Variant #0000570029 (NC_000020.10:g.57016058C>T, NM_004738.4:c.492C>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.57016058C>T
DNA change (hg38) g.58441002C>T
Published as VAPB(NM_004738.4):c.492C>T (p.T164=), VAPB(NM_004738.5):c.492C>T (p.T164=)
ISCN -
DB-ID VAPB_000008 See all 3 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) 0.00016 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 2023-01-11 15:44:22 +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.212-3075C>T r.(=) p.(=)
VAPB NM_004738.4 ?/. - c.492C>T r.(?) p.(Thr164=)


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