Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42128846A>C | CA411773908 | CYP2D6 | c.451T>G (p.Phe151Val) c.604T>G (p.Phe202Val) c.271T>G (p.Phe91Val) c.538T>G (p.Phe180Val) n.1328T>G c.460T>G (p.Phe154Val) | |
22 | g.42128846A>G | CA411773909 | CYP2D6 | c.451T>C (p.Phe151Leu) c.604T>C (p.Phe202Leu) c.271T>C (p.Phe91Leu) c.538T>C (p.Phe180Leu) n.1328T>C c.460T>C (p.Phe154Leu) | |
22 | g.42128846A>T | CA411773910 | CYP2D6 | c.451T>A (p.Phe151Ile) c.604T>A (p.Phe202Ile) c.271T>A (p.Phe91Ile) c.538T>A (p.Phe180Ile) n.1328T>A c.460T>A (p.Phe154Ile) | dbSNP |
22 | g.42128847G>A | CA514696914 | CYP2D6 | c.450C>T (p.Arg150=) c.603C>T (p.Arg201=) c.270C>T (p.Arg90=) c.537C>T (p.Arg179=) n.1327C>T c.459C>T (p.Arg153=) | dbSNP |
22 | g.42128847G>C | CA514696916 | CYP2D6 | c.450C>G (p.Arg150=) c.603C>G (p.Arg201=) c.270C>G (p.Arg90=) c.537C>G (p.Arg179=) n.1327C>G c.459C>G (p.Arg153=) | |
22 | g.42128847G= | CA2406579516 | CYP2D6 | c.450C= (p.Arg150=) c.603C= (p.Arg201=) c.270C= (p.Arg90=) c.537C= (p.Arg179=) n.1327C= c.459C= (p.Arg153=) | |
22 | g.42128847G>T | CA514696918 | CYP2D6 | c.450C>A (p.Arg150=) c.603C>A (p.Arg201=) c.270C>A (p.Arg90=) c.537C>A (p.Arg179=) n.1327C>A c.459C>A (p.Arg153=) | dbSNP |
22 | g.42128848C>A | CA411773911 | CYP2D6 | c.449G>T (p.Arg150Leu) c.602G>T (p.Arg201Leu) c.269G>T (p.Arg90Leu) c.536G>T (p.Arg179Leu) n.1326G>T c.458G>T (p.Arg153Leu) | dbSNP gnomAD v4 |
22 | g.42128848C= | CA2406579517 | CYP2D6 | c.449G= (p.Arg150=) c.602G= (p.Arg201=) c.269G= (p.Arg90=) c.536G= (p.Arg179=) n.1326G= c.458G= (p.Arg153=) | |
22 | g.42128848C>G | CA10265009 | CYP2D6 | c.449G>C (p.Arg150Pro) c.602G>C (p.Arg201Pro) c.269G>C (p.Arg90Pro) c.536G>C (p.Arg179Pro) n.1326G>C c.458G>C (p.Arg153Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128848C>T | CA10265010 | CYP2D6 | c.449G>A (p.Arg150His) c.602G>A (p.Arg201His) c.269G>A (p.Arg90His) c.536G>A (p.Arg179His) n.1326G>A c.458G>A (p.Arg153His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128849G>A | CA411773912 | CYP2D6 | c.448C>T (p.Arg150Cys) c.601C>T (p.Arg201Cys) c.268C>T (p.Arg90Cys) c.535C>T (p.Arg179Cys) n.1325C>T c.457C>T (p.Arg153Cys) | dbSNP gnomAD v3 gnomAD v4 |
22 | g.42128849G>C | CA10265012 | CYP2D6 | c.448C>G (p.Arg150Gly) c.601C>G (p.Arg201Gly) c.268C>G (p.Arg90Gly) c.535C>G (p.Arg179Gly) n.1325C>G c.457C>G (p.Arg153Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128849G= | CA2406579518 | CYP2D6 | c.448C= (p.Arg150=) c.601C= (p.Arg201=) c.268C= (p.Arg90=) c.535C= (p.Arg179=) n.1325C= c.457C= (p.Arg153=) | |
22 | g.42128849G>T | CA10265011 | CYP2D6 | c.448C>A (p.Arg150Ser) c.601C>A (p.Arg201Ser) c.268C>A (p.Arg90Ser) c.535C>A (p.Arg179Ser) n.1325C>A c.457C>A (p.Arg153Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128850A>C | CA514696932 | CYP2D6 | c.447T>G (p.Pro149=) c.600T>G (p.Pro200=) c.267T>G (p.Pro89=) c.534T>G (p.Pro178=) n.1324T>G c.456T>G (p.Pro152=) | |
22 | g.42128850A>G | CA514696934 | CYP2D6 | c.447T>C (p.Pro149=) c.600T>C (p.Pro200=) c.267T>C (p.Pro89=) c.534T>C (p.Pro178=) n.1324T>C c.456T>C (p.Pro152=) | |
22 | g.42128850A>T | CA514696936 | CYP2D6 | c.447T>A (p.Pro149=) c.600T>A (p.Pro200=) c.267T>A (p.Pro89=) c.534T>A (p.Pro178=) n.1324T>A c.456T>A (p.Pro152=) | dbSNP |
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=) |