| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.18222363A= | CA1768101108 | NAT1 | c.316A= (p.Ile106=) c.502A= (p.Ile168=) n.668A= | |
| 8 | g.18222363A>C | CA370445051 | NAT1 | c.316A>C (p.Ile106Leu) c.502A>C (p.Ile168Leu) n.668A>C | |
| 8 | g.18222363A>G | CA370445052 | NAT1 | c.316A>G (p.Ile106Val) c.502A>G (p.Ile168Val) n.668A>G | |
| 8 | g.18222363A>T | CA370445053 | NAT1 | c.316A>T (p.Ile106Phe) c.502A>T (p.Ile168Phe) n.668A>T | dbSNP |
| 8 | g.18222364T>A | CA370445054 | NAT1 | c.317T>A (p.Ile106Asn) c.503T>A (p.Ile168Asn) n.669T>A | dbSNP gnomAD v2 |
| 8 | g.18222364T>C | CA370445055 | NAT1 | c.317T>C (p.Ile106Thr) c.503T>C (p.Ile168Thr) n.669T>C | |
| 8 | g.18222364T>G | CA370445056 | NAT1 | c.317T>G (p.Ile106Ser) c.503T>G (p.Ile168Ser) n.669T>G | dbSNP |
| 8 | g.18222364T= | CA1768101109 | NAT1 | c.317T= (p.Ile106=) c.503T= (p.Ile168=) n.669T= | |
| 8 | g.18222365T>A | CA459877570 | NAT1 | c.318T>A (p.Ile106=) c.504T>A (p.Ile168=) n.670T>A | |
| 8 | g.18222365T>C | CA173180328 | NAT1 | c.318T>C (p.Ile106=) c.504T>C (p.Ile168=) n.670T>C | dbSNP gnomAD v4 |
| 8 | g.18222365T>G | CA4651374 | NAT1 | c.318T>G (p.Ile106Met) c.504T>G (p.Ile168Met) n.670T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222365T= | CA1768101110 | NAT1 | c.318T= (p.Ile106=) c.504T= (p.Ile168=) n.670T= | |
| 8 | g.18222366C>A | CA370445057 | NAT1 | c.319C>A (p.His107Asn) c.505C>A (p.His169Asn) n.671C>A | |
| 8 | g.18222366C>G | CA370445058 | NAT1 | c.319C>G (p.His107Asp) c.505C>G (p.His169Asp) n.671C>G | |
| 8 | g.18222366C>T | CA370445059 | NAT1 | c.319C>T (p.His107Tyr) c.505C>T (p.His169Tyr) n.671C>T | |
| 8 | g.18222367A>C | CA370445060 | NAT1 | c.320A>C (p.His107Pro) c.506A>C (p.His169Pro) n.672A>C | |
| 8 | g.18222367A>G | CA370445061 | NAT1 | c.320A>G (p.His107Arg) c.506A>G (p.His169Arg) n.672A>G | |
| 8 | g.18222367A>T | CA370445062 | NAT1 | c.320A>T (p.His107Leu) c.506A>T (p.His169Leu) n.672A>T | |
| 8 | g.18222368C>A | CA370445063 | NAT1 | c.321C>A (p.His107Gln) c.507C>A (p.His169Gln) n.673C>A | |
| 8 | g.18222368C= | CA1768101111 | NAT1 | c.321C= (p.His107=) c.507C= (p.His169=) n.673C= | |
| 8 | g.18222368C>G | CA370445064 | NAT1 | c.321C>G (p.His107Gln) c.507C>G (p.His169Gln) n.673C>G | dbSNP gnomAD v4 |
| 8 | g.18222368C>T | CA4651375 | NAT1 | c.321C>T (p.His107=) c.507C>T (p.His169=) n.673C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222369C>A | CA4651376 | NAT1 | c.322C>A (p.Leu108Ile) c.508C>A (p.Leu170Ile) n.674C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222369C= | CA1768101113 | NAT1 | c.322C= (p.Leu108=) c.508C= (p.Leu170=) n.674C= | |
| 8 | g.18222369C>G | CA370445065 | NAT1 | c.322C>G (p.Leu108Val) c.508C>G (p.Leu170Val) n.674C>G | |
| 8 | g.18222369C>T | CA370445066 | NAT1 | c.322C>T (p.Leu108Phe) c.508C>T (p.Leu170Phe) n.674C>T | |
| 8 | g.18222371_18222373dup | CA1768101112 | NAT1 | c.324_326dup (p.Leu109_Leu110insLeu) c.510_512dup (p.Leu171_Leu172insLeu) n.676_678dup | dbSNP |
| 8 | g.18222370T>A | CA370445067 | NAT1 | c.323T>A (p.Leu108His) c.509T>A (p.Leu170His) n.675T>A | |
| 8 | g.18222370T>C | CA370445068 | NAT1 | c.323T>C (p.Leu108Pro) c.509T>C (p.Leu170Pro) n.675T>C | |
| 8 | g.18222370T>G | CA370445069 | NAT1 | c.323T>G (p.Leu108Arg) c.509T>G (p.Leu170Arg) n.675T>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222370T= | CA1768101114 | NAT1 | c.323T= (p.Leu108=) c.509T= (p.Leu170=) n.675T= | |
| 8 | g.18222371T>A | CA459877572 | NAT1 | c.324T>A (p.Leu108=) c.510T>A (p.Leu170=) n.676T>A | |
| 8 | g.18222371T>C | CA459877573 | NAT1 | c.324T>C (p.Leu108=) c.510T>C (p.Leu170=) n.676T>C | |
| 8 | g.18222371T>G | CA459877571 | NAT1 | c.324T>G (p.Leu108=) c.510T>G (p.Leu170=) n.676T>G | |
| 8 | g.18222372C>A | CA370445070 | NAT1 | c.325C>A (p.Leu109Ile) c.511C>A (p.Leu171Ile) n.677C>A | |
| 8 | g.18222372C>G | CA370445071 | NAT1 | c.325C>G (p.Leu109Val) c.511C>G (p.Leu171Val) n.677C>G | |
| 8 | g.18222372C>T | CA370445072 | NAT1 | c.325C>T (p.Leu109Phe) c.511C>T (p.Leu171Phe) n.677C>T | |
| 8 | g.18222373T>A | CA370445073 | NAT1 | c.326T>A (p.Leu109His) c.512T>A (p.Leu171His) n.678T>A | |
| 8 | g.18222373T>C | CA370445074 | NAT1 | c.326T>C (p.Leu109Pro) c.512T>C (p.Leu171Pro) n.678T>C | |
| 8 | g.18222373T>G | CA370445075 | NAT1 | c.326T>G (p.Leu109Arg) c.512T>G (p.Leu171Arg) n.678T>G | |
| 8 | g.18222374C>A | CA459877576 | NAT1 | c.327C>A (p.Leu109=) c.513C>A (p.Leu171=) n.679C>A | |
| 8 | g.18222374C>G | CA459877574 | NAT1 | c.327C>G (p.Leu109=) c.513C>G (p.Leu171=) n.679C>G | |
| 8 | g.18222374C>T | CA459877575 | NAT1 | c.327C>T (p.Leu109=) c.513C>T (p.Leu171=) n.679C>T | gnomAD v4 |
| 8 | g.18222375C>A | CA370445077 | NAT1 | c.328C>A (p.Leu110Met) c.514C>A (p.Leu172Met) n.680C>A | |
| 8 | g.18222375C>G | CA370445076 | NAT1 | c.328C>G (p.Leu110Val) c.514C>G (p.Leu172Val) n.680C>G | |
| 8 | g.18222375C>T | CA459877577 | NAT1 | c.328C>T (p.Leu110=) c.514C>T (p.Leu172=) n.680C>T | gnomAD v4 |
| 8 | g.18222376T>A | CA370445078 | NAT1 | c.329T>A (p.Leu110Gln) c.515T>A (p.Leu172Gln) n.681T>A | |
| 8 | g.18222376T>C | CA370445079 | NAT1 | c.329T>C (p.Leu110Pro) c.515T>C (p.Leu172Pro) n.681T>C | |
| 8 | g.18222376T>G | CA370445080 | NAT1 | c.329T>G (p.Leu110Arg) c.515T>G (p.Leu172Arg) n.681T>G | gnomAD v4 |
| 8 | g.18222377G>A | CA459877579 | NAT1 | c.330G>A (p.Leu110=) c.516G>A (p.Leu172=) n.682G>A | |
| 8 | g.18222377G>C | CA459877580 | NAT1 | c.330G>C (p.Leu110=) c.516G>C (p.Leu172=) n.682G>C | |
| 8 | g.18222377G>T | CA459877578 | NAT1 | c.330G>T (p.Leu110=) c.516G>T (p.Leu172=) n.682G>T | gnomAD v4 |
| 8 | g.18222378C>A | CA370445081 | NAT1 | c.331C>A (p.Gln111Lys) c.517C>A (p.Gln173Lys) n.683C>A | |
| 8 | g.18222378C>G | CA370445082 | NAT1 | c.331C>G (p.Gln111Glu) c.517C>G (p.Gln173Glu) n.683C>G | |
| 8 | g.18222378C>T | CA370445083 | NAT1 | c.331C>T (p.Gln111Ter) c.517C>T (p.Gln173Ter) n.683C>T | |
| 8 | g.18222379A= | CA1768101115 | NAT1 | c.332A= (p.Gln111=) c.518A= (p.Gln173=) n.684A= | |
| 8 | g.18222379A>C | CA370445084 | NAT1 | c.332A>C (p.Gln111Pro) c.518A>C (p.Gln173Pro) n.684A>C | |
| 8 | g.18222379A>G | CA370445085 | NAT1 | c.332A>G (p.Gln111Arg) c.518A>G (p.Gln173Arg) n.684A>G | |
| 8 | g.18222379A>T | CA4651377 | NAT1 | c.332A>T (p.Gln111Leu) c.518A>T (p.Gln173Leu) n.684A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222381_18222382insAGAAGG | CA2830544404 | NAT1 | c.334_335insAGAAGG (p.Gln111_Val112insGluLys) c.520_521insAGAAGG (p.Gln173_Val174insGluLys) n.686_687insAGAAGG | |
| 8 | g.18222380G>A | CA4651378 | NAT1 | c.333G>A (p.Gln111=) c.519G>A (p.Gln173=) n.685G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222380G>C | CA370445086 | NAT1 | c.333G>C (p.Gln111His) c.519G>C (p.Gln173His) n.685G>C | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222380G= | CA1768101116 | NAT1 | c.333G= (p.Gln111=) c.519G= (p.Gln173=) n.685G= | |
| 8 | g.18222380G>T | CA370445087 | NAT1 | c.333G>T (p.Gln111His) c.519G>T (p.Gln173His) n.685G>T | |
| 8 | g.18222381G>A | CA370445089 | NAT1 | c.334G>A (p.Val112Met) c.520G>A (p.Val174Met) n.686G>A | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222381G>C | CA370445090 | NAT1 | c.334G>C (p.Val112Leu) c.520G>C (p.Val174Leu) n.686G>C | |
| 8 | g.18222381G= | CA1768101117 | NAT1 | c.334G= (p.Val112=) c.520G= (p.Val174=) n.686G= | |
| 8 | g.18222381G>T | CA370445088 | NAT1 | c.334G>T (p.Val112Leu) c.520G>T (p.Val174Leu) n.686G>T | gnomAD v4 |
| 8 | g.18222382T>A | CA370445092 | NAT1 | c.335T>A (p.Val112Glu) c.521T>A (p.Val174Glu) n.687T>A | |
| 8 | g.18222382T>C | CA173180336 | NAT1 | c.335T>C (p.Val112Ala) c.521T>C (p.Val174Ala) n.687T>C | dbSNP |
| 8 | g.18222382T>G | CA370445091 | NAT1 | c.335T>G (p.Val112Gly) c.521T>G (p.Val174Gly) n.687T>G | |
| 8 | g.18222382T= | CA1768101118 | NAT1 | c.335T= (p.Val112=) c.521T= (p.Val174=) n.687T= | |
| 8 | g.18222383G>A | CA459877581 | NAT1 | c.336G>A (p.Val112=) c.522G>A (p.Val174=) n.688G>A | |
| 8 | g.18222383G>C | CA459877582 | NAT1 | c.336G>C (p.Val112=) c.522G>C (p.Val174=) n.688G>C | |
| 8 | g.18222383G>T | CA459877583 | NAT1 | c.336G>T (p.Val112=) c.522G>T (p.Val174=) n.688G>T | COSMIC COSMIC |
| 8 | g.18222384A= | CA1768101119 | NAT1 | c.337A= (p.Thr113=) c.523A= (p.Thr175=) n.689A= | |
| 8 | g.18222384A>C | CA370445093 | NAT1 | c.337A>C (p.Thr113Pro) c.523A>C (p.Thr175Pro) n.689A>C | |
| 8 | g.18222384A>G | CA370445094 | NAT1 | c.337A>G (p.Thr113Ala) c.523A>G (p.Thr175Ala) n.689A>G | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222384A>T | CA370445095 | NAT1 | c.337A>T (p.Thr113Ser) c.523A>T (p.Thr175Ser) n.689A>T | |
| 8 | g.18222385C>A | CA370445096 | NAT1 | c.338C>A (p.Thr113Asn) c.524C>A (p.Thr175Asn) n.690C>A | |
| 8 | g.18222385C= | CA1768101120 | NAT1 | c.338C= (p.Thr113=) c.524C= (p.Thr175=) n.690C= | |
| 8 | g.18222385C>G | CA4651379 | NAT1 | c.338C>G (p.Thr113Ser) c.524C>G (p.Thr175Ser) n.690C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222385C>T | CA370445097 | NAT1 | c.338C>T (p.Thr113Ile) c.524C>T (p.Thr175Ile) n.690C>T | |
| 8 | g.18222386C>A | CA459877584 | NAT1 | c.339C>A (p.Thr113=) c.525C>A (p.Thr175=) n.691C>A | |
| 8 | g.18222386C= | CA1768101121 | NAT1 | c.339C= (p.Thr113=) c.525C= (p.Thr175=) n.691C= | |
| 8 | g.18222386C>G | CA459877585 | NAT1 | c.339C>G (p.Thr113=) c.525C>G (p.Thr175=) n.691C>G | dbSNP gnomAD v4 |
| 8 | g.18222386C>T | CA459877586 | NAT1 | c.339C>T (p.Thr113=) c.525C>T (p.Thr175=) n.691C>T | |
| 8 | g.18222387A= | CA1768101122 | NAT1 | c.340A= (p.Ile114=) c.526A= (p.Ile176=) n.692A= | |
| 8 | g.18222387A>C | CA370445098 | NAT1 | c.340A>C (p.Ile114Leu) c.526A>C (p.Ile176Leu) n.692A>C | |
| 8 | g.18222387A>G | CA4651380 | NAT1 | c.340A>G (p.Ile114Val) c.526A>G (p.Ile176Val) n.692A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222387A>T | CA370445099 | NAT1 | c.340A>T (p.Ile114Phe) c.526A>T (p.Ile176Phe) n.692A>T | |
| 8 | g.18222388T>A | CA4651382 | NAT1 | c.341T>A (p.Ile114Asn) c.527T>A (p.Ile176Asn) n.693T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222388T>C | CA4651381 | NAT1 | c.341T>C (p.Ile114Thr) c.527T>C (p.Ile176Thr) n.693T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222388T>G | CA370445100 | NAT1 | c.341T>G (p.Ile114Ser) c.527T>G (p.Ile176Ser) n.693T>G | |
| 8 | g.18222388T= | CA1768101123 | NAT1 | c.341T= (p.Ile114=) c.527T= (p.Ile176=) n.693T= | |
| 8 | g.18222389T>A | CA459877588 | NAT1 | c.342T>A (p.Ile114=) c.528T>A (p.Ile176=) n.694T>A | |
| 8 | g.18222389T>C | CA4651383 | NAT1 | c.342T>C (p.Ile114=) c.528T>C (p.Ile176=) n.694T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222389T>G | CA370445101 | NAT1 | c.342T>G (p.Ile114Met) c.528T>G (p.Ile176Met) n.694T>G | |
| 8 | g.18222389T= | CA1768101124 | NAT1 | c.342T= (p.Ile114=) c.528T= (p.Ile176=) n.694T= | |
| 8 | g.18222390G>A | CA370445102 | NAT1 | c.343G>A (p.Asp115Asn) c.529G>A (p.Asp177Asn) n.695G>A | dbSNP |
| 8 | g.18222390G>C | CA370445103 | NAT1 | c.343G>C (p.Asp115His) c.529G>C (p.Asp177His) n.695G>C | |
| 8 | g.18222390G= | CA1768101125 | NAT1 | c.343G= (p.Asp115=) c.529G= (p.Asp177=) n.695G= | |
| 8 | g.18222390G>T | CA370445104 | NAT1 | c.343G>T (p.Asp115Tyr) c.529G>T (p.Asp177Tyr) n.695G>T | |
| 8 | g.18222391A>C | CA370445105 | NAT1 | c.344A>C (p.Asp115Ala) c.530A>C (p.Asp177Ala) n.696A>C | |
| 8 | g.18222391A>G | CA370445106 | NAT1 | c.344A>G (p.Asp115Gly) c.530A>G (p.Asp177Gly) n.696A>G | |
| 8 | g.18222391A>T | CA370445107 | NAT1 | c.344A>T (p.Asp115Val) c.530A>T (p.Asp177Val) n.696A>T | |
| 8 | g.18222392T>A | CA4651384 | NAT1 | c.345T>A (p.Asp115Glu) c.531T>A (p.Asp177Glu) n.697T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222392T>C | CA459877590 | NAT1 | c.345T>C (p.Asp115=) c.531T>C (p.Asp177=) n.697T>C | |
| 8 | g.18222392T>G | CA370445108 | NAT1 | c.345T>G (p.Asp115Glu) c.531T>G (p.Asp177Glu) n.697T>G | |
| 8 | g.18222392T= | CA1768101126 | NAT1 | c.345T= (p.Asp115=) c.531T= (p.Asp177=) n.697T= | |
| 8 | g.18222393G>A | CA370445109 | NAT1 | c.346G>A (p.Gly116Ser) c.532G>A (p.Gly178Ser) n.698G>A | gnomAD v4 |
| 8 | g.18222393G>C | CA370445110 | NAT1 | c.346G>C (p.Gly116Arg) c.532G>C (p.Gly178Arg) n.698G>C | |
| 8 | g.18222393G>T | CA370445111 | NAT1 | c.346G>T (p.Gly116Cys) c.532G>T (p.Gly178Cys) n.698G>T | |
| 8 | g.18222394G>A | CA370445113 | NAT1 | c.347G>A (p.Gly116Asp) c.533G>A (p.Gly178Asp) n.699G>A | COSMIC COSMIC |
| 8 | g.18222394G>C | CA370445114 | NAT1 | c.347G>C (p.Gly116Ala) c.533G>C (p.Gly178Ala) n.699G>C | gnomAD v4 |
| 8 | g.18222394G>T | CA370445112 | NAT1 | c.347G>T (p.Gly116Val) c.533G>T (p.Gly178Val) n.699G>T | |
| 8 | g.18222395C>A | CA459877591 | NAT1 | c.348C>A (p.Gly116=) c.534C>A (p.Gly178=) n.700C>A | |
| 8 | g.18222395C= | CA1768101127 | NAT1 | c.348C= (p.Gly116=) c.534C= (p.Gly178=) n.700C= | |
| 8 | g.18222395C>G | CA459877592 | NAT1 | c.348C>G (p.Gly116=) c.534C>G (p.Gly178=) n.700C>G | |
| 8 | g.18222395C>T | CA459877593 | NAT1 | c.348C>T (p.Gly116=) c.534C>T (p.Gly178=) n.700C>T | dbSNP |
| 8 | g.18222396A>C | CA459877697 | NAT1 | c.349A>C (p.Arg117=) c.535A>C (p.Arg179=) n.701A>C | |
| 8 | g.18222396A>G | CA370445115 | NAT1 | c.349A>G (p.Arg117Gly) c.535A>G (p.Arg179Gly) n.701A>G | |
| 8 | g.18222396A>T | CA370445116 | NAT1 | c.349A>T (p.Arg117Trp) c.535A>T (p.Arg179Trp) n.701A>T | |
| 8 | g.18222397G>A | CA370445117 | NAT1 | c.350G>A (p.Arg117Lys) c.536G>A (p.Arg179Lys) n.702G>A | dbSNP gnomAD v4 |
| 8 | g.18222397G>C | CA173180346 | NAT1 | c.350G>C (p.Arg117Thr) c.536G>C (p.Arg179Thr) n.702G>C | dbSNP gnomAD v4 |
| 8 | g.18222397G= | CA1768101128 | NAT1 | c.350G= (p.Arg117=) c.536G= (p.Arg179=) n.702G= | |
| 8 | g.18222397G>T | CA370445118 | NAT1 | c.350G>T (p.Arg117Met) c.536G>T (p.Arg179Met) n.702G>T | |
| 8 | g.18222397_18222398delinsCC | CA173180344 | NAT1 | c.350_351delinsCC (p.Arg117Thr) c.536_537delinsCC (p.Arg179Thr) n.702_703delinsCC | dbSNP |
| 8 | g.18222397_18222398delinsGG | CA1768101129 | NAT1 | c.350_351delinsGG (p.Arg117=) c.536_537delinsGG (p.Arg179=) n.702_703delinsGG | |
| 8 | g.18222398G>A | CA459877702 | NAT1 | c.351G>A (p.Arg117=) c.537G>A (p.Arg179=) n.703G>A | |
| 8 | g.18222398G>C | CA173180347 | NAT1 | c.351G>C (p.Arg117Ser) c.537G>C (p.Arg179Ser) n.703G>C | dbSNP |
| 8 | g.18222398G= | CA1768101130 | NAT1 | c.351G= (p.Arg117=) c.537G= (p.Arg179=) n.703G= | |
| 8 | g.18222398G>T | CA370445119 | NAT1 | c.351G>T (p.Arg117Ser) c.537G>T (p.Arg179Ser) n.703G>T | |
| 8 | g.18222399A>C | CA370445120 | NAT1 | c.352A>C (p.Asn118His) c.538A>C (p.Asn180His) n.704A>C | |
| 8 | g.18222399A>G | CA370445122 | NAT1 | c.352A>G (p.Asn118Asp) c.538A>G (p.Asn180Asp) n.704A>G | |
| 8 | g.18222399A>T | CA370445121 | NAT1 | c.352A>T (p.Asn118Tyr) c.538A>T (p.Asn180Tyr) n.704A>T | |
| 8 | g.18222400A>C | CA370445123 | NAT1 | c.353A>C (p.Asn118Thr) c.539A>C (p.Asn180Thr) n.705A>C | |
| 8 | g.18222400A>G | CA370445124 | NAT1 | c.353A>G (p.Asn118Ser) c.539A>G (p.Asn180Ser) n.705A>G | COSMIC COSMIC |
| 8 | g.18222400A>T | CA370445125 | NAT1 | c.353A>T (p.Asn118Ile) c.539A>T (p.Asn180Ile) n.705A>T | |
| 8 | g.18222401C>A | CA4651385 | NAT1 | c.354C>A (p.Asn118Lys) c.540C>A (p.Asn180Lys) n.706C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222401C= | CA1768101131 | NAT1 | c.354C= (p.Asn118=) c.540C= (p.Asn180=) n.706C= | |
| 8 | g.18222401C>G | CA370445126 | NAT1 | c.354C>G (p.Asn118Lys) c.540C>G (p.Asn180Lys) n.706C>G | |
| 8 | g.18222401C>T | CA459877706 | NAT1 | c.354C>T (p.Asn118=) c.540C>T (p.Asn180=) n.706C>T | |
| 8 | g.18222402T>A | CA370445127 | NAT1 | c.355T>A (p.Tyr119Asn) c.541T>A (p.Tyr181Asn) n.707T>A | gnomAD v4 |
| 8 | g.18222402T>C | CA4651386 | NAT1 | c.355T>C (p.Tyr119His) c.541T>C (p.Tyr181His) n.707T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222402T>G | CA370445128 | NAT1 | c.355T>G (p.Tyr119Asp) c.541T>G (p.Tyr181Asp) n.707T>G | |
| 8 | g.18222402T= | CA1768101132 | NAT1 | c.355T= (p.Tyr119=) c.541T= (p.Tyr181=) n.707T= | |
| 8 | g.18222403A>C | CA370445129 | NAT1 | c.356A>C (p.Tyr119Ser) c.542A>C (p.Tyr181Ser) n.708A>C | |
| 8 | g.18222403A>G | CA370445130 | NAT1 | c.356A>G (p.Tyr119Cys) c.542A>G (p.Tyr181Cys) n.708A>G | dbSNP |
| 8 | g.18222403A>T | CA370445131 | NAT1 | c.356A>T (p.Tyr119Phe) c.542A>T (p.Tyr181Phe) n.708A>T | |
| 8 | g.18222404C>A | CA370445132 | NAT1 | c.357C>A (p.Tyr119Ter) c.543C>A (p.Tyr181Ter) n.709C>A | |
| 8 | g.18222404C= | CA1768101133 | NAT1 | c.357C= (p.Tyr119=) c.543C= (p.Tyr181=) n.709C= | |
| 8 | g.18222404C>G | CA370445133 | NAT1 | c.357C>G (p.Tyr119Ter) c.543C>G (p.Tyr181Ter) n.709C>G | |
| 8 | g.18222404C>T | CA459877708 | NAT1 | c.357C>T (p.Tyr119=) c.543C>T (p.Tyr181=) n.709C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222405A= | CA1768101134 | NAT1 | c.358A= (p.Ile120=) c.544A= (p.Ile182=) n.710A= | |
| 8 | g.18222405A>C | CA370445134 | NAT1 | c.358A>C (p.Ile120Leu) c.544A>C (p.Ile182Leu) n.710A>C | |
| 8 | g.18222405A>G | CA370445135 | NAT1 | c.358A>G (p.Ile120Val) c.544A>G (p.Ile182Val) n.710A>G | dbSNP gnomAD v4 |
| 8 | g.18222405A>T | CA4651387 | NAT1 | c.358A>T (p.Ile120Phe) c.544A>T (p.Ile182Phe) n.710A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222406T>A | CA370445136 | NAT1 | c.359T>A (p.Ile120Asn) c.545T>A (p.Ile182Asn) n.711T>A | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222406T>C | CA370445137 | NAT1 | c.359T>C (p.Ile120Thr) c.545T>C (p.Ile182Thr) n.711T>C | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222406T>G | CA4651388 | NAT1 | c.359T>G (p.Ile120Ser) c.545T>G (p.Ile182Ser) n.711T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222406T= | CA1768101135 | NAT1 | c.359T= (p.Ile120=) c.545T= (p.Ile182=) n.711T= | |
| 8 | g.18222407T>A | CA459877713 | NAT1 | c.360T>A (p.Ile120=) c.546T>A (p.Ile182=) n.712T>A | |
| 8 | g.18222407T>C | CA459877715 | NAT1 | c.360T>C (p.Ile120=) c.546T>C (p.Ile182=) n.712T>C | |
| 8 | g.18222407T>G | CA370445138 | NAT1 | c.360T>G (p.Ile120Met) c.546T>G (p.Ile182Met) n.712T>G | |
| 8 | g.18222408G>A | CA370445141 | NAT1 | c.361G>A (p.Val121Ile) c.547G>A (p.Val183Ile) n.713G>A | |
| 8 | g.18222408G>C | CA370445139 | NAT1 | c.361G>C (p.Val121Leu) c.547G>C (p.Val183Leu) n.713G>C | |
| 8 | g.18222408G>T | CA370445140 | NAT1 | c.361G>T (p.Val121Phe) c.547G>T (p.Val183Phe) n.713G>T | |
| 8 | g.18222409T>A | CA370445142 | NAT1 | c.362T>A (p.Val121Asp) c.548T>A (p.Val183Asp) n.714T>A | |
| 8 | g.18222409T>C | CA370445144 | NAT1 | c.362T>C (p.Val121Ala) c.548T>C (p.Val183Ala) n.714T>C | |
| 8 | g.18222409T>G | CA370445143 | NAT1 | c.362T>G (p.Val121Gly) c.548T>G (p.Val183Gly) n.714T>G | |
| 8 | g.18222410C>A | CA459877720 | NAT1 | c.363C>A (p.Val121=) c.549C>A (p.Val183=) n.715C>A | gnomAD v4 |
| 8 | g.18222410C= | CA1768101136 | NAT1 | c.363C= (p.Val121=) c.549C= (p.Val183=) n.715C= | |
| 8 | g.18222410C>G | CA459877722 | NAT1 | c.363C>G (p.Val121=) c.549C>G (p.Val183=) n.715C>G | gnomAD v4 |
| 8 | g.18222410C>T | CA4651389 | NAT1 | c.363C>T (p.Val121=) c.549C>T (p.Val183=) n.715C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222411G>A | CA370445145 | NAT1 | c.364G>A (p.Asp122Asn) c.550G>A (p.Asp184Asn) n.716G>A | gnomAD v4 COSMIC COSMIC |
| 8 | g.18222411G>C | CA370445146 | NAT1 | c.364G>C (p.Asp122His) c.550G>C (p.Asp184His) n.716G>C | |
| 8 | g.18222411G>T | CA370445147 | NAT1 | c.364G>T (p.Asp122Tyr) c.550G>T (p.Asp184Tyr) n.716G>T | |
| 8 | g.18222412A>C | CA370445148 | NAT1 | c.365A>C (p.Asp122Ala) c.551A>C (p.Asp184Ala) n.717A>C | |
| 8 | g.18222412A>G | CA370445149 | NAT1 | c.365A>G (p.Asp122Gly) c.551A>G (p.Asp184Gly) n.717A>G | |
| 8 | g.18222412A>T | CA370445150 | NAT1 | c.365A>T (p.Asp122Val) c.551A>T (p.Asp184Val) n.717A>T | |
| 8 | g.18222413T>A | CA370445151 | NAT1 | c.366T>A (p.Asp122Glu) c.552T>A (p.Asp184Glu) n.718T>A | |
| 8 | g.18222413T>C | CA459877727 | NAT1 | c.366T>C (p.Asp122=) c.552T>C (p.Asp184=) n.718T>C | |
| 8 | g.18222413T>G | CA370445152 | NAT1 | c.366T>G (p.Asp122Glu) c.552T>G (p.Asp184Glu) n.718T>G | gnomAD v4 |
| 8 | g.18222414G>A | CA370445153 | NAT1 | c.367G>A (p.Ala123Thr) c.553G>A (p.Ala185Thr) n.719G>A | gnomAD v4 |
| 8 | g.18222414G>C | CA370445154 | NAT1 | c.367G>C (p.Ala123Pro) c.553G>C (p.Ala185Pro) n.719G>C | gnomAD v4 |
| 8 | g.18222414G>T | CA370445155 | NAT1 | c.367G>T (p.Ala123Ser) c.553G>T (p.Ala185Ser) n.719G>T | |
| 8 | g.18222415C>A | CA370445157 | NAT1 | c.368C>A (p.Ala123Asp) c.554C>A (p.Ala185Asp) n.720C>A | |
| 8 | g.18222415C= | CA1768101137 | NAT1 | c.368C= (p.Ala123=) c.554C= (p.Ala185=) n.720C= | |
| 8 | g.18222415C>G | CA370445156 | NAT1 | c.368C>G (p.Ala123Gly) c.554C>G (p.Ala185Gly) n.720C>G | |
| 8 | g.18222415C>T | CA4651390 | NAT1 | c.368C>T (p.Ala123Val) c.554C>T (p.Ala185Val) n.720C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222416T>A | CA459877733 | NAT1 | c.369T>A (p.Ala123=) c.555T>A (p.Ala185=) n.721T>A | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222416T>C | CA459877731 | NAT1 | c.369T>C (p.Ala123=) c.555T>C (p.Ala185=) n.721T>C | |
| 8 | g.18222416T>G | CA459877732 | NAT1 | c.369T>G (p.Ala123=) c.555T>G (p.Ala185=) n.721T>G | |
| 8 | g.18222416T= | CA1768101138 | NAT1 | c.369T= (p.Ala123=) c.555T= (p.Ala185=) n.721T= | |
| 8 | g.18222417G>A | CA370445158 | NAT1 | c.370G>A (p.Gly124Arg) c.556G>A (p.Gly186Arg) n.722G>A | |
| 8 | g.18222417G>C | CA370445159 | NAT1 | c.370G>C (p.Gly124Arg) c.556G>C (p.Gly186Arg) n.722G>C | |
| 8 | g.18222417G>T | CA370445160 | NAT1 | c.370G>T (p.Gly124Trp) c.556G>T (p.Gly186Trp) n.722G>T | |
| 8 | g.18222418G>A | CA370445161 | NAT1 | c.371G>A (p.Gly124Glu) c.557G>A (p.Gly186Glu) n.723G>A | |
| 8 | g.18222418G>C | CA370445162 | NAT1 | c.371G>C (p.Gly124Ala) c.557G>C (p.Gly186Ala) n.723G>C | gnomAD v4 |
| 8 | g.18222418G>T | CA370445163 | NAT1 | c.371G>T (p.Gly124Val) c.557G>T (p.Gly186Val) n.723G>T | |
| 8 | g.18222419G>A | CA459877735 | NAT1 | c.372G>A (p.Gly124=) c.558G>A (p.Gly186=) n.724G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222419G>C | CA4651391 | NAT1 | c.372G>C (p.Gly124=) c.558G>C (p.Gly186=) n.724G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222419G= | CA1768101139 | NAT1 | c.372G= (p.Gly124=) c.558G= (p.Gly186=) n.724G= | |
| 8 | g.18222419G>T | CA459877734 | NAT1 | c.372G>T (p.Gly124=) c.558G>T (p.Gly186=) n.724G>T | |
| 8 | g.18222420T>A | CA370445164 | NAT1 | c.373T>A (p.Phe125Ile) c.559T>A (p.Phe187Ile) n.725T>A | |
| 8 | g.18222420T>C | CA370445165 | NAT1 | c.373T>C (p.Phe125Leu) c.559T>C (p.Phe187Leu) n.725T>C | |
| 8 | g.18222420T>G | CA370445166 | NAT1 | c.373T>G (p.Phe125Val) c.559T>G (p.Phe187Val) n.725T>G | |
| 8 | g.18222421T>A | CA370445167 | NAT1 | c.374T>A (p.Phe125Tyr) c.560T>A (p.Phe187Tyr) n.726T>A | |
| 8 | g.18222421T>C | CA370445168 | NAT1 | c.374T>C (p.Phe125Ser) c.560T>C (p.Phe187Ser) n.726T>C | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222421T>G | CA370445169 | NAT1 | c.374T>G (p.Phe125Cys) c.560T>G (p.Phe187Cys) n.726T>G | |
| 8 | g.18222421T= | CA1768101140 | NAT1 | c.374T= (p.Phe125=) c.560T= (p.Phe187=) n.726T= | |
| 8 | g.18222422T>A | CA370445171 | NAT1 | c.375T>A (p.Phe125Leu) c.561T>A (p.Phe187Leu) n.727T>A | |
| 8 | g.18222422T>C | CA459877740 | NAT1 | c.375T>C (p.Phe125=) c.561T>C (p.Phe187=) n.727T>C | gnomAD v4 |
| 8 | g.18222422T>G | CA370445170 | NAT1 | c.375T>G (p.Phe125Leu) c.561T>G (p.Phe187Leu) n.727T>G | dbSNP |
| 8 | g.18222422T= | CA1768101141 | NAT1 | c.375T= (p.Phe125=) c.561T= (p.Phe187=) n.727T= | |
| 8 | g.18222423G>A | CA370445172 | NAT1 | c.376G>A (p.Gly126Arg) c.562G>A (p.Gly188Arg) n.728G>A | |
| 8 | g.18222423G>C | CA370445173 | NAT1 | c.376G>C (p.Gly126Arg) c.562G>C (p.Gly188Arg) n.728G>C | |
| 8 | g.18222423G>T | CA370445174 | NAT1 | c.376G>T (p.Gly126Ter) c.562G>T (p.Gly188Ter) n.728G>T | |
| 8 | g.18222424G>A | CA370445175 | NAT1 | c.377G>A (p.Gly126Glu) c.563G>A (p.Gly188Glu) n.729G>A | |
| 8 | g.18222424G>C | CA370445176 | NAT1 | c.377G>C (p.Gly126Ala) c.563G>C (p.Gly188Ala) n.729G>C | |
| 8 | g.18222424G>T | CA370445177 | NAT1 | c.377G>T (p.Gly126Val) c.563G>T (p.Gly188Val) n.729G>T | |
| 8 | g.18222425A>C | CA459877747 | NAT1 | c.378A>C (p.Gly126=) c.564A>C (p.Gly188=) n.730A>C | |
| 8 | g.18222425A>G | CA459877745 | NAT1 | c.378A>G (p.Gly126=) c.564A>G (p.Gly188=) n.730A>G | |
| 8 | g.18222425A>T | CA459877746 | NAT1 | c.378A>T (p.Gly126=) c.564A>T (p.Gly188=) n.730A>T | |
| 8 | g.18222426C>A | CA370445179 | NAT1 | c.379C>A (p.Arg127Ser) c.565C>A (p.Arg189Ser) n.731C>A | |
| 8 | g.18222426C= | CA1768101142 | NAT1 | c.379C= (p.Arg127=) c.565C= (p.Arg189=) n.731C= | |
| 8 | g.18222426C>G | CA370445178 | NAT1 | c.379C>G (p.Arg127Gly) c.565C>G (p.Arg189Gly) n.731C>G | |
| 8 | g.18222426C>T | CA4651392 | NAT1 | c.379C>T (p.Arg127Cys) c.565C>T (p.Arg189Cys) n.731C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 8 | g.18222427G>A | CA4651394 | NAT1 | c.380G>A (p.Arg127His) c.566G>A (p.Arg189His) n.732G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222427G>C | CA370445180 | NAT1 | c.380G>C (p.Arg127Pro) c.566G>C (p.Arg189Pro) n.732G>C | |
| 8 | g.18222427G= | CA1768101143 | NAT1 | c.380G= (p.Arg127=) c.566G= (p.Arg189=) n.732G= | |
| 8 | g.18222427G>T | CA4651393 | NAT1 | c.380G>T (p.Arg127Leu) c.566G>T (p.Arg189Leu) n.732G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222428C>A | CA459877751 | NAT1 | c.381C>A (p.Arg127=) c.567C>A (p.Arg189=) n.733C>A | |
| 8 | g.18222428C= | CA1768101144 | NAT1 | c.381C= (p.Arg127=) c.567C= (p.Arg189=) n.733C= | |
| 8 | g.18222428C>G | CA459877752 | NAT1 | c.381C>G (p.Arg127=) c.567C>G (p.Arg189=) n.733C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222428C>T | CA459877753 | NAT1 | c.381C>T (p.Arg127=) c.567C>T (p.Arg189=) n.733C>T | |
| 8 | g.18222429T>A | CA370445181 | NAT1 | c.382T>A (p.Ser128Thr) c.568T>A (p.Ser190Thr) n.734T>A | |
| 8 | g.18222429T>C | CA370445182 | NAT1 | c.382T>C (p.Ser128Pro) c.568T>C (p.Ser190Pro) n.734T>C | |
| 8 | g.18222429T>G | CA370445183 | NAT1 | c.382T>G (p.Ser128Ala) c.568T>G (p.Ser190Ala) n.734T>G | |
| 8 | g.18222430C>A | CA370445184 | NAT1 | c.383C>A (p.Ser128Ter) c.569C>A (p.Ser190Ter) n.735C>A | |
| 8 | g.18222430C= | CA1768101145 | NAT1 | c.383C= (p.Ser128=) c.569C= (p.Ser190=) n.735C= | |
| 8 | g.18222430C>G | CA370445185 | NAT1 | c.383C>G (p.Ser128Ter) c.569C>G (p.Ser190Ter) n.735C>G | |
| 8 | g.18222430C>T | CA4651395 | NAT1 | c.383C>T (p.Ser128Leu) c.569C>T (p.Ser190Leu) n.735C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222431A= | CA1768101146 | NAT1 | c.384A= (p.Ser128=) c.570A= (p.Ser190=) n.736A= | |
| 8 | g.18222431A>C | CA459877757 | NAT1 | c.384A>C (p.Ser128=) c.570A>C (p.Ser190=) n.736A>C | |
| 8 | g.18222431A>G | CA459877758 | NAT1 | c.384A>G (p.Ser128=) c.570A>G (p.Ser190=) n.736A>G | dbSNP gnomAD v4 |
| 8 | g.18222431A>T | CA459877759 | NAT1 | c.384A>T (p.Ser128=) c.570A>T (p.Ser190=) n.736A>T | |
| 8 | g.18222432T>A | CA370445186 | NAT1 | c.385T>A (p.Tyr129Asn) c.571T>A (p.Tyr191Asn) n.737T>A | |
| 8 | g.18222432T>C | CA370445187 | NAT1 | c.385T>C (p.Tyr129His) c.571T>C (p.Tyr191His) n.737T>C | |
| 8 | g.18222432T>G | CA370445188 | NAT1 | c.385T>G (p.Tyr129Asp) c.571T>G (p.Tyr191Asp) n.737T>G | |
| 8 | g.18222433A= | CA1768101147 | NAT1 | c.386A= (p.Tyr129=) c.572A= (p.Tyr191=) n.738A= | |
| 8 | g.18222433A>C | CA370445189 | NAT1 | c.386A>C (p.Tyr129Ser) c.572A>C (p.Tyr191Ser) n.738A>C | dbSNP |
| 8 | g.18222433A>G | CA4651396 | NAT1 | c.386A>G (p.Tyr129Cys) c.572A>G (p.Tyr191Cys) n.738A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222433A>T | CA173180361 | NAT1 | c.386A>T (p.Tyr129Phe) c.572A>T (p.Tyr191Phe) n.738A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222434C>A | CA370445190 | NAT1 | c.387C>A (p.Tyr129Ter) c.573C>A (p.Tyr191Ter) n.739C>A | |
| 8 | g.18222434C= | CA1768101148 | NAT1 | c.387C= (p.Tyr129=) c.573C= (p.Tyr191=) n.739C= | |
| 8 | g.18222434C>G | CA370445191 | NAT1 | c.387C>G (p.Tyr129Ter) c.573C>G (p.Tyr191Ter) n.739C>G | dbSNP |
| 8 | g.18222434C>T | CA4651397 | NAT1 | c.387C>T (p.Tyr129=) c.573C>T (p.Tyr191=) n.739C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222435C>A | CA370445192 | NAT1 | c.388C>A (p.Gln130Lys) c.574C>A (p.Gln192Lys) n.740C>A | |
| 8 | g.18222435C>G | CA370445193 | NAT1 | c.388C>G (p.Gln130Glu) c.574C>G (p.Gln192Glu) n.740C>G | |
| 8 | g.18222435C>T | CA370445194 | NAT1 | c.388C>T (p.Gln130Ter) c.574C>T (p.Gln192Ter) n.740C>T | gnomAD v4 |
| 8 | g.18222436A>C | CA370445197 | NAT1 | c.389A>C (p.Gln130Pro) c.575A>C (p.Gln192Pro) n.741A>C | |
| 8 | g.18222436A>G | CA370445195 | NAT1 | c.389A>G (p.Gln130Arg) c.575A>G (p.Gln192Arg) n.741A>G | gnomAD v4 |
| 8 | g.18222436A>T | CA370445196 | NAT1 | c.389A>T (p.Gln130Leu) c.575A>T (p.Gln192Leu) n.741A>T | |
| 8 | g.18222437G>A | CA4651399 | NAT1 | c.390G>A (p.Gln130=) c.576G>A (p.Gln192=) n.742G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222437G>C | CA4651398 | NAT1 | c.390G>C (p.Gln130His) c.576G>C (p.Gln192His) n.742G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222437G= | CA1768101149 | NAT1 | c.390G= (p.Gln130=) c.576G= (p.Gln192=) n.742G= | |
| 8 | g.18222437G>T | CA370445198 | NAT1 | c.390G>T (p.Gln130His) c.576G>T (p.Gln192His) n.742G>T | |
| 8 | g.18222438A>C | CA370445199 | NAT1 | c.391A>C (p.Met131Leu) c.577A>C (p.Met193Leu) n.743A>C | |
| 8 | g.18222438A>G | CA370445200 | NAT1 | c.391A>G (p.Met131Val) c.577A>G (p.Met193Val) n.743A>G | |
| 8 | g.18222438A>T | CA370445201 | NAT1 | c.391A>T (p.Met131Leu) c.577A>T (p.Met193Leu) n.743A>T | gnomAD v4 |
| 8 | g.18222439T>A | CA370445202 | NAT1 | c.392T>A (p.Met131Lys) c.578T>A (p.Met193Lys) n.744T>A | gnomAD v4 |
| 8 | g.18222439T>C | CA370445203 | NAT1 | c.392T>C (p.Met131Thr) c.578T>C (p.Met193Thr) n.744T>C | |
| 8 | g.18222439T>G | CA370445204 | NAT1 | c.392T>G (p.Met131Arg) c.578T>G (p.Met193Arg) n.744T>G | |
| 8 | g.18222440G>A | CA370445205 | NAT1 | c.393G>A (p.Met131Ile) c.579G>A (p.Met193Ile) n.745G>A | |
| 8 | g.18222440G>C | CA370445206 | NAT1 | c.393G>C (p.Met131Ile) c.579G>C (p.Met193Ile) n.745G>C | |
| 8 | g.18222440G>T | CA370445207 | NAT1 | c.393G>T (p.Met131Ile) c.579G>T (p.Met193Ile) n.745G>T | |
| 8 | g.18222441T>A | CA370445208 | NAT1 | c.394T>A (p.Trp132Arg) c.580T>A (p.Trp194Arg) n.746T>A | |
| 8 | g.18222441T>C | CA4651400 | NAT1 | c.394T>C (p.Trp132Arg) c.580T>C (p.Trp194Arg) n.746T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222441T>G | CA370445209 | NAT1 | c.394T>G (p.Trp132Gly) c.580T>G (p.Trp194Gly) n.746T>G | |
| 8 | g.18222441T= | CA1768101150 | NAT1 | c.394T= (p.Trp132=) c.580T= (p.Trp194=) n.746T= | |
| 8 | g.18222442G>A | CA370445212 | NAT1 | c.395G>A (p.Trp132Ter) c.581G>A (p.Trp194Ter) n.747G>A | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222442G>C | CA370445210 | NAT1 | c.395G>C (p.Trp132Ser) c.581G>C (p.Trp194Ser) n.747G>C | |
| 8 | g.18222442G= | CA1768101151 | NAT1 | c.395G= (p.Trp132=) c.581G= (p.Trp194=) n.747G= | |
| 8 | g.18222442G>T | CA370445211 | NAT1 | c.395G>T (p.Trp132Leu) c.581G>T (p.Trp194Leu) n.747G>T | |
| 8 | g.18222443G>A | CA370445213 | NAT1 | c.396G>A (p.Trp132Ter) c.582G>A (p.Trp194Ter) n.748G>A | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222443G>C | CA370445214 | NAT1 | c.396G>C (p.Trp132Cys) c.582G>C (p.Trp194Cys) n.748G>C | dbSNP gnomAD v2 |
| 8 | g.18222443G= | CA1768101152 | NAT1 | c.396G= (p.Trp132=) c.582G= (p.Trp194=) n.748G= | |
| 8 | g.18222443G>T | CA4651401 | NAT1 | c.396G>T (p.Trp132Cys) c.582G>T (p.Trp194Cys) n.748G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222444C>A | CA370445215 | NAT1 | c.397C>A (p.Gln133Lys) c.583C>A (p.Gln195Lys) n.749C>A | |
| 8 | g.18222444C= | CA1768101153 | NAT1 | c.397C= (p.Gln133=) c.583C= (p.Gln195=) n.749C= | |
| 8 | g.18222444C>G | CA370445216 | NAT1 | c.397C>G (p.Gln133Glu) c.583C>G (p.Gln195Glu) n.749C>G | |
| 8 | g.18222444C>T | CA370445217 | NAT1 | c.397C>T (p.Gln133Ter) c.583C>T (p.Gln195Ter) n.749C>T | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222445A>C | CA370445218 | NAT1 | c.398A>C (p.Gln133Pro) c.584A>C (p.Gln195Pro) n.750A>C | |
| 8 | g.18222445A>G | CA370445219 | NAT1 | c.398A>G (p.Gln133Arg) c.584A>G (p.Gln195Arg) n.750A>G | |
| 8 | g.18222445A>T | CA370445220 | NAT1 | c.398A>T (p.Gln133Leu) c.584A>T (p.Gln195Leu) n.750A>T | |
| 8 | g.18222446G>A | CA459877774 | NAT1 | c.399G>A (p.Gln133=) c.585G>A (p.Gln195=) n.751G>A | |
| 8 | g.18222446G>C | CA370445221 | NAT1 | c.399G>C (p.Gln133His) c.585G>C (p.Gln195His) n.751G>C | |
| 8 | g.18222446G>T | CA370445222 | NAT1 | c.399G>T (p.Gln133His) c.585G>T (p.Gln195His) n.751G>T | gnomAD v4 |
| 8 | g.18222447C>A | CA370445225 | NAT1 | c.400C>A (p.Pro134Thr) c.586C>A (p.Pro196Thr) n.752C>A | |
| 8 | g.18222447C= | CA1768101154 | NAT1 | c.400C= (p.Pro134=) c.586C= (p.Pro196=) n.752C= | |
| 8 | g.18222447C>G | CA370445224 | NAT1 | c.400C>G (p.Pro134Ala) c.586C>G (p.Pro196Ala) n.752C>G | dbSNP |
| 8 | g.18222447C>T | CA370445223 | NAT1 | c.400C>T (p.Pro134Ser) c.586C>T (p.Pro196Ser) n.752C>T | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222448C>A | CA173180369 | NAT1 | c.401C>A (p.Pro134His) c.587C>A (p.Pro196His) n.753C>A | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222448C= | CA1768101155 | NAT1 | c.401C= (p.Pro134=) c.587C= (p.Pro196=) n.753C= | |
| 8 | g.18222448C>G | CA370445226 | NAT1 | c.401C>G (p.Pro134Arg) c.587C>G (p.Pro196Arg) n.753C>G | |
| 8 | g.18222448C>T | CA370445227 | NAT1 | c.401C>T (p.Pro134Leu) c.587C>T (p.Pro196Leu) n.753C>T | gnomAD v4 |
| 8 | g.18222449T>A | CA459877777 | NAT1 | c.402T>A (p.Pro134=) c.588T>A (p.Pro196=) n.754T>A | |
| 8 | g.18222449T>C | CA4651402 | NAT1 | c.402T>C (p.Pro134=) c.588T>C (p.Pro196=) n.754T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222449T>G | CA459877778 | NAT1 | c.402T>G (p.Pro134=) c.588T>G (p.Pro196=) n.754T>G | |
| 8 | g.18222449T= | CA1768101156 | NAT1 | c.402T= (p.Pro134=) c.588T= (p.Pro196=) n.754T= | |
| 8 | g.18222450C>A | CA370445228 | NAT1 | c.403C>A (p.Leu135Met) c.589C>A (p.Leu197Met) n.755C>A | |
| 8 | g.18222450C>G | CA370445229 | NAT1 | c.403C>G (p.Leu135Val) c.589C>G (p.Leu197Val) n.755C>G | gnomAD v4 |
| 8 | g.18222450C>T | CA459877780 | NAT1 | c.403C>T (p.Leu135=) c.589C>T (p.Leu197=) n.755C>T | |
| 8 | g.18222451T>A | CA370445230 | NAT1 | c.404T>A (p.Leu135Gln) c.590T>A (p.Leu197Gln) n.756T>A | |
| 8 | g.18222451T>C | CA370445231 | NAT1 | c.404T>C (p.Leu135Pro) c.590T>C (p.Leu197Pro) n.756T>C | dbSNP gnomAD v4 |
| 8 | g.18222451T>G | CA370445232 | NAT1 | c.404T>G (p.Leu135Arg) c.590T>G (p.Leu197Arg) n.756T>G | |
| 8 | g.18222451T= | CA1768101157 | NAT1 | c.404T= (p.Leu135=) c.590T= (p.Leu197=) n.756T= | |
| 8 | g.18222452G>A | CA4651403 | NAT1 | c.405G>A (p.Leu135=) c.591G>A (p.Leu197=) n.757G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222452G>C | CA459877782 | NAT1 | c.405G>C (p.Leu135=) c.591G>C (p.Leu197=) n.757G>C | |
| 8 | g.18222452G= | CA1768101158 | NAT1 | c.405G= (p.Leu135=) c.591G= (p.Leu197=) n.757G= | |
| 8 | g.18222452G>T | CA459877783 | NAT1 | c.405G>T (p.Leu135=) c.591G>T (p.Leu197=) n.757G>T | |
| 8 | g.18222453G>A | CA370445233 | NAT1 | c.406G>A (p.Glu136Lys) c.592G>A (p.Glu198Lys) n.758G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222453G>C | CA370445234 | NAT1 | c.406G>C (p.Glu136Gln) c.592G>C (p.Glu198Gln) n.758G>C | |
| 8 | g.18222453G= | CA1768101159 | NAT1 | c.406G= (p.Glu136=) c.592G= (p.Glu198=) n.758G= | |
| 8 | g.18222453G>T | CA370445235 | NAT1 | c.406G>T (p.Glu136Ter) c.592G>T (p.Glu198Ter) n.758G>T | |
| 8 | g.18222454A= | CA1768101160 | NAT1 | c.407A= (p.Glu136=) c.593A= (p.Glu198=) n.759A= | |
| 8 | g.18222454A>C | CA370445238 | NAT1 | c.407A>C (p.Glu136Ala) c.593A>C (p.Glu198Ala) n.759A>C | |
| 8 | g.18222454A>G | CA370445237 | NAT1 | c.407A>G (p.Glu136Gly) c.593A>G (p.Glu198Gly) n.759A>G | dbSNP |
| 8 | g.18222454A>T | CA370445236 | NAT1 | c.407A>T (p.Glu136Val) c.593A>T (p.Glu198Val) n.759A>T | |
| 8 | g.18222455G>A | CA459877785 | NAT1 | c.408G>A (p.Glu136=) c.594G>A (p.Glu198=) n.760G>A | |
| 8 | g.18222455G>C | CA4651404 | NAT1 | c.408G>C (p.Glu136Asp) c.594G>C (p.Glu198Asp) n.760G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222455G= | CA1768101161 | NAT1 | c.408G= (p.Glu136=) c.594G= (p.Glu198=) n.760G= | |
| 8 | g.18222455G>T | CA370445239 | NAT1 | c.408G>T (p.Glu136Asp) c.594G>T (p.Glu198Asp) n.760G>T | |
| 8 | g.18222456T>A | CA370445240 | NAT1 | c.409T>A (p.Leu137Ile) c.595T>A (p.Leu199Ile) n.761T>A | |
| 8 | g.18222456T>C | CA4651405 | NAT1 | c.409T>C (p.Leu137=) c.595T>C (p.Leu199=) n.761T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222456T>G | CA370445241 | NAT1 | c.409T>G (p.Leu137Val) c.595T>G (p.Leu199Val) n.761T>G | dbSNP |
| 8 | g.18222456T= | CA1768101162 | NAT1 | c.409T= (p.Leu137=) c.595T= (p.Leu199=) n.761T= | |
| 8 | g.18222457T>A | CA370445242 | NAT1 | c.410T>A (p.Leu137Ter) c.596T>A (p.Leu199Ter) n.762T>A | |
| 8 | g.18222457T>C | CA370445243 | NAT1 | c.410T>C (p.Leu137Ser) c.596T>C (p.Leu199Ser) n.762T>C | |
| 8 | g.18222457T>G | CA370445244 | NAT1 | c.410T>G (p.Leu137Ter) c.596T>G (p.Leu199Ter) n.762T>G | |
| 8 | g.18222458A>C | CA370445245 | NAT1 | c.411A>C (p.Leu137Phe) c.597A>C (p.Leu199Phe) n.763A>C | |
| 8 | g.18222458A>G | CA459877792 | NAT1 | c.411A>G (p.Leu137=) c.597A>G (p.Leu199=) n.763A>G | |
| 8 | g.18222458A>T | CA370445246 | NAT1 | c.411A>T (p.Leu137Phe) c.597A>T (p.Leu199Phe) n.763A>T | |
| 8 | g.18222459A>C | CA370445247 | NAT1 | c.412A>C (p.Ile138Leu) c.598A>C (p.Ile200Leu) n.764A>C | |
| 8 | g.18222459A>G | CA370445248 | NAT1 | c.412A>G (p.Ile138Val) c.598A>G (p.Ile200Val) n.764A>G | |
| 8 | g.18222459A>T | CA370445249 | NAT1 | c.412A>T (p.Ile138Phe) c.598A>T (p.Ile200Phe) n.764A>T | |
| 8 | g.18222460T>A | CA370445251 | NAT1 | c.413T>A (p.Ile138Asn) c.599T>A (p.Ile200Asn) n.765T>A | |
| 8 | g.18222460T>C | CA4651406 | NAT1 | c.413T>C (p.Ile138Thr) c.599T>C (p.Ile200Thr) n.765T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222460T>G | CA370445250 | NAT1 | c.413T>G (p.Ile138Ser) c.599T>G (p.Ile200Ser) n.765T>G | |
| 8 | g.18222460T= | CA1768101163 | NAT1 | c.413T= (p.Ile138=) c.599T= (p.Ile200=) n.765T= | |
| 8 | g.18222461T>A | CA459877795 | NAT1 | c.414T>A (p.Ile138=) c.600T>A (p.Ile200=) n.766T>A | |
| 8 | g.18222461T>C | CA459877796 | NAT1 | c.414T>C (p.Ile138=) c.600T>C (p.Ile200=) n.766T>C | |
| 8 | g.18222461T>G | CA370445252 | NAT1 | c.414T>G (p.Ile138Met) c.600T>G (p.Ile200Met) n.766T>G | |
| 8 | g.18222462T>A | CA370445254 | NAT1 | c.415T>A (p.Ser139Thr) c.601T>A (p.Ser201Thr) n.767T>A | |
| 8 | g.18222462T>C | CA370445253 | NAT1 | c.415T>C (p.Ser139Pro) c.601T>C (p.Ser201Pro) n.767T>C | |
| 8 | g.18222462T>G | CA370445255 | NAT1 | c.415T>G (p.Ser139Ala) c.601T>G (p.Ser201Ala) n.767T>G | |
| 8 | g.18222463C>A | CA370445256 | NAT1 | c.416C>A (p.Ser139Tyr) c.602C>A (p.Ser201Tyr) n.768C>A | dbSNP gnomAD v2 |
| 8 | g.18222463C= | CA1768101164 | NAT1 | c.416C= (p.Ser139=) c.602C= (p.Ser201=) n.768C= | |
| 8 | g.18222463C>G | CA370445257 | NAT1 | c.416C>G (p.Ser139Cys) c.602C>G (p.Ser201Cys) n.768C>G | |
| 8 | g.18222463C>T | CA370445258 | NAT1 | c.416C>T (p.Ser139Phe) c.602C>T (p.Ser201Phe) n.768C>T |