Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.34859485C>TCA248610RUNX1c.602G>A (p.Arg201Gln)
c.521G>A (p.Arg174Gln)
c.566G>A (p.Arg189Gln)
n.94G>A
c.*192G>A (n.*192G>A)
c.563G>A (p.Arg188Gln)
n.781G>A
c.449G>A (p.Arg150Gln)
n.828G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
21g.34859485C=CA2387284472RUNX1c.602G= (p.Arg201=)
c.521G= (p.Arg174=)
c.566G= (p.Arg189=)
n.94G=
c.*192G= (n.*192G=)
c.563G= (p.Arg188=)
n.781G=
c.449G= (p.Arg150=)
n.828G=
dbSNP
21g.34859485C>GCA410207956RUNX1c.602G>C (p.Arg201Pro)
c.521G>C (p.Arg174Pro)
c.566G>C (p.Arg189Pro)
n.94G>C
c.*192G>C (n.*192G>C)
c.563G>C (p.Arg188Pro)
n.781G>C
c.449G>C (p.Arg150Pro)
n.828G>C
dbSNP

Number of alleles fetched