Variant #0000895112 (NC_000019.9:g.51848627_51848629del, NM_001985.2:c.614_616del (ETFB))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51848627_51848629del
DNA change (hg38) -
Published as ETFB(NM_001985.3):c.614_616delAGA (p.K205del)
ISCN -
DB-ID ETFB_000019
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +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     
ETFB NM_001014763.1 +?/. - c.887_889del r.(?) p.(Lys296del)
VSIG10L NM_001163922.1 +?/. - c.-3241_-3239del r.(?) p.(=)
ETFB NM_001985.2 +?/. - c.614_616del r.(?) p.(Lys205del)


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