Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.45850995C>G | CA384480560 | ARID2 | c.2872C>G (p.Gln958Glu) c.2793C>G c.2425C>G (p.Gln809Glu) c.1702C>G (p.Gln568Glu) n.2163C>G c.1240C>G (p.Gln414Glu) n.3020C>G n.3003C>G | dbSNP |
12 | g.45850995C>A | CA384480557 | ARID2 | c.2872C>A (p.Gln958Lys) c.2793C>A c.2425C>A (p.Gln809Lys) c.1702C>A (p.Gln568Lys) n.2163C>A c.1240C>A (p.Gln414Lys) n.3020C>A n.3003C>A | dbSNP |
12 | g.45850995C>T | CA16607287 | ARID2 | c.2872C>T (p.Gln958Ter) c.2793C>T c.2425C>T (p.Gln809Ter) c.1702C>T (p.Gln568Ter) n.2163C>T c.1240C>T (p.Gln414Ter) n.3020C>T n.3003C>T | ClinVar dbSNP COSMIC |