| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42128847G>A | CA514696914 | CYP2D6 | c.603C>T (p.Arg201=) c.450C>T (p.Arg150=) n.270C>T (p.Arg90=) c.537C>T (p.Arg179=) n.1327C>T c.459C>T (p.Arg153=) | |
| 22 | g.42128847G>C | CA514696916 | CYP2D6 | c.603C>G (p.Arg201=) c.450C>G (p.Arg150=) n.270C>G (p.Arg90=) c.537C>G (p.Arg179=) n.1327C>G c.459C>G (p.Arg153=) | |
| 22 | g.42128847G= | CA2406579516 | CYP2D6 | c.603C= (p.Arg201=) c.450C= (p.Arg150=) n.270C= (p.Arg90=) c.537C= (p.Arg179=) n.1327C= c.459C= (p.Arg153=) | |
| 22 | g.42128847G>T | CA514696918 | CYP2D6 | c.603C>A (p.Arg201=) c.450C>A (p.Arg150=) n.270C>A (p.Arg90=) c.537C>A (p.Arg179=) n.1327C>A c.459C>A (p.Arg153=) | |
| 22 | g.42128848C>A | CA411773911 | CYP2D6 | c.602G>T (p.Arg201Leu) c.449G>T (p.Arg150Leu) n.269G>T (p.Arg90Leu) c.536G>T (p.Arg179Leu) n.1326G>T c.458G>T (p.Arg153Leu) | |
| 22 | g.42128848C= | CA2406579517 | CYP2D6 | c.602G= (p.Arg201=) c.449G= (p.Arg150=) n.269G= (p.Arg90=) c.536G= (p.Arg179=) n.1326G= c.458G= (p.Arg153=) | |
| 22 | g.42128848C>G | CA10265009 | CYP2D6 | c.602G>C (p.Arg201Pro) c.449G>C (p.Arg150Pro) n.269G>C (p.Arg90Pro) c.536G>C (p.Arg179Pro) n.1326G>C c.458G>C (p.Arg153Pro) | dbSNP ExAC gnomAD |
| 22 | g.42128848C>T | CA10265010 | CYP2D6 | c.602G>A (p.Arg201His) c.449G>A (p.Arg150His) n.269G>A (p.Arg90His) c.536G>A (p.Arg179His) n.1326G>A c.458G>A (p.Arg153His) | dbSNP ExAC gnomAD |
| 22 | g.42128849G>A | CA411773912 | CYP2D6 | c.601C>T (p.Arg201Cys) c.448C>T (p.Arg150Cys) n.268C>T (p.Arg90Cys) c.535C>T (p.Arg179Cys) n.1325C>T c.457C>T (p.Arg153Cys) | |
| 22 | g.42128849G>C | CA10265012 | CYP2D6 | c.601C>G (p.Arg201Gly) c.448C>G (p.Arg150Gly) n.268C>G (p.Arg90Gly) c.535C>G (p.Arg179Gly) n.1325C>G c.457C>G (p.Arg153Gly) | dbSNP ExAC gnomAD |
| 22 | g.42128849G= | CA2406579518 | CYP2D6 | c.601C= (p.Arg201=) c.448C= (p.Arg150=) n.268C= (p.Arg90=) c.535C= (p.Arg179=) n.1325C= c.457C= (p.Arg153=) | |
| 22 | g.42128849G>T | CA10265011 | CYP2D6 | c.601C>A (p.Arg201Ser) c.448C>A (p.Arg150Ser) n.268C>A (p.Arg90Ser) c.535C>A (p.Arg179Ser) n.1325C>A c.457C>A (p.Arg153Ser) | dbSNP ExAC gnomAD |
| 22 | g.42128850A>C | CA514696932 | CYP2D6 | c.600T>G (p.Pro200=) c.447T>G (p.Pro149=) n.267T>G (p.Pro89=) c.534T>G (p.Pro178=) n.1324T>G c.456T>G (p.Pro152=) | |
| 22 | g.42128850A>G | CA514696934 | CYP2D6 | c.600T>C (p.Pro200=) c.447T>C (p.Pro149=) n.267T>C (p.Pro89=) c.534T>C (p.Pro178=) n.1324T>C c.456T>C (p.Pro152=) | |
| 22 | g.42128850A>T | CA514696936 | CYP2D6 | c.600T>A (p.Pro200=) c.447T>A (p.Pro149=) n.267T>A (p.Pro89=) c.534T>A (p.Pro178=) n.1324T>A c.456T>A (p.Pro152=) | |
| 22 | g.42128851G>A | CA411773913 | CYP2D6 | c.599C>T (p.Pro200Leu) c.446C>T (p.Pro149Leu) n.266C>T (p.Pro89Leu) c.533C>T (p.Pro178Leu) n.1323C>T c.455C>T (p.Pro152Leu) | |
| 22 | g.42128851G>C | CA411773914 | CYP2D6 | c.599C>G (p.Pro200Arg) c.446C>G (p.Pro149Arg) n.266C>G (p.Pro89Arg) c.533C>G (p.Pro178Arg) n.1323C>G c.455C>G (p.Pro152Arg) | |
| 22 | g.42128851G= | CA2406579519 | CYP2D6 | c.599C= (p.Pro200=) c.446C= (p.Pro149=) n.266C= (p.Pro89=) c.533C= (p.Pro178=) n.1323C= c.455C= (p.Pro152=) | |
| 22 | g.42128851G>T | CA411773915 | CYP2D6 | c.599C>A (p.Pro200His) c.446C>A (p.Pro149His) n.266C>A (p.Pro89His) c.533C>A (p.Pro178His) n.1323C>A c.455C>A (p.Pro152His) | gnomAD |
| 22 | g.42128852G>A | CA411773916 | CYP2D6 | c.598C>T (p.Pro200Ser) c.445C>T (p.Pro149Ser) n.265C>T (p.Pro89Ser) c.532C>T (p.Pro178Ser) n.1322C>T c.454C>T (p.Pro152Ser) | |
| 22 | g.42128852G>C | CA10265013 | CYP2D6 | c.598C>G (p.Pro200Ala) c.445C>G (p.Pro149Ala) n.265C>G (p.Pro89Ala) c.532C>G (p.Pro178Ala) n.1322C>G c.454C>G (p.Pro152Ala) | dbSNP ExAC gnomAD |
| 22 | g.42128852G= | CA2406579520 | CYP2D6 | c.598C= (p.Pro200=) c.445C= (p.Pro149=) n.265C= (p.Pro89=) c.532C= (p.Pro178=) n.1322C= c.454C= (p.Pro152=) | |
| 22 | g.42128852G>T | CA411773917 | CYP2D6 | c.598C>A (p.Pro200Thr) c.445C>A (p.Pro149Thr) n.265C>A (p.Pro89Thr) c.532C>A (p.Pro178Thr) n.1322C>A c.454C>A (p.Pro152Thr) | gnomAD |
| 22 | g.42128853G>A | CA10265014 | CYP2D6 | c.597C>T (p.Asp199=) c.444C>T (p.Asp148=) n.264C>T (p.Asp88=) c.531C>T (p.Asp177=) n.1321C>T c.453C>T (p.Asp151=) | dbSNP ExAC gnomAD |
| 22 | g.42128853G>C | CA411773918 | CYP2D6 | c.597C>G (p.Asp199Glu) c.444C>G (p.Asp148Glu) n.264C>G (p.Asp88Glu) c.531C>G (p.Asp177Glu) n.1321C>G c.453C>G (p.Asp151Glu) | |
| 22 | g.42128853G= | CA2406579521 | CYP2D6 | c.597C= (p.Asp199=) c.444C= (p.Asp148=) n.264C= (p.Asp88=) c.531C= (p.Asp177=) n.1321C= c.453C= (p.Asp151=) | |
| 22 | g.42128853G>T | CA411773919 | CYP2D6 | c.597C>A (p.Asp199Glu) c.444C>A (p.Asp148Glu) n.264C>A (p.Asp88Glu) c.531C>A (p.Asp177Glu) n.1321C>A c.453C>A (p.Asp151Glu) | |
| 22 | g.42128854T>A | CA411773920 | CYP2D6 | c.596A>T (p.Asp199Val) c.443A>T (p.Asp148Val) n.263A>T (p.Asp88Val) c.530A>T (p.Asp177Val) n.1320A>T c.452A>T (p.Asp151Val) | |
| 22 | g.42128854T>C | CA411773921 | CYP2D6 | c.596A>G (p.Asp199Gly) c.443A>G (p.Asp148Gly) n.263A>G (p.Asp88Gly) c.530A>G (p.Asp177Gly) n.1320A>G c.452A>G (p.Asp151Gly) | |
| 22 | g.42128854T>G | CA10265015 | CYP2D6 | c.596A>C (p.Asp199Ala) c.443A>C (p.Asp148Ala) n.263A>C (p.Asp88Ala) c.530A>C (p.Asp177Ala) n.1320A>C c.452A>C (p.Asp151Ala) | dbSNP ExAC gnomAD |
| 22 | g.42128854T= | CA2406579522 | CYP2D6 | c.596A= (p.Asp199=) c.443A= (p.Asp148=) n.263A= (p.Asp88=) c.530A= (p.Asp177=) n.1320A= c.452A= (p.Asp151=) | |
| 22 | g.42128855C>A | CA10265016 | CYP2D6 | c.595G>T (p.Asp199Tyr) c.442G>T (p.Asp148Tyr) n.262G>T (p.Asp88Tyr) c.529G>T (p.Asp177Tyr) n.1319G>T c.451G>T (p.Asp151Tyr) | dbSNP ExAC gnomAD |
| 22 | g.42128855C= | CA2406579523 | CYP2D6 | c.595G= (p.Asp199=) c.442G= (p.Asp148=) n.262G= (p.Asp88=) c.529G= (p.Asp177=) n.1319G= c.451G= (p.Asp151=) | |
| 22 | g.42128855C>G | CA411773923 | CYP2D6 | c.595G>C (p.Asp199His) c.442G>C (p.Asp148His) n.262G>C (p.Asp88His) c.529G>C (p.Asp177His) n.1319G>C c.451G>C (p.Asp151His) | |
| 22 | g.42128855C>T | CA411773922 | CYP2D6 | c.595G>A (p.Asp199Asn) c.442G>A (p.Asp148Asn) n.262G>A (p.Asp88Asn) c.529G>A (p.Asp177Asn) n.1319G>A c.451G>A (p.Asp151Asn) | |
| 22 | g.42128856G>A | CA10265017 | CYP2D6 | c.594C>T (p.Asp198=) c.441C>T (p.Asp147=) n.261C>T (p.Asp87=) c.528C>T (p.Asp176=) n.1318C>T c.450C>T (p.Asp150=) | dbSNP ExAC gnomAD |
| 22 | g.42128856G>C | CA411773924 | CYP2D6 | c.594C>G (p.Asp198Glu) c.441C>G (p.Asp147Glu) n.261C>G (p.Asp87Glu) c.528C>G (p.Asp176Glu) n.1318C>G c.450C>G (p.Asp150Glu) | |
| 22 | g.42128856G= | CA2406579524 | CYP2D6 | c.594C= (p.Asp198=) c.441C= (p.Asp147=) n.261C= (p.Asp87=) c.528C= (p.Asp176=) n.1318C= c.450C= (p.Asp150=) | |
| 22 | g.42128856G>T | CA411773925 | CYP2D6 | c.594C>A (p.Asp198Glu) c.441C>A (p.Asp147Glu) n.261C>A (p.Asp87Glu) c.528C>A (p.Asp176Glu) n.1318C>A c.450C>A (p.Asp150Glu) | |
| 22 | g.42128857T>A | CA411773926 | CYP2D6 | c.593A>T (p.Asp198Val) c.440A>T (p.Asp147Val) n.260A>T (p.Asp87Val) c.527A>T (p.Asp176Val) n.1317A>T c.449A>T (p.Asp150Val) | |
| 22 | g.42128857T>C | CA411773927 | CYP2D6 | c.593A>G (p.Asp198Gly) c.440A>G (p.Asp147Gly) n.260A>G (p.Asp87Gly) c.527A>G (p.Asp176Gly) n.1317A>G c.449A>G (p.Asp150Gly) | |
| 22 | g.42128857T>G | CA411773928 | CYP2D6 | c.593A>C (p.Asp198Ala) c.440A>C (p.Asp147Ala) n.260A>C (p.Asp87Ala) c.527A>C (p.Asp176Ala) n.1317A>C c.449A>C (p.Asp150Ala) | |
| 22 | g.42128857T= | CA2406579525 | CYP2D6 | c.593A= (p.Asp198=) c.440A= (p.Asp147=) n.260A= (p.Asp87=) c.527A= (p.Asp176=) n.1317A= c.449A= (p.Asp150=) | |
| 22 | g.42128858C>A | CA411773930 | CYP2D6 | c.592G>T (p.Asp198Tyr) c.439G>T (p.Asp147Tyr) n.259G>T (p.Asp87Tyr) c.526G>T (p.Asp176Tyr) n.1316G>T c.448G>T (p.Asp150Tyr) | |
| 22 | g.42128858C= | CA2406579526 | CYP2D6 | c.592G= (p.Asp198=) c.439G= (p.Asp147=) n.259G= (p.Asp87=) c.526G= (p.Asp176=) n.1316G= c.448G= (p.Asp150=) | |
| 22 | g.42128858C>G | CA411773929 | CYP2D6 | c.592G>C (p.Asp198His) c.439G>C (p.Asp147His) n.259G>C (p.Asp87His) c.526G>C (p.Asp176His) n.1316G>C c.448G>C (p.Asp150His) | |
| 22 | g.42128858C>T | CA10265018 | CYP2D6 | c.592G>A (p.Asp198Asn) c.439G>A (p.Asp147Asn) n.259G>A (p.Asp87Asn) c.526G>A (p.Asp176Asn) n.1316G>A c.448G>A (p.Asp150Asn) | dbSNP ExAC gnomAD |
| 22 | g.42128859G>A | CA10265019 | CYP2D6 | c.591C>T (p.Tyr197=) c.438C>T (p.Tyr146=) n.258C>T (p.Tyr86=) c.525C>T (p.Tyr175=) n.1315C>T c.447C>T (p.Tyr149=) | dbSNP ExAC gnomAD |
| 22 | g.42128859G>C | CA411773931 | CYP2D6 | c.591C>G (p.Tyr197Ter) c.438C>G (p.Tyr146Ter) n.258C>G (p.Tyr86Ter) c.525C>G (p.Tyr175Ter) n.1315C>G c.447C>G (p.Tyr149Ter) | gnomAD |
| 22 | g.42128859G= | CA2406579527 | CYP2D6 | c.591C= (p.Tyr197=) c.438C= (p.Tyr146=) n.258C= (p.Tyr86=) c.525C= (p.Tyr175=) n.1315C= c.447C= (p.Tyr149=) |