Variant #0000046675 (NC_000017.10:g.56772284A>G, NC_000017.10(NM_058216.1):c.146-8A>G (RAD51C))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56772284A>G |
| DNA change (hg38) |
g.58694923A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RAD51C_000028 See all 7 reported entries |
| Variant remarks |
DNA from FFPE tumor tissue: no abnormal promotor methylation detected; RNA/cDNA: no abnormalities |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00122 View details |
| Owner |
Christine Rappaport |
| Database submission license |
No license selected |
| Created by |
Christine Rappaport |
| Date created |
2014-11-02 12:02:12 +01:00 (CET) |
| Date last edited |
2020-07-14 21:59:34 +02:00 (CEST) |

Variant on transcripts
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