Variant #0000289551 (NC_000023.10:g.153770626C>T, NC_000023.10(NM_000402.3):c.210+3625G>A (G6PD))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153770626C>T
DNA change (hg38) g.154542411C>T
Published as IKBKG(NM_001099856.4):c.148C>T (p.R50C)
ISCN -
DB-ID G6PD_000199
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) 0.00156 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Protein level     
G6PD NM_000402.3 -/. 2i c.210+3625G>A r.(=) p.(=) - -
G6PD NM_001042351.1 -/. 2i c.120+3625G>A r.(=) p.(=) - -
IKBKG NM_003639.3 -/. - c.-5694C>T r.(?) p.(=) - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.