| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.112835165G>T | CA16025598 | APC | c.1623G>T (n.1623G>T) c.2012G>T (p.Arg671Met) c.*1964G>T (n.*1964G>T) c.1904G>T (p.Arg635Met) c.1958G>T (p.Arg653Met) c.311G>T c.647G>T (p.Arg216Met) c.*1280G>T (n.*1280G>T) c.230+6193G>T c.1988G>T (p.Arg663Met) c.1883G>T (p.Arg628Met) c.1874G>T (p.Arg625Met) c.1835G>T (p.Arg612Met) c.1781G>T (p.Arg594Met) c.1685G>T (p.Arg562Met) c.1655G>T (p.Arg552Met) c.1580G>T (p.Arg527Met) c.1478G>T (p.Arg493Met) c.1109G>T (p.Arg370Met) | ClinVar dbSNP COSMIC |
| 5 | g.112835165G>C | CA16025597 | APC | c.1623G>C (n.1623G>C) c.2012G>C (p.Arg671Thr) c.*1964G>C (n.*1964G>C) c.1904G>C (p.Arg635Thr) c.1958G>C (p.Arg653Thr) c.311G>C c.647G>C (p.Arg216Thr) c.*1280G>C (n.*1280G>C) c.230+6193G>C c.1988G>C (p.Arg663Thr) c.1883G>C (p.Arg628Thr) c.1874G>C (p.Arg625Thr) c.1835G>C (p.Arg612Thr) c.1781G>C (p.Arg594Thr) c.1685G>C (p.Arg562Thr) c.1655G>C (p.Arg552Thr) c.1580G>C (p.Arg527Thr) c.1478G>C (p.Arg493Thr) c.1109G>C (p.Arg370Thr) | ClinVar dbSNP |
| 5 | g.112835165G>A | CA16025596 | APC | c.1623G>A (n.1623G>A) c.2012G>A (p.Arg671Lys) c.*1964G>A (n.*1964G>A) c.1904G>A (p.Arg635Lys) c.1958G>A (p.Arg653Lys) c.311G>A c.647G>A (p.Arg216Lys) c.*1280G>A (n.*1280G>A) c.230+6193G>A c.1988G>A (p.Arg663Lys) c.1883G>A (p.Arg628Lys) c.1874G>A (p.Arg625Lys) c.1835G>A (p.Arg612Lys) c.1781G>A (p.Arg594Lys) c.1685G>A (p.Arg562Lys) c.1655G>A (p.Arg552Lys) c.1580G>A (p.Arg527Lys) c.1478G>A (p.Arg493Lys) c.1109G>A (p.Arg370Lys) | ClinVar dbSNP COSMIC |