Variant #0000562106 (NC_000017.10:g.466004dup, NC_000017.10(NM_018289.3):c.1227-9dup (VPS53))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.466004dup
DNA change (hg38) g.562764dup
Published as VPS53(NM_001128159.3):c.1314-9dupT
ISCN -
DB-ID VPS53_000018
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
VPS53 NM_001128159.2 -/. - c.1314-9dup r.(=) p.(=)
VPS53 NM_018289.3 -/. - c.1227-9dup r.(=) p.(=)


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