Variant #0000485531 (NC_000013.10:g.48877837G>A, NM_000321.2:c.-212G>A (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.48877837G>A |
| DNA change (hg38) |
g.48303701G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RB1_000926 |
| 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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