Variant #0000256543 (NC_000020.10:g.57019199A>C, NM_004738.4:c.640A>C (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.57019199A>C
DNA change (hg38) g.58444143A>C
Published as VAPB(NM_004738.4):c.640A>C (p.T214P)
ISCN -
DB-ID VAPB_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.278A>C r.(?) p.(Asn93Thr)
VAPB NM_004738.4 ?/. - c.640A>C r.(?) p.(Thr214Pro)


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