Variant #0000680939 (NC_000017.10:g.56772522G>A, NM_058216.1:c.376G>A (RAD51C))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56772522G>A |
DNA change (hg38) |
- |
Published as |
RAD51C(NM_002876.2):c.376G>A (p.(Ala126Thr)), RAD51C(NM_058216.1):c.376G>A (p.A126T), RAD51C(NM_058216.3):c.376G>A (p.A126T) |
ISCN |
- |
DB-ID |
RAD51C_000008 See all 15 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.0035 View details |
Owner |
VKGL-NL_NKI |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_NKI |
Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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