Variant #0000009627 (NC_000003.12:g.14147333C>T, NM_004628.5:c.2561G>A (XPC))
Individual ID |
00002313 |
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.14147333C>T |
Reference |
- |
DB-ID |
XPC_000001 |
dbSNP ID |
rs372943289 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Claudia Martin-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2023-12-06 14:59:17 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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