Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.19353085G>ACA203852PDHA1c.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
Xg.19353085G=CA2418222781PDHA1c.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

Number of alleles fetched