| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 | |
| 8 | g.18222361T>A | CA370445047 | NAT1 | c.314T>A (p.Met105Lys) c.500T>A (p.Met167Lys) n.666T>A | |
| 8 | g.18222361T>C | CA370445048 | NAT1 | c.314T>C (p.Met105Thr) c.500T>C (p.Met167Thr) n.666T>C | |
| 8 | g.18222361T>G | CA370445049 | NAT1 | c.314T>G (p.Met105Arg) c.500T>G (p.Met167Arg) n.666T>G | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18222361T= | CA1768101106 | NAT1 | c.314T= (p.Met105=) c.500T= (p.Met167=) n.666T= | |
| 8 | g.18222362G>A | CA4651373 | NAT1 | c.315G>A (p.Met105Ile) c.501G>A (p.Met167Ile) n.667G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18222362G>C | CA370445050 | NAT1 | c.315G>C (p.Met105Ile) c.501G>C (p.Met167Ile) n.667G>C | |
| 8 | g.18222362G= | CA1768101107 | NAT1 | c.315G= (p.Met105=) c.501G= (p.Met167=) n.667G= | |
| 8 | g.18222362G>T | CA4651372 | NAT1 | c.315G>T (p.Met105Ile) c.501G>T (p.Met167Ile) n.667G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 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 |