Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.11117039C>A | CA338383476 | MTOR | c.*2356G>T (n.*2356G>T) n.2935-1571G>T c.1769G>T c.6768G>T (p.Met2256Ile) c.*2498G>T (n.*2498G>T) c.*3811G>T (n.*3811G>T) c.6981G>T (p.Met2327Ile) c.1596G>T (p.Met532Ile) n.7055-1571G>T c.6300G>T (p.Met2100Ile) c.5733G>T (p.Met1911Ile) | dbSNP COSMIC |
1 | g.11117039C>T | CA10583991 | MTOR | c.*2356G>A (n.*2356G>A) n.2935-1571G>A c.1769G>A c.6768G>A (p.Met2256Ile) c.*2498G>A (n.*2498G>A) c.*3811G>A (n.*3811G>A) c.6981G>A (p.Met2327Ile) c.1596G>A (p.Met532Ile) n.7055-1571G>A c.6300G>A (p.Met2100Ile) c.5733G>A (p.Met1911Ile) | ClinVar dbSNP COSMIC |