| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121488035C>G | CA378314515 | FGFR2 | c.1945G>C (p.Ala649Pro) c.1936G>C (p.Ala646Pro) c.766G>C (p.Ala256Pro) n.1284G>C c.1591G>C (p.Ala531Pro) n.762G>C n.354G>C c.*644G>C (n.*644G>C) n.4283G>C n.2955G>C c.1942G>C (p.Ala648Pro) c.1669G>C (p.Ala557Pro) c.1675G>C (p.Ala559Pro) c.1678G>C (p.Ala560Pro) c.1600G>C (p.Ala534Pro) c.1594G>C (p.Ala532Pro) c.1606G>C (p.Ala536Pro) c.718G>C (p.Ala240Pro) c.1258G>C (p.Ala420Pro) c.*989G>C (n.*989G>C) c.1597G>C (p.Ala533Pro) n.2392G>C c.1996G>C (p.Ala666Pro) c.1993G>C (p.Ala665Pro) c.2002G>C (p.Ala668Pro) c.1735G>C (p.Ala579Pro) c.1657G>C (p.Ala553Pro) c.1999G>C (p.Ala667Pro) c.1654G>C (p.Ala552Pro) c.1648G>C (p.Ala550Pro) c.1732G>C (p.Ala578Pro) c.1729G>C (p.Ala577Pro) c.1726G>C (p.Ala576Pro) c.772G>C (p.Ala258Pro) n.2378G>C | dbSNP |
| 10 | g.121488035C>T | CA122998 | FGFR2 | c.1945G>A (p.Ala649Thr) c.1936G>A (p.Ala646Thr) c.766G>A (p.Ala256Thr) n.1284G>A c.1591G>A (p.Ala531Thr) n.762G>A n.354G>A c.*644G>A (n.*644G>A) n.4283G>A n.2955G>A c.1942G>A (p.Ala648Thr) c.1669G>A (p.Ala557Thr) c.1675G>A (p.Ala559Thr) c.1678G>A (p.Ala560Thr) c.1600G>A (p.Ala534Thr) c.1594G>A (p.Ala532Thr) c.1606G>A (p.Ala536Thr) c.718G>A (p.Ala240Thr) c.1258G>A (p.Ala420Thr) c.*989G>A (n.*989G>A) c.1597G>A (p.Ala533Thr) n.2392G>A c.1996G>A (p.Ala666Thr) c.1993G>A (p.Ala665Thr) c.2002G>A (p.Ala668Thr) c.1735G>A (p.Ala579Thr) c.1657G>A (p.Ala553Thr) c.1999G>A (p.Ala667Thr) c.1654G>A (p.Ala552Thr) c.1648G>A (p.Ala550Thr) c.1732G>A (p.Ala578Thr) c.1729G>A (p.Ala577Thr) c.1726G>A (p.Ala576Thr) c.772G>A (p.Ala258Thr) n.2378G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
| 10 | g.121488035C>A | CA378314513 | FGFR2 | c.1945G>T (p.Ala649Ser) c.1936G>T (p.Ala646Ser) c.766G>T (p.Ala256Ser) n.1284G>T c.1591G>T (p.Ala531Ser) n.762G>T n.354G>T c.*644G>T (n.*644G>T) n.4283G>T n.2955G>T c.1942G>T (p.Ala648Ser) c.1669G>T (p.Ala557Ser) c.1675G>T (p.Ala559Ser) c.1678G>T (p.Ala560Ser) c.1600G>T (p.Ala534Ser) c.1594G>T (p.Ala532Ser) c.1606G>T (p.Ala536Ser) c.718G>T (p.Ala240Ser) c.1258G>T (p.Ala420Ser) c.*989G>T (n.*989G>T) c.1597G>T (p.Ala533Ser) n.2392G>T c.1996G>T (p.Ala666Ser) c.1993G>T (p.Ala665Ser) c.2002G>T (p.Ala668Ser) c.1735G>T (p.Ala579Ser) c.1657G>T (p.Ala553Ser) c.1999G>T (p.Ala667Ser) c.1654G>T (p.Ala552Ser) c.1648G>T (p.Ala550Ser) c.1732G>T (p.Ala578Ser) c.1729G>T (p.Ala577Ser) c.1726G>T (p.Ala576Ser) c.772G>T (p.Ala258Ser) n.2378G>T | dbSNP |