Variant #0001055759 (NC_000017.10:g.423155G>C, NM_018289.3:c.*12912C>G (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.423155G>C
DNA change (hg38) -
Published as VPS53(NM_001128159.3):c.2239C>G (p.(His747Asp))
ISCN -
DB-ID VPS53_000040
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS53 NM_001128159.2 ?/. - c.2239C>G r.(?) p.(His747Asp)
VPS53 NM_018289.3 ?/. - c.*12912C>G r.(=) p.(=)


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