| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.39723405G>A | CA16602787 | ERBB2 | c.2033G>A (p.Arg678Gln) c.1943G>A (p.Arg648Gln) c.1205G>A (p.Arg402Gln) c.1988G>A (p.Arg663Gln) c.*1823G>A (n.*1823G>A) n.642G>A c.139G>A c.351G>A n.3167G>A n.2357G>A c.2171G>A (p.Arg724Gln) c.2126G>A (p.Arg709Gln) c.2081G>A (p.Arg694Gln) c.2150G>A (p.Arg717Gln) c.2135G>A (p.Arg712Gln) c.2108G>A (p.Arg703Gln) c.2063G>A (p.Arg688Gln) c.2054G>A (p.Arg685Gln) c.2030G>A (p.Arg677Gln) c.2024G>A (p.Arg675Gln) c.1985G>A (p.Arg662Gln) c.1853G>A (p.Arg618Gln) c.1775G>A (p.Arg592Gln) c.1223-559G>A (n.1223-559G>A) n.2271G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 17 | g.39723405G= | CA2259227317 | ERBB2 | c.2033G= (p.Arg678=) c.1943G= (p.Arg648=) c.1205G= (p.Arg402=) c.1988G= (p.Arg663=) c.*1823G= (n.*1823G=) n.642G= c.139G= c.351G= n.3167G= n.2357G= c.2171G= (p.Arg724=) c.2126G= (p.Arg709=) c.2081G= (p.Arg694=) c.2150G= (p.Arg717=) c.2135G= (p.Arg712=) c.2108G= (p.Arg703=) c.2063G= (p.Arg688=) c.2054G= (p.Arg685=) c.2030G= (p.Arg677=) c.2024G= (p.Arg675=) c.1985G= (p.Arg662=) c.1853G= (p.Arg618=) c.1775G= (p.Arg592=) c.1223-559G= (n.1223-559G=) n.2271G= | dbSNP |