Variant #0000569293 (NC_000020.10:g.2819734_2819735insCCCCCC, NM_022575.2:c.-1687_-1686insCCCCCC (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.2819734_2819735insCCCCCC
DNA change (hg38) g.2839088_2839089insCCCCCC
Published as PCED1A(NM_022760.5):c.205-4_205-3insGGGGGG
ISCN -
DB-ID PCED1A_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 14:41:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRA NM_002836.3 -?/. - c.-25782_-25781insCCCCCC r.(?) p.(=)
VPS16 NM_022575.2 -?/. - c.-1687_-1686insCCCCCC r.(?) p.(=)
PCED1A NM_022760.4 -?/. - c.205-4_205-3insGGGGGG r.spl? p.?


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