Variant #0000646538 (NC_000015.9:g.91560607del, NC_000015.9(NM_018668.3):c.178-353del (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.91560607del |
DNA change (hg38) |
g.91017377del |
Published as |
- |
ISCN |
- |
DB-ID |
VPS33B_000119 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs11314057 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
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 11:16:39 +02:00 (CEST) |
Date last edited |
2021-09-09 14:41:03 +02:00 (CEST) |

Variant on transcripts
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