Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.121498597T>C | CA16603155 | FGFR2 | c.1573A>G (p.Thr525Ala) c.1564A>G (p.Thr522Ala) c.394A>G (p.Thr132Ala) n.912A>G c.1219A>G (p.Thr407Ala) n.390A>G c.*272A>G (n.*272A>G) n.3911A>G n.2583A>G c.1570A>G (p.Thr524Ala) c.1297A>G (p.Thr433Ala) c.1303A>G (p.Thr435Ala) c.1306A>G (p.Thr436Ala) c.1228A>G (p.Thr410Ala) c.1222A>G (p.Thr408Ala) c.1234A>G (p.Thr412Ala) c.346A>G (p.Thr116Ala) c.886A>G (p.Thr296Ala) c.*617A>G (n.*617A>G) c.1225A>G (p.Thr409Ala) n.2020A>G c.1624A>G (p.Thr542Ala) c.1621A>G (p.Thr541Ala) c.1630A>G (p.Thr544Ala) c.1363A>G (p.Thr455Ala) c.1285A>G (p.Thr429Ala) c.1627A>G (p.Thr543Ala) c.1282A>G (p.Thr428Ala) c.1276A>G (p.Thr426Ala) c.1360A>G (p.Thr454Ala) c.1357A>G (p.Thr453Ala) c.1354A>G (p.Thr452Ala) c.400A>G (p.Thr134Ala) n.2006A>G | ClinVar dbSNP |
10 | g.121498597T>A | CA378321786 | FGFR2 | c.1573A>T (p.Thr525Ser) c.1564A>T (p.Thr522Ser) c.394A>T (p.Thr132Ser) n.912A>T c.1219A>T (p.Thr407Ser) n.390A>T c.*272A>T (n.*272A>T) n.3911A>T n.2583A>T c.1570A>T (p.Thr524Ser) c.1297A>T (p.Thr433Ser) c.1303A>T (p.Thr435Ser) c.1306A>T (p.Thr436Ser) c.1228A>T (p.Thr410Ser) c.1222A>T (p.Thr408Ser) c.1234A>T (p.Thr412Ser) c.346A>T (p.Thr116Ser) c.886A>T (p.Thr296Ser) c.*617A>T (n.*617A>T) c.1225A>T (p.Thr409Ser) n.2020A>T c.1624A>T (p.Thr542Ser) c.1621A>T (p.Thr541Ser) c.1630A>T (p.Thr544Ser) c.1363A>T (p.Thr455Ser) c.1285A>T (p.Thr429Ser) c.1627A>T (p.Thr543Ser) c.1282A>T (p.Thr428Ser) c.1276A>T (p.Thr426Ser) c.1360A>T (p.Thr454Ser) c.1357A>T (p.Thr453Ser) c.1354A>T (p.Thr452Ser) c.400A>T (p.Thr134Ser) n.2006A>T | dbSNP |