Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66435071_66435118del | CA645570529 | MAP2K1 | c.59_106del (p.Leu20_Lys35del) c.125_172del (p.Leu42_Lys57del) n.561_608del n.636_683del | COSMIC |
15 | g.66435076_66435108del | CA2573151054 | MAP2K1 | c.64_96del (p.Glu22_Leu32del) c.130_162del (p.Glu44_Leu54del) n.566_598del n.641_673del | ClinVar dbSNP |
15 | g.66435097G>A | CA392929164 | MAP2K1 | c.85G>A (p.Glu29Lys) c.151G>A (p.Glu51Lys) n.587G>A n.662G>A | dbSNP |
15 | g.66435097G>C | CA392929165 | MAP2K1 | c.85G>C (p.Glu29Gln) c.151G>C (p.Glu51Gln) n.587G>C n.662G>C | dbSNP |
15 | g.66435097G>T | CA392929167 | MAP2K1 | c.85G>T (p.Glu29Ter) c.151G>T (p.Glu51Ter) n.587G>T n.662G>T | |
15 | g.66435098A>C | CA392929169 | MAP2K1 | c.86A>C (p.Glu29Ala) c.152A>C (p.Glu51Ala) n.588A>C n.663A>C | |
15 | g.66435098A>G | CA392929171 | MAP2K1 | c.86A>G (p.Glu29Gly) c.152A>G (p.Glu51Gly) n.588A>G n.663A>G | |
15 | g.66435098A>T | CA392929172 | MAP2K1 | c.86A>T (p.Glu29Val) c.152A>T (p.Glu51Val) n.588A>T n.663A>T | |
15 | g.66435099G>A | CA490855924 | MAP2K1 | c.87G>A (p.Glu29=) c.153G>A (p.Glu51=) n.589G>A n.664G>A | ClinVar dbSNP gnomAD v4 |
15 | g.66435099G>C | CA392929174 | MAP2K1 | c.87G>C (p.Glu29Asp) c.153G>C (p.Glu51Asp) n.589G>C n.664G>C | dbSNP |
15 | g.66435099G= | CA2184071735 | MAP2K1 | c.87G= (p.Glu29=) c.153G= (p.Glu51=) n.589G= n.664G= | |
15 | g.66435099G>T | CA392929176 | MAP2K1 | c.87G>T (p.Glu29Asp) c.153G>T (p.Glu51Asp) n.589G>T n.664G>T | dbSNP |
15 | g.66435100G>A | CA392929181 | MAP2K1 | c.88G>A (p.Ala30Thr) c.154G>A (p.Ala52Thr) n.590G>A n.665G>A | ClinVar dbSNP gnomAD v4 |
15 | g.66435100G>C | CA392929179 | MAP2K1 | c.88G>C (p.Ala30Pro) c.154G>C (p.Ala52Pro) n.590G>C n.665G>C | dbSNP |
15 | g.66435100G>T | CA392929178 | MAP2K1 | c.88G>T (p.Ala30Ser) c.154G>T (p.Ala52Ser) n.590G>T n.665G>T | |
15 | g.66435101C>A | CA392929186 | MAP2K1 | c.89C>A (p.Ala30Asp) c.155C>A (p.Ala52Asp) n.591C>A n.666C>A | dbSNP |
15 | g.66435101C>G | CA392929183 | MAP2K1 | c.89C>G (p.Ala30Gly) c.155C>G (p.Ala52Gly) n.591C>G n.666C>G | dbSNP |
15 | g.66435101C>T | CA392929185 | MAP2K1 | c.89C>T (p.Ala30Val) c.155C>T (p.Ala52Val) n.591C>T n.666C>T | dbSNP |
15 | g.66435102C>A | CA490855925 | MAP2K1 | c.90C>A (p.Ala30=) c.156C>A (p.Ala52=) n.592C>A n.667C>A | |
15 | g.66435102C= | CA2184071736 | MAP2K1 | c.90C= (p.Ala30=) c.156C= (p.Ala52=) n.592C= n.667C= | |
15 | g.66435102C>G | CA490855926 | MAP2K1 | c.90C>G (p.Ala30=) c.156C>G (p.Ala52=) n.592C>G n.667C>G | ClinVar dbSNP |
15 | g.66435102C>T | CA176700 | MAP2K1 | c.90C>T (p.Ala30=) c.156C>T (p.Ala52=) n.592C>T n.667C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435103T>A | CA16602882 | MAP2K1 | c.91T>A (p.Phe31Ile) c.157T>A (p.Phe53Ile) n.593T>A n.668T>A | ClinVar dbSNP COSMIC |
15 | g.66435103T>C | CA16602452 | MAP2K1 | c.91T>C (p.Phe31Leu) c.157T>C (p.Phe53Leu) n.593T>C n.668T>C | ClinVar dbSNP COSMIC |
15 | g.66435103T>G | CA16602881 | MAP2K1 | c.91T>G (p.Phe31Val) c.157T>G (p.Phe53Val) n.593T>G n.668T>G | ClinVar dbSNP COSMIC |
15 | g.66435103T= | CA2184071737 | MAP2K1 | c.91T= (p.Phe31=) c.157T= (p.Phe53=) n.593T= n.668T= | |
15 | g.66435104T>A | CA392929195 | MAP2K1 | c.92T>A (p.Phe31Tyr) c.158T>A (p.Phe53Tyr) n.594T>A n.669T>A | dbSNP COSMIC |
15 | g.66435104T>C | CA279966 | MAP2K1 | c.92T>C (p.Phe31Ser) c.158T>C (p.Phe53Ser) n.594T>C n.669T>C | ClinVar dbSNP |
15 | g.66435104T>G | CA392929193 | MAP2K1 | c.92T>G (p.Phe31Cys) c.158T>G (p.Phe53Cys) n.594T>G n.669T>G | dbSNP COSMIC |
15 | g.66435104T= | CA2184071738 | MAP2K1 | c.92T= (p.Phe31=) c.158T= (p.Phe53=) n.594T= n.669T= | |
15 | g.66435106_66435108del | CA2695220906 | MAP2K1 | c.94_96del (p.Leu32del) c.160_162del (p.Leu54del) n.596_598del n.671_673del | |
15 | g.66435105_66435134del | CA2580618255 | MAP2K1 | c.93_122del (p.Phe31_Glu40del) c.159_188del (p.Phe53_Glu62del) n.595_624del n.670_699del | |
15 | g.66435105T>A | CA392929197 | MAP2K1 | c.93T>A (p.Phe31Leu) c.159T>A (p.Phe53Leu) n.595T>A n.670T>A | dbSNP COSMIC |
15 | g.66435105T>C | CA490855927 | MAP2K1 | c.93T>C (p.Phe31=) c.159T>C (p.Phe53=) n.595T>C n.670T>C | dbSNP |
15 | g.66435105T>G | CA16602880 | MAP2K1 | c.93T>G (p.Phe31Leu) c.159T>G (p.Phe53Leu) n.595T>G n.670T>G | ClinVar dbSNP COSMIC |
15 | g.66435105T= | CA2184071739 | MAP2K1 | c.93T= (p.Phe31=) c.159T= (p.Phe53=) n.595T= n.670T= | |
15 | g.66435105_66435119del | CA645570532 | MAP2K1 | c.93_107del (p.Phe31_Gln36delinsLeu) c.159_173del (p.Phe53_Gln58delinsLeu) n.595_609del n.670_684del | COSMIC |
15 | g.66435106C>A | CA392929198 | MAP2K1 | c.94C>A (p.Leu32Ile) c.160C>A (p.Leu54Ile) n.596C>A n.671C>A | |
15 | g.66435106C>G | CA392929200 | MAP2K1 | c.94C>G (p.Leu32Val) c.160C>G (p.Leu54Val) n.596C>G n.671C>G | gnomAD v4 |
15 | g.66435106C>T | CA392929202 | MAP2K1 | c.94C>T (p.Leu32Phe) c.160C>T (p.Leu54Phe) n.596C>T n.671C>T | |
15 | g.66435107T>A | CA392929204 | MAP2K1 | c.95T>A (p.Leu32His) c.161T>A (p.Leu54His) n.597T>A n.672T>A | dbSNP |
15 | g.66435107T>C | CA392929208 | MAP2K1 | c.95T>C (p.Leu32Pro) c.161T>C (p.Leu54Pro) n.597T>C n.672T>C | ClinVar dbSNP COSMIC |
15 | g.66435107T>G | CA392929206 | MAP2K1 | c.95T>G (p.Leu32Arg) c.161T>G (p.Leu54Arg) n.597T>G n.672T>G | |
15 | g.66435108T>A | CA490855930 | MAP2K1 | c.96T>A (p.Leu32=) c.162T>A (p.Leu54=) n.598T>A n.673T>A | |
15 | g.66435108T>C | CA490855931 | MAP2K1 | c.96T>C (p.Leu32=) c.162T>C (p.Leu54=) n.598T>C n.673T>C | |
15 | g.66435108T>G | CA7623877 | MAP2K1 | c.96T>G (p.Leu32=) c.162T>G (p.Leu54=) n.598T>G n.673T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.66435108T= | CA2184071740 | MAP2K1 | c.96T= (p.Leu32=) c.162T= (p.Leu54=) n.598T= n.673T= | |
15 | g.66435109del | CA2731113720 | MAP2K1 | c.97del (p.Thr33ProfsTer9) c.163del (p.Thr55ProfsTer9) n.599del n.674del | dbSNP |
15 | g.66435109A>C | CA392929211 | MAP2K1 | c.97A>C (p.Thr33Pro) c.163A>C (p.Thr55Pro) n.599A>C n.674A>C | |
15 | g.66435109A>G | CA392929213 | MAP2K1 | c.97A>G (p.Thr33Ala) c.163A>G (p.Thr55Ala) n.599A>G n.674A>G | |
15 | g.66435109A>T | CA392929215 | MAP2K1 | c.97A>T (p.Thr33Ser) c.163A>T (p.Thr55Ser) n.599A>T n.674A>T | |
15 | g.66435110C>A | CA392929216 | MAP2K1 | c.98C>A (p.Thr33Asn) c.164C>A (p.Thr55Asn) n.600C>A n.675C>A | dbSNP |
15 | g.66435110C>G | CA392929218 | MAP2K1 | c.98C>G (p.Thr33Ser) c.164C>G (p.Thr55Ser) n.600C>G n.675C>G | dbSNP |
15 | g.66435110C>T | CA392929220 | MAP2K1 | c.98C>T (p.Thr33Ile) c.164C>T (p.Thr55Ile) n.600C>T n.675C>T | dbSNP |
15 | g.66435112del | CA2731113721 | MAP2K1 | c.100del (p.Gln34ArgfsTer8) c.166del (p.Gln56ArgfsTer8) n.602del n.677del | dbSNP |
15 | g.66435111C>A | CA490855935 | MAP2K1 | c.99C>A (p.Thr33=) c.165C>A (p.Thr55=) n.601C>A n.676C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435111C= | CA2184071741 | MAP2K1 | c.99C= (p.Thr33=) c.165C= (p.Thr55=) n.601C= n.676C= | |
15 | g.66435111C>G | CA7623878 | MAP2K1 | c.99C>G (p.Thr33=) c.165C>G (p.Thr55=) n.601C>G n.676C>G | dbSNP ExAC gnomAD v2 |
15 | g.66435111C>T | CA490855937 | MAP2K1 | c.99C>T (p.Thr33=) c.165C>T (p.Thr55=) n.601C>T n.676C>T | dbSNP gnomAD v4 |
15 | g.66435111_66435125del | CA912992484 | MAP2K1 | c.99_113del (p.Gln34_Val38del) c.165_179del (p.Gln56_Val60del) n.601_615del n.676_690del | ClinVar |
15 | g.66435112C>A | CA392929222 | MAP2K1 | c.100C>A (p.Gln34Lys) c.166C>A (p.Gln56Lys) n.602C>A n.677C>A | dbSNP |
15 | g.66435112C= | CA2184071742 | MAP2K1 | c.100C= (p.Gln34=) c.166C= (p.Gln56=) n.602C= n.677C= | |
15 | g.66435112C>G | CA392929224 | MAP2K1 | c.100C>G (p.Gln34Glu) c.166C>G (p.Gln56Glu) n.602C>G n.677C>G | dbSNP |
15 | g.66435112C>T | CA392929226 | MAP2K1 | c.100C>T (p.Gln34Ter) c.166C>T (p.Gln56Ter) n.602C>T n.677C>T | dbSNP gnomAD v4 |
15 | g.66435113A= | CA2184071743 | MAP2K1 | c.101A= (p.Gln34=) c.167A= (p.Gln56=) n.603A= n.678A= | |
15 | g.66435113A>C | CA16602453 | MAP2K1 | c.101A>C (p.Gln34Pro) c.167A>C (p.Gln56Pro) n.603A>C n.678A>C | ClinVar dbSNP |
15 | g.66435113A>G | CA392929230 | MAP2K1 | c.101A>G (p.Gln34Arg) c.167A>G (p.Gln56Arg) n.603A>G n.678A>G | dbSNP |
15 | g.66435113A>T | CA392929227 | MAP2K1 | c.101A>T (p.Gln34Leu) c.167A>T (p.Gln56Leu) n.603A>T n.678A>T | dbSNP |
15 | g.66435113_66435127del | CA645570533 | MAP2K1 | c.101_115del (p.Gln34_Gly39delinsArg) c.167_181del (p.Gln56_Gly61delinsArg) n.603_617del n.678_692del | COSMIC |
15 | g.66435114G>A | CA490855939 | MAP2K1 | c.102G>A (p.Gln34=) c.168G>A (p.Gln56=) n.604G>A n.679G>A | dbSNP |
15 | g.66435114G>C | CA392929232 | MAP2K1 | c.102G>C (p.Gln34His) c.168G>C (p.Gln56His) n.604G>C n.679G>C | dbSNP |
15 | g.66435114G>T | CA392929234 | MAP2K1 | c.102G>T (p.Gln34His) c.168G>T (p.Gln56His) n.604G>T n.679G>T | |
15 | g.66435114_66435128del | CA645570535 | MAP2K1 | c.102_116del (p.Lys35_Gly39del) c.168_182del (p.Lys57_Gly61del) n.604_618del n.679_693del | COSMIC |
15 | g.66435115A= | CA2184071744 | MAP2K1 | c.103A= (p.Lys35=) c.169A= (p.Lys57=) n.605A= n.680A= | |
15 | g.66435115A>C | CA134595 | MAP2K1 | c.103A>C (p.Lys35Gln) c.169A>C (p.Lys57Gln) n.605A>C n.680A>C | ClinVar dbSNP |
15 | g.66435115A>G | CA16602628 | MAP2K1 | c.103A>G (p.Lys35Glu) c.169A>G (p.Lys57Glu) n.605A>G n.680A>G | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.66435115A>T | CA392929237 | MAP2K1 | c.103A>T (p.Lys35Ter) c.169A>T (p.Lys57Ter) n.605A>T n.680A>T | |
15 | g.66435116A= | CA2184071745 | MAP2K1 | c.104A= (p.Lys35=) c.170A= (p.Lys57=) n.606A= n.681A= | |
15 | g.66435116A>C | CA16602883 | MAP2K1 | c.104A>C (p.Lys35Thr) c.170A>C (p.Lys57Thr) n.606A>C n.681A>C | ClinVar dbSNP COSMIC |
15 | g.66435116A>G | CA392929239 | MAP2K1 | c.104A>G (p.Lys35Arg) c.170A>G (p.Lys57Arg) n.606A>G n.681A>G | dbSNP |
15 | g.66435116A>T | CA392929241 | MAP2K1 | c.104A>T (p.Lys35Met) c.170A>T (p.Lys57Met) n.606A>T n.681A>T | ClinVar dbSNP |
15 | g.66435117_66435131del | CA645570536 | MAP2K1 | c.105_119del (p.Gln36_Glu40del) c.171_185del (p.Gln58_Glu62del) n.607_621del n.682_696del | COSMIC |
15 | g.66435117G>A | CA490855943 | MAP2K1 | c.105G>A (p.Lys35=) c.171G>A (p.Lys57=) n.607G>A n.682G>A | dbSNP gnomAD v4 |
15 | g.66435117G>C | CA16602629 | MAP2K1 | c.105G>C (p.Lys35Asn) c.171G>C (p.Lys57Asn) n.607G>C n.682G>C | ClinVar dbSNP COSMIC |
15 | g.66435117G= | CA2184071746 | MAP2K1 | c.105G= (p.Lys35=) c.171G= (p.Lys57=) n.607G= n.682G= | |
15 | g.66435117G>T | CA356995 | MAP2K1 | c.105G>T (p.Lys35Asn) c.171G>T (p.Lys57Asn) n.607G>T n.682G>T | ClinVar dbSNP COSMIC |
15 | g.66435118C>A | CA392929244 | MAP2K1 | c.106C>A (p.Gln36Lys) c.172C>A (p.Gln58Lys) n.608C>A n.683C>A | dbSNP |
15 | g.66435118C>G | CA392929245 | MAP2K1 | c.106C>G (p.Gln36Glu) c.172C>G (p.Gln58Glu) n.608C>G n.683C>G | dbSNP |
15 | g.66435118C>T | CA392929247 | MAP2K1 | c.106C>T (p.Gln36Ter) c.172C>T (p.Gln58Ter) n.608C>T n.683C>T | dbSNP COSMIC |
15 | g.66435118_66435121delinsCAGA | CA2184071747 | MAP2K1 | c.106_109delinsCAGA (p.Gln36=) c.172_175delinsCAGA (p.Gln58=) n.608_611delinsCAGA n.683_686delinsCAGA | |
15 | g.66435119_66435133del | CA645570537 | MAP2K1 | c.107_121del (p.Gln36_Glu40del) c.173_187del (p.Gln58_Glu62del) n.609_623del n.684_698del | ClinVar dbSNP COSMIC |
15 | g.66435119A>C | CA392929255 | MAP2K1 | c.107A>C (p.Gln36Pro) c.173A>C (p.Gln58Pro) n.609A>C n.684A>C | |
15 | g.66435119A>G | CA392929253 | MAP2K1 | c.107A>G (p.Gln36Arg) c.173A>G (p.Gln58Arg) n.609A>G n.684A>G | ClinVar gnomAD v4 |
15 | g.66435119A>T | CA392929250 | MAP2K1 | c.107A>T (p.Gln36Leu) c.173A>T (p.Gln58Leu) n.609A>T n.684A>T | dbSNP |
15 | g.66435121_66435123del | CA354831 | MAP2K1 | c.109_111del (p.Lys37del) c.175_177del (p.Lys59del) n.611_613del n.686_688del | ClinVar dbSNP |
15 | g.66435119_66435134delinsAGAAGGTGGGAGAACT | CA2184071748 | MAP2K1 | c.107_122delinsAGAAGGTGGGAGAACT (p.Gln36=) c.173_188delinsAGAAGGTGGGAGAACT (p.Gln58=) n.609_624delinsAGAAGGTGGGAGAACT n.684_699delinsAGAAGGTGGGAGAACT | |
15 | g.66435120G>A | CA490855947 | MAP2K1 | c.108G>A (p.Gln36=) c.174G>A (p.Gln58=) n.610G>A n.685G>A | |
15 | g.66435120G>C | CA392929256 | MAP2K1 | c.108G>C (p.Gln36His) c.174G>C (p.Gln58His) n.610G>C n.685G>C | |
15 | g.66435120G= | CA2184071749 | MAP2K1 | c.108G= (p.Gln36=) c.174G= (p.Gln58=) n.610G= n.685G= | |
15 | g.66435120G>T | CA392929258 | MAP2K1 | c.108G>T (p.Gln36His) c.174G>T (p.Gln58His) n.610G>T n.685G>T | ClinVar dbSNP |
15 | g.66435125_66435139del | CA16042952 | MAP2K1 | c.113_127del (p.Val38_Lys42del) c.179_193del (p.Val60_Lys64del) n.615_629del n.690_704del | ClinVar dbSNP |
15 | g.66435121A>C | CA392929261 | MAP2K1 | c.109A>C (p.Lys37Gln) c.175A>C (p.Lys59Gln) n.611A>C n.686A>C | |
15 | g.66435121A>G | CA392929262 | MAP2K1 | c.109A>G (p.Lys37Glu) c.175A>G (p.Lys59Glu) n.611A>G n.686A>G | dbSNP |
15 | g.66435121A>T | CA392929263 | MAP2K1 | c.109A>T (p.Lys37Ter) c.175A>T (p.Lys59Ter) n.611A>T n.686A>T | dbSNP |
15 | g.66435122A>C | CA392929264 | MAP2K1 | c.110A>C (p.Lys37Thr) c.176A>C (p.Lys59Thr) n.612A>C n.687A>C | |
15 | g.66435122A>G | CA392929265 | MAP2K1 | c.110A>G (p.Lys37Arg) c.176A>G (p.Lys59Arg) n.612A>G n.687A>G | dbSNP |
15 | g.66435122A>T | CA392929266 | MAP2K1 | c.110A>T (p.Lys37Met) c.176A>T (p.Lys59Met) n.612A>T n.687A>T | dbSNP |
15 | g.66435123G>A | CA7623879 | MAP2K1 | c.111G>A (p.Lys37=) c.177G>A (p.Lys59=) n.613G>A n.688G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435123G>C | CA392929267 | MAP2K1 | c.111G>C (p.Lys37Asn) c.177G>C (p.Lys59Asn) n.613G>C n.688G>C | dbSNP gnomAD v3 gnomAD v4 |
15 | g.66435123G= | CA2184071750 | MAP2K1 | c.111G= (p.Lys37=) c.177G= (p.Lys59=) n.613G= n.688G= | |
15 | g.66435123G>T | CA392929268 | MAP2K1 | c.111G>T (p.Lys37Asn) c.177G>T (p.Lys59Asn) n.613G>T n.688G>T | dbSNP |
15 | g.66435124G>A | CA392929270 | MAP2K1 | c.112G>A (p.Val38Met) c.178G>A (p.Val60Met) n.614G>A n.689G>A | dbSNP |
15 | g.66435124G>C | CA392929269 | MAP2K1 | c.112G>C (p.Val38Leu) c.178G>C (p.Val60Leu) n.614G>C n.689G>C | dbSNP |
15 | g.66435124G= | CA2184071751 | MAP2K1 | c.112G= (p.Val38=) c.178G= (p.Val60=) n.614G= n.689G= | |
15 | g.66435124G>T | CA392929271 | MAP2K1 | c.112G>T (p.Val38Leu) c.178G>T (p.Val60Leu) n.614G>T n.689G>T | dbSNP gnomAD v4 |
15 | g.66435125T>A | CA392929272 | MAP2K1 | c.113T>A (p.Val38Glu) c.179T>A (p.Val60Glu) n.615T>A n.690T>A | dbSNP COSMIC |
15 | g.66435125T>C | CA392929273 | MAP2K1 | c.113T>C (p.Val38Ala) c.179T>C (p.Val60Ala) n.615T>C n.690T>C | |
15 | g.66435125T>G | CA296106 | MAP2K1 | c.113T>G (p.Val38Gly) c.179T>G (p.Val60Gly) n.615T>G n.690T>G | ClinVar dbSNP |
15 | g.66435125T= | CA2184071752 | MAP2K1 | c.113T= (p.Val38=) c.179T= (p.Val60=) n.615T= n.690T= | |
15 | g.66435126G>A | CA490855953 | MAP2K1 | c.114G>A (p.Val38=) c.180G>A (p.Val60=) n.616G>A n.691G>A | dbSNP |
15 | g.66435126G>C | CA490855955 | MAP2K1 | c.114G>C (p.Val38=) c.180G>C (p.Val60=) n.616G>C n.691G>C | dbSNP |
15 | g.66435126G>T | CA490855957 | MAP2K1 | c.114G>T (p.Val38=) c.180G>T (p.Val60=) n.616G>T n.691G>T | dbSNP |
15 | g.66435128del | CA2731114367 | MAP2K1 | c.116del (p.Gly39GlufsTer3) c.182del (p.Gly61GlufsTer3) n.618del n.693del | dbSNP |
15 | g.66435127G>A | CA392929274 | MAP2K1 | c.115G>A (p.Gly39Arg) c.181G>A (p.Gly61Arg) n.617G>A n.692G>A | dbSNP |
15 | g.66435127G>C | CA392929275 | MAP2K1 | c.115G>C (p.Gly39Arg) c.181G>C (p.Gly61Arg) n.617G>C n.692G>C | dbSNP |
15 | g.66435127G>T | CA392929276 | MAP2K1 | c.115G>T (p.Gly39Ter) c.181G>T (p.Gly61Ter) n.617G>T n.692G>T | dbSNP |
15 | g.66435128_66435142del | CA645570539 | MAP2K1 | c.116_130del (p.Gly39_Asp43del) c.182_196del (p.Gly61_Asp65del) n.618_632del n.693_707del | COSMIC |
15 | g.66435128G>A | CA392929277 | MAP2K1 | c.116G>A (p.Gly39Glu) c.182G>A (p.Gly61Glu) n.618G>A n.693G>A | dbSNP |
15 | g.66435128G>C | CA392929278 | MAP2K1 | c.116G>C (p.Gly39Ala) c.182G>C (p.Gly61Ala) n.618G>C n.693G>C | dbSNP |
15 | g.66435128G>T | CA392929279 | MAP2K1 | c.116G>T (p.Gly39Val) c.182G>T (p.Gly61Val) n.618G>T n.693G>T | dbSNP |
15 | g.66435129A>C | CA490855962 | MAP2K1 | c.117A>C (p.Gly39=) c.183A>C (p.Gly61=) n.619A>C n.694A>C | |
15 | g.66435129A>G | CA490855961 | MAP2K1 | c.117A>G (p.Gly39=) c.183A>G (p.Gly61=) n.619A>G n.694A>G | dbSNP |
15 | g.66435129A>T | CA490855960 | MAP2K1 | c.117A>T (p.Gly39=) c.183A>T (p.Gly61=) n.619A>T n.694A>T | |
15 | g.66435129_66435144delinsAGAACTGAAGGATGAC | CA2184071753 | MAP2K1 | c.117_132delinsAGAACTGAAGGATGAC (p.Gly39=) c.183_198delinsAGAACTGAAGGATGAC (p.Gly61=) n.619_634delinsAGAACTGAAGGATGAC n.694_709delinsAGAACTGAAGGATGAC | |
15 | g.66435130G>A | CA392929280 | MAP2K1 | c.118G>A (p.Glu40Lys) c.184G>A (p.Glu62Lys) n.620G>A n.695G>A | dbSNP |
15 | g.66435130G>C | CA392929281 | MAP2K1 | c.118G>C (p.Glu40Gln) c.184G>C (p.Glu62Gln) n.620G>C n.695G>C | dbSNP |
15 | g.66435130G>T | CA392929282 | MAP2K1 | c.118G>T (p.Glu40Ter) c.184G>T (p.Glu62Ter) n.620G>T n.695G>T | |
15 | g.66435132_66435146del | CA16042894 | MAP2K1 | c.120_134del (p.Glu40_Asp44del) c.186_200del (p.Glu62_Asp66del) n.622_636del n.697_711del | ClinVar dbSNP |
15 | g.66435131A>C | CA392929285 | MAP2K1 | c.119A>C (p.Glu40Ala) c.185A>C (p.Glu62Ala) n.621A>C n.696A>C | |
15 | g.66435131A>G | CA392929283 | MAP2K1 | c.119A>G (p.Glu40Gly) c.185A>G (p.Glu62Gly) n.621A>G n.696A>G | |
15 | g.66435131A>T | CA392929284 | MAP2K1 | c.119A>T (p.Glu40Val) c.185A>T (p.Glu62Val) n.621A>T n.696A>T | |
15 | g.66435132A>C | CA392929286 | MAP2K1 | c.120A>C (p.Glu40Asp) c.186A>C (p.Glu62Asp) n.622A>C n.697A>C | |
15 | g.66435132A>G | CA490855964 | MAP2K1 | c.120A>G (p.Glu40=) c.186A>G (p.Glu62=) n.622A>G n.697A>G | |
15 | g.66435132A>T | CA392929287 | MAP2K1 | c.120A>T (p.Glu40Asp) c.186A>T (p.Glu62Asp) n.622A>T n.697A>T | dbSNP |
15 | g.66435133C>A | CA392929288 | MAP2K1 | c.121C>A (p.Leu41Met) c.187C>A (p.Leu63Met) n.623C>A n.698C>A | dbSNP |
15 | g.66435133C= | CA2184071754 | MAP2K1 | c.121C= (p.Leu41=) c.187C= (p.Leu63=) n.623C= n.698C= | |
15 | g.66435133C>G | CA392929289 | MAP2K1 | c.121C>G (p.Leu41Val) c.187C>G (p.Leu63Val) n.623C>G n.698C>G | dbSNP |
15 | g.66435133C>T | CA490855965 | MAP2K1 | c.121C>T (p.Leu41=) c.187C>T (p.Leu63=) n.623C>T n.698C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.66435133_66435147del | CA645570540 | MAP2K1 | c.121_135del (p.Leu41_Asp45del) c.187_201del (p.Leu63_Asp67del) n.623_637del n.698_712del | COSMIC |
15 | g.66435134T>A | CA392929290 | MAP2K1 | c.122T>A (p.Leu41Gln) c.188T>A (p.Leu63Gln) n.624T>A n.699T>A | dbSNP |
15 | g.66435134T>C | CA392929291 | MAP2K1 | c.122T>C (p.Leu41Pro) c.188T>C (p.Leu63Pro) n.624T>C n.699T>C | |
15 | g.66435134T>G | CA392929292 | MAP2K1 | c.122T>G (p.Leu41Arg) c.188T>G (p.Leu63Arg) n.624T>G n.699T>G | |
15 | g.66435135G>A | CA490855972 | MAP2K1 | c.123G>A (p.Leu41=) c.189G>A (p.Leu63=) n.625G>A n.700G>A | dbSNP |
15 | g.66435135G>C | CA490855970 | MAP2K1 | c.123G>C (p.Leu41=) c.189G>C (p.Leu63=) n.625G>C n.700G>C | dbSNP |
15 | g.66435135G>T | CA490855969 | MAP2K1 | c.123G>T (p.Leu41=) c.189G>T (p.Leu63=) n.625G>T n.700G>T | |
15 | g.66435136A>C | CA392929293 | MAP2K1 | c.124A>C (p.Lys42Gln) c.190A>C (p.Lys64Gln) n.626A>C n.701A>C | |
15 | g.66435136A>G | CA392929294 | MAP2K1 | c.124A>G (p.Lys42Glu) c.190A>G (p.Lys64Glu) n.626A>G n.701A>G | |
15 | g.66435136A>T | CA392929295 | MAP2K1 | c.124A>T (p.Lys42Ter) c.190A>T (p.Lys64Ter) n.626A>T n.701A>T | dbSNP |
15 | g.66435137A>C | CA392929298 | MAP2K1 | c.125A>C (p.Lys42Thr) c.191A>C (p.Lys64Thr) n.627A>C n.702A>C | |
15 | g.66435137A>G | CA392929297 | MAP2K1 | c.125A>G (p.Lys42Arg) c.191A>G (p.Lys64Arg) n.627A>G n.702A>G | dbSNP |
15 | g.66435137A>T | CA392929296 | MAP2K1 | c.125A>T (p.Lys42Met) c.191A>T (p.Lys64Met) n.627A>T n.702A>T | dbSNP |
15 | g.66435138G>A | CA490855973 | MAP2K1 | c.126G>A (p.Lys42=) c.192G>A (p.Lys64=) n.628G>A n.703G>A | dbSNP gnomAD v4 |
15 | g.66435138G>C | CA392929299 | MAP2K1 | c.126G>C (p.Lys42Asn) c.192G>C (p.Lys64Asn) n.628G>C n.703G>C | |
15 | g.66435138G>T | CA392929300 | MAP2K1 | c.126G>T (p.Lys42Asn) c.192G>T (p.Lys64Asn) n.628G>T n.703G>T | dbSNP |
15 | g.66435139G>A | CA392929301 | MAP2K1 | c.127G>A (p.Asp43Asn) c.193G>A (p.Asp65Asn) n.629G>A n.704G>A | |
15 | g.66435139G>C | CA392929303 | MAP2K1 | c.127G>C (p.Asp43His) c.193G>C (p.Asp65His) n.629G>C n.704G>C | |
15 | g.66435139G>T | CA392929302 | MAP2K1 | c.127G>T (p.Asp43Tyr) c.193G>T (p.Asp65Tyr) n.629G>T n.704G>T | |
15 | g.66435140A>C | CA392929304 | MAP2K1 | c.128A>C (p.Asp43Ala) c.194A>C (p.Asp65Ala) n.630A>C n.705A>C | |
15 | g.66435140A>G | CA392929305 | MAP2K1 | c.128A>G (p.Asp43Gly) c.194A>G (p.Asp65Gly) n.630A>G n.705A>G | |
15 | g.66435140A>T | CA392929306 | MAP2K1 | c.128A>T (p.Asp43Val) c.194A>T (p.Asp65Val) n.630A>T n.705A>T | dbSNP |
15 | g.66435141T>A | CA392929307 | MAP2K1 | c.129T>A (p.Asp43Glu) c.195T>A (p.Asp65Glu) n.631T>A n.706T>A | dbSNP |
15 | g.66435141T>C | CA490855975 | MAP2K1 | c.129T>C (p.Asp43=) c.195T>C (p.Asp65=) n.631T>C n.706T>C | dbSNP gnomAD v4 |
15 | g.66435141T>G | CA392929308 | MAP2K1 | c.129T>G (p.Asp43Glu) c.195T>G (p.Asp65Glu) n.631T>G n.706T>G | |
15 | g.66435142G>A | CA392929309 | MAP2K1 | c.130G>A (p.Asp44Asn) c.196G>A (p.Asp66Asn) n.632G>A n.707G>A | dbSNP |
15 | g.66435142G>C | CA392929310 | MAP2K1 | c.130G>C (p.Asp44His) c.196G>C (p.Asp66His) n.632G>C n.707G>C | dbSNP |
15 | g.66435142G= | CA2184071755 | MAP2K1 | c.130G= (p.Asp44=) c.196G= (p.Asp66=) n.632G= n.707G= | |
15 | g.66435142G>T | CA392929311 | MAP2K1 | c.130G>T (p.Asp44Tyr) c.196G>T (p.Asp66Tyr) n.632G>T n.707G>T | dbSNP |
15 | g.66435143A>C | CA392929312 | MAP2K1 | c.131A>C (p.Asp44Ala) c.197A>C (p.Asp66Ala) n.633A>C n.708A>C | dbSNP |
15 | g.66435143A>G | CA392929313 | MAP2K1 | c.131A>G (p.Asp44Gly) c.197A>G (p.Asp66Gly) n.633A>G n.708A>G | dbSNP |
15 | g.66435143A>T | CA392929314 | MAP2K1 | c.131A>T (p.Asp44Val) c.197A>T (p.Asp66Val) n.633A>T n.708A>T | dbSNP |
15 | g.66435144C>A | CA392929316 | MAP2K1 | c.132C>A (p.Asp44Glu) c.198C>A (p.Asp66Glu) n.634C>A n.709C>A | ClinVar dbSNP |
15 | g.66435144C= | CA2184071756 | MAP2K1 | c.132C= (p.Asp44=) c.198C= (p.Asp66=) n.634C= n.709C= | |
15 | g.66435144C>G | CA392929315 | MAP2K1 | c.132C>G (p.Asp44Glu) c.198C>G (p.Asp66Glu) n.634C>G n.709C>G | dbSNP gnomAD v4 |
15 | g.66435144C>T | CA7623880 | MAP2K1 | c.132C>T (p.Asp44=) c.198C>T (p.Asp66=) n.634C>T n.709C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66435145G>A | CA180743 | MAP2K1 | c.133G>A (p.Asp45Asn) c.199G>A (p.Asp67Asn) n.635G>A n.710G>A | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.66435145G>C | CA392929317 | MAP2K1 | c.133G>C (p.Asp45His) c.199G>C (p.Asp67His) n.635G>C n.710G>C | dbSNP |
15 | g.66435145G= | CA2184071757 | MAP2K1 | c.133G= (p.Asp45=) c.199G= (p.Asp67=) n.635G= n.710G= | |
15 | g.66435145G>T | CA392929318 | MAP2K1 | c.133G>T (p.Asp45Tyr) c.199G>T (p.Asp67Tyr) n.635G>T n.710G>T | dbSNP gnomAD v4 COSMIC |
15 | g.66435146A>C | CA392929319 | MAP2K1 | c.134A>C (p.Asp45Ala) c.200A>C (p.Asp67Ala) n.636A>C n.711A>C | dbSNP |
15 | g.66435146A>G | CA392929320 | MAP2K1 | c.134A>G (p.Asp45Gly) c.200A>G (p.Asp67Gly) n.636A>G n.711A>G | |
15 | g.66435146A>T | CA392929321 | MAP2K1 | c.134A>T (p.Asp45Val) c.200A>T (p.Asp67Val) n.636A>T n.711A>T | dbSNP |
15 | g.66435147C>A | CA392929322 | MAP2K1 | c.135C>A (p.Asp45Glu) c.201C>A (p.Asp67Glu) n.637C>A n.712C>A | dbSNP |
15 | g.66435147C>G | CA392929323 | MAP2K1 | c.135C>G (p.Asp45Glu) c.201C>G (p.Asp67Glu) n.637C>G n.712C>G | dbSNP |
15 | g.66435147C>T | CA490855981 | MAP2K1 | c.135C>T (p.Asp45=) c.201C>T (p.Asp67=) n.637C>T n.712C>T | |
15 | g.66435148T>A | CA392929324 | MAP2K1 | c.136T>A (p.Phe46Ile) c.202T>A (p.Phe68Ile) n.638T>A n.713T>A | |
15 | g.66435148T>C | CA392929325 | MAP2K1 | c.136T>C (p.Phe46Leu) c.202T>C (p.Phe68Leu) n.638T>C n.713T>C | |
15 | g.66435148T>G | CA392929326 | MAP2K1 | c.136T>G (p.Phe46Val) c.202T>G (p.Phe68Val) n.638T>G n.713T>G | |
15 | g.66435149T>A | CA392929328 | MAP2K1 | c.137T>A (p.Phe46Tyr) c.203T>A (p.Phe68Tyr) n.639T>A n.714T>A | |
15 | g.66435149T>C | CA392929329 | MAP2K1 | c.137T>C (p.Phe46Ser) c.203T>C (p.Phe68Ser) n.639T>C n.714T>C | |
15 | g.66435149T>G | CA392929327 | MAP2K1 | c.137T>G (p.Phe46Cys) c.203T>G (p.Phe68Cys) n.639T>G n.714T>G | |
15 | g.66435150T>A | CA392929330 | MAP2K1 | c.138T>A (p.Phe46Leu) c.204T>A (p.Phe68Leu) n.640T>A n.715T>A | dbSNP |
15 | g.66435150T>C | CA490855986 | MAP2K1 | c.138T>C (p.Phe46=) c.204T>C (p.Phe68=) n.640T>C n.715T>C | |
15 | g.66435150T>G | CA392929331 | MAP2K1 | c.138T>G (p.Phe46Leu) c.204T>G (p.Phe68Leu) n.640T>G n.715T>G | |
15 | g.66435151G>A | CA392929332 | MAP2K1 | c.139G>A (p.Glu47Lys) c.205G>A (p.Glu69Lys) n.641G>A n.716G>A | ClinVar dbSNP |
15 | g.66435151G>C | CA392929333 | MAP2K1 | c.139G>C (p.Glu47Gln) c.205G>C (p.Glu69Gln) n.641G>C n.716G>C | dbSNP |
15 | g.66435151G= | CA2184071758 | MAP2K1 | c.139G= (p.Glu47=) c.205G= (p.Glu69=) n.641G= n.716G= | |
15 | g.66435151G>T | CA392929334 | MAP2K1 | c.139G>T (p.Glu47Ter) c.205G>T (p.Glu69Ter) n.641G>T n.716G>T | |
15 | g.66435152A>C | CA392929335 | MAP2K1 | c.140A>C (p.Glu47Ala) c.206A>C (p.Glu69Ala) n.642A>C n.717A>C | |
15 | g.66435152A>G | CA392929336 | MAP2K1 | c.140A>G (p.Glu47Gly) c.206A>G (p.Glu69Gly) n.642A>G n.717A>G | dbSNP |
15 | g.66435152A>T | CA392929337 | MAP2K1 | c.140A>T (p.Glu47Val) c.206A>T (p.Glu69Val) n.642A>T n.717A>T | dbSNP |
15 | g.66435153G>A | CA490855989 | MAP2K1 | c.141G>A (p.Glu47=) c.207G>A (p.Glu69=) n.643G>A n.718G>A | dbSNP |
15 | g.66435153G>C | CA392929338 | MAP2K1 | c.141G>C (p.Glu47Asp) c.207G>C (p.Glu69Asp) n.643G>C n.718G>C | dbSNP |
15 | g.66435153G>T | CA392929339 | MAP2K1 | c.141G>T (p.Glu47Asp) c.207G>T (p.Glu69Asp) n.643G>T n.718G>T | |
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 |