Full data view for gene ETFDH

Information The variants shown are described using the NM_004453.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.1366C>T r.(?) p.(Pro456Ser) Both (homozygous) ACMG likely pathogenic g.159627421C>T g.158706269C>T - - ETFDH_000084 ACMG PM2, PP3, PM5, PM1, PM3 PubMed: Molaei 2025 SCV006075021 - Germline - - - - - DNA SEQ, SEQ-NG - WES MYOP Fam202769Pat541 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - 1 Johan den Dunnen
+/. - c.1366C>T r.(?) p.(Pro456Ser) Both (homozygous) ACMG pathogenic g.159627421C>T g.158706269C>T - - ETFDH_000084 ACMG PM3, PM2, PP3, PM5 PubMed: Molaei 2025 SCV006075021 - Germline - - - - - DNA SEQ, SEQ-NG - WES MYOP Fam203315Pat557 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history F yes Iran - - - - - 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.