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.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.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 |