Variant #0000016288 (NC_000008.10:g.(?_100013161)_(100133463_?)del, NM_017890.3:c.(?-12444)_996+?del (VPS13B))

Chromosome 8
Allele Both (homozygous)
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.(?_100013161)_(100133463_?)del
DNA change (hg38) -
Published as a 140-kb homozygous deletion with breakpoints between probes A_14_p12741-normal, A_16_p18412462-deleted, A_16_p01978354-deleted, and A_16_p18412663-normal: deletion of exons 1-7.
ISCN -
DB-ID VPS13B_000006
Variant remarks 1 COH1 family (hom)
Reference PubMed: Balikova 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 2012-11-14 13:00:16 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+ 01-09a c.(?-12444)_996+?del r.? p.?


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