Variant #0000646520 (NC_000015.9:g.91562005A>G, NC_000015.9(NM_018668.3):c.97-890T>C (VPS33B))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.91562005A>G |
DNA change (hg38) |
g.91018775A>G |
Published as |
- |
ISCN |
- |
DB-ID |
VPS33B_000181 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs8026678 |
Origin |
Unknown |
Segregation |
- |
Frequency |
0.338 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Paul Gissen |
Database submission license |
No license selected |
Created by |
Paul Gissen |
Date created |
2011-08-22 11:16:40 +02:00 (CEST) |
Date last edited |
2021-09-09 14:41:03 +02:00 (CEST) |

Variant on transcripts
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