Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.112838793C>T | CA008153 | APC | c.2864C>T (n.2864C>T) c.3253C>T (p.Gln1085Ter) c.*3205C>T (n.*3205C>T) c.3145C>T (p.Gln1049Ter) c.3199C>T (p.Gln1067Ter) c.1552C>T c.*2521C>T (n.*2521C>T) c.230+9821C>T c.3229C>T (p.Gln1077Ter) c.3124C>T (p.Gln1042Ter) c.3115C>T (p.Gln1039Ter) c.3076C>T (p.Gln1026Ter) c.3022C>T (p.Gln1008Ter) c.2926C>T (p.Gln976Ter) c.2896C>T (p.Gln966Ter) c.2821C>T (p.Gln941Ter) c.2719C>T (p.Gln907Ter) c.2350C>T (p.Gln784Ter) | ClinVar dbSNP COSMIC |
5 | g.112838793C>A | CA16028350 | APC | c.2864C>A (n.2864C>A) c.3253C>A (p.Gln1085Lys) c.*3205C>A (n.*3205C>A) c.3145C>A (p.Gln1049Lys) c.3199C>A (p.Gln1067Lys) c.1552C>A c.*2521C>A (n.*2521C>A) c.230+9821C>A c.3229C>A (p.Gln1077Lys) c.3124C>A (p.Gln1042Lys) c.3115C>A (p.Gln1039Lys) c.3076C>A (p.Gln1026Lys) c.3022C>A (p.Gln1008Lys) c.2926C>A (p.Gln976Lys) c.2896C>A (p.Gln966Lys) c.2821C>A (p.Gln941Lys) c.2719C>A (p.Gln907Lys) c.2350C>A (p.Gln784Lys) | dbSNP |