Variant #0000658166 (NC_000017.10:g.455184G>A, NM_018289.3:c.1707C>T (VPS53))

Chromosome 17
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.455184G>A
DNA change (hg38) g.551944G>A
Published as VPS53(NM_001128159.2):c.1794C>T (p.I598=)
ISCN -
DB-ID VPS53_000022
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) 0.00065 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 2020-03-23 16:13:27 +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.1794C>T r.(?) p.(Ile598=)
VPS53 NM_018289.3 -?/. - c.1707C>T r.(?) p.(Ile569=)


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