Variant #0000016399 (NC_000008.10:g.100865698dup, NM_017890.3:c.10156dupA (VPS13B))
Chromosome |
8 |
Allele |
Paternal (confirmed) |
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.100865698dup |
DNA change (hg38) |
g.99853470dup |
Published as |
c.10156dup: p.T3361NfsX3 |
ISCN |
- |
DB-ID |
VPS13B_000117 See all 2 reported entries |
Variant remarks |
1 Italian COH1 family (com-het) |
Reference |
PubMed: Athanasakis et al. 2012 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
0/200 |
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 14:59:55 +02:00 (CEST) |

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