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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