Variant #0000016289 (NC_000008.10:g.100001615_100141005del, NC_000008.10(NM_017890.3):c.-23990_1207-5855del (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.100001615_100141005del |
| DNA change (hg38) |
g.98989387_99128777del |
| Published as |
Del promotor - 8: 100070791 - 100210181 bp (hg18) |
| ISCN |
- |
| DB-ID |
VPS13B_000007 |
| Variant remarks |
2 Belgian COH1 families (hom); Deletion of exons 1-9a |
| Reference |
PubMed: Balikova et al. 2009 |
| 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 |
2012-11-14 13:00:16 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

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