Variant #0000570035 (NC_000020.10:g.57019259G>A, NM_004738.4:c.700G>A (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.57019259G>A
DNA change (hg38) g.58444203G>A
Published as VAPB(NM_004738.4):c.700G>A (p.V234I)
ISCN -
DB-ID VAPB_000011
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) 6.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
VAPB NM_001195677.1 ?/. - c.*38G>A r.(=) p.(=)
VAPB NM_004738.4 ?/. - c.700G>A r.(?) p.(Val234Ile)


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