Variant #0000614208 (NC_000012.11:g.50232682C>T, NM_181708.2:c.351G>A (BCDIN3D))

Chromosome 12
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.50232682C>T
DNA change (hg38) g.49838899C>T
Published as BCDIN3D(NM_181708.2):c.351G>A (p.K117=)
ISCN -
DB-ID BCDIN3D_000001
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) 2.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCDIN3D NM_181708.2 -?/. - c.351G>A r.(?) p.(Lys117=)
BCDIN3D-AS1 NR_027499.1 -?/. - n.833C>T r.(?) -


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