Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.40062808G>A | CA278976 | BCOR | c.4111C>T (p.Gln1371Ter) c.4009C>T (p.Gln1337Ter) c.4057C>T (p.Gln1353Ter) c.3955C>T (p.Gln1319Ter) c.640C>T (p.Gln214Ter) c.721C>T (p.Gln241Ter) c.195C>T c.130C>T (p.Gln44Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC |
X | g.40062808G= | CA2425440753 | BCOR | c.4111C= (p.Gln1371=) c.4009C= (p.Gln1337=) c.4057C= (p.Gln1353=) c.3955C= (p.Gln1319=) c.640C= (p.Gln214=) c.721C= (p.Gln241=) c.195C= c.130C= (p.Gln44=) | dbSNP |