Variant #0000801559 (NC_000004.11:g.159627845T>C, NM_004453.2:c.1533T>C (ETFDH))

Chromosome 4
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.159627845T>C
DNA change (hg38) -
Published as ETFDH(NM_004453.3):c.1533T>C (p.D511=)
ISCN -
DB-ID ETFDH_000052
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) 0.00675 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 2021-09-17 14:40:49 +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.1533T>C r.(?) p.(Asp511=)
PPID NM_005038.2 -?/. - c.*3043A>G r.(=) p.(=)


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