Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42128851G>A | CA411773913 | CYP2D6 | c.446C>T (p.Pro149Leu) c.599C>T (p.Pro200Leu) c.266C>T (p.Pro89Leu) c.533C>T (p.Pro178Leu) n.1323C>T c.455C>T (p.Pro152Leu) | |
22 | g.42128851G>C | CA411773914 | CYP2D6 | c.446C>G (p.Pro149Arg) c.599C>G (p.Pro200Arg) c.266C>G (p.Pro89Arg) c.533C>G (p.Pro178Arg) n.1323C>G c.455C>G (p.Pro152Arg) | |
22 | g.42128851G= | CA2406579519 | CYP2D6 | c.446C= (p.Pro149=) c.599C= (p.Pro200=) c.266C= (p.Pro89=) c.533C= (p.Pro178=) n.1323C= c.455C= (p.Pro152=) | |
22 | g.42128851G>T | CA411773915 | CYP2D6 | c.446C>A (p.Pro149His) c.599C>A (p.Pro200His) c.266C>A (p.Pro89His) c.533C>A (p.Pro178His) n.1323C>A c.455C>A (p.Pro152His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128852G>A | CA411773916 | CYP2D6 | c.445C>T (p.Pro149Ser) c.598C>T (p.Pro200Ser) c.265C>T (p.Pro89Ser) c.532C>T (p.Pro178Ser) n.1322C>T c.454C>T (p.Pro152Ser) | ClinVar dbSNP gnomAD v4 |
22 | g.42128852G>C | CA10265013 | CYP2D6 | c.445C>G (p.Pro149Ala) c.598C>G (p.Pro200Ala) c.265C>G (p.Pro89Ala) c.532C>G (p.Pro178Ala) n.1322C>G c.454C>G (p.Pro152Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
22 | g.42128852G= | CA2406579520 | CYP2D6 | c.445C= (p.Pro149=) c.598C= (p.Pro200=) c.265C= (p.Pro89=) c.532C= (p.Pro178=) n.1322C= c.454C= (p.Pro152=) | |
22 | g.42128852G>T | CA411773917 | CYP2D6 | c.445C>A (p.Pro149Thr) c.598C>A (p.Pro200Thr) c.265C>A (p.Pro89Thr) c.532C>A (p.Pro178Thr) n.1322C>A c.454C>A (p.Pro152Thr) | dbSNP gnomAD v2 gnomAD v4 |
22 | g.42128853G>A | CA10265014 | CYP2D6 | c.444C>T (p.Asp148=) c.597C>T (p.Asp199=) c.264C>T (p.Asp88=) c.531C>T (p.Asp177=) n.1321C>T c.453C>T (p.Asp151=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
22 | g.42128853G>C | CA411773918 | CYP2D6 | c.444C>G (p.Asp148Glu) c.597C>G (p.Asp199Glu) c.264C>G (p.Asp88Glu) c.531C>G (p.Asp177Glu) n.1321C>G c.453C>G (p.Asp151Glu) | dbSNP |
22 | g.42128853G= | CA2406579521 | CYP2D6 | c.444C= (p.Asp148=) c.597C= (p.Asp199=) c.264C= (p.Asp88=) c.531C= (p.Asp177=) n.1321C= c.453C= (p.Asp151=) | |
22 | g.42128853G>T | CA411773919 | CYP2D6 | c.444C>A (p.Asp148Glu) c.597C>A (p.Asp199Glu) c.264C>A (p.Asp88Glu) c.531C>A (p.Asp177Glu) n.1321C>A c.453C>A (p.Asp151Glu) | |
22 | g.42128858_42128860del | CA2657033654 | CYP2D6 | c.442_444del (p.Asp148del) c.595_597del (p.Asp199del) c.262_264del (p.Asp88del) c.529_531del (p.Asp177del) n.1319_1321del c.451_453del (p.Asp151del) | gnomAD v4 |
22 | g.42128854T>A | CA411773920 | CYP2D6 | c.443A>T (p.Asp148Val) c.596A>T (p.Asp199Val) c.263A>T (p.Asp88Val) c.530A>T (p.Asp177Val) n.1320A>T c.452A>T (p.Asp151Val) | dbSNP |
22 | g.42128854T>C | CA411773921 | CYP2D6 | c.443A>G (p.Asp148Gly) c.596A>G (p.Asp199Gly) c.263A>G (p.Asp88Gly) c.530A>G (p.Asp177Gly) n.1320A>G c.452A>G (p.Asp151Gly) | |
22 | g.42128854T>G | CA10265015 | CYP2D6 | c.443A>C (p.Asp148Ala) c.596A>C (p.Asp199Ala) c.263A>C (p.Asp88Ala) c.530A>C (p.Asp177Ala) n.1320A>C c.452A>C (p.Asp151Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
22 | g.42128854T= | CA2406579522 | CYP2D6 | c.443A= (p.Asp148=) c.596A= (p.Asp199=) c.263A= (p.Asp88=) c.530A= (p.Asp177=) n.1320A= c.452A= (p.Asp151=) | |
22 | g.42128855C>A | CA10265016 | CYP2D6 | c.442G>T (p.Asp148Tyr) c.595G>T (p.Asp199Tyr) c.262G>T (p.Asp88Tyr) c.529G>T (p.Asp177Tyr) n.1319G>T c.451G>T (p.Asp151Tyr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128855C= | CA2406579523 | CYP2D6 | c.442G= (p.Asp148=) c.595G= (p.Asp199=) c.262G= (p.Asp88=) c.529G= (p.Asp177=) n.1319G= c.451G= (p.Asp151=) | |
22 | g.42128855C>G | CA411773923 | CYP2D6 | c.442G>C (p.Asp148His) c.595G>C (p.Asp199His) c.262G>C (p.Asp88His) c.529G>C (p.Asp177His) n.1319G>C c.451G>C (p.Asp151His) | dbSNP gnomAD v4 |
22 | g.42128855C>T | CA411773922 | CYP2D6 | c.442G>A (p.Asp148Asn) c.595G>A (p.Asp199Asn) c.262G>A (p.Asp88Asn) c.529G>A (p.Asp177Asn) n.1319G>A c.451G>A (p.Asp151Asn) | dbSNP gnomAD v4 |
22 | g.42128855_42128862del | CA2738247943 | CYP2D6 | c.435_442del (p.Tyr146ProfsTer?) c.588_595del (p.Tyr197ProfsTer?) c.255_262del (p.Tyr86ProfsTer?) c.522_529del (p.Tyr175ProfsTer?) n.1312_1319del c.444_451del (p.Tyr149ProfsTer?) | dbSNP |
22 | g.42128856G>A | CA10265017 | CYP2D6 | c.441C>T (p.Asp147=) c.594C>T (p.Asp198=) c.261C>T (p.Asp87=) c.528C>T (p.Asp176=) n.1318C>T c.450C>T (p.Asp150=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128856G>C | CA411773924 | CYP2D6 | c.441C>G (p.Asp147Glu) c.594C>G (p.Asp198Glu) c.261C>G (p.Asp87Glu) c.528C>G (p.Asp176Glu) n.1318C>G c.450C>G (p.Asp150Glu) | dbSNP gnomAD v4 |
22 | g.42128856G= | CA2406579524 | CYP2D6 | c.441C= (p.Asp147=) c.594C= (p.Asp198=) c.261C= (p.Asp87=) c.528C= (p.Asp176=) n.1318C= c.450C= (p.Asp150=) | |
22 | g.42128856G>T | CA411773925 | CYP2D6 | c.441C>A (p.Asp147Glu) c.594C>A (p.Asp198Glu) c.261C>A (p.Asp87Glu) c.528C>A (p.Asp176Glu) n.1318C>A c.450C>A (p.Asp150Glu) | dbSNP |
22 | g.42128857T>A | CA411773926 | CYP2D6 | c.440A>T (p.Asp147Val) c.593A>T (p.Asp198Val) c.260A>T (p.Asp87Val) c.527A>T (p.Asp176Val) n.1317A>T c.449A>T (p.Asp150Val) | dbSNP |
22 | g.42128857T>C | CA411773927 | CYP2D6 | c.440A>G (p.Asp147Gly) c.593A>G (p.Asp198Gly) c.260A>G (p.Asp87Gly) c.527A>G (p.Asp176Gly) n.1317A>G c.449A>G (p.Asp150Gly) | dbSNP gnomAD v3 gnomAD v4 |
22 | g.42128857T>G | CA411773928 | CYP2D6 | c.440A>C (p.Asp147Ala) c.593A>C (p.Asp198Ala) c.260A>C (p.Asp87Ala) c.527A>C (p.Asp176Ala) n.1317A>C c.449A>C (p.Asp150Ala) | dbSNP |
22 | g.42128857T= | CA2406579525 | CYP2D6 | c.440A= (p.Asp147=) c.593A= (p.Asp198=) c.260A= (p.Asp87=) c.527A= (p.Asp176=) n.1317A= c.449A= (p.Asp150=) | |
22 | g.42128858C>A | CA411773930 | CYP2D6 | c.439G>T (p.Asp147Tyr) c.592G>T (p.Asp198Tyr) c.259G>T (p.Asp87Tyr) c.526G>T (p.Asp176Tyr) n.1316G>T c.448G>T (p.Asp150Tyr) | dbSNP |
22 | g.42128858C= | CA2406579526 | CYP2D6 | c.439G= (p.Asp147=) c.592G= (p.Asp198=) c.259G= (p.Asp87=) c.526G= (p.Asp176=) n.1316G= c.448G= (p.Asp150=) | |
22 | g.42128858C>G | CA411773929 | CYP2D6 | c.439G>C (p.Asp147His) c.592G>C (p.Asp198His) c.259G>C (p.Asp87His) c.526G>C (p.Asp176His) n.1316G>C c.448G>C (p.Asp150His) | dbSNP gnomAD v4 |
22 | g.42128858C>T | CA10265018 | CYP2D6 | c.439G>A (p.Asp147Asn) c.592G>A (p.Asp198Asn) c.259G>A (p.Asp87Asn) c.526G>A (p.Asp176Asn) n.1316G>A c.448G>A (p.Asp150Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
22 | g.42128859G>A | CA10265019 | CYP2D6 | c.438C>T (p.Tyr146=) c.591C>T (p.Tyr197=) c.258C>T (p.Tyr86=) c.525C>T (p.Tyr175=) n.1315C>T c.447C>T (p.Tyr149=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128859G>C | CA411773931 | CYP2D6 | c.438C>G (p.Tyr146Ter) c.591C>G (p.Tyr197Ter) c.258C>G (p.Tyr86Ter) c.525C>G (p.Tyr175Ter) n.1315C>G c.447C>G (p.Tyr149Ter) | dbSNP gnomAD v2 gnomAD v4 |
22 | g.42128859G= | CA2406579527 | CYP2D6 | c.438C= (p.Tyr146=) c.591C= (p.Tyr197=) c.258C= (p.Tyr86=) c.525C= (p.Tyr175=) n.1315C= c.447C= (p.Tyr149=) | |
22 | g.42128859G>T | CA411773932 | CYP2D6 | c.438C>A (p.Tyr146Ter) c.591C>A (p.Tyr197Ter) c.258C>A (p.Tyr86Ter) c.525C>A (p.Tyr175Ter) n.1315C>A c.447C>A (p.Tyr149Ter) | |
22 | g.42128860T>A | CA411773933 | CYP2D6 | c.437A>T (p.Tyr146Phe) c.590A>T (p.Tyr197Phe) c.257A>T (p.Tyr86Phe) c.524A>T (p.Tyr175Phe) n.1314A>T c.446A>T (p.Tyr149Phe) | dbSNP |
22 | g.42128860T>C | CA411773934 | CYP2D6 | c.437A>G (p.Tyr146Cys) c.590A>G (p.Tyr197Cys) c.257A>G (p.Tyr86Cys) c.524A>G (p.Tyr175Cys) n.1314A>G c.446A>G (p.Tyr149Cys) | dbSNP |
22 | g.42128860T>G | CA411773935 | CYP2D6 | c.437A>C (p.Tyr146Ser) c.590A>C (p.Tyr197Ser) c.257A>C (p.Tyr86Ser) c.524A>C (p.Tyr175Ser) n.1314A>C c.446A>C (p.Tyr149Ser) | dbSNP |
22 | g.42128860T= | CA2406579528 | CYP2D6 | c.437A= (p.Tyr146=) c.590A= (p.Tyr197=) c.257A= (p.Tyr86=) c.524A= (p.Tyr175=) n.1314A= c.446A= (p.Tyr149=) | |
22 | g.42128861A= | CA2406579529 | CYP2D6 | c.436T= (p.Tyr146=) c.589T= (p.Tyr197=) c.256T= (p.Tyr86=) c.523T= (p.Tyr175=) n.1313T= c.445T= (p.Tyr149=) | |
22 | g.42128861A>C | CA411773936 | CYP2D6 | c.436T>G (p.Tyr146Asp) c.589T>G (p.Tyr197Asp) c.256T>G (p.Tyr86Asp) c.523T>G (p.Tyr175Asp) n.1313T>G c.445T>G (p.Tyr149Asp) | |
22 | g.42128861A>G | CA411773938 | CYP2D6 | c.436T>C (p.Tyr146His) c.589T>C (p.Tyr197His) c.256T>C (p.Tyr86His) c.523T>C (p.Tyr175His) n.1313T>C c.445T>C (p.Tyr149His) | dbSNP gnomAD v3 gnomAD v4 |
22 | g.42128861A>T | CA411773937 | CYP2D6 | c.436T>A (p.Tyr146Asn) c.589T>A (p.Tyr197Asn) c.256T>A (p.Tyr86Asn) c.523T>A (p.Tyr175Asn) n.1313T>A c.445T>A (p.Tyr149Asn) | dbSNP |
22 | g.42128862C>A | CA411773939 | CYP2D6 | c.435G>T (p.Glu145Asp) c.588G>T (p.Glu196Asp) c.255G>T (p.Glu85Asp) c.522G>T (p.Glu174Asp) n.1312G>T c.444G>T (p.Glu148Asp) | dbSNP gnomAD v4 |
22 | g.42128862C= | CA2406579530 | CYP2D6 | c.435G= (p.Glu145=) c.588G= (p.Glu196=) c.255G= (p.Glu85=) c.522G= (p.Glu174=) n.1312G= c.444G= (p.Glu148=) | |
22 | g.42128862C>G | CA411773940 | CYP2D6 | c.435G>C (p.Glu145Asp) c.588G>C (p.Glu196Asp) c.255G>C (p.Glu85Asp) c.522G>C (p.Glu174Asp) n.1312G>C c.444G>C (p.Glu148Asp) | dbSNP gnomAD v4 |
22 | g.42128862C>T | CA10265020 | CYP2D6 | c.435G>A (p.Glu145=) c.588G>A (p.Glu196=) c.255G>A (p.Glu85=) c.522G>A (p.Glu174=) n.1312G>A c.444G>A (p.Glu148=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |