Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.90088605C>GCA16602460IDH2c.516G>C (p.Arg172Ser)
c.360G>C (p.Arg120Ser)
c.208-103G>C (n.208-103G>C)
c.*141G>C (n.*141G>C)
c.126G>C (p.Arg42Ser)
ClinVar dbSNP gnomAD v4 COSMIC
15g.90088605C>ACA393802238IDH2c.516G>T (p.Arg172Ser)
c.360G>T (p.Arg120Ser)
c.208-103G>T (n.208-103G>T)
c.*141G>T (n.*141G>T)
c.126G>T (p.Arg42Ser)
ClinVar dbSNP COSMIC
15g.90088605C>TCA492298026IDH2c.516G>A (p.Arg172=)
c.360G>A (p.Arg120=)
c.208-103G>A (n.208-103G>A)
c.*141G>A (n.*141G>A)
c.126G>A (p.Arg42=)
dbSNP gnomAD v4 COSMIC

Number of alleles fetched