Variant #0000567441 (NC_000019.9:g.41928621G>A, NM_000709.3:c.941G>A (BCKDHA))

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.41928621G>A
DNA change (hg38) g.41422716G>A
Published as BCKDHA(NM_000709.3):c.941G>A (p.R314Q)
ISCN -
DB-ID BCKDHA_000032
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCKDHA NM_000709.3 ?/. - c.941G>A r.(?) p.(Arg314Gln)
B3GNT8 NM_198540.2 ?/. - c.*2869C>T r.(=) p.(=)


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