Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.4110576G>A | CA9091012 | MAP2K2 | n.822C>T c.383C>T (p.Pro128Leu) c.92C>T (p.Pro31Leu) n.580C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
19 | g.4110576G>C | CA180731 | MAP2K2 | n.822C>G c.383C>G (p.Pro128Arg) c.92C>G (p.Pro31Arg) n.580C>G | ClinVar dbSNP |
19 | g.4110576G= | CA2319230228 | MAP2K2 | n.822C= c.383C= (p.Pro128=) c.92C= (p.Pro31=) n.580C= | |
19 | g.4110576G>T | CA279962 | MAP2K2 | n.822C>A c.383C>A (p.Pro128Gln) c.92C>A (p.Pro31Gln) n.580C>A | ClinVar dbSNP |
19 | g.4110577del | CA2585249275 | MAP2K2 | n.822del c.383del (p.Pro128ArgfsTer?) c.92del (p.Pro31ArgfsTer?) n.580del | gnomAD v4 |
19 | g.4110577G>A | CA403391477 | MAP2K2 | n.821C>T c.382C>T (p.Pro128Ser) c.91C>T (p.Pro31Ser) n.579C>T | dbSNP gnomAD v4 |
19 | g.4110577G>C | CA403391479 | MAP2K2 | n.821C>G c.382C>G (p.Pro128Ala) c.91C>G (p.Pro31Ala) n.579C>G | dbSNP |
19 | g.4110577G>T | CA403391481 | MAP2K2 | n.821C>A c.382C>A (p.Pro128Thr) c.91C>A (p.Pro31Thr) n.579C>A | |
19 | g.4110578C>A | CA9091014 | MAP2K2 | n.820G>T c.381G>T (p.Ser127=) c.90G>T (p.Ser30=) n.578G>T | dbSNP ExAC |
19 | g.4110578C= | CA2319230238 | MAP2K2 | n.820G= c.381G= (p.Ser127=) c.90G= (p.Ser30=) n.578G= | |
19 | g.4110578C>G | CA504987500 | MAP2K2 | n.820G>C c.381G>C (p.Ser127=) c.90G>C (p.Ser30=) n.578G>C | dbSNP |
19 | g.4110578C>T | CA9091013 | MAP2K2 | n.820G>A c.381G>A (p.Ser127=) c.90G>A (p.Ser30=) n.578G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.4110579G>A | CA403391488 | MAP2K2 | n.819C>T c.380C>T (p.Ser127Leu) c.89C>T (p.Ser30Leu) n.577C>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
19 | g.4110579G>C | CA403391490 | MAP2K2 | n.819C>G c.380C>G (p.Ser127Trp) c.89C>G (p.Ser30Trp) n.577C>G | dbSNP |
19 | g.4110579G= | CA2319230243 | MAP2K2 | n.819C= c.380C= (p.Ser127=) c.89C= (p.Ser30=) n.577C= | |
19 | g.4110579G>T | CA403391486 | MAP2K2 | n.819C>A c.380C>A (p.Ser127Ter) c.89C>A (p.Ser30Ter) n.577C>A | dbSNP gnomAD v4 |
19 | g.4110580A>C | CA403391493 | MAP2K2 | n.818T>G c.379T>G (p.Ser127Ala) c.88T>G (p.Ser30Ala) n.576T>G | |
19 | g.4110580A>G | CA403391495 | MAP2K2 | n.818T>C c.379T>C (p.Ser127Pro) c.88T>C (p.Ser30Pro) n.576T>C | dbSNP |
19 | g.4110580A>T | CA403391497 | MAP2K2 | n.818T>A c.379T>A (p.Ser127Thr) c.88T>A (p.Ser30Thr) n.576T>A | dbSNP gnomAD v4 |
19 | g.4110581G>A | CA504987502 | MAP2K2 | n.817C>T c.378C>T (p.Asn126=) c.87C>T (p.Asn29=) n.575C>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.4110581G>C | CA403391499 | MAP2K2 | n.817C>G c.378C>G (p.Asn126Lys) c.87C>G (p.Asn29Lys) n.575C>G | dbSNP |
19 | g.4110581G= | CA2319230248 | MAP2K2 | n.817C= c.378C= (p.Asn126=) c.87C= (p.Asn29=) n.575C= | |
19 | g.4110581G>T | CA403391500 | MAP2K2 | n.817C>A c.378C>A (p.Asn126Lys) c.87C>A (p.Asn29Lys) n.575C>A | |
19 | g.4110582T>A | CA403391503 | MAP2K2 | n.816A>T c.377A>T (p.Asn126Ile) c.86A>T (p.Asn29Ile) n.574A>T | dbSNP |
19 | g.4110582T>C | CA403391504 | MAP2K2 | n.816A>G c.377A>G (p.Asn126Ser) c.86A>G (p.Asn29Ser) n.574A>G | ClinVar gnomAD v4 |
19 | g.4110582T>G | CA403391506 | MAP2K2 | n.816A>C c.377A>C (p.Asn126Thr) c.86A>C (p.Asn29Thr) n.574A>C | dbSNP |
19 | g.4110583T>A | CA403391508 | MAP2K2 | n.815A>T c.376A>T (p.Asn126Tyr) c.85A>T (p.Asn29Tyr) n.573A>T | |
19 | g.4110583T>C | CA16602631 | MAP2K2 | n.815A>G c.376A>G (p.Asn126Asp) c.85A>G (p.Asn29Asp) n.573A>G | ClinVar dbSNP COSMIC COSMIC |
19 | g.4110583T>G | CA403391510 | MAP2K2 | n.815A>C c.376A>C (p.Asn126His) c.85A>C (p.Asn29His) n.573A>C | ClinVar dbSNP gnomAD v4 |
19 | g.4110583T= | CA2319230252 | MAP2K2 | n.815A= c.376A= (p.Asn126=) c.85A= (p.Asn29=) n.573A= | |
19 | g.4110584G>A | CA504987503 | MAP2K2 | n.814C>T c.375C>T (p.Cys125=) c.84C>T (p.Cys28=) n.572C>T | dbSNP COSMIC COSMIC |
19 | g.4110584G>C | CA403391512 | MAP2K2 | n.814C>G c.375C>G (p.Cys125Trp) c.84C>G (p.Cys28Trp) n.572C>G | dbSNP |
19 | g.4110584G>T | CA403391514 | MAP2K2 | n.814C>A c.375C>A (p.Cys125Ter) c.84C>A (p.Cys28Ter) n.572C>A | |
19 | g.4110585C>A | CA403391521 | MAP2K2 | n.813G>T c.374G>T (p.Cys125Phe) c.83G>T (p.Cys28Phe) n.571G>T | |
19 | g.4110585C>G | CA403391519 | MAP2K2 | n.813G>C c.374G>C (p.Cys125Ser) c.83G>C (p.Cys28Ser) n.571G>C | COSMIC |
19 | g.4110585C>T | CA403391517 | MAP2K2 | n.813G>A c.374G>A (p.Cys125Tyr) c.83G>A (p.Cys28Tyr) n.571G>A | |
19 | g.4110586A= | CA2319230261 | MAP2K2 | n.812T= c.373T= (p.Cys125=) c.82T= (p.Cys28=) n.570T= | |
19 | g.4110586A>C | CA403391522 | MAP2K2 | n.812T>G c.373T>G (p.Cys125Gly) c.82T>G (p.Cys28Gly) n.570T>G | dbSNP |
19 | g.4110586A>G | CA403391525 | MAP2K2 | n.812T>C c.373T>C (p.Cys125Arg) c.82T>C (p.Cys28Arg) n.570T>C | |
19 | g.4110586A>T | CA16602632 | MAP2K2 | n.812T>A c.373T>A (p.Cys125Ser) c.82T>A (p.Cys28Ser) n.570T>A | ClinVar dbSNP COSMIC COSMIC |
19 | g.4110587T>A | CA403391528 | MAP2K2 | n.811A>T c.372A>T (p.Glu124Asp) c.81A>T (p.Glu27Asp) n.569A>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.4110587T>C | CA504987504 | MAP2K2 | n.811A>G c.372A>G (p.Glu124=) c.81A>G (p.Glu27=) n.569A>G | |
19 | g.4110587T>G | CA403391529 | MAP2K2 | n.811A>C c.372A>C (p.Glu124Asp) c.81A>C (p.Glu27Asp) n.569A>C | dbSNP |
19 | g.4110587T= | CA2319230269 | MAP2K2 | n.811A= c.372A= (p.Glu124=) c.81A= (p.Glu27=) n.569A= | |
19 | g.4110588T>A | CA403391531 | MAP2K2 | n.810A>T c.371A>T (p.Glu124Val) c.80A>T (p.Glu27Val) n.568A>T | |
19 | g.4110588T>C | CA9091015 | MAP2K2 | n.810A>G c.371A>G (p.Glu124Gly) c.80A>G (p.Glu27Gly) n.568A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.4110588T>G | CA403391534 | MAP2K2 | n.810A>C c.371A>C (p.Glu124Ala) c.80A>C (p.Glu27Ala) n.568A>C | |
19 | g.4110588T= | CA2319230272 | MAP2K2 | n.810A= c.371A= (p.Glu124=) c.80A= (p.Glu27=) n.568A= | |
19 | g.4110589C>A | CA403391536 | MAP2K2 | n.809G>T c.370G>T (p.Glu124Ter) c.79G>T (p.Glu27Ter) n.567G>T | dbSNP |
19 | g.4110589C= | CA2319230275 | MAP2K2 | n.809G= c.370G= (p.Glu124=) c.79G= (p.Glu27=) n.567G= |