Variant #0000009551 (NC_000012.12:g.132649392T>C, NM_006231.3:c.3919A>G (POLE))
Individual ID |
00002309 |
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.132649392T>C |
Reference |
- |
DB-ID |
POLE_000017 |
dbSNP ID |
rs1000912264 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2023-11-27 11:31:24 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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