Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112450398C>T | CA256752 | PTPN11 | c.218C>T (p.Thr73Ile) c.215C>T (p.Thr72Ile) | ClinVar dbSNP COSMIC |
12 | g.112450398C>A | CA386777862 | PTPN11 | c.218C>A (p.Thr73Asn) c.215C>A (p.Thr72Asn) | dbSNP |
12 | g.112450398C>G | CA386777865 | PTPN11 | c.218C>G (p.Thr73Ser) c.215C>G (p.Thr72Ser) | dbSNP |