Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.21970995C>TCA190729820CDKN2Ac.364G>A (p.Gly122Ser)
c.*8G>A (p.=)
n.638G>A (p.=)
c.211G>A (p.Gly71Ser)
n.765G>A
n.554G>A
n.503G>A
n.286G>A
n.694G>A
c.406G>A (p.Gly136Ser)
n.338G>A
c.348-58438C>T (p.=)
dbSNP COSMIC
9g.21970995C>GCA120400CDKN2Ac.364G>C (p.Gly122Arg)
c.*8G>C (p.=)
n.638G>C (p.=)
c.211G>C (p.Gly71Arg)
n.765G>C
n.554G>C
n.503G>C
n.286G>C
n.694G>C
c.406G>C (p.Gly136Arg)
n.338G>C
c.348-58438C>G (p.=)
ClinVar dbSNP

Number of alleles fetched