Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.39724747G>A | CA16602843 | ERBB2 | c.2329G>A (p.Val777Met) c.2239G>A (p.Val747Met) c.1501G>A (p.Val501Met) c.2284G>A (p.Val762Met) c.*2119G>A (n.*2119G>A) c.435G>A n.3463G>A n.2653G>A c.2467G>A (p.Val823Met) c.2422G>A (p.Val808Met) c.2377G>A (p.Val793Met) c.2446G>A (p.Val816Met) c.2431G>A (p.Val811Met) c.2410G>A (p.Val804Met) c.2404G>A (p.Val802Met) c.2359G>A (p.Val787Met) c.2350G>A (p.Val784Met) c.2326G>A (p.Val776Met) c.2320G>A (p.Val774Met) c.2293G>A (p.Val765Met) c.2287G>A (p.Val763Met) c.2281G>A (p.Val761Met) c.2230G>A (p.Val744Met) c.2149G>A (p.Val717Met) c.2308-302G>A (n.2308-302G>A) c.2071G>A (p.Val691Met) c.2208+1087G>A (n.2208+1087G>A) c.1291G>A (p.Val431Met) n.2567G>A | ClinVar dbSNP COSMIC |
17 | g.39724747G>C | CA16602503 | ERBB2 | c.2329G>C (p.Val777Leu) c.2239G>C (p.Val747Leu) c.1501G>C (p.Val501Leu) c.2284G>C (p.Val762Leu) c.*2119G>C (n.*2119G>C) c.435G>C n.3463G>C n.2653G>C c.2467G>C (p.Val823Leu) c.2422G>C (p.Val808Leu) c.2377G>C (p.Val793Leu) c.2446G>C (p.Val816Leu) c.2431G>C (p.Val811Leu) c.2410G>C (p.Val804Leu) c.2404G>C (p.Val802Leu) c.2359G>C (p.Val787Leu) c.2350G>C (p.Val784Leu) c.2326G>C (p.Val776Leu) c.2320G>C (p.Val774Leu) c.2293G>C (p.Val765Leu) c.2287G>C (p.Val763Leu) c.2281G>C (p.Val761Leu) c.2230G>C (p.Val744Leu) c.2149G>C (p.Val717Leu) c.2308-302G>C (n.2308-302G>C) c.2071G>C (p.Val691Leu) c.2208+1087G>C (n.2208+1087G>C) c.1291G>C (p.Val431Leu) n.2567G>C | ClinVar dbSNP COSMIC COSMIC |
17 | g.39724747G>T | CA135387 | ERBB2 | c.2329G>T (p.Val777Leu) c.2239G>T (p.Val747Leu) c.1501G>T (p.Val501Leu) c.2284G>T (p.Val762Leu) c.*2119G>T (n.*2119G>T) c.435G>T n.3463G>T n.2653G>T c.2467G>T (p.Val823Leu) c.2422G>T (p.Val808Leu) c.2377G>T (p.Val793Leu) c.2446G>T (p.Val816Leu) c.2431G>T (p.Val811Leu) c.2410G>T (p.Val804Leu) c.2404G>T (p.Val802Leu) c.2359G>T (p.Val787Leu) c.2350G>T (p.Val784Leu) c.2326G>T (p.Val776Leu) c.2320G>T (p.Val774Leu) c.2293G>T (p.Val765Leu) c.2287G>T (p.Val763Leu) c.2281G>T (p.Val761Leu) c.2230G>T (p.Val744Leu) c.2149G>T (p.Val717Leu) c.2308-302G>T (n.2308-302G>T) c.2071G>T (p.Val691Leu) c.2208+1087G>T (n.2208+1087G>T) c.1291G>T (p.Val431Leu) n.2567G>T | ClinVar dbSNP COSMIC COSMIC |