| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66435071_66435118del | CA645570529 | MAP2K1 | c.59_106del (p.Leu20_Lys35del) c.125_172del (p.Leu42_Lys57del) n.561_608del n.636_683del | COSMIC |
| 15 | g.66435076_66435108del | CA2573151054 | MAP2K1 | c.64_96del (p.Glu22_Leu32del) c.130_162del (p.Glu44_Leu54del) n.566_598del n.641_673del | ClinVar dbSNP |
| 15 | g.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 | |
| 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= |