Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.99762077T>A | CA368368874 | CYP3A4 | c.1217A>T (p.Lys406Met) n.652A>T c.758A>T (p.Lys253Met) c.1070A>T (p.Lys357Met) c.767A>T (p.Lys256Met) c.1214A>T (p.Lys405Met) | COSMIC |
7 | g.99762077T>C | CA368368875 | CYP3A4 | c.1217A>G (p.Lys406Arg) n.652A>G c.758A>G (p.Lys253Arg) c.1070A>G (p.Lys357Arg) c.767A>G (p.Lys256Arg) c.1214A>G (p.Lys405Arg) | |
7 | g.99762077T>G | CA368368876 | CYP3A4 | c.1217A>C (p.Lys406Thr) n.652A>C c.758A>C (p.Lys253Thr) c.1070A>C (p.Lys357Thr) c.767A>C (p.Lys256Thr) c.1214A>C (p.Lys405Thr) | |
7 | g.99762078T>A | CA368368879 | CYP3A4 | c.1216A>T (p.Lys406Ter) n.651A>T c.757A>T (p.Lys253Ter) c.1069A>T (p.Lys357Ter) c.766A>T (p.Lys256Ter) c.1213A>T (p.Lys405Ter) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.99762078T>C | CA368368878 | CYP3A4 | c.1216A>G (p.Lys406Glu) n.651A>G c.757A>G (p.Lys253Glu) c.1069A>G (p.Lys357Glu) c.766A>G (p.Lys256Glu) c.1213A>G (p.Lys405Glu) | gnomAD v4 |
7 | g.99762078T>G | CA368368877 | CYP3A4 | c.1216A>C (p.Lys406Gln) n.651A>C c.757A>C (p.Lys253Gln) c.1069A>C (p.Lys357Gln) c.766A>C (p.Lys256Gln) c.1213A>C (p.Lys405Gln) | |
7 | g.99762078T= | CA1729177297 | CYP3A4 | c.1216A= (p.Lys406=) n.651A= c.757A= (p.Lys253=) c.1069A= (p.Lys357=) c.766A= (p.Lys256=) c.1213A= (p.Lys405=) | |
7 | g.99762079T>A | CA456687145 | CYP3A4 | c.1215A>T (p.Pro405=) n.650A>T c.756A>T (p.Pro252=) c.1068A>T (p.Pro356=) c.765A>T (p.Pro255=) c.1212A>T (p.Pro404=) | |
7 | g.99762079T>C | CA456687146 | CYP3A4 | c.1215A>G (p.Pro405=) n.650A>G c.756A>G (p.Pro252=) c.1068A>G (p.Pro356=) c.765A>G (p.Pro255=) c.1212A>G (p.Pro404=) | |
7 | g.99762079T>G | CA456687147 | CYP3A4 | c.1215A>C (p.Pro405=) n.650A>C c.756A>C (p.Pro252=) c.1068A>C (p.Pro356=) c.765A>C (p.Pro255=) c.1212A>C (p.Pro404=) | |
7 | g.99762080G>A | CA368368881 | CYP3A4 | c.1214C>T (p.Pro405Leu) n.649C>T c.755C>T (p.Pro252Leu) c.1067C>T (p.Pro356Leu) c.764C>T (p.Pro255Leu) c.1211C>T (p.Pro404Leu) | |
7 | g.99762080G>C | CA368368880 | CYP3A4 | c.1214C>G (p.Pro405Arg) n.649C>G c.755C>G (p.Pro252Arg) c.1067C>G (p.Pro356Arg) c.764C>G (p.Pro255Arg) c.1211C>G (p.Pro404Arg) | |
7 | g.99762080G>T | CA368368882 | CYP3A4 | c.1214C>A (p.Pro405Gln) n.649C>A c.755C>A (p.Pro252Gln) c.1067C>A (p.Pro356Gln) c.764C>A (p.Pro255Gln) c.1211C>A (p.Pro404Gln) | |
7 | g.99762081G>A | CA368368883 | CYP3A4 | c.1213C>T (p.Pro405Ser) n.648C>T c.754C>T (p.Pro252Ser) c.1066C>T (p.Pro356Ser) c.763C>T (p.Pro255Ser) c.1210C>T (p.Pro404Ser) | |
7 | g.99762081G>C | CA368368885 | CYP3A4 | c.1213C>G (p.Pro405Ala) n.648C>G c.754C>G (p.Pro252Ala) c.1066C>G (p.Pro356Ala) c.763C>G (p.Pro255Ala) c.1210C>G (p.Pro404Ala) | |
7 | g.99762081G= | CA1729177298 | CYP3A4 | c.1213C= (p.Pro405=) n.648C= c.754C= (p.Pro252=) c.1066C= (p.Pro356=) c.763C= (p.Pro255=) c.1210C= (p.Pro404=) | |
7 | g.99762081G>T | CA368368884 | CYP3A4 | c.1213C>A (p.Pro405Thr) n.648C>A c.754C>A (p.Pro252Thr) c.1066C>A (p.Pro356Thr) c.763C>A (p.Pro255Thr) c.1210C>A (p.Pro404Thr) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.99762082G>A | CA456687148 | CYP3A4 | c.1212C>T (p.Asp404=) n.647C>T c.753C>T (p.Asp251=) c.1065C>T (p.Asp355=) c.762C>T (p.Asp254=) c.1209C>T (p.Asp403=) | |
7 | g.99762082G>C | CA368368886 | CYP3A4 | c.1212C>G (p.Asp404Glu) n.647C>G c.753C>G (p.Asp251Glu) c.1065C>G (p.Asp355Glu) c.762C>G (p.Asp254Glu) c.1209C>G (p.Asp403Glu) | |
7 | g.99762082G>T | CA368368887 | CYP3A4 | c.1212C>A (p.Asp404Glu) n.647C>A c.753C>A (p.Asp251Glu) c.1065C>A (p.Asp355Glu) c.762C>A (p.Asp254Glu) c.1209C>A (p.Asp403Glu) | |
7 | g.99762083T>A | CA368368888 | CYP3A4 | c.1211A>T (p.Asp404Val) n.646A>T c.752A>T (p.Asp251Val) c.1064A>T (p.Asp355Val) c.761A>T (p.Asp254Val) c.1208A>T (p.Asp403Val) | |
7 | g.99762083T>C | CA368368889 | CYP3A4 | c.1211A>G (p.Asp404Gly) n.646A>G c.752A>G (p.Asp251Gly) c.1064A>G (p.Asp355Gly) c.761A>G (p.Asp254Gly) c.1208A>G (p.Asp403Gly) | |
7 | g.99762083T>G | CA368368890 | CYP3A4 | c.1211A>C (p.Asp404Ala) n.646A>C c.752A>C (p.Asp251Ala) c.1064A>C (p.Asp355Ala) c.761A>C (p.Asp254Ala) c.1208A>C (p.Asp403Ala) | |
7 | g.99762084C>A | CA368368891 | CYP3A4 | c.1210G>T (p.Asp404Tyr) n.645G>T c.751G>T (p.Asp251Tyr) c.1063G>T (p.Asp355Tyr) c.760G>T (p.Asp254Tyr) c.1207G>T (p.Asp403Tyr) | |
7 | g.99762084C>G | CA368368892 | CYP3A4 | c.1210G>C (p.Asp404His) n.645G>C c.751G>C (p.Asp251His) c.1063G>C (p.Asp355His) c.760G>C (p.Asp254His) c.1207G>C (p.Asp403His) | |
7 | g.99762084C>T | CA368368893 | CYP3A4 | c.1210G>A (p.Asp404Asn) n.645G>A c.751G>A (p.Asp251Asn) c.1063G>A (p.Asp355Asn) c.760G>A (p.Asp254Asn) c.1207G>A (p.Asp403Asn) | |
7 | g.99762085A>C | CA456687149 | CYP3A4 | c.1209T>G (p.Arg403=) n.644T>G c.750T>G (p.Arg250=) c.1062T>G (p.Arg354=) c.759T>G (p.Arg253=) c.1206T>G (p.Arg402=) | |
7 | g.99762085A>G | CA456687150 | CYP3A4 | c.1209T>C (p.Arg403=) n.644T>C c.750T>C (p.Arg250=) c.1062T>C (p.Arg354=) c.759T>C (p.Arg253=) c.1206T>C (p.Arg402=) | |
7 | g.99762085A>T | CA456687151 | CYP3A4 | c.1209T>A (p.Arg403=) n.644T>A c.750T>A (p.Arg250=) c.1062T>A (p.Arg354=) c.759T>A (p.Arg253=) c.1206T>A (p.Arg402=) | |
7 | g.99762086C>A | CA368368894 | CYP3A4 | c.1208G>T (p.Arg403Leu) n.643G>T c.749G>T (p.Arg250Leu) c.1061G>T (p.Arg354Leu) c.758G>T (p.Arg253Leu) c.1205G>T (p.Arg402Leu) | |
7 | g.99762086C= | CA1729177299 | CYP3A4 | c.1208G= (p.Arg403=) n.643G= c.749G= (p.Arg250=) c.1061G= (p.Arg354=) c.758G= (p.Arg253=) c.1205G= (p.Arg402=) | |
7 | g.99762086C>G | CA4369539 | CYP3A4 | c.1208G>C (p.Arg403Pro) n.643G>C c.749G>C (p.Arg250Pro) c.1061G>C (p.Arg354Pro) c.758G>C (p.Arg253Pro) c.1205G>C (p.Arg402Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.99762086C>T | CA163151529 | CYP3A4 | c.1208G>A (p.Arg403His) n.643G>A c.749G>A (p.Arg250His) c.1061G>A (p.Arg354His) c.758G>A (p.Arg253His) c.1205G>A (p.Arg402His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.99762087G>A | CA4369540 | CYP3A4 | c.1207C>T (p.Arg403Cys) n.642C>T c.748C>T (p.Arg250Cys) c.1060C>T (p.Arg354Cys) c.757C>T (p.Arg253Cys) c.1204C>T (p.Arg402Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.99762087G>C | CA368368896 | CYP3A4 | c.1207C>G (p.Arg403Gly) n.642C>G c.748C>G (p.Arg250Gly) c.1060C>G (p.Arg354Gly) c.757C>G (p.Arg253Gly) c.1204C>G (p.Arg402Gly) | |
7 | g.99762087G= | CA1729177300 | CYP3A4 | c.1207C= (p.Arg403=) n.642C= c.748C= (p.Arg250=) c.1060C= (p.Arg354=) c.757C= (p.Arg253=) c.1204C= (p.Arg402=) | |
7 | g.99762087G>T | CA368368895 | CYP3A4 | c.1207C>A (p.Arg403Ser) n.642C>A c.748C>A (p.Arg250Ser) c.1060C>A (p.Arg354Ser) c.757C>A (p.Arg253Ser) c.1204C>A (p.Arg402Ser) | |
7 | g.99762088G>A | CA163151530 | CYP3A4 | c.1206C>T (p.His402=) n.641C>T c.747C>T (p.His249=) c.1059C>T (p.His353=) c.756C>T (p.His252=) c.1203C>T (p.His401=) | dbSNP gnomAD v4 |
7 | g.99762088G>C | CA368368897 | CYP3A4 | c.1206C>G (p.His402Gln) n.641C>G c.747C>G (p.His249Gln) c.1059C>G (p.His353Gln) c.756C>G (p.His252Gln) c.1203C>G (p.His401Gln) | |
7 | g.99762088G= | CA1729177301 | CYP3A4 | c.1206C= (p.His402=) n.641C= c.747C= (p.His249=) c.1059C= (p.His353=) c.756C= (p.His252=) c.1203C= (p.His401=) | |
7 | g.99762088G>T | CA368368898 | CYP3A4 | c.1206C>A (p.His402Gln) n.641C>A c.747C>A (p.His249Gln) c.1059C>A (p.His353Gln) c.756C>A (p.His252Gln) c.1203C>A (p.His401Gln) | |
7 | g.99762089T>A | CA368368899 | CYP3A4 | c.1205A>T (p.His402Leu) n.640A>T c.746A>T (p.His249Leu) c.1058A>T (p.His353Leu) c.755A>T (p.His252Leu) c.1202A>T (p.His401Leu) | |
7 | g.99762089T>C | CA368368900 | CYP3A4 | c.1205A>G (p.His402Arg) n.640A>G c.746A>G (p.His249Arg) c.1058A>G (p.His353Arg) c.755A>G (p.His252Arg) c.1202A>G (p.His401Arg) | |
7 | g.99762089T>G | CA368368901 | CYP3A4 | c.1205A>C (p.His402Pro) n.640A>C c.746A>C (p.His249Pro) c.1058A>C (p.His353Pro) c.755A>C (p.His252Pro) c.1202A>C (p.His401Pro) | |
7 | g.99762090G>A | CA368368902 | CYP3A4 | c.1204C>T (p.His402Tyr) n.639C>T c.745C>T (p.His249Tyr) c.1057C>T (p.His353Tyr) c.754C>T (p.His252Tyr) c.1201C>T (p.His401Tyr) | gnomAD v4 |
7 | g.99762090G>C | CA368368903 | CYP3A4 | c.1204C>G (p.His402Asp) n.639C>G c.745C>G (p.His249Asp) c.1057C>G (p.His353Asp) c.754C>G (p.His252Asp) c.1201C>G (p.His401Asp) | |
7 | g.99762090G>T | CA368368904 | CYP3A4 | c.1204C>A (p.His402Asn) n.639C>A c.745C>A (p.His249Asn) c.1057C>A (p.His353Asn) c.754C>A (p.His252Asn) c.1201C>A (p.His401Asn) | |
7 | g.99762091A>C | CA456687152 | CYP3A4 | c.1203T>G (p.Leu401=) n.638T>G c.744T>G (p.Leu248=) c.1056T>G (p.Leu352=) c.753T>G (p.Leu251=) c.1200T>G (p.Leu400=) | |
7 | g.99762091A>G | CA456687153 | CYP3A4 | c.1203T>C (p.Leu401=) n.638T>C c.744T>C (p.Leu248=) c.1056T>C (p.Leu352=) c.753T>C (p.Leu251=) c.1200T>C (p.Leu400=) | |
7 | g.99762091A>T | CA456687154 | CYP3A4 | c.1203T>A (p.Leu401=) n.638T>A c.744T>A (p.Leu248=) c.1056T>A (p.Leu352=) c.753T>A (p.Leu251=) c.1200T>A (p.Leu400=) |