Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.43120162C>G | CA376557232 | RET | c.2293C>G (p.Arg765Gly) n.2263C>G n.2254C>G c.2689C>G (p.Arg897Gly) c.*1283C>G (n.*1283C>G) c.*38C>G (n.*38C>G) c.1927C>G (p.Arg643Gly) | ClinVar dbSNP |
10 | g.43120162C>T | CA16612889 | RET | c.2293C>T (p.Arg765Ter) n.2263C>T n.2254C>T c.2689C>T (p.Arg897Ter) c.*1283C>T (n.*1283C>T) c.*38C>T (n.*38C>T) c.1927C>T (p.Arg643Ter) | ClinVar dbSNP |
10 | g.43120162C>A | CA469028911 | RET | c.2293C>A (p.Arg765=) n.2263C>A n.2254C>A c.2689C>A (p.Arg897=) c.*1283C>A (n.*1283C>A) c.*38C>A (n.*38C>A) c.1927C>A (p.Arg643=) | dbSNP |