Variant #0000016410 (NC_000008.10:g.100883101dup, NM_017890.3:c.11556dup (VPS13B))

Chromosome 8
Allele Maternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.100883101dup
DNA change (hg38) g.99870873dup
Published as 11556insT
ISCN -
DB-ID VPS13B_000128 See all 2 reported entries
Variant remarks 1 COH1 family (com-het)
Reference -
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 Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-14 13:00:16 +01:00 (CET)
Date last edited 2019-03-08 10:20:16 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+ 58 c.11556dup r.(11556dup) p.(Val3853Cysfs*33)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.