Variant #0000016290 (NC_000008.10:g.99945853_100278670del, NC_000008.10(NM_017890.3):c.-79752_2516-7756del (VPS13B))
| Chromosome |
8 |
| Allele |
Maternal (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.99945853_100278670del |
| DNA change (hg38) |
g.98933625_99266442del |
| Published as |
315 kb del: exons 1-17: chr8(hg18):100015029...100347846; c.1-2515del |
| ISCN |
- |
| DB-ID |
VPS13B_000008 |
| Variant remarks |
1 German/African COH1 family (com-het); Chr8(hg18):g.100015029_100347846del = Chr8(hg19):g.99945853_100278670del |
| Reference |
Rivera-Brugués 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/1612 CON |
| 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
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