Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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.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.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.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.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.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.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.66435128dup | CA2838198301 | MAP2K1 | c.116dup (p.Glu40ArgfsTer5) c.182dup (p.Glu62ArgfsTer5) n.618dup n.693dup | |
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 |
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.66435214dup | CA2843335960 | MAP2K1 | c.202dup (p.Ser68PhefsTer?) c.268dup (p.Ser90PhefsTer?) c.268dup (p.Ser90PhefsTer25) n.704dup n.779dup | |
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 |