Variant #0000485609 (NC_000013.10:g.48934298A>T, NC_000013.10(NM_000321.2):c.718+35A>T (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.48934298A>T |
DNA change (hg38) |
g.48360162A>T |
Published as |
- |
ISCN |
- |
DB-ID |
RB1_001023 See all 2 reported entries |
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) |
0.00228 View details |
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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