| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.39723967T>G | CA16602786 | ERBB2 | c.2264T>G (p.Leu755Trp) c.2174T>G (p.Leu725Trp) c.1436T>G (p.Leu479Trp) c.2219T>G (p.Leu740Trp) c.*2054T>G (n.*2054T>G) n.873T>G c.370T>G n.3398T>G n.2588T>G c.2402T>G (p.Leu801Trp) c.2357T>G (p.Leu786Trp) c.2312T>G (p.Leu771Trp) c.2381T>G (p.Leu794Trp) c.2366T>G (p.Leu789Trp) c.2345T>G (p.Leu782Trp) c.2339T>G (p.Leu780Trp) c.2294T>G (p.Leu765Trp) c.2285T>G (p.Leu762Trp) c.2261T>G (p.Leu754Trp) c.2255T>G (p.Leu752Trp) c.2228T>G (p.Leu743Trp) c.2222T>G (p.Leu741Trp) c.2216T>G (p.Leu739Trp) c.2208+307T>G (n.2208+307T>G) c.2084T>G (p.Leu695Trp) c.2006T>G (p.Leu669Trp) c.1226T>G (p.Leu409Trp) n.2502T>G | ClinVar dbSNP COSMIC COSMIC |
| 17 | g.39723967T>C | CA16602502 | ERBB2 | c.2264T>C (p.Leu755Ser) c.2174T>C (p.Leu725Ser) c.1436T>C (p.Leu479Ser) c.2219T>C (p.Leu740Ser) c.*2054T>C (n.*2054T>C) n.873T>C c.370T>C n.3398T>C n.2588T>C c.2402T>C (p.Leu801Ser) c.2357T>C (p.Leu786Ser) c.2312T>C (p.Leu771Ser) c.2381T>C (p.Leu794Ser) c.2366T>C (p.Leu789Ser) c.2345T>C (p.Leu782Ser) c.2339T>C (p.Leu780Ser) c.2294T>C (p.Leu765Ser) c.2285T>C (p.Leu762Ser) c.2261T>C (p.Leu754Ser) c.2255T>C (p.Leu752Ser) c.2228T>C (p.Leu743Ser) c.2222T>C (p.Leu741Ser) c.2216T>C (p.Leu739Ser) c.2208+307T>C (n.2208+307T>C) c.2084T>C (p.Leu695Ser) c.2006T>C (p.Leu669Ser) c.1226T>C (p.Leu409Ser) n.2502T>C | ClinVar dbSNP COSMIC COSMIC |
| 17 | g.39723967T>A | CA399302590 | ERBB2 | c.2264T>A (p.Leu755Ter) c.2174T>A (p.Leu725Ter) c.1436T>A (p.Leu479Ter) c.2219T>A (p.Leu740Ter) c.*2054T>A (n.*2054T>A) n.873T>A c.370T>A n.3398T>A n.2588T>A c.2402T>A (p.Leu801Ter) c.2357T>A (p.Leu786Ter) c.2312T>A (p.Leu771Ter) c.2381T>A (p.Leu794Ter) c.2366T>A (p.Leu789Ter) c.2345T>A (p.Leu782Ter) c.2339T>A (p.Leu780Ter) c.2294T>A (p.Leu765Ter) c.2285T>A (p.Leu762Ter) c.2261T>A (p.Leu754Ter) c.2255T>A (p.Leu752Ter) c.2228T>A (p.Leu743Ter) c.2222T>A (p.Leu741Ter) c.2216T>A (p.Leu739Ter) c.2208+307T>A (n.2208+307T>A) c.2084T>A (p.Leu695Ter) c.2006T>A (p.Leu669Ter) c.1226T>A (p.Leu409Ter) n.2502T>A | dbSNP |