Variant #0000263631 (NC_000019.9:g.41928655C>T, NM_000709.3:c.975C>T (BCKDHA))

Chromosome 19
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.41928655C>T
DNA change (hg38) g.41422750C>T
Published as BCKDHA(NM_000709.3):c.975C>T (p.L325=)
ISCN -
DB-ID BCKDHA_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) 0.00323 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCKDHA NM_000709.3 -?/. - c.975C>T r.(?) p.(Leu325=)
B3GNT8 NM_198540.2 -?/. - c.*2835G>A r.(=) p.(=)


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