Variant #0000680927 (NC_000017.10:g.526814C>G, NM_018289.3:c.988G>C (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.526814C>G
DNA change (hg38) -
Published as VPS53(NM_001128159.2):c.1075G>C (p.A359P)
ISCN -
DB-ID VPS53_000023
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) 2.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
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.1075G>C r.(?) p.(Ala359Pro)
VPS53 NM_018289.3 ?/. - c.988G>C r.(?) p.(Ala330Pro)


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