Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66435154A>C | CA392929340 | MAP2K1 | c.142A>C (p.Lys48Gln) c.208A>C (p.Lys70Gln) n.644A>C n.719A>C | |
15 | g.66435154A>G | CA392929341 | MAP2K1 | c.142A>G (p.Lys48Glu) c.208A>G (p.Lys70Glu) n.644A>G n.719A>G | dbSNP |
15 | g.66435154A>T | CA392929342 | MAP2K1 | c.142A>T (p.Lys48Ter) c.208A>T (p.Lys70Ter) n.644A>T n.719A>T | |
15 | g.66435155A>C | CA392929345 | MAP2K1 | c.143A>C (p.Lys48Thr) c.209A>C (p.Lys70Thr) n.645A>C n.720A>C | |
15 | g.66435155A>G | CA392929344 | MAP2K1 | c.143A>G (p.Lys48Arg) c.209A>G (p.Lys70Arg) n.645A>G n.720A>G | dbSNP gnomAD v4 |
15 | g.66435155A>T | CA392929343 | MAP2K1 | c.143A>T (p.Lys48Met) c.209A>T (p.Lys70Met) n.645A>T n.720A>T | dbSNP |
15 | g.66435156G>A | CA490855997 | MAP2K1 | c.144G>A (p.Lys48=) c.210G>A (p.Lys70=) n.646G>A n.721G>A | dbSNP |
15 | g.66435156G>C | CA392929346 | MAP2K1 | c.144G>C (p.Lys48Asn) c.210G>C (p.Lys70Asn) n.646G>C n.721G>C | dbSNP gnomAD v4 |
15 | g.66435156G>T | CA392929347 | MAP2K1 | c.144G>T (p.Lys48Asn) c.210G>T (p.Lys70Asn) n.646G>T n.721G>T | |
15 | g.66435157A>C | CA392929348 | MAP2K1 | c.145A>C (p.Ile49Leu) c.211A>C (p.Ile71Leu) n.647A>C n.722A>C | |
15 | g.66435157A>G | CA392929349 | MAP2K1 | c.145A>G (p.Ile49Val) c.211A>G (p.Ile71Val) n.647A>G n.722A>G | gnomAD v4 |
15 | g.66435157A>T | CA392929350 | MAP2K1 | c.145A>T (p.Ile49Phe) c.211A>T (p.Ile71Phe) n.647A>T n.722A>T | |
15 | g.66435158T>A | CA392929351 | MAP2K1 | c.146T>A (p.Ile49Asn) c.212T>A (p.Ile71Asn) n.648T>A n.723T>A | dbSNP |
15 | g.66435158T>C | CA392929352 | MAP2K1 | c.146T>C (p.Ile49Thr) c.212T>C (p.Ile71Thr) n.648T>C n.723T>C | ClinVar dbSNP |
15 | g.66435158T>G | CA392929353 | MAP2K1 | c.146T>G (p.Ile49Ser) c.212T>G (p.Ile71Ser) n.648T>G n.723T>G | ClinVar dbSNP |
15 | g.66435159C>A | CA490855999 | MAP2K1 | c.147C>A (p.Ile49=) c.213C>A (p.Ile71=) n.649C>A n.724C>A | dbSNP |
15 | g.66435159C>G | CA392929354 | MAP2K1 | c.147C>G (p.Ile49Met) c.213C>G (p.Ile71Met) n.649C>G n.724C>G | dbSNP |
15 | g.66435159C>T | CA490856000 | MAP2K1 | c.147C>T (p.Ile49=) c.213C>T (p.Ile71=) n.649C>T n.724C>T | dbSNP gnomAD v4 |
15 | g.66435160A= | CA2184071759 | MAP2K1 | c.148A= (p.Ser50=) c.214A= (p.Ser72=) n.650A= n.725A= | |
15 | g.66435160A>C | CA392929355 | MAP2K1 | c.148A>C (p.Ser50Arg) c.214A>C (p.Ser72Arg) n.650A>C n.725A>C | gnomAD v4 |
15 | g.66435160A>G | CA392929356 | MAP2K1 | c.148A>G (p.Ser50Gly) c.214A>G (p.Ser72Gly) n.650A>G n.725A>G | dbSNP gnomAD v3 gnomAD v4 COSMIC |
15 | g.66435160A>T | CA392929357 | MAP2K1 | c.148A>T (p.Ser50Cys) c.214A>T (p.Ser72Cys) n.650A>T n.725A>T | dbSNP |
15 | g.66435161G>A | CA271640782 | MAP2K1 | c.149G>A (p.Ser50Asn) c.215G>A (p.Ser72Asn) n.651G>A n.726G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.66435161G>C | CA392929359 | MAP2K1 | c.149G>C (p.Ser50Thr) c.215G>C (p.Ser72Thr) n.651G>C n.726G>C | dbSNP gnomAD v4 |
15 | g.66435161G= | CA2184071760 | MAP2K1 | c.149G= (p.Ser50=) c.215G= (p.Ser72=) n.651G= n.726G= | |
15 | g.66435161G>T | CA392929358 | MAP2K1 | c.149G>T (p.Ser50Ile) c.215G>T (p.Ser72Ile) n.651G>T n.726G>T | dbSNP |
15 | g.66435162T>A | CA392929360 | MAP2K1 | c.150T>A (p.Ser50Arg) c.216T>A (p.Ser72Arg) n.652T>A n.727T>A | dbSNP |
15 | g.66435162T>C | CA490856001 | MAP2K1 | c.150T>C (p.Ser50=) c.216T>C (p.Ser72=) n.652T>C n.727T>C | |
15 | g.66435162T>G | CA392929361 | MAP2K1 | c.150T>G (p.Ser50Arg) c.216T>G (p.Ser72Arg) n.652T>G n.727T>G | |
15 | g.66435162T= | CA2184071761 | MAP2K1 | c.150T= (p.Ser50=) c.216T= (p.Ser72=) n.652T= n.727T= | |
15 | g.66435163G>A | CA392929362 | MAP2K1 | c.151G>A (p.Glu51Lys) c.217G>A (p.Glu73Lys) n.653G>A n.728G>A | dbSNP |
15 | g.66435163G>C | CA392929363 | MAP2K1 | c.151G>C (p.Glu51Gln) c.217G>C (p.Glu73Gln) n.653G>C n.728G>C | dbSNP |
15 | g.66435163G>T | CA392929364 | MAP2K1 | c.151G>T (p.Glu51Ter) c.217G>T (p.Glu73Ter) n.653G>T n.728G>T | dbSNP |
15 | g.66435164A>C | CA392929365 | MAP2K1 | c.152A>C (p.Glu51Ala) c.218A>C (p.Glu73Ala) n.654A>C n.729A>C | |
15 | g.66435164A>G | CA392929366 | MAP2K1 | c.152A>G (p.Glu51Gly) c.218A>G (p.Glu73Gly) n.654A>G n.729A>G | dbSNP |
15 | g.66435164A>T | CA392929367 | MAP2K1 | c.152A>T (p.Glu51Val) c.218A>T (p.Glu73Val) n.654A>T n.729A>T | dbSNP |
15 | g.66435165G>A | CA490856002 | MAP2K1 | c.153G>A (p.Glu51=) c.219G>A (p.Glu73=) n.655G>A n.730G>A | COSMIC |
15 | g.66435165G>C | CA392929369 | MAP2K1 | c.153G>C (p.Glu51Asp) c.219G>C (p.Glu73Asp) n.655G>C n.730G>C | dbSNP |
15 | g.66435165G>T | CA392929370 | MAP2K1 | c.153G>T (p.Glu51Asp) c.219G>T (p.Glu73Asp) n.655G>T n.730G>T | |
15 | g.66435166C>A | CA392929371 | MAP2K1 | c.154C>A (p.Leu52Met) c.220C>A (p.Leu74Met) n.656C>A n.731C>A | dbSNP |
15 | g.66435166C>G | CA392929372 | MAP2K1 | c.154C>G (p.Leu52Val) c.220C>G (p.Leu74Val) n.656C>G n.731C>G | dbSNP |
15 | g.66435166C>T | CA490856003 | MAP2K1 | c.154C>T (p.Leu52=) c.220C>T (p.Leu74=) n.656C>T n.731C>T | dbSNP |
15 | g.66435167T>A | CA392929373 | MAP2K1 | c.155T>A (p.Leu52Gln) c.221T>A (p.Leu74Gln) n.657T>A n.732T>A | |
15 | g.66435167T>C | CA392929374 | MAP2K1 | c.155T>C (p.Leu52Pro) c.221T>C (p.Leu74Pro) n.657T>C n.732T>C | |
15 | g.66435167T>G | CA392929375 | MAP2K1 | c.155T>G (p.Leu52Arg) c.221T>G (p.Leu74Arg) n.657T>G n.732T>G | |
15 | g.66435168G>A | CA490856005 | MAP2K1 | c.156G>A (p.Leu52=) c.222G>A (p.Leu74=) n.658G>A n.733G>A | dbSNP |
15 | g.66435168G>C | CA490856004 | MAP2K1 | c.156G>C (p.Leu52=) c.222G>C (p.Leu74=) n.658G>C n.733G>C | dbSNP |
15 | g.66435168G= | CA2184071762 | MAP2K1 | c.156G= (p.Leu52=) c.222G= (p.Leu74=) n.658G= n.733G= | |
15 | g.66435168G>T | CA490856006 | MAP2K1 | c.156G>T (p.Leu52=) c.222G>T (p.Leu74=) n.658G>T n.733G>T | |
15 | g.66435172dup | CA2731115417 | MAP2K1 | c.160dup (p.Ala54GlyfsTer?) c.226dup (p.Ala76GlyfsTer?) n.662dup n.737dup | dbSNP |
15 | g.66435169G>A | CA392929376 | MAP2K1 | c.157G>A (p.Gly53Arg) c.223G>A (p.Gly75Arg) n.659G>A n.734G>A | |
15 | g.66435169G>C | CA392929378 | MAP2K1 | c.157G>C (p.Gly53Arg) c.223G>C (p.Gly75Arg) n.659G>C n.734G>C | |
15 | g.66435169G>T | CA392929377 | MAP2K1 | c.157G>T (p.Gly53Trp) c.223G>T (p.Gly75Trp) n.659G>T n.734G>T | |
15 | g.66435170G>A | CA392929381 | MAP2K1 | c.158G>A (p.Gly53Glu) c.224G>A (p.Gly75Glu) n.660G>A n.735G>A | dbSNP |
15 | g.66435170G>C | CA392929383 | MAP2K1 | c.158G>C (p.Gly53Ala) c.224G>C (p.Gly75Ala) n.660G>C n.735G>C | dbSNP |
15 | g.66435170G>T | CA392929384 | MAP2K1 | c.158G>T (p.Gly53Val) c.224G>T (p.Gly75Val) n.660G>T n.735G>T | |
15 | g.66435171G>A | CA490856007 | MAP2K1 | c.159G>A (p.Gly53=) c.225G>A (p.Gly75=) n.661G>A n.736G>A | |
15 | g.66435171G>C | CA490856008 | MAP2K1 | c.159G>C (p.Gly53=) c.225G>C (p.Gly75=) n.661G>C n.736G>C | |
15 | g.66435171G>T | CA490856009 | MAP2K1 | c.159G>T (p.Gly53=) c.225G>T (p.Gly75=) n.661G>T n.736G>T | |
15 | g.66435172G>A | CA392929387 | MAP2K1 | c.160G>A (p.Ala54Thr) c.226G>A (p.Ala76Thr) n.662G>A n.737G>A | dbSNP |
15 | g.66435172G>C | CA392929388 | MAP2K1 | c.160G>C (p.Ala54Pro) c.226G>C (p.Ala76Pro) n.662G>C n.737G>C | dbSNP |
15 | g.66435172G>T | CA392929390 | MAP2K1 | c.160G>T (p.Ala54Ser) c.226G>T (p.Ala76Ser) n.662G>T n.737G>T | dbSNP gnomAD v4 |
15 | g.66435173C>A | CA392929392 | MAP2K1 | c.161C>A (p.Ala54Asp) c.227C>A (p.Ala76Asp) n.663C>A n.738C>A | dbSNP |
15 | g.66435173C>G | CA392929394 | MAP2K1 | c.161C>G (p.Ala54Gly) c.227C>G (p.Ala76Gly) n.663C>G n.738C>G | dbSNP |
15 | g.66435173C>T | CA392929396 | MAP2K1 | c.161C>T (p.Ala54Val) c.227C>T (p.Ala76Val) n.663C>T n.738C>T | dbSNP COSMIC |
15 | g.66435174T>A | CA490856011 | MAP2K1 | c.162T>A (p.Ala54=) c.228T>A (p.Ala76=) n.664T>A n.739T>A | |
15 | g.66435174T>C | CA490856010 | MAP2K1 | c.162T>C (p.Ala54=) c.228T>C (p.Ala76=) n.664T>C n.739T>C | |
15 | g.66435174T>G | CA490856012 | MAP2K1 | c.162T>G (p.Ala54=) c.228T>G (p.Ala76=) n.664T>G n.739T>G | |
15 | g.66435175G>A | CA392929399 | MAP2K1 | c.163G>A (p.Gly55Ser) c.229G>A (p.Gly77Ser) n.665G>A n.740G>A | dbSNP gnomAD v4 |
15 | g.66435175G>C | CA392929400 | MAP2K1 | c.163G>C (p.Gly55Arg) c.229G>C (p.Gly77Arg) n.665G>C n.740G>C | |
15 | g.66435175G>T | CA392929402 | MAP2K1 | c.163G>T (p.Gly55Cys) c.229G>T (p.Gly77Cys) n.665G>T n.740G>T | |
15 | g.66435176G>A | CA392929405 | MAP2K1 | c.164G>A (p.Gly55Asp) c.230G>A (p.Gly77Asp) n.666G>A n.741G>A | |
15 | g.66435176G>C | CA392929409 | MAP2K1 | c.164G>C (p.Gly55Ala) c.230G>C (p.Gly77Ala) n.666G>C n.741G>C | |
15 | g.66435176G>T | CA392929406 | MAP2K1 | c.164G>T (p.Gly55Val) c.230G>T (p.Gly77Val) n.666G>T n.741G>T | dbSNP |
15 | g.66435177C>A | CA490856014 | MAP2K1 | c.165C>A (p.Gly55=) c.231C>A (p.Gly77=) n.667C>A n.742C>A | |
15 | g.66435177C= | CA2184071763 | MAP2K1 | c.165C= (p.Gly55=) c.231C= (p.Gly77=) n.667C= n.742C= | |
15 | g.66435177C>G | CA490856013 | MAP2K1 | c.165C>G (p.Gly55=) c.231C>G (p.Gly77=) n.667C>G n.742C>G | dbSNP gnomAD v4 |
15 | g.66435177C>T | CA490856015 | MAP2K1 | c.165C>T (p.Gly55=) c.231C>T (p.Gly77=) n.667C>T n.742C>T | |
15 | g.66435178A>C | CA392929411 | MAP2K1 | c.166A>C (p.Asn56His) c.232A>C (p.Asn78His) n.668A>C n.743A>C | |
15 | g.66435178A>G | CA392929413 | MAP2K1 | c.166A>G (p.Asn56Asp) c.232A>G (p.Asn78Asp) n.668A>G n.743A>G | |
15 | g.66435178A>T | CA392929415 | MAP2K1 | c.166A>T (p.Asn56Tyr) c.232A>T (p.Asn78Tyr) n.668A>T n.743A>T | dbSNP |
15 | g.66435179A>C | CA392929417 | MAP2K1 | c.167A>C (p.Asn56Thr) c.233A>C (p.Asn78Thr) n.669A>C n.744A>C | dbSNP |
15 | g.66435179A>G | CA392929419 | MAP2K1 | c.167A>G (p.Asn56Ser) c.233A>G (p.Asn78Ser) n.669A>G n.744A>G | |
15 | g.66435179A>T | CA392929420 | MAP2K1 | c.167A>T (p.Asn56Ile) c.233A>T (p.Asn78Ile) n.669A>T n.744A>T | dbSNP |
15 | g.66435180T>A | CA392929421 | MAP2K1 | c.168T>A (p.Asn56Lys) c.234T>A (p.Asn78Lys) n.670T>A n.745T>A | dbSNP |
15 | g.66435180T>C | CA490856016 | MAP2K1 | c.168T>C (p.Asn56=) c.234T>C (p.Asn78=) n.670T>C n.745T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435180T>G | CA392929422 | MAP2K1 | c.168T>G (p.Asn56Lys) c.234T>G (p.Asn78Lys) n.670T>G n.745T>G | dbSNP |
15 | g.66435180T= | CA2184071764 | MAP2K1 | c.168T= (p.Asn56=) c.234T= (p.Asn78=) n.670T= n.745T= | |
15 | g.66435181G>A | CA392929424 | MAP2K1 | c.169G>A (p.Gly57Ser) c.235G>A (p.Gly79Ser) n.671G>A n.746G>A | dbSNP |
15 | g.66435181G>C | CA392929425 | MAP2K1 | c.169G>C (p.Gly57Arg) c.235G>C (p.Gly79Arg) n.671G>C n.746G>C | |
15 | g.66435181G>T | CA392929427 | MAP2K1 | c.169G>T (p.Gly57Cys) c.235G>T (p.Gly79Cys) n.671G>T n.746G>T | dbSNP |
15 | g.66435182G>A | CA392929433 | MAP2K1 | c.170G>A (p.Gly57Asp) c.236G>A (p.Gly79Asp) n.672G>A n.747G>A | dbSNP |
15 | g.66435182G>C | CA392929431 | MAP2K1 | c.170G>C (p.Gly57Ala) c.236G>C (p.Gly79Ala) n.672G>C n.747G>C | dbSNP |
15 | g.66435182G>T | CA392929429 | MAP2K1 | c.170G>T (p.Gly57Val) c.236G>T (p.Gly79Val) n.672G>T n.747G>T | dbSNP COSMIC |
15 | g.66435183C>A | CA490856018 | MAP2K1 | c.171C>A (p.Gly57=) c.237C>A (p.Gly79=) n.673C>A n.748C>A | dbSNP |
15 | g.66435183C= | CA2184071765 | MAP2K1 | c.171C= (p.Gly57=) c.237C= (p.Gly79=) n.673C= n.748C= | |
15 | g.66435183C>G | CA490856017 | MAP2K1 | c.171C>G (p.Gly57=) c.237C>G (p.Gly79=) n.673C>G n.748C>G | dbSNP |
15 | g.66435183C>T | CA134598 | MAP2K1 | c.171C>T (p.Gly57=) c.237C>T (p.Gly79=) n.673C>T n.748C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435184G>A | CA392929437 | MAP2K1 | c.172G>A (p.Gly58Ser) c.238G>A (p.Gly80Ser) n.674G>A n.749G>A | ClinVar dbSNP COSMIC |
15 | g.66435184G>C | CA392929440 | MAP2K1 | c.172G>C (p.Gly58Arg) c.238G>C (p.Gly80Arg) n.674G>C n.749G>C | |
15 | g.66435184G>T | CA392929442 | MAP2K1 | c.172G>T (p.Gly58Cys) c.238G>T (p.Gly80Cys) n.674G>T n.749G>T | |
15 | g.66435185G>A | CA392929444 | MAP2K1 | c.173G>A (p.Gly58Asp) c.239G>A (p.Gly80Asp) n.675G>A n.750G>A | ClinVar dbSNP |
15 | g.66435185G>C | CA392929446 | MAP2K1 | c.173G>C (p.Gly58Ala) c.239G>C (p.Gly80Ala) n.675G>C n.750G>C | dbSNP |
15 | g.66435185G>T | CA392929448 | MAP2K1 | c.173G>T (p.Gly58Val) c.239G>T (p.Gly80Val) n.675G>T n.750G>T | |
15 | g.66435186T>A | CA490856019 | MAP2K1 | c.174T>A (p.Gly58=) c.240T>A (p.Gly80=) n.676T>A n.751T>A | dbSNP |
15 | g.66435186T>C | CA490856020 | MAP2K1 | c.174T>C (p.Gly58=) c.240T>C (p.Gly80=) n.676T>C n.751T>C | dbSNP |
15 | g.66435186T>G | CA490856021 | MAP2K1 | c.174T>G (p.Gly58=) c.240T>G (p.Gly80=) n.676T>G n.751T>G | dbSNP |
15 | g.66435186T= | CA2184071766 | MAP2K1 | c.174T= (p.Gly58=) c.240T= (p.Gly80=) n.676T= n.751T= | |
15 | g.66435187G>A | CA392929450 | MAP2K1 | c.175G>A (p.Val59Met) c.241G>A (p.Val81Met) n.677G>A n.752G>A | dbSNP |
15 | g.66435187G>C | CA392929452 | MAP2K1 | c.175G>C (p.Val59Leu) c.241G>C (p.Val81Leu) n.677G>C n.752G>C | dbSNP |
15 | g.66435187G>T | CA392929454 | MAP2K1 | c.175G>T (p.Val59Leu) c.241G>T (p.Val81Leu) n.677G>T n.752G>T | |
15 | g.66435188T>A | CA392929457 | MAP2K1 | c.176T>A (p.Val59Glu) c.242T>A (p.Val81Glu) n.678T>A n.753T>A | |
15 | g.66435188T>C | CA392929458 | MAP2K1 | c.176T>C (p.Val59Ala) c.242T>C (p.Val81Ala) n.678T>C n.753T>C | gnomAD v4 |
15 | g.66435188T>G | CA392929461 | MAP2K1 | c.176T>G (p.Val59Gly) c.242T>G (p.Val81Gly) n.678T>G n.753T>G | |
15 | g.66435189G>A | CA490856023 | MAP2K1 | c.177G>A (p.Val59=) c.243G>A (p.Val81=) n.679G>A n.754G>A | dbSNP |
15 | g.66435189G>C | CA490856024 | MAP2K1 | c.177G>C (p.Val59=) c.243G>C (p.Val81=) n.679G>C n.754G>C | dbSNP |
15 | g.66435189G>T | CA490856022 | MAP2K1 | c.177G>T (p.Val59=) c.243G>T (p.Val81=) n.679G>T n.754G>T | dbSNP |
15 | g.66435189_66435190insT | CA2731115882 | MAP2K1 | c.177_178insT (p.Val60CysfsTer?) c.243_244insT (p.Val82CysfsTer?) n.679_680insT n.754_755insT | dbSNP |
15 | g.66435190G>A | CA392929465 | MAP2K1 | c.178G>A (p.Val60Met) c.244G>A (p.Val82Met) n.680G>A n.755G>A | dbSNP |
15 | g.66435190G>C | CA392929467 | MAP2K1 | c.178G>C (p.Val60Leu) c.244G>C (p.Val82Leu) n.680G>C n.755G>C | dbSNP |
15 | g.66435190G>T | CA392929463 | MAP2K1 | c.178G>T (p.Val60Leu) c.244G>T (p.Val82Leu) n.680G>T n.755G>T | |
15 | g.66435191T>A | CA392929469 | MAP2K1 | c.179T>A (p.Val60Glu) c.245T>A (p.Val82Glu) n.681T>A n.756T>A | dbSNP |
15 | g.66435191T>C | CA392929468 | MAP2K1 | c.179T>C (p.Val60Ala) c.245T>C (p.Val82Ala) n.681T>C n.756T>C | dbSNP gnomAD v3 gnomAD v4 |
15 | g.66435191T>G | CA392929470 | MAP2K1 | c.179T>G (p.Val60Gly) c.245T>G (p.Val82Gly) n.681T>G n.756T>G | |
15 | g.66435191T= | CA2184071767 | MAP2K1 | c.179T= (p.Val60=) c.245T= (p.Val82=) n.681T= n.756T= | |
15 | g.66435192G>A | CA490856026 | MAP2K1 | c.180G>A (p.Val60=) c.246G>A (p.Val82=) n.682G>A n.757G>A | dbSNP |
15 | g.66435192G>C | CA490856025 | MAP2K1 | c.180G>C (p.Val60=) c.246G>C (p.Val82=) n.682G>C n.757G>C | dbSNP |
15 | g.66435192G>T | CA490856027 | MAP2K1 | c.180G>T (p.Val60=) c.246G>T (p.Val82=) n.682G>T n.757G>T | |
15 | g.66435193T>A | CA392929473 | MAP2K1 | c.181T>A (p.Phe61Ile) c.247T>A (p.Phe83Ile) n.683T>A n.758T>A | dbSNP |
15 | g.66435193T>C | CA392929475 | MAP2K1 | c.181T>C (p.Phe61Leu) c.247T>C (p.Phe83Leu) n.683T>C n.758T>C | ClinVar dbSNP |
15 | g.66435193T>G | CA392929474 | MAP2K1 | c.181T>G (p.Phe61Val) c.247T>G (p.Phe83Val) n.683T>G n.758T>G | dbSNP |
15 | g.66435193T= | CA2184071768 | MAP2K1 | c.181T= (p.Phe61=) c.247T= (p.Phe83=) n.683T= n.758T= | |
15 | g.66435194T>A | CA392929478 | MAP2K1 | c.182T>A (p.Phe61Tyr) c.248T>A (p.Phe83Tyr) n.684T>A n.759T>A | dbSNP |
15 | g.66435194T>C | CA392929481 | MAP2K1 | c.182T>C (p.Phe61Ser) c.248T>C (p.Phe83Ser) n.684T>C n.759T>C | dbSNP |
15 | g.66435194T>G | CA392929479 | MAP2K1 | c.182T>G (p.Phe61Cys) c.248T>G (p.Phe83Cys) n.684T>G n.759T>G | |
15 | g.66435195C>A | CA392929483 | MAP2K1 | c.183C>A (p.Phe61Leu) c.249C>A (p.Phe83Leu) n.685C>A n.760C>A | |
15 | g.66435195C>G | CA392929485 | MAP2K1 | c.183C>G (p.Phe61Leu) c.249C>G (p.Phe83Leu) n.685C>G n.760C>G | |
15 | g.66435195C>T | CA490856028 | MAP2K1 | c.183C>T (p.Phe61=) c.249C>T (p.Phe83=) n.685C>T n.760C>T | gnomAD v4 |
15 | g.66435196A>C | CA392929487 | MAP2K1 | c.184A>C (p.Lys62Gln) c.250A>C (p.Lys84Gln) n.686A>C n.761A>C | |
15 | g.66435196A>G | CA392929489 | MAP2K1 | c.184A>G (p.Lys62Glu) c.250A>G (p.Lys84Glu) n.686A>G n.761A>G | |
15 | g.66435196A>T | CA392929491 | MAP2K1 | c.184A>T (p.Lys62Ter) c.250A>T (p.Lys84Ter) n.686A>T n.761A>T | dbSNP |
15 | g.66435197A= | CA2184071769 | MAP2K1 | c.185A= (p.Lys62=) c.251A= (p.Lys84=) n.687A= n.762A= | |
15 | g.66435197A>C | CA392929493 | MAP2K1 | c.185A>C (p.Lys62Thr) c.251A>C (p.Lys84Thr) n.687A>C n.762A>C | |
15 | g.66435197A>G | CA7623881 | MAP2K1 | c.185A>G (p.Lys62Arg) c.251A>G (p.Lys84Arg) n.687A>G n.762A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435197A>T | CA392929496 | MAP2K1 | c.185A>T (p.Lys62Met) c.251A>T (p.Lys84Met) n.687A>T n.762A>T | dbSNP |
15 | g.66435198G>A | CA490856029 | MAP2K1 | c.186G>A (p.Lys62=) c.252G>A (p.Lys84=) n.688G>A n.763G>A | dbSNP |
15 | g.66435198G>C | CA392929499 | MAP2K1 | c.186G>C (p.Lys62Asn) c.252G>C (p.Lys84Asn) n.688G>C n.763G>C | dbSNP |
15 | g.66435198G>T | CA392929500 | MAP2K1 | c.186G>T (p.Lys62Asn) c.252G>T (p.Lys84Asn) n.688G>T n.763G>T | dbSNP |
15 | g.66435199G>A | CA392929502 | MAP2K1 | c.187G>A (p.Val63Ile) c.253G>A (p.Val85Ile) n.689G>A n.764G>A | dbSNP |
15 | g.66435199G>C | CA392929503 | MAP2K1 | c.187G>C (p.Val63Leu) c.253G>C (p.Val85Leu) n.689G>C n.764G>C | dbSNP |
15 | g.66435199G>T | CA392929505 | MAP2K1 | c.187G>T (p.Val63Phe) c.253G>T (p.Val85Phe) n.689G>T n.764G>T | dbSNP |
15 | g.66435200T>A | CA392929511 | MAP2K1 | c.188T>A (p.Val63Asp) c.254T>A (p.Val85Asp) n.690T>A n.765T>A | dbSNP |
15 | g.66435200T>C | CA392929510 | MAP2K1 | c.188T>C (p.Val63Ala) c.254T>C (p.Val85Ala) n.690T>C n.765T>C | dbSNP |
15 | g.66435200T>G | CA392929508 | MAP2K1 | c.188T>G (p.Val63Gly) c.254T>G (p.Val85Gly) n.690T>G n.765T>G | dbSNP gnomAD v4 |
15 | g.66435201C>A | CA490856030 | MAP2K1 | c.189C>A (p.Val63=) c.255C>A (p.Val85=) n.691C>A n.766C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.66435201C= | CA2184071770 | MAP2K1 | c.189C= (p.Val63=) c.255C= (p.Val85=) n.691C= n.766C= | |
15 | g.66435201C>G | CA490856031 | MAP2K1 | c.189C>G (p.Val63=) c.255C>G (p.Val85=) n.691C>G n.766C>G | dbSNP |
15 | g.66435201C>T | CA271640820 | MAP2K1 | c.189C>T (p.Val63=) c.255C>T (p.Val85=) n.691C>T n.766C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435202T>A | CA392929514 | MAP2K1 | c.190T>A (p.Ser64Thr) c.256T>A (p.Ser86Thr) n.692T>A n.767T>A | ClinVar |
15 | g.66435202T>C | CA392929516 | MAP2K1 | c.190T>C (p.Ser64Pro) c.256T>C (p.Ser86Pro) n.692T>C n.767T>C | |
15 | g.66435202T>G | CA392929517 | MAP2K1 | c.190T>G (p.Ser64Ala) c.256T>G (p.Ser86Ala) n.692T>G n.767T>G | COSMIC |
15 | g.66435203C>A | CA392929520 | MAP2K1 | c.191C>A (p.Ser64Tyr) c.257C>A (p.Ser86Tyr) n.693C>A n.768C>A | |
15 | g.66435203C>G | CA392929521 | MAP2K1 | c.191C>G (p.Ser64Cys) c.257C>G (p.Ser86Cys) n.693C>G n.768C>G | |
15 | g.66435203C>T | CA392929523 | MAP2K1 | c.191C>T (p.Ser64Phe) c.257C>T (p.Ser86Phe) n.693C>T n.768C>T | |
15 | g.66435204C>A | CA490856032 | MAP2K1 | c.192C>A (p.Ser64=) c.258C>A (p.Ser86=) n.694C>A n.769C>A | |
15 | g.66435204C>G | CA490856034 | MAP2K1 | c.192C>G (p.Ser64=) c.258C>G (p.Ser86=) n.694C>G n.769C>G | |
15 | g.66435204C>T | CA490856033 | MAP2K1 | c.192C>T (p.Ser64=) c.258C>T (p.Ser86=) n.694C>T n.769C>T | |
15 | g.66435205C>A | CA392929524 | MAP2K1 | c.193C>A (p.His65Asn) c.259C>A (p.His87Asn) n.695C>A n.770C>A | dbSNP |
15 | g.66435205C>G | CA392929526 | MAP2K1 | c.193C>G (p.His65Asp) c.259C>G (p.His87Asp) n.695C>G n.770C>G | dbSNP |
15 | g.66435205C>T | CA392929528 | MAP2K1 | c.193C>T (p.His65Tyr) c.259C>T (p.His87Tyr) n.695C>T n.770C>T | dbSNP |
15 | g.66435206A>C | CA392929530 | MAP2K1 | c.194A>C (p.His65Pro) c.260A>C (p.His87Pro) n.696A>C n.771A>C | dbSNP |
15 | g.66435206A>G | CA392929532 | MAP2K1 | c.194A>G (p.His65Arg) c.260A>G (p.His87Arg) n.696A>G n.771A>G | dbSNP |
15 | g.66435206A>T | CA392929534 | MAP2K1 | c.194A>T (p.His65Leu) c.260A>T (p.His87Leu) n.696A>T n.771A>T | dbSNP |
15 | g.66435207C>A | CA392929536 | MAP2K1 | c.195C>A (p.His65Gln) c.261C>A (p.His87Gln) n.697C>A n.772C>A | dbSNP |
15 | g.66435207C= | CA2184071771 | MAP2K1 | c.195C= (p.His65=) c.261C= (p.His87=) n.697C= n.772C= | |
15 | g.66435207C>G | CA392929538 | MAP2K1 | c.195C>G (p.His65Gln) c.261C>G (p.His87Gln) n.697C>G n.772C>G | dbSNP |
15 | g.66435207C>T | CA490856035 | MAP2K1 | c.195C>T (p.His65=) c.261C>T (p.His87=) n.697C>T n.772C>T | dbSNP gnomAD v3 gnomAD v4 |
15 | g.66435208A>C | CA392929541 | MAP2K1 | c.196A>C (p.Lys66Gln) c.262A>C (p.Lys88Gln) n.698A>C n.773A>C | dbSNP |
15 | g.66435208A>G | CA392929543 | MAP2K1 | c.196A>G (p.Lys66Glu) c.262A>G (p.Lys88Glu) n.698A>G n.773A>G | gnomAD v4 |
15 | g.66435208A>T | CA392929544 | MAP2K1 | c.196A>T (p.Lys66Ter) c.262A>T (p.Lys88Ter) n.698A>T n.773A>T | dbSNP |
15 | g.66435209A= | CA2184071772 | MAP2K1 | c.197A= (p.Lys66=) c.263A= (p.Lys88=) n.699A= n.774A= | |
15 | g.66435209A>C | CA392929547 | MAP2K1 | c.197A>C (p.Lys66Thr) c.263A>C (p.Lys88Thr) n.699A>C n.774A>C | |
15 | g.66435209A>G | CA7623882 | MAP2K1 | c.197A>G (p.Lys66Arg) c.263A>G (p.Lys88Arg) n.699A>G n.774A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435209A>T | CA392929550 | MAP2K1 | c.197A>T (p.Lys66Met) c.263A>T (p.Lys88Met) n.699A>T n.774A>T | dbSNP |
15 | g.66435210G>A | CA7623883 | MAP2K1 | c.198G>A (p.Lys66=) c.264G>A (p.Lys88=) n.700G>A n.775G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435210G>C | CA392929552 | MAP2K1 | c.198G>C (p.Lys66Asn) c.264G>C (p.Lys88Asn) n.700G>C n.775G>C | dbSNP |
15 | g.66435210G= | CA2184071773 | MAP2K1 | c.198G= (p.Lys66=) c.264G= (p.Lys88=) n.700G= n.775G= | |
15 | g.66435210G>T | CA392929553 | MAP2K1 | c.198G>T (p.Lys66Asn) c.264G>T (p.Lys88Asn) n.700G>T n.775G>T | |
15 | g.66435211C>A | CA392929555 | MAP2K1 | c.199C>A (p.Pro67Thr) c.265C>A (p.Pro89Thr) n.701C>A n.776C>A | ClinVar dbSNP gnomAD v4 |
15 | g.66435211C= | CA2184071774 | MAP2K1 | c.199C= (p.Pro67=) c.265C= (p.Pro89=) n.701C= n.776C= | |
15 | g.66435211C>G | CA392929556 | MAP2K1 | c.199C>G (p.Pro67Ala) c.265C>G (p.Pro89Ala) n.701C>G n.776C>G | dbSNP gnomAD v4 |
15 | g.66435211C>T | CA392929558 | MAP2K1 | c.199C>T (p.Pro67Ser) c.265C>T (p.Pro89Ser) n.701C>T n.776C>T | ClinVar dbSNP gnomAD v2 |
15 | g.66435212C>A | CA392929563 | MAP2K1 | c.200C>A (p.Pro67His) c.266C>A (p.Pro89His) n.702C>A n.777C>A | |
15 | g.66435212C>G | CA392929559 | MAP2K1 | c.200C>G (p.Pro67Arg) c.266C>G (p.Pro89Arg) n.702C>G n.777C>G | |
15 | g.66435212C>T | CA392929561 | MAP2K1 | c.200C>T (p.Pro67Leu) c.266C>T (p.Pro89Leu) n.702C>T n.777C>T | gnomAD v4 |
15 | g.66435213T>A | CA490856038 | MAP2K1 | c.201T>A (p.Pro67=) c.267T>A (p.Pro89=) n.703T>A n.778T>A | dbSNP |
15 | g.66435213T>C | CA490856037 | MAP2K1 | c.201T>C (p.Pro67=) c.267T>C (p.Pro89=) n.703T>C n.778T>C | dbSNP |
15 | g.66435213T>G | CA490856036 | MAP2K1 | c.201T>G (p.Pro67=) c.267T>G (p.Pro89=) n.703T>G n.778T>G | dbSNP |
15 | g.66435213_66435218delinsTTCTGG | CA2184071775 | MAP2K1 | c.201_206delinsTTCTGG (p.Pro67=) c.267_272delinsTTCTGG (p.Pro89=) n.703_708delinsTTCTGG n.778_783delinsTTCTGG | |
15 | g.66435214T>A | CA392929565 | MAP2K1 | c.202T>A (p.Ser68Thr) c.268T>A (p.Ser90Thr) n.704T>A n.779T>A | dbSNP |
15 | g.66435214T>C | CA392929566 | MAP2K1 | c.202T>C (p.Ser68Pro) c.268T>C (p.Ser90Pro) n.704T>C n.779T>C | dbSNP |
15 | g.66435214T>G | CA392929568 | MAP2K1 | c.202T>G (p.Ser68Ala) c.268T>G (p.Ser90Ala) n.704T>G n.779T>G | |
15 | g.66435214_66435218del | CA715007314 | MAP2K1 | c.202_206del (p.Ser68ProfsTer29) c.268_272del (p.Ser90ProfsTer29) c.268_272del (p.Ser90ProfsTer23) n.704_708del n.779_783del | dbSNP |
15 | g.66435215C>A | CA392929570 | MAP2K1 | c.203C>A (p.Ser68Tyr) c.269C>A (p.Ser90Tyr) n.705C>A n.780C>A | |
15 | g.66435215C>G | CA392929571 | MAP2K1 | c.203C>G (p.Ser68Cys) c.269C>G (p.Ser90Cys) n.705C>G n.780C>G | dbSNP |
15 | g.66435215C>T | CA392929573 | MAP2K1 | c.203C>T (p.Ser68Phe) c.269C>T (p.Ser90Phe) n.705C>T n.780C>T | dbSNP |
15 | g.66435216T>A | CA490856040 | MAP2K1 | c.204T>A (p.Ser68=) c.270T>A (p.Ser90=) n.706T>A n.781T>A | |
15 | g.66435216T>C | CA490856039 | MAP2K1 | c.204T>C (p.Ser68=) c.270T>C (p.Ser90=) n.706T>C n.781T>C | gnomAD v4 |
15 | g.66435216T>G | CA490856041 | MAP2K1 | c.204T>G (p.Ser68=) c.270T>G (p.Ser90=) n.706T>G n.781T>G | |
15 | g.66435217G>A | CA392929575 | MAP2K1 | c.205G>A (p.Gly69Ser) c.271G>A (p.Gly91Ser) n.707G>A n.782G>A | |
15 | g.66435217G>C | CA392929577 | MAP2K1 | c.205G>C (p.Gly69Arg) c.271G>C (p.Gly91Arg) n.707G>C n.782G>C | |
15 | g.66435217G>T | CA392929579 | MAP2K1 | c.205G>T (p.Gly69Cys) c.271G>T (p.Gly91Cys) n.707G>T n.782G>T | |
15 | g.66435218G>A | CA392929582 | MAP2K1 | c.206G>A (p.Gly69Asp) c.272G>A (p.Gly91Asp) n.708G>A n.783G>A | dbSNP |
15 | g.66435218G>C | CA392929583 | MAP2K1 | c.206G>C (p.Gly69Ala) c.272G>C (p.Gly91Ala) n.708G>C n.783G>C | dbSNP |
15 | g.66435218G>T | CA392929585 | MAP2K1 | c.206G>T (p.Gly69Val) c.272G>T (p.Gly91Val) n.708G>T n.783G>T | dbSNP |
15 | g.66435219C>A | CA490856042 | MAP2K1 | c.207C>A (p.Gly69=) c.273C>A (p.Gly91=) n.709C>A n.784C>A | |
15 | g.66435219C>G | CA490856044 | MAP2K1 | c.207C>G (p.Gly69=) c.273C>G (p.Gly91=) n.709C>G n.784C>G | dbSNP |
15 | g.66435219C>T | CA490856043 | MAP2K1 | c.207C>T (p.Gly69=) c.273C>T (p.Gly91=) n.709C>T n.784C>T | gnomAD v4 COSMIC |
15 | g.66435220C>A | CA392929589 | MAP2K1 | c.208C>A (p.Leu70Met) c.274C>A (p.Leu92Met) n.710C>A n.785C>A | |
15 | g.66435220C>G | CA392929588 | MAP2K1 | c.208C>G (p.Leu70Val) c.274C>G (p.Leu92Val) n.710C>G n.785C>G | |
15 | g.66435220C>T | CA490856045 | MAP2K1 | c.208C>T (p.Leu70=) c.274C>T (p.Leu92=) n.710C>T n.785C>T | |
15 | g.66435220_66435221insA | CA2804543903 | MAP2K1 | c.208_209insA (p.Leu70HisfsTer29) c.274_275insA (p.Leu92HisfsTer29) c.274_275insA (p.Leu92HisfsTer23) n.710_711insA n.785_786insA | |
15 | g.66435221T>A | CA392929591 | MAP2K1 | c.209T>A (p.Leu70Gln) c.275T>A (p.Leu92Gln) n.711T>A n.786T>A | |
15 | g.66435221T>C | CA392929593 | MAP2K1 | c.209T>C (p.Leu70Pro) c.275T>C (p.Leu92Pro) n.711T>C n.786T>C | |
15 | g.66435221T>G | CA134601 | MAP2K1 | c.209T>G (p.Leu70Arg) c.275T>G (p.Leu92Arg) n.711T>G n.786T>G | ClinVar dbSNP |
15 | g.66435221T= | CA2184071776 | MAP2K1 | c.209T= (p.Leu70=) c.275T= (p.Leu92=) n.711T= n.786T= | |
15 | g.66435222G>A | CA490856046 | MAP2K1 | c.210G>A (p.Leu70=) c.276G>A (p.Leu92=) n.712G>A n.787G>A | dbSNP gnomAD v2 gnomAD v4 |
15 | g.66435222G>C | CA7623884 | MAP2K1 | c.210G>C (p.Leu70=) c.276G>C (p.Leu92=) n.712G>C n.787G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.66435222G= | CA2184071777 | MAP2K1 | c.210G= (p.Leu70=) c.276G= (p.Leu92=) n.712G= n.787G= | |
15 | g.66435222G>T | CA490856047 | MAP2K1 | c.210G>T (p.Leu70=) c.276G>T (p.Leu92=) n.712G>T n.787G>T | |
15 | g.66435223G>A | CA296099 | MAP2K1 | c.211G>A (p.Val71Ile) c.277G>A (p.Val93Ile) n.713G>A n.788G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435223G>C | CA392929597 | MAP2K1 | c.211G>C (p.Val71Leu) c.277G>C (p.Val93Leu) n.713G>C n.788G>C | dbSNP |
15 | g.66435223G= | CA2184071778 | MAP2K1 | c.211G= (p.Val71=) c.277G= (p.Val93=) n.713G= n.788G= | |
15 | g.66435223G>T | CA392929599 | MAP2K1 | c.211G>T (p.Val71Phe) c.277G>T (p.Val93Phe) n.713G>T n.788G>T | dbSNP COSMIC |
15 | g.66435224T>A | CA392929601 | MAP2K1 | c.212T>A (p.Val71Asp) c.278T>A (p.Val93Asp) n.714T>A n.789T>A | dbSNP |
15 | g.66435224T>C | CA392929603 | MAP2K1 | c.212T>C (p.Val71Ala) c.278T>C (p.Val93Ala) n.714T>C n.789T>C | dbSNP |
15 | g.66435224T>G | CA392929605 | MAP2K1 | c.212T>G (p.Val71Gly) c.278T>G (p.Val93Gly) n.714T>G n.789T>G | dbSNP |
15 | g.66435225C>A | CA490856048 | MAP2K1 | c.213C>A (p.Val71=) c.279C>A (p.Val93=) n.715C>A n.790C>A | gnomAD v4 |
15 | g.66435225C= | CA2184071779 | MAP2K1 | c.213C= (p.Val71=) c.279C= (p.Val93=) n.715C= n.790C= | |
15 | g.66435225C>G | CA271640881 | MAP2K1 | c.213C>G (p.Val71=) c.279C>G (p.Val93=) n.715C>G n.790C>G | dbSNP |
15 | g.66435225C>T | CA7623885 | MAP2K1 | c.213C>T (p.Val71=) c.279C>T (p.Val93=) n.715C>T n.790C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435226A= | CA2184071780 | MAP2K1 | c.214A= (p.Met72=) c.280A= (p.Met94=) n.716A= n.791A= | |
15 | g.66435226A>C | CA392929609 | MAP2K1 | c.214A>C (p.Met72Leu) c.280A>C (p.Met94Leu) n.716A>C n.791A>C | |
15 | g.66435226A>G | CA271640885 | MAP2K1 | c.214A>G (p.Met72Val) c.280A>G (p.Met94Val) n.716A>G n.791A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.66435226A>T | CA392929612 | MAP2K1 | c.214A>T (p.Met72Leu) c.280A>T (p.Met94Leu) n.716A>T n.791A>T | gnomAD v4 |
15 | g.66435227del | CA2629081330 | MAP2K1 | c.215del (p.Met72ArgfsTer5) c.281del (p.Met94ArgfsTer5) c.281del (p.Met94ArgfsTer13) n.717del n.792del | gnomAD v4 |
15 | g.66435227T>A | CA392929617 | MAP2K1 | c.215T>A (p.Met72Lys) c.281T>A (p.Met94Lys) n.717T>A n.792T>A | |
15 | g.66435227T>C | CA392929614 | MAP2K1 | c.215T>C (p.Met72Thr) c.281T>C (p.Met94Thr) n.717T>C n.792T>C | dbSNP |
15 | g.66435227T>G | CA271640899 | MAP2K1 | c.215T>G (p.Met72Arg) c.281T>G (p.Met94Arg) n.717T>G n.792T>G | dbSNP |
15 | g.66435227T= | CA2184071781 | MAP2K1 | c.215T= (p.Met72=) c.281T= (p.Met94=) n.717T= n.792T= | |
15 | g.66435228G>A | CA392929619 | MAP2K1 | c.216G>A (p.Met72Ile) c.282G>A (p.Met94Ile) n.718G>A n.793G>A | COSMIC |
15 | g.66435228G>C | CA392929620 | MAP2K1 | c.216G>C (p.Met72Ile) c.282G>C (p.Met94Ile) n.718G>C n.793G>C | dbSNP |
15 | g.66435228G>T | CA392929622 | MAP2K1 | c.216G>T (p.Met72Ile) c.282G>T (p.Met94Ile) n.718G>T n.793G>T | dbSNP |
15 | g.66435229G>A | CA392929624 | MAP2K1 | c.217G>A (p.Ala73Thr) c.283G>A (p.Ala95Thr) n.719G>A n.794G>A | |
15 | g.66435229G>C | CA392929626 | MAP2K1 | c.217G>C (p.Ala73Pro) c.283G>C (p.Ala95Pro) n.719G>C n.794G>C | |
15 | g.66435229G>T | CA392929628 | MAP2K1 | c.217G>T (p.Ala73Ser) c.283G>T (p.Ala95Ser) n.719G>T n.794G>T | |
15 | g.66435230C>A | CA392929630 | MAP2K1 | c.218C>A (p.Ala73Asp) c.284C>A (p.Ala95Asp) n.720C>A n.795C>A | dbSNP gnomAD v4 |
15 | g.66435230C>G | CA392929632 | MAP2K1 | c.218C>G (p.Ala73Gly) c.284C>G (p.Ala95Gly) n.720C>G n.795C>G | dbSNP |
15 | g.66435230C>T | CA392929634 | MAP2K1 | c.218C>T (p.Ala73Val) c.284C>T (p.Ala95Val) n.720C>T n.795C>T | dbSNP |
15 | g.66435231C>A | CA490856051 | MAP2K1 | c.219C>A (p.Ala73=) c.285C>A (p.Ala95=) n.721C>A n.796C>A | dbSNP |
15 | g.66435231C>G | CA490856050 | MAP2K1 | c.219C>G (p.Ala73=) c.285C>G (p.Ala95=) n.721C>G n.796C>G | dbSNP |
15 | g.66435231C>T | CA490856049 | MAP2K1 | c.219C>T (p.Ala73=) c.285C>T (p.Ala95=) n.721C>T n.796C>T | COSMIC |
15 | g.66435232A= | CA2184071782 | MAP2K1 | c.220A= (p.Arg74=) c.286A= (p.Arg96=) n.722A= n.797A= | |
15 | g.66435232A>C | CA490856052 | MAP2K1 | c.220A>C (p.Arg74=) c.286A>C (p.Arg96=) n.722A>C n.797A>C | |
15 | g.66435232A>G | CA7623886 | MAP2K1 | c.220A>G (p.Arg74Gly) c.286A>G (p.Arg96Gly) n.722A>G n.797A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.66435232A>T | CA392929637 | MAP2K1 | c.220A>T (p.Arg74Ter) c.286A>T (p.Arg96Ter) n.722A>T n.797A>T | |
15 | g.66435233G>A | CA392929641 | MAP2K1 | c.221G>A (p.Arg74Lys) c.287G>A (p.Arg96Lys) n.723G>A n.798G>A | COSMIC |
15 | g.66435233G>C | CA392929644 | MAP2K1 | c.221G>C (p.Arg74Thr) c.287G>C (p.Arg96Thr) n.723G>C n.798G>C | dbSNP |
15 | g.66435233G>T | CA392929640 | MAP2K1 | c.221G>T (p.Arg74Ile) c.287G>T (p.Arg96Ile) n.723G>T n.798G>T | |
15 | g.66435234A>C | CA392929646 | MAP2K1 | c.222A>C (p.Arg74Ser) c.288A>C (p.Arg96Ser) n.724A>C n.799A>C | |
15 | g.66435234A>G | CA490856053 | MAP2K1 | c.222A>G (p.Arg74=) c.288A>G (p.Arg96=) n.724A>G n.799A>G | ClinVar dbSNP |
15 | g.66435234A>T | CA392929647 | MAP2K1 | c.222A>T (p.Arg74Ser) c.288A>T (p.Arg96Ser) n.724A>T n.799A>T | |
15 | g.66435235A>C | CA392929651 | MAP2K1 | c.223A>C (p.Lys75Gln) c.289A>C (p.Lys97Gln) n.725A>C n.800A>C | |
15 | g.66435235A>G | CA392929652 | MAP2K1 | c.223A>G (p.Lys75Glu) c.289A>G (p.Lys97Glu) n.725A>G n.800A>G | |
15 | g.66435235A>T | CA392929654 | MAP2K1 | c.223A>T (p.Lys75Ter) c.289A>T (p.Lys97Ter) n.725A>T n.800A>T | |
15 | g.66435236A>C | CA392929656 | MAP2K1 | c.224A>C (p.Lys75Thr) c.290A>C (p.Lys97Thr) n.726A>C n.801A>C | |
15 | g.66435236A>G | CA392929657 | MAP2K1 | c.224A>G (p.Lys75Arg) c.290A>G (p.Lys97Arg) n.726A>G n.801A>G | dbSNP |
15 | g.66435236A>T | CA392929659 | MAP2K1 | c.224A>T (p.Lys75Met) c.290A>T (p.Lys97Met) n.726A>T n.801A>T | dbSNP |
15 | g.66435237G>A | CA490856058 | MAP2K1 | c.225G>A (p.Lys75=) c.291G>A (p.Lys97=) n.727G>A n.802G>A | dbSNP |
15 | g.66435237G>C | CA392929661 | MAP2K1 | c.225G>C (p.Lys75Asn) c.291G>C (p.Lys97Asn) n.727G>C n.802G>C | dbSNP |
15 | g.66435237G>T | CA392929663 | MAP2K1 | c.225G>T (p.Lys75Asn) c.291G>T (p.Lys97Asn) n.727G>T n.802G>T | |
15 | g.66435237_66435238insCTT | CA2804543905 | MAP2K1 | c.225_225+1insCTT (n.225_225+1insCTT) c.291_291+1insCTT (n.291_291+1insCTT) n.727_727+1insCTT n.802_802+1insCTT | |
15 | g.66435238G>A | CA392929666 | MAP2K1 | c.225+1G>A (n.225+1G>A) c.291+1G>A (n.291+1G>A) n.727+1G>A n.802+1G>A | dbSNP |
15 | g.66435238G>C | CA392929668 | MAP2K1 | c.225+1G>C (n.225+1G>C) c.291+1G>C (n.291+1G>C) n.727+1G>C n.802+1G>C | dbSNP |
15 | g.66435238G>T | CA392929670 | MAP2K1 | c.225+1G>T (n.225+1G>T) c.291+1G>T (n.291+1G>T) n.727+1G>T n.802+1G>T | |
15 | g.66435239T>A | CA392929676 | MAP2K1 | c.225+2T>A (n.225+2T>A) c.291+2T>A (n.291+2T>A) n.727+2T>A n.802+2T>A | dbSNP |
15 | g.66435239T>C | CA392929674 | MAP2K1 | c.225+2T>C (n.225+2T>C) c.291+2T>C (n.291+2T>C) n.727+2T>C n.802+2T>C | |
15 | g.66435239T>G | CA392929672 | MAP2K1 | c.225+2T>G (n.225+2T>G) c.291+2T>G (n.291+2T>G) n.727+2T>G n.802+2T>G | dbSNP |
15 | g.66435239T= | CA2184071783 | MAP2K1 | c.225+2T= (n.225+2T=) c.291+2T= (n.291+2T=) n.727+2T= n.802+2T= | |
15 | g.66435239_66435241delinsTGA | CA2184071784 | MAP2K1 | c.225+2_225+4delinsTGA (n.225+2_225+4delinsTGA) c.291+2_291+4delinsTGA (n.291+2_291+4delinsTGA) n.727+2_727+4delinsTGA n.802+2_802+4delinsTGA | |
15 | g.66435240G>A | CA2730933679 | MAP2K1 | c.225+3G>A (n.225+3G>A) c.291+3G>A (n.291+3G>A) n.727+3G>A n.802+3G>A | dbSNP |
15 | g.66435240G>C | CA2730933680 | MAP2K1 | c.225+3G>C (n.225+3G>C) c.291+3G>C (n.291+3G>C) n.727+3G>C n.802+3G>C | dbSNP |
15 | g.66435240G= | CA2184071786 | MAP2K1 | c.225+3G= (n.225+3G=) c.291+3G= (n.291+3G=) n.727+3G= n.802+3G= | |
15 | g.66435240G>T | CA618958552 | MAP2K1 | c.225+3G>T (n.225+3G>T) c.291+3G>T (n.291+3G>T) n.727+3G>T n.802+3G>T | dbSNP gnomAD v2 gnomAD v4 |
15 | g.66435241_66435242del | CA2184071785 | MAP2K1 | c.225+4_225+5del (n.225+4_225+5del) c.291+4_291+5del (n.291+4_291+5del) n.727+4_727+5del n.802+4_802+5del | dbSNP |
15 | g.66435241A>G | CA2731117181 | MAP2K1 | c.225+4A>G (n.225+4A>G) c.291+4A>G (n.291+4A>G) n.727+4A>G n.802+4A>G | dbSNP |
15 | g.66435241A>T | CA2731117227 | MAP2K1 | c.225+4A>T (n.225+4A>T) c.291+4A>T (n.291+4A>T) n.727+4A>T n.802+4A>T | dbSNP |
15 | g.66435242G>A | CA2731117259 | MAP2K1 | c.225+5G>A (n.225+5G>A) c.291+5G>A (n.291+5G>A) n.727+5G>A n.802+5G>A | dbSNP |
15 | g.66435242G>C | CA2731117268 | MAP2K1 | c.225+5G>C (n.225+5G>C) c.291+5G>C (n.291+5G>C) n.727+5G>C n.802+5G>C | dbSNP |
15 | g.66435242G>T | CA645570543 | MAP2K1 | c.225+5G>T (n.225+5G>T) c.291+5G>T (n.291+5G>T) n.727+5G>T n.802+5G>T | COSMIC |
15 | g.66435243T>A | CA2730937753 | MAP2K1 | c.225+6T>A (n.225+6T>A) c.291+6T>A (n.291+6T>A) n.727+6T>A n.802+6T>A | dbSNP |
15 | g.66435243T>C | CA618958553 | MAP2K1 | c.225+6T>C (n.225+6T>C) c.291+6T>C (n.291+6T>C) n.727+6T>C n.802+6T>C | dbSNP gnomAD v2 gnomAD v4 |
15 | g.66435243T>G | CA2730937752 | MAP2K1 | c.225+6T>G (n.225+6T>G) c.291+6T>G (n.291+6T>G) n.727+6T>G n.802+6T>G | dbSNP |
15 | g.66435243T= | CA2184071787 | MAP2K1 | c.225+6T= (n.225+6T=) c.291+6T= (n.291+6T=) n.727+6T= n.802+6T= | |
15 | g.66435244T>A | CA2629081331 | MAP2K1 | c.225+7T>A (n.225+7T>A) c.291+7T>A (n.291+7T>A) n.727+7T>A n.802+7T>A | dbSNP gnomAD v4 |
15 | g.66435244T>C | CA2629081332 | MAP2K1 | c.225+7T>C (n.225+7T>C) c.291+7T>C (n.291+7T>C) n.727+7T>C n.802+7T>C | gnomAD v4 |
15 | g.66435245T>A | CA2731117280 | MAP2K1 | c.225+8T>A (n.225+8T>A) c.291+8T>A (n.291+8T>A) n.727+8T>A n.802+8T>A | dbSNP |
15 | g.66435246G>A | CA618958554 | MAP2K1 | c.225+9G>A (n.225+9G>A) c.291+9G>A (n.291+9G>A) n.727+9G>A n.802+9G>A | dbSNP gnomAD v2 gnomAD v4 |
15 | g.66435246G>C | CA2730953337 | MAP2K1 | c.225+9G>C (n.225+9G>C) c.291+9G>C (n.291+9G>C) n.727+9G>C n.802+9G>C | dbSNP |
15 | g.66435246G= | CA2184071788 | MAP2K1 | c.225+9G= (n.225+9G=) c.291+9G= (n.291+9G=) n.727+9G= n.802+9G= | |
15 | g.66435246G>T | CA2575765956 | MAP2K1 | c.225+9G>T (n.225+9G>T) c.291+9G>T (n.291+9G>T) n.727+9G>T n.802+9G>T | ClinVar gnomAD v4 |
15 | g.66435247C>A | CA2629081333 | MAP2K1 | c.225+10C>A (n.225+10C>A) c.291+10C>A (n.291+10C>A) n.727+10C>A n.802+10C>A | dbSNP gnomAD v4 |
15 | g.66435247C= | CA2184071789 | MAP2K1 | c.225+10C= (n.225+10C=) c.291+10C= (n.291+10C=) n.727+10C= n.802+10C= | |
15 | g.66435247C>G | CA2731033609 | MAP2K1 | c.225+10C>G (n.225+10C>G) c.291+10C>G (n.291+10C>G) n.727+10C>G n.802+10C>G | dbSNP |
15 | g.66435247C>T | CA2184071790 | MAP2K1 | c.225+10C>T (n.225+10C>T) c.291+10C>T (n.291+10C>T) n.727+10C>T n.802+10C>T | dbSNP |
15 | g.66435248C>A | CA2629081334 | MAP2K1 | c.225+11C>A (n.225+11C>A) c.291+11C>A (n.291+11C>A) n.727+11C>A n.802+11C>A | dbSNP gnomAD v4 |
15 | g.66435248C>G | CA2731117365 | MAP2K1 | c.225+11C>G (n.225+11C>G) c.291+11C>G (n.291+11C>G) n.727+11C>G n.802+11C>G | dbSNP |
15 | g.66435248C>T | CA2731117286 | MAP2K1 | c.225+11C>T (n.225+11C>T) c.291+11C>T (n.291+11C>T) n.727+11C>T n.802+11C>T | dbSNP |
15 | g.66435249T>A | CA2731117373 | MAP2K1 | c.225+12T>A (n.225+12T>A) c.291+12T>A (n.291+12T>A) n.727+12T>A n.802+12T>A | dbSNP |
15 | g.66435249T>C | CA2629081335 | MAP2K1 | c.225+12T>C (n.225+12T>C) c.291+12T>C (n.291+12T>C) n.727+12T>C n.802+12T>C | dbSNP gnomAD v4 |
15 | g.66435249_66435252delinsTTGA | CA2184071791 | MAP2K1 | c.225+12_225+15delinsTTGA (n.225+12_225+15delinsTTGA) c.291+12_291+15delinsTTGA (n.291+12_291+15delinsTTGA) n.727+12_727+15delinsTTGA n.802+12_802+15delinsTTGA | |
15 | g.66435250T>A | CA2731033610 | MAP2K1 | c.225+13T>A (n.225+13T>A) c.291+13T>A (n.291+13T>A) n.727+13T>A n.802+13T>A | dbSNP |
15 | g.66435250T>C | CA2184071796 | MAP2K1 | c.225+13T>C (n.225+13T>C) c.291+13T>C (n.291+13T>C) n.727+13T>C n.802+13T>C | dbSNP gnomAD v4 |
15 | g.66435250T= | CA2184071795 | MAP2K1 | c.225+13T= (n.225+13T=) c.291+13T= (n.291+13T=) n.727+13T= n.802+13T= | |
15 | g.66435250_66435252delinsTGA | CA2184071793 | MAP2K1 | c.225+13_225+15delinsTGA (n.225+13_225+15delinsTGA) c.291+13_291+15delinsTGA (n.291+13_291+15delinsTGA) n.727+13_727+15delinsTGA n.802+13_802+15delinsTGA | |
15 | g.66435251_66435253del | CA2184071792 | MAP2K1 | c.225+14_225+16del (n.225+14_225+16del) c.291+14_291+16del (n.291+14_291+16del) n.727+14_727+16del n.802+14_802+16del | ClinVar dbSNP |
15 | g.66435250_66435257delinsTGATTAAC | CA2184071794 | MAP2K1 | c.225+13_225+20delinsTGATTAAC (n.225+13_225+20delinsTGATTAAC) c.291+13_291+20delinsTGATTAAC (n.291+13_291+20delinsTGATTAAC) n.727+13_727+20delinsTGATTAAC n.802+13_802+20delinsTGATTAAC | |
15 | g.66435251G>A | CA2629081336 | MAP2K1 | c.225+14G>A (n.225+14G>A) c.291+14G>A (n.291+14G>A) n.727+14G>A n.802+14G>A | dbSNP gnomAD v4 |
15 | g.66435251G>C | CA2730935208 | MAP2K1 | c.225+14G>C (n.225+14G>C) c.291+14G>C (n.291+14G>C) n.727+14G>C n.802+14G>C | dbSNP |
15 | g.66435251G= | CA2184071797 | MAP2K1 | c.225+14G= (n.225+14G=) c.291+14G= (n.291+14G=) n.727+14G= n.802+14G= | |
15 | g.66435251G>T | CA715007395 | MAP2K1 | c.225+14G>T (n.225+14G>T) c.291+14G>T (n.291+14G>T) n.727+14G>T n.802+14G>T | ClinVar dbSNP gnomAD v4 |
15 | g.66435251_66435252del | CA7623887 | MAP2K1 | c.225+14_225+15del (n.225+14_225+15del) c.291+14_291+15del (n.291+14_291+15del) n.727+14_727+15del n.802+14_802+15del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435251_66435252delinsTC | CA1139664040 | MAP2K1 | c.225+14_225+15delinsTC (n.225+14_225+15delinsTC) c.291+14_291+15delinsTC (n.291+14_291+15delinsTC) n.727+14_727+15delinsTC n.802+14_802+15delinsTC | ClinVar |
15 | g.66435251_66435256delinsTCTCAC | CA2697549136 | MAP2K1 | c.225+14_225+19delinsTCTCAC (n.225+14_225+19delinsTCTCAC) c.291+14_291+19delinsTCTCAC (n.291+14_291+19delinsTCTCAC) n.727+14_727+19delinsTCTCAC n.802+14_802+19delinsTCTCAC | ClinVar |
15 | g.66435251_66435257delinsTCTCACCAATCACCA | CA16619989 | MAP2K1 | c.225+14_225+20delinsTCTCACCAATCACCA (n.225+14_225+20delinsTCTCACCAATCACCA) c.291+14_291+20delinsTCTCACCAATCACCA (n.291+14_291+20delinsTCTCACCAATCACCA) n.727+14_727+20delinsTCTCACCAATCACCA n.802+14_802+20delinsTCTCACCAATCACCA | ClinVar dbSNP |
15 | g.66435252A= | CA2184071798 | MAP2K1 | c.225+15A= (n.225+15A=) c.291+15A= (n.291+15A=) n.727+15A= n.802+15A= | |
15 | g.66435252A>C | CA715007400 | MAP2K1 | c.225+15A>C (n.225+15A>C) c.291+15A>C (n.291+15A>C) n.727+15A>C n.802+15A>C | ClinVar dbSNP |
15 | g.66435253T>A | CA2731117418 | MAP2K1 | c.225+16T>A (n.225+16T>A) c.291+16T>A (n.291+16T>A) n.727+16T>A n.802+16T>A | dbSNP |
15 | g.66435253T= | CA2184071799 | MAP2K1 | c.225+16T= (n.225+16T=) c.291+16T= (n.291+16T=) n.727+16T= n.802+16T= | |
15 | g.66435254del | CA2575765957 | MAP2K1 | c.225+17del (n.225+17del) c.291+17del (n.291+17del) n.727+17del n.802+17del | |
15 | g.66435253_66435254insC | CA7623888 | MAP2K1 | c.225+16_225+17insC (n.225+16_225+17insC) c.291+16_291+17insC (n.291+16_291+17insC) n.727+16_727+17insC n.802+16_802+17insC | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435254T>A | CA2575765958 | MAP2K1 | c.225+17T>A (n.225+17T>A) c.291+17T>A (n.291+17T>A) n.727+17T>A n.802+17T>A | dbSNP gnomAD v4 |
15 | g.66435254T>C | CA715007405 | MAP2K1 | c.225+17T>C (n.225+17T>C) c.291+17T>C (n.291+17T>C) n.727+17T>C n.802+17T>C | ClinVar dbSNP |
15 | g.66435254T= | CA2184071800 | MAP2K1 | c.225+17T= (n.225+17T=) c.291+17T= (n.291+17T=) n.727+17T= n.802+17T= |