Variant #0000016414 (NC_000008.10:g.100883800_100883803del, NM_017890.3:c.11695_11698del (VPS13B))

Chromosome 8
Allele Unknown
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.100883800_100883803del
DNA change (hg38) g.99871572_99871575del
Published as 11695delAGTG
ISCN -
DB-ID VPS13B_000132 See all 2 reported entries
Variant remarks 2 COH1 patients (com-het)
Reference PubMed: El Chehadeh-Djebbar et al. 2013
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 10:15:44 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+ 64 c.11695_11698del r.(11695_11698del) p.(Ser3901Argfs*40)


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