Variant #0000570031 (NC_000020.10:g.57016076G>A, NM_004738.4:c.510G>A (VAPB))

Chromosome 20
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.57016076G>A
DNA change (hg38) g.58441020G>A
Published as VAPB(NM_004738.4):c.510G>A (p.M170I, p.(Met170Ile)), VAPB(NM_004738.5):c.510G>A (p.M170I)
ISCN -
DB-ID VAPB_000009 See all 5 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) 0.00129 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAPB NM_001195677.1 -?/. - c.212-3057G>A r.(=) p.(=)
VAPB NM_004738.4 -?/. - c.510G>A r.(?) p.(Met170Ile)


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