Variant #0000016291 (NC_000008.10:g.100026038_100026039delinsA, NM_017890.3:c.22_23delCCinsA (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.100026038_100026039delinsA
DNA change (hg38) g.99013810_99013811delinsA
Published as c.22_23delCCinsA: p.Pro8fsX3
ISCN -
DB-ID VPS13B_000009
Variant remarks 1 Danish COH1 patient (com-het)
Reference PubMed: Kolehmainen et al. 2004
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 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 +/+ 02 c.22_23delCCinsA r.22_23delccinsa p.Pro8Lysfs*3


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