UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) | 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.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.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) | |
| 8 | g.18400851C>A | CA370636752 | NAT2 | c.848C>A (p.Pro283His) c.458C>A (p.Pro153His) | |
| 8 | g.18400851C= | CA1768219183 | NAT2 | c.848C= (p.Pro283=) c.458C= (p.Pro153=) | |
| 8 | g.18400851C>G | CA4651714 | NAT2 | c.848C>G (p.Pro283Arg) c.458C>G (p.Pro153Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18400851C>T | CA370636753 | NAT2 | c.848C>T (p.Pro283Leu) c.458C>T (p.Pro153Leu) | |
| 8 | g.18400852T>A | CA459700090 | NAT2 | c.849T>A (p.Pro283=) c.459T>A (p.Pro153=) | |
| 8 | g.18400852T>C | CA459700088 | NAT2 | c.849T>C (p.Pro283=) c.459T>C (p.Pro153=) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18400852T>G | CA459700087 | NAT2 | c.849T>G (p.Pro283=) c.459T>G (p.Pro153=) | |
| 8 | g.18400852T= | CA1768219184 | NAT2 | c.849T= (p.Pro283=) c.459T= (p.Pro153=) | |
| 8 | g.18400853G>A | CA370636754 | NAT2 | c.850G>A (p.Gly284Ser) c.460G>A (p.Gly154Ser) | |
| 8 | g.18400853G>C | CA370636755 | NAT2 | c.850G>C (p.Gly284Arg) c.460G>C (p.Gly154Arg) | gnomAD v4 |
| 8 | g.18400853G>T | CA370636756 | NAT2 | c.850G>T (p.Gly284Cys) c.460G>T (p.Gly154Cys) | |
| 8 | g.18400854G>A | CA370636757 | NAT2 | c.851G>A (p.Gly284Asp) c.461G>A (p.Gly154Asp) | |
| 8 | g.18400854G>C | CA370636758 | NAT2 | c.851G>C (p.Gly284Ala) c.461G>C (p.Gly154Ala) | |
| 8 | g.18400854G>T | CA370636759 | NAT2 | c.851G>T (p.Gly284Val) c.461G>T (p.Gly154Val) | |
| 8 | g.18400855T>A | CA459700101 | NAT2 | c.852T>A (p.Gly284=) c.462T>A (p.Gly154=) | |
| 8 | g.18400855T>C | CA459700103 | NAT2 | c.852T>C (p.Gly284=) c.462T>C (p.Gly154=) | |
| 8 | g.18400855T>G | CA459700109 | NAT2 | c.852T>G (p.Gly284=) c.462T>G (p.Gly154=) | |
| 8 | g.18400856G>A | CA370636760 | NAT2 | c.853G>A (p.Asp285Asn) c.463G>A (p.Asp155Asn) | COSMIC |
| 8 | g.18400856G>C | CA370636761 | NAT2 | c.853G>C (p.Asp285His) c.463G>C (p.Asp155His) | |
| 8 | g.18400856G>T | CA370636762 | NAT2 | c.853G>T (p.Asp285Tyr) c.463G>T (p.Asp155Tyr) | |
| 8 | g.18400857A= | CA1768219185 | NAT2 | c.854A= (p.Asp285=) c.464A= (p.Asp155=) | |
| 8 | g.18400857A>C | CA370636765 | NAT2 | c.854A>C (p.Asp285Ala) c.464A>C (p.Asp155Ala) | |
| 8 | g.18400857A>G | CA370636764 | NAT2 | c.854A>G (p.Asp285Gly) c.464A>G (p.Asp155Gly) | dbSNP gnomAD v4 COSMIC |
| 8 | g.18400857A>T | CA370636763 | NAT2 | c.854A>T (p.Asp285Val) c.464A>T (p.Asp155Val) | |
| 8 | g.18400858T>A | CA370636766 | NAT2 | c.855T>A (p.Asp285Glu) c.465T>A (p.Asp155Glu) | |
| 8 | g.18400858T>C | CA459700125 | NAT2 | c.855T>C (p.Asp285=) c.465T>C (p.Asp155=) | |
| 8 | g.18400858T>G | CA370636767 | NAT2 | c.855T>G (p.Asp285Glu) c.465T>G (p.Asp155Glu) | |
| 8 | g.18400859G>A | CA370636768 | NAT2 | c.856G>A (p.Gly286Arg) c.466G>A (p.Gly156Arg) | |
| 8 | g.18400859G>C | CA370636769 | NAT2 | c.856G>C (p.Gly286Arg) c.466G>C (p.Gly156Arg) | |
| 8 | g.18400859G>T | CA370636770 | NAT2 | c.856G>T (p.Gly286Ter) c.466G>T (p.Gly156Ter) | |
| 8 | g.18400860G>A | CA114453 | NAT2 | c.857G>A (p.Gly286Glu) c.467G>A (p.Gly156Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18400860G>C | CA370636771 | NAT2 | c.857G>C (p.Gly286Ala) c.467G>C (p.Gly156Ala) | dbSNP |
| 8 | g.18400860G= | CA1768219186 | NAT2 | c.857G= (p.Gly286=) c.467G= (p.Gly156=) | |
| 8 | g.18400860G>T | CA370636772 | NAT2 | c.857G>T (p.Gly286Val) c.467G>T (p.Gly156Val) | |
| 8 | g.18400861A= | CA1768219187 | NAT2 | c.858A= (p.Gly286=) c.468A= (p.Gly156=) | |
| 8 | g.18400861A>C | CA459700137 | NAT2 | c.858A>C (p.Gly286=) c.468A>C (p.Gly156=) | |
| 8 | g.18400861A>G | CA459700139 | NAT2 | c.858A>G (p.Gly286=) c.468A>G (p.Gly156=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18400861A>T | CA459700142 | NAT2 | c.858A>T (p.Gly286=) c.468A>T (p.Gly156=) | |
| 8 | g.18400862del | CA2695208956 | NAT2 | c.859del (p.Ser287ProfsTer?) c.469del (p.Ser157ProfsTer?) | |
| 8 | g.18400862T>A | CA370636773 | NAT2 | c.859T>A (p.Ser287Thr) c.469T>A (p.Ser157Thr) | |
| 8 | g.18400862T>C | CA4651715 | NAT2 | c.859T>C (p.Ser287Pro) c.469T>C (p.Ser157Pro) | dbSNP ExAC gnomAD v4 |
| 8 | g.18400862T>G | CA370636774 | NAT2 | c.859T>G (p.Ser287Ala) c.469T>G (p.Ser157Ala) | |
| 8 | g.18400862T= | CA1768219188 | NAT2 | c.859T= (p.Ser287=) c.469T= (p.Ser157=) | |
| 8 | g.18400863C>A | CA370636775 | NAT2 | c.860C>A (p.Ser287Tyr) c.470C>A (p.Ser157Tyr) | |
| 8 | g.18400863C= | CA1768219189 | NAT2 | c.860C= (p.Ser287=) c.470C= (p.Ser157=) | |
| 8 | g.18400863C>G | CA370636776 | NAT2 | c.860C>G (p.Ser287Cys) c.470C>G (p.Ser157Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18400863C>T | CA370636777 | NAT2 | c.860C>T (p.Ser287Phe) c.470C>T (p.Ser157Phe) | COSMIC |
| 8 | g.18400864C>A | CA459700154 | NAT2 | c.861C>A (p.Ser287=) c.471C>A (p.Ser157=) | |
| 8 | g.18400864C= | CA1768219190 | NAT2 | c.861C= (p.Ser287=) c.471C= (p.Ser157=) | |
| 8 | g.18400864C>G | CA459700156 | NAT2 | c.861C>G (p.Ser287=) c.471C>G (p.Ser157=) | |
| 8 | g.18400864C>T | CA4651716 | NAT2 | c.861C>T (p.Ser287=) c.471C>T (p.Ser157=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18400865C>A | CA370636778 | NAT2 | c.862C>A (p.Leu288Ile) c.472C>A (p.Leu158Ile) | |
| 8 | g.18400865C>G | CA370636779 | NAT2 | c.862C>G (p.Leu288Val) c.472C>G (p.Leu158Val) | |
| 8 | g.18400865C>T | CA370636780 | NAT2 | c.862C>T (p.Leu288Phe) c.472C>T (p.Leu158Phe) | gnomAD v4 |
| 8 | g.18400866T>A | CA370636781 | NAT2 | c.863T>A (p.Leu288His) c.473T>A (p.Leu158His) | |
| 8 | g.18400866T>C | CA370636782 | NAT2 | c.863T>C (p.Leu288Pro) c.473T>C (p.Leu158Pro) | |
| 8 | g.18400866T>G | CA370636783 | NAT2 | c.863T>G (p.Leu288Arg) c.473T>G (p.Leu158Arg) |