Variant #0000016306 (NC_000008.10:g.100146922_100146926del, NM_017890.3:c.1269_1273delATTGT (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.100146922_100146926del |
| DNA change (hg38) |
g.99134694_99134698del |
| Published as |
c.1269_1273delATTGT: p.Cys425GlyfsX8 (exon 9) |
| ISCN |
- |
| DB-ID |
VPS13B_000024 |
| Variant remarks |
1 Belgian/ Italian COH1 family (com-het) |
| Reference |
PubMed: Sheifert et al. 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/50 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 |
2020-06-24 14:18:38 +02:00 (CEST) |

Variant on transcripts
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