Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.99764003A>GCA4369608CYP3A4c.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
7g.99764003A>CCA368369941CYP3A4c.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
7g.99764003A=CA1729178094CYP3A4c.878T= (p.Leu293=)
n.313T=
c.419T= (p.Leu140=)
c.731T= (p.Leu244=)
c.428T= (p.Leu143=)
c.875T= (p.Leu292=)
dbSNP
7g.99764003A>TCA368369942CYP3A4c.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

Number of alleles fetched