Variant #0000016390 (NC_000008.10:g.100832259A>G, NM_017890.3:c.8978A>G (VPS13B))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100832259A>G
DNA change (hg38) g.99820031A>G
Published as c.8978A>G: p.Asn2993Ser
ISCN -
DB-ID VPS13B_000108 See all 8 reported entries
Variant remarks 1 Belgian sib pair (hom) with COH1
Reference PubMed: Kolehmainen et al. 2004
ClinVar ID -
dbSNP ID rs28940272
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00323 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 +?/+? 52 c.8978A>G r.8978a>g p.Asn2993Ser


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