| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.55228999C>A | CA402528922 | TCF4 | c.1727G>T (p.Arg576Leu) c.1607G>T (p.Arg536Leu) n.1407G>T c.1655G>T (p.Arg552Leu) c.*1435G>T (n.*1435G>T) c.1337G>T (p.Arg446Leu) c.*1605G>T (n.*1605G>T) c.1079G>T (p.Arg360Leu) n.1782G>T n.1421G>T c.1325G>T c.1754G>T (p.Arg585Leu) c.*1338G>T (n.*1338G>T) c.1715G>T (p.Arg572Leu) c.2033G>T (p.Arg678Leu) c.1247G>T (p.Arg416Leu) c.1325G>T (p.Arg442Leu) c.1643G>T (p.Arg548Leu) c.1589G>T (p.Arg530Leu) c.1514G>T (p.Arg505Leu) c.1235G>T (p.Arg412Leu) n.5250G>T c.1502G>T (p.Arg501Leu) c.1745G>T (p.Arg582Leu) c.1463G>T (p.Arg488Leu) c.1547G>T (p.Arg516Leu) c.1706G>T (p.Arg569Leu) c.1535G>T (p.Arg512Leu) c.1640G>T (p.Arg547Leu) n.750G>T c.1067G>T (p.Arg356Leu) c.1724G>T (p.Arg575Leu) c.1652G>T (p.Arg551Leu) c.1601G>T (p.Arg534Leu) c.1517G>T (p.Arg506Leu) c.1244G>T (p.Arg415Leu) c.2030G>T (p.Arg677Leu) c.2021G>T (p.Arg674Leu) c.2018G>T (p.Arg673Leu) c.1721G>T (p.Arg574Leu) c.1232G>T (p.Arg411Leu) c.1712G>T (p.Arg571Leu) c.1637G>T (p.Arg546Leu) c.1598G>T (p.Arg533Leu) c.1511G>T (p.Arg504Leu) c.1505G>T (p.Arg502Leu) c.1334G>T (p.Arg445Leu) c.1490G>T (p.Arg497Leu) c.1658G>T (p.Arg553Leu) | ClinVar dbSNP |
| 18 | g.55228999C>T | CA16607615 | TCF4 | c.1727G>A (p.Arg576Gln) c.1607G>A (p.Arg536Gln) n.1407G>A c.1655G>A (p.Arg552Gln) c.*1435G>A (n.*1435G>A) c.1337G>A (p.Arg446Gln) c.*1605G>A (n.*1605G>A) c.1079G>A (p.Arg360Gln) n.1782G>A n.1421G>A c.1325G>A c.1754G>A (p.Arg585Gln) c.*1338G>A (n.*1338G>A) c.1715G>A (p.Arg572Gln) c.2033G>A (p.Arg678Gln) c.1247G>A (p.Arg416Gln) c.1325G>A (p.Arg442Gln) c.1643G>A (p.Arg548Gln) c.1589G>A (p.Arg530Gln) c.1514G>A (p.Arg505Gln) c.1235G>A (p.Arg412Gln) n.5250G>A c.1502G>A (p.Arg501Gln) c.1745G>A (p.Arg582Gln) c.1463G>A (p.Arg488Gln) c.1547G>A (p.Arg516Gln) c.1706G>A (p.Arg569Gln) c.1535G>A (p.Arg512Gln) c.1640G>A (p.Arg547Gln) n.750G>A c.1067G>A (p.Arg356Gln) c.1724G>A (p.Arg575Gln) c.1652G>A (p.Arg551Gln) c.1601G>A (p.Arg534Gln) c.1517G>A (p.Arg506Gln) c.1244G>A (p.Arg415Gln) c.2030G>A (p.Arg677Gln) c.2021G>A (p.Arg674Gln) c.2018G>A (p.Arg673Gln) c.1721G>A (p.Arg574Gln) c.1232G>A (p.Arg411Gln) c.1712G>A (p.Arg571Gln) c.1637G>A (p.Arg546Gln) c.1598G>A (p.Arg533Gln) c.1511G>A (p.Arg504Gln) c.1505G>A (p.Arg502Gln) c.1334G>A (p.Arg445Gln) c.1490G>A (p.Arg497Gln) c.1658G>A (p.Arg553Gln) | ClinVar dbSNP |