Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.112839777A>T | CA008937 | APC | c.3848A>T (n.3848A>T) c.4237A>T (p.Ser1413Cys) c.*4189A>T (n.*4189A>T) c.4129A>T (p.Ser1377Cys) c.4183A>T (p.Ser1395Cys) c.2536A>T c.*3505A>T (n.*3505A>T) c.230+10805A>T c.4213A>T (p.Ser1405Cys) c.4108A>T (p.Ser1370Cys) c.4099A>T (p.Ser1367Cys) c.4060A>T (p.Ser1354Cys) c.4006A>T (p.Ser1336Cys) c.3910A>T (p.Ser1304Cys) c.3880A>T (p.Ser1294Cys) c.3805A>T (p.Ser1269Cys) c.3703A>T (p.Ser1235Cys) c.3334A>T (p.Ser1112Cys) | ClinVar dbSNP COSMIC |
5 | g.112839777A>G | CA16030496 | APC | c.3848A>G (n.3848A>G) c.4237A>G (p.Ser1413Gly) c.*4189A>G (n.*4189A>G) c.4129A>G (p.Ser1377Gly) c.4183A>G (p.Ser1395Gly) c.2536A>G c.*3505A>G (n.*3505A>G) c.230+10805A>G c.4213A>G (p.Ser1405Gly) c.4108A>G (p.Ser1370Gly) c.4099A>G (p.Ser1367Gly) c.4060A>G (p.Ser1354Gly) c.4006A>G (p.Ser1336Gly) c.3910A>G (p.Ser1304Gly) c.3880A>G (p.Ser1294Gly) c.3805A>G (p.Ser1269Gly) c.3703A>G (p.Ser1235Gly) c.3334A>G (p.Ser1112Gly) | ClinVar dbSNP |
5 | g.112839777A= | CA1573466750 | APC | c.3848A= (n.3848A=) c.4237A= (p.Ser1413=) c.*4189A= (n.*4189A=) c.4129A= (p.Ser1377=) c.4183A= (p.Ser1395=) c.2536A= c.*3505A= (n.*3505A=) c.230+10805A= c.4213A= (p.Ser1405=) c.4108A= (p.Ser1370=) c.4099A= (p.Ser1367=) c.4060A= (p.Ser1354=) c.4006A= (p.Ser1336=) c.3910A= (p.Ser1304=) c.3880A= (p.Ser1294=) c.3805A= (p.Ser1269=) c.3703A= (p.Ser1235=) c.3334A= (p.Ser1112=) | dbSNP |