Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.34799407G>TCA248619RUNX1c.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
21g.34799407G>CCA410150112RUNX1c.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
21g.34799407G>ACA512232261RUNX1c.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

Number of alleles fetched