Variant #0001005307 (NC_000020.10:g.2840930G>A, NM_022575.2:c.286G>A (VPS16))

Chromosome 20
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.2840930G>A
DNA change (hg38) -
Published as VPS16(NM_022575.4):c.286G>A (p.E96K)
ISCN -
DB-ID PCED1A_000020
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) 0.00025 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRA NM_002836.3 -?/. - c.-4586G>A r.(?) p.(=)
VPS16 NM_022575.2 -?/. - c.286G>A r.(?) p.(Glu96Lys)
PCED1A NM_022760.4 -?/. - c.-20095C>T r.(?) p.(=)


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