Variant #0000721121 (NC_000006.11:g.80838884_80838894del, NM_000056.3:c.281_291del (BCKDHB))

Chromosome 6
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.80838884_80838894del
DNA change (hg38) -
Published as BCKDHB(NM_183050.4):c.281_291delTTGGTGAAGAT (p.F94Cfs*8)
ISCN -
DB-ID BCKDHB_000010
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCKDHB NM_000056.3 +?/. - c.281_291del r.(?) p.(Phe94CysfsTer8)
BCKDHB NM_183050.2 +?/. - c.281_291del r.(?) p.(Phe94CysfsTer8)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.