Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112450358G>ACA235370PTPN11c.178G>A (p.Gly60Ser)
c.175G>A (p.Gly59Ser)
ClinVar dbSNP gnomAD v4
12g.112450358G>TCA215448PTPN11c.178G>T (p.Gly60Cys)
c.175G>T (p.Gly59Cys)
ClinVar dbSNP
12g.112450358G>CCA16042862PTPN11c.178G>C (p.Gly60Arg)
c.175G>C (p.Gly59Arg)
ClinVar dbSNP COSMIC

Number of alleles fetched