| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121498556C>G | CA16602617 | FGFR2 | c.1614G>C (p.Met538Ile) c.1605G>C (p.Met535Ile) c.435G>C (p.Met145Ile) n.953G>C c.1260G>C (p.Met420Ile) n.431G>C c.*313G>C (n.*313G>C) n.3952G>C n.2624G>C c.1611G>C (p.Met537Ile) c.1338G>C (p.Met446Ile) c.1344G>C (p.Met448Ile) c.1347G>C (p.Met449Ile) c.1269G>C (p.Met423Ile) c.1263G>C (p.Met421Ile) c.1275G>C (p.Met425Ile) c.387G>C (p.Met129Ile) c.927G>C (p.Met309Ile) c.*658G>C (n.*658G>C) c.1266G>C (p.Met422Ile) n.2061G>C c.1665G>C (p.Met555Ile) c.1662G>C (p.Met554Ile) c.1671G>C (p.Met557Ile) c.1404G>C (p.Met468Ile) c.1326G>C (p.Met442Ile) c.1668G>C (p.Met556Ile) c.1323G>C (p.Met441Ile) c.1317G>C (p.Met439Ile) c.1401G>C (p.Met467Ile) c.1398G>C (p.Met466Ile) c.1395G>C (p.Met465Ile) c.441G>C (p.Met147Ile) n.2047G>C | ClinVar dbSNP |
| 10 | g.121498556C>A | CA16602616 | FGFR2 | c.1614G>T (p.Met538Ile) c.1605G>T (p.Met535Ile) c.435G>T (p.Met145Ile) n.953G>T c.1260G>T (p.Met420Ile) n.431G>T c.*313G>T (n.*313G>T) n.3952G>T n.2624G>T c.1611G>T (p.Met537Ile) c.1338G>T (p.Met446Ile) c.1344G>T (p.Met448Ile) c.1347G>T (p.Met449Ile) c.1269G>T (p.Met423Ile) c.1263G>T (p.Met421Ile) c.1275G>T (p.Met425Ile) c.387G>T (p.Met129Ile) c.927G>T (p.Met309Ile) c.*658G>T (n.*658G>T) c.1266G>T (p.Met422Ile) n.2061G>T c.1665G>T (p.Met555Ile) c.1662G>T (p.Met554Ile) c.1671G>T (p.Met557Ile) c.1404G>T (p.Met468Ile) c.1326G>T (p.Met442Ile) c.1668G>T (p.Met556Ile) c.1323G>T (p.Met441Ile) c.1317G>T (p.Met439Ile) c.1401G>T (p.Met467Ile) c.1398G>T (p.Met466Ile) c.1395G>T (p.Met465Ile) c.441G>T (p.Met147Ile) n.2047G>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
| 10 | g.121498556C>T | CA16602618 | FGFR2 | c.1614G>A (p.Met538Ile) c.1605G>A (p.Met535Ile) c.435G>A (p.Met145Ile) n.953G>A c.1260G>A (p.Met420Ile) n.431G>A c.*313G>A (n.*313G>A) n.3952G>A n.2624G>A c.1611G>A (p.Met537Ile) c.1338G>A (p.Met446Ile) c.1344G>A (p.Met448Ile) c.1347G>A (p.Met449Ile) c.1269G>A (p.Met423Ile) c.1263G>A (p.Met421Ile) c.1275G>A (p.Met425Ile) c.387G>A (p.Met129Ile) c.927G>A (p.Met309Ile) c.*658G>A (n.*658G>A) c.1266G>A (p.Met422Ile) n.2061G>A c.1665G>A (p.Met555Ile) c.1662G>A (p.Met554Ile) c.1671G>A (p.Met557Ile) c.1404G>A (p.Met468Ile) c.1326G>A (p.Met442Ile) c.1668G>A (p.Met556Ile) c.1323G>A (p.Met441Ile) c.1317G>A (p.Met439Ile) c.1401G>A (p.Met467Ile) c.1398G>A (p.Met466Ile) c.1395G>A (p.Met465Ile) c.441G>A (p.Met147Ile) n.2047G>A | ClinVar dbSNP |
| 10 | g.121498556C= | CA1941017714 | FGFR2 | c.1614G= (p.Met538=) c.1605G= (p.Met535=) c.435G= (p.Met145=) n.953G= c.1260G= (p.Met420=) n.431G= c.*313G= (n.*313G=) n.3952G= n.2624G= c.1611G= (p.Met537=) c.1338G= (p.Met446=) c.1344G= (p.Met448=) c.1347G= (p.Met449=) c.1269G= (p.Met423=) c.1263G= (p.Met421=) c.1275G= (p.Met425=) c.387G= (p.Met129=) c.927G= (p.Met309=) c.*658G= (n.*658G=) c.1266G= (p.Met422=) n.2061G= c.1665G= (p.Met555=) c.1662G= (p.Met554=) c.1671G= (p.Met557=) c.1404G= (p.Met468=) c.1326G= (p.Met442=) c.1668G= (p.Met556=) c.1323G= (p.Met441=) c.1317G= (p.Met439=) c.1401G= (p.Met467=) c.1398G= (p.Met466=) c.1395G= (p.Met465=) c.441G= (p.Met147=) n.2047G= | dbSNP |