| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.38417879T>C | CA16602865 | FGFR1 | c.1543A>G (p.Met515Val) c.1531A>G (p.Met511Val) n.2436A>G c.1723A>G (p.Met575Val) n.2231A>G c.1264A>G (p.Met422Val) c.*1189A>G (n.*1189A>G) c.*1510A>G (n.*1510A>G) n.3037A>G c.1270A>G (p.Met424Val) c.1513A>G (p.Met505Val) c.*593A>G (n.*593A>G) c.1276A>G (p.Met426Val) c.1537A>G (p.Met513Val) c.1636A>G (p.Met546Val) n.710A>G c.1420A>G (n.1420A>G) n.3822A>G n.1065A>G n.771A>G c.*438A>G (n.*438A>G) c.1519A>G (p.Met507Val) c.1642A>G (p.Met548Val) c.1375A>G (p.Met459Val) c.1369A>G (p.Met457Val) c.1252A>G (p.Met418Val) c.1630A>G (p.Met544Val) c.1363A>G (p.Met455Val) c.571A>G (p.Met191Val) n.1791A>G | ClinVar dbSNP |
| 8 | g.38417879T>A | CA370732927 | FGFR1 | c.1543A>T (p.Met515Leu) c.1531A>T (p.Met511Leu) n.2436A>T c.1723A>T (p.Met575Leu) n.2231A>T c.1264A>T (p.Met422Leu) c.*1189A>T (n.*1189A>T) c.*1510A>T (n.*1510A>T) n.3037A>T c.1270A>T (p.Met424Leu) c.1513A>T (p.Met505Leu) c.*593A>T (n.*593A>T) c.1276A>T (p.Met426Leu) c.1537A>T (p.Met513Leu) c.1636A>T (p.Met546Leu) n.710A>T c.1420A>T (n.1420A>T) n.3822A>T n.1065A>T n.771A>T c.*438A>T (n.*438A>T) c.1519A>T (p.Met507Leu) c.1642A>T (p.Met548Leu) c.1375A>T (p.Met459Leu) c.1369A>T (p.Met457Leu) c.1252A>T (p.Met418Leu) c.1630A>T (p.Met544Leu) c.1363A>T (p.Met455Leu) c.571A>T (p.Met191Leu) n.1791A>T | dbSNP |
| 8 | g.38417879T= | CA1777536509 | FGFR1 | c.1543A= (p.Met515=) c.1531A= (p.Met511=) n.2436A= c.1723A= (p.Met575=) n.2231A= c.1264A= (p.Met422=) c.*1189A= (n.*1189A=) c.*1510A= (n.*1510A=) n.3037A= c.1270A= (p.Met424=) c.1513A= (p.Met505=) c.*593A= (n.*593A=) c.1276A= (p.Met426=) c.1537A= (p.Met513=) c.1636A= (p.Met546=) n.710A= c.1420A= (n.1420A=) n.3822A= n.1065A= n.771A= c.*438A= (n.*438A=) c.1519A= (p.Met507=) c.1642A= (p.Met548=) c.1375A= (p.Met459=) c.1369A= (p.Met457=) c.1252A= (p.Met418=) c.1630A= (p.Met544=) c.1363A= (p.Met455=) c.571A= (p.Met191=) n.1791A= | dbSNP |