Variant #0000024455 (NC_000008.10:g.100133678_100155175dup, NC_000008.10(NM_017890.3):c.1206+5_1652-27dup (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.100133678_100155175dup
DNA change (hg38) g.99121450_99142947dup
Published as DupEX9-12 (g.100202854_100224351dup)
ISCN -
DB-ID VPS13B_000148
Variant remarks 2 French siblings with COH1 (com-het)
Reference PubMed: El Chehadeh-Djebbar et al. 2011
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 2014-02-03 19:29:52 +01:00 (CET)
Date last edited 2017-05-05 18:33:04 +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 +/+ 10-13 c.1206+5_1652-27dup r.spl? p.?


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