Variant #0000982648 (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) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56772284A>G |
DNA change (hg38) |
- |
Published as |
RAD51C(NM_002876.2):c.146-8A>G (p.(=)), RAD51C(NM_058216.1):c.146-8A>G, RAD51C(NM_058216.3):c.146-8A>G |
ISCN |
- |
DB-ID |
RAD51C_000028 See all 7 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) |
0.00122 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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