Variant #0000624528 (NC_000023.10:g.153792583C>T, NM_000402.3:c.-17498G>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.153792583C>T
DNA change (hg38) g.154564368C>T
Published as IKBKG(NM_001099857.5):c.1167C>T (p.P389=)
ISCN -
DB-ID IKBKG_000096
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
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 -?/. - c.-17498G>A r.(?) p.(=) - -
G6PD NM_001042351.1 -?/. - c.-16909G>A r.(?) p.(=) - -
IKBKG NM_003639.3 -?/. - c.1167C>T r.(?) p.(Pro389=) - -


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