Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.30674127C>A | CA323900 | TGFBR2 | c.1277C>A (p.Ala426Asp) n.2873C>A n.155C>A c.1352C>A (p.Ala451Asp) c.1304C>A (p.Ala435Asp) c.1229C>A (p.Ala410Asp) c.1172C>A (p.Ala391Asp) | ClinVar dbSNP |
3 | g.30674127C>G | CA351808914 | TGFBR2 | c.1277C>G (p.Ala426Gly) n.2873C>G n.155C>G c.1352C>G (p.Ala451Gly) c.1304C>G (p.Ala435Gly) c.1229C>G (p.Ala410Gly) c.1172C>G (p.Ala391Gly) | dbSNP |
3 | g.30674127C>T | CA020644 | TGFBR2 | c.1277C>T (p.Ala426Val) n.2873C>T n.155C>T c.1352C>T (p.Ala451Val) c.1304C>T (p.Ala435Val) c.1229C>T (p.Ala410Val) c.1172C>T (p.Ala391Val) | ClinVar dbSNP COSMIC COSMIC |