Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.1220627G>C | CA402949588 | STK11 | c.644G>C (p.Gly215Ala) c.272G>C (p.Gly91Ala) c.470G>C (p.Gly157Ala) n.542G>C n.734G>C n.615G>C c.422G>C (p.Gly141Ala) n.1269G>C | dbSNP COSMIC COSMIC |
19 | g.1220627G>A | CA16603147 | STK11 | c.644G>A (p.Gly215Asp) c.272G>A (p.Gly91Asp) c.470G>A (p.Gly157Asp) n.542G>A n.734G>A n.615G>A c.422G>A (p.Gly141Asp) n.1269G>A | ClinVar dbSNP gnomAD v4 COSMIC |