Variant #0000016302 (NC_000008.10:g.100128081_100128082del, NM_017890.3:c.916_917delGA (VPS13B))

Chromosome 8
Allele Unknown
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.100128081_100128082del
DNA change (hg38) g.99115853_99115854del
Published as c.916_917delGA: p.Asp306TyrfsX9 (exon 7)
ISCN -
DB-ID VPS13B_000020
Variant remarks 1 Belgian COH1 family (com-het), 2 French siblings with COH1 (com-het)
Reference PubMed: Sheifert et al. 2008, PubMed: El Chehadeh et al. 2010
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/50 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2020-06-24 14:16:24 +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 +/+ 08 c.916_917delGA r.(916_917delga) p.(Asp306Tyrfs*9)


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