Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.34880568C>GCA410202489RUNX1c.497G>C (p.Arg166Pro)
c.416G>C (p.Arg139Pro)
c.461G>C (p.Arg154Pro)
c.*87G>C (n.*87G>C)
c.458G>C (p.Arg153Pro)
n.676G>C
c.344G>C (p.Arg115Pro)
n.723G>C
dbSNP COSMIC
21g.34880568C>TCA16616941RUNX1c.497G>A (p.Arg166Gln)
c.416G>A (p.Arg139Gln)
c.461G>A (p.Arg154Gln)
c.*87G>A (n.*87G>A)
c.458G>A (p.Arg153Gln)
n.676G>A
c.344G>A (p.Arg115Gln)
n.723G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
21g.34880568C>ACA410202488RUNX1c.497G>T (p.Arg166Leu)
c.416G>T (p.Arg139Leu)
c.461G>T (p.Arg154Leu)
c.*87G>T (n.*87G>T)
c.458G>T (p.Arg153Leu)
n.676G>T
c.344G>T (p.Arg115Leu)
n.723G>T
dbSNP COSMIC

Number of alleles fetched