Variant #0000016298 (NC_000008.10:g.(?_100115181)_(100160238_?)del, NC_000008.10(NM_017890.3):c.413-?_2013+?del (VPS13B))

Chromosome 8
Allele Both (homozygous)
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.(?_100115181)_(100160238_?)del
DNA change (hg38) -
Published as c.413_2013del: p.Gly138GlufsX4 (exon 5-14)
ISCN -
DB-ID VPS13B_000016
Variant remarks 1 Iranian COH1 family (hom); Deletion of exons 6-15
Reference PubMed: Sheifert et al. 2008
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 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+ 06-15 c.413-?_2013+?del r.(413_2013del) p.(Gly138Glufs*4)


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