Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.1220623C>T | CA402949571 | STK11 | c.640C>T (p.Gln214Ter) c.268C>T (p.Gln90Ter) c.466C>T (p.Gln156Ter) n.538C>T n.730C>T n.611C>T c.418C>T (p.Gln140Ter) n.1265C>T | ClinVar dbSNP |
19 | g.1220623C>A | CA402949569 | STK11 | c.640C>A (p.Gln214Lys) c.268C>A (p.Gln90Lys) c.466C>A (p.Gln156Lys) n.538C>A n.730C>A n.611C>A c.418C>A (p.Gln140Lys) n.1265C>A | dbSNP |
19 | g.1220623C= | CA2317589909 | STK11 | c.640C= (p.Gln214=) c.268C= (p.Gln90=) c.466C= (p.Gln156=) n.538C= n.730C= n.611C= c.418C= (p.Gln140=) n.1265C= | dbSNP |