Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.19353085G>A | CA203852 | PDHA1 | c.443G>A (p.Arg148Gln) c.422G>A (p.Arg141Gln) c.506G>A (p.Arg169Gln) c.536G>A (p.Arg179Gln) c.418+1678G>A (n.418+1678G>A) c.419-1406G>A (n.419-1406G>A) n.257G>A c.557G>A (p.Arg186Gln) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
X | g.19353085G= | CA2418222781 | PDHA1 | c.443G= (p.Arg148=) c.422G= (p.Arg141=) c.506G= (p.Arg169=) c.536G= (p.Arg179=) c.418+1678G= (n.418+1678G=) c.419-1406G= (n.419-1406G=) n.257G= c.557G= (p.Arg186=) | dbSNP |