Variant #0000007888 (NC_000010.11:g.87957920_87957921delinsC, NM_000314.6:c.702_703delinsC (PTEN))
Individual ID |
00001384 |
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.87957920_87957921delinsC |
Reference |
- |
DB-ID |
PTEN_000009 |
dbSNP ID |
- |
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 |
2020-08-28 16:59:59 -03:00 (-03) |
Date last edited |
2020-12-07 19:26:18 -02:00 (-02) |
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Variant on transcripts
Screenings
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