Variant #0000533317 (NC_000008.10:g.100887867_100887870dup, NM_017890.3:c.12042_12045dup (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.100887867_100887870dup |
DNA change (hg38) |
g.99875639_99875642dup |
Published as |
VPS13B(NM_017890.4):c.12038_12039insAAAT (p.(Ala4016Ter)), VPS13B(NM_017890.4):c.12042_12045dupTAAA (p.A4016*) |
ISCN |
- |
DB-ID |
COX6C_000093 See all 2 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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