Variant #0000618219 (NC_000020.10:g.56964571G>T, NM_004738.4:c.56G>T (VAPB))

Chromosome 20
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.56964571G>T
DNA change (hg38) g.58389515G>T
Published as VAPB(NM_004738.4):c.56G>T (p.R19L)
ISCN -
DB-ID VAPB_000006 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAPB NM_001195677.1 ?/. - c.56G>T r.(?) p.(Arg19Leu)
VAPB NM_004738.4 ?/. - c.56G>T r.(?) p.(Arg19Leu)


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