Variant #0000486454 (NC_000013.10:g.48878088dup, NM_000321.2:c.40dup (RB1))
Chromosome |
13 |
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.48878088dup |
DNA change (hg38) |
g.48303952dup |
Published as |
- |
ISCN |
- |
DB-ID |
RB1_002017 |
Variant remarks |
- |
Reference |
data copied from the RB1-LSDB |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Dietmar Lohmann |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2019-06-08 19:09:47 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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