Variant #0000024443 (NC_000008.10:g.100115204C>T, NM_017890.3:c.436C>T (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.100115204C>T
DNA change (hg38) g.99102976C>T
Published as EX5
ISCN -
DB-ID VPS13B_000138 See all 2 reported entries
Variant remarks 1 French COH1 patient (com-het)
Reference PubMed: El Chehadeh et al. 2010
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2014-02-03 14:59:38 +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 +/+ 06 c.436C>T r.(?) p.(Arg146*)


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