Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.34799407G>T | CA248619 | RUNX1 | c.861C>A (p.Tyr287Ter) c.780C>A (p.Tyr260Ter) c.588C>A (p.Tyr196Ter) c.*451C>A (n.*451C>A) c.825C>A (p.Tyr275Ter) c.669C>A (p.Tyr223Ter) c.822C>A (p.Tyr274Ter) c.630C>A (p.Tyr210Ter) n.1040C>A c.708C>A (p.Tyr236Ter) n.1087C>A | ClinVar dbSNP |
21 | g.34799407G>C | CA410150112 | RUNX1 | c.861C>G (p.Tyr287Ter) c.780C>G (p.Tyr260Ter) c.588C>G (p.Tyr196Ter) c.*451C>G (n.*451C>G) c.825C>G (p.Tyr275Ter) c.669C>G (p.Tyr223Ter) c.822C>G (p.Tyr274Ter) c.630C>G (p.Tyr210Ter) n.1040C>G c.708C>G (p.Tyr236Ter) n.1087C>G | ClinVar dbSNP COSMIC |
21 | g.34799407G>A | CA512232261 | RUNX1 | c.861C>T (p.Tyr287=) c.780C>T (p.Tyr260=) c.588C>T (p.Tyr196=) c.*451C>T (n.*451C>T) c.825C>T (p.Tyr275=) c.669C>T (p.Tyr223=) c.822C>T (p.Tyr274=) c.630C>T (p.Tyr210=) n.1040C>T c.708C>T (p.Tyr236=) n.1087C>T | ClinVar dbSNP |