| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.18222258_18222260dup | CA580501892 | NAT1 | c.211_213dup (p.Val71_Asn72insVal) c.397_399dup (p.Val133_Asn134insVal) n.563_565dup n.472_474dup n.738_740dup | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222260C>A | CA459877566 | NAT1 | c.213C>A (p.Val71=) c.399C>A (p.Val133=) n.565C>A n.474C>A n.740C>A | gnomAD v4 |
| 8 | g.18222260C>G | CA459877567 | NAT1 | c.213C>G (p.Val71=) c.399C>G (p.Val133=) n.565C>G n.474C>G n.740C>G | |
| 8 | g.18222260C>T | CA459877568 | NAT1 | c.213C>T (p.Val71=) c.399C>T (p.Val133=) n.565C>T n.474C>T n.740C>T | |
| 8 | g.18222261A>C | CA370444834 | NAT1 | c.214A>C (p.Asn72His) c.400A>C (p.Asn134His) n.566A>C n.475A>C n.741A>C | |
| 8 | g.18222261A>G | CA370444835 | NAT1 | c.214A>G (p.Asn72Asp) c.400A>G (p.Asn134Asp) n.566A>G n.475A>G n.741A>G | |
| 8 | g.18222261A>T | CA370444836 | NAT1 | c.214A>T (p.Asn72Tyr) c.400A>T (p.Asn134Tyr) n.566A>T n.475A>T n.741A>T | |
| 8 | g.18222262A>C | CA370444837 | NAT1 | c.215A>C (p.Asn72Thr) c.401A>C (p.Asn134Thr) n.567A>C n.476A>C n.742A>C | |
| 8 | g.18222262A>G | CA370444839 | NAT1 | c.215A>G (p.Asn72Ser) c.401A>G (p.Asn134Ser) n.567A>G n.476A>G n.742A>G | |
| 8 | g.18222262A>T | CA370444838 | NAT1 | c.215A>T (p.Asn72Ile) c.401A>T (p.Asn134Ile) n.567A>T n.476A>T n.742A>T | |
| 8 | g.18222263T>A | CA370444840 | NAT1 | c.216T>A (p.Asn72Lys) c.402T>A (p.Asn134Lys) n.568T>A n.477T>A n.743T>A | |
| 8 | g.18222263T>C | CA459877569 | NAT1 | c.216T>C (p.Asn72=) c.402T>C (p.Asn134=) n.568T>C n.477T>C n.743T>C | |
| 8 | g.18222263T>G | CA370444841 | NAT1 | c.216T>G (p.Asn72Lys) c.402T>G (p.Asn134Lys) n.568T>G n.477T>G n.743T>G | gnomAD v4 |
| 8 | g.18222264C>A | CA370444842 | NAT1 | c.217C>A (p.His73Asn) c.403C>A (p.His135Asn) n.569C>A n.478C>A n.744C>A | |
| 8 | g.18222264C= | CA1768101062 | NAT1 | c.217C= (p.His73=) c.403C= (p.His135=) n.569C= n.478C= n.744C= | |
| 8 | g.18222264C>G | CA370444843 | NAT1 | c.217C>G (p.His73Asp) c.403C>G (p.His135Asp) n.569C>G n.478C>G n.744C>G | |
| 8 | g.18222264C>T | CA370444844 | NAT1 | c.217C>T (p.His73Tyr) c.403C>T (p.His135Tyr) n.569C>T n.478C>T n.744C>T | dbSNP gnomAD v4 |
| 8 | g.18222265A>C | CA370444845 | NAT1 | c.218A>C (p.His73Pro) c.404A>C (p.His135Pro) n.570A>C n.479A>C n.745A>C | |
| 8 | g.18222265A>G | CA370444846 | NAT1 | c.218A>G (p.His73Arg) c.404A>G (p.His135Arg) n.570A>G n.479A>G n.745A>G | |
| 8 | g.18222265A>T | CA370444847 | NAT1 | c.218A>T (p.His73Leu) c.404A>T (p.His135Leu) n.570A>T n.479A>T n.745A>T | |
| 8 | g.18222266T>A | CA370444848 | NAT1 | c.219T>A (p.His73Gln) c.405T>A (p.His135Gln) n.571T>A n.480T>A n.746T>A | gnomAD v4 |
| 8 | g.18222266T>C | CA4651351 | NAT1 | c.219T>C (p.His73=) c.405T>C (p.His135=) n.571T>C n.480T>C n.746T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222266T>G | CA370444849 | NAT1 | c.219T>G (p.His73Gln) c.405T>G (p.His135Gln) n.571T>G n.480T>G n.746T>G | |
| 8 | g.18222266T= | CA1768101063 | NAT1 | c.219T= (p.His73=) c.405T= (p.His135=) n.571T= n.480T= n.746T= | |
| 8 | g.18222269_18222271del | CA645553238 | NAT1 | c.222_224del (p.Leu75del) c.408_410del (p.Leu137del) n.574_576del n.483_485del n.749_751del | COSMIC COSMIC |
| 8 | g.18222267C>A | CA370444852 | NAT1 | c.220C>A (p.Leu74Ile) c.406C>A (p.Leu136Ile) n.572C>A n.481C>A n.747C>A | |
| 8 | g.18222267C>G | CA370444851 | NAT1 | c.220C>G (p.Leu74Val) c.406C>G (p.Leu136Val) n.572C>G n.481C>G n.747C>G | |
| 8 | g.18222267C>T | CA370444850 | NAT1 | c.220C>T (p.Leu74Phe) c.406C>T (p.Leu136Phe) n.572C>T n.481C>T n.747C>T | |
| 8 | g.18222268T>A | CA370444853 | NAT1 | c.221T>A (p.Leu74His) c.407T>A (p.Leu136His) n.573T>A n.482T>A n.748T>A | |
| 8 | g.18222268T>C | CA370444854 | NAT1 | c.221T>C (p.Leu74Pro) c.407T>C (p.Leu136Pro) n.573T>C n.482T>C n.748T>C | |
| 8 | g.18222268T>G | CA370444855 | NAT1 | c.221T>G (p.Leu74Arg) c.407T>G (p.Leu136Arg) n.573T>G n.482T>G n.748T>G | |
| 8 | g.18222269T>A | CA459877416 | NAT1 | c.222T>A (p.Leu74=) c.408T>A (p.Leu136=) n.574T>A n.483T>A n.749T>A | |
| 8 | g.18222269T>C | CA4651352 | NAT1 | c.222T>C (p.Leu74=) c.408T>C (p.Leu136=) n.574T>C n.483T>C n.749T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222269T>G | CA459877417 | NAT1 | c.222T>G (p.Leu74=) c.408T>G (p.Leu136=) n.574T>G n.483T>G n.749T>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222269T= | CA1768101064 | NAT1 | c.222T= (p.Leu74=) c.408T= (p.Leu136=) n.574T= n.483T= n.749T= | |
| 8 | g.18222270C>A | CA370444856 | NAT1 | c.223C>A (p.Leu75Met) c.409C>A (p.Leu137Met) n.575C>A n.484C>A n.750C>A | |
| 8 | g.18222270C= | CA1768101065 | NAT1 | c.223C= (p.Leu75=) c.409C= (p.Leu137=) n.575C= n.484C= n.750C= | |
| 8 | g.18222270C>G | CA370444857 | NAT1 | c.223C>G (p.Leu75Val) c.409C>G (p.Leu137Val) n.575C>G n.484C>G n.750C>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222270C>T | CA459877421 | NAT1 | c.223C>T (p.Leu75=) c.409C>T (p.Leu137=) n.575C>T n.484C>T n.750C>T | |
| 8 | g.18222271T>A | CA370444858 | NAT1 | c.224T>A (p.Leu75Gln) c.410T>A (p.Leu137Gln) n.576T>A n.485T>A n.751T>A | |
| 8 | g.18222271T>C | CA370444859 | NAT1 | c.224T>C (p.Leu75Pro) c.410T>C (p.Leu137Pro) n.576T>C n.485T>C n.751T>C | |
| 8 | g.18222271T>G | CA370444860 | NAT1 | c.224T>G (p.Leu75Arg) c.410T>G (p.Leu137Arg) n.576T>G n.485T>G n.751T>G | |
| 8 | g.18222272G>A | CA459877425 | NAT1 | c.225G>A (p.Leu75=) c.411G>A (p.Leu137=) n.577G>A n.486G>A n.752G>A | |
| 8 | g.18222272G>C | CA459877424 | NAT1 | c.225G>C (p.Leu75=) c.411G>C (p.Leu137=) n.577G>C n.486G>C n.752G>C | |
| 8 | g.18222272G>T | CA459877423 | NAT1 | c.225G>T (p.Leu75=) c.411G>T (p.Leu137=) n.577G>T n.486G>T n.752G>T | |
| 8 | g.18222273T>A | CA370444861 | NAT1 | c.226T>A (p.Tyr76Asn) c.412T>A (p.Tyr138Asn) n.578T>A n.487T>A n.753T>A | |
| 8 | g.18222273T>C | CA370444862 | NAT1 | c.226T>C (p.Tyr76His) c.412T>C (p.Tyr138His) n.578T>C n.487T>C n.753T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222273T>G | CA370444863 | NAT1 | c.226T>G (p.Tyr76Asp) c.412T>G (p.Tyr138Asp) n.578T>G n.487T>G n.753T>G | |
| 8 | g.18222273T= | CA1768101066 | NAT1 | c.226T= (p.Tyr76=) c.412T= (p.Tyr138=) n.578T= n.487T= n.753T= | |
| 8 | g.18222274A= | CA1768101067 | NAT1 | c.227A= (p.Tyr76=) c.413A= (p.Tyr138=) n.579A= n.488A= n.754A= | |
| 8 | g.18222274A>C | CA370444865 | NAT1 | c.227A>C (p.Tyr76Ser) c.413A>C (p.Tyr138Ser) n.579A>C n.488A>C n.754A>C | |
| 8 | g.18222274A>G | CA370444866 | NAT1 | c.227A>G (p.Tyr76Cys) c.413A>G (p.Tyr138Cys) n.579A>G n.488A>G n.754A>G | |
| 8 | g.18222274A>T | CA370444864 | NAT1 | c.227A>T (p.Tyr76Phe) c.413A>T (p.Tyr138Phe) n.579A>T n.488A>T n.754A>T | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222275C>A | CA4651353 | NAT1 | c.228C>A (p.Tyr76Ter) c.414C>A (p.Tyr138Ter) n.580C>A n.489C>A n.755C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222275C= | CA1768101068 | NAT1 | c.228C= (p.Tyr76=) c.414C= (p.Tyr138=) n.580C= n.489C= n.755C= | |
| 8 | g.18222275C>G | CA370444867 | NAT1 | c.228C>G (p.Tyr76Ter) c.414C>G (p.Tyr138Ter) n.580C>G n.489C>G n.755C>G | dbSNP gnomAD v4 |
| 8 | g.18222275C>T | CA173180292 | NAT1 | c.228C>T (p.Tyr76=) c.414C>T (p.Tyr138=) n.580C>T n.489C>T n.755C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222276T>A | CA370444868 | NAT1 | c.229T>A (p.Trp77Arg) c.415T>A (p.Trp139Arg) n.581T>A n.490T>A n.756T>A | |
| 8 | g.18222276T>C | CA370444869 | NAT1 | c.229T>C (p.Trp77Arg) c.415T>C (p.Trp139Arg) n.581T>C n.490T>C n.756T>C | |
| 8 | g.18222276T>G | CA370444870 | NAT1 | c.229T>G (p.Trp77Gly) c.415T>G (p.Trp139Gly) n.581T>G n.490T>G n.756T>G | |
| 8 | g.18222277G>A | CA173180294 | NAT1 | c.230G>A (p.Trp77Ter) c.416G>A (p.Trp139Ter) n.582G>A n.491G>A n.757G>A | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222277G>C | CA370444872 | NAT1 | c.230G>C (p.Trp77Ser) c.416G>C (p.Trp139Ser) n.582G>C n.491G>C n.757G>C | |
| 8 | g.18222277G= | CA1768101069 | NAT1 | c.230G= (p.Trp77=) c.416G= (p.Trp139=) n.582G= n.491G= n.757G= | |
| 8 | g.18222277G>T | CA370444871 | NAT1 | c.230G>T (p.Trp77Leu) c.416G>T (p.Trp139Leu) n.582G>T n.491G>T n.757G>T | |
| 8 | g.18222278G>A | CA4651354 | NAT1 | c.231G>A (p.Trp77Ter) c.417G>A (p.Trp139Ter) n.583G>A n.492G>A n.758G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222278G>C | CA370444873 | NAT1 | c.231G>C (p.Trp77Cys) c.417G>C (p.Trp139Cys) n.583G>C n.492G>C n.758G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222278G= | CA1768101070 | NAT1 | c.231G= (p.Trp77=) c.417G= (p.Trp139=) n.583G= n.492G= n.758G= | |
| 8 | g.18222278G>T | CA370444874 | NAT1 | c.231G>T (p.Trp77Cys) c.417G>T (p.Trp139Cys) n.583G>T n.492G>T n.758G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222279G>A | CA370444875 | NAT1 | c.232G>A (p.Ala78Thr) c.418G>A (p.Ala140Thr) n.584G>A n.493G>A n.759G>A | |
| 8 | g.18222279G>C | CA370444876 | NAT1 | c.232G>C (p.Ala78Pro) c.418G>C (p.Ala140Pro) n.584G>C n.493G>C n.759G>C | |
| 8 | g.18222279G>T | CA370444877 | NAT1 | c.232G>T (p.Ala78Ser) c.418G>T (p.Ala140Ser) n.584G>T n.493G>T n.759G>T | |
| 8 | g.18222280C>A | CA370444878 | NAT1 | c.233C>A (p.Ala78Asp) c.419C>A (p.Ala140Asp) n.585C>A n.494C>A n.760C>A | |
| 8 | g.18222280C= | CA1768101071 | NAT1 | c.233C= (p.Ala78=) c.419C= (p.Ala140=) n.585C= n.494C= n.760C= | |
| 8 | g.18222280C>G | CA370444880 | NAT1 | c.233C>G (p.Ala78Gly) c.419C>G (p.Ala140Gly) n.585C>G n.494C>G n.760C>G | |
| 8 | g.18222280C>T | CA370444879 | NAT1 | c.233C>T (p.Ala78Val) c.419C>T (p.Ala140Val) n.585C>T n.494C>T n.760C>T | dbSNP |
| 8 | g.18222281T>A | CA459877435 | NAT1 | c.234T>A (p.Ala78=) c.420T>A (p.Ala140=) n.586T>A n.495T>A n.761T>A | |
| 8 | g.18222281T>C | CA459877436 | NAT1 | c.234T>C (p.Ala78=) c.420T>C (p.Ala140=) n.586T>C n.495T>C n.761T>C | |
| 8 | g.18222281T>G | CA459877437 | NAT1 | c.234T>G (p.Ala78=) c.420T>G (p.Ala140=) n.586T>G n.495T>G n.761T>G | |
| 8 | g.18222282C>A | CA370444881 | NAT1 | c.235C>A (p.Leu79Met) c.421C>A (p.Leu141Met) n.587C>A n.496C>A n.762C>A | |
| 8 | g.18222282C>G | CA370444882 | NAT1 | c.235C>G (p.Leu79Val) c.421C>G (p.Leu141Val) n.587C>G n.496C>G n.762C>G | gnomAD v4 |
| 8 | g.18222282C>T | CA459877438 | NAT1 | c.235C>T (p.Leu79=) c.421C>T (p.Leu141=) n.587C>T n.496C>T n.762C>T | |
| 8 | g.18222283T>A | CA370444883 | NAT1 | c.236T>A (p.Leu79Gln) c.422T>A (p.Leu141Gln) n.588T>A n.497T>A n.763T>A | |
| 8 | g.18222283T>C | CA370444884 | NAT1 | c.236T>C (p.Leu79Pro) c.422T>C (p.Leu141Pro) n.588T>C n.497T>C n.763T>C | |
| 8 | g.18222283T>G | CA370444885 | NAT1 | c.236T>G (p.Leu79Arg) c.422T>G (p.Leu141Arg) n.588T>G n.497T>G n.763T>G | |
| 8 | g.18222284G>A | CA459877440 | NAT1 | c.237G>A (p.Leu79=) c.423G>A (p.Leu141=) n.589G>A n.498G>A n.764G>A | |
| 8 | g.18222284G>C | CA4651355 | NAT1 | c.237G>C (p.Leu79=) c.423G>C (p.Leu141=) n.589G>C n.498G>C n.764G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222284G= | CA1768101072 | NAT1 | c.237G= (p.Leu79=) c.423G= (p.Leu141=) n.589G= n.498G= n.764G= | |
| 8 | g.18222284G>T | CA459877441 | NAT1 | c.237G>T (p.Leu79=) c.423G>T (p.Leu141=) n.589G>T n.498G>T n.764G>T | |
| 8 | g.18222285A>C | CA370444886 | NAT1 | c.238A>C (p.Thr80Pro) c.424A>C (p.Thr142Pro) n.590A>C n.499A>C n.765A>C | |
| 8 | g.18222285A>G | CA370444887 | NAT1 | c.238A>G (p.Thr80Ala) c.424A>G (p.Thr142Ala) n.590A>G n.499A>G n.765A>G | |
| 8 | g.18222285A>T | CA370444888 | NAT1 | c.238A>T (p.Thr80Ser) c.424A>T (p.Thr142Ser) n.590A>T n.499A>T n.765A>T | |
| 8 | g.18222286C>A | CA370444889 | NAT1 | c.239C>A (p.Thr80Asn) c.425C>A (p.Thr142Asn) n.591C>A n.500C>A n.766C>A | |
| 8 | g.18222286C>G | CA370444890 | NAT1 | c.239C>G (p.Thr80Ser) c.425C>G (p.Thr142Ser) n.591C>G n.500C>G n.766C>G | |
| 8 | g.18222286C>T | CA370444891 | NAT1 | c.239C>T (p.Thr80Ile) c.425C>T (p.Thr142Ile) n.591C>T n.500C>T n.766C>T | |
| 8 | g.18222287C>A | CA459877443 | NAT1 | c.240C>A (p.Thr80=) c.426C>A (p.Thr142=) n.592C>A n.501C>A n.767C>A | gnomAD v4 |
| 8 | g.18222287C= | CA1768101073 | NAT1 | c.240C= (p.Thr80=) c.426C= (p.Thr142=) n.592C= n.501C= n.767C= | |
| 8 | g.18222287C>G | CA459877445 | NAT1 | c.240C>G (p.Thr80=) c.426C>G (p.Thr142=) n.592C>G n.501C>G n.767C>G | |
| 8 | g.18222287C>T | CA4651356 | NAT1 | c.240C>T (p.Thr80=) c.426C>T (p.Thr142=) n.592C>T n.501C>T n.767C>T | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 8 | g.18222288A= | CA1768101074 | NAT1 | c.241A= (p.Thr81=) c.427A= (p.Thr143=) n.593A= n.502A= n.768A= | |
| 8 | g.18222288A>C | CA370444894 | NAT1 | c.241A>C (p.Thr81Pro) c.427A>C (p.Thr143Pro) n.593A>C n.502A>C n.768A>C | |
| 8 | g.18222288A>G | CA370444892 | NAT1 | c.241A>G (p.Thr81Ala) c.427A>G (p.Thr143Ala) n.593A>G n.502A>G n.768A>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222288A>T | CA370444893 | NAT1 | c.241A>T (p.Thr81Ser) c.427A>T (p.Thr143Ser) n.593A>T n.502A>T n.768A>T | dbSNP |
| 8 | g.18222289C>A | CA370444895 | NAT1 | c.242C>A (p.Thr81Asn) c.428C>A (p.Thr143Asn) n.594C>A n.503C>A n.769C>A | |
| 8 | g.18222289C>G | CA370444896 | NAT1 | c.242C>G (p.Thr81Ser) c.428C>G (p.Thr143Ser) n.594C>G n.503C>G n.769C>G | |
| 8 | g.18222289C>T | CA370444897 | NAT1 | c.242C>T (p.Thr81Ile) c.428C>T (p.Thr143Ile) n.594C>T n.503C>T n.769C>T | gnomAD v4 |
| 8 | g.18222290T>A | CA459877451 | NAT1 | c.243T>A (p.Thr81=) c.429T>A (p.Thr143=) n.595T>A n.504T>A n.770T>A | |
| 8 | g.18222290T>C | CA459877452 | NAT1 | c.243T>C (p.Thr81=) c.429T>C (p.Thr143=) n.595T>C n.504T>C n.770T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222290T>G | CA459877453 | NAT1 | c.243T>G (p.Thr81=) c.429T>G (p.Thr143=) n.595T>G n.504T>G n.770T>G | |
| 8 | g.18222290T= | CA1768101075 | NAT1 | c.243T= (p.Thr81=) c.429T= (p.Thr143=) n.595T= n.504T= n.770T= | |
| 8 | g.18222291A= | CA1768101076 | NAT1 | c.244A= (p.Ile82=) c.430A= (p.Ile144=) n.596A= n.505A= n.771A= | |
| 8 | g.18222291A>C | CA370444898 | NAT1 | c.244A>C (p.Ile82Leu) c.430A>C (p.Ile144Leu) n.596A>C n.505A>C n.771A>C | |
| 8 | g.18222291A>G | CA173180299 | NAT1 | c.244A>G (p.Ile82Val) c.430A>G (p.Ile144Val) n.596A>G n.505A>G n.771A>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222291A>T | CA370444899 | NAT1 | c.244A>T (p.Ile82Phe) c.430A>T (p.Ile144Phe) n.596A>T n.505A>T n.771A>T | |
| 8 | g.18222292T>A | CA4651358 | NAT1 | c.245T>A (p.Ile82Asn) c.431T>A (p.Ile144Asn) n.597T>A n.506T>A n.772T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222292T>C | CA4651357 | NAT1 | c.245T>C (p.Ile82Thr) c.431T>C (p.Ile144Thr) n.597T>C n.506T>C n.772T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222292T>G | CA370444900 | NAT1 | c.245T>G (p.Ile82Ser) c.431T>G (p.Ile144Ser) n.597T>G n.506T>G n.772T>G | |
| 8 | g.18222292T= | CA1768101077 | NAT1 | c.245T= (p.Ile82=) c.431T= (p.Ile144=) n.597T= n.506T= n.772T= | |
| 8 | g.18222293T>A | CA459877461 | NAT1 | c.246T>A (p.Ile82=) c.432T>A (p.Ile144=) n.598T>A n.507T>A n.773T>A | |
| 8 | g.18222293T>C | CA459877460 | NAT1 | c.246T>C (p.Ile82=) c.432T>C (p.Ile144=) n.598T>C n.507T>C n.773T>C | |
| 8 | g.18222293T>G | CA370444901 | NAT1 | c.246T>G (p.Ile82Met) c.432T>G (p.Ile144Met) n.598T>G n.507T>G n.773T>G | |
| 8 | g.18222294G>A | CA370444902 | NAT1 | c.247G>A (p.Gly83Ser) c.433G>A (p.Gly145Ser) n.599G>A n.508G>A n.774G>A | |
| 8 | g.18222294G>C | CA370444903 | NAT1 | c.247G>C (p.Gly83Arg) c.433G>C (p.Gly145Arg) n.599G>C n.508G>C n.774G>C | |
| 8 | g.18222294G>T | CA370444904 | NAT1 | c.247G>T (p.Gly83Cys) c.433G>T (p.Gly145Cys) n.599G>T n.508G>T n.774G>T | |
| 8 | g.18222295G>A | CA370444905 | NAT1 | c.248G>A (p.Gly83Asp) c.434G>A (p.Gly145Asp) n.600G>A n.509G>A n.775G>A | |
| 8 | g.18222295G>C | CA370444907 | NAT1 | c.248G>C (p.Gly83Ala) c.434G>C (p.Gly145Ala) n.600G>C n.509G>C n.775G>C | |
| 8 | g.18222295G>T | CA370444906 | NAT1 | c.248G>T (p.Gly83Val) c.434G>T (p.Gly145Val) n.600G>T n.509G>T n.775G>T | gnomAD v4 |
| 8 | g.18222296T>A | CA459877465 | NAT1 | c.249T>A (p.Gly83=) c.435T>A (p.Gly145=) n.601T>A n.510T>A n.776T>A | |
| 8 | g.18222296T>C | CA459877467 | NAT1 | c.249T>C (p.Gly83=) c.435T>C (p.Gly145=) n.601T>C n.510T>C n.776T>C | |
| 8 | g.18222296T>G | CA459877466 | NAT1 | c.249T>G (p.Gly83=) c.435T>G (p.Gly145=) n.601T>G n.510T>G n.776T>G | gnomAD v4 |
| 8 | g.18222297T>A | CA370444908 | NAT1 | c.250T>A (p.Phe84Ile) c.436T>A (p.Phe146Ile) n.602T>A n.511T>A n.777T>A | |
| 8 | g.18222297T>C | CA370444909 | NAT1 | c.250T>C (p.Phe84Leu) c.436T>C (p.Phe146Leu) n.602T>C n.511T>C n.777T>C | |
| 8 | g.18222297T>G | CA370444910 | NAT1 | c.250T>G (p.Phe84Val) c.436T>G (p.Phe146Val) n.602T>G n.511T>G n.777T>G | |
| 8 | g.18222298T>A | CA370444911 | NAT1 | c.251T>A (p.Phe84Tyr) c.437T>A (p.Phe146Tyr) n.603T>A n.512T>A n.778T>A | |
| 8 | g.18222298T>C | CA370444912 | NAT1 | c.251T>C (p.Phe84Ser) c.437T>C (p.Phe146Ser) n.603T>C n.512T>C n.778T>C | |
| 8 | g.18222298T>G | CA370444913 | NAT1 | c.251T>G (p.Phe84Cys) c.437T>G (p.Phe146Cys) n.603T>G n.512T>G n.778T>G | |
| 8 | g.18222299T>A | CA370444914 | NAT1 | c.252T>A (p.Phe84Leu) c.438T>A (p.Phe146Leu) n.604T>A n.513T>A n.779T>A | |
| 8 | g.18222299T>C | CA459877470 | NAT1 | c.252T>C (p.Phe84=) c.438T>C (p.Phe146=) n.604T>C n.513T>C n.779T>C | |
| 8 | g.18222299T>G | CA370444915 | NAT1 | c.252T>G (p.Phe84Leu) c.438T>G (p.Phe146Leu) n.604T>G n.513T>G n.779T>G | gnomAD v4 |
| 8 | g.18222300G>A | CA370444916 | NAT1 | c.253G>A (p.Glu85Lys) c.439G>A (p.Glu147Lys) n.605G>A n.514G>A n.780G>A | |
| 8 | g.18222300G>C | CA370444917 | NAT1 | c.253G>C (p.Glu85Gln) c.439G>C (p.Glu147Gln) n.605G>C n.514G>C n.780G>C | |
| 8 | g.18222300G>T | CA370444918 | NAT1 | c.253G>T (p.Glu85Ter) c.439G>T (p.Glu147Ter) n.605G>T n.514G>T n.780G>T | |
| 8 | g.18222301A>C | CA370444921 | NAT1 | c.254A>C (p.Glu85Ala) c.440A>C (p.Glu147Ala) n.606A>C n.515A>C n.781A>C | |
| 8 | g.18222301A>G | CA370444920 | NAT1 | c.254A>G (p.Glu85Gly) c.440A>G (p.Glu147Gly) n.606A>G n.515A>G n.781A>G | |
| 8 | g.18222301A>T | CA370444919 | NAT1 | c.254A>T (p.Glu85Val) c.440A>T (p.Glu147Val) n.606A>T n.515A>T n.781A>T | |
| 8 | g.18222302G>A | CA459877472 | NAT1 | c.255G>A (p.Glu85=) c.441G>A (p.Glu147=) n.607G>A n.516G>A n.782G>A | |
| 8 | g.18222302G>C | CA370444922 | NAT1 | c.255G>C (p.Glu85Asp) c.441G>C (p.Glu147Asp) n.607G>C n.516G>C n.782G>C | |
| 8 | g.18222302G>T | CA370444923 | NAT1 | c.255G>T (p.Glu85Asp) c.441G>T (p.Glu147Asp) n.607G>T n.516G>T n.782G>T | gnomAD v4 |
| 8 | g.18222303A= | CA1768101078 | NAT1 | c.256A= (p.Thr86=) c.442A= (p.Thr148=) n.608A= n.517A= n.783A= | |
| 8 | g.18222303A>C | CA370444924 | NAT1 | c.256A>C (p.Thr86Pro) c.442A>C (p.Thr148Pro) n.608A>C n.517A>C n.783A>C | |
| 8 | g.18222303A>G | CA370444925 | NAT1 | c.256A>G (p.Thr86Ala) c.442A>G (p.Thr148Ala) n.608A>G n.517A>G n.783A>G | dbSNP gnomAD v4 |
| 8 | g.18222303A>T | CA370444926 | NAT1 | c.256A>T (p.Thr86Ser) c.442A>T (p.Thr148Ser) n.608A>T n.517A>T n.783A>T | |
| 8 | g.18222304C>A | CA370444927 | NAT1 | c.257C>A (p.Thr86Asn) c.443C>A (p.Thr148Asn) n.609C>A n.518C>A n.784C>A | gnomAD v4 |
| 8 | g.18222304C= | CA1768101079 | NAT1 | c.257C= (p.Thr86=) c.443C= (p.Thr148=) n.609C= n.518C= n.784C= | |
| 8 | g.18222304C>G | CA370444928 | NAT1 | c.257C>G (p.Thr86Ser) c.443C>G (p.Thr148Ser) n.609C>G n.518C>G n.784C>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222304C>T | CA370444929 | NAT1 | c.257C>T (p.Thr86Ile) c.443C>T (p.Thr148Ile) n.609C>T n.518C>T n.784C>T | gnomAD v4 |
| 8 | g.18222305C>A | CA459877479 | NAT1 | c.258C>A (p.Thr86=) c.444C>A (p.Thr148=) n.610C>A n.519C>A n.785C>A | |
| 8 | g.18222305C>G | CA459877478 | NAT1 | c.258C>G (p.Thr86=) c.444C>G (p.Thr148=) n.610C>G n.519C>G n.785C>G | |
| 8 | g.18222305C>T | CA459877476 | NAT1 | c.258C>T (p.Thr86=) c.444C>T (p.Thr148=) n.610C>T n.519C>T n.785C>T | |
| 8 | g.18222306A>C | CA370444930 | NAT1 | c.259A>C (p.Thr87Pro) c.445A>C (p.Thr149Pro) n.611A>C n.520A>C n.786A>C | |
| 8 | g.18222306A>G | CA370444932 | NAT1 | c.259A>G (p.Thr87Ala) c.445A>G (p.Thr149Ala) n.611A>G n.520A>G n.786A>G | gnomAD v4 |
| 8 | g.18222306A>T | CA370444931 | NAT1 | c.259A>T (p.Thr87Ser) c.445A>T (p.Thr149Ser) n.611A>T n.520A>T n.786A>T | COSMIC |
| 8 | g.18222307C>A | CA370444933 | NAT1 | c.260C>A (p.Thr87Lys) c.446C>A (p.Thr149Lys) n.612C>A n.521C>A n.787C>A | |
| 8 | g.18222307C= | CA1768101080 | NAT1 | c.260C= (p.Thr87=) c.446C= (p.Thr149=) n.612C= n.521C= n.787C= | |
| 8 | g.18222307C>G | CA370444934 | NAT1 | c.260C>G (p.Thr87Arg) c.446C>G (p.Thr149Arg) n.612C>G n.521C>G n.787C>G | |
| 8 | g.18222307C>T | CA4651359 | NAT1 | c.260C>T (p.Thr87Met) c.446C>T (p.Thr149Met) n.612C>T n.521C>T n.787C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222308G>A | CA4651360 | NAT1 | c.261G>A (p.Thr87=) c.447G>A (p.Thr149=) n.613G>A n.522G>A n.788G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222308G>C | CA459877482 | NAT1 | c.261G>C (p.Thr87=) c.447G>C (p.Thr149=) n.613G>C n.522G>C n.788G>C | |
| 8 | g.18222308G= | CA1768101081 | NAT1 | c.261G= (p.Thr87=) c.447G= (p.Thr149=) n.613G= n.522G= n.788G= | |
| 8 | g.18222308G>T | CA173180305 | NAT1 | c.261G>T (p.Thr87=) c.447G>T (p.Thr149=) n.613G>T n.522G>T n.788G>T | dbSNP gnomAD v4 |
| 8 | g.18222309A>C | CA370444935 | NAT1 | c.262A>C (p.Met88Leu) c.448A>C (p.Met150Leu) n.614A>C n.523A>C n.789A>C | |
| 8 | g.18222309A>G | CA370444937 | NAT1 | c.262A>G (p.Met88Val) c.448A>G (p.Met150Val) n.614A>G n.523A>G n.789A>G | gnomAD v4 |
| 8 | g.18222309A>T | CA370444936 | NAT1 | c.262A>T (p.Met88Leu) c.448A>T (p.Met150Leu) n.614A>T n.523A>T n.789A>T | gnomAD v4 |
| 8 | g.18222310T>A | CA370444938 | NAT1 | c.263T>A (p.Met88Lys) c.449T>A (p.Met150Lys) n.615T>A n.524T>A n.790T>A | |
| 8 | g.18222310T>C | CA370444939 | NAT1 | c.263T>C (p.Met88Thr) c.449T>C (p.Met150Thr) n.615T>C n.524T>C n.790T>C | gnomAD v4 |
| 8 | g.18222310T>G | CA370444940 | NAT1 | c.263T>G (p.Met88Arg) c.449T>G (p.Met150Arg) n.615T>G n.524T>G n.790T>G | |
| 8 | g.18222311G>A | CA370444941 | NAT1 | c.264G>A (p.Met88Ile) c.450G>A (p.Met150Ile) n.616G>A n.525G>A n.791G>A | |
| 8 | g.18222311G>C | CA370444942 | NAT1 | c.264G>C (p.Met88Ile) c.450G>C (p.Met150Ile) n.616G>C n.525G>C n.791G>C | gnomAD v4 |
| 8 | g.18222311G>T | CA370444943 | NAT1 | c.264G>T (p.Met88Ile) c.450G>T (p.Met150Ile) n.616G>T n.525G>T n.791G>T | |
| 8 | g.18222312T>A | CA370444944 | NAT1 | c.265T>A (p.Leu89Met) c.451T>A (p.Leu151Met) n.617T>A n.526T>A n.792T>A | |
| 8 | g.18222312T>C | CA459877485 | NAT1 | c.265T>C (p.Leu89=) c.451T>C (p.Leu151=) n.617T>C n.526T>C n.792T>C | |
| 8 | g.18222312T>G | CA370444945 | NAT1 | c.265T>G (p.Leu89Val) c.451T>G (p.Leu151Val) n.617T>G n.526T>G n.792T>G | gnomAD v4 |
| 8 | g.18222313T>A | CA4651361 | NAT1 | c.266T>A (p.Leu89Ter) c.452T>A (p.Leu151Ter) n.618T>A n.527T>A n.793T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222313T>C | CA370444946 | NAT1 | c.266T>C (p.Leu89Ser) c.452T>C (p.Leu151Ser) n.618T>C n.527T>C n.793T>C | gnomAD v4 |
| 8 | g.18222313T>G | CA370444947 | NAT1 | c.266T>G (p.Leu89Trp) c.452T>G (p.Leu151Trp) n.618T>G n.527T>G n.793T>G | |
| 8 | g.18222313T= | CA1768101082 | NAT1 | c.266T= (p.Leu89=) c.452T= (p.Leu151=) n.618T= n.527T= n.793T= | |
| 8 | g.18222314G>A | CA459877489 | NAT1 | c.267G>A (p.Leu89=) c.453G>A (p.Leu151=) n.619G>A n.528G>A n.794G>A | |
| 8 | g.18222314G>C | CA370444948 | NAT1 | c.267G>C (p.Leu89Phe) c.453G>C (p.Leu151Phe) n.619G>C n.528G>C n.794G>C | gnomAD v4 |
| 8 | g.18222314G= | CA1768101083 | NAT1 | c.267G= (p.Leu89=) c.453G= (p.Leu151=) n.619G= n.528G= n.794G= | |
| 8 | g.18222314G>T | CA370444949 | NAT1 | c.267G>T (p.Leu89Phe) c.453G>T (p.Leu151Phe) n.619G>T n.528G>T n.794G>T | dbSNP |
| 8 | g.18222315G>A | CA370444950 | NAT1 | c.268G>A (p.Gly90Arg) c.454G>A (p.Gly152Arg) n.620G>A n.529G>A n.795G>A | |
| 8 | g.18222315G>C | CA370444952 | NAT1 | c.268G>C (p.Gly90Arg) c.454G>C (p.Gly152Arg) n.620G>C n.529G>C n.795G>C | |
| 8 | g.18222315G>T | CA370444951 | NAT1 | c.268G>T (p.Gly90Ter) c.454G>T (p.Gly152Ter) n.620G>T n.529G>T n.795G>T | |
| 8 | g.18222316G>A | CA370444953 | NAT1 | c.269G>A (p.Gly90Glu) c.455G>A (p.Gly152Glu) n.621G>A n.530G>A n.796G>A | dbSNP gnomAD v4 |
| 8 | g.18222316G>C | CA370444954 | NAT1 | c.269G>C (p.Gly90Ala) c.455G>C (p.Gly152Ala) n.621G>C n.530G>C n.796G>C | dbSNP |
| 8 | g.18222316G= | CA1768101084 | NAT1 | c.269G= (p.Gly90=) c.455G= (p.Gly152=) n.621G= n.530G= n.796G= | |
| 8 | g.18222316G>T | CA370444955 | NAT1 | c.269G>T (p.Gly90Val) c.455G>T (p.Gly152Val) n.621G>T n.530G>T n.796G>T | |
| 8 | g.18222317A>C | CA459877494 | NAT1 | c.270A>C (p.Gly90=) c.456A>C (p.Gly152=) n.622A>C n.531A>C n.797A>C | |
| 8 | g.18222317A>G | CA459877495 | NAT1 | c.270A>G (p.Gly90=) c.456A>G (p.Gly152=) n.622A>G n.531A>G n.797A>G | gnomAD v4 |
| 8 | g.18222317A>T | CA459877496 | NAT1 | c.270A>T (p.Gly90=) c.456A>T (p.Gly152=) n.622A>T n.531A>T n.797A>T | |
| 8 | g.18222318G>A | CA370444956 | NAT1 | c.271G>A (p.Gly91Arg) c.457G>A (p.Gly153Arg) n.623G>A n.532G>A n.798G>A | gnomAD v4 |
| 8 | g.18222318G>C | CA370444957 | NAT1 | c.271G>C (p.Gly91Arg) c.457G>C (p.Gly153Arg) n.623G>C n.532G>C n.798G>C | |
| 8 | g.18222318G= | CA1768101085 | NAT1 | c.271G= (p.Gly91=) c.457G= (p.Gly153=) n.623G= n.532G= n.798G= | |
| 8 | g.18222318G>T | CA173180308 | NAT1 | c.271G>T (p.Gly91Trp) c.457G>T (p.Gly153Trp) n.623G>T n.532G>T n.798G>T | dbSNP |
| 8 | g.18222319G>A | CA370444958 | NAT1 | c.272G>A (p.Gly91Glu) c.458G>A (p.Gly153Glu) n.624G>A n.533G>A n.799G>A | |
| 8 | g.18222319G>C | CA370444959 | NAT1 | c.272G>C (p.Gly91Ala) c.458G>C (p.Gly153Ala) n.624G>C n.533G>C n.799G>C | gnomAD v4 |
| 8 | g.18222319G>T | CA370444960 | NAT1 | c.272G>T (p.Gly91Val) c.458G>T (p.Gly153Val) n.624G>T n.533G>T n.799G>T | |
| 8 | g.18222320G>A | CA459877497 | NAT1 | c.273G>A (p.Gly91=) c.459G>A (p.Gly153=) n.625G>A n.534G>A n.800G>A | |
| 8 | g.18222320G>C | CA459877498 | NAT1 | c.273G>C (p.Gly91=) c.459G>C (p.Gly153=) n.625G>C n.534G>C n.800G>C | dbSNP gnomAD v4 |
| 8 | g.18222320G= | CA1768101086 | NAT1 | c.273G= (p.Gly91=) c.459G= (p.Gly153=) n.625G= n.534G= n.800G= | |
| 8 | g.18222320G>T | CA459877499 | NAT1 | c.273G>T (p.Gly91=) c.459G>T (p.Gly153=) n.625G>T n.534G>T n.800G>T | gnomAD v4 |
| 8 | g.18222321T>A | CA370444961 | NAT1 | c.274T>A (p.Tyr92Asn) c.460T>A (p.Tyr154Asn) n.626T>A n.535T>A n.801T>A | |
| 8 | g.18222321T>C | CA370444962 | NAT1 | c.274T>C (p.Tyr92His) c.460T>C (p.Tyr154His) n.626T>C n.535T>C n.801T>C | |
| 8 | g.18222321T>G | CA370444963 | NAT1 | c.274T>G (p.Tyr92Asp) c.460T>G (p.Tyr154Asp) n.626T>G n.535T>G n.801T>G | |
| 8 | g.18222322A= | CA1768101087 | NAT1 | c.275A= (p.Tyr92=) c.461A= (p.Tyr154=) n.627A= n.536A= n.802A= | |
| 8 | g.18222322A>C | CA370444965 | NAT1 | c.275A>C (p.Tyr92Ser) c.461A>C (p.Tyr154Ser) n.627A>C n.536A>C n.802A>C | |
| 8 | g.18222322A>G | CA4651362 | NAT1 | c.275A>G (p.Tyr92Cys) c.461A>G (p.Tyr154Cys) n.627A>G n.536A>G n.802A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222322A>T | CA370444964 | NAT1 | c.275A>T (p.Tyr92Phe) c.461A>T (p.Tyr154Phe) n.627A>T n.536A>T n.802A>T | |
| 8 | g.18222323T>A | CA370444966 | NAT1 | c.276T>A (p.Tyr92Ter) c.462T>A (p.Tyr154Ter) n.628T>A n.537T>A n.803T>A | |
| 8 | g.18222323T>C | CA4651364 | NAT1 | c.276T>C (p.Tyr92=) c.462T>C (p.Tyr154=) n.628T>C n.537T>C n.803T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222323T>G | CA370444967 | NAT1 | c.276T>G (p.Tyr92Ter) c.462T>G (p.Tyr154Ter) n.628T>G n.537T>G n.803T>G | |
| 8 | g.18222323T= | CA1768101088 | NAT1 | c.276T= (p.Tyr92=) c.462T= (p.Tyr154=) n.628T= n.537T= n.803T= | |
| 8 | g.18222324_18222326dup | CA4651363 | NAT1 | c.277_279dup (p.Val93_Tyr94insVal) c.463_465dup (p.Val155_Tyr156insVal) n.629_631dup | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222324G>A | CA370444969 | NAT1 | c.277G>A (p.Val93Ile) c.463G>A (p.Val155Ile) n.629G>A n.538G>A n.804G>A | |
| 8 | g.18222324G>C | CA173180314 | NAT1 | c.277G>C (p.Val93Leu) c.463G>C (p.Val155Leu) n.629G>C n.538G>C n.804G>C | dbSNP |
| 8 | g.18222324G= | CA1768101089 | NAT1 | c.277G= (p.Val93=) c.463G= (p.Val155=) n.629G= n.538G= n.804G= | |
| 8 | g.18222324G>T | CA370444968 | NAT1 | c.277G>T (p.Val93Phe) c.463G>T (p.Val155Phe) n.629G>T n.538G>T n.804G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222325T>A | CA370444970 | NAT1 | c.278T>A (p.Val93Asp) c.464T>A (p.Val155Asp) n.630T>A | |
| 8 | g.18222325T>C | CA370444971 | NAT1 | c.278T>C (p.Val93Ala) c.464T>C (p.Val155Ala) n.630T>C | |
| 8 | g.18222325T>G | CA370444972 | NAT1 | c.278T>G (p.Val93Gly) c.464T>G (p.Val155Gly) n.630T>G | |
| 8 | g.18222326T>A | CA459877508 | NAT1 | c.279T>A (p.Val93=) c.465T>A (p.Val155=) n.631T>A | |
| 8 | g.18222326T>C | CA459877510 | NAT1 | c.279T>C (p.Val93=) c.465T>C (p.Val155=) n.631T>C | dbSNP gnomAD v4 |
| 8 | g.18222326T>G | CA459877509 | NAT1 | c.279T>G (p.Val93=) c.465T>G (p.Val155=) n.631T>G | |
| 8 | g.18222326T= | CA1768101090 | NAT1 | c.279T= (p.Val93=) c.465T= (p.Val155=) n.631T= | |
| 8 | g.18222327T>A | CA370444973 | NAT1 | c.280T>A (p.Tyr94Asn) c.466T>A (p.Tyr156Asn) n.632T>A | |
| 8 | g.18222327T>C | CA370444974 | NAT1 | c.280T>C (p.Tyr94His) c.466T>C (p.Tyr156His) n.632T>C | gnomAD v4 |
| 8 | g.18222327T>G | CA370444975 | NAT1 | c.280T>G (p.Tyr94Asp) c.466T>G (p.Tyr156Asp) n.632T>G | |
| 8 | g.18222328A>C | CA370444978 | NAT1 | c.281A>C (p.Tyr94Ser) c.467A>C (p.Tyr156Ser) n.633A>C | |
| 8 | g.18222328A>G | CA370444976 | NAT1 | c.281A>G (p.Tyr94Cys) c.467A>G (p.Tyr156Cys) n.633A>G | |
| 8 | g.18222328A>T | CA370444977 | NAT1 | c.281A>T (p.Tyr94Phe) c.467A>T (p.Tyr156Phe) n.633A>T | |
| 8 | g.18222329C>A | CA370444979 | NAT1 | c.282C>A (p.Tyr94Ter) c.468C>A (p.Tyr156Ter) n.634C>A | |
| 8 | g.18222329C>G | CA370444980 | NAT1 | c.282C>G (p.Tyr94Ter) c.468C>G (p.Tyr156Ter) n.634C>G | |
| 8 | g.18222329C>T | CA459877512 | NAT1 | c.282C>T (p.Tyr94=) c.468C>T (p.Tyr156=) n.634C>T | gnomAD v4 |
| 8 | g.18222330A>C | CA370444981 | NAT1 | c.283A>C (p.Ser95Arg) c.469A>C (p.Ser157Arg) n.635A>C | |
| 8 | g.18222330A>G | CA370444982 | NAT1 | c.283A>G (p.Ser95Gly) c.469A>G (p.Ser157Gly) n.635A>G | |
| 8 | g.18222330A>T | CA370444983 | NAT1 | c.283A>T (p.Ser95Cys) c.469A>T (p.Ser157Cys) n.635A>T | gnomAD v4 |
| 8 | g.18222331G>A | CA370444984 | NAT1 | c.284G>A (p.Ser95Asn) c.470G>A (p.Ser157Asn) n.636G>A | |
| 8 | g.18222331G>C | CA370444985 | NAT1 | c.284G>C (p.Ser95Thr) c.470G>C (p.Ser157Thr) n.636G>C | |
| 8 | g.18222331G>T | CA370444986 | NAT1 | c.284G>T (p.Ser95Ile) c.470G>T (p.Ser157Ile) n.636G>T | |
| 8 | g.18222332C>A | CA370444987 | NAT1 | c.285C>A (p.Ser95Arg) c.471C>A (p.Ser157Arg) n.637C>A | |
| 8 | g.18222332C>G | CA370444988 | NAT1 | c.285C>G (p.Ser95Arg) c.471C>G (p.Ser157Arg) n.637C>G | |
| 8 | g.18222332C>T | CA459877518 | NAT1 | c.285C>T (p.Ser95=) c.471C>T (p.Ser157=) n.637C>T | |
| 8 | g.18222333A= | CA1768101091 | NAT1 | c.286A= (p.Thr96=) c.472A= (p.Thr158=) n.638A= | |
| 8 | g.18222333A>C | CA370444989 | NAT1 | c.286A>C (p.Thr96Pro) c.472A>C (p.Thr158Pro) n.638A>C | dbSNP |
| 8 | g.18222333A>G | CA370444990 | NAT1 | c.286A>G (p.Thr96Ala) c.472A>G (p.Thr158Ala) n.638A>G | |
| 8 | g.18222333A>T | CA370444991 | NAT1 | c.286A>T (p.Thr96Ser) c.472A>T (p.Thr158Ser) n.638A>T | |
| 8 | g.18222334C>A | CA370444993 | NAT1 | c.287C>A (p.Thr96Asn) c.473C>A (p.Thr158Asn) n.639C>A | |
| 8 | g.18222334C= | CA1768101092 | NAT1 | c.287C= (p.Thr96=) c.473C= (p.Thr158=) n.639C= | |
| 8 | g.18222334C>G | CA370444992 | NAT1 | c.287C>G (p.Thr96Ser) c.473C>G (p.Thr158Ser) n.639C>G | |
| 8 | g.18222334C>T | CA4651365 | NAT1 | c.287C>T (p.Thr96Ile) c.473C>T (p.Thr158Ile) n.639C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222335T>A | CA459877520 | NAT1 | c.288T>A (p.Thr96=) c.474T>A (p.Thr158=) n.640T>A | |
| 8 | g.18222335T>C | CA459877521 | NAT1 | c.288T>C (p.Thr96=) c.474T>C (p.Thr158=) n.640T>C | |
| 8 | g.18222335T>G | CA459877522 | NAT1 | c.288T>G (p.Thr96=) c.474T>G (p.Thr158=) n.640T>G | |
| 8 | g.18222336C>A | CA370444994 | NAT1 | c.289C>A (p.Pro97Thr) c.475C>A (p.Pro159Thr) n.641C>A | gnomAD v4 |
| 8 | g.18222336C= | CA1768101093 | NAT1 | c.289C= (p.Pro97=) c.475C= (p.Pro159=) n.641C= | |
| 8 | g.18222336C>G | CA4651366 | NAT1 | c.289C>G (p.Pro97Ala) c.475C>G (p.Pro159Ala) n.641C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222336C>T | CA370444995 | NAT1 | c.289C>T (p.Pro97Ser) c.475C>T (p.Pro159Ser) n.641C>T | dbSNP gnomAD v4 |
| 8 | g.18222337C>A | CA370444996 | NAT1 | c.290C>A (p.Pro97Gln) c.476C>A (p.Pro159Gln) n.642C>A | |
| 8 | g.18222337C>G | CA370444997 | NAT1 | c.290C>G (p.Pro97Arg) c.476C>G (p.Pro159Arg) n.642C>G | |
| 8 | g.18222337C>T | CA370444998 | NAT1 | c.290C>T (p.Pro97Leu) c.476C>T (p.Pro159Leu) n.642C>T | |
| 8 | g.18222338A>C | CA459877525 | NAT1 | c.291A>C (p.Pro97=) c.477A>C (p.Pro159=) n.643A>C | |
| 8 | g.18222338A>G | CA459877527 | NAT1 | c.291A>G (p.Pro97=) c.477A>G (p.Pro159=) n.643A>G | |
| 8 | g.18222338A>T | CA459877526 | NAT1 | c.291A>T (p.Pro97=) c.477A>T (p.Pro159=) n.643A>T | |
| 8 | g.18222339G>A | CA370444999 | NAT1 | c.292G>A (p.Ala98Thr) c.478G>A (p.Ala160Thr) n.644G>A | |
| 8 | g.18222339G>C | CA370445000 | NAT1 | c.292G>C (p.Ala98Pro) c.478G>C (p.Ala160Pro) n.644G>C | |
| 8 | g.18222339G>T | CA370445001 | NAT1 | c.292G>T (p.Ala98Ser) c.478G>T (p.Ala160Ser) n.644G>T | |
| 8 | g.18222340C>A | CA370445002 | NAT1 | c.293C>A (p.Ala98Asp) c.479C>A (p.Ala160Asp) n.645C>A | gnomAD v4 |
| 8 | g.18222340C= | CA1768101094 | NAT1 | c.293C= (p.Ala98=) c.479C= (p.Ala160=) n.645C= | |
| 8 | g.18222340C>G | CA370445003 | NAT1 | c.293C>G (p.Ala98Gly) c.479C>G (p.Ala160Gly) n.645C>G | dbSNP gnomAD v2 |
| 8 | g.18222340C>T | CA4651367 | NAT1 | c.293C>T (p.Ala98Val) c.479C>T (p.Ala160Val) n.645C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222341C>A | CA459877531 | NAT1 | c.294C>A (p.Ala98=) c.480C>A (p.Ala160=) n.646C>A | |
| 8 | g.18222341C= | CA1768101095 | NAT1 | c.294C= (p.Ala98=) c.480C= (p.Ala160=) n.646C= | |
| 8 | g.18222341C>G | CA459877532 | NAT1 | c.294C>G (p.Ala98=) c.480C>G (p.Ala160=) n.646C>G | |
| 8 | g.18222341C>T | CA459877535 | NAT1 | c.294C>T (p.Ala98=) c.480C>T (p.Ala160=) n.646C>T | |
| 8 | g.18222342A>C | CA370445006 | NAT1 | c.295A>C (p.Lys99Gln) c.481A>C (p.Lys161Gln) n.647A>C | |
| 8 | g.18222342A>G | CA370445005 | NAT1 | c.295A>G (p.Lys99Glu) c.481A>G (p.Lys161Glu) n.647A>G | |
| 8 | g.18222342A>T | CA370445004 | NAT1 | c.295A>T (p.Lys99Ter) c.481A>T (p.Lys161Ter) n.647A>T | |
| 8 | g.18222347dup | CA4651368 | NAT1 | c.300dup (p.Tyr101IlefsTer15) c.486dup (p.Tyr163IlefsTer15) n.652dup | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 8 | g.18222347del | CA2686324948 | NAT1 | c.300del (p.Lys100AsnfsTer6) c.486del (p.Lys162AsnfsTer6) n.652del | gnomAD v4 |
| 8 | g.18222343A= | CA1768101096 | NAT1 | c.296A= (p.Lys99=) c.482A= (p.Lys161=) n.648A= | |
| 8 | g.18222343A>C | CA370445009 | NAT1 | c.296A>C (p.Lys99Thr) c.482A>C (p.Lys161Thr) n.648A>C | |
| 8 | g.18222343A>G | CA370445007 | NAT1 | c.296A>G (p.Lys99Arg) c.482A>G (p.Lys161Arg) n.648A>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222343A>T | CA370445008 | NAT1 | c.296A>T (p.Lys99Ile) c.482A>T (p.Lys161Ile) n.648A>T | |
| 8 | g.18222344A= | CA1768101097 | NAT1 | c.297A= (p.Lys99=) c.483A= (p.Lys161=) n.649A= | |
| 8 | g.18222344A>C | CA370445010 | NAT1 | c.297A>C (p.Lys99Asn) c.483A>C (p.Lys161Asn) n.649A>C | dbSNP gnomAD v2 |
| 8 | g.18222344A>G | CA459877540 | NAT1 | c.297A>G (p.Lys99=) c.483A>G (p.Lys161=) n.649A>G | |
| 8 | g.18222344A>T | CA370445011 | NAT1 | c.297A>T (p.Lys99Asn) c.483A>T (p.Lys161Asn) n.649A>T | |
| 8 | g.18222345A>C | CA370445012 | NAT1 | c.298A>C (p.Lys100Gln) c.484A>C (p.Lys162Gln) n.650A>C | |
| 8 | g.18222345A>G | CA370445013 | NAT1 | c.298A>G (p.Lys100Glu) c.484A>G (p.Lys162Glu) n.650A>G | gnomAD v4 |
| 8 | g.18222345A>T | CA370445014 | NAT1 | c.298A>T (p.Lys100Ter) c.484A>T (p.Lys162Ter) n.650A>T | |
| 8 | g.18222346A>C | CA370445015 | NAT1 | c.299A>C (p.Lys100Thr) c.485A>C (p.Lys162Thr) n.651A>C | |
| 8 | g.18222346A>G | CA370445016 | NAT1 | c.299A>G (p.Lys100Arg) c.485A>G (p.Lys162Arg) n.651A>G | gnomAD v4 |
| 8 | g.18222346A>T | CA370445017 | NAT1 | c.299A>T (p.Lys100Ile) c.485A>T (p.Lys162Ile) n.651A>T | |
| 8 | g.18222347A= | CA1768101098 | NAT1 | c.300A= (p.Lys100=) c.486A= (p.Lys162=) n.652A= | |
| 8 | g.18222347A>C | CA173180322 | NAT1 | c.300A>C (p.Lys100Asn) c.486A>C (p.Lys162Asn) n.652A>C | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222347A>G | CA459877544 | NAT1 | c.300A>G (p.Lys100=) c.486A>G (p.Lys162=) n.652A>G | gnomAD v4 |
| 8 | g.18222347A>T | CA370445018 | NAT1 | c.300A>T (p.Lys100Asn) c.486A>T (p.Lys162Asn) n.652A>T | |
| 8 | g.18222348T>A | CA370445021 | NAT1 | c.301T>A (p.Tyr101Asn) c.487T>A (p.Tyr163Asn) n.653T>A | |
| 8 | g.18222348T>C | CA370445020 | NAT1 | c.301T>C (p.Tyr101His) c.487T>C (p.Tyr163His) n.653T>C | |
| 8 | g.18222348T>G | CA370445019 | NAT1 | c.301T>G (p.Tyr101Asp) c.487T>G (p.Tyr163Asp) n.653T>G | |
| 8 | g.18222349A>C | CA370445022 | NAT1 | c.302A>C (p.Tyr101Ser) c.488A>C (p.Tyr163Ser) n.654A>C | |
| 8 | g.18222349A>G | CA370445023 | NAT1 | c.302A>G (p.Tyr101Cys) c.488A>G (p.Tyr163Cys) n.654A>G | |
| 8 | g.18222349A>T | CA370445024 | NAT1 | c.302A>T (p.Tyr101Phe) c.488A>T (p.Tyr163Phe) n.654A>T | |
| 8 | g.18222350C>A | CA370445025 | NAT1 | c.303C>A (p.Tyr101Ter) c.489C>A (p.Tyr163Ter) n.655C>A | gnomAD v4 |
| 8 | g.18222350C>G | CA370445026 | NAT1 | c.303C>G (p.Tyr101Ter) c.489C>G (p.Tyr163Ter) n.655C>G | gnomAD v4 |
| 8 | g.18222350C>T | CA459877549 | NAT1 | c.303C>T (p.Tyr101=) c.489C>T (p.Tyr163=) n.655C>T | gnomAD v4 |
| 8 | g.18222351A>C | CA370445027 | NAT1 | c.304A>C (p.Ser102Arg) c.490A>C (p.Ser164Arg) n.656A>C | |
| 8 | g.18222351A>G | CA370445028 | NAT1 | c.304A>G (p.Ser102Gly) c.490A>G (p.Ser164Gly) n.656A>G | |
| 8 | g.18222351A>T | CA370445029 | NAT1 | c.304A>T (p.Ser102Cys) c.490A>T (p.Ser164Cys) n.656A>T | |
| 8 | g.18222352G>A | CA370445030 | NAT1 | c.305G>A (p.Ser102Asn) c.491G>A (p.Ser164Asn) n.657G>A | COSMIC COSMIC |
| 8 | g.18222352G>C | CA370445031 | NAT1 | c.305G>C (p.Ser102Thr) c.491G>C (p.Ser164Thr) n.657G>C | |
| 8 | g.18222352G>T | CA370445032 | NAT1 | c.305G>T (p.Ser102Ile) c.491G>T (p.Ser164Ile) n.657G>T | |
| 8 | g.18222353C>A | CA370445033 | NAT1 | c.306C>A (p.Ser102Arg) c.492C>A (p.Ser164Arg) n.658C>A | |
| 8 | g.18222353C= | CA1768101099 | NAT1 | c.306C= (p.Ser102=) c.492C= (p.Ser164=) n.658C= | |
| 8 | g.18222353C>G | CA370445034 | NAT1 | c.306C>G (p.Ser102Arg) c.492C>G (p.Ser164Arg) n.658C>G | |
| 8 | g.18222353C>T | CA459877554 | NAT1 | c.306C>T (p.Ser102=) c.492C>T (p.Ser164=) n.658C>T | dbSNP gnomAD v4 |
| 8 | g.18222354A= | CA1768101100 | NAT1 | c.307A= (p.Thr103=) c.493A= (p.Thr165=) n.659A= | |
| 8 | g.18222354A>C | CA370445036 | NAT1 | c.307A>C (p.Thr103Pro) c.493A>C (p.Thr165Pro) n.659A>C | gnomAD v4 |
| 8 | g.18222354A>G | CA370445037 | NAT1 | c.307A>G (p.Thr103Ala) c.493A>G (p.Thr165Ala) n.659A>G | dbSNP gnomAD v4 |
| 8 | g.18222354A>T | CA370445035 | NAT1 | c.307A>T (p.Thr103Ser) c.493A>T (p.Thr165Ser) n.659A>T | |
| 8 | g.18222355C>A | CA370445038 | NAT1 | c.308C>A (p.Thr103Asn) c.494C>A (p.Thr165Asn) n.660C>A | |
| 8 | g.18222355C>G | CA370445040 | NAT1 | c.308C>G (p.Thr103Ser) c.494C>G (p.Thr165Ser) n.660C>G | |
| 8 | g.18222355C>T | CA370445039 | NAT1 | c.308C>T (p.Thr103Ile) c.494C>T (p.Thr165Ile) n.660C>T | |
| 8 | g.18222356T>A | CA459877556 | NAT1 | c.309T>A (p.Thr103=) c.495T>A (p.Thr165=) n.661T>A | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222356T>C | CA459877557 | NAT1 | c.309T>C (p.Thr103=) c.495T>C (p.Thr165=) n.661T>C | |
| 8 | g.18222356T>G | CA459877555 | NAT1 | c.309T>G (p.Thr103=) c.495T>G (p.Thr165=) n.661T>G | |
| 8 | g.18222356T= | CA1768101101 | NAT1 | c.309T= (p.Thr103=) c.495T= (p.Thr165=) n.661T= | |
| 8 | g.18222357G>A | CA4651369 | NAT1 | c.310G>A (p.Gly104Ser) c.496G>A (p.Gly166Ser) n.662G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222357G>C | CA370445041 | NAT1 | c.310G>C (p.Gly104Arg) c.496G>C (p.Gly166Arg) n.662G>C | |
| 8 | g.18222357G= | CA1768101102 | NAT1 | c.310G= (p.Gly104=) c.496G= (p.Gly166=) n.662G= | |
| 8 | g.18222357G>T | CA370445042 | NAT1 | c.310G>T (p.Gly104Cys) c.496G>T (p.Gly166Cys) n.662G>T | |
| 8 | g.18222358G>A | CA4651370 | NAT1 | c.311G>A (p.Gly104Asp) c.497G>A (p.Gly166Asp) n.663G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222358G>C | CA370445043 | NAT1 | c.311G>C (p.Gly104Ala) c.497G>C (p.Gly166Ala) n.663G>C | |
| 8 | g.18222358G= | CA1768101103 | NAT1 | c.311G= (p.Gly104=) c.497G= (p.Gly166=) n.663G= | |
| 8 | g.18222358G>T | CA4651371 | NAT1 | c.311G>T (p.Gly104Val) c.497G>T (p.Gly166Val) n.663G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18222359C>A | CA459877562 | NAT1 | c.312C>A (p.Gly104=) c.498C>A (p.Gly166=) n.664C>A | |
| 8 | g.18222359C= | CA1768101104 | NAT1 | c.312C= (p.Gly104=) c.498C= (p.Gly166=) n.664C= | |
| 8 | g.18222359C>G | CA459877563 | NAT1 | c.312C>G (p.Gly104=) c.498C>G (p.Gly166=) n.664C>G | |
| 8 | g.18222359C>T | CA459877564 | NAT1 | c.312C>T (p.Gly104=) c.498C>T (p.Gly166=) n.664C>T | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18222360A= | CA1768101105 | NAT1 | c.313A= (p.Met105=) c.499A= (p.Met167=) n.665A= | |
| 8 | g.18222360A>C | CA370445044 | NAT1 | c.313A>C (p.Met105Leu) c.499A>C (p.Met167Leu) n.665A>C | |
| 8 | g.18222360A>G | CA370445045 | NAT1 | c.313A>G (p.Met105Val) c.499A>G (p.Met167Val) n.665A>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222360A>T | CA370445046 | NAT1 | c.313A>T (p.Met105Leu) c.499A>T (p.Met167Leu) n.665A>T |