Variant #0000016289 (NC_000008.10:g.100001615_100141005del, NC_000008.10(NM_017890.3):c.-23990_1207-5855del (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.100001615_100141005del
DNA change (hg38) g.98989387_99128777del
Published as Del promotor - 8: 100070791 - 100210181 bp (hg18)
ISCN -
DB-ID VPS13B_000007
Variant remarks 2 Belgian COH1 families (hom); Deletion of exons 1-9a
Reference PubMed: Balikova et al. 2009
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+ 01-09a c.-23990_1207-5855del r.? p.?


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