Variant #0000016306 (NC_000008.10:g.100146922_100146926del, NM_017890.3:c.1269_1273delATTGT (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.100146922_100146926del
DNA change (hg38) g.99134694_99134698del
Published as c.1269_1273delATTGT: p.Cys425GlyfsX8 (exon 9)
ISCN -
DB-ID VPS13B_000024
Variant remarks 1 Belgian/ Italian COH1 family (com-het)
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 2020-06-24 14:18:38 +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 +/+ 10 c.1269_1273delATTGT r.(1269_1273delauugu) p.(Cys425Glyfs*8)


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