Variant #0000009905 (NC_000010.11:g.87960892A>T, PTEN(NM_000314.6):c.802-2A>T)
Individual ID |
00002770 |
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.87960892A>T |
Reference |
- |
DB-ID |
PTEN_000011 |
dbSNP ID |
rs587782455 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Guillermo Alberto-Instituto Fleming |
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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