Variant #0000010486 (NC_000012.12:g.?, POLE(NM_006231.4):c.1473+5G>A)
Individual ID |
00003425 |
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.? |
Reference |
- |
DB-ID |
POLE_000047 |
dbSNP ID |
rs2135995568 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Claudia Martin-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Variant on transcripts
Screenings
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