Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.112839693C>G | CA16030308 | APC | c.3764C>G (n.3764C>G) c.4153C>G (p.Gln1385Glu) c.*4105C>G (n.*4105C>G) c.4045C>G (p.Gln1349Glu) c.4099C>G (p.Gln1367Glu) c.2452C>G c.*3421C>G (n.*3421C>G) c.230+10721C>G c.4129C>G (p.Gln1377Glu) c.4024C>G (p.Gln1342Glu) c.4015C>G (p.Gln1339Glu) c.3976C>G (p.Gln1326Glu) c.3922C>G (p.Gln1308Glu) c.3826C>G (p.Gln1276Glu) c.3796C>G (p.Gln1266Glu) c.3721C>G (p.Gln1241Glu) c.3619C>G (p.Gln1207Glu) c.3250C>G (p.Gln1084Glu) | dbSNP COSMIC |
5 | g.112839693C>T | CA16030309 | APC | c.3764C>T (n.3764C>T) c.4153C>T (p.Gln1385Ter) c.*4105C>T (n.*4105C>T) c.4045C>T (p.Gln1349Ter) c.4099C>T (p.Gln1367Ter) c.2452C>T c.*3421C>T (n.*3421C>T) c.230+10721C>T c.4129C>T (p.Gln1377Ter) c.4024C>T (p.Gln1342Ter) c.4015C>T (p.Gln1339Ter) c.3976C>T (p.Gln1326Ter) c.3922C>T (p.Gln1308Ter) c.3826C>T (p.Gln1276Ter) c.3796C>T (p.Gln1266Ter) c.3721C>T (p.Gln1241Ter) c.3619C>T (p.Gln1207Ter) c.3250C>T (p.Gln1084Ter) | ClinVar dbSNP COSMIC |