Variant #0000721737 (NC_000008.10:g.100887650_100887652dup, NM_017890.3:c.11825_11827dup (VPS13B))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.100887650_100887652dup |
| DNA change (hg38) |
- |
| Published as |
VPS13B(NM_017890.4):c.11825_11827dupATG (p.D3942dup), VPS13B(NM_017890.5):c.11825_11827dupATG (p.D3942dup), VPS13B(NM_152564.4):c.11750_11752dupATG... |
| ISCN |
- |
| DB-ID |
VPS13B_000134 See all 4 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2021-02-08 18:36:18 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
|