Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.18400750T>A | CA370636544 | NAT2 | c.747T>A (p.Asn249Lys) c.357T>A (p.Asn119Lys) | |
8 | g.18400750T>C | CA459699544 | NAT2 | c.747T>C (p.Asn249=) c.357T>C (p.Asn119=) | |
8 | g.18400750T>G | CA370636545 | NAT2 | c.747T>G (p.Asn249Lys) c.357T>G (p.Asn119Lys) | |
8 | g.18400751A= | CA1768219131 | NAT2 | c.748A= (p.Thr250=) c.358A= (p.Thr120=) | |
8 | g.18400751A>C | CA370636546 | NAT2 | c.748A>C (p.Thr250Pro) c.358A>C (p.Thr120Pro) | |
8 | g.18400751A>G | CA370636547 | NAT2 | c.748A>G (p.Thr250Ala) c.358A>G (p.Thr120Ala) | gnomAD v4 |
8 | g.18400751A>T | CA370636548 | NAT2 | c.748A>T (p.Thr250Ser) c.358A>T (p.Thr120Ser) | dbSNP |
8 | g.18400752C>A | CA173519941 | NAT2 | c.749C>A (p.Thr250Lys) c.359C>A (p.Thr120Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400752C= | CA1768219132 | NAT2 | c.749C= (p.Thr250=) c.359C= (p.Thr120=) | |
8 | g.18400752C>G | CA370636549 | NAT2 | c.749C>G (p.Thr250Arg) c.359C>G (p.Thr120Arg) | |
8 | g.18400752C>T | CA370636550 | NAT2 | c.749C>T (p.Thr250Ile) c.359C>T (p.Thr120Ile) | |
8 | g.18400753A>C | CA459699559 | NAT2 | c.750A>C (p.Thr250=) c.360A>C (p.Thr120=) | |
8 | g.18400753A>G | CA459699563 | NAT2 | c.750A>G (p.Thr250=) c.360A>G (p.Thr120=) | gnomAD v4 |
8 | g.18400753A>T | CA459699560 | NAT2 | c.750A>T (p.Thr250=) c.360A>T (p.Thr120=) | |
8 | g.18400754G>A | CA4651690 | NAT2 | c.751G>A (p.Asp251Asn) c.361G>A (p.Asp121Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.18400754G>C | CA370636551 | NAT2 | c.751G>C (p.Asp251His) c.361G>C (p.Asp121His) | |
8 | g.18400754G= | CA1768219133 | NAT2 | c.751G= (p.Asp251=) c.361G= (p.Asp121=) | |
8 | g.18400754G>T | CA370636552 | NAT2 | c.751G>T (p.Asp251Tyr) c.361G>T (p.Asp121Tyr) | gnomAD v4 |
8 | g.18400755A>C | CA370636554 | NAT2 | c.752A>C (p.Asp251Ala) c.362A>C (p.Asp121Ala) | |
8 | g.18400755A>G | CA370636555 | NAT2 | c.752A>G (p.Asp251Gly) c.362A>G (p.Asp121Gly) | gnomAD v4 |
8 | g.18400755A>T | CA370636553 | NAT2 | c.752A>T (p.Asp251Val) c.362A>T (p.Asp121Val) | |
8 | g.18400756T>A | CA370636556 | NAT2 | c.753T>A (p.Asp251Glu) c.363T>A (p.Asp121Glu) | |
8 | g.18400756T>C | CA459699578 | NAT2 | c.753T>C (p.Asp251=) c.363T>C (p.Asp121=) | |
8 | g.18400756T>G | CA370636557 | NAT2 | c.753T>G (p.Asp251Glu) c.363T>G (p.Asp121Glu) | gnomAD v4 |
8 | g.18400757C>A | CA370636558 | NAT2 | c.754C>A (p.Leu252Met) c.364C>A (p.Leu122Met) | |
8 | g.18400757C>G | CA370636559 | NAT2 | c.754C>G (p.Leu252Val) c.364C>G (p.Leu122Val) | |
8 | g.18400757C>T | CA459699584 | NAT2 | c.754C>T (p.Leu252=) c.364C>T (p.Leu122=) | |
8 | g.18400758T>A | CA370636562 | NAT2 | c.755T>A (p.Leu252Gln) c.365T>A (p.Leu122Gln) | |
8 | g.18400758T>C | CA370636561 | NAT2 | c.755T>C (p.Leu252Pro) c.365T>C (p.Leu122Pro) | |
8 | g.18400758T>G | CA370636560 | NAT2 | c.755T>G (p.Leu252Arg) c.365T>G (p.Leu122Arg) | |
8 | g.18400759G>A | CA459699594 | NAT2 | c.756G>A (p.Leu252=) c.366G>A (p.Leu122=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400759G>C | CA459699596 | NAT2 | c.756G>C (p.Leu252=) c.366G>C (p.Leu122=) | |
8 | g.18400759G= | CA1768219134 | NAT2 | c.756G= (p.Leu252=) c.366G= (p.Leu122=) | |
8 | g.18400759G>T | CA459699598 | NAT2 | c.756G>T (p.Leu252=) c.366G>T (p.Leu122=) | gnomAD v4 |
8 | g.18400760G>A | CA370636563 | NAT2 | c.757G>A (p.Val253Ile) c.367G>A (p.Val123Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400760G>C | CA370636564 | NAT2 | c.757G>C (p.Val253Leu) c.367G>C (p.Val123Leu) | |
8 | g.18400760G= | CA1768219135 | NAT2 | c.757G= (p.Val253=) c.367G= (p.Val123=) | |
8 | g.18400760G>T | CA370636565 | NAT2 | c.757G>T (p.Val253Phe) c.367G>T (p.Val123Phe) | dbSNP gnomAD v4 |
8 | g.18400761T>A | CA370636566 | NAT2 | c.758T>A (p.Val253Asp) c.368T>A (p.Val123Asp) | |
8 | g.18400761T>C | CA4651691 | NAT2 | c.758T>C (p.Val253Ala) c.368T>C (p.Val123Ala) | dbSNP ExAC gnomAD v2 |
8 | g.18400761T>G | CA370636567 | NAT2 | c.758T>G (p.Val253Gly) c.368T>G (p.Val123Gly) | |
8 | g.18400761T= | CA1768219136 | NAT2 | c.758T= (p.Val253=) c.368T= (p.Val123=) | |
8 | g.18400762C>A | CA459699616 | NAT2 | c.759C>A (p.Val253=) c.369C>A (p.Val123=) | |
8 | g.18400762C= | CA1768219137 | NAT2 | c.759C= (p.Val253=) c.369C= (p.Val123=) | |
8 | g.18400762C>G | CA459699612 | NAT2 | c.759C>G (p.Val253=) c.369C>G (p.Val123=) | |
8 | g.18400762C>T | CA4651692 | NAT2 | c.759C>T (p.Val253=) c.369C>T (p.Val123=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400763G>A | CA4651693 | NAT2 | c.760G>A (p.Glu254Lys) c.370G>A (p.Glu124Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.18400763G>C | CA370636569 | NAT2 | c.760G>C (p.Glu254Gln) c.370G>C (p.Glu124Gln) | dbSNP |
8 | g.18400763G= | CA1768219138 | NAT2 | c.760G= (p.Glu254=) c.370G= (p.Glu124=) | |
8 | g.18400763G>T | CA370636568 | NAT2 | c.760G>T (p.Glu254Ter) c.370G>T (p.Glu124Ter) | gnomAD v4 COSMIC |
8 | g.18400764A>C | CA370636570 | NAT2 | c.761A>C (p.Glu254Ala) c.371A>C (p.Glu124Ala) | |
8 | g.18400764A>G | CA370636572 | NAT2 | c.761A>G (p.Glu254Gly) c.371A>G (p.Glu124Gly) | gnomAD v4 |
8 | g.18400764A>T | CA370636571 | NAT2 | c.761A>T (p.Glu254Val) c.371A>T (p.Glu124Val) | |
8 | g.18400765G>A | CA173519942 | NAT2 | c.762G>A (p.Glu254=) c.372G>A (p.Glu124=) | dbSNP |
8 | g.18400765G>C | CA370636573 | NAT2 | c.762G>C (p.Glu254Asp) c.372G>C (p.Glu124Asp) | |
8 | g.18400765G= | CA1768219139 | NAT2 | c.762G= (p.Glu254=) c.372G= (p.Glu124=) | |
8 | g.18400765G>T | CA370636574 | NAT2 | c.762G>T (p.Glu254Asp) c.372G>T (p.Glu124Asp) | |
8 | g.18400765dup | CA2539107248 | NAT2 | c.762dup (p.Phe255ValfsTer2) c.372dup (p.Phe125ValfsTer2) | |
8 | g.18400766T>A | CA370636575 | NAT2 | c.763T>A (p.Phe255Ile) c.373T>A (p.Phe125Ile) | |
8 | g.18400766T>C | CA370636576 | NAT2 | c.763T>C (p.Phe255Leu) c.373T>C (p.Phe125Leu) | |
8 | g.18400766T>G | CA370636577 | NAT2 | c.763T>G (p.Phe255Val) c.373T>G (p.Phe125Val) | |
8 | g.18400767T>A | CA370636578 | NAT2 | c.764T>A (p.Phe255Tyr) c.374T>A (p.Phe125Tyr) | |
8 | g.18400767T>C | CA370636579 | NAT2 | c.764T>C (p.Phe255Ser) c.374T>C (p.Phe125Ser) | |
8 | g.18400767T>G | CA370636580 | NAT2 | c.764T>G (p.Phe255Cys) c.374T>G (p.Phe125Cys) | |
8 | g.18400767_18400768insCAAGCGTAAA | CA2550720478 | NAT2 | c.764_765insCAAGCGTAAA (p.Thr257ArgfsTer3) c.374_375insCAAGCGTAAA (p.Thr127ArgfsTer3) | |
8 | g.18400768T>A | CA370636581 | NAT2 | c.765T>A (p.Phe255Leu) c.375T>A (p.Phe125Leu) | |
8 | g.18400768T>C | CA459699646 | NAT2 | c.765T>C (p.Phe255=) c.375T>C (p.Phe125=) | |
8 | g.18400768T>G | CA370636582 | NAT2 | c.765T>G (p.Phe255Leu) c.375T>G (p.Phe125Leu) | gnomAD v3 gnomAD v4 |
8 | g.18400769A= | CA1768219140 | NAT2 | c.766A= (p.Lys256=) c.376A= (p.Lys126=) | |
8 | g.18400769A>C | CA370636584 | NAT2 | c.766A>C (p.Lys256Gln) c.376A>C (p.Lys126Gln) | |
8 | g.18400769A>G | CA4651694 | NAT2 | c.766A>G (p.Lys256Glu) c.376A>G (p.Lys126Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400769A>T | CA370636583 | NAT2 | c.766A>T (p.Lys256Ter) c.376A>T (p.Lys126Ter) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400770A>C | CA370636585 | NAT2 | c.767A>C (p.Lys256Thr) c.377A>C (p.Lys126Thr) | |
8 | g.18400770A>G | CA370636586 | NAT2 | c.767A>G (p.Lys256Arg) c.377A>G (p.Lys126Arg) | gnomAD v4 |
8 | g.18400770A>T | CA370636587 | NAT2 | c.767A>T (p.Lys256Ile) c.377A>T (p.Lys126Ile) | |
8 | g.18400771A>C | CA370636588 | NAT2 | c.768A>C (p.Lys256Asn) c.378A>C (p.Lys126Asn) | gnomAD v4 |
8 | g.18400771A>G | CA459699661 | NAT2 | c.768A>G (p.Lys256=) c.378A>G (p.Lys126=) | |
8 | g.18400771A>T | CA370636589 | NAT2 | c.768A>T (p.Lys256Asn) c.378A>T (p.Lys126Asn) | |
8 | g.18400772A= | CA1768219141 | NAT2 | c.769A= (p.Thr257=) c.379A= (p.Thr127=) | |
8 | g.18400772A>C | CA370636590 | NAT2 | c.769A>C (p.Thr257Pro) c.379A>C (p.Thr127Pro) | |
8 | g.18400772A>G | CA4651696 | NAT2 | c.769A>G (p.Thr257Ala) c.379A>G (p.Thr127Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18400772A>T | CA4651695 | NAT2 | c.769A>T (p.Thr257Ser) c.379A>T (p.Thr127Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400772_18400774delinsACT | CA1768219142 | NAT2 | c.769_771delinsACT (p.Thr257=) c.379_381delinsACT (p.Thr127=) | |
8 | g.18400773C>A | CA370636591 | NAT2 | c.770C>A (p.Thr257Asn) c.380C>A (p.Thr127Asn) | |
8 | g.18400773C= | CA1768219143 | NAT2 | c.770C= (p.Thr257=) c.380C= (p.Thr127=) | |
8 | g.18400773C>G | CA4651697 | NAT2 | c.770C>G (p.Thr257Ser) c.380C>G (p.Thr127Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18400773C>T | CA370636592 | NAT2 | c.770C>T (p.Thr257Ile) c.380C>T (p.Thr127Ile) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400776_18400777del | CA580502475 | NAT2 | c.773_774del (p.Leu258HisfsTer2) c.383_384del (p.Leu128HisfsTer2) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400774T>A | CA459699679 | NAT2 | c.771T>A (p.Thr257=) c.381T>A (p.Thr127=) | |
8 | g.18400774T>C | CA459699680 | NAT2 | c.771T>C (p.Thr257=) c.381T>C (p.Thr127=) | |
8 | g.18400774T>G | CA459699683 | NAT2 | c.771T>G (p.Thr257=) c.381T>G (p.Thr127=) | |
8 | g.18400775C>A | CA370636594 | NAT2 | c.772C>A (p.Leu258Ile) c.382C>A (p.Leu128Ile) | |
8 | g.18400775C= | CA1768219144 | NAT2 | c.772C= (p.Leu258=) c.382C= (p.Leu128=) | |
8 | g.18400775C>G | CA4651698 | NAT2 | c.772C>G (p.Leu258Val) c.382C>G (p.Leu128Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18400775C>T | CA370636593 | NAT2 | c.772C>T (p.Leu258Phe) c.382C>T (p.Leu128Phe) | |
8 | g.18400776T>A | CA370636595 | NAT2 | c.773T>A (p.Leu258His) c.383T>A (p.Leu128His) | |
8 | g.18400776T>C | CA370636596 | NAT2 | c.773T>C (p.Leu258Pro) c.383T>C (p.Leu128Pro) | gnomAD v4 |
8 | g.18400776T>G | CA370636597 | NAT2 | c.773T>G (p.Leu258Arg) c.383T>G (p.Leu128Arg) | |
8 | g.18400777C>A | CA173519943 | NAT2 | c.774C>A (p.Leu258=) c.384C>A (p.Leu128=) | dbSNP gnomAD v4 |
8 | g.18400777C= | CA1768219145 | NAT2 | c.774C= (p.Leu258=) c.384C= (p.Leu128=) | |
8 | g.18400777C>G | CA459699695 | NAT2 | c.774C>G (p.Leu258=) c.384C>G (p.Leu128=) | dbSNP |
8 | g.18400777C>T | CA459699698 | NAT2 | c.774C>T (p.Leu258=) c.384C>T (p.Leu128=) | |
8 | g.18400778A= | CA1768219146 | NAT2 | c.775A= (p.Thr259=) c.385A= (p.Thr129=) | |
8 | g.18400778A>C | CA370636598 | NAT2 | c.775A>C (p.Thr259Pro) c.385A>C (p.Thr129Pro) | gnomAD v4 |
8 | g.18400778A>G | CA370636599 | NAT2 | c.775A>G (p.Thr259Ala) c.385A>G (p.Thr129Ala) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
8 | g.18400778A>T | CA370636600 | NAT2 | c.775A>T (p.Thr259Ser) c.385A>T (p.Thr129Ser) | |
8 | g.18400779C>A | CA370636601 | NAT2 | c.776C>A (p.Thr259Asn) c.386C>A (p.Thr129Asn) | dbSNP |
8 | g.18400779C= | CA1768219147 | NAT2 | c.776C= (p.Thr259=) c.386C= (p.Thr129=) | |
8 | g.18400779C>G | CA370636602 | NAT2 | c.776C>G (p.Thr259Ser) c.386C>G (p.Thr129Ser) | |
8 | g.18400779C>T | CA370636603 | NAT2 | c.776C>T (p.Thr259Ile) c.386C>T (p.Thr129Ile) | dbSNP gnomAD v4 |
8 | g.18400780T>A | CA459699712 | NAT2 | c.777T>A (p.Thr259=) c.387T>A (p.Thr129=) | |
8 | g.18400780T>C | CA459699714 | NAT2 | c.777T>C (p.Thr259=) c.387T>C (p.Thr129=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400780T>G | CA459699716 | NAT2 | c.777T>G (p.Thr259=) c.387T>G (p.Thr129=) | gnomAD v4 |
8 | g.18400780T= | CA1768219148 | NAT2 | c.777T= (p.Thr259=) c.387T= (p.Thr129=) | |
8 | g.18400781G>A | CA4651699 | NAT2 | c.778G>A (p.Glu260Lys) c.388G>A (p.Glu130Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
8 | g.18400781G>C | CA370636604 | NAT2 | c.778G>C (p.Glu260Gln) c.388G>C (p.Glu130Gln) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400781G= | CA1768219149 | NAT2 | c.778G= (p.Glu260=) c.388G= (p.Glu130=) | |
8 | g.18400781G>T | CA370636605 | NAT2 | c.778G>T (p.Glu260Ter) c.388G>T (p.Glu130Ter) | gnomAD v4 |
8 | g.18400782A= | CA1768219150 | NAT2 | c.779A= (p.Glu260=) c.389A= (p.Glu130=) | |
8 | g.18400782A>C | CA370636607 | NAT2 | c.779A>C (p.Glu260Ala) c.389A>C (p.Glu130Ala) | |
8 | g.18400782A>G | CA370636608 | NAT2 | c.779A>G (p.Glu260Gly) c.389A>G (p.Glu130Gly) | |
8 | g.18400782A>T | CA370636606 | NAT2 | c.779A>T (p.Glu260Val) c.389A>T (p.Glu130Val) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400783G>A | CA459699732 | NAT2 | c.780G>A (p.Glu260=) c.390G>A (p.Glu130=) | |
8 | g.18400783G>C | CA4651701 | NAT2 | c.780G>C (p.Glu260Asp) c.390G>C (p.Glu130Asp) | dbSNP ExAC gnomAD v2 |
8 | g.18400783G= | CA1768219151 | NAT2 | c.780G= (p.Glu260=) c.390G= (p.Glu130=) | |
8 | g.18400783G>T | CA370636609 | NAT2 | c.780G>T (p.Glu260Asp) c.390G>T (p.Glu130Asp) | |
8 | g.18400784dup | CA4651700 | NAT2 | c.781dup (p.Glu261GlyfsTer4) c.391dup (p.Glu131GlyfsTer4) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18400784G>A | CA173519944 | NAT2 | c.781G>A (p.Glu261Lys) c.391G>A (p.Glu131Lys) | dbSNP |
8 | g.18400784G>C | CA370636610 | NAT2 | c.781G>C (p.Glu261Gln) c.391G>C (p.Glu131Gln) | |
8 | g.18400784G= | CA1768219152 | NAT2 | c.781G= (p.Glu261=) c.391G= (p.Glu131=) | |
8 | g.18400784G>T | CA370636611 | NAT2 | c.781G>T (p.Glu261Ter) c.391G>T (p.Glu131Ter) | gnomAD v4 |
8 | g.18400785A= | CA1768219153 | NAT2 | c.782A= (p.Glu261=) c.392A= (p.Glu131=) | |
8 | g.18400785A>C | CA370636614 | NAT2 | c.782A>C (p.Glu261Ala) c.392A>C (p.Glu131Ala) | |
8 | g.18400785A>G | CA370636612 | NAT2 | c.782A>G (p.Glu261Gly) c.392A>G (p.Glu131Gly) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400785A>T | CA370636613 | NAT2 | c.782A>T (p.Glu261Val) c.392A>T (p.Glu131Val) | |
8 | g.18400786A>C | CA370636615 | NAT2 | c.783A>C (p.Glu261Asp) c.393A>C (p.Glu131Asp) | |
8 | g.18400786A>G | CA459699751 | NAT2 | c.783A>G (p.Glu261=) c.393A>G (p.Glu131=) | |
8 | g.18400786A>T | CA370636616 | NAT2 | c.783A>T (p.Glu261Asp) c.393A>T (p.Glu131Asp) | |
8 | g.18400787G>A | CA370636617 | NAT2 | c.784G>A (p.Glu262Lys) c.394G>A (p.Glu132Lys) | gnomAD v4 |
8 | g.18400787G>C | CA370636618 | NAT2 | c.784G>C (p.Glu262Gln) c.394G>C (p.Glu132Gln) | |
8 | g.18400787G>T | CA370636619 | NAT2 | c.784G>T (p.Glu262Ter) c.394G>T (p.Glu132Ter) | |
8 | g.18400788del | CA2686326442 | NAT2 | c.785del (p.Glu262GlyfsTer6) c.395del (p.Glu132GlyfsTer6) | gnomAD v4 |
8 | g.18400788A>C | CA370636620 | NAT2 | c.785A>C (p.Glu262Ala) c.395A>C (p.Glu132Ala) | |
8 | g.18400788A>G | CA370636622 | NAT2 | c.785A>G (p.Glu262Gly) c.395A>G (p.Glu132Gly) | |
8 | g.18400788A>T | CA370636621 | NAT2 | c.785A>T (p.Glu262Val) c.395A>T (p.Glu132Val) | |
8 | g.18400789G>A | CA459699766 | NAT2 | c.786G>A (p.Glu262=) c.396G>A (p.Glu132=) | gnomAD v4 |
8 | g.18400789G>C | CA4651702 | NAT2 | c.786G>C (p.Glu262Asp) c.396G>C (p.Glu132Asp) | dbSNP ExAC |
8 | g.18400789G= | CA1768219154 | NAT2 | c.786G= (p.Glu262=) c.396G= (p.Glu132=) | |
8 | g.18400789G>T | CA370636623 | NAT2 | c.786G>T (p.Glu262Asp) c.396G>T (p.Glu132Asp) | |
8 | g.18400790G>A | CA370636624 | NAT2 | c.787G>A (p.Val263Ile) c.397G>A (p.Val133Ile) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400790G>C | CA370636625 | NAT2 | c.787G>C (p.Val263Leu) c.397G>C (p.Val133Leu) | |
8 | g.18400790G= | CA1768219155 | NAT2 | c.787G= (p.Val263=) c.397G= (p.Val133=) | |
8 | g.18400790G>T | CA370636626 | NAT2 | c.787G>T (p.Val263Phe) c.397G>T (p.Val133Phe) | gnomAD v4 |
8 | g.18400791T>A | CA370636627 | NAT2 | c.788T>A (p.Val263Asp) c.398T>A (p.Val133Asp) | |
8 | g.18400791T>C | CA173519945 | NAT2 | c.788T>C (p.Val263Ala) c.398T>C (p.Val133Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400791T>G | CA370636628 | NAT2 | c.788T>G (p.Val263Gly) c.398T>G (p.Val133Gly) | gnomAD v4 |
8 | g.18400791T= | CA1768219156 | NAT2 | c.788T= (p.Val263=) c.398T= (p.Val133=) | |
8 | g.18400792T>A | CA459699776 | NAT2 | c.789T>A (p.Val263=) c.399T>A (p.Val133=) | |
8 | g.18400792T>C | CA459699778 | NAT2 | c.789T>C (p.Val263=) c.399T>C (p.Val133=) | |
8 | g.18400792T>G | CA459699780 | NAT2 | c.789T>G (p.Val263=) c.399T>G (p.Val133=) | |
8 | g.18400793G>A | CA173519946 | NAT2 | c.790G>A (p.Glu264Lys) c.400G>A (p.Glu134Lys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
8 | g.18400793G>C | CA370636629 | NAT2 | c.790G>C (p.Glu264Gln) c.400G>C (p.Glu134Gln) | |
8 | g.18400793G= | CA1768219157 | NAT2 | c.790G= (p.Glu264=) c.400G= (p.Glu134=) | |
8 | g.18400793G>T | CA370636630 | NAT2 | c.790G>T (p.Glu264Ter) c.400G>T (p.Glu134Ter) | |
8 | g.18400797_18400799del | CA2686326443 | NAT2 | c.794_796del (p.Glu265del) c.404_406del (p.Glu135del) | gnomAD v4 |
8 | g.18400794A>C | CA370636631 | NAT2 | c.791A>C (p.Glu264Ala) c.401A>C (p.Glu134Ala) | |
8 | g.18400794A>G | CA370636632 | NAT2 | c.791A>G (p.Glu264Gly) c.401A>G (p.Glu134Gly) | |
8 | g.18400794A>T | CA370636633 | NAT2 | c.791A>T (p.Glu264Val) c.401A>T (p.Glu134Val) | |
8 | g.18400795del | CA2686326444 | NAT2 | c.792del (p.Glu265LysfsTer3) c.402del (p.Glu135LysfsTer3) | gnomAD v4 |
8 | g.18400795A>C | CA370636634 | NAT2 | c.792A>C (p.Glu264Asp) c.402A>C (p.Glu134Asp) | |
8 | g.18400795A>G | CA459699794 | NAT2 | c.792A>G (p.Glu264=) c.402A>G (p.Glu134=) | gnomAD v4 |
8 | g.18400795A>T | CA370636635 | NAT2 | c.792A>T (p.Glu264Asp) c.402A>T (p.Glu134Asp) | |
8 | g.18400796G>A | CA370636638 | NAT2 | c.793G>A (p.Glu265Lys) c.403G>A (p.Glu135Lys) | |
8 | g.18400796G>C | CA370636636 | NAT2 | c.793G>C (p.Glu265Gln) c.403G>C (p.Glu135Gln) | gnomAD v4 |
8 | g.18400796G>T | CA370636637 | NAT2 | c.793G>T (p.Glu265Ter) c.403G>T (p.Glu135Ter) | |
8 | g.18400797A>C | CA370636639 | NAT2 | c.794A>C (p.Glu265Ala) c.404A>C (p.Glu135Ala) | |
8 | g.18400797A>G | CA370636640 | NAT2 | c.794A>G (p.Glu265Gly) c.404A>G (p.Glu135Gly) | |
8 | g.18400797A>T | CA370636641 | NAT2 | c.794A>T (p.Glu265Val) c.404A>T (p.Glu135Val) | |
8 | g.18400798A>C | CA370636642 | NAT2 | c.795A>C (p.Glu265Asp) c.405A>C (p.Glu135Asp) | |
8 | g.18400798A>G | CA459699809 | NAT2 | c.795A>G (p.Glu265=) c.405A>G (p.Glu135=) | gnomAD v4 |
8 | g.18400798A>T | CA370636643 | NAT2 | c.795A>T (p.Glu265Asp) c.405A>T (p.Glu135Asp) | |
8 | g.18400799G>A | CA4651703 | NAT2 | c.796G>A (p.Val266Met) c.406G>A (p.Val136Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400799G>C | CA370636644 | NAT2 | c.796G>C (p.Val266Leu) c.406G>C (p.Val136Leu) | |
8 | g.18400799G= | CA1768219158 | NAT2 | c.796G= (p.Val266=) c.406G= (p.Val136=) | |
8 | g.18400799G>T | CA370636645 | NAT2 | c.796G>T (p.Val266Leu) c.406G>T (p.Val136Leu) | gnomAD v4 |
8 | g.18400800T>A | CA370636646 | NAT2 | c.797T>A (p.Val266Glu) c.407T>A (p.Val136Glu) | |
8 | g.18400800T>C | CA370636647 | NAT2 | c.797T>C (p.Val266Ala) c.407T>C (p.Val136Ala) | |
8 | g.18400800T>G | CA370636648 | NAT2 | c.797T>G (p.Val266Gly) c.407T>G (p.Val136Gly) | |
8 | g.18400801G>A | CA459699822 | NAT2 | c.798G>A (p.Val266=) c.408G>A (p.Val136=) | |
8 | g.18400801G>C | CA459699823 | NAT2 | c.798G>C (p.Val266=) c.408G>C (p.Val136=) | |
8 | g.18400801G>T | CA459699826 | NAT2 | c.798G>T (p.Val266=) c.408G>T (p.Val136=) | gnomAD v4 |
8 | g.18400802C>A | CA370636649 | NAT2 | c.799C>A (p.Leu267Met) c.409C>A (p.Leu137Met) | |
8 | g.18400802C>G | CA370636650 | NAT2 | c.799C>G (p.Leu267Val) c.409C>G (p.Leu137Val) | gnomAD v4 |
8 | g.18400802C>T | CA459699831 | NAT2 | c.799C>T (p.Leu267=) c.409C>T (p.Leu137=) | |
8 | g.18400803T>A | CA370636651 | NAT2 | c.800T>A (p.Leu267Gln) c.410T>A (p.Leu137Gln) | |
8 | g.18400803T>C | CA370636653 | NAT2 | c.800T>C (p.Leu267Pro) c.410T>C (p.Leu137Pro) | |
8 | g.18400803T>G | CA370636652 | NAT2 | c.800T>G (p.Leu267Arg) c.410T>G (p.Leu137Arg) | |
8 | g.18400804G>A | CA459699840 | NAT2 | c.801G>A (p.Leu267=) c.411G>A (p.Leu137=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400804G>C | CA459699838 | NAT2 | c.801G>C (p.Leu267=) c.411G>C (p.Leu137=) | gnomAD v4 |
8 | g.18400804G= | CA1768219159 | NAT2 | c.801G= (p.Leu267=) c.411G= (p.Leu137=) | |
8 | g.18400804G>T | CA459699837 | NAT2 | c.801G>T (p.Leu267=) c.411G>T (p.Leu137=) | |
8 | g.18400805A= | CA1768219160 | NAT2 | c.802A= (p.Arg268=) c.412A= (p.Arg138=) | |
8 | g.18400805A>C | CA459699843 | NAT2 | c.802A>C (p.Arg268=) c.412A>C (p.Arg138=) | |
8 | g.18400805A>G | CA173519947 | NAT2 | c.802A>G (p.Arg268Gly) c.412A>G (p.Arg138Gly) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400805A>T | CA370636654 | NAT2 | c.802A>T (p.Arg268Ter) c.412A>T (p.Arg138Ter) | |
8 | g.18400806G>A | CA4651704 | NAT2 | c.803G>A (p.Arg268Lys) c.413G>A (p.Arg138Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400806G>C | CA370636655 | NAT2 | c.803G>C (p.Arg268Thr) c.413G>C (p.Arg138Thr) | dbSNP gnomAD v4 |
8 | g.18400806G= | CA114451 | NAT2 | c.803G= (p.Arg268=) c.413G= (p.Arg138=) | |
8 | g.18400806G>T | CA370636656 | NAT2 | c.803G>T (p.Arg268Ile) c.413G>T (p.Arg138Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400807A>C | CA370636657 | NAT2 | c.804A>C (p.Arg268Ser) c.414A>C (p.Arg138Ser) | |
8 | g.18400807A>G | CA459699856 | NAT2 | c.804A>G (p.Arg268=) c.414A>G (p.Arg138=) | |
8 | g.18400807A>T | CA370636658 | NAT2 | c.804A>T (p.Arg268Ser) c.414A>T (p.Arg138Ser) | |
8 | g.18400808A>C | CA370636659 | NAT2 | c.805A>C (p.Asn269His) c.415A>C (p.Asn139His) | |
8 | g.18400808A>G | CA370636660 | NAT2 | c.805A>G (p.Asn269Asp) c.415A>G (p.Asn139Asp) | |
8 | g.18400808A>T | CA370636661 | NAT2 | c.805A>T (p.Asn269Tyr) c.415A>T (p.Asn139Tyr) | |
8 | g.18400809A= | CA1768219161 | NAT2 | c.806A= (p.Asn269=) c.416A= (p.Asn139=) | |
8 | g.18400809A>C | CA370636664 | NAT2 | c.806A>C (p.Asn269Thr) c.416A>C (p.Asn139Thr) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400809A>G | CA370636663 | NAT2 | c.806A>G (p.Asn269Ser) c.416A>G (p.Asn139Ser) | |
8 | g.18400809A>T | CA370636662 | NAT2 | c.806A>T (p.Asn269Ile) c.416A>T (p.Asn139Ile) | |
8 | g.18400810T>A | CA370636665 | NAT2 | c.807T>A (p.Asn269Lys) c.417T>A (p.Asn139Lys) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400810T>C | CA459699866 | NAT2 | c.807T>C (p.Asn269=) c.417T>C (p.Asn139=) | |
8 | g.18400810T>G | CA370636666 | NAT2 | c.807T>G (p.Asn269Lys) c.417T>G (p.Asn139Lys) | |
8 | g.18400810T= | CA1768219162 | NAT2 | c.807T= (p.Asn269=) c.417T= (p.Asn139=) | |
8 | g.18400811A>C | CA370636667 | NAT2 | c.808A>C (p.Ile270Leu) c.418A>C (p.Ile140Leu) | gnomAD v4 |
8 | g.18400811A>G | CA370636668 | NAT2 | c.808A>G (p.Ile270Val) c.418A>G (p.Ile140Val) | |
8 | g.18400811A>T | CA370636669 | NAT2 | c.808A>T (p.Ile270Leu) c.418A>T (p.Ile140Leu) | |
8 | g.18400812T>A | CA370636670 | NAT2 | c.809T>A (p.Ile270Lys) c.419T>A (p.Ile140Lys) | |
8 | g.18400812T>C | CA173519948 | NAT2 | c.809T>C (p.Ile270Thr) c.419T>C (p.Ile140Thr) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400812T>G | CA370636671 | NAT2 | c.809T>G (p.Ile270Arg) c.419T>G (p.Ile140Arg) | dbSNP |
8 | g.18400812T= | CA1768219163 | NAT2 | c.809T= (p.Ile270=) c.419T= (p.Ile140=) | |
8 | g.18400813A= | CA1768219164 | NAT2 | c.810A= (p.Ile270=) c.420A= (p.Ile140=) | |
8 | g.18400813A>C | CA459699879 | NAT2 | c.810A>C (p.Ile270=) c.420A>C (p.Ile140=) | |
8 | g.18400813A>G | CA370636672 | NAT2 | c.810A>G (p.Ile270Met) c.420A>G (p.Ile140Met) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400813A>T | CA459699883 | NAT2 | c.810A>T (p.Ile270=) c.420A>T (p.Ile140=) | |
8 | g.18400814T>A | CA370636673 | NAT2 | c.811T>A (p.Phe271Ile) c.421T>A (p.Phe141Ile) | |
8 | g.18400814T>C | CA4651705 | NAT2 | c.811T>C (p.Phe271Leu) c.421T>C (p.Phe141Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400814T>G | CA370636674 | NAT2 | c.811T>G (p.Phe271Val) c.421T>G (p.Phe141Val) | |
8 | g.18400814T= | CA1768219165 | NAT2 | c.811T= (p.Phe271=) c.421T= (p.Phe141=) | |
8 | g.18400815T>A | CA370636677 | NAT2 | c.812T>A (p.Phe271Tyr) c.422T>A (p.Phe141Tyr) | |
8 | g.18400815T>C | CA370636676 | NAT2 | c.812T>C (p.Phe271Ser) c.422T>C (p.Phe141Ser) | |
8 | g.18400815T>G | CA370636675 | NAT2 | c.812T>G (p.Phe271Cys) c.422T>G (p.Phe141Cys) | |
8 | g.18400816T>A | CA370636678 | NAT2 | c.813T>A (p.Phe271Leu) c.423T>A (p.Phe141Leu) | |
8 | g.18400816T>C | CA459699893 | NAT2 | c.813T>C (p.Phe271=) c.423T>C (p.Phe141=) | |
8 | g.18400816T>G | CA370636679 | NAT2 | c.813T>G (p.Phe271Leu) c.423T>G (p.Phe141Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400816T= | CA1768219166 | NAT2 | c.813T= (p.Phe271=) c.423T= (p.Phe141=) | |
8 | g.18400817A= | CA1768219167 | NAT2 | c.814A= (p.Lys272=) c.424A= (p.Lys142=) | |
8 | g.18400817A>C | CA370636680 | NAT2 | c.814A>C (p.Lys272Gln) c.424A>C (p.Lys142Gln) | |
8 | g.18400817A>G | CA370636681 | NAT2 | c.814A>G (p.Lys272Glu) c.424A>G (p.Lys142Glu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400817A>T | CA370636682 | NAT2 | c.814A>T (p.Lys272Ter) c.424A>T (p.Lys142Ter) | |
8 | g.18400818A>C | CA370636683 | NAT2 | c.815A>C (p.Lys272Thr) c.425A>C (p.Lys142Thr) | |
8 | g.18400818A>G | CA370636684 | NAT2 | c.815A>G (p.Lys272Arg) c.425A>G (p.Lys142Arg) | |
8 | g.18400818A>T | CA370636685 | NAT2 | c.815A>T (p.Lys272Met) c.425A>T (p.Lys142Met) | |
8 | g.18400819G>A | CA459699906 | NAT2 | c.816G>A (p.Lys272=) c.426G>A (p.Lys142=) | |
8 | g.18400819G>C | CA370636686 | NAT2 | c.816G>C (p.Lys272Asn) c.426G>C (p.Lys142Asn) | |
8 | g.18400819G>T | CA370636687 | NAT2 | c.816G>T (p.Lys272Asn) c.426G>T (p.Lys142Asn) | COSMIC |
8 | g.18400820A>C | CA370636688 | NAT2 | c.817A>C (p.Ile273Leu) c.427A>C (p.Ile143Leu) | |
8 | g.18400820A>G | CA370636689 | NAT2 | c.817A>G (p.Ile273Val) c.427A>G (p.Ile143Val) | |
8 | g.18400820A>T | CA370636690 | NAT2 | c.817A>T (p.Ile273Phe) c.427A>T (p.Ile143Phe) | |
8 | g.18400821T>A | CA370636693 | NAT2 | c.818T>A (p.Ile273Asn) c.428T>A (p.Ile143Asn) | |
8 | g.18400821T>C | CA370636692 | NAT2 | c.818T>C (p.Ile273Thr) c.428T>C (p.Ile143Thr) | |
8 | g.18400821T>G | CA370636691 | NAT2 | c.818T>G (p.Ile273Ser) c.428T>G (p.Ile143Ser) | |
8 | g.18400822T>A | CA459699919 | NAT2 | c.819T>A (p.Ile273=) c.429T>A (p.Ile143=) | |
8 | g.18400822T>C | CA459699921 | NAT2 | c.819T>C (p.Ile273=) c.429T>C (p.Ile143=) | |
8 | g.18400822T>G | CA370636694 | NAT2 | c.819T>G (p.Ile273Met) c.429T>G (p.Ile143Met) | |
8 | g.18400823T>A | CA370636695 | NAT2 | c.820T>A (p.Ser274Thr) c.430T>A (p.Ser144Thr) | |
8 | g.18400823T>C | CA370636696 | NAT2 | c.820T>C (p.Ser274Pro) c.430T>C (p.Ser144Pro) | |
8 | g.18400823T>G | CA370636697 | NAT2 | c.820T>G (p.Ser274Ala) c.430T>G (p.Ser144Ala) | |
8 | g.18400824C>A | CA370636698 | NAT2 | c.821C>A (p.Ser274Tyr) c.431C>A (p.Ser144Tyr) | |
8 | g.18400824C>G | CA370636699 | NAT2 | c.821C>G (p.Ser274Cys) c.431C>G (p.Ser144Cys) | |
8 | g.18400824C>T | CA370636700 | NAT2 | c.821C>T (p.Ser274Phe) c.431C>T (p.Ser144Phe) | COSMIC |
8 | g.18400825C>A | CA459699933 | NAT2 | c.822C>A (p.Ser274=) c.432C>A (p.Ser144=) | |
8 | g.18400825C>G | CA459699935 | NAT2 | c.822C>G (p.Ser274=) c.432C>G (p.Ser144=) | |
8 | g.18400825C>T | CA459699936 | NAT2 | c.822C>T (p.Ser274=) c.432C>T (p.Ser144=) | gnomAD v4 |
8 | g.18400826T>A | CA4651706 | NAT2 | c.823T>A (p.Leu275Met) c.433T>A (p.Leu145Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400826T>C | CA459699939 | NAT2 | c.823T>C (p.Leu275=) c.433T>C (p.Leu145=) | gnomAD v4 |
8 | g.18400826T>G | CA370636701 | NAT2 | c.823T>G (p.Leu275Val) c.433T>G (p.Leu145Val) | gnomAD v4 |
8 | g.18400826T= | CA1768219168 | NAT2 | c.823T= (p.Leu275=) c.433T= (p.Leu145=) | |
8 | g.18400827T>A | CA370636702 | NAT2 | c.824T>A (p.Leu275Ter) c.434T>A (p.Leu145Ter) | |
8 | g.18400827T>C | CA370636703 | NAT2 | c.824T>C (p.Leu275Ser) c.434T>C (p.Leu145Ser) | |
8 | g.18400827T>G | CA370636704 | NAT2 | c.824T>G (p.Leu275Trp) c.434T>G (p.Leu145Trp) | dbSNP |
8 | g.18400827T= | CA1768219169 | NAT2 | c.824T= (p.Leu275=) c.434T= (p.Leu145=) | |
8 | g.18400828G>A | CA459699950 | NAT2 | c.825G>A (p.Leu275=) c.435G>A (p.Leu145=) | gnomAD v4 |
8 | g.18400828G>C | CA370636705 | NAT2 | c.825G>C (p.Leu275Phe) c.435G>C (p.Leu145Phe) | |
8 | g.18400828G>T | CA370636706 | NAT2 | c.825G>T (p.Leu275Phe) c.435G>T (p.Leu145Phe) | gnomAD v4 |
8 | g.18400829G>A | CA370636708 | NAT2 | c.826G>A (p.Gly276Arg) c.436G>A (p.Gly146Arg) | gnomAD v4 |
8 | g.18400829G>C | CA370636709 | NAT2 | c.826G>C (p.Gly276Arg) c.436G>C (p.Gly146Arg) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400829G= | CA1768219170 | NAT2 | c.826G= (p.Gly276=) c.436G= (p.Gly146=) | |
8 | g.18400829G>T | CA370636707 | NAT2 | c.826G>T (p.Gly276Trp) c.436G>T (p.Gly146Trp) | gnomAD v4 |
8 | g.18400830G>A | CA370636710 | NAT2 | c.827G>A (p.Gly276Glu) c.437G>A (p.Gly146Glu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400830G>C | CA370636711 | NAT2 | c.827G>C (p.Gly276Ala) c.437G>C (p.Gly146Ala) | |
8 | g.18400830G= | CA1768219171 | NAT2 | c.827G= (p.Gly276=) c.437G= (p.Gly146=) | |
8 | g.18400830G>T | CA370636712 | NAT2 | c.827G>T (p.Gly276Val) c.437G>T (p.Gly146Val) | |
8 | g.18400830_18400831insCAC | CA2830536285 | NAT2 | c.827_828insCAC (p.Gly276_Arg277insThr) c.437_438insCAC (p.Gly146_Arg147insThr) | |
8 | g.18400831G>A | CA4651707 | NAT2 | c.828G>A (p.Gly276=) c.438G>A (p.Gly146=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18400831G>C | CA459699969 | NAT2 | c.828G>C (p.Gly276=) c.438G>C (p.Gly146=) | |
8 | g.18400831G= | CA1768219172 | NAT2 | c.828G= (p.Gly276=) c.438G= (p.Gly146=) | |
8 | g.18400831G>T | CA459699966 | NAT2 | c.828G>T (p.Gly276=) c.438G>T (p.Gly146=) | |
8 | g.18400832A= | CA1768219173 | NAT2 | c.829A= (p.Arg277=) c.439A= (p.Arg147=) | |
8 | g.18400832A>C | CA459699972 | NAT2 | c.829A>C (p.Arg277=) c.439A>C (p.Arg147=) | |
8 | g.18400832A>G | CA370636713 | NAT2 | c.829A>G (p.Arg277Gly) c.439A>G (p.Arg147Gly) | |
8 | g.18400832A>T | CA173519949 | NAT2 | c.829A>T (p.Arg277Ter) c.439A>T (p.Arg147Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400833G>A | CA370636714 | NAT2 | c.830G>A (p.Arg277Lys) c.440G>A (p.Arg147Lys) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400833G>C | CA370636715 | NAT2 | c.830G>C (p.Arg277Thr) c.440G>C (p.Arg147Thr) | |
8 | g.18400833G= | CA1768219174 | NAT2 | c.830G= (p.Arg277=) c.440G= (p.Arg147=) | |
8 | g.18400833G>T | CA370636716 | NAT2 | c.830G>T (p.Arg277Ile) c.440G>T (p.Arg147Ile) | |
8 | g.18400834_18400835insTTTCTCCCCAAGGA | CA2830536290 | NAT2 | c.831_832insTTTCTCCCCAAGGA (p.Asn278PhefsTer?) c.441_442insTTTCTCCCCAAGGA (p.Asn148PhefsTer?) | |
8 | g.18400834A>C | CA370636717 | NAT2 | c.831A>C (p.Arg277Ser) c.441A>C (p.Arg147Ser) | |
8 | g.18400834A>G | CA459699980 | NAT2 | c.831A>G (p.Arg277=) c.441A>G (p.Arg147=) | |
8 | g.18400834A>T | CA370636718 | NAT2 | c.831A>T (p.Arg277Ser) c.441A>T (p.Arg147Ser) | |
8 | g.18400835A>C | CA370636721 | NAT2 | c.832A>C (p.Asn278His) c.442A>C (p.Asn148His) | |
8 | g.18400835A>G | CA370636720 | NAT2 | c.832A>G (p.Asn278Asp) c.442A>G (p.Asn148Asp) | |
8 | g.18400835A>T | CA370636719 | NAT2 | c.832A>T (p.Asn278Tyr) c.442A>T (p.Asn148Tyr) | |
8 | g.18400836A>C | CA370636722 | NAT2 | c.833A>C (p.Asn278Thr) c.443A>C (p.Asn148Thr) | |
8 | g.18400836A>G | CA370636723 | NAT2 | c.833A>G (p.Asn278Ser) c.443A>G (p.Asn148Ser) | |
8 | g.18400836A>T | CA370636724 | NAT2 | c.833A>T (p.Asn278Ile) c.443A>T (p.Asn148Ile) | |
8 | g.18400837T>A | CA370636725 | NAT2 | c.834T>A (p.Asn278Lys) c.444T>A (p.Asn148Lys) | |
8 | g.18400837T>C | CA459699997 | NAT2 | c.834T>C (p.Asn278=) c.444T>C (p.Asn148=) | COSMIC |
8 | g.18400837T>G | CA370636726 | NAT2 | c.834T>G (p.Asn278Lys) c.444T>G (p.Asn148Lys) | dbSNP |
8 | g.18400838C>A | CA370636728 | NAT2 | c.835C>A (p.Leu279Ile) c.445C>A (p.Leu149Ile) | ClinVar gnomAD v4 |
8 | g.18400838C>G | CA370636729 | NAT2 | c.835C>G (p.Leu279Val) c.445C>G (p.Leu149Val) | |
8 | g.18400838C>T | CA370636730 | NAT2 | c.835C>T (p.Leu279Phe) c.445C>T (p.Leu149Phe) | gnomAD v4 |
8 | g.18400839T>A | CA370636731 | NAT2 | c.836T>A (p.Leu279His) c.446T>A (p.Leu149His) | |
8 | g.18400839T>C | CA370636732 | NAT2 | c.836T>C (p.Leu279Pro) c.446T>C (p.Leu149Pro) | gnomAD v4 |
8 | g.18400839T>G | CA4651708 | NAT2 | c.836T>G (p.Leu279Arg) c.446T>G (p.Leu149Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18400839T= | CA1768219175 | NAT2 | c.836T= (p.Leu279=) c.446T= (p.Leu149=) | |
8 | g.18400840C>A | CA459700010 | NAT2 | c.837C>A (p.Leu279=) c.447C>A (p.Leu149=) | gnomAD v4 |
8 | g.18400840C= | CA1768219176 | NAT2 | c.837C= (p.Leu279=) c.447C= (p.Leu149=) | |
8 | g.18400840C>G | CA459700012 | NAT2 | c.837C>G (p.Leu279=) c.447C>G (p.Leu149=) | |
8 | g.18400840C>T | CA4651709 | NAT2 | c.837C>T (p.Leu279=) c.447C>T (p.Leu149=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.18400841G>A | CA4651710 | NAT2 | c.838G>A (p.Val280Met) c.448G>A (p.Val150Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.18400841G>C | CA370636734 | NAT2 | c.838G>C (p.Val280Leu) c.448G>C (p.Val150Leu) | |
8 | g.18400841G= | CA1768219177 | NAT2 | c.838G= (p.Val280=) c.448G= (p.Val150=) | |
8 | g.18400841G>T | CA370636733 | NAT2 | c.838G>T (p.Val280Leu) c.448G>T (p.Val150Leu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400842T>A | CA370636735 | NAT2 | c.839T>A (p.Val280Glu) c.449T>A (p.Val150Glu) | |
8 | g.18400842T>C | CA370636737 | NAT2 | c.839T>C (p.Val280Ala) c.449T>C (p.Val150Ala) | |
8 | g.18400842T>G | CA370636736 | NAT2 | c.839T>G (p.Val280Gly) c.449T>G (p.Val150Gly) | |
8 | g.18400843G>A | CA4651711 | NAT2 | c.840G>A (p.Val280=) c.450G>A (p.Val150=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400843G>C | CA459700029 | NAT2 | c.840G>C (p.Val280=) c.450G>C (p.Val150=) | gnomAD v4 |
8 | g.18400843G= | CA1768219178 | NAT2 | c.840G= (p.Val280=) c.450G= (p.Val150=) | |
8 | g.18400843G>T | CA459700031 | NAT2 | c.840G>T (p.Val280=) c.450G>T (p.Val150=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400844C>A | CA370636739 | NAT2 | c.841C>A (p.Pro281Thr) c.451C>A (p.Pro151Thr) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400844C= | CA1768219179 | NAT2 | c.841C= (p.Pro281=) c.451C= (p.Pro151=) | |
8 | g.18400844C>G | CA370636738 | NAT2 | c.841C>G (p.Pro281Ala) c.451C>G (p.Pro151Ala) | |
8 | g.18400844C>T | CA370636740 | NAT2 | c.841C>T (p.Pro281Ser) c.451C>T (p.Pro151Ser) | |
8 | g.18400845C>A | CA370636741 | NAT2 | c.842C>A (p.Pro281His) c.452C>A (p.Pro151His) | |
8 | g.18400845C>G | CA370636742 | NAT2 | c.842C>G (p.Pro281Arg) c.452C>G (p.Pro151Arg) | |
8 | g.18400845C>T | CA370636743 | NAT2 | c.842C>T (p.Pro281Leu) c.452C>T (p.Pro151Leu) | |
8 | g.18400846C>A | CA459700044 | NAT2 | c.843C>A (p.Pro281=) c.453C>A (p.Pro151=) | |
8 | g.18400846C= | CA1768219180 | NAT2 | c.843C= (p.Pro281=) c.453C= (p.Pro151=) | |
8 | g.18400846C>G | CA459700053 | NAT2 | c.843C>G (p.Pro281=) c.453C>G (p.Pro151=) | |
8 | g.18400846C>T | CA173519950 | NAT2 | c.843C>T (p.Pro281=) c.453C>T (p.Pro151=) | dbSNP COSMIC |
8 | g.18400847A>C | CA370636744 | NAT2 | c.844A>C (p.Lys282Gln) c.454A>C (p.Lys152Gln) | |
8 | g.18400847A>G | CA370636745 | NAT2 | c.844A>G (p.Lys282Glu) c.454A>G (p.Lys152Glu) | |
8 | g.18400847A>T | CA370636746 | NAT2 | c.844A>T (p.Lys282Ter) c.454A>T (p.Lys152Ter) | |
8 | g.18400848A= | CA1768219181 | NAT2 | c.845A= (p.Lys282=) c.455A= (p.Lys152=) | |
8 | g.18400848A>C | CA173519951 | NAT2 | c.845A>C (p.Lys282Thr) c.455A>C (p.Lys152Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400848A>G | CA4651712 | NAT2 | c.845A>G (p.Lys282Arg) c.455A>G (p.Lys152Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400848A>T | CA370636747 | NAT2 | c.845A>T (p.Lys282Ile) c.455A>T (p.Lys152Ile) | |
8 | g.18400849A>C | CA370636748 | NAT2 | c.846A>C (p.Lys282Asn) c.456A>C (p.Lys152Asn) | gnomAD v4 |
8 | g.18400849A>G | CA459700069 | NAT2 | c.846A>G (p.Lys282=) c.456A>G (p.Lys152=) | |
8 | g.18400849A>T | CA370636749 | NAT2 | c.846A>T (p.Lys282Asn) c.456A>T (p.Lys152Asn) | |
8 | g.18400850C>A | CA370636751 | NAT2 | c.847C>A (p.Pro283Thr) c.457C>A (p.Pro153Thr) | |
8 | g.18400850C= | CA1768219182 | NAT2 | c.847C= (p.Pro283=) c.457C= (p.Pro153=) | |
8 | g.18400850C>G | CA4651713 | NAT2 | c.847C>G (p.Pro283Ala) c.457C>G (p.Pro153Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400850C>T | CA370636750 | NAT2 | c.847C>T (p.Pro283Ser) c.457C>T (p.Pro153Ser) |