Variant #0000866256 (NC_000019.9:g.51857502G>T, NM_001985.2:c.118C>A (ETFB))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.51857502G>T
DNA change (hg38) -
Published as ETFB(NM_001014763.1):c.391C>A (p.(Pro131Thr))
ISCN -
DB-ID ETFB_000018
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +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     
ETFB NM_001014763.1 ?/. - c.391C>A r.(?) p.(Pro131Thr)
ETFB NM_001985.2 ?/. - c.118C>A r.(?) p.(Pro40Thr)


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