Variant #0000950959 (NC_000017.10:g.56772370dup, NM_058216.1:c.224dup (RAD51C))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56772370dup |
DNA change (hg38) |
- |
Published as |
RAD51C(NM_058216.1):c.224dupA (p.Y75*), RAD51C(NM_058216.3):c.224dupA (p.Y75*) |
ISCN |
- |
DB-ID |
RAD51C_000029 See all 6 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) |
Retrieve |
Owner |
VKGL-NL_NKI |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_NKI |
Date created |
2023-11-27 17:35:39 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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