Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.99764003A>G | CA4369608 | CYP3A4 | c.878T>C (p.Leu293Pro) n.313T>C c.419T>C (p.Leu140Pro) c.731T>C (p.Leu244Pro) c.428T>C (p.Leu143Pro) c.875T>C (p.Leu292Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.99764003A>C | CA368369941 | CYP3A4 | c.878T>G (p.Leu293Arg) n.313T>G c.419T>G (p.Leu140Arg) c.731T>G (p.Leu244Arg) c.428T>G (p.Leu143Arg) c.875T>G (p.Leu292Arg) | dbSNP |
7 | g.99764003A= | CA1729178094 | CYP3A4 | c.878T= (p.Leu293=) n.313T= c.419T= (p.Leu140=) c.731T= (p.Leu244=) c.428T= (p.Leu143=) c.875T= (p.Leu292=) | dbSNP |
7 | g.99764003A>T | CA368369942 | CYP3A4 | c.878T>A (p.Leu293Gln) n.313T>A c.419T>A (p.Leu140Gln) c.731T>A (p.Leu244Gln) c.428T>A (p.Leu143Gln) c.875T>A (p.Leu292Gln) | dbSNP |