Variant #0000046673 (NC_000017.10:g.56774077A>G, NM_058216.1:c.428A>G (RAD51C))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56774077A>G |
| DNA change (hg38) |
g.58696716A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RAD51C_000032 See all 8 reported entries |
| Variant remarks |
DNA from FFPE tumor tissue: no LOH, no abnormal promotor methylation detected |
| Reference |
- |
| ClinVar ID |
SCV001365258.1 |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 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 |
2023-12-15 11:34:47 +01:00 (CET) |

Variant on transcripts
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