Variant #0000653630 (NC_000001.10:g.12398365A>G, NC_000001.10(NM_015378.2):c.8626+3A>G (VPS13D))
| Chromosome |
1 |
| 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.12398365A>G |
| DNA change (hg38) |
g.12338308A>G |
| Published as |
VPS13D(NM_015378.4):c.8626+3A>G |
| ISCN |
- |
| DB-ID |
VPS13D_000060 |
| 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 |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-06-03 15:45:51 +02:00 (CEST) |

Variant on transcripts
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