Variant #0001046934 (NC_000004.11:g.159629677T>C, NM_004453.2:c.1852T>C (ETFDH))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.159629677T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ETFDH_000011 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs765742496
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-07-13 15:30:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ETFDH NM_004453.2 +/. - c.1852T>C r.(?) p.(Ter618GlnextTer13)


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