Variant #0000574955 (NC_000023.10:g.153770497G>A, NC_000023.10(NM_000402.3):c.210+3754C>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.153770497G>A
DNA change (hg38) g.154542282G>A
Published as IKBKG(NM_001099856.4):c.19G>A (p.V7M), IKBKG(NM_001099856.6):c.19G>A (p.V7M)
ISCN -
DB-ID G6PD_000198 See all 2 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) 0.00011 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)
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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+3754C>T r.(=) p.(=) - -
G6PD NM_001042351.1 -?/. 2i c.120+3754C>T r.(=) p.(=) - -
IKBKG NM_003639.3 -?/. - c.-5823G>A r.(?) p.(=) - -


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