Variant #0000863107 (NC_000012.11:g.6568016C>A, NM_014231.3:c.*5620G>T (VAMP1))

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.6568016C>A
DNA change (hg38) -
Published as TAPBPL(NM_001351355.1):c.720C>A (p.T240=)
ISCN -
DB-ID TAPBPL_000006
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 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAMP1 NM_014231.3 -?/. - c.*5620G>T r.(=) p.(=)
TAPBPL NM_018009.4 -?/. - c.1110C>A r.(?) p.(Thr370=)


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