Variant #0000024446 (NC_000008.10:g.100115246_100115249del, NM_017890.3:c.478_481delCTAA (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.100115246_100115249del |
| DNA change (hg38) |
g.99103018_99103021del |
| Published as |
c.477_480delACTA (p.I159fsX21) |
| ISCN |
- |
| DB-ID |
VPS13B_000141 |
| Variant remarks |
1 French COH1 patient (com-het) |
| Reference |
PubMed: El Chehadeh et al. 2010 |
| 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 International |
| Created by |
Anne Polvi |
| Date created |
2014-02-03 16:58:31 +01:00 (CET) |
| Date last edited |
2020-06-24 14:14:33 +02:00 (CEST) |

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