| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121488095C>T | CA123000 | FGFR2 | c.1885G>A (p.Ala629Thr) c.1876G>A (p.Ala626Thr) c.706G>A (p.Ala236Thr) n.1224G>A c.1531G>A (p.Ala511Thr) n.702G>A n.294G>A c.*584G>A (n.*584G>A) n.4223G>A n.2895G>A c.1882G>A (p.Ala628Thr) c.1609G>A (p.Ala537Thr) c.1615G>A (p.Ala539Thr) c.1618G>A (p.Ala540Thr) c.1540G>A (p.Ala514Thr) c.1534G>A (p.Ala512Thr) c.1546G>A (p.Ala516Thr) c.658G>A (p.Ala220Thr) c.1198G>A (p.Ala400Thr) c.*929G>A (n.*929G>A) c.1537G>A (p.Ala513Thr) n.2332G>A c.1936G>A (p.Ala646Thr) c.1933G>A (p.Ala645Thr) c.1942G>A (p.Ala648Thr) c.1675G>A (p.Ala559Thr) c.1597G>A (p.Ala533Thr) c.1939G>A (p.Ala647Thr) c.1594G>A (p.Ala532Thr) c.1588G>A (p.Ala530Thr) c.1672G>A (p.Ala558Thr) c.1669G>A (p.Ala557Thr) c.1666G>A (p.Ala556Thr) c.712G>A (p.Ala238Thr) n.2318G>A | ClinVar dbSNP |
| 10 | g.121488095C>G | CA378315010 | FGFR2 | c.1885G>C (p.Ala629Pro) c.1876G>C (p.Ala626Pro) c.706G>C (p.Ala236Pro) n.1224G>C c.1531G>C (p.Ala511Pro) n.702G>C n.294G>C c.*584G>C (n.*584G>C) n.4223G>C n.2895G>C c.1882G>C (p.Ala628Pro) c.1609G>C (p.Ala537Pro) c.1615G>C (p.Ala539Pro) c.1618G>C (p.Ala540Pro) c.1540G>C (p.Ala514Pro) c.1534G>C (p.Ala512Pro) c.1546G>C (p.Ala516Pro) c.658G>C (p.Ala220Pro) c.1198G>C (p.Ala400Pro) c.*929G>C (n.*929G>C) c.1537G>C (p.Ala513Pro) n.2332G>C c.1936G>C (p.Ala646Pro) c.1933G>C (p.Ala645Pro) c.1942G>C (p.Ala648Pro) c.1675G>C (p.Ala559Pro) c.1597G>C (p.Ala533Pro) c.1939G>C (p.Ala647Pro) c.1594G>C (p.Ala532Pro) c.1588G>C (p.Ala530Pro) c.1672G>C (p.Ala558Pro) c.1669G>C (p.Ala557Pro) c.1666G>C (p.Ala556Pro) c.712G>C (p.Ala238Pro) n.2318G>C | dbSNP |
| 10 | g.121488095C>A | CA378315007 | FGFR2 | c.1885G>T (p.Ala629Ser) c.1876G>T (p.Ala626Ser) c.706G>T (p.Ala236Ser) n.1224G>T c.1531G>T (p.Ala511Ser) n.702G>T n.294G>T c.*584G>T (n.*584G>T) n.4223G>T n.2895G>T c.1882G>T (p.Ala628Ser) c.1609G>T (p.Ala537Ser) c.1615G>T (p.Ala539Ser) c.1618G>T (p.Ala540Ser) c.1540G>T (p.Ala514Ser) c.1534G>T (p.Ala512Ser) c.1546G>T (p.Ala516Ser) c.658G>T (p.Ala220Ser) c.1198G>T (p.Ala400Ser) c.*929G>T (n.*929G>T) c.1537G>T (p.Ala513Ser) n.2332G>T c.1936G>T (p.Ala646Ser) c.1933G>T (p.Ala645Ser) c.1942G>T (p.Ala648Ser) c.1675G>T (p.Ala559Ser) c.1597G>T (p.Ala533Ser) c.1939G>T (p.Ala647Ser) c.1594G>T (p.Ala532Ser) c.1588G>T (p.Ala530Ser) c.1672G>T (p.Ala558Ser) c.1669G>T (p.Ala557Ser) c.1666G>T (p.Ala556Ser) c.712G>T (p.Ala238Ser) n.2318G>T | dbSNP |