Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.138013781G>A | CA348472852 | HNMT | c.530G>A (p.Ser177Asn) n.462G>A c.428G>A (p.Ser143Asn) c.152G>A (p.Ser51Asn) n.232-5985C>T n.917G>A | |
2 | g.138013781G>C | CA348472846 | HNMT | c.530G>C (p.Ser177Thr) n.462G>C c.428G>C (p.Ser143Thr) c.152G>C (p.Ser51Thr) n.232-5985C>G n.917G>C | |
2 | g.138013781G>T | CA348472847 | HNMT | c.530G>T (p.Ser177Ile) n.462G>T c.428G>T (p.Ser143Ile) c.152G>T (p.Ser51Ile) n.232-5985C>A n.917G>T | |
2 | g.138013782T>A | CA348472857 | HNMT | c.531T>A (p.Ser177Arg) n.463T>A c.429T>A (p.Ser143Arg) c.153T>A (p.Ser51Arg) n.232-5986A>T n.918T>A | |
2 | g.138013782T>C | CA429193176 | HNMT | c.531T>C (p.Ser177=) n.463T>C c.429T>C (p.Ser143=) c.153T>C (p.Ser51=) n.232-5986A>G n.918T>C | |
2 | g.138013782T>G | CA348472860 | HNMT | c.531T>G (p.Ser177Arg) n.463T>G c.429T>G (p.Ser143Arg) c.153T>G (p.Ser51Arg) n.232-5986A>C n.918T>G | |
2 | g.138013783G>A | CA348472865 | HNMT | c.532G>A (p.Gly178Ser) n.464G>A c.430G>A (p.Gly144Ser) c.154G>A (p.Gly52Ser) n.232-5987C>T n.919G>A | |
2 | g.138013783G>C | CA348472868 | HNMT | c.532G>C (p.Gly178Arg) n.464G>C c.430G>C (p.Gly144Arg) c.154G>C (p.Gly52Arg) n.232-5987C>G n.919G>C | |
2 | g.138013783G>T | CA348472871 | HNMT | c.532G>T (p.Gly178Cys) n.464G>T c.430G>T (p.Gly144Cys) c.154G>T (p.Gly52Cys) n.232-5987C>A n.919G>T | |
2 | g.138013784G>A | CA348472875 | HNMT | c.533G>A (p.Gly178Asp) n.465G>A c.431G>A (p.Gly144Asp) c.155G>A (p.Gly52Asp) n.232-5988C>T n.920G>A | |
2 | g.138013784G>C | CA348472877 | HNMT | c.533G>C (p.Gly178Ala) n.465G>C c.431G>C (p.Gly144Ala) c.155G>C (p.Gly52Ala) n.232-5988C>G n.920G>C | |
2 | g.138013784G= | CA1291857861 | HNMT | c.533G= (p.Gly178=) n.465G= c.431G= (p.Gly144=) c.155G= (p.Gly52=) n.232-5988C= n.920G= | |
2 | g.138013784G>T | CA348472880 | HNMT | c.533G>T (p.Gly178Val) n.465G>T c.431G>T (p.Gly144Val) c.155G>T (p.Gly52Val) n.232-5988C>A n.920G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013785C>A | CA429193177 | HNMT | c.534C>A (p.Gly178=) n.466C>A c.432C>A (p.Gly144=) c.156C>A (p.Gly52=) n.232-5989G>T n.921C>A | |
2 | g.138013785C= | CA1291857867 | HNMT | c.534C= (p.Gly178=) n.466C= c.432C= (p.Gly144=) c.156C= (p.Gly52=) n.232-5989G= n.921C= | |
2 | g.138013785C>G | CA429193178 | HNMT | c.534C>G (p.Gly178=) n.466C>G c.432C>G (p.Gly144=) c.156C>G (p.Gly52=) n.232-5989G>C n.921C>G | |
2 | g.138013785C>T | CA1891810 | HNMT | c.534C>T (p.Gly178=) n.466C>T c.432C>T (p.Gly144=) c.156C>T (p.Gly52=) n.232-5989G>A n.921C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013786T>A | CA1891811 | HNMT | c.535T>A (p.Trp179Arg) n.467T>A c.433T>A (p.Trp145Arg) c.157T>A (p.Trp53Arg) n.232-5990A>T n.922T>A | dbSNP ExAC |
2 | g.138013786T>C | CA348472890 | HNMT | c.535T>C (p.Trp179Arg) n.467T>C c.433T>C (p.Trp145Arg) c.157T>C (p.Trp53Arg) n.232-5990A>G n.922T>C | |
2 | g.138013786T>G | CA348472894 | HNMT | c.535T>G (p.Trp179Gly) n.467T>G c.433T>G (p.Trp145Gly) c.157T>G (p.Trp53Gly) n.232-5990A>C n.922T>G | |
2 | g.138013786T= | CA1291857870 | HNMT | c.535T= (p.Trp179=) n.467T= c.433T= (p.Trp145=) c.157T= (p.Trp53=) n.232-5990A= n.922T= | |
2 | g.138013787G>A | CA348472905 | HNMT | c.536G>A (p.Trp179Ter) n.468G>A c.434G>A (p.Trp145Ter) c.158G>A (p.Trp53Ter) n.232-5991C>T n.923G>A | |
2 | g.138013787G>C | CA348472898 | HNMT | c.536G>C (p.Trp179Ser) n.468G>C c.434G>C (p.Trp145Ser) c.158G>C (p.Trp53Ser) n.232-5991C>G n.923G>C | |
2 | g.138013787G>T | CA348472902 | HNMT | c.536G>T (p.Trp179Leu) n.468G>T c.434G>T (p.Trp145Leu) c.158G>T (p.Trp53Leu) n.232-5991C>A n.923G>T | |
2 | g.138013788G>A | CA348472912 | HNMT | c.537G>A (p.Trp179Ter) n.469G>A c.435G>A (p.Trp145Ter) c.159G>A (p.Trp53Ter) n.232-5992C>T n.924G>A | gnomAD v4 |
2 | g.138013788G>C | CA348472915 | HNMT | c.537G>C (p.Trp179Cys) n.469G>C c.435G>C (p.Trp145Cys) c.159G>C (p.Trp53Cys) n.232-5992C>G n.924G>C | |
2 | g.138013788G= | CA1291857873 | HNMT | c.537G= (p.Trp179=) n.469G= c.435G= (p.Trp145=) c.159G= (p.Trp53=) n.232-5992C= n.924G= | |
2 | g.138013788G>T | CA348472918 | HNMT | c.537G>T (p.Trp179Cys) n.469G>T c.435G>T (p.Trp145Cys) c.159G>T (p.Trp53Cys) n.232-5992C>A n.924G>T | dbSNP |
2 | g.138013789G>A | CA348472923 | HNMT | c.538G>A (p.Asp180Asn) n.470G>A c.436G>A (p.Asp146Asn) c.160G>A (p.Asp54Asn) n.232-5993C>T n.925G>A | |
2 | g.138013789G>C | CA348472926 | HNMT | c.538G>C (p.Asp180His) n.470G>C c.436G>C (p.Asp146His) c.160G>C (p.Asp54His) n.232-5993C>G n.925G>C | |
2 | g.138013789G= | CA1291857876 | HNMT | c.538G= (p.Asp180=) n.470G= c.436G= (p.Asp146=) c.160G= (p.Asp54=) n.232-5993C= n.925G= | |
2 | g.138013789G>T | CA348472930 | HNMT | c.538G>T (p.Asp180Tyr) n.470G>T c.436G>T (p.Asp146Tyr) c.160G>T (p.Asp54Tyr) n.232-5993C>A n.925G>T | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013790A= | CA1291857880 | HNMT | c.539A= (p.Asp180=) n.471A= c.437A= (p.Asp146=) c.161A= (p.Asp54=) n.232-5994T= n.926A= | |
2 | g.138013790A>C | CA348472941 | HNMT | c.539A>C (p.Asp180Ala) n.471A>C c.437A>C (p.Asp146Ala) c.161A>C (p.Asp54Ala) n.232-5994T>G n.926A>C | |
2 | g.138013790A>G | CA348472934 | HNMT | c.539A>G (p.Asp180Gly) n.471A>G c.437A>G (p.Asp146Gly) c.161A>G (p.Asp54Gly) n.232-5994T>C n.926A>G | dbSNP gnomAD v4 |
2 | g.138013790A>T | CA348472939 | HNMT | c.539A>T (p.Asp180Val) n.471A>T c.437A>T (p.Asp146Val) c.161A>T (p.Asp54Val) n.232-5994T>A n.926A>T | |
2 | g.138013791C>A | CA348472944 | HNMT | c.540C>A (p.Asp180Glu) n.472C>A c.438C>A (p.Asp146Glu) c.162C>A (p.Asp54Glu) n.232-5995G>T n.927C>A | |
2 | g.138013791C= | CA1291857886 | HNMT | c.540C= (p.Asp180=) n.472C= c.438C= (p.Asp146=) c.162C= (p.Asp54=) n.232-5995G= n.927C= | |
2 | g.138013791C>G | CA348472948 | HNMT | c.540C>G (p.Asp180Glu) n.472C>G c.438C>G (p.Asp146Glu) c.162C>G (p.Asp54Glu) n.232-5995G>C n.927C>G | |
2 | g.138013791C>T | CA429193179 | HNMT | c.540C>T (p.Asp180=) n.472C>T c.438C>T (p.Asp146=) c.162C>T (p.Asp54=) n.232-5995G>A n.927C>T | dbSNP gnomAD v2 |
2 | g.138013792A>C | CA348472952 | HNMT | c.541A>C (p.Lys181Gln) n.473A>C c.439A>C (p.Lys147Gln) c.163A>C (p.Lys55Gln) n.232-5996T>G n.928A>C | |
2 | g.138013792A>G | CA348472955 | HNMT | c.541A>G (p.Lys181Glu) n.473A>G c.439A>G (p.Lys147Glu) c.163A>G (p.Lys55Glu) n.232-5996T>C n.928A>G | |
2 | g.138013792A>T | CA348472958 | HNMT | c.541A>T (p.Lys181Ter) n.473A>T c.439A>T (p.Lys147Ter) c.163A>T (p.Lys55Ter) n.232-5996T>A n.928A>T | |
2 | g.138013793A>C | CA348472963 | HNMT | c.542A>C (p.Lys181Thr) n.474A>C c.440A>C (p.Lys147Thr) c.164A>C (p.Lys55Thr) n.232-5997T>G n.929A>C | |
2 | g.138013793A>G | CA348472971 | HNMT | c.542A>G (p.Lys181Arg) n.474A>G c.440A>G (p.Lys147Arg) c.164A>G (p.Lys55Arg) n.232-5997T>C n.929A>G | |
2 | g.138013793A>T | CA348472965 | HNMT | c.542A>T (p.Lys181Met) n.474A>T c.440A>T (p.Lys147Met) c.164A>T (p.Lys55Met) n.232-5997T>A n.929A>T | |
2 | g.138013794G>A | CA429193180 | HNMT | c.543G>A (p.Lys181=) n.475G>A c.441G>A (p.Lys147=) c.165G>A (p.Lys55=) n.232-5998C>T n.930G>A | |
2 | g.138013794G>C | CA348472974 | HNMT | c.543G>C (p.Lys181Asn) n.475G>C c.441G>C (p.Lys147Asn) c.165G>C (p.Lys55Asn) n.232-5998C>G n.930G>C | |
2 | g.138013794G>T | CA348472979 | HNMT | c.543G>T (p.Lys181Asn) n.475G>T c.441G>T (p.Lys147Asn) c.165G>T (p.Lys55Asn) n.232-5998C>A n.930G>T | |
2 | g.138013795C>A | CA348472981 | HNMT | c.544C>A (p.Leu182Met) n.476C>A c.442C>A (p.Leu148Met) c.166C>A (p.Leu56Met) n.232-5999G>T n.931C>A | |
2 | g.138013795C>G | CA348472984 | HNMT | c.544C>G (p.Leu182Val) n.476C>G c.442C>G (p.Leu148Val) c.166C>G (p.Leu56Val) n.232-5999G>C n.931C>G | |
2 | g.138013795C>T | CA429193181 | HNMT | c.544C>T (p.Leu182=) n.476C>T c.442C>T (p.Leu148=) c.166C>T (p.Leu56=) n.232-5999G>A n.931C>T | |
2 | g.138013796T>A | CA348472988 | HNMT | c.545T>A (p.Leu182Gln) n.477T>A c.443T>A (p.Leu148Gln) c.167T>A (p.Leu56Gln) n.232-6000A>T n.932T>A | |
2 | g.138013796T>C | CA348472993 | HNMT | c.545T>C (p.Leu182Pro) n.477T>C c.443T>C (p.Leu148Pro) c.167T>C (p.Leu56Pro) n.232-6000A>G n.932T>C | |
2 | g.138013796T>G | CA348472997 | HNMT | c.545T>G (p.Leu182Arg) n.477T>G c.443T>G (p.Leu148Arg) c.167T>G (p.Leu56Arg) n.232-6000A>C n.932T>G | |
2 | g.138013797G>A | CA429193183 | HNMT | c.546G>A (p.Leu182=) n.478G>A c.444G>A (p.Leu148=) c.168G>A (p.Leu56=) n.232-6001C>T n.933G>A | gnomAD v4 |
2 | g.138013797G>C | CA1891812 | HNMT | c.546G>C (p.Leu182=) n.478G>C c.444G>C (p.Leu148=) c.168G>C (p.Leu56=) n.232-6001C>G n.933G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013797G= | CA1291857889 | HNMT | c.546G= (p.Leu182=) n.478G= c.444G= (p.Leu148=) c.168G= (p.Leu56=) n.232-6001C= n.933G= | |
2 | g.138013797G>T | CA429193182 | HNMT | c.546G>T (p.Leu182=) n.478G>T c.444G>T (p.Leu148=) c.168G>T (p.Leu56=) n.232-6001C>A n.933G>T | |
2 | g.138013798T>A | CA348473006 | HNMT | c.547T>A (p.Trp183Arg) n.479T>A c.445T>A (p.Trp149Arg) c.169T>A (p.Trp57Arg) n.232-6002A>T n.934T>A | |
2 | g.138013798T>C | CA348473008 | HNMT | c.547T>C (p.Trp183Arg) n.479T>C c.445T>C (p.Trp149Arg) c.169T>C (p.Trp57Arg) n.232-6002A>G n.934T>C | |
2 | g.138013798T>G | CA348473010 | HNMT | c.547T>G (p.Trp183Gly) n.479T>G c.445T>G (p.Trp149Gly) c.169T>G (p.Trp57Gly) n.232-6002A>C n.934T>G | |
2 | g.138013799G>A | CA348473013 | HNMT | c.548G>A (p.Trp183Ter) n.480G>A c.446G>A (p.Trp149Ter) c.170G>A (p.Trp57Ter) n.232-6003C>T n.935G>A | |
2 | g.138013799G>C | CA348473018 | HNMT | c.548G>C (p.Trp183Ser) n.480G>C c.446G>C (p.Trp149Ser) c.170G>C (p.Trp57Ser) n.232-6003C>G n.935G>C | |
2 | g.138013799G>T | CA348473015 | HNMT | c.548G>T (p.Trp183Leu) n.480G>T c.446G>T (p.Trp149Leu) c.170G>T (p.Trp57Leu) n.232-6003C>A n.935G>T | |
2 | g.138013800G>A | CA348473019 | HNMT | c.549G>A (p.Trp183Ter) n.481G>A c.447G>A (p.Trp149Ter) c.171G>A (p.Trp57Ter) n.232-6004C>T n.936G>A | |
2 | g.138013800G>C | CA348473021 | HNMT | c.549G>C (p.Trp183Cys) n.481G>C c.447G>C (p.Trp149Cys) c.171G>C (p.Trp57Cys) n.232-6004C>G n.936G>C | |
2 | g.138013800G>T | CA348473020 | HNMT | c.549G>T (p.Trp183Cys) n.481G>T c.447G>T (p.Trp149Cys) c.171G>T (p.Trp57Cys) n.232-6004C>A n.936G>T | |
2 | g.138013801A= | CA1291857894 | HNMT | c.550A= (p.Lys184=) n.482A= c.448A= (p.Lys150=) c.172A= (p.Lys58=) n.232-6005T= n.937A= | |
2 | g.138013801A>C | CA348473022 | HNMT | c.550A>C (p.Lys184Gln) n.482A>C c.448A>C (p.Lys150Gln) c.172A>C (p.Lys58Gln) n.232-6005T>G n.937A>C | dbSNP gnomAD v2 gnomAD v4 |
2 | g.138013801A>G | CA348473023 | HNMT | c.550A>G (p.Lys184Glu) n.482A>G c.448A>G (p.Lys150Glu) c.172A>G (p.Lys58Glu) n.232-6005T>C n.937A>G | dbSNP |
2 | g.138013801A>T | CA348473024 | HNMT | c.550A>T (p.Lys184Ter) n.482A>T c.448A>T (p.Lys150Ter) c.172A>T (p.Lys58Ter) n.232-6005T>A n.937A>T | |
2 | g.138013805dup | CA645532939 | HNMT | c.554dup (p.Tyr186ValfsTer9) n.486dup c.452dup (p.Tyr152ValfsTer9) c.176dup (p.Tyr60ValfsTer9) n.232-6005dup n.941dup | COSMIC |
2 | g.138013805del | CA2661303317 | HNMT | c.554del (p.Lys185SerfsTer27) n.486del c.452del (p.Lys151SerfsTer27) c.176del (p.Lys59SerfsTer27) n.232-6005del n.941del | gnomAD v4 |
2 | g.138013802A>C | CA348473027 | HNMT | c.551A>C (p.Lys184Thr) n.483A>C c.449A>C (p.Lys150Thr) c.173A>C (p.Lys58Thr) n.232-6006T>G n.938A>C | gnomAD v4 |
2 | g.138013802A>G | CA348473028 | HNMT | c.551A>G (p.Lys184Arg) n.483A>G c.449A>G (p.Lys150Arg) c.173A>G (p.Lys58Arg) n.232-6006T>C n.938A>G | |
2 | g.138013802A>T | CA348473031 | HNMT | c.551A>T (p.Lys184Ile) n.483A>T c.449A>T (p.Lys150Ile) c.173A>T (p.Lys58Ile) n.232-6006T>A n.938A>T | |
2 | g.138013803A>C | CA348473033 | HNMT | c.552A>C (p.Lys184Asn) n.484A>C c.450A>C (p.Lys150Asn) c.174A>C (p.Lys58Asn) n.232-6007T>G n.939A>C | |
2 | g.138013803A>G | CA429193184 | HNMT | c.552A>G (p.Lys184=) n.484A>G c.450A>G (p.Lys150=) c.174A>G (p.Lys58=) n.232-6007T>C n.939A>G | |
2 | g.138013803A>T | CA348473035 | HNMT | c.552A>T (p.Lys184Asn) n.484A>T c.450A>T (p.Lys150Asn) c.174A>T (p.Lys58Asn) n.232-6007T>A n.939A>T | |
2 | g.138013804A>C | CA348473036 | HNMT | c.553A>C (p.Lys185Gln) n.485A>C c.451A>C (p.Lys151Gln) c.175A>C (p.Lys59Gln) n.232-6008T>G n.940A>C | |
2 | g.138013804A>G | CA348473037 | HNMT | c.553A>G (p.Lys185Glu) n.485A>G c.451A>G (p.Lys151Glu) c.175A>G (p.Lys59Glu) n.232-6008T>C n.940A>G | |
2 | g.138013804A>T | CA348473038 | HNMT | c.553A>T (p.Lys185Ter) n.485A>T c.451A>T (p.Lys151Ter) c.175A>T (p.Lys59Ter) n.232-6008T>A n.940A>T | |
2 | g.138013805A>C | CA348473046 | HNMT | c.554A>C (p.Lys185Thr) n.486A>C c.452A>C (p.Lys151Thr) c.176A>C (p.Lys59Thr) n.232-6009T>G n.941A>C | |
2 | g.138013805A>G | CA348473044 | HNMT | c.554A>G (p.Lys185Arg) n.486A>G c.452A>G (p.Lys151Arg) c.176A>G (p.Lys59Arg) n.232-6009T>C n.941A>G | |
2 | g.138013805A>T | CA348473042 | HNMT | c.554A>T (p.Lys185Met) n.486A>T c.452A>T (p.Lys151Met) c.176A>T (p.Lys59Met) n.232-6009T>A n.941A>T | |
2 | g.138013806G>A | CA429193185 | HNMT | c.555G>A (p.Lys185=) n.487G>A c.453G>A (p.Lys151=) c.177G>A (p.Lys59=) n.232-6010C>T n.942G>A | |
2 | g.138013806G>C | CA57015577 | HNMT | c.555G>C (p.Lys185Asn) n.487G>C c.453G>C (p.Lys151Asn) c.177G>C (p.Lys59Asn) n.232-6010C>G n.942G>C | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013806G= | CA1291857896 | HNMT | c.555G= (p.Lys185=) n.487G= c.453G= (p.Lys151=) c.177G= (p.Lys59=) n.232-6010C= n.942G= | |
2 | g.138013806G>T | CA348473050 | HNMT | c.555G>T (p.Lys185Asn) n.487G>T c.453G>T (p.Lys151Asn) c.177G>T (p.Lys59Asn) n.232-6010C>A n.942G>T | |
2 | g.138013807T>A | CA348473053 | HNMT | c.556T>A (p.Tyr186Asn) n.488T>A c.454T>A (p.Tyr152Asn) c.178T>A (p.Tyr60Asn) n.232-6011A>T n.943T>A | |
2 | g.138013807T>C | CA348473055 | HNMT | c.556T>C (p.Tyr186His) n.488T>C c.454T>C (p.Tyr152His) c.178T>C (p.Tyr60His) n.232-6011A>G n.943T>C | |
2 | g.138013807T>G | CA348473058 | HNMT | c.556T>G (p.Tyr186Asp) n.488T>G c.454T>G (p.Tyr152Asp) c.178T>G (p.Tyr60Asp) n.232-6011A>C n.943T>G | |
2 | g.138013808A>C | CA348473060 | HNMT | c.557A>C (p.Tyr186Ser) n.489A>C c.455A>C (p.Tyr152Ser) c.179A>C (p.Tyr60Ser) n.232-6012T>G n.944A>C | |
2 | g.138013808A>G | CA348473061 | HNMT | c.557A>G (p.Tyr186Cys) n.489A>G c.455A>G (p.Tyr152Cys) c.179A>G (p.Tyr60Cys) n.232-6012T>C n.944A>G | |
2 | g.138013808A>T | CA348473062 | HNMT | c.557A>T (p.Tyr186Phe) n.489A>T c.455A>T (p.Tyr152Phe) c.179A>T (p.Tyr60Phe) n.232-6012T>A n.944A>T | |
2 | g.138013809C>A | CA348473064 | HNMT | c.558C>A (p.Tyr186Ter) n.490C>A c.456C>A (p.Tyr152Ter) c.180C>A (p.Tyr60Ter) n.232-6013G>T n.945C>A | gnomAD v4 |
2 | g.138013809C= | CA1291857903 | HNMT | c.558C= (p.Tyr186=) n.490C= c.456C= (p.Tyr152=) c.180C= (p.Tyr60=) n.232-6013G= n.945C= | |
2 | g.138013809C>G | CA348473066 | HNMT | c.558C>G (p.Tyr186Ter) n.490C>G c.456C>G (p.Tyr152Ter) c.180C>G (p.Tyr60Ter) n.232-6013G>C n.945C>G | gnomAD v4 |
2 | g.138013809C>T | CA1891813 | HNMT | c.558C>T (p.Tyr186=) n.490C>T c.456C>T (p.Tyr152=) c.180C>T (p.Tyr60=) n.232-6013G>A n.945C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.138013810G>A | CA1891814 | HNMT | c.559G>A (p.Gly187Arg) n.491G>A c.457G>A (p.Gly153Arg) c.181G>A (p.Gly61Arg) n.232-6014C>T n.946G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013810G>C | CA348473072 | HNMT | c.559G>C (p.Gly187Arg) n.491G>C c.457G>C (p.Gly153Arg) c.181G>C (p.Gly61Arg) n.232-6014C>G n.946G>C | gnomAD v4 |
2 | g.138013810G= | CA1291857912 | HNMT | c.559G= (p.Gly187=) n.491G= c.457G= (p.Gly153=) c.181G= (p.Gly61=) n.232-6014C= n.946G= | |
2 | g.138013810G>T | CA348473071 | HNMT | c.559G>T (p.Gly187Ter) n.491G>T c.457G>T (p.Gly153Ter) c.181G>T (p.Gly61Ter) n.232-6014C>A n.946G>T | gnomAD v4 |
2 | g.138013811G>A | CA348473077 | HNMT | c.560G>A (p.Gly187Glu) n.492G>A c.458G>A (p.Gly153Glu) c.182G>A (p.Gly61Glu) n.232-6015C>T n.947G>A | dbSNP |
2 | g.138013811G>C | CA348473079 | HNMT | c.560G>C (p.Gly187Ala) n.492G>C c.458G>C (p.Gly153Ala) c.182G>C (p.Gly61Ala) n.232-6015C>G n.947G>C | |
2 | g.138013811G>T | CA348473080 | HNMT | c.560G>T (p.Gly187Val) n.492G>T c.458G>T (p.Gly153Val) c.182G>T (p.Gly61Val) n.232-6015C>A n.947G>T | |
2 | g.138013812A= | CA1291857917 | HNMT | c.561A= (p.Gly187=) n.493A= c.459A= (p.Gly153=) c.183A= (p.Gly61=) n.232-6016T= n.948A= | |
2 | g.138013812A>C | CA429193186 | HNMT | c.561A>C (p.Gly187=) n.493A>C c.459A>C (p.Gly153=) c.183A>C (p.Gly61=) n.232-6016T>G n.948A>C | |
2 | g.138013812A>G | CA429193187 | HNMT | c.561A>G (p.Gly187=) n.493A>G c.459A>G (p.Gly153=) c.183A>G (p.Gly61=) n.232-6016T>C n.948A>G | dbSNP |
2 | g.138013812A>T | CA429193188 | HNMT | c.561A>T (p.Gly187=) n.493A>T c.459A>T (p.Gly153=) c.183A>T (p.Gly61=) n.232-6016T>A n.948A>T | gnomAD v4 |
2 | g.138013813T>A | CA348473082 | HNMT | c.562T>A (p.Ser188Thr) n.494T>A c.460T>A (p.Ser154Thr) c.184T>A (p.Ser62Thr) n.232-6017A>T n.949T>A | |
2 | g.138013813T>C | CA348473084 | HNMT | c.562T>C (p.Ser188Pro) n.494T>C c.460T>C (p.Ser154Pro) c.184T>C (p.Ser62Pro) n.232-6017A>G n.949T>C | |
2 | g.138013813T>G | CA348473086 | HNMT | c.562T>G (p.Ser188Ala) n.494T>G c.460T>G (p.Ser154Ala) c.184T>G (p.Ser62Ala) n.232-6017A>C n.949T>G | |
2 | g.138013814C>A | CA348473088 | HNMT | c.563C>A (p.Ser188Ter) n.495C>A c.461C>A (p.Ser154Ter) c.185C>A (p.Ser62Ter) n.232-6018G>T n.950C>A | |
2 | g.138013814C>G | CA348473091 | HNMT | c.563C>G (p.Ser188Ter) n.495C>G c.461C>G (p.Ser154Ter) c.185C>G (p.Ser62Ter) n.232-6018G>C n.950C>G | |
2 | g.138013814C>T | CA348473097 | HNMT | c.563C>T (p.Ser188Leu) n.495C>T c.461C>T (p.Ser154Leu) c.185C>T (p.Ser62Leu) n.232-6018G>A n.950C>T | |
2 | g.138013815A>C | CA429193191 | HNMT | c.564A>C (p.Ser188=) n.496A>C c.462A>C (p.Ser154=) c.186A>C (p.Ser62=) n.232-6019T>G n.951A>C | |
2 | g.138013815A>G | CA429193189 | HNMT | c.564A>G (p.Ser188=) n.496A>G c.462A>G (p.Ser154=) c.186A>G (p.Ser62=) n.232-6019T>C n.951A>G | |
2 | g.138013815A>T | CA429193190 | HNMT | c.564A>T (p.Ser188=) n.496A>T c.462A>T (p.Ser154=) c.186A>T (p.Ser62=) n.232-6019T>A n.951A>T | |
2 | g.138013816C>A | CA348473100 | HNMT | c.565C>A (p.Arg189Ser) n.497C>A c.463C>A (p.Arg155Ser) c.187C>A (p.Arg63Ser) n.232-6020G>T n.952C>A | |
2 | g.138013816C= | CA1291857923 | HNMT | c.565C= (p.Arg189=) n.497C= c.463C= (p.Arg155=) c.187C= (p.Arg63=) n.232-6020G= n.952C= | |
2 | g.138013816C>G | CA348473102 | HNMT | c.565C>G (p.Arg189Gly) n.497C>G c.463C>G (p.Arg155Gly) c.187C>G (p.Arg63Gly) n.232-6020G>C n.952C>G | |
2 | g.138013816C>T | CA1891815 | HNMT | c.565C>T (p.Arg189Cys) n.497C>T c.463C>T (p.Arg155Cys) c.187C>T (p.Arg63Cys) n.232-6020G>A n.952C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.138013817G>A | CA348473106 | HNMT | c.566G>A (p.Arg189His) n.498G>A c.464G>A (p.Arg155His) c.188G>A (p.Arg63His) n.232-6021C>T n.953G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013817G>C | CA348473104 | HNMT | c.566G>C (p.Arg189Pro) n.498G>C c.464G>C (p.Arg155Pro) c.188G>C (p.Arg63Pro) n.232-6021C>G n.953G>C | |
2 | g.138013817G= | CA1291857928 | HNMT | c.566G= (p.Arg189=) n.498G= c.464G= (p.Arg155=) c.188G= (p.Arg63=) n.232-6021C= n.953G= | |
2 | g.138013817G>T | CA348473105 | HNMT | c.566G>T (p.Arg189Leu) n.498G>T c.464G>T (p.Arg155Leu) c.188G>T (p.Arg63Leu) n.232-6021C>A n.953G>T | gnomAD v4 |
2 | g.138013818C>A | CA429193192 | HNMT | c.567C>A (p.Arg189=) n.499C>A c.465C>A (p.Arg155=) c.189C>A (p.Arg63=) n.232-6022G>T n.954C>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013818C= | CA1291857934 | HNMT | c.567C= (p.Arg189=) n.499C= c.465C= (p.Arg155=) c.189C= (p.Arg63=) n.232-6022G= n.954C= | |
2 | g.138013818C>G | CA429193193 | HNMT | c.567C>G (p.Arg189=) n.499C>G c.465C>G (p.Arg155=) c.189C>G (p.Arg63=) n.232-6022G>C n.954C>G | |
2 | g.138013818C>T | CA1891816 | HNMT | c.567C>T (p.Arg189=) n.499C>T c.465C>T (p.Arg155=) c.189C>T (p.Arg63=) n.232-6022G>A n.954C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013819T>A | CA348473109 | HNMT | c.568T>A (p.Phe190Ile) n.500T>A c.466T>A (p.Phe156Ile) c.190T>A (p.Phe64Ile) n.232-6023A>T n.955T>A | |
2 | g.138013819T>C | CA348473111 | HNMT | c.568T>C (p.Phe190Leu) n.500T>C c.466T>C (p.Phe156Leu) c.190T>C (p.Phe64Leu) n.232-6023A>G n.955T>C | |
2 | g.138013819T>G | CA348473113 | HNMT | c.568T>G (p.Phe190Val) n.500T>G c.466T>G (p.Phe156Val) c.190T>G (p.Phe64Val) n.232-6023A>C n.955T>G | |
2 | g.138013820T>A | CA348473116 | HNMT | c.569T>A (p.Phe190Tyr) n.501T>A c.467T>A (p.Phe156Tyr) c.191T>A (p.Phe64Tyr) n.232-6024A>T n.956T>A | |
2 | g.138013820T>C | CA348473117 | HNMT | c.569T>C (p.Phe190Ser) n.501T>C c.467T>C (p.Phe156Ser) c.191T>C (p.Phe64Ser) n.232-6024A>G n.956T>C | |
2 | g.138013820T>G | CA348473120 | HNMT | c.569T>G (p.Phe190Cys) n.501T>G c.467T>G (p.Phe156Cys) c.191T>G (p.Phe64Cys) n.232-6024A>C n.956T>G | |
2 | g.138013821T>A | CA348473123 | HNMT | c.570T>A (p.Phe190Leu) n.502T>A c.468T>A (p.Phe156Leu) c.192T>A (p.Phe64Leu) n.232-6025A>T n.957T>A | gnomAD v4 |
2 | g.138013821T>C | CA429193197 | HNMT | c.570T>C (p.Phe190=) n.502T>C c.468T>C (p.Phe156=) c.192T>C (p.Phe64=) n.232-6025A>G n.957T>C | |
2 | g.138013821T>G | CA348473125 | HNMT | c.570T>G (p.Phe190Leu) n.502T>G c.468T>G (p.Phe156Leu) c.192T>G (p.Phe64Leu) n.232-6025A>C n.957T>G | |
2 | g.138013822C>A | CA348473127 | HNMT | c.571C>A (p.Pro191Thr) n.503C>A c.469C>A (p.Pro157Thr) c.193C>A (p.Pro65Thr) n.232-6026G>T n.958C>A | |
2 | g.138013822C= | CA1291857941 | HNMT | c.571C= (p.Pro191=) n.503C= c.469C= (p.Pro157=) c.193C= (p.Pro65=) n.232-6026G= n.958C= | |
2 | g.138013822C>G | CA348473129 | HNMT | c.571C>G (p.Pro191Ala) n.503C>G c.469C>G (p.Pro157Ala) c.193C>G (p.Pro65Ala) n.232-6026G>C n.958C>G | |
2 | g.138013822C>T | CA348473131 | HNMT | c.571C>T (p.Pro191Ser) n.503C>T c.469C>T (p.Pro157Ser) c.193C>T (p.Pro65Ser) n.232-6026G>A n.958C>T | |
2 | g.138013825dup | CA429193199 | HNMT | c.574dup (p.Gln192ProfsTer3) n.506dup c.472dup (p.Gln158ProfsTer3) c.196dup (p.Gln66ProfsTer3) n.232-6026dup n.961dup | COSMIC |
2 | g.138013822_138013823insT | CA916660781 | HNMT | c.571_572insT (p.Pro191LeufsTer4) n.503_504insT c.469_470insT (p.Pro157LeufsTer4) c.193_194insT (p.Pro65LeufsTer4) n.232-6027_232-6026insA n.958_959insT | dbSNP |
2 | g.138013823C>A | CA348473137 | HNMT | c.572C>A (p.Pro191His) n.504C>A c.470C>A (p.Pro157His) c.194C>A (p.Pro65His) n.232-6027G>T n.959C>A | |
2 | g.138013823C>G | CA348473138 | HNMT | c.572C>G (p.Pro191Arg) n.504C>G c.470C>G (p.Pro157Arg) c.194C>G (p.Pro65Arg) n.232-6027G>C n.959C>G | |
2 | g.138013823C>T | CA348473135 | HNMT | c.572C>T (p.Pro191Leu) n.504C>T c.470C>T (p.Pro157Leu) c.194C>T (p.Pro65Leu) n.232-6027G>A n.959C>T | |
2 | g.138013824C>A | CA429193204 | HNMT | c.573C>A (p.Pro191=) n.505C>A c.471C>A (p.Pro157=) c.195C>A (p.Pro65=) n.232-6028G>T n.960C>A | |
2 | g.138013824C>G | CA429193205 | HNMT | c.573C>G (p.Pro191=) n.505C>G c.471C>G (p.Pro157=) c.195C>G (p.Pro65=) n.232-6028G>C n.960C>G | |
2 | g.138013824C>T | CA429193203 | HNMT | c.573C>T (p.Pro191=) n.505C>T c.471C>T (p.Pro157=) c.195C>T (p.Pro65=) n.232-6028G>A n.960C>T | |
2 | g.138013825C>A | CA348473144 | HNMT | c.574C>A (p.Gln192Lys) n.506C>A c.472C>A (p.Gln158Lys) c.196C>A (p.Gln66Lys) n.232-6029G>T n.961C>A | |
2 | g.138013825C>G | CA348473140 | HNMT | c.574C>G (p.Gln192Glu) n.506C>G c.472C>G (p.Gln158Glu) c.196C>G (p.Gln66Glu) n.232-6029G>C n.961C>G | |
2 | g.138013825C>T | CA348473143 | HNMT | c.574C>T (p.Gln192Ter) n.506C>T c.472C>T (p.Gln158Ter) c.196C>T (p.Gln66Ter) n.232-6029G>A n.961C>T | |
2 | g.138013826A>C | CA348473148 | HNMT | c.575A>C (p.Gln192Pro) n.507A>C c.473A>C (p.Gln158Pro) c.197A>C (p.Gln66Pro) n.232-6030T>G n.962A>C | |
2 | g.138013826A>G | CA348473150 | HNMT | c.575A>G (p.Gln192Arg) n.507A>G c.473A>G (p.Gln158Arg) c.197A>G (p.Gln66Arg) n.232-6030T>C n.962A>G | gnomAD v4 |
2 | g.138013826A>T | CA348473151 | HNMT | c.575A>T (p.Gln192Leu) n.507A>T c.473A>T (p.Gln158Leu) c.197A>T (p.Gln66Leu) n.232-6030T>A n.962A>T | |
2 | g.138013827G>A | CA429193209 | HNMT | c.576G>A (p.Gln192=) n.508G>A c.474G>A (p.Gln158=) c.198G>A (p.Gln66=) n.232-6031C>T n.963G>A | |
2 | g.138013827G>C | CA348473154 | HNMT | c.576G>C (p.Gln192His) n.508G>C c.474G>C (p.Gln158His) c.198G>C (p.Gln66His) n.232-6031C>G n.963G>C | |
2 | g.138013827G= | CA1291857948 | HNMT | c.576G= (p.Gln192=) n.508G= c.474G= (p.Gln158=) c.198G= (p.Gln66=) n.232-6031C= n.963G= | |
2 | g.138013827G>T | CA57015578 | HNMT | c.576G>T (p.Gln192His) n.508G>T c.474G>T (p.Gln158His) c.198G>T (p.Gln66His) n.232-6031C>A n.963G>T | dbSNP |
2 | g.138013828G>A | CA348473166 | HNMT | c.577G>A (p.Asp193Asn) n.509G>A c.475G>A (p.Asp159Asn) c.199G>A (p.Asp67Asn) n.232-6032C>T n.964G>A | COSMIC |
2 | g.138013828G>C | CA348473158 | HNMT | c.577G>C (p.Asp193His) n.509G>C c.475G>C (p.Asp159His) c.199G>C (p.Asp67His) n.232-6032C>G n.964G>C | |
2 | g.138013828G= | CA1291857953 | HNMT | c.577G= (p.Asp193=) n.509G= c.475G= (p.Asp159=) c.199G= (p.Asp67=) n.232-6032C= n.964G= | |
2 | g.138013828G>T | CA348473164 | HNMT | c.577G>T (p.Asp193Tyr) n.509G>T c.475G>T (p.Asp159Tyr) c.199G>T (p.Asp67Tyr) n.232-6032C>A n.964G>T | dbSNP COSMIC |
2 | g.138013829A= | CA1291857956 | HNMT | c.578A= (p.Asp193=) n.510A= c.476A= (p.Asp159=) c.200A= (p.Asp67=) n.232-6033T= n.965A= | |
2 | g.138013829A>C | CA348473169 | HNMT | c.578A>C (p.Asp193Ala) n.510A>C c.476A>C (p.Asp159Ala) c.200A>C (p.Asp67Ala) n.232-6033T>G n.965A>C | |
2 | g.138013829A>G | CA348473172 | HNMT | c.578A>G (p.Asp193Gly) n.510A>G c.476A>G (p.Asp159Gly) c.200A>G (p.Asp67Gly) n.232-6033T>C n.965A>G | |
2 | g.138013829A>T | CA348473174 | HNMT | c.578A>T (p.Asp193Val) n.510A>T c.476A>T (p.Asp159Val) c.200A>T (p.Asp67Val) n.232-6033T>A n.965A>T | dbSNP |
2 | g.138013830T>A | CA348473176 | HNMT | c.579T>A (p.Asp193Glu) n.511T>A c.477T>A (p.Asp159Glu) c.201T>A (p.Asp67Glu) n.232-6034A>T n.966T>A | |
2 | g.138013830T>C | CA429193211 | HNMT | c.579T>C (p.Asp193=) n.511T>C c.477T>C (p.Asp159=) c.201T>C (p.Asp67=) n.232-6034A>G n.966T>C | gnomAD v4 |
2 | g.138013830T>G | CA348473178 | HNMT | c.579T>G (p.Asp193Glu) n.511T>G c.477T>G (p.Asp159Glu) c.201T>G (p.Asp67Glu) n.232-6034A>C n.966T>G | |
2 | g.138013831G>A | CA348473179 | HNMT | c.580G>A (p.Asp194Asn) n.512G>A c.478G>A (p.Asp160Asn) c.202G>A (p.Asp68Asn) n.232-6035C>T n.967G>A | gnomAD v4 |
2 | g.138013831G>C | CA348473181 | HNMT | c.580G>C (p.Asp194His) n.512G>C c.478G>C (p.Asp160His) c.202G>C (p.Asp68His) n.232-6035C>G n.967G>C | |
2 | g.138013831G>T | CA348473180 | HNMT | c.580G>T (p.Asp194Tyr) n.512G>T c.478G>T (p.Asp160Tyr) c.202G>T (p.Asp68Tyr) n.232-6035C>A n.967G>T | |
2 | g.138013832A>C | CA348473182 | HNMT | c.581A>C (p.Asp194Ala) n.513A>C c.479A>C (p.Asp160Ala) c.203A>C (p.Asp68Ala) n.232-6036T>G n.968A>C | |
2 | g.138013832A>G | CA348473184 | HNMT | c.581A>G (p.Asp194Gly) n.513A>G c.479A>G (p.Asp160Gly) c.203A>G (p.Asp68Gly) n.232-6036T>C n.968A>G | |
2 | g.138013832A>T | CA348473185 | HNMT | c.581A>T (p.Asp194Val) n.513A>T c.479A>T (p.Asp160Val) c.203A>T (p.Asp68Val) n.232-6036T>A n.968A>T | |
2 | g.138013833C>A | CA1891817 | HNMT | c.582C>A (p.Asp194Glu) n.514C>A c.480C>A (p.Asp160Glu) c.204C>A (p.Asp68Glu) n.232-6037G>T n.969C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013833C= | CA1291857958 | HNMT | c.582C= (p.Asp194=) n.514C= c.480C= (p.Asp160=) c.204C= (p.Asp68=) n.232-6037G= n.969C= | |
2 | g.138013833C>G | CA348473188 | HNMT | c.582C>G (p.Asp194Glu) n.514C>G c.480C>G (p.Asp160Glu) c.204C>G (p.Asp68Glu) n.232-6037G>C n.969C>G | |
2 | g.138013833C>T | CA1891818 | HNMT | c.582C>T (p.Asp194=) n.514C>T c.480C>T (p.Asp160=) c.204C>T (p.Asp68=) n.232-6037G>A n.969C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013834C>A | CA57015579 | HNMT | c.583C>A (p.Leu195Ile) n.515C>A c.481C>A (p.Leu161Ile) c.205C>A (p.Leu69Ile) n.232-6038G>T n.970C>A | dbSNP gnomAD v4 |
2 | g.138013834C= | CA1291857961 | HNMT | c.583C= (p.Leu195=) n.515C= c.481C= (p.Leu161=) c.205C= (p.Leu69=) n.232-6038G= n.970C= | |
2 | g.138013834C>G | CA348473193 | HNMT | c.583C>G (p.Leu195Val) n.515C>G c.481C>G (p.Leu161Val) c.205C>G (p.Leu69Val) n.232-6038G>C n.970C>G | |
2 | g.138013834C>T | CA1891819 | HNMT | c.583C>T (p.Leu195Phe) n.515C>T c.481C>T (p.Leu161Phe) c.205C>T (p.Leu69Phe) n.232-6038G>A n.970C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.138013835T>A | CA348473196 | HNMT | c.584T>A (p.Leu195His) n.516T>A c.482T>A (p.Leu161His) c.206T>A (p.Leu69His) n.232-6039A>T n.971T>A | |
2 | g.138013835T>C | CA348473197 | HNMT | c.584T>C (p.Leu195Pro) n.516T>C c.482T>C (p.Leu161Pro) c.206T>C (p.Leu69Pro) n.232-6039A>G n.971T>C | |
2 | g.138013835T>G | CA348473198 | HNMT | c.584T>G (p.Leu195Arg) n.516T>G c.482T>G (p.Leu161Arg) c.206T>G (p.Leu69Arg) n.232-6039A>C n.971T>G | |
2 | g.138013836C>A | CA429193219 | HNMT | c.585C>A (p.Leu195=) n.517C>A c.483C>A (p.Leu161=) c.207C>A (p.Leu69=) n.232-6040G>T n.972C>A | |
2 | g.138013836C>G | CA429193220 | HNMT | c.585C>G (p.Leu195=) n.517C>G c.483C>G (p.Leu161=) c.207C>G (p.Leu69=) n.232-6040G>C n.972C>G | gnomAD v4 |
2 | g.138013836C>T | CA429193221 | HNMT | c.585C>T (p.Leu195=) n.517C>T c.483C>T (p.Leu161=) c.207C>T (p.Leu69=) n.232-6040G>A n.972C>T | |
2 | g.138013837T>A | CA348473202 | HNMT | c.586T>A (p.Cys196Ser) n.518T>A c.484T>A (p.Cys162Ser) c.208T>A (p.Cys70Ser) n.232-6041A>T n.973T>A | |
2 | g.138013837T>C | CA348473205 | HNMT | c.586T>C (p.Cys196Arg) n.518T>C c.484T>C (p.Cys162Arg) c.208T>C (p.Cys70Arg) n.232-6041A>G n.973T>C | |
2 | g.138013837T>G | CA348473203 | HNMT | c.586T>G (p.Cys196Gly) n.518T>G c.484T>G (p.Cys162Gly) c.208T>G (p.Cys70Gly) n.232-6041A>C n.973T>G | |
2 | g.138013838G>A | CA348473207 | HNMT | c.587G>A (p.Cys196Tyr) n.519G>A c.485G>A (p.Cys162Tyr) c.209G>A (p.Cys70Tyr) n.232-6042C>T n.974G>A | |
2 | g.138013838G>C | CA348473208 | HNMT | c.587G>C (p.Cys196Ser) n.519G>C c.485G>C (p.Cys162Ser) c.209G>C (p.Cys70Ser) n.232-6042C>G n.974G>C | |
2 | g.138013838G= | CA1291857965 | HNMT | c.587G= (p.Cys196=) n.519G= c.485G= (p.Cys162=) c.209G= (p.Cys70=) n.232-6042C= n.974G= | |
2 | g.138013838G>T | CA348473210 | HNMT | c.587G>T (p.Cys196Phe) n.519G>T c.485G>T (p.Cys162Phe) c.209G>T (p.Cys70Phe) n.232-6042C>A n.974G>T | dbSNP |
2 | g.138013839C>A | CA348473213 | HNMT | c.588C>A (p.Cys196Ter) n.520C>A c.486C>A (p.Cys162Ter) c.210C>A (p.Cys70Ter) n.232-6043G>T n.975C>A | |
2 | g.138013839C>G | CA348473215 | HNMT | c.588C>G (p.Cys196Trp) n.520C>G c.486C>G (p.Cys162Trp) c.210C>G (p.Cys70Trp) n.232-6043G>C n.975C>G | |
2 | g.138013839C>T | CA429193224 | HNMT | c.588C>T (p.Cys196=) n.520C>T c.486C>T (p.Cys162=) c.210C>T (p.Cys70=) n.232-6043G>A n.975C>T | |
2 | g.138013840C>A | CA348473217 | HNMT | c.589C>A (p.Gln197Lys) n.521C>A c.487C>A (p.Gln163Lys) c.211C>A (p.Gln71Lys) n.232-6044G>T n.976C>A | |
2 | g.138013840C>G | CA348473219 | HNMT | c.589C>G (p.Gln197Glu) n.521C>G c.487C>G (p.Gln163Glu) c.211C>G (p.Gln71Glu) n.232-6044G>C n.976C>G | |
2 | g.138013840C>T | CA348473221 | HNMT | c.589C>T (p.Gln197Ter) n.521C>T c.487C>T (p.Gln163Ter) c.211C>T (p.Gln71Ter) n.232-6044G>A n.976C>T | |
2 | g.138013841A>C | CA348473224 | HNMT | c.590A>C (p.Gln197Pro) n.522A>C c.488A>C (p.Gln163Pro) c.212A>C (p.Gln71Pro) n.232-6045T>G n.977A>C | |
2 | g.138013841A>G | CA348473226 | HNMT | c.590A>G (p.Gln197Arg) n.522A>G c.488A>G (p.Gln163Arg) c.212A>G (p.Gln71Arg) n.232-6045T>C n.977A>G | COSMIC |
2 | g.138013841A>T | CA348473230 | HNMT | c.590A>T (p.Gln197Leu) n.522A>T c.488A>T (p.Gln163Leu) c.212A>T (p.Gln71Leu) n.232-6045T>A n.977A>T | |
2 | g.138013842G>A | CA429193228 | HNMT | c.591G>A (p.Gln197=) n.523G>A c.489G>A (p.Gln163=) c.213G>A (p.Gln71=) n.232-6046C>T n.978G>A | gnomAD v4 |
2 | g.138013842G>C | CA348473233 | HNMT | c.591G>C (p.Gln197His) n.523G>C c.489G>C (p.Gln163His) c.213G>C (p.Gln71His) n.232-6046C>G n.978G>C | |
2 | g.138013842G>T | CA348473234 | HNMT | c.591G>T (p.Gln197His) n.523G>T c.489G>T (p.Gln163His) c.213G>T (p.Gln71His) n.232-6046C>A n.978G>T | |
2 | g.138013843T>A | CA348473238 | HNMT | c.592T>A (p.Tyr198Asn) n.524T>A c.490T>A (p.Tyr164Asn) c.214T>A (p.Tyr72Asn) n.232-6047A>T n.979T>A | |
2 | g.138013843T>C | CA348473235 | HNMT | c.592T>C (p.Tyr198His) n.524T>C c.490T>C (p.Tyr164His) c.214T>C (p.Tyr72His) n.232-6047A>G n.979T>C | |
2 | g.138013843T>G | CA348473237 | HNMT | c.592T>G (p.Tyr198Asp) n.524T>G c.490T>G (p.Tyr164Asp) c.214T>G (p.Tyr72Asp) n.232-6047A>C n.979T>G | |
2 | g.138013844A= | CA1291857969 | HNMT | c.593A= (p.Tyr198=) n.525A= c.491A= (p.Tyr164=) c.215A= (p.Tyr72=) n.232-6048T= n.980A= | |
2 | g.138013844A>C | CA348473240 | HNMT | c.593A>C (p.Tyr198Ser) n.525A>C c.491A>C (p.Tyr164Ser) c.215A>C (p.Tyr72Ser) n.232-6048T>G n.980A>C | |
2 | g.138013844A>G | CA348473245 | HNMT | c.593A>G (p.Tyr198Cys) n.525A>G c.491A>G (p.Tyr164Cys) c.215A>G (p.Tyr72Cys) n.232-6048T>C n.980A>G | dbSNP gnomAD v4 |
2 | g.138013844A>T | CA348473248 | HNMT | c.593A>T (p.Tyr198Phe) n.525A>T c.491A>T (p.Tyr164Phe) c.215A>T (p.Tyr72Phe) n.232-6048T>A n.980A>T | |
2 | g.138013845T>A | CA348473254 | HNMT | c.594T>A (p.Tyr198Ter) n.526T>A c.492T>A (p.Tyr164Ter) c.216T>A (p.Tyr72Ter) n.232-6049A>T n.981T>A | |
2 | g.138013845T>C | CA1891820 | HNMT | c.594T>C (p.Tyr198=) n.526T>C c.492T>C (p.Tyr164=) c.216T>C (p.Tyr72=) n.232-6049A>G n.981T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013845T>G | CA348473259 | HNMT | c.594T>G (p.Tyr198Ter) n.526T>G c.492T>G (p.Tyr164Ter) c.216T>G (p.Tyr72Ter) n.232-6049A>C n.981T>G | |
2 | g.138013845T= | CA1291857973 | HNMT | c.594T= (p.Tyr198=) n.526T= c.492T= (p.Tyr164=) c.216T= (p.Tyr72=) n.232-6049A= n.981T= | |
2 | g.138013846A>C | CA348473262 | HNMT | c.595A>C (p.Ile199Leu) n.527A>C c.493A>C (p.Ile165Leu) c.217A>C (p.Ile73Leu) n.232-6050T>G n.982A>C | |
2 | g.138013846A>G | CA348473265 | HNMT | c.595A>G (p.Ile199Val) n.527A>G c.493A>G (p.Ile165Val) c.217A>G (p.Ile73Val) n.232-6050T>C n.982A>G | |
2 | g.138013846A>T | CA348473268 | HNMT | c.595A>T (p.Ile199Phe) n.527A>T c.493A>T (p.Ile165Phe) c.217A>T (p.Ile73Phe) n.232-6050T>A n.982A>T | |
2 | g.138013847T>A | CA348473272 | HNMT | c.596T>A (p.Ile199Asn) n.528T>A c.494T>A (p.Ile165Asn) c.218T>A (p.Ile73Asn) n.232-6051A>T n.983T>A | dbSNP |
2 | g.138013847T>C | CA348473274 | HNMT | c.596T>C (p.Ile199Thr) n.528T>C c.494T>C (p.Ile165Thr) c.218T>C (p.Ile73Thr) n.232-6051A>G n.983T>C | |
2 | g.138013847T>G | CA57015580 | HNMT | c.596T>G (p.Ile199Ser) n.528T>G c.494T>G (p.Ile165Ser) c.218T>G (p.Ile73Ser) n.232-6051A>C n.983T>G | dbSNP gnomAD v4 |
2 | g.138013847T= | CA1291857977 | HNMT | c.596T= (p.Ile199=) n.528T= c.494T= (p.Ile165=) c.218T= (p.Ile73=) n.232-6051A= n.983T= | |
2 | g.138013848C>A | CA429193232 | HNMT | c.597C>A (p.Ile199=) n.529C>A c.495C>A (p.Ile165=) c.219C>A (p.Ile73=) n.232-6052G>T n.984C>A | gnomAD v4 |
2 | g.138013848C>G | CA348473280 | HNMT | c.597C>G (p.Ile199Met) n.529C>G c.495C>G (p.Ile165Met) c.219C>G (p.Ile73Met) n.232-6052G>C n.984C>G | gnomAD v4 |
2 | g.138013848C>T | CA429193233 | HNMT | c.597C>T (p.Ile199=) n.529C>T c.495C>T (p.Ile165=) c.219C>T (p.Ile73=) n.232-6052G>A n.984C>T | gnomAD v4 |
2 | g.138013849A>C | CA348473292 | HNMT | c.598A>C (p.Thr200Pro) n.530A>C c.496A>C (p.Thr166Pro) c.220A>C (p.Thr74Pro) n.232-6053T>G n.985A>C | |
2 | g.138013849A>G | CA348473283 | HNMT | c.598A>G (p.Thr200Ala) n.530A>G c.496A>G (p.Thr166Ala) c.220A>G (p.Thr74Ala) n.232-6053T>C n.985A>G | |
2 | g.138013849A>T | CA348473286 | HNMT | c.598A>T (p.Thr200Ser) n.530A>T c.496A>T (p.Thr166Ser) c.220A>T (p.Thr74Ser) n.232-6053T>A n.985A>T | |
2 | g.138013850C>A | CA348473297 | HNMT | c.599C>A (p.Thr200Lys) n.531C>A c.497C>A (p.Thr166Lys) c.221C>A (p.Thr74Lys) n.232-6054G>T n.986C>A | |
2 | g.138013850C= | CA1291857979 | HNMT | c.599C= (p.Thr200=) n.531C= c.497C= (p.Thr166=) c.221C= (p.Thr74=) n.232-6054G= n.986C= | |
2 | g.138013850C>G | CA348473300 | HNMT | c.599C>G (p.Thr200Arg) n.531C>G c.497C>G (p.Thr166Arg) c.221C>G (p.Thr74Arg) n.232-6054G>C n.986C>G | |
2 | g.138013850C>T | CA348473302 | HNMT | c.599C>T (p.Thr200Ile) n.531C>T c.497C>T (p.Thr166Ile) c.221C>T (p.Thr74Ile) n.232-6054G>A n.986C>T | dbSNP gnomAD v2 gnomAD v4 |
2 | g.138013851A>C | CA429193237 | HNMT | c.600A>C (p.Thr200=) n.532A>C c.498A>C (p.Thr166=) c.222A>C (p.Thr74=) n.232-6055T>G n.987A>C | |
2 | g.138013851A>G | CA429193238 | HNMT | c.600A>G (p.Thr200=) n.532A>G c.498A>G (p.Thr166=) c.222A>G (p.Thr74=) n.232-6055T>C n.987A>G | ClinVar |
2 | g.138013851A>T | CA429193239 | HNMT | c.600A>T (p.Thr200=) n.532A>T c.498A>T (p.Thr166=) c.222A>T (p.Thr74=) n.232-6055T>A n.987A>T | |
2 | g.138013852T>A | CA348473311 | HNMT | c.601T>A (p.Ser201Thr) n.533T>A c.499T>A (p.Ser167Thr) c.223T>A (p.Ser75Thr) n.232-6056A>T n.988T>A | COSMIC |
2 | g.138013852T>C | CA348473310 | HNMT | c.601T>C (p.Ser201Pro) n.533T>C c.499T>C (p.Ser167Pro) c.223T>C (p.Ser75Pro) n.232-6056A>G n.988T>C | |
2 | g.138013852T>G | CA348473307 | HNMT | c.601T>G (p.Ser201Ala) n.533T>G c.499T>G (p.Ser167Ala) c.223T>G (p.Ser75Ala) n.232-6056A>C n.988T>G | |
2 | g.138013853C>A | CA348473312 | HNMT | c.602C>A (p.Ser201Ter) n.534C>A c.500C>A (p.Ser167Ter) c.224C>A (p.Ser75Ter) n.232-6057G>T n.989C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013853C= | CA1291857982 | HNMT | c.602C= (p.Ser201=) n.534C= c.500C= (p.Ser167=) c.224C= (p.Ser75=) n.232-6057G= n.989C= | |
2 | g.138013853C>G | CA348473313 | HNMT | c.602C>G (p.Ser201Ter) n.534C>G c.500C>G (p.Ser167Ter) c.224C>G (p.Ser75Ter) n.232-6057G>C n.989C>G | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013853C>T | CA348473314 | HNMT | c.602C>T (p.Ser201Leu) n.534C>T c.500C>T (p.Ser167Leu) c.224C>T (p.Ser75Leu) n.232-6057G>A n.989C>T | |
2 | g.138013854A>C | CA429193241 | HNMT | c.603A>C (p.Ser201=) n.535A>C c.501A>C (p.Ser167=) c.225A>C (p.Ser75=) n.232-6058T>G n.990A>C | |
2 | g.138013854A>G | CA429193243 | HNMT | c.603A>G (p.Ser201=) n.535A>G c.501A>G (p.Ser167=) c.225A>G (p.Ser75=) n.232-6058T>C n.990A>G | |
2 | g.138013854A>T | CA429193242 | HNMT | c.603A>T (p.Ser201=) n.535A>T c.501A>T (p.Ser167=) c.225A>T (p.Ser75=) n.232-6058T>A n.990A>T | |
2 | g.138013855G>A | CA348473318 | HNMT | c.604G>A (p.Asp202Asn) n.536G>A c.502G>A (p.Asp168Asn) c.226G>A (p.Asp76Asn) n.232-6059C>T n.991G>A | |
2 | g.138013855G>C | CA348473322 | HNMT | c.604G>C (p.Asp202His) n.536G>C c.502G>C (p.Asp168His) c.226G>C (p.Asp76His) n.232-6059C>G n.991G>C | |
2 | g.138013855G>T | CA348473326 | HNMT | c.604G>T (p.Asp202Tyr) n.536G>T c.502G>T (p.Asp168Tyr) c.226G>T (p.Asp76Tyr) n.232-6059C>A n.991G>T | |
2 | g.138013856A>C | CA348473334 | HNMT | c.605A>C (p.Asp202Ala) n.537A>C c.503A>C (p.Asp168Ala) c.227A>C (p.Asp76Ala) n.232-6060T>G n.992A>C | |
2 | g.138013856A>G | CA348473329 | HNMT | c.605A>G (p.Asp202Gly) n.537A>G c.503A>G (p.Asp168Gly) c.227A>G (p.Asp76Gly) n.232-6060T>C n.992A>G | |
2 | g.138013856A>T | CA348473331 | HNMT | c.605A>T (p.Asp202Val) n.537A>T c.503A>T (p.Asp168Val) c.227A>T (p.Asp76Val) n.232-6060T>A n.992A>T | |
2 | g.138013857T>A | CA348473337 | HNMT | c.606T>A (p.Asp202Glu) n.538T>A c.504T>A (p.Asp168Glu) c.228T>A (p.Asp76Glu) n.232-6061A>T n.993T>A | |
2 | g.138013857T>C | CA429193247 | HNMT | c.606T>C (p.Asp202=) n.538T>C c.504T>C (p.Asp168=) c.228T>C (p.Asp76=) n.232-6061A>G n.993T>C | gnomAD v4 |
2 | g.138013857T>G | CA348473339 | HNMT | c.606T>G (p.Asp202Glu) n.538T>G c.504T>G (p.Asp168Glu) c.228T>G (p.Asp76Glu) n.232-6061A>C n.993T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013857T= | CA1291857984 | HNMT | c.606T= (p.Asp202=) n.538T= c.504T= (p.Asp168=) c.228T= (p.Asp76=) n.232-6061A= n.993T= | |
2 | g.138013858del | CA2661303318 | HNMT | c.607del (p.Asp203ThrfsTer9) n.539del c.505del (p.Asp169ThrfsTer9) c.229del (p.Asp77ThrfsTer9) n.232-6062del n.994del | gnomAD v4 |
2 | g.138013858G>A | CA348473342 | HNMT | c.607G>A (p.Asp203Asn) n.539G>A c.505G>A (p.Asp169Asn) c.229G>A (p.Asp77Asn) n.232-6062C>T n.994G>A | |
2 | g.138013858G>C | CA348473345 | HNMT | c.607G>C (p.Asp203His) n.539G>C c.505G>C (p.Asp169His) c.229G>C (p.Asp77His) n.232-6062C>G n.994G>C | |
2 | g.138013858G>T | CA348473347 | HNMT | c.607G>T (p.Asp203Tyr) n.539G>T c.505G>T (p.Asp169Tyr) c.229G>T (p.Asp77Tyr) n.232-6062C>A n.994G>T | |
2 | g.138013859A>C | CA348473351 | HNMT | c.608A>C (p.Asp203Ala) n.540A>C c.506A>C (p.Asp169Ala) c.230A>C (p.Asp77Ala) n.232-6063T>G n.995A>C | |
2 | g.138013859A>G | CA348473352 | HNMT | c.608A>G (p.Asp203Gly) n.540A>G c.506A>G (p.Asp169Gly) c.230A>G (p.Asp77Gly) n.232-6063T>C n.995A>G | |
2 | g.138013859A>T | CA348473353 | HNMT | c.608A>T (p.Asp203Val) n.540A>T c.506A>T (p.Asp169Val) c.230A>T (p.Asp77Val) n.232-6063T>A n.995A>T | |
2 | g.138013860C>A | CA348473356 | HNMT | c.609C>A (p.Asp203Glu) n.541C>A c.507C>A (p.Asp169Glu) c.231C>A (p.Asp77Glu) n.232-6064G>T n.996C>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013860C= | CA1291857987 | HNMT | c.609C= (p.Asp203=) n.541C= c.507C= (p.Asp169=) c.231C= (p.Asp77=) n.232-6064G= n.996C= | |
2 | g.138013860C>G | CA348473360 | HNMT | c.609C>G (p.Asp203Glu) n.541C>G c.507C>G (p.Asp169Glu) c.231C>G (p.Asp77Glu) n.232-6064G>C n.996C>G | |
2 | g.138013860C>T | CA429193249 | HNMT | c.609C>T (p.Asp203=) n.541C>T c.507C>T (p.Asp169=) c.231C>T (p.Asp77=) n.232-6064G>A n.996C>T | gnomAD v4 |
2 | g.138013861C>A | CA348473363 | HNMT | c.610C>A (p.Leu204Ile) n.542C>A c.508C>A (p.Leu170Ile) c.232C>A (p.Leu78Ile) n.232-6065G>T n.997C>A | |
2 | g.138013861C>G | CA348473365 | HNMT | c.610C>G (p.Leu204Val) n.542C>G c.508C>G (p.Leu170Val) c.232C>G (p.Leu78Val) n.232-6065G>C n.997C>G | |
2 | g.138013861C>T | CA348473368 | HNMT | c.610C>T (p.Leu204Phe) n.542C>T c.508C>T (p.Leu170Phe) c.232C>T (p.Leu78Phe) n.232-6065G>A n.997C>T | |
2 | g.138013862T>A | CA348473371 | HNMT | c.611T>A (p.Leu204His) n.543T>A c.509T>A (p.Leu170His) c.233T>A (p.Leu78His) n.232-6066A>T n.998T>A | |
2 | g.138013862T>C | CA348473378 | HNMT | c.611T>C (p.Leu204Pro) n.543T>C c.509T>C (p.Leu170Pro) c.233T>C (p.Leu78Pro) n.232-6066A>G n.998T>C | |
2 | g.138013862T>G | CA348473374 | HNMT | c.611T>G (p.Leu204Arg) n.543T>G c.509T>G (p.Leu170Arg) c.233T>G (p.Leu78Arg) n.232-6066A>C n.998T>G | |
2 | g.138013863C>A | CA429193255 | HNMT | c.612C>A (p.Leu204=) n.544C>A c.510C>A (p.Leu170=) c.234C>A (p.Leu78=) n.232-6067G>T n.999C>A | |
2 | g.138013863C>G | CA429193256 | HNMT | c.612C>G (p.Leu204=) n.544C>G c.510C>G (p.Leu170=) c.234C>G (p.Leu78=) n.232-6067G>C n.999C>G | |
2 | g.138013863C>T | CA429193254 | HNMT | c.612C>T (p.Leu204=) n.544C>T c.510C>T (p.Leu170=) c.234C>T (p.Leu78=) n.232-6067G>A n.999C>T | |
2 | g.138013864A= | CA1291857989 | HNMT | c.613A= (p.Thr205=) n.545A= c.511A= (p.Thr171=) c.235A= (p.Thr79=) n.232-6068T= n.1000A= | |
2 | g.138013864A>C | CA348473382 | HNMT | c.613A>C (p.Thr205Pro) n.545A>C c.511A>C (p.Thr171Pro) c.235A>C (p.Thr79Pro) n.232-6068T>G n.1000A>C | |
2 | g.138013864A>G | CA348473384 | HNMT | c.613A>G (p.Thr205Ala) n.545A>G c.511A>G (p.Thr171Ala) c.235A>G (p.Thr79Ala) n.232-6068T>C n.1000A>G | dbSNP |
2 | g.138013864A>T | CA348473386 | HNMT | c.613A>T (p.Thr205Ser) n.545A>T c.511A>T (p.Thr171Ser) c.235A>T (p.Thr79Ser) n.232-6068T>A n.1000A>T | |
2 | g.138013865C>A | CA348473391 | HNMT | c.614C>A (p.Thr205Asn) n.546C>A c.512C>A (p.Thr171Asn) c.236C>A (p.Thr79Asn) n.232-6069G>T n.1001C>A | gnomAD v4 |
2 | g.138013865C= | CA1291857991 | HNMT | c.614C= (p.Thr205=) n.546C= c.512C= (p.Thr171=) c.236C= (p.Thr79=) n.232-6069G= n.1001C= | |
2 | g.138013865C>G | CA348473395 | HNMT | c.614C>G (p.Thr205Ser) n.546C>G c.512C>G (p.Thr171Ser) c.236C>G (p.Thr79Ser) n.232-6069G>C n.1001C>G | |
2 | g.138013865C>T | CA1891821 | HNMT | c.614C>T (p.Thr205Ile) n.546C>T c.512C>T (p.Thr171Ile) c.236C>T (p.Thr79Ile) n.232-6069G>A n.1001C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013866T>A | CA429193258 | HNMT | c.615T>A (p.Thr205=) n.547T>A c.513T>A (p.Thr171=) c.237T>A (p.Thr79=) n.232-6070A>T n.1002T>A | |
2 | g.138013866T>C | CA429193259 | HNMT | c.615T>C (p.Thr205=) n.547T>C c.513T>C (p.Thr171=) c.237T>C (p.Thr79=) n.232-6070A>G n.1002T>C | |
2 | g.138013866T>G | CA429193260 | HNMT | c.615T>G (p.Thr205=) n.547T>G c.513T>G (p.Thr171=) c.237T>G (p.Thr79=) n.232-6070A>C n.1002T>G | |
2 | g.138013867C>A | CA348473402 | HNMT | c.616C>A (p.Gln206Lys) n.548C>A c.514C>A (p.Gln172Lys) c.238C>A (p.Gln80Lys) n.232-6071G>T n.1003C>A | |
2 | g.138013867C= | CA1291857993 | HNMT | c.616C= (p.Gln206=) n.548C= c.514C= (p.Gln172=) c.238C= (p.Gln80=) n.232-6071G= n.1003C= | |
2 | g.138013867C>G | CA348473398 | HNMT | c.616C>G (p.Gln206Glu) n.548C>G c.514C>G (p.Gln172Glu) c.238C>G (p.Gln80Glu) n.232-6071G>C n.1003C>G | |
2 | g.138013867C>T | CA348473400 | HNMT | c.616C>T (p.Gln206Ter) n.548C>T c.514C>T (p.Gln172Ter) c.238C>T (p.Gln80Ter) n.232-6071G>A n.1003C>T | dbSNP gnomAD v2 gnomAD v4 |
2 | g.138013868A= | CA1291857997 | HNMT | c.617A= (p.Gln206=) n.549A= c.515A= (p.Gln172=) c.239A= (p.Gln80=) n.232-6072T= n.1004A= | |
2 | g.138013868A>C | CA57015581 | HNMT | c.617A>C (p.Gln206Pro) n.549A>C c.515A>C (p.Gln172Pro) c.239A>C (p.Gln80Pro) n.232-6072T>G n.1004A>C | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013868A>G | CA348473409 | HNMT | c.617A>G (p.Gln206Arg) n.549A>G c.515A>G (p.Gln172Arg) c.239A>G (p.Gln80Arg) n.232-6072T>C n.1004A>G | |
2 | g.138013868A>T | CA57015582 | HNMT | c.617A>T (p.Gln206Leu) n.549A>T c.515A>T (p.Gln172Leu) c.239A>T (p.Gln80Leu) n.232-6072T>A n.1004A>T | dbSNP gnomAD v3 gnomAD v4 |
2 | g.138013869G>A | CA429193261 | HNMT | c.618G>A (p.Gln206=) n.550G>A c.516G>A (p.Gln172=) c.240G>A (p.Gln80=) n.232-6073C>T n.1005G>A | |
2 | g.138013869G>C | CA348473415 | HNMT | c.618G>C (p.Gln206His) n.550G>C c.516G>C (p.Gln172His) c.240G>C (p.Gln80His) n.232-6073C>G n.1005G>C | |
2 | g.138013869G>T | CA348473418 | HNMT | c.618G>T (p.Gln206His) n.550G>T c.516G>T (p.Gln172His) c.240G>T (p.Gln80His) n.232-6073C>A n.1005G>T | |
2 | g.138013870A>C | CA348473424 | HNMT | c.619A>C (p.Met207Leu) n.551A>C c.517A>C (p.Met173Leu) c.241A>C (p.Met81Leu) n.232-6074T>G n.1006A>C | |
2 | g.138013870A>G | CA348473430 | HNMT | c.619A>G (p.Met207Val) n.551A>G c.517A>G (p.Met173Val) c.241A>G (p.Met81Val) n.232-6074T>C n.1006A>G | |
2 | g.138013870A>T | CA348473427 | HNMT | c.619A>T (p.Met207Leu) n.551A>T c.517A>T (p.Met173Leu) c.241A>T (p.Met81Leu) n.232-6074T>A n.1006A>T | |
2 | g.138013871T>A | CA348473433 | HNMT | c.620T>A (p.Met207Lys) n.552T>A c.518T>A (p.Met173Lys) c.242T>A (p.Met81Lys) n.232-6075A>T n.1007T>A | |
2 | g.138013871T>C | CA1891822 | HNMT | c.620T>C (p.Met207Thr) n.552T>C c.518T>C (p.Met173Thr) c.242T>C (p.Met81Thr) n.232-6075A>G n.1007T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.138013871T>G | CA348473437 | HNMT | c.620T>G (p.Met207Arg) n.552T>G c.518T>G (p.Met173Arg) c.242T>G (p.Met81Arg) n.232-6075A>C n.1007T>G | |
2 | g.138013871T= | CA1291858000 | HNMT | c.620T= (p.Met207=) n.552T= c.518T= (p.Met173=) c.242T= (p.Met81=) n.232-6075A= n.1007T= | |
2 | g.138013872G>A | CA348473440 | HNMT | c.621G>A (p.Met207Ile) n.553G>A c.519G>A (p.Met173Ile) c.243G>A (p.Met81Ile) n.232-6076C>T n.1008G>A | dbSNP gnomAD v4 |
2 | g.138013872G>C | CA348473443 | HNMT | c.621G>C (p.Met207Ile) n.553G>C c.519G>C (p.Met173Ile) c.243G>C (p.Met81Ile) n.232-6076C>G n.1008G>C | |
2 | g.138013872G= | CA1291858002 | HNMT | c.621G= (p.Met207=) n.553G= c.519G= (p.Met173=) c.243G= (p.Met81=) n.232-6076C= n.1008G= | |
2 | g.138013872G>T | CA348473446 | HNMT | c.621G>T (p.Met207Ile) n.553G>T c.519G>T (p.Met173Ile) c.243G>T (p.Met81Ile) n.232-6076C>A n.1008G>T | dbSNP gnomAD v4 |
2 | g.138013873C>A | CA348473450 | HNMT | c.622C>A (p.Leu208Met) n.554C>A c.520C>A (p.Leu174Met) c.244C>A (p.Leu82Met) n.232-6077G>T n.1009C>A | |
2 | g.138013873C>G | CA348473452 | HNMT | c.622C>G (p.Leu208Val) n.554C>G c.520C>G (p.Leu174Val) c.244C>G (p.Leu82Val) n.232-6077G>C n.1009C>G | |
2 | g.138013873C>T | CA429193263 | HNMT | c.622C>T (p.Leu208=) n.554C>T c.520C>T (p.Leu174=) c.244C>T (p.Leu82=) n.232-6077G>A n.1009C>T | |
2 | g.138013874T>A | CA348473454 | HNMT | c.623T>A (p.Leu208Gln) n.555T>A c.521T>A (p.Leu174Gln) c.245T>A (p.Leu82Gln) n.232-6078A>T n.1010T>A | |
2 | g.138013874T>C | CA347928 | HNMT | c.623T>C (p.Leu208Pro) n.555T>C c.521T>C (p.Leu174Pro) c.245T>C (p.Leu82Pro) n.232-6078A>G n.1010T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.138013874T>G | CA348473468 | HNMT | c.623T>G (p.Leu208Arg) n.555T>G c.521T>G (p.Leu174Arg) c.245T>G (p.Leu82Arg) n.232-6078A>C n.1010T>G | |
2 | g.138013874T= | CA1291858005 | HNMT | c.623T= (p.Leu208=) n.555T= c.521T= (p.Leu174=) c.245T= (p.Leu82=) n.232-6078A= n.1010T= | |
2 | g.138013875G>A | CA429193265 | HNMT | c.624G>A (p.Leu208=) n.556G>A c.522G>A (p.Leu174=) c.246G>A (p.Leu82=) n.232-6079C>T n.1011G>A | |
2 | g.138013875G>C | CA429193267 | HNMT | c.624G>C (p.Leu208=) n.556G>C c.522G>C (p.Leu174=) c.246G>C (p.Leu82=) n.232-6079C>G n.1011G>C | |
2 | g.138013875G>T | CA429193268 | HNMT | c.624G>T (p.Leu208=) n.556G>T c.522G>T (p.Leu174=) c.246G>T (p.Leu82=) n.232-6079C>A n.1011G>T | |
2 | g.138013876G>A | CA348473473 | HNMT | c.625G>A (p.Asp209Asn) n.557G>A c.523G>A (p.Asp175Asn) c.247G>A (p.Asp83Asn) n.232-6080C>T n.1012G>A | |
2 | g.138013876G>C | CA348473476 | HNMT | c.625G>C (p.Asp209His) n.557G>C c.523G>C (p.Asp175His) c.247G>C (p.Asp83His) n.232-6080C>G n.1012G>C | |
2 | g.138013876G>T | CA348473471 | HNMT | c.625G>T (p.Asp209Tyr) n.557G>T c.523G>T (p.Asp175Tyr) c.247G>T (p.Asp83Tyr) n.232-6080C>A n.1012G>T | |
2 | g.138013877A>C | CA348473482 | HNMT | c.626A>C (p.Asp209Ala) n.558A>C c.524A>C (p.Asp175Ala) c.248A>C (p.Asp83Ala) n.232-6081T>G n.1013A>C | |
2 | g.138013877A>G | CA348473480 | HNMT | c.626A>G (p.Asp209Gly) n.558A>G c.524A>G (p.Asp175Gly) c.248A>G (p.Asp83Gly) n.232-6081T>C n.1013A>G | |
2 | g.138013877A>T | CA348473484 | HNMT | c.626A>T (p.Asp209Val) n.558A>T c.524A>T (p.Asp175Val) c.248A>T (p.Asp83Val) n.232-6081T>A n.1013A>T | |
2 | g.138013878C>A | CA348473490 | HNMT | c.627C>A (p.Asp209Glu) n.559C>A c.525C>A (p.Asp175Glu) c.249C>A (p.Asp83Glu) n.232-6082G>T n.1014C>A | |
2 | g.138013878C>G | CA348473493 | HNMT | c.627C>G (p.Asp209Glu) n.559C>G c.525C>G (p.Asp175Glu) c.249C>G (p.Asp83Glu) n.232-6082G>C n.1014C>G | |
2 | g.138013878C>T | CA429193270 | HNMT | c.627C>T (p.Asp209=) n.559C>T c.525C>T (p.Asp175=) c.249C>T (p.Asp83=) n.232-6082G>A n.1014C>T | |
2 | g.138013879A= | CA1291858013 | HNMT | c.628A= (p.Asn210=) n.560A= c.526A= (p.Asn176=) c.250A= (p.Asn84=) n.232-6083T= n.1015A= | |
2 | g.138013879A>C | CA1891823 | HNMT | c.628A>C (p.Asn210His) n.560A>C c.526A>C (p.Asn176His) c.250A>C (p.Asn84His) n.232-6083T>G n.1015A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.138013879A>G | CA1891824 | HNMT | c.628A>G (p.Asn210Asp) n.560A>G c.526A>G (p.Asn176Asp) c.250A>G (p.Asn84Asp) n.232-6083T>C n.1015A>G | dbSNP ExAC gnomAD v2 |
2 | g.138013879A>T | CA348473500 | HNMT | c.628A>T (p.Asn210Tyr) n.560A>T c.526A>T (p.Asn176Tyr) c.250A>T (p.Asn84Tyr) n.232-6083T>A n.1015A>T | |
2 | g.138013880A>C | CA348473503 | HNMT | c.629A>C (p.Asn210Thr) n.561A>C c.527A>C (p.Asn176Thr) c.251A>C (p.Asn84Thr) n.232-6084T>G n.1016A>C | |
2 | g.138013880A>G | CA348473506 | HNMT | c.629A>G (p.Asn210Ser) n.561A>G c.527A>G (p.Asn176Ser) c.251A>G (p.Asn84Ser) n.232-6084T>C n.1016A>G | |
2 | g.138013880A>T | CA348473509 | HNMT | c.629A>T (p.Asn210Ile) n.561A>T c.527A>T (p.Asn176Ile) c.251A>T (p.Asn84Ile) n.232-6084T>A n.1016A>T | |
2 | g.138013881C>A | CA348473512 | HNMT | c.630C>A (p.Asn210Lys) n.562C>A c.528C>A (p.Asn176Lys) c.252C>A (p.Asn84Lys) n.232-6085G>T n.1017C>A | |
2 | g.138013881C= | CA1291858016 | HNMT | c.630C= (p.Asn210=) n.562C= c.528C= (p.Asn176=) c.252C= (p.Asn84=) n.232-6085G= n.1017C= | |
2 | g.138013881C>G | CA57015583 | HNMT | c.630C>G (p.Asn210Lys) n.562C>G c.528C>G (p.Asn176Lys) c.252C>G (p.Asn84Lys) n.232-6085G>C n.1017C>G | dbSNP |
2 | g.138013881C>T | CA429193274 | HNMT | c.630C>T (p.Asn210=) n.562C>T c.528C>T (p.Asn176=) c.252C>T (p.Asn84=) n.232-6085G>A n.1017C>T |