Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.121498522T>G | CA16043908 | FGFR2 | c.1648A>C (p.Asn550His) c.1639A>C (p.Asn547His) c.469A>C (p.Asn157His) n.987A>C c.1294A>C (p.Asn432His) n.465A>C c.*347A>C (n.*347A>C) n.3986A>C n.2658A>C c.1645A>C (p.Asn549His) c.1372A>C (p.Asn458His) c.1378A>C (p.Asn460His) c.1381A>C (p.Asn461His) c.1303A>C (p.Asn435His) c.1297A>C (p.Asn433His) c.1309A>C (p.Asn437His) c.421A>C (p.Asn141His) c.961A>C (p.Asn321His) c.*692A>C (n.*692A>C) c.1300A>C (p.Asn434His) n.2095A>C c.1699A>C (p.Asn567His) c.1696A>C (p.Asn566His) c.1705A>C (p.Asn569His) c.1438A>C (p.Asn480His) c.1360A>C (p.Asn454His) c.1702A>C (p.Asn568His) c.1357A>C (p.Asn453His) c.1351A>C (p.Asn451His) c.1435A>C (p.Asn479His) c.1432A>C (p.Asn478His) c.1429A>C (p.Asn477His) c.475A>C (p.Asn159His) n.2081A>C | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
10 | g.121498522T>C | CA378321436 | FGFR2 | c.1648A>G (p.Asn550Asp) c.1639A>G (p.Asn547Asp) c.469A>G (p.Asn157Asp) n.987A>G c.1294A>G (p.Asn432Asp) n.465A>G c.*347A>G (n.*347A>G) n.3986A>G n.2658A>G c.1645A>G (p.Asn549Asp) c.1372A>G (p.Asn458Asp) c.1378A>G (p.Asn460Asp) c.1381A>G (p.Asn461Asp) c.1303A>G (p.Asn435Asp) c.1297A>G (p.Asn433Asp) c.1309A>G (p.Asn437Asp) c.421A>G (p.Asn141Asp) c.961A>G (p.Asn321Asp) c.*692A>G (n.*692A>G) c.1300A>G (p.Asn434Asp) n.2095A>G c.1699A>G (p.Asn567Asp) c.1696A>G (p.Asn566Asp) c.1705A>G (p.Asn569Asp) c.1438A>G (p.Asn480Asp) c.1360A>G (p.Asn454Asp) c.1702A>G (p.Asn568Asp) c.1357A>G (p.Asn453Asp) c.1351A>G (p.Asn451Asp) c.1435A>G (p.Asn479Asp) c.1432A>G (p.Asn478Asp) c.1429A>G (p.Asn477Asp) c.475A>G (p.Asn159Asp) n.2081A>G | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |