| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66435057G>A | CA490855899 | MAP2K1 | c.45G>A (p.Leu15=) c.111G>A (p.Leu37=) n.547G>A n.622G>A | dbSNP |
| 15 | g.66435057G>C | CA490855900 | MAP2K1 | c.45G>C (p.Leu15=) c.111G>C (p.Leu37=) n.547G>C n.622G>C | dbSNP |
| 15 | g.66435057G>T | CA490855898 | MAP2K1 | c.45G>T (p.Leu15=) c.111G>T (p.Leu37=) n.547G>T n.622G>T | dbSNP |
| 15 | g.66435058G>A | CA392928993 | MAP2K1 | c.46G>A (p.Glu16Lys) c.112G>A (p.Glu38Lys) n.548G>A n.623G>A | dbSNP |
| 15 | g.66435058G>C | CA392928994 | MAP2K1 | c.46G>C (p.Glu16Gln) c.112G>C (p.Glu38Gln) n.548G>C n.623G>C | dbSNP |
| 15 | g.66435058G>T | CA392928996 | MAP2K1 | c.46G>T (p.Glu16Ter) c.112G>T (p.Glu38Ter) n.548G>T n.623G>T | dbSNP |
| 15 | g.66435059del | CA2563258997 | MAP2K1 | c.47del (p.Glu16GlyfsTer3) c.113del (p.Glu38GlyfsTer3) n.549del n.624del | |
| 15 | g.66435059A>C | CA392928998 | MAP2K1 | c.47A>C (p.Glu16Ala) c.113A>C (p.Glu38Ala) n.549A>C n.624A>C | |
| 15 | g.66435059A>G | CA392929000 | MAP2K1 | c.47A>G (p.Glu16Gly) c.113A>G (p.Glu38Gly) n.549A>G n.624A>G | dbSNP |
| 15 | g.66435059A>T | CA392929001 | MAP2K1 | c.47A>T (p.Glu16Val) c.113A>T (p.Glu38Val) n.549A>T n.624A>T | dbSNP |
| 15 | g.66435060G>A | CA490855901 | MAP2K1 | c.48G>A (p.Glu16=) c.114G>A (p.Glu38=) n.550G>A n.625G>A | dbSNP |
| 15 | g.66435060G>C | CA392929003 | MAP2K1 | c.48G>C (p.Glu16Asp) c.114G>C (p.Glu38Asp) n.550G>C n.625G>C | dbSNP |
| 15 | g.66435060G>T | CA392929004 | MAP2K1 | c.48G>T (p.Glu16Asp) c.114G>T (p.Glu38Asp) n.550G>T n.625G>T | |
| 15 | g.66435061G>A | CA392929005 | MAP2K1 | c.49G>A (p.Glu17Lys) c.115G>A (p.Glu39Lys) n.551G>A n.626G>A | dbSNP |
| 15 | g.66435061G>C | CA392929008 | MAP2K1 | c.49G>C (p.Glu17Gln) c.115G>C (p.Glu39Gln) n.551G>C n.626G>C | dbSNP |
| 15 | g.66435061G>T | CA392929006 | MAP2K1 | c.49G>T (p.Glu17Ter) c.115G>T (p.Glu39Ter) n.551G>T n.626G>T | |
| 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 |