Variant #0000016346 (NC_000008.10:g.100587947C>T, NM_017890.3:c.5086C>T (VPS13B))

Chromosome 8
Allele Paternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100587947C>T
DNA change (hg38) g.99575719C>T
Published as c.5086C/T/p.R1696X, exon 32
ISCN -
DB-ID VPS13B_000049 See all 3 reported entries
Variant remarks 1 Arabian COH1 family (com-het)
Reference Rivera-Brugués 2011
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/676 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-11-14 13:00:16 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+ 35 c.5086C>T r.(5086c>u) p.(Arg1696*)


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