UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66435062A>C | CA392929010 | MAP2K1 | c.50A>C (p.Glu17Ala) c.116A>C (p.Glu39Ala) n.552A>C n.627A>C | |
| 15 | g.66435062A>G | CA392929011 | MAP2K1 | c.50A>G (p.Glu17Gly) c.116A>G (p.Glu39Gly) n.552A>G n.627A>G | dbSNP |
| 15 | g.66435062A>T | CA392929013 | MAP2K1 | c.50A>T (p.Glu17Val) c.116A>T (p.Glu39Val) n.552A>T n.627A>T | dbSNP |
| 15 | g.66435063G>A | CA490855902 | MAP2K1 | c.51G>A (p.Glu17=) c.117G>A (p.Glu39=) n.553G>A n.628G>A | dbSNP gnomAD v4 |
| 15 | g.66435063G>C | CA392929014 | MAP2K1 | c.51G>C (p.Glu17Asp) c.117G>C (p.Glu39Asp) n.553G>C n.628G>C | dbSNP |
| 15 | g.66435063G>T | CA392929015 | MAP2K1 | c.51G>T (p.Glu17Asp) c.117G>T (p.Glu39Asp) n.553G>T n.628G>T | |
| 15 | g.66435063_66435064delinsGC | CA2184071716 | MAP2K1 | c.51_52delinsGC (p.Glu17=) c.117_118delinsGC (p.Glu39=) n.553_554delinsGC n.628_629delinsGC | |
| 15 | g.66435064del | CA7623874 | MAP2K1 | c.52del (p.Leu18Ter) c.118del (p.Leu40Ter) n.554del n.629del | dbSNP ExAC gnomAD v2 |
| 15 | g.66435064C>A | CA392929017 | MAP2K1 | c.52C>A (p.Leu18Ile) c.118C>A (p.Leu40Ile) n.554C>A n.629C>A | dbSNP |
| 15 | g.66435064C= | CA2184071717 | MAP2K1 | c.52C= (p.Leu18=) c.118C= (p.Leu40=) n.554C= n.629C= | |
| 15 | g.66435064C>G | CA392929019 | MAP2K1 | c.52C>G (p.Leu18Val) c.118C>G (p.Leu40Val) n.554C>G n.629C>G | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.66435064C>T | CA490855903 | MAP2K1 | c.52C>T (p.Leu18=) c.118C>T (p.Leu40=) n.554C>T n.629C>T | gnomAD v4 |
| 15 | g.66435064dup | CA2629081329 | MAP2K1 | c.52dup (p.Leu18ProfsTer4) c.118dup (p.Leu40ProfsTer4) n.554dup n.629dup | gnomAD v4 |
| 15 | g.66435065T>A | CA392929021 | MAP2K1 | c.53T>A (p.Leu18Gln) c.119T>A (p.Leu40Gln) n.555T>A n.630T>A | |
| 15 | g.66435065T>C | CA392929023 | MAP2K1 | c.53T>C (p.Leu18Pro) c.119T>C (p.Leu40Pro) n.555T>C n.630T>C | dbSNP |
| 15 | g.66435065T>G | CA392929025 | MAP2K1 | c.53T>G (p.Leu18Arg) c.119T>G (p.Leu40Arg) n.555T>G n.630T>G | |
| 15 | g.66435066A>C | CA490855905 | MAP2K1 | c.54A>C (p.Leu18=) c.120A>C (p.Leu40=) n.556A>C n.631A>C | |
| 15 | g.66435066A>G | CA490855904 | MAP2K1 | c.54A>G (p.Leu18=) c.120A>G (p.Leu40=) n.556A>G n.631A>G | dbSNP |
| 15 | g.66435066A>T | CA490855906 | MAP2K1 | c.54A>T (p.Leu18=) c.120A>T (p.Leu40=) n.556A>T n.631A>T | dbSNP |
| 15 | g.66435067G>A | CA392929031 | MAP2K1 | c.55G>A (p.Glu19Lys) c.121G>A (p.Glu41Lys) n.557G>A n.632G>A | dbSNP |
| 15 | g.66435067G>C | CA392929029 | MAP2K1 | c.55G>C (p.Glu19Gln) c.121G>C (p.Glu41Gln) n.557G>C n.632G>C | dbSNP |
| 15 | g.66435067G>T | CA392929027 | MAP2K1 | c.55G>T (p.Glu19Ter) c.121G>T (p.Glu41Ter) n.557G>T n.632G>T | |
| 15 | g.66435068A>C | CA392929034 | MAP2K1 | c.56A>C (p.Glu19Ala) c.122A>C (p.Glu41Ala) n.558A>C n.633A>C | |
| 15 | g.66435068A>G | CA392929035 | MAP2K1 | c.56A>G (p.Glu19Gly) c.122A>G (p.Glu41Gly) n.558A>G n.633A>G | dbSNP |
| 15 | g.66435068A>T | CA392929036 | MAP2K1 | c.56A>T (p.Glu19Val) c.122A>T (p.Glu41Val) n.558A>T n.633A>T | dbSNP |
| 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.66435069G>A | CA490855907 | MAP2K1 | c.57G>A (p.Glu19=) c.123G>A (p.Glu41=) n.559G>A n.634G>A | dbSNP |
| 15 | g.66435069G>C | CA392929038 | MAP2K1 | c.57G>C (p.Glu19Asp) c.123G>C (p.Glu41Asp) n.559G>C n.634G>C | dbSNP gnomAD v4 |
| 15 | g.66435069G= | CA2184071718 | MAP2K1 | c.57G= (p.Glu19=) c.123G= (p.Glu41=) n.559G= n.634G= | |
| 15 | g.66435069G>T | CA392929040 | MAP2K1 | c.57G>T (p.Glu19Asp) c.123G>T (p.Glu41Asp) n.559G>T n.634G>T | dbSNP |
| 15 | g.66435070C>A | CA392929042 | MAP2K1 | c.58C>A (p.Leu20Ile) c.124C>A (p.Leu42Ile) n.560C>A n.635C>A | |
| 15 | g.66435070C= | CA2184071719 | MAP2K1 | c.58C= (p.Leu20=) c.124C= (p.Leu42=) n.560C= n.635C= | |
| 15 | g.66435070C>G | CA392929043 | MAP2K1 | c.58C>G (p.Leu20Val) c.124C>G (p.Leu42Val) n.560C>G n.635C>G | dbSNP |
| 15 | g.66435070C>T | CA279993 | MAP2K1 | c.58C>T (p.Leu20Phe) c.124C>T (p.Leu42Phe) n.560C>T n.635C>T | ClinVar dbSNP COSMIC |
| 15 | g.66435071T>A | CA392929046 | MAP2K1 | c.59T>A (p.Leu20His) c.125T>A (p.Leu42His) n.561T>A n.636T>A | COSMIC |
| 15 | g.66435071T>C | CA392929048 | MAP2K1 | c.59T>C (p.Leu20Pro) c.125T>C (p.Leu42Pro) n.561T>C n.636T>C | |
| 15 | g.66435071T>G | CA392929050 | MAP2K1 | c.59T>G (p.Leu20Arg) c.125T>G (p.Leu42Arg) n.561T>G n.636T>G | ClinVar dbSNP |
| 15 | g.66435071T= | CA2184071721 | MAP2K1 | c.59T= (p.Leu20=) c.125T= (p.Leu42=) n.561T= n.636T= | |
| 15 | g.66435072dup | CA2731112622 | MAP2K1 | c.60dup (p.Asp21Ter) c.126dup (p.Asp43Ter) n.562dup n.637dup | dbSNP |
| 15 | g.66435071_66435074delinsTTGA | CA2184071720 | MAP2K1 | c.59_62delinsTTGA (p.Leu20=) c.125_128delinsTTGA (p.Leu42=) n.561_564delinsTTGA n.636_639delinsTTGA | |
| 15 | g.66435072T>A | CA490855909 | MAP2K1 | c.60T>A (p.Leu20=) c.126T>A (p.Leu42=) n.562T>A n.637T>A | dbSNP |
| 15 | g.66435072T>C | CA7623875 | MAP2K1 | c.60T>C (p.Leu20=) c.126T>C (p.Leu42=) n.562T>C n.637T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435072T>G | CA490855908 | MAP2K1 | c.60T>G (p.Leu20=) c.126T>G (p.Leu42=) n.562T>G n.637T>G | dbSNP |
| 15 | g.66435072T= | CA2184071722 | MAP2K1 | c.60T= (p.Leu20=) c.126T= (p.Leu42=) n.562T= n.637T= | |
| 15 | g.66435075_66435077del | CA658656490 | MAP2K1 | c.63_65del (p.Asp21del) c.129_131del (p.Asp43del) n.565_567del n.640_642del | ClinVar dbSNP |
| 15 | g.66435073G>A | CA392929056 | MAP2K1 | c.61G>A (p.Asp21Asn) c.127G>A (p.Asp43Asn) n.563G>A n.638G>A | dbSNP |
| 15 | g.66435073G>C | CA392929054 | MAP2K1 | c.61G>C (p.Asp21His) c.127G>C (p.Asp43His) n.563G>C n.638G>C | dbSNP |
| 15 | g.66435073G>T | CA392929053 | MAP2K1 | c.61G>T (p.Asp21Tyr) c.127G>T (p.Asp43Tyr) n.563G>T n.638G>T | dbSNP |
| 15 | g.66435074A>C | CA392929058 | MAP2K1 | c.62A>C (p.Asp21Ala) c.128A>C (p.Asp43Ala) n.564A>C n.639A>C | |
| 15 | g.66435074A>G | CA392929060 | MAP2K1 | c.62A>G (p.Asp21Gly) c.128A>G (p.Asp43Gly) n.564A>G n.639A>G | dbSNP |
| 15 | g.66435074A>T | CA392929062 | MAP2K1 | c.62A>T (p.Asp21Val) c.128A>T (p.Asp43Val) n.564A>T n.639A>T | dbSNP |
| 15 | g.66435075T>A | CA392929064 | MAP2K1 | c.63T>A (p.Asp21Glu) c.129T>A (p.Asp43Glu) n.565T>A n.640T>A | |
| 15 | g.66435075T>C | CA490855910 | MAP2K1 | c.63T>C (p.Asp21=) c.129T>C (p.Asp43=) n.565T>C n.640T>C | |
| 15 | g.66435075T>G | CA392929065 | MAP2K1 | c.63T>G (p.Asp21Glu) c.129T>G (p.Asp43Glu) n.565T>G n.640T>G | |
| 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.66435076G>A | CA392929068 | MAP2K1 | c.64G>A (p.Glu22Lys) c.130G>A (p.Glu44Lys) n.566G>A n.641G>A | dbSNP |
| 15 | g.66435076G>C | CA392929069 | MAP2K1 | c.64G>C (p.Glu22Gln) c.130G>C (p.Glu44Gln) n.566G>C n.641G>C | dbSNP |
| 15 | g.66435076G>T | CA392929071 | MAP2K1 | c.64G>T (p.Glu22Ter) c.130G>T (p.Glu44Ter) n.566G>T n.641G>T | dbSNP gnomAD v4 |
| 15 | g.66435077A= | CA2184071723 | MAP2K1 | c.65A= (p.Glu22=) c.131A= (p.Glu44=) n.567A= n.642A= | |
| 15 | g.66435077A>C | CA392929073 | MAP2K1 | c.65A>C (p.Glu22Ala) c.131A>C (p.Glu44Ala) n.567A>C n.642A>C | |
| 15 | g.66435077A>G | CA392929075 | MAP2K1 | c.65A>G (p.Glu22Gly) c.131A>G (p.Glu44Gly) n.567A>G n.642A>G | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.66435077A>T | CA392929077 | MAP2K1 | c.65A>T (p.Glu22Val) c.131A>T (p.Glu44Val) n.567A>T n.642A>T | dbSNP |
| 15 | g.66435078G>A | CA490855911 | MAP2K1 | c.66G>A (p.Glu22=) c.132G>A (p.Glu44=) n.568G>A n.643G>A | dbSNP gnomAD v4 |
| 15 | g.66435078G>C | CA392929079 | MAP2K1 | c.66G>C (p.Glu22Asp) c.132G>C (p.Glu44Asp) n.568G>C n.643G>C | dbSNP |
| 15 | g.66435078G= | CA2184071724 | MAP2K1 | c.66G= (p.Glu22=) c.132G= (p.Glu44=) n.568G= n.643G= | |
| 15 | g.66435078G>T | CA392929080 | MAP2K1 | c.66G>T (p.Glu22Asp) c.132G>T (p.Glu44Asp) n.568G>T n.643G>T | |
| 15 | g.66435079C>A | CA392929086 | MAP2K1 | c.67C>A (p.Gln23Lys) c.133C>A (p.Gln45Lys) n.569C>A n.644C>A | |
| 15 | g.66435079C>G | CA392929083 | MAP2K1 | c.67C>G (p.Gln23Glu) c.133C>G (p.Gln45Glu) n.569C>G n.644C>G | dbSNP |
| 15 | g.66435079C>T | CA392929084 | MAP2K1 | c.67C>T (p.Gln23Ter) c.133C>T (p.Gln45Ter) n.569C>T n.644C>T | dbSNP |
| 15 | g.66435080A>C | CA392929087 | MAP2K1 | c.68A>C (p.Gln23Pro) c.134A>C (p.Gln45Pro) n.570A>C n.645A>C | |
| 15 | g.66435080A>G | CA392929089 | MAP2K1 | c.68A>G (p.Gln23Arg) c.134A>G (p.Gln45Arg) n.570A>G n.645A>G | |
| 15 | g.66435080A>T | CA392929091 | MAP2K1 | c.68A>T (p.Gln23Leu) c.134A>T (p.Gln45Leu) n.570A>T n.645A>T | dbSNP |
| 15 | g.66435081G>A | CA490855912 | MAP2K1 | c.69G>A (p.Gln23=) c.135G>A (p.Gln45=) n.571G>A n.646G>A | dbSNP gnomAD v4 |
| 15 | g.66435081G>C | CA392929092 | MAP2K1 | c.69G>C (p.Gln23His) c.135G>C (p.Gln45His) n.571G>C n.646G>C | dbSNP |
| 15 | g.66435081G= | CA2184071725 | MAP2K1 | c.69G= (p.Gln23=) c.135G= (p.Gln45=) n.571G= n.646G= | |
| 15 | g.66435081G>T | CA392929095 | MAP2K1 | c.69G>T (p.Gln23His) c.135G>T (p.Gln45His) n.571G>T n.646G>T | ClinVar dbSNP gnomAD v4 |
| 15 | g.66435082C>A | CA392929097 | MAP2K1 | c.70C>A (p.Gln24Lys) c.136C>A (p.Gln46Lys) n.572C>A n.647C>A | |
| 15 | g.66435082C>G | CA392929098 | MAP2K1 | c.70C>G (p.Gln24Glu) c.136C>G (p.Gln46Glu) n.572C>G n.647C>G | dbSNP |
| 15 | g.66435082C>T | CA392929101 | MAP2K1 | c.70C>T (p.Gln24Ter) c.136C>T (p.Gln46Ter) n.572C>T n.647C>T | dbSNP |
| 15 | g.66435083A= | CA2184071726 | MAP2K1 | c.71A= (p.Gln24=) c.137A= (p.Gln46=) n.573A= n.648A= | |
| 15 | g.66435083A>C | CA392929103 | MAP2K1 | c.71A>C (p.Gln24Pro) c.137A>C (p.Gln46Pro) n.573A>C n.648A>C | |
| 15 | g.66435083A>G | CA392929104 | MAP2K1 | c.71A>G (p.Gln24Arg) c.137A>G (p.Gln46Arg) n.573A>G n.648A>G | |
| 15 | g.66435083A>T | CA392929105 | MAP2K1 | c.71A>T (p.Gln24Leu) c.137A>T (p.Gln46Leu) n.573A>T n.648A>T | ClinVar dbSNP |
| 15 | g.66435084del | CA2697549135 | MAP2K1 | c.72del (p.Gln24HisfsTer18) c.138del (p.Gln46HisfsTer18) n.574del n.649del | ClinVar |
| 15 | g.66435084G>A | CA490855913 | MAP2K1 | c.72G>A (p.Gln24=) c.138G>A (p.Gln46=) n.574G>A n.649G>A | dbSNP |
| 15 | g.66435084G>C | CA392929117 | MAP2K1 | c.72G>C (p.Gln24His) c.138G>C (p.Gln46His) n.574G>C n.649G>C | dbSNP |
| 15 | g.66435084G>T | CA392929118 | MAP2K1 | c.72G>T (p.Gln24His) c.138G>T (p.Gln46His) n.574G>T n.649G>T | |
| 15 | g.66435085C>A | CA490855914 | MAP2K1 | c.73C>A (p.Arg25=) c.139C>A (p.Arg47=) n.575C>A n.650C>A | ClinVar dbSNP |
| 15 | g.66435085C= | CA2184071727 | MAP2K1 | c.73C= (p.Arg25=) c.139C= (p.Arg47=) n.575C= n.650C= | |
| 15 | g.66435085C>G | CA392929120 | MAP2K1 | c.73C>G (p.Arg25Gly) c.139C>G (p.Arg47Gly) n.575C>G n.650C>G | dbSNP |
| 15 | g.66435085C>T | CA271640690 | MAP2K1 | c.73C>T (p.Arg25Ter) c.139C>T (p.Arg47Ter) n.575C>T n.650C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435086G>A | CA392929123 | MAP2K1 | c.74G>A (p.Arg25Gln) c.140G>A (p.Arg47Gln) n.576G>A n.651G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.66435086G>C | CA392929127 | MAP2K1 | c.74G>C (p.Arg25Pro) c.140G>C (p.Arg47Pro) n.576G>C n.651G>C | dbSNP |
| 15 | g.66435086G= | CA2184071728 | MAP2K1 | c.74G= (p.Arg25=) c.140G= (p.Arg47=) n.576G= n.651G= | |
| 15 | g.66435086G>T | CA392929125 | MAP2K1 | c.74G>T (p.Arg25Leu) c.140G>T (p.Arg47Leu) n.576G>T n.651G>T | |
| 15 | g.66435087A= | CA2184071729 | MAP2K1 | c.75A= (p.Arg25=) c.141A= (p.Arg47=) n.577A= n.652A= | |
| 15 | g.66435087A>C | CA490855917 | MAP2K1 | c.75A>C (p.Arg25=) c.141A>C (p.Arg47=) n.577A>C n.652A>C | |
| 15 | g.66435087A>G | CA490855916 | MAP2K1 | c.75A>G (p.Arg25=) c.141A>G (p.Arg47=) n.577A>G n.652A>G | dbSNP |
| 15 | g.66435087A>T | CA490855915 | MAP2K1 | c.75A>T (p.Arg25=) c.141A>T (p.Arg47=) n.577A>T n.652A>T | dbSNP |
| 15 | g.66435088A= | CA2184071730 | MAP2K1 | c.76A= (p.Lys26=) c.142A= (p.Lys48=) n.578A= n.653A= | |
| 15 | g.66435088A>C | CA392929129 | MAP2K1 | c.76A>C (p.Lys26Gln) c.142A>C (p.Lys48Gln) n.578A>C n.653A>C | |
| 15 | g.66435088A>G | CA392929133 | MAP2K1 | c.76A>G (p.Lys26Glu) c.142A>G (p.Lys48Glu) n.578A>G n.653A>G | dbSNP |
| 15 | g.66435088A>T | CA392929131 | MAP2K1 | c.76A>T (p.Lys26Ter) c.142A>T (p.Lys48Ter) n.578A>T n.653A>T | dbSNP |
| 15 | g.66435089A>C | CA392929134 | MAP2K1 | c.77A>C (p.Lys26Thr) c.143A>C (p.Lys48Thr) n.579A>C n.654A>C | dbSNP |
| 15 | g.66435089A>G | CA392929136 | MAP2K1 | c.77A>G (p.Lys26Arg) c.143A>G (p.Lys48Arg) n.579A>G n.654A>G | dbSNP |
| 15 | g.66435089A>T | CA392929138 | MAP2K1 | c.77A>T (p.Lys26Met) c.143A>T (p.Lys48Met) n.579A>T n.654A>T | dbSNP |
| 15 | g.66435090G>A | CA490855918 | MAP2K1 | c.78G>A (p.Lys26=) c.144G>A (p.Lys48=) n.580G>A n.655G>A | dbSNP |
| 15 | g.66435090G>C | CA392929139 | MAP2K1 | c.78G>C (p.Lys26Asn) c.144G>C (p.Lys48Asn) n.580G>C n.655G>C | dbSNP |
| 15 | g.66435090G>T | CA392929140 | MAP2K1 | c.78G>T (p.Lys26Asn) c.144G>T (p.Lys48Asn) n.580G>T n.655G>T | |
| 15 | g.66435090_66435091delinsA | CA2695220905 | MAP2K1 | c.78_79delinsA (p.Arg27AlafsTer15) c.144_145delinsA (p.Arg49AlafsTer15) n.580_581delinsA n.655_656delinsA | |
| 15 | g.66435091C>A | CA392929141 | MAP2K1 | c.79C>A (p.Arg27Ser) c.145C>A (p.Arg49Ser) n.581C>A n.656C>A | dbSNP |
| 15 | g.66435091C>G | CA392929143 | MAP2K1 | c.79C>G (p.Arg27Gly) c.145C>G (p.Arg49Gly) n.581C>G n.656C>G | dbSNP |
| 15 | g.66435091C>T | CA392929144 | MAP2K1 | c.79C>T (p.Arg27Cys) c.145C>T (p.Arg49Cys) n.581C>T n.656C>T | dbSNP gnomAD v4 COSMIC |
| 15 | g.66435092G>A | CA271640694 | MAP2K1 | c.80G>A (p.Arg27His) c.146G>A (p.Arg49His) n.582G>A n.657G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.66435092G>C | CA392929148 | MAP2K1 | c.80G>C (p.Arg27Pro) c.146G>C (p.Arg49Pro) n.582G>C n.657G>C | |
| 15 | g.66435092G= | CA2184071731 | MAP2K1 | c.80G= (p.Arg27=) c.146G= (p.Arg49=) n.582G= n.657G= | |
| 15 | g.66435092G>T | CA392929149 | MAP2K1 | c.80G>T (p.Arg27Leu) c.146G>T (p.Arg49Leu) n.582G>T n.657G>T | COSMIC |
| 15 | g.66435093C>A | CA7623876 | MAP2K1 | c.81C>A (p.Arg27=) c.147C>A (p.Arg49=) n.583C>A n.658C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.66435093C= | CA2184071732 | MAP2K1 | c.81C= (p.Arg27=) c.147C= (p.Arg49=) n.583C= n.658C= | |
| 15 | g.66435093C>G | CA490855920 | MAP2K1 | c.81C>G (p.Arg27=) c.147C>G (p.Arg49=) n.583C>G n.658C>G | |
| 15 | g.66435093C>T | CA490855919 | MAP2K1 | c.81C>T (p.Arg27=) c.147C>T (p.Arg49=) n.583C>T n.658C>T | dbSNP |
| 15 | g.66435094C>A | CA392929157 | MAP2K1 | c.82C>A (p.Leu28Ile) c.148C>A (p.Leu50Ile) n.584C>A n.659C>A | dbSNP |
| 15 | g.66435094C= | CA2184071733 | MAP2K1 | c.82C= (p.Leu28=) c.148C= (p.Leu50=) n.584C= n.659C= | |
| 15 | g.66435094C>G | CA392929153 | MAP2K1 | c.82C>G (p.Leu28Val) c.148C>G (p.Leu50Val) n.584C>G n.659C>G | dbSNP |
| 15 | g.66435094C>T | CA392929155 | MAP2K1 | c.82C>T (p.Leu28Phe) c.148C>T (p.Leu50Phe) n.584C>T n.659C>T | dbSNP |
| 15 | g.66435095T>A | CA392929159 | MAP2K1 | c.83T>A (p.Leu28His) c.149T>A (p.Leu50His) n.585T>A n.660T>A | dbSNP |
| 15 | g.66435095T>C | CA392929161 | MAP2K1 | c.83T>C (p.Leu28Pro) c.149T>C (p.Leu50Pro) n.585T>C n.660T>C | ClinVar dbSNP |
| 15 | g.66435095T>G | CA392929163 | MAP2K1 | c.83T>G (p.Leu28Arg) c.149T>G (p.Leu50Arg) n.585T>G n.660T>G | |
| 15 | g.66435096T>A | CA490855921 | MAP2K1 | c.84T>A (p.Leu28=) c.150T>A (p.Leu50=) n.586T>A n.661T>A | |
| 15 | g.66435096T>C | CA490855923 | MAP2K1 | c.84T>C (p.Leu28=) c.150T>C (p.Leu50=) n.586T>C n.661T>C | dbSNP |
| 15 | g.66435096T>G | CA490855922 | MAP2K1 | c.84T>G (p.Leu28=) c.150T>G (p.Leu50=) n.586T>G n.661T>G | |
| 15 | g.66435096T= | CA2184071734 | MAP2K1 | c.84T= (p.Leu28=) c.150T= (p.Leu50=) n.586T= n.661T= | |
| 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 | 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= |