Variant #0000785923 (NC_000017.10:g.56772289C>T, NC_000017.10(NM_058216.1):c.146-3C>T (RAD51C))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56772289C>T |
| DNA change (hg38) |
g.58694928C>T |
| Published as |
ACMG BS3 |
| ISCN |
- |
| DB-ID |
RAD51C_000240 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Sanoguera-Miralles 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-05-19 14:00:58 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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