Variant #0000326528 (NC_000019.9:g.41931741G>A, NM_000709.3:c.*1228G>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.41931741G>A
DNA change (hg38) g.41425836G>A
Published as B3GNT8(NM_198540.2):c.943C>T (p.(Arg315Cys))
ISCN -
DB-ID B3GNT8_000002
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCKDHA NM_000709.3 ?/. - c.*1228G>A r.(=) p.(=)
B3GNT8 NM_198540.2 ?/. - c.943C>T r.(?) p.(Arg315Cys)


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