Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.129766800A= | CA1944921593 | MGMT | c.520A= (p.Ile174=) c.427A= (p.Ile143=) c.250A= (p.Ile84=) c.436A= (p.Ile146=) | |
10 | g.129766800A>C | CA378712948 | MGMT | c.520A>C (p.Ile174Leu) c.427A>C (p.Ile143Leu) c.250A>C (p.Ile84Leu) c.436A>C (p.Ile146Leu) | |
10 | g.129766800A>G | CA5748123 | MGMT | c.520A>G (p.Ile174Val) c.427A>G (p.Ile143Val) c.250A>G (p.Ile84Val) c.436A>G (p.Ile146Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.129766800A>T | CA378712949 | MGMT | c.520A>T (p.Ile174Phe) c.427A>T (p.Ile143Phe) c.250A>T (p.Ile84Phe) c.436A>T (p.Ile146Phe) | |
10 | g.129766801T>A | CA378712950 | MGMT | c.521T>A (p.Ile174Asn) c.428T>A (p.Ile143Asn) c.251T>A (p.Ile84Asn) c.437T>A (p.Ile146Asn) | gnomAD v4 |
10 | g.129766801T>C | CA378712951 | MGMT | c.521T>C (p.Ile174Thr) c.428T>C (p.Ile143Thr) c.251T>C (p.Ile84Thr) c.437T>C (p.Ile146Thr) | |
10 | g.129766801T>G | CA378712952 | MGMT | c.521T>G (p.Ile174Ser) c.428T>G (p.Ile143Ser) c.251T>G (p.Ile84Ser) c.437T>G (p.Ile146Ser) | |
10 | g.129766802C>A | CA471816453 | MGMT | c.522C>A (p.Ile174=) c.429C>A (p.Ile143=) c.252C>A (p.Ile84=) c.438C>A (p.Ile146=) | |
10 | g.129766802C= | CA1944921594 | MGMT | c.522C= (p.Ile174=) c.429C= (p.Ile143=) c.252C= (p.Ile84=) c.438C= (p.Ile146=) | |
10 | g.129766802C>G | CA378712953 | MGMT | c.522C>G (p.Ile174Met) c.429C>G (p.Ile143Met) c.252C>G (p.Ile84Met) c.438C>G (p.Ile146Met) | |
10 | g.129766802C>T | CA471816454 | MGMT | c.522C>T (p.Ile174=) c.429C>T (p.Ile143=) c.252C>T (p.Ile84=) c.438C>T (p.Ile146=) | dbSNP gnomAD v3 gnomAD v4 |
10 | g.129766803C>A | CA378712954 | MGMT | c.523C>A (p.Pro175Thr) c.430C>A (p.Pro144Thr) c.253C>A (p.Pro85Thr) c.439C>A (p.Pro147Thr) | |
10 | g.129766803C= | CA1944921595 | MGMT | c.523C= (p.Pro175=) c.430C= (p.Pro144=) c.253C= (p.Pro85=) c.439C= (p.Pro147=) | |
10 | g.129766803C>G | CA378712955 | MGMT | c.523C>G (p.Pro175Ala) c.430C>G (p.Pro144Ala) c.253C>G (p.Pro85Ala) c.439C>G (p.Pro147Ala) | dbSNP |
10 | g.129766803C>T | CA378712956 | MGMT | c.523C>T (p.Pro175Ser) c.430C>T (p.Pro144Ser) c.253C>T (p.Pro85Ser) c.439C>T (p.Pro147Ser) | COSMIC COSMIC |
10 | g.129766804C>A | CA378712957 | MGMT | c.524C>A (p.Pro175Gln) c.431C>A (p.Pro144Gln) c.254C>A (p.Pro85Gln) c.440C>A (p.Pro147Gln) | gnomAD v4 |
10 | g.129766804C= | CA1944921596 | MGMT | c.524C= (p.Pro175=) c.431C= (p.Pro144=) c.254C= (p.Pro85=) c.440C= (p.Pro147=) | |
10 | g.129766804C>G | CA5748125 | MGMT | c.524C>G (p.Pro175Arg) c.431C>G (p.Pro144Arg) c.254C>G (p.Pro85Arg) c.440C>G (p.Pro147Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.129766804C>T | CA5748124 | MGMT | c.524C>T (p.Pro175Leu) c.431C>T (p.Pro144Leu) c.254C>T (p.Pro85Leu) c.440C>T (p.Pro147Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
10 | g.129766805G>A | CA5748126 | MGMT | c.525G>A (p.Pro175=) c.432G>A (p.Pro144=) c.255G>A (p.Pro85=) c.441G>A (p.Pro147=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.129766805G>C | CA471816455 | MGMT | c.525G>C (p.Pro175=) c.432G>C (p.Pro144=) c.255G>C (p.Pro85=) c.441G>C (p.Pro147=) | |
10 | g.129766805G= | CA1944921597 | MGMT | c.525G= (p.Pro175=) c.432G= (p.Pro144=) c.255G= (p.Pro85=) c.441G= (p.Pro147=) | |
10 | g.129766805G>T | CA471816456 | MGMT | c.525G>T (p.Pro175=) c.432G>T (p.Pro144=) c.255G>T (p.Pro85=) c.441G>T (p.Pro147=) | |
10 | g.129766806T>A | CA378712958 | MGMT | c.526T>A (p.Cys176Ser) c.433T>A (p.Cys145Ser) c.256T>A (p.Cys86Ser) c.442T>A (p.Cys148Ser) | |
10 | g.129766806T>C | CA378712960 | MGMT | c.526T>C (p.Cys176Arg) c.433T>C (p.Cys145Arg) c.256T>C (p.Cys86Arg) c.442T>C (p.Cys148Arg) | |
10 | g.129766806T>G | CA378712959 | MGMT | c.526T>G (p.Cys176Gly) c.433T>G (p.Cys145Gly) c.256T>G (p.Cys86Gly) c.442T>G (p.Cys148Gly) | |
10 | g.129766807G>A | CA378712961 | MGMT | c.527G>A (p.Cys176Tyr) c.434G>A (p.Cys145Tyr) c.257G>A (p.Cys86Tyr) c.443G>A (p.Cys148Tyr) | |
10 | g.129766807G>C | CA378712962 | MGMT | c.527G>C (p.Cys176Ser) c.434G>C (p.Cys145Ser) c.257G>C (p.Cys86Ser) c.443G>C (p.Cys148Ser) | |
10 | g.129766807G>T | CA378712963 | MGMT | c.527G>T (p.Cys176Phe) c.434G>T (p.Cys145Phe) c.257G>T (p.Cys86Phe) c.443G>T (p.Cys148Phe) | |
10 | g.129766808C>A | CA378712964 | MGMT | c.528C>A (p.Cys176Ter) c.435C>A (p.Cys145Ter) c.258C>A (p.Cys86Ter) c.444C>A (p.Cys148Ter) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
10 | g.129766808C= | CA1944921598 | MGMT | c.528C= (p.Cys176=) c.435C= (p.Cys145=) c.258C= (p.Cys86=) c.444C= (p.Cys148=) | |
10 | g.129766808C>G | CA378712965 | MGMT | c.528C>G (p.Cys176Trp) c.435C>G (p.Cys145Trp) c.258C>G (p.Cys86Trp) c.444C>G (p.Cys148Trp) | |
10 | g.129766808C>T | CA471816457 | MGMT | c.528C>T (p.Cys176=) c.435C>T (p.Cys145=) c.258C>T (p.Cys86=) c.444C>T (p.Cys148=) | |
10 | g.129766809C>A | CA378712966 | MGMT | c.529C>A (p.His177Asn) c.436C>A (p.His146Asn) c.259C>A (p.His87Asn) c.445C>A (p.His149Asn) | |
10 | g.129766809C= | CA1944921599 | MGMT | c.529C= (p.His177=) c.436C= (p.His146=) c.259C= (p.His87=) c.445C= (p.His149=) | |
10 | g.129766809C>G | CA378712967 | MGMT | c.529C>G (p.His177Asp) c.436C>G (p.His146Asp) c.259C>G (p.His87Asp) c.445C>G (p.His149Asp) | COSMIC |
10 | g.129766809C>T | CA378712968 | MGMT | c.529C>T (p.His177Tyr) c.436C>T (p.His146Tyr) c.259C>T (p.His87Tyr) c.445C>T (p.His149Tyr) | dbSNP gnomAD v4 |
10 | g.129766810A>C | CA378712969 | MGMT | c.530A>C (p.His177Pro) c.437A>C (p.His146Pro) c.260A>C (p.His87Pro) c.446A>C (p.His149Pro) | |
10 | g.129766810A>G | CA378712971 | MGMT | c.530A>G (p.His177Arg) c.437A>G (p.His146Arg) c.260A>G (p.His87Arg) c.446A>G (p.His149Arg) | |
10 | g.129766810A>T | CA378712970 | MGMT | c.530A>T (p.His177Leu) c.437A>T (p.His146Leu) c.260A>T (p.His87Leu) c.446A>T (p.His149Leu) | |
10 | g.129766811C>A | CA378712972 | MGMT | c.531C>A (p.His177Gln) c.438C>A (p.His146Gln) c.261C>A (p.His87Gln) c.447C>A (p.His149Gln) | |
10 | g.129766811C>G | CA378712973 | MGMT | c.531C>G (p.His177Gln) c.438C>G (p.His146Gln) c.261C>G (p.His87Gln) c.447C>G (p.His149Gln) | |
10 | g.129766811C>T | CA471816458 | MGMT | c.531C>T (p.His177=) c.438C>T (p.His146=) c.261C>T (p.His87=) c.447C>T (p.His149=) | |
10 | g.129766812A>C | CA471816459 | MGMT | c.532A>C (p.Arg178=) c.439A>C (p.Arg147=) c.262A>C (p.Arg88=) c.448A>C (p.Arg150=) | |
10 | g.129766812A>G | CA378712974 | MGMT | c.532A>G (p.Arg178Gly) c.439A>G (p.Arg147Gly) c.262A>G (p.Arg88Gly) c.448A>G (p.Arg150Gly) | gnomAD v4 |
10 | g.129766812A>T | CA378712975 | MGMT | c.532A>T (p.Arg178Ter) c.439A>T (p.Arg147Ter) c.262A>T (p.Arg88Ter) c.448A>T (p.Arg150Ter) | |
10 | g.129766813G>A | CA378712976 | MGMT | c.533G>A (p.Arg178Lys) c.440G>A (p.Arg147Lys) c.263G>A (p.Arg88Lys) c.449G>A (p.Arg150Lys) | |
10 | g.129766813G>C | CA378712978 | MGMT | c.533G>C (p.Arg178Thr) c.440G>C (p.Arg147Thr) c.263G>C (p.Arg88Thr) c.449G>C (p.Arg150Thr) | gnomAD v4 |
10 | g.129766813G>T | CA378712977 | MGMT | c.533G>T (p.Arg178Ile) c.440G>T (p.Arg147Ile) c.263G>T (p.Arg88Ile) c.449G>T (p.Arg150Ile) | gnomAD v4 |
10 | g.129766814A>C | CA378712979 | MGMT | c.534A>C (p.Arg178Ser) c.441A>C (p.Arg147Ser) c.264A>C (p.Arg88Ser) c.450A>C (p.Arg150Ser) |