| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121498562C>A | CA16602619 | FGFR2 | c.1608G>T (p.Met536Ile) c.1599G>T (p.Met533Ile) c.429G>T (p.Met143Ile) n.947G>T c.1254G>T (p.Met418Ile) n.425G>T c.*307G>T (n.*307G>T) n.3946G>T n.2618G>T c.1605G>T (p.Met535Ile) c.1332G>T (p.Met444Ile) c.1338G>T (p.Met446Ile) c.1341G>T (p.Met447Ile) c.1263G>T (p.Met421Ile) c.1257G>T (p.Met419Ile) c.1269G>T (p.Met423Ile) c.381G>T (p.Met127Ile) c.921G>T (p.Met307Ile) c.*652G>T (n.*652G>T) c.1260G>T (p.Met420Ile) n.2055G>T c.1659G>T (p.Met553Ile) c.1656G>T (p.Met552Ile) c.1665G>T (p.Met555Ile) c.1398G>T (p.Met466Ile) c.1320G>T (p.Met440Ile) c.1662G>T (p.Met554Ile) c.1317G>T (p.Met439Ile) c.1311G>T (p.Met437Ile) c.1395G>T (p.Met465Ile) c.1392G>T (p.Met464Ile) c.1389G>T (p.Met463Ile) c.435G>T (p.Met145Ile) n.2041G>T | ClinVar dbSNP |
| 10 | g.121498562C>G | CA16602620 | FGFR2 | c.1608G>C (p.Met536Ile) c.1599G>C (p.Met533Ile) c.429G>C (p.Met143Ile) n.947G>C c.1254G>C (p.Met418Ile) n.425G>C c.*307G>C (n.*307G>C) n.3946G>C n.2618G>C c.1605G>C (p.Met535Ile) c.1332G>C (p.Met444Ile) c.1338G>C (p.Met446Ile) c.1341G>C (p.Met447Ile) c.1263G>C (p.Met421Ile) c.1257G>C (p.Met419Ile) c.1269G>C (p.Met423Ile) c.381G>C (p.Met127Ile) c.921G>C (p.Met307Ile) c.*652G>C (n.*652G>C) c.1260G>C (p.Met420Ile) n.2055G>C c.1659G>C (p.Met553Ile) c.1656G>C (p.Met552Ile) c.1665G>C (p.Met555Ile) c.1398G>C (p.Met466Ile) c.1320G>C (p.Met440Ile) c.1662G>C (p.Met554Ile) c.1317G>C (p.Met439Ile) c.1311G>C (p.Met437Ile) c.1395G>C (p.Met465Ile) c.1392G>C (p.Met464Ile) c.1389G>C (p.Met463Ile) c.435G>C (p.Met145Ile) n.2041G>C | ClinVar dbSNP |
| 10 | g.121498562C>T | CA16602621 | FGFR2 | c.1608G>A (p.Met536Ile) c.1599G>A (p.Met533Ile) c.429G>A (p.Met143Ile) n.947G>A c.1254G>A (p.Met418Ile) n.425G>A c.*307G>A (n.*307G>A) n.3946G>A n.2618G>A c.1605G>A (p.Met535Ile) c.1332G>A (p.Met444Ile) c.1338G>A (p.Met446Ile) c.1341G>A (p.Met447Ile) c.1263G>A (p.Met421Ile) c.1257G>A (p.Met419Ile) c.1269G>A (p.Met423Ile) c.381G>A (p.Met127Ile) c.921G>A (p.Met307Ile) c.*652G>A (n.*652G>A) c.1260G>A (p.Met420Ile) n.2055G>A c.1659G>A (p.Met553Ile) c.1656G>A (p.Met552Ile) c.1665G>A (p.Met555Ile) c.1398G>A (p.Met466Ile) c.1320G>A (p.Met440Ile) c.1662G>A (p.Met554Ile) c.1317G>A (p.Met439Ile) c.1311G>A (p.Met437Ile) c.1395G>A (p.Met465Ile) c.1392G>A (p.Met464Ile) c.1389G>A (p.Met463Ile) c.435G>A (p.Met145Ile) n.2041G>A | ClinVar dbSNP gnomAD v4 |
| 10 | g.121498562C= | CA1941017718 | FGFR2 | c.1608G= (p.Met536=) c.1599G= (p.Met533=) c.429G= (p.Met143=) n.947G= c.1254G= (p.Met418=) n.425G= c.*307G= (n.*307G=) n.3946G= n.2618G= c.1605G= (p.Met535=) c.1332G= (p.Met444=) c.1338G= (p.Met446=) c.1341G= (p.Met447=) c.1263G= (p.Met421=) c.1257G= (p.Met419=) c.1269G= (p.Met423=) c.381G= (p.Met127=) c.921G= (p.Met307=) c.*652G= (n.*652G=) c.1260G= (p.Met420=) n.2055G= c.1659G= (p.Met553=) c.1656G= (p.Met552=) c.1665G= (p.Met555=) c.1398G= (p.Met466=) c.1320G= (p.Met440=) c.1662G= (p.Met554=) c.1317G= (p.Met439=) c.1311G= (p.Met437=) c.1395G= (p.Met465=) c.1392G= (p.Met464=) c.1389G= (p.Met463=) c.435G= (p.Met145=) n.2041G= | dbSNP |