Variant #0000016293 (NC_000008.10:g.100057231_100201680del, NC_000008.10(NM_017890.3):c.291+6437_2334-3424del (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.100057231_100201680del |
| DNA change (hg38) |
g.99045003_99189452del |
| Published as |
Del 4-16: 100126407 - 100270856 bp (hg18) |
| ISCN |
- |
| DB-ID |
VPS13B_000011 |
| Variant remarks |
1 COH1 family (com-het); Deletion of exons 4-17 |
| 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
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