM_001099856.2):c.185G>C (p.(Gly62Ala))
ISCN -
DB-ID G6PD_000200
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 2018-01-15 20:58:59 +01:00 (CET)
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 -?/. 2i c.210+3588C>G r.(=) p.(=) - -
G6PD NM_001042351.1 -?/. 2i c.120+3588C>G r.(=) p.(=) - -
IKBKG NM_003639.3 -?/. - c.-5657G>C r.(?) p.(=) - -


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