Variant #0001016815 (NC_000002.11:g.26502111C>T, NM_000183.2:c.739C>T (HADHB))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.26502111C>T
DNA change (hg38) g.26279243C>T
Published as (R214C)
ISCN -
DB-ID HADHB_000001 See all 6 reported entries
Variant remarks cDNA expression cloning 0.05 enzyme activity
Reference PubMed: Purevsuren 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-12 22:11:58 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HADHB NM_000183.2 +/. - c.739C>T - p.Arg247Cys


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