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.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.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 |