Variant #0000623719 (NC_000017.10:g.530438G>A, NM_018289.3:c.863C>T (VPS53))

Chromosome 17
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.530438G>A
DNA change (hg38) g.627198G>A
Published as VPS53(NM_001128159.2):c.950C>T (p.A317V)
ISCN -
DB-ID VPS53_000021
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) 0.00014 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS53 NM_001128159.2 ?/. - c.950C>T r.(?) p.(Ala317Val)
VPS53 NM_018289.3 ?/. - c.863C>T r.(?) p.(Ala288Val)


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