Variant #0000016302 (NC_000008.10:g.100128081_100128082del, NM_017890.3:c.916_917delGA (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.100128081_100128082del |
DNA change (hg38) |
g.99115853_99115854del |
Published as |
c.916_917delGA: p.Asp306TyrfsX9 (exon 7) |
ISCN |
- |
DB-ID |
VPS13B_000020 |
Variant remarks |
1 Belgian COH1 family (com-het), 2 French siblings with COH1 (com-het) |
Reference |
PubMed: Sheifert et al. 2008, PubMed: El Chehadeh et al. 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
0/50 CON |
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 |
2020-06-24 14:16:24 +02:00 (CEST) |

Variant on transcripts
|