Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.129766811C>ACA378712972MGMTc.531C>A (p.His177Gln)
c.438C>A (p.His146Gln)
c.261C>A (p.His87Gln)
c.447C>A (p.His149Gln)
10g.129766811C>GCA378712973MGMTc.531C>G (p.His177Gln)
c.438C>G (p.His146Gln)
c.261C>G (p.His87Gln)
c.447C>G (p.His149Gln)
10g.129766811C>TCA471816458MGMTc.531C>T (p.His177=)
c.438C>T (p.His146=)
c.261C>T (p.His87=)
c.447C>T (p.His149=)
10g.129766812A>CCA471816459MGMTc.532A>C (p.Arg178=)
c.439A>C (p.Arg147=)
c.262A>C (p.Arg88=)
c.448A>C (p.Arg150=)
10g.129766812A>GCA378712974MGMTc.532A>G (p.Arg178Gly)
c.439A>G (p.Arg147Gly)
c.262A>G (p.Arg88Gly)
c.448A>G (p.Arg150Gly)
 gnomAD v4
10g.129766812A>TCA378712975MGMTc.532A>T (p.Arg178Ter)
c.439A>T (p.Arg147Ter)
c.262A>T (p.Arg88Ter)
c.448A>T (p.Arg150Ter)
10g.129766813G>ACA378712976MGMTc.533G>A (p.Arg178Lys)
c.440G>A (p.Arg147Lys)
c.263G>A (p.Arg88Lys)
c.449G>A (p.Arg150Lys)
10g.129766813G>CCA378712978MGMTc.533G>C (p.Arg178Thr)
c.440G>C (p.Arg147Thr)
c.263G>C (p.Arg88Thr)
c.449G>C (p.Arg150Thr)
 gnomAD v4
10g.129766813G>TCA378712977MGMTc.533G>T (p.Arg178Ile)
c.440G>T (p.Arg147Ile)
c.263G>T (p.Arg88Ile)
c.449G>T (p.Arg150Ile)
 gnomAD v4
10g.129766814A>CCA378712979MGMTc.534A>C (p.Arg178Ser)
c.441A>C (p.Arg147Ser)
c.264A>C (p.Arg88Ser)
c.450A>C (p.Arg150Ser)
10g.129766814A>GCA471816461MGMTc.534A>G (p.Arg178=)
c.441A>G (p.Arg147=)
c.264A>G (p.Arg88=)
c.450A>G (p.Arg150=)
10g.129766814A>TCA378712980MGMTc.534A>T (p.Arg178Ser)
c.441A>T (p.Arg147Ser)
c.264A>T (p.Arg88Ser)
c.450A>T (p.Arg150Ser)
10g.129766815G>ACA5748127MGMTc.535G>A (p.Val179Met)
c.442G>A (p.Val148Met)
c.265G>A (p.Val89Met)
c.451G>A (p.Val151Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766815G>CCA378712981MGMTc.535G>C (p.Val179Leu)
c.442G>C (p.Val148Leu)
c.265G>C (p.Val89Leu)
c.451G>C (p.Val151Leu)
10g.129766815G=CA1944921600MGMTc.535G= (p.Val179=)
c.442G= (p.Val148=)
c.265G= (p.Val89=)
c.451G= (p.Val151=)
10g.129766815G>TCA378712982MGMTc.535G>T (p.Val179Leu)
c.442G>T (p.Val148Leu)
c.265G>T (p.Val89Leu)
c.451G>T (p.Val151Leu)
 gnomAD v4
10g.129766816_129766817dupCA2574707796MGMTc.536_537dup (p.Val180TrpfsTer17)
c.443_444dup (p.Val149TrpfsTer17)
c.266_267dup (p.Val90TrpfsTer17)
c.452_453dup (p.Val152TrpfsTer17)
10g.129766816T>ACA378712983MGMTc.536T>A (p.Val179Glu)
c.443T>A (p.Val148Glu)
c.266T>A (p.Val89Glu)
c.452T>A (p.Val151Glu)
10g.129766816T>CCA378712984MGMTc.536T>C (p.Val179Ala)
c.443T>C (p.Val148Ala)
c.266T>C (p.Val89Ala)
c.452T>C (p.Val151Ala)
 gnomAD v4
10g.129766816T>GCA378712985MGMTc.536T>G (p.Val179Gly)
c.443T>G (p.Val148Gly)
c.266T>G (p.Val89Gly)
c.452T>G (p.Val151Gly)
10g.129766817G>ACA471816463MGMTc.537G>A (p.Val179=)
c.444G>A (p.Val148=)
c.267G>A (p.Val89=)
c.453G>A (p.Val151=)
 dbSNP gnomAD v3 gnomAD v4
10g.129766817G>CCA471816464MGMTc.537G>C (p.Val179=)
c.444G>C (p.Val148=)
c.267G>C (p.Val89=)
c.453G>C (p.Val151=)
 dbSNP
10g.129766817G=CA1944921601MGMTc.537G= (p.Val179=)
c.444G= (p.Val148=)
c.267G= (p.Val89=)
c.453G= (p.Val151=)
10g.129766817G>TCA471816466MGMTc.537G>T (p.Val179=)
c.444G>T (p.Val148=)
c.267G>T (p.Val89=)
c.453G>T (p.Val151=)
 gnomAD v4 COSMIC COSMIC
10g.129766818G>ACA378712986MGMTc.538G>A (p.Val180Ile)
c.445G>A (p.Val149Ile)
c.268G>A (p.Val90Ile)
c.454G>A (p.Val152Ile)
10g.129766818G>CCA378712987MGMTc.538G>C (p.Val180Leu)
c.445G>C (p.Val149Leu)
c.268G>C (p.Val90Leu)
c.454G>C (p.Val152Leu)
10g.129766818G>TCA378712988MGMTc.538G>T (p.Val180Phe)
c.445G>T (p.Val149Phe)
c.268G>T (p.Val90Phe)
c.454G>T (p.Val152Phe)
 gnomAD v4 COSMIC COSMIC
10g.129766819T>ACA378712991MGMTc.539T>A (p.Val180Asp)
c.446T>A (p.Val149Asp)
c.269T>A (p.Val90Asp)
c.455T>A (p.Val152Asp)
10g.129766819T>CCA378712989MGMTc.539T>C (p.Val180Ala)
c.446T>C (p.Val149Ala)
c.269T>C (p.Val90Ala)
c.455T>C (p.Val152Ala)
10g.129766819T>GCA378712990MGMTc.539T>G (p.Val180Gly)
c.446T>G (p.Val149Gly)
c.269T>G (p.Val90Gly)
c.455T>G (p.Val152Gly)
10g.129766820C>ACA471816469MGMTc.540C>A (p.Val180=)
c.447C>A (p.Val149=)
c.270C>A (p.Val90=)
c.456C>A (p.Val152=)
10g.129766820C>GCA471816470MGMTc.540C>G (p.Val180=)
c.447C>G (p.Val149=)
c.270C>G (p.Val90=)
c.456C>G (p.Val152=)
10g.129766820C>TCA471816471MGMTc.540C>T (p.Val180=)
c.447C>T (p.Val149=)
c.270C>T (p.Val90=)
c.456C>T (p.Val152=)
10g.129766821T>ACA378712992MGMTc.541T>A (p.Cys181Ser)
c.448T>A (p.Cys150Ser)
c.271T>A (p.Cys91Ser)
c.457T>A (p.Cys153Ser)
10g.129766821T>CCA378712993MGMTc.541T>C (p.Cys181Arg)
c.448T>C (p.Cys150Arg)
c.271T>C (p.Cys91Arg)
c.457T>C (p.Cys153Arg)
10g.129766821T>GCA378712994MGMTc.541T>G (p.Cys181Gly)
c.448T>G (p.Cys150Gly)
c.271T>G (p.Cys91Gly)
c.457T>G (p.Cys153Gly)
10g.129766822G>ACA378712995MGMTc.542G>A (p.Cys181Tyr)
c.449G>A (p.Cys150Tyr)
c.272G>A (p.Cys91Tyr)
c.458G>A (p.Cys153Tyr)
10g.129766822G>CCA378712996MGMTc.542G>C (p.Cys181Ser)
c.449G>C (p.Cys150Ser)
c.272G>C (p.Cys91Ser)
c.458G>C (p.Cys153Ser)
10g.129766822G>TCA378712997MGMTc.542G>T (p.Cys181Phe)
c.449G>T (p.Cys150Phe)
c.272G>T (p.Cys91Phe)
c.458G>T (p.Cys153Phe)
10g.129766823C>ACA378712998MGMTc.543C>A (p.Cys181Ter)
c.450C>A (p.Cys150Ter)
c.273C>A (p.Cys91Ter)
c.459C>A (p.Cys153Ter)
10g.129766823C=CA1944921602MGMTc.543C= (p.Cys181=)
c.450C= (p.Cys150=)
c.273C= (p.Cys91=)
c.459C= (p.Cys153=)
10g.129766823C>GCA378712999MGMTc.543C>G (p.Cys181Trp)
c.450C>G (p.Cys150Trp)
c.273C>G (p.Cys91Trp)
c.459C>G (p.Cys153Trp)
10g.129766823C>TCA5748128MGMTc.543C>T (p.Cys181=)
c.450C>T (p.Cys150=)
c.273C>T (p.Cys91=)
c.459C>T (p.Cys153=)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766824A=CA1944921603MGMTc.544A= (p.Ser182=)
c.451A= (p.Ser151=)
c.274A= (p.Ser92=)
c.460A= (p.Ser154=)
10g.129766824A>CCA378713000MGMTc.544A>C (p.Ser182Arg)
c.451A>C (p.Ser151Arg)
c.274A>C (p.Ser92Arg)
c.460A>C (p.Ser154Arg)
10g.129766824A>GCA378713001MGMTc.544A>G (p.Ser182Gly)
c.451A>G (p.Ser151Gly)
c.274A>G (p.Ser92Gly)
c.460A>G (p.Ser154Gly)
 dbSNP gnomAD v2 gnomAD v4
10g.129766824A>TCA378713002MGMTc.544A>T (p.Ser182Cys)
c.451A>T (p.Ser151Cys)
c.274A>T (p.Ser92Cys)
c.460A>T (p.Ser154Cys)
10g.129766825G>ACA378713005MGMTc.545G>A (p.Ser182Asn)
c.452G>A (p.Ser151Asn)
c.275G>A (p.Ser92Asn)
c.461G>A (p.Ser154Asn)
 COSMIC COSMIC
10g.129766825G>CCA378713004MGMTc.545G>C (p.Ser182Thr)
c.452G>C (p.Ser151Thr)
c.275G>C (p.Ser92Thr)
c.461G>C (p.Ser154Thr)
10g.129766825G>TCA378713003MGMTc.545G>T (p.Ser182Ile)
c.452G>T (p.Ser151Ile)
c.275G>T (p.Ser92Ile)
c.461G>T (p.Ser154Ile)
10g.129766826C>ACA215499774MGMTc.546C>A (p.Ser182Arg)
c.453C>A (p.Ser151Arg)
c.276C>A (p.Ser92Arg)
c.462C>A (p.Ser154Arg)
 dbSNP
10g.129766826C=CA1944921604MGMTc.546C= (p.Ser182=)
c.453C= (p.Ser151=)
c.276C= (p.Ser92=)
c.462C= (p.Ser154=)
10g.129766826C>GCA378713006MGMTc.546C>G (p.Ser182Arg)
c.453C>G (p.Ser151Arg)
c.276C>G (p.Ser92Arg)
c.462C>G (p.Ser154Arg)
10g.129766826C>TCA471816476MGMTc.546C>T (p.Ser182=)
c.453C>T (p.Ser151=)
c.276C>T (p.Ser92=)
c.462C>T (p.Ser154=)
 dbSNP gnomAD v4
10g.129766827A>CCA378713007MGMTc.547A>C (p.Ser183Arg)
c.454A>C (p.Ser152Arg)
c.277A>C (p.Ser93Arg)
c.463A>C (p.Ser155Arg)
10g.129766827A>GCA378713008MGMTc.547A>G (p.Ser183Gly)
c.454A>G (p.Ser152Gly)
c.277A>G (p.Ser93Gly)
c.463A>G (p.Ser155Gly)
10g.129766827A>TCA378713009MGMTc.547A>T (p.Ser183Cys)
c.454A>T (p.Ser152Cys)
c.277A>T (p.Ser93Cys)
c.463A>T (p.Ser155Cys)
10g.129766828G>ACA5748129MGMTc.548G>A (p.Ser183Asn)
c.455G>A (p.Ser152Asn)
c.278G>A (p.Ser93Asn)
c.464G>A (p.Ser155Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766828G>CCA378713010MGMTc.548G>C (p.Ser183Thr)
c.455G>C (p.Ser152Thr)
c.278G>C (p.Ser93Thr)
c.464G>C (p.Ser155Thr)
10g.129766828G=CA1944921605MGMTc.548G= (p.Ser183=)
c.455G= (p.Ser152=)
c.278G= (p.Ser93=)
c.464G= (p.Ser155=)
10g.129766828G>TCA378713011MGMTc.548G>T (p.Ser183Ile)
c.455G>T (p.Ser152Ile)
c.278G>T (p.Ser93Ile)
c.464G>T (p.Ser155Ile)
10g.129766829C>ACA378713012MGMTc.549C>A (p.Ser183Arg)
c.456C>A (p.Ser152Arg)
c.279C>A (p.Ser93Arg)
c.465C>A (p.Ser155Arg)
10g.129766829C=CA1944921606MGMTc.549C= (p.Ser183=)
c.456C= (p.Ser152=)
c.279C= (p.Ser93=)
c.465C= (p.Ser155=)
10g.129766829C>GCA378713013MGMTc.549C>G (p.Ser183Arg)
c.456C>G (p.Ser152Arg)
c.279C>G (p.Ser93Arg)
c.465C>G (p.Ser155Arg)
10g.129766829C>TCA471816479MGMTc.549C>T (p.Ser183=)
c.456C>T (p.Ser152=)
c.279C>T (p.Ser93=)
c.465C>T (p.Ser155=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
10g.129766830G>ACA5748130MGMTc.550G>A (p.Gly184Arg)
c.457G>A (p.Gly153Arg)
c.280G>A (p.Gly94Arg)
c.466G>A (p.Gly156Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766830G>CCA378713014MGMTc.550G>C (p.Gly184Arg)
c.457G>C (p.Gly153Arg)
c.280G>C (p.Gly94Arg)
c.466G>C (p.Gly156Arg)
10g.129766830G=CA1944921607MGMTc.550G= (p.Gly184=)
c.457G= (p.Gly153=)
c.280G= (p.Gly94=)
c.466G= (p.Gly156=)
10g.129766830G>TCA378713015MGMTc.550G>T (p.Gly184Ter)
c.457G>T (p.Gly153Ter)
c.280G>T (p.Gly94Ter)
c.466G>T (p.Gly156Ter)
 gnomAD v4
10g.129766831G>ACA378713017MGMTc.551G>A (p.Gly184Glu)
c.458G>A (p.Gly153Glu)
c.281G>A (p.Gly94Glu)
c.467G>A (p.Gly156Glu)
10g.129766831G>CCA378713018MGMTc.551G>C (p.Gly184Ala)
c.458G>C (p.Gly153Ala)
c.281G>C (p.Gly94Ala)
c.467G>C (p.Gly156Ala)
10g.129766831G>TCA378713016MGMTc.551G>T (p.Gly184Val)
c.458G>T (p.Gly153Val)
c.281G>T (p.Gly94Val)
c.467G>T (p.Gly156Val)
10g.129766832A=CA1944921608MGMTc.552A= (p.Gly184=)
c.459A= (p.Gly153=)
c.282A= (p.Gly94=)
c.468A= (p.Gly156=)
10g.129766832A>CCA471816482MGMTc.552A>C (p.Gly184=)
c.459A>C (p.Gly153=)
c.282A>C (p.Gly94=)
c.468A>C (p.Gly156=)
10g.129766832A>GCA5748131MGMTc.552A>G (p.Gly184=)
c.459A>G (p.Gly153=)
c.282A>G (p.Gly94=)
c.468A>G (p.Gly156=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766832A>TCA471816483MGMTc.552A>T (p.Gly184=)
c.459A>T (p.Gly153=)
c.282A>T (p.Gly94=)
c.468A>T (p.Gly156=)
 COSMIC COSMIC
10g.129766833G>ACA378713019MGMTc.553G>A (p.Ala185Thr)
c.460G>A (p.Ala154Thr)
c.283G>A (p.Ala95Thr)
c.469G>A (p.Ala157Thr)
10g.129766833G>CCA378713020MGMTc.553G>C (p.Ala185Pro)
c.460G>C (p.Ala154Pro)
c.283G>C (p.Ala95Pro)
c.469G>C (p.Ala157Pro)
10g.129766833G>TCA378713021MGMTc.553G>T (p.Ala185Ser)
c.460G>T (p.Ala154Ser)
c.283G>T (p.Ala95Ser)
c.469G>T (p.Ala157Ser)
10g.129766834C>ACA378713022MGMTc.554C>A (p.Ala185Asp)
c.461C>A (p.Ala154Asp)
c.284C>A (p.Ala95Asp)
c.470C>A (p.Ala157Asp)
10g.129766834C>GCA378713023MGMTc.554C>G (p.Ala185Gly)
c.461C>G (p.Ala154Gly)
c.284C>G (p.Ala95Gly)
c.470C>G (p.Ala157Gly)
10g.129766834C>TCA378713024MGMTc.554C>T (p.Ala185Val)
c.461C>T (p.Ala154Val)
c.284C>T (p.Ala95Val)
c.470C>T (p.Ala157Val)
10g.129766835C>ACA471816486MGMTc.555C>A (p.Ala185=)
c.462C>A (p.Ala154=)
c.285C>A (p.Ala95=)
c.471C>A (p.Ala157=)
10g.129766835C=CA1944921609MGMTc.555C= (p.Ala185=)
c.462C= (p.Ala154=)
c.285C= (p.Ala95=)
c.471C= (p.Ala157=)
10g.129766835C>GCA471816487MGMTc.555C>G (p.Ala185=)
c.462C>G (p.Ala154=)
c.285C>G (p.Ala95=)
c.471C>G (p.Ala157=)
10g.129766835C>TCA5748132MGMTc.555C>T (p.Ala185=)
c.462C>T (p.Ala154=)
c.285C>T (p.Ala95=)
c.471C>T (p.Ala157=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766836G>ACA5748133MGMTc.556G>A (p.Val186Met)
c.463G>A (p.Val155Met)
c.286G>A (p.Val96Met)
c.472G>A (p.Val158Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766836G>CCA378713026MGMTc.556G>C (p.Val186Leu)
c.463G>C (p.Val155Leu)
c.286G>C (p.Val96Leu)
c.472G>C (p.Val158Leu)
10g.129766836G=CA1944921610MGMTc.556G= (p.Val186=)
c.463G= (p.Val155=)
c.286G= (p.Val96=)
c.472G= (p.Val158=)
10g.129766836G>TCA378713025MGMTc.556G>T (p.Val186Leu)
c.463G>T (p.Val155Leu)
c.286G>T (p.Val96Leu)
c.472G>T (p.Val158Leu)
10g.129766837T>ACA378713027MGMTc.557T>A (p.Val186Glu)
c.464T>A (p.Val155Glu)
c.287T>A (p.Val96Glu)
c.473T>A (p.Val158Glu)
10g.129766837T>CCA378713028MGMTc.557T>C (p.Val186Ala)
c.464T>C (p.Val155Ala)
c.287T>C (p.Val96Ala)
c.473T>C (p.Val158Ala)
10g.129766837T>GCA378713029MGMTc.557T>G (p.Val186Gly)
c.464T>G (p.Val155Gly)
c.287T>G (p.Val96Gly)
c.473T>G (p.Val158Gly)
10g.129766838G>ACA5748134MGMTc.558G>A (p.Val186=)
c.465G>A (p.Val155=)
c.288G>A (p.Val96=)
c.474G>A (p.Val158=)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766838G>CCA471816490MGMTc.558G>C (p.Val186=)
c.465G>C (p.Val155=)
c.288G>C (p.Val96=)
c.474G>C (p.Val158=)
10g.129766838G=CA1944921611MGMTc.558G= (p.Val186=)
c.465G= (p.Val155=)
c.288G= (p.Val96=)
c.474G= (p.Val158=)
10g.129766838G>TCA471816491MGMTc.558G>T (p.Val186=)
c.465G>T (p.Val155=)
c.288G>T (p.Val96=)
c.474G>T (p.Val158=)
10g.129766839G>ACA378713030MGMTc.559G>A (p.Gly187Ser)
c.466G>A (p.Gly156Ser)
c.289G>A (p.Gly97Ser)
c.475G>A (p.Gly159Ser)
 dbSNP gnomAD v3 gnomAD v4
10g.129766839G>CCA378713032MGMTc.559G>C (p.Gly187Arg)
c.466G>C (p.Gly156Arg)
c.289G>C (p.Gly97Arg)
c.475G>C (p.Gly159Arg)
 gnomAD v4
10g.129766839G=CA1944921612MGMTc.559G= (p.Gly187=)
c.466G= (p.Gly156=)
c.289G= (p.Gly97=)
c.475G= (p.Gly159=)
10g.129766839G>TCA378713031MGMTc.559G>T (p.Gly187Cys)
c.466G>T (p.Gly156Cys)
c.289G>T (p.Gly97Cys)
c.475G>T (p.Gly159Cys)
 COSMIC COSMIC
10g.129766840G>ACA378713033MGMTc.560G>A (p.Gly187Asp)
c.467G>A (p.Gly156Asp)
c.290G>A (p.Gly97Asp)
c.476G>A (p.Gly159Asp)
10g.129766840G>CCA378713034MGMTc.560G>C (p.Gly187Ala)
c.467G>C (p.Gly156Ala)
c.290G>C (p.Gly97Ala)
c.476G>C (p.Gly159Ala)
10g.129766840G>TCA378713035MGMTc.560G>T (p.Gly187Val)
c.467G>T (p.Gly156Val)
c.290G>T (p.Gly97Val)
c.476G>T (p.Gly159Val)
10g.129766841C>ACA471816495MGMTc.561C>A (p.Gly187=)
c.468C>A (p.Gly156=)
c.291C>A (p.Gly97=)
c.477C>A (p.Gly159=)
10g.129766841C>GCA471816496MGMTc.561C>G (p.Gly187=)
c.468C>G (p.Gly156=)
c.291C>G (p.Gly97=)
c.477C>G (p.Gly159=)
10g.129766841C>TCA471816497MGMTc.561C>T (p.Gly187=)
c.468C>T (p.Gly156=)
c.291C>T (p.Gly97=)
c.477C>T (p.Gly159=)
10g.129766842A>CCA378713036MGMTc.562A>C (p.Asn188His)
c.469A>C (p.Asn157His)
c.292A>C (p.Asn98His)
c.478A>C (p.Asn160His)
10g.129766842A>GCA378713037MGMTc.562A>G (p.Asn188Asp)
c.469A>G (p.Asn157Asp)
c.292A>G (p.Asn98Asp)
c.478A>G (p.Asn160Asp)
10g.129766842A>TCA378713038MGMTc.562A>T (p.Asn188Tyr)
c.469A>T (p.Asn157Tyr)
c.292A>T (p.Asn98Tyr)
c.478A>T (p.Asn160Tyr)
10g.129766843A>CCA378713039MGMTc.563A>C (p.Asn188Thr)
c.470A>C (p.Asn157Thr)
c.293A>C (p.Asn98Thr)
c.479A>C (p.Asn160Thr)
10g.129766843A>GCA378713040MGMTc.563A>G (p.Asn188Ser)
c.470A>G (p.Asn157Ser)
c.293A>G (p.Asn98Ser)
c.479A>G (p.Asn160Ser)
 gnomAD v4
10g.129766843A>TCA378713041MGMTc.563A>T (p.Asn188Ile)
c.470A>T (p.Asn157Ile)
c.293A>T (p.Asn98Ile)
c.479A>T (p.Asn160Ile)
10g.129766844C>ACA378713042MGMTc.564C>A (p.Asn188Lys)
c.471C>A (p.Asn157Lys)
c.294C>A (p.Asn98Lys)
c.480C>A (p.Asn160Lys)
10g.129766844C=CA1944921613MGMTc.564C= (p.Asn188=)
c.471C= (p.Asn157=)
c.294C= (p.Asn98=)
c.480C= (p.Asn160=)
10g.129766844C>GCA378713043MGMTc.564C>G (p.Asn188Lys)
c.471C>G (p.Asn157Lys)
c.294C>G (p.Asn98Lys)
c.480C>G (p.Asn160Lys)
 dbSNP gnomAD v2 gnomAD v4
10g.129766844C>TCA471816499MGMTc.564C>T (p.Asn188=)
c.471C>T (p.Asn157=)
c.294C>T (p.Asn98=)
c.480C>T (p.Asn160=)
10g.129766845T>ACA378713044MGMTc.565T>A (p.Tyr189Asn)
c.472T>A (p.Tyr158Asn)
c.295T>A (p.Tyr99Asn)
c.481T>A (p.Tyr161Asn)
10g.129766845T>CCA378713046MGMTc.565T>C (p.Tyr189His)
c.472T>C (p.Tyr158His)
c.295T>C (p.Tyr99His)
c.481T>C (p.Tyr161His)
10g.129766845T>GCA378713045MGMTc.565T>G (p.Tyr189Asp)
c.472T>G (p.Tyr158Asp)
c.295T>G (p.Tyr99Asp)
c.481T>G (p.Tyr161Asp)
10g.129766846A>CCA378713047MGMTc.566A>C (p.Tyr189Ser)
c.473A>C (p.Tyr158Ser)
c.296A>C (p.Tyr99Ser)
c.482A>C (p.Tyr161Ser)
10g.129766846A>GCA378713048MGMTc.566A>G (p.Tyr189Cys)
c.473A>G (p.Tyr158Cys)
c.296A>G (p.Tyr99Cys)
c.482A>G (p.Tyr161Cys)
10g.129766846A>TCA378713049MGMTc.566A>T (p.Tyr189Phe)
c.473A>T (p.Tyr158Phe)
c.296A>T (p.Tyr99Phe)
c.482A>T (p.Tyr161Phe)
10g.129766847C>ACA378713050MGMTc.567C>A (p.Tyr189Ter)
c.474C>A (p.Tyr158Ter)
c.297C>A (p.Tyr99Ter)
c.483C>A (p.Tyr161Ter)
10g.129766847C=CA1944921614MGMTc.567C= (p.Tyr189=)
c.474C= (p.Tyr158=)
c.297C= (p.Tyr99=)
c.483C= (p.Tyr161=)
10g.129766847C>GCA378713051MGMTc.567C>G (p.Tyr189Ter)
c.474C>G (p.Tyr158Ter)
c.297C>G (p.Tyr99Ter)
c.483C>G (p.Tyr161Ter)
10g.129766847C>TCA471816503MGMTc.567C>T (p.Tyr189=)
c.474C>T (p.Tyr158=)
c.297C>T (p.Tyr99=)
c.483C>T (p.Tyr161=)
 dbSNP gnomAD v4
10g.129766848T>ACA378713052MGMTc.568T>A (p.Ser190Thr)
c.475T>A (p.Ser159Thr)
c.298T>A (p.Ser100Thr)
c.484T>A (p.Ser162Thr)
10g.129766848T>CCA378713053MGMTc.568T>C (p.Ser190Pro)
c.475T>C (p.Ser159Pro)
c.298T>C (p.Ser100Pro)
c.484T>C (p.Ser162Pro)
10g.129766848T>GCA378713054MGMTc.568T>G (p.Ser190Ala)
c.475T>G (p.Ser159Ala)
c.298T>G (p.Ser100Ala)
c.484T>G (p.Ser162Ala)
10g.129766849C>ACA378713055MGMTc.569C>A (p.Ser190Tyr)
c.476C>A (p.Ser159Tyr)
c.299C>A (p.Ser100Tyr)
c.485C>A (p.Ser162Tyr)
 gnomAD v4
10g.129766849C>GCA378713056MGMTc.569C>G (p.Ser190Cys)
c.476C>G (p.Ser159Cys)
c.299C>G (p.Ser100Cys)
c.485C>G (p.Ser162Cys)
10g.129766849C>TCA378713057MGMTc.569C>T (p.Ser190Phe)
c.476C>T (p.Ser159Phe)
c.299C>T (p.Ser100Phe)
c.485C>T (p.Ser162Phe)
 gnomAD v4
10g.129766850C>ACA471816505MGMTc.570C>A (p.Ser190=)
c.477C>A (p.Ser159=)
c.300C>A (p.Ser100=)
c.486C>A (p.Ser162=)
10g.129766850C=CA1944921615MGMTc.570C= (p.Ser190=)
c.477C= (p.Ser159=)
c.300C= (p.Ser100=)
c.486C= (p.Ser162=)
10g.129766850C>GCA471816506MGMTc.570C>G (p.Ser190=)
c.477C>G (p.Ser159=)
c.300C>G (p.Ser100=)
c.486C>G (p.Ser162=)
10g.129766850C>TCA5748135MGMTc.570C>T (p.Ser190=)
c.477C>T (p.Ser159=)
c.300C>T (p.Ser100=)
c.486C>T (p.Ser162=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766851G>ACA5748136MGMTc.571G>A (p.Gly191Arg)
c.478G>A (p.Gly160Arg)
c.301G>A (p.Gly101Arg)
c.487G>A (p.Gly163Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766851G>CCA378713058MGMTc.571G>C (p.Gly191Arg)
c.478G>C (p.Gly160Arg)
c.301G>C (p.Gly101Arg)
c.487G>C (p.Gly163Arg)
10g.129766851G=CA1944921616MGMTc.571G= (p.Gly191=)
c.478G= (p.Gly160=)
c.301G= (p.Gly101=)
c.487G= (p.Gly163=)
10g.129766851G>TCA378713059MGMTc.571G>T (p.Gly191Ter)
c.478G>T (p.Gly160Ter)
c.301G>T (p.Gly101Ter)
c.487G>T (p.Gly163Ter)
10g.129766852G>ACA378713060MGMTc.572G>A (p.Gly191Glu)
c.479G>A (p.Gly160Glu)
c.302G>A (p.Gly101Glu)
c.488G>A (p.Gly163Glu)
 COSMIC COSMIC
10g.129766852G>CCA378713061MGMTc.572G>C (p.Gly191Ala)
c.479G>C (p.Gly160Ala)
c.302G>C (p.Gly101Ala)
c.488G>C (p.Gly163Ala)
10g.129766852G>TCA378713062MGMTc.572G>T (p.Gly191Val)
c.479G>T (p.Gly160Val)
c.302G>T (p.Gly101Val)
c.488G>T (p.Gly163Val)
 dbSNP
10g.129766853A>CCA471816508MGMTc.573A>C (p.Gly191=)
c.480A>C (p.Gly160=)
c.303A>C (p.Gly101=)
c.489A>C (p.Gly163=)
10g.129766853A>GCA471816510MGMTc.573A>G (p.Gly191=)
c.480A>G (p.Gly160=)
c.303A>G (p.Gly101=)
c.489A>G (p.Gly163=)
 gnomAD v4
10g.129766853A>TCA471816511MGMTc.573A>T (p.Gly191=)
c.480A>T (p.Gly160=)
c.303A>T (p.Gly101=)
c.489A>T (p.Gly163=)
10g.129766854G>ACA378713063MGMTc.574G>A (p.Gly192Arg)
c.481G>A (p.Gly161Arg)
c.304G>A (p.Gly102Arg)
c.490G>A (p.Gly164Arg)
 dbSNP
10g.129766854G>CCA378713064MGMTc.574G>C (p.Gly192Arg)
c.481G>C (p.Gly161Arg)
c.304G>C (p.Gly102Arg)
c.490G>C (p.Gly164Arg)
 gnomAD v4
10g.129766854G=CA1944921617MGMTc.574G= (p.Gly192=)
c.481G= (p.Gly161=)
c.304G= (p.Gly102=)
c.490G= (p.Gly164=)
10g.129766854G>TCA378713065MGMTc.574G>T (p.Gly192Ter)
c.481G>T (p.Gly161Ter)
c.304G>T (p.Gly102Ter)
c.490G>T (p.Gly164Ter)
10g.129766855G>ACA378713066MGMTc.575G>A (p.Gly192Glu)
c.482G>A (p.Gly161Glu)
c.305G>A (p.Gly102Glu)
c.491G>A (p.Gly164Glu)
10g.129766855G>CCA378713067MGMTc.575G>C (p.Gly192Ala)
c.482G>C (p.Gly161Ala)
c.305G>C (p.Gly102Ala)
c.491G>C (p.Gly164Ala)
 gnomAD v4
10g.129766855G>TCA378713068MGMTc.575G>T (p.Gly192Val)
c.482G>T (p.Gly161Val)
c.305G>T (p.Gly102Val)
c.491G>T (p.Gly164Val)
 gnomAD v4
10g.129766856A=CA1944921618MGMTc.576A= (p.Gly192=)
c.483A= (p.Gly161=)
c.306A= (p.Gly102=)
c.492A= (p.Gly164=)
10g.129766856A>CCA471816516MGMTc.576A>C (p.Gly192=)
c.483A>C (p.Gly161=)
c.306A>C (p.Gly102=)
c.492A>C (p.Gly164=)
 dbSNP
10g.129766856A>GCA471816517MGMTc.576A>G (p.Gly192=)
c.483A>G (p.Gly161=)
c.306A>G (p.Gly102=)
c.492A>G (p.Gly164=)
 gnomAD v4
10g.129766856A>TCA471816518MGMTc.576A>T (p.Gly192=)
c.483A>T (p.Gly161=)
c.306A>T (p.Gly102=)
c.492A>T (p.Gly164=)
10g.129766857C>ACA378713069MGMTc.577C>A (p.Leu193Met)
c.484C>A (p.Leu162Met)
c.307C>A (p.Leu103Met)
c.493C>A (p.Leu165Met)
10g.129766857C>GCA378713070MGMTc.577C>G (p.Leu193Val)
c.484C>G (p.Leu162Val)
c.307C>G (p.Leu103Val)
c.493C>G (p.Leu165Val)
10g.129766857C>TCA471816522MGMTc.577C>T (p.Leu193=)
c.484C>T (p.Leu162=)
c.307C>T (p.Leu103=)
c.493C>T (p.Leu165=)
10g.129766858T>ACA378713072MGMTc.578T>A (p.Leu193Gln)
c.485T>A (p.Leu162Gln)
c.308T>A (p.Leu103Gln)
c.494T>A (p.Leu165Gln)
10g.129766858T>CCA378713073MGMTc.578T>C (p.Leu193Pro)
c.485T>C (p.Leu162Pro)
c.308T>C (p.Leu103Pro)
c.494T>C (p.Leu165Pro)
 dbSNP gnomAD v3 gnomAD v4
10g.129766858T>GCA378713071MGMTc.578T>G (p.Leu193Arg)
c.485T>G (p.Leu162Arg)
c.308T>G (p.Leu103Arg)
c.494T>G (p.Leu165Arg)
10g.129766858T=CA1944921619MGMTc.578T= (p.Leu193=)
c.485T= (p.Leu162=)
c.308T= (p.Leu103=)
c.494T= (p.Leu165=)
10g.129766859G>ACA471816523MGMTc.579G>A (p.Leu193=)
c.486G>A (p.Leu162=)
c.309G>A (p.Leu103=)
c.495G>A (p.Leu165=)
 dbSNP gnomAD v4
10g.129766859G>CCA471816525MGMTc.579G>C (p.Leu193=)
c.486G>C (p.Leu162=)
c.309G>C (p.Leu103=)
c.495G>C (p.Leu165=)
10g.129766859G=CA1944921620MGMTc.579G= (p.Leu193=)
c.486G= (p.Leu162=)
c.309G= (p.Leu103=)
c.495G= (p.Leu165=)
10g.129766859G>TCA471816527MGMTc.579G>T (p.Leu193=)
c.486G>T (p.Leu162=)
c.309G>T (p.Leu103=)
c.495G>T (p.Leu165=)
10g.129766860G>ACA378713076MGMTc.580G>A (p.Ala194Thr)
c.487G>A (p.Ala163Thr)
c.310G>A (p.Ala104Thr)
c.496G>A (p.Ala166Thr)
10g.129766860G>CCA378713074MGMTc.580G>C (p.Ala194Pro)
c.487G>C (p.Ala163Pro)
c.310G>C (p.Ala104Pro)
c.496G>C (p.Ala166Pro)
10g.129766860G>TCA378713075MGMTc.580G>T (p.Ala194Ser)
c.487G>T (p.Ala163Ser)
c.310G>T (p.Ala104Ser)
c.496G>T (p.Ala166Ser)
10g.129766861C>ACA378713077MGMTc.581C>A (p.Ala194Asp)
c.488C>A (p.Ala163Asp)
c.311C>A (p.Ala104Asp)
c.497C>A (p.Ala166Asp)
 gnomAD v4
10g.129766861C=CA1944921621MGMTc.581C= (p.Ala194=)
c.488C= (p.Ala163=)
c.311C= (p.Ala104=)
c.497C= (p.Ala166=)
10g.129766861C>GCA378713078MGMTc.581C>G (p.Ala194Gly)
c.488C>G (p.Ala163Gly)
c.311C>G (p.Ala104Gly)
c.497C>G (p.Ala166Gly)
10g.129766861C>TCA215499786MGMTc.581C>T (p.Ala194Val)
c.488C>T (p.Ala163Val)
c.311C>T (p.Ala104Val)
c.497C>T (p.Ala166Val)
 dbSNP gnomAD v4
10g.129766862C>ACA471816530MGMTc.582C>A (p.Ala194=)
c.489C>A (p.Ala163=)
c.312C>A (p.Ala104=)
c.498C>A (p.Ala166=)
10g.129766862C=CA1944921622MGMTc.582C= (p.Ala194=)
c.489C= (p.Ala163=)
c.312C= (p.Ala104=)
c.498C= (p.Ala166=)
10g.129766862C>GCA471816531MGMTc.582C>G (p.Ala194=)
c.489C>G (p.Ala163=)
c.312C>G (p.Ala104=)
c.498C>G (p.Ala166=)
 dbSNP gnomAD v4
10g.129766862C>TCA5748137MGMTc.582C>T (p.Ala194=)
c.489C>T (p.Ala163=)
c.312C>T (p.Ala104=)
c.498C>T (p.Ala166=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766863G>ACA5748138MGMTc.583G>A (p.Val195Met)
c.490G>A (p.Val164Met)
c.313G>A (p.Val105Met)
c.499G>A (p.Val167Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766863G>CCA378713079MGMTc.583G>C (p.Val195Leu)
c.490G>C (p.Val164Leu)
c.313G>C (p.Val105Leu)
c.499G>C (p.Val167Leu)
10g.129766863G=CA1944921623MGMTc.583G= (p.Val195=)
c.490G= (p.Val164=)
c.313G= (p.Val105=)
c.499G= (p.Val167=)
10g.129766863G>TCA5748139MGMTc.583G>T (p.Val195Leu)
c.490G>T (p.Val164Leu)
c.313G>T (p.Val105Leu)
c.499G>T (p.Val167Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766864T>ACA378713080MGMTc.584T>A (p.Val195Glu)
c.491T>A (p.Val164Glu)
c.314T>A (p.Val105Glu)
c.500T>A (p.Val167Glu)
10g.129766864T>CCA378713081MGMTc.584T>C (p.Val195Ala)
c.491T>C (p.Val164Ala)
c.314T>C (p.Val105Ala)
c.500T>C (p.Val167Ala)
10g.129766864T>GCA378713082MGMTc.584T>G (p.Val195Gly)
c.491T>G (p.Val164Gly)
c.314T>G (p.Val105Gly)
c.500T>G (p.Val167Gly)
10g.129766865G>ACA471816534MGMTc.585G>A (p.Val195=)
c.492G>A (p.Val164=)
c.315G>A (p.Val105=)
c.501G>A (p.Val167=)
10g.129766865G>CCA471816535MGMTc.585G>C (p.Val195=)
c.492G>C (p.Val164=)
c.315G>C (p.Val105=)
c.501G>C (p.Val167=)
10g.129766865G>TCA471816536MGMTc.585G>T (p.Val195=)
c.492G>T (p.Val164=)
c.315G>T (p.Val105=)
c.501G>T (p.Val167=)
10g.129766866A>CCA378713085MGMTc.586A>C (p.Lys196Gln)
c.493A>C (p.Lys165Gln)
c.316A>C (p.Lys106Gln)
c.502A>C (p.Lys168Gln)
10g.129766866A>GCA378713084MGMTc.586A>G (p.Lys196Glu)
c.493A>G (p.Lys165Glu)
c.316A>G (p.Lys106Glu)
c.502A>G (p.Lys168Glu)
10g.129766866A>TCA378713083MGMTc.586A>T (p.Lys196Ter)
c.493A>T (p.Lys165Ter)
c.316A>T (p.Lys106Ter)
c.502A>T (p.Lys168Ter)
10g.129766867A>CCA378713086MGMTc.587A>C (p.Lys196Thr)
c.494A>C (p.Lys165Thr)
c.317A>C (p.Lys106Thr)
c.503A>C (p.Lys168Thr)
10g.129766867A>GCA378713087MGMTc.587A>G (p.Lys196Arg)
c.494A>G (p.Lys165Arg)
c.317A>G (p.Lys106Arg)
c.503A>G (p.Lys168Arg)
10g.129766867A>TCA378713088MGMTc.587A>T (p.Lys196Met)
c.494A>T (p.Lys165Met)
c.317A>T (p.Lys106Met)
c.503A>T (p.Lys168Met)
10g.129766868G>ACA471816539MGMTc.588G>A (p.Lys196=)
c.495G>A (p.Lys165=)
c.318G>A (p.Lys106=)
c.504G>A (p.Lys168=)
 dbSNP gnomAD v2 gnomAD v4
10g.129766868G>CCA378713089MGMTc.588G>C (p.Lys196Asn)
c.495G>C (p.Lys165Asn)
c.318G>C (p.Lys106Asn)
c.504G>C (p.Lys168Asn)
10g.129766868G=CA1944921624MGMTc.588G= (p.Lys196=)
c.495G= (p.Lys165=)
c.318G= (p.Lys106=)
c.504G= (p.Lys168=)
10g.129766868G>TCA378713090MGMTc.588G>T (p.Lys196Asn)
c.495G>T (p.Lys165Asn)
c.318G>T (p.Lys106Asn)
c.504G>T (p.Lys168Asn)
10g.129766869G>ACA378713091MGMTc.589G>A (p.Glu197Lys)
c.496G>A (p.Glu166Lys)
c.319G>A (p.Glu107Lys)
c.505G>A (p.Glu169Lys)
10g.129766869G>CCA378713092MGMTc.589G>C (p.Glu197Gln)
c.496G>C (p.Glu166Gln)
c.319G>C (p.Glu107Gln)
c.505G>C (p.Glu169Gln)
10g.129766869G>TCA378713093MGMTc.589G>T (p.Glu197Ter)
c.496G>T (p.Glu166Ter)
c.319G>T (p.Glu107Ter)
c.505G>T (p.Glu169Ter)
10g.129766870A=CA1944921625MGMTc.590A= (p.Glu197=)
c.497A= (p.Glu166=)
c.320A= (p.Glu107=)
c.506A= (p.Glu169=)
10g.129766870A>CCA378713094MGMTc.590A>C (p.Glu197Ala)
c.497A>C (p.Glu166Ala)
c.320A>C (p.Glu107Ala)
c.506A>C (p.Glu169Ala)
10g.129766870A>GCA378713095MGMTc.590A>G (p.Glu197Gly)
c.497A>G (p.Glu166Gly)
c.320A>G (p.Glu107Gly)
c.506A>G (p.Glu169Gly)
 dbSNP
10g.129766870A>TCA378713096MGMTc.590A>T (p.Glu197Val)
c.497A>T (p.Glu166Val)
c.320A>T (p.Glu107Val)
c.506A>T (p.Glu169Val)
10g.129766871A=CA1944921626MGMTc.591A= (p.Glu197=)
c.498A= (p.Glu166=)
c.321A= (p.Glu107=)
c.507A= (p.Glu169=)
10g.129766871A>CCA378713097MGMTc.591A>C (p.Glu197Asp)
c.498A>C (p.Glu166Asp)
c.321A>C (p.Glu107Asp)
c.507A>C (p.Glu169Asp)
10g.129766871A>GCA471816541MGMTc.591A>G (p.Glu197=)
c.498A>G (p.Glu166=)
c.321A>G (p.Glu107=)
c.507A>G (p.Glu169=)
 gnomAD v4
10g.129766871A>TCA5748140MGMTc.591A>T (p.Glu197Asp)
c.498A>T (p.Glu166Asp)
c.321A>T (p.Glu107Asp)
c.507A>T (p.Glu169Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766872T>ACA378713100MGMTc.592T>A (p.Trp198Arg)
c.499T>A (p.Trp167Arg)
c.322T>A (p.Trp108Arg)
c.508T>A (p.Trp170Arg)
10g.129766872T>CCA378713099MGMTc.592T>C (p.Trp198Arg)
c.499T>C (p.Trp167Arg)
c.322T>C (p.Trp108Arg)
c.508T>C (p.Trp170Arg)
 gnomAD v4
10g.129766872T>GCA378713098MGMTc.592T>G (p.Trp198Gly)
c.499T>G (p.Trp167Gly)
c.322T>G (p.Trp108Gly)
c.508T>G (p.Trp170Gly)
10g.129766873G>ACA5748141MGMTc.593G>A (p.Trp198Ter)
c.500G>A (p.Trp167Ter)
c.323G>A (p.Trp108Ter)
c.509G>A (p.Trp170Ter)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766873G>CCA378713101MGMTc.593G>C (p.Trp198Ser)
c.500G>C (p.Trp167Ser)
c.323G>C (p.Trp108Ser)
c.509G>C (p.Trp170Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.129766873G=CA1944921627MGMTc.593G= (p.Trp198=)
c.500G= (p.Trp167=)
c.323G= (p.Trp108=)
c.509G= (p.Trp170=)
10g.129766873G>TCA378713102MGMTc.593G>T (p.Trp198Leu)
c.500G>T (p.Trp167Leu)
c.323G>T (p.Trp108Leu)
c.509G>T (p.Trp170Leu)
10g.129766874G>ACA378713103MGMTc.594G>A (p.Trp198Ter)
c.501G>A (p.Trp167Ter)
c.324G>A (p.Trp108Ter)
c.510G>A (p.Trp170Ter)
10g.129766874G>CCA378713104MGMTc.594G>C (p.Trp198Cys)
c.501G>C (p.Trp167Cys)
c.324G>C (p.Trp108Cys)
c.510G>C (p.Trp170Cys)
10g.129766874G>TCA378713105MGMTc.594G>T (p.Trp198Cys)
c.501G>T (p.Trp167Cys)
c.324G>T (p.Trp108Cys)
c.510G>T (p.Trp170Cys)
 gnomAD v4
10g.129766875C>ACA378713108MGMTc.595C>A (p.Leu199Ile)
c.502C>A (p.Leu168Ile)
c.325C>A (p.Leu109Ile)
c.511C>A (p.Leu171Ile)
10g.129766875C>GCA378713107MGMTc.595C>G (p.Leu199Val)
c.502C>G (p.Leu168Val)
c.325C>G (p.Leu109Val)
c.511C>G (p.Leu171Val)
10g.129766875C>TCA378713106MGMTc.595C>T (p.Leu199Phe)
c.502C>T (p.Leu168Phe)
c.325C>T (p.Leu109Phe)
c.511C>T (p.Leu171Phe)
 gnomAD v4
10g.129766876T>ACA378713109MGMTc.596T>A (p.Leu199His)
c.503T>A (p.Leu168His)
c.326T>A (p.Leu109His)
c.512T>A (p.Leu171His)
10g.129766876T>CCA378713110MGMTc.596T>C (p.Leu199Pro)
c.503T>C (p.Leu168Pro)
c.326T>C (p.Leu109Pro)
c.512T>C (p.Leu171Pro)
 dbSNP
10g.129766876T>GCA378713111MGMTc.596T>G (p.Leu199Arg)
c.503T>G (p.Leu168Arg)
c.326T>G (p.Leu109Arg)
c.512T>G (p.Leu171Arg)
 gnomAD v4
10g.129766876T=CA1944921628MGMTc.596T= (p.Leu199=)
c.503T= (p.Leu168=)
c.326T= (p.Leu109=)
c.512T= (p.Leu171=)
10g.129766877T>ACA471816550MGMTc.597T>A (p.Leu199=)
c.504T>A (p.Leu168=)
c.327T>A (p.Leu109=)
c.513T>A (p.Leu171=)
10g.129766877T>CCA471816554MGMTc.597T>C (p.Leu199=)
c.504T>C (p.Leu168=)
c.327T>C (p.Leu109=)
c.513T>C (p.Leu171=)
10g.129766877T>GCA471816555MGMTc.597T>G (p.Leu199=)
c.504T>G (p.Leu168=)
c.327T>G (p.Leu109=)
c.513T>G (p.Leu171=)
10g.129766878C>ACA378713112MGMTc.598C>A (p.Leu200Met)
c.505C>A (p.Leu169Met)
c.328C>A (p.Leu110Met)
c.514C>A (p.Leu172Met)
10g.129766878C=CA1944921629MGMTc.598C= (p.Leu200=)
c.505C= (p.Leu169=)
c.328C= (p.Leu110=)
c.514C= (p.Leu172=)
10g.129766878C>GCA378713113MGMTc.598C>G (p.Leu200Val)
c.505C>G (p.Leu169Val)
c.328C>G (p.Leu110Val)
c.514C>G (p.Leu172Val)
10g.129766878C>TCA5748142MGMTc.598C>T (p.Leu200=)
c.505C>T (p.Leu169=)
c.328C>T (p.Leu110=)
c.514C>T (p.Leu172=)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766879T>ACA378713114MGMTc.599T>A (p.Leu200Gln)
c.506T>A (p.Leu169Gln)
c.329T>A (p.Leu110Gln)
c.515T>A (p.Leu172Gln)
10g.129766879T>CCA378713116MGMTc.599T>C (p.Leu200Pro)
c.506T>C (p.Leu169Pro)
c.329T>C (p.Leu110Pro)
c.515T>C (p.Leu172Pro)
10g.129766879T>GCA378713115MGMTc.599T>G (p.Leu200Arg)
c.506T>G (p.Leu169Arg)
c.329T>G (p.Leu110Arg)
c.515T>G (p.Leu172Arg)
10g.129766880G>ACA471816557MGMTc.600G>A (p.Leu200=)
c.507G>A (p.Leu169=)
c.330G>A (p.Leu110=)
c.516G>A (p.Leu172=)
 gnomAD v4
10g.129766880G>CCA471816558MGMTc.600G>C (p.Leu200=)
c.507G>C (p.Leu169=)
c.330G>C (p.Leu110=)
c.516G>C (p.Leu172=)
10g.129766880G>TCA471816559MGMTc.600G>T (p.Leu200=)
c.507G>T (p.Leu169=)
c.330G>T (p.Leu110=)
c.516G>T (p.Leu172=)
10g.129766881G>ACA378713117MGMTc.601G>A (p.Ala201Thr)
c.508G>A (p.Ala170Thr)
c.331G>A (p.Ala111Thr)
c.517G>A (p.Ala173Thr)
 gnomAD v4
10g.129766881G>CCA378713118MGMTc.601G>C (p.Ala201Pro)
c.508G>C (p.Ala170Pro)
c.331G>C (p.Ala111Pro)
c.517G>C (p.Ala173Pro)
10g.129766881G>TCA378713119MGMTc.601G>T (p.Ala201Ser)
c.508G>T (p.Ala170Ser)
c.331G>T (p.Ala111Ser)
c.517G>T (p.Ala173Ser)
10g.129766882C>ACA378713120MGMTc.602C>A (p.Ala201Asp)
c.509C>A (p.Ala170Asp)
c.332C>A (p.Ala111Asp)
c.518C>A (p.Ala173Asp)
10g.129766882C=CA1944921630MGMTc.602C= (p.Ala201=)
c.509C= (p.Ala170=)
c.332C= (p.Ala111=)
c.518C= (p.Ala173=)
10g.129766882C>GCA378713121MGMTc.602C>G (p.Ala201Gly)
c.509C>G (p.Ala170Gly)
c.332C>G (p.Ala111Gly)
c.518C>G (p.Ala173Gly)
 gnomAD v4
10g.129766882C>TCA378713122MGMTc.602C>T (p.Ala201Val)
c.509C>T (p.Ala170Val)
c.332C>T (p.Ala111Val)
c.518C>T (p.Ala173Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.129766883C>ACA471816563MGMTc.603C>A (p.Ala201=)
c.510C>A (p.Ala170=)
c.333C>A (p.Ala111=)
c.519C>A (p.Ala173=)
10g.129766883C>GCA471816564MGMTc.603C>G (p.Ala201=)
c.510C>G (p.Ala170=)
c.333C>G (p.Ala111=)
c.519C>G (p.Ala173=)
10g.129766883C>TCA471816565MGMTc.603C>T (p.Ala201=)
c.510C>T (p.Ala170=)
c.333C>T (p.Ala111=)
c.519C>T (p.Ala173=)
10g.129766884C>ACA378713123MGMTc.604C>A (p.His202Asn)
c.511C>A (p.His171Asn)
c.334C>A (p.His112Asn)
c.520C>A (p.His174Asn)
10g.129766884C>GCA378713124MGMTc.604C>G (p.His202Asp)
c.511C>G (p.His171Asp)
c.334C>G (p.His112Asp)
c.520C>G (p.His174Asp)
10g.129766884C>TCA378713125MGMTc.604C>T (p.His202Tyr)
c.511C>T (p.His171Tyr)
c.334C>T (p.His112Tyr)
c.520C>T (p.His174Tyr)
10g.129766885A=CA1944891109MGMTc.605A= (p.His202=)
c.512A= (p.His171=)
c.335A= (p.His112=)
c.521A= (p.His174=)
10g.129766885A>CCA378713126MGMTc.605A>C (p.His202Pro)
c.512A>C (p.His171Pro)
c.335A>C (p.His112Pro)
c.521A>C (p.His174Pro)
 dbSNP gnomAD v2 gnomAD v4
10g.129766885A>GCA378713127MGMTc.605A>G (p.His202Arg)
c.512A>G (p.His171Arg)
c.335A>G (p.His112Arg)
c.521A>G (p.His174Arg)
10g.129766885A>TCA378713128MGMTc.605A>T (p.His202Leu)
c.512A>T (p.His171Leu)
c.335A>T (p.His112Leu)
c.521A>T (p.His174Leu)
10g.129766886T>ACA378713130MGMTc.606T>A (p.His202Gln)
c.513T>A (p.His171Gln)
c.336T>A (p.His112Gln)
c.522T>A (p.His174Gln)
10g.129766886T>CCA5748143MGMTc.606T>C (p.His202=)
c.513T>C (p.His171=)
c.336T>C (p.His112=)
c.522T>C (p.His174=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766886T>GCA378713129MGMTc.606T>G (p.His202Gln)
c.513T>G (p.His171Gln)
c.336T>G (p.His112Gln)
c.522T>G (p.His174Gln)
10g.129766886T=CA1944891120MGMTc.606T= (p.His202=)
c.513T= (p.His171=)
c.336T= (p.His112=)
c.522T= (p.His174=)
10g.129766887G>ACA378713131MGMTc.607G>A (p.Glu203Lys)
c.514G>A (p.Glu172Lys)
c.337G>A (p.Glu113Lys)
c.523G>A (p.Glu175Lys)
10g.129766887G>CCA378713132MGMTc.607G>C (p.Glu203Gln)
c.514G>C (p.Glu172Gln)
c.337G>C (p.Glu113Gln)
c.523G>C (p.Glu175Gln)
10g.129766887G>TCA378713133MGMTc.607G>T (p.Glu203Ter)
c.514G>T (p.Glu172Ter)
c.337G>T (p.Glu113Ter)
c.523G>T (p.Glu175Ter)
10g.129766888A=CA1944891127MGMTc.608A= (p.Glu203=)
c.515A= (p.Glu172=)
c.338A= (p.Glu113=)
c.524A= (p.Glu175=)
10g.129766888A>CCA215499796MGMTc.608A>C (p.Glu203Ala)
c.515A>C (p.Glu172Ala)
c.338A>C (p.Glu113Ala)
c.524A>C (p.Glu175Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.129766888A>GCA215499797MGMTc.608A>G (p.Glu203Gly)
c.515A>G (p.Glu172Gly)
c.338A>G (p.Glu113Gly)
c.524A>G (p.Glu175Gly)
 dbSNP gnomAD v3 gnomAD v4
10g.129766888A>TCA378713134MGMTc.608A>T (p.Glu203Val)
c.515A>T (p.Glu172Val)
c.338A>T (p.Glu113Val)
c.524A>T (p.Glu175Val)
10g.129766889A>CCA378713136MGMTc.609A>C (p.Glu203Asp)
c.516A>C (p.Glu172Asp)
c.339A>C (p.Glu113Asp)
c.525A>C (p.Glu175Asp)
10g.129766889A>GCA471816570MGMTc.609A>G (p.Glu203=)
c.516A>G (p.Glu172=)
c.339A>G (p.Glu113=)
c.525A>G (p.Glu175=)
 dbSNP gnomAD v4
10g.129766889A>TCA378713135MGMTc.609A>T (p.Glu203Asp)
c.516A>T (p.Glu172Asp)
c.339A>T (p.Glu113Asp)
c.525A>T (p.Glu175Asp)
10g.129766890G>ACA378713137MGMTc.610G>A (p.Gly204Ser)
c.517G>A (p.Gly173Ser)
c.340G>A (p.Gly114Ser)
c.526G>A (p.Gly176Ser)
10g.129766890G>CCA378713138MGMTc.610G>C (p.Gly204Arg)
c.517G>C (p.Gly173Arg)
c.340G>C (p.Gly114Arg)
c.526G>C (p.Gly176Arg)
 COSMIC COSMIC
10g.129766890G>TCA378713139MGMTc.610G>T (p.Gly204Cys)
c.517G>T (p.Gly173Cys)
c.340G>T (p.Gly114Cys)
c.526G>T (p.Gly176Cys)
10g.129766891G>ACA378713140MGMTc.611G>A (p.Gly204Asp)
c.518G>A (p.Gly173Asp)
c.341G>A (p.Gly114Asp)
c.527G>A (p.Gly176Asp)
10g.129766891G>CCA378713141MGMTc.611G>C (p.Gly204Ala)
c.518G>C (p.Gly173Ala)
c.341G>C (p.Gly114Ala)
c.527G>C (p.Gly176Ala)
 gnomAD v4
10g.129766891G=CA1944891135MGMTc.611G= (p.Gly204=)
c.518G= (p.Gly173=)
c.341G= (p.Gly114=)
c.527G= (p.Gly176=)
10g.129766891G>TCA5748144MGMTc.611G>T (p.Gly204Val)
c.518G>T (p.Gly173Val)
c.341G>T (p.Gly114Val)
c.527G>T (p.Gly176Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766892C>ACA471816574MGMTc.612C>A (p.Gly204=)
c.519C>A (p.Gly173=)
c.342C>A (p.Gly114=)
c.528C>A (p.Gly176=)
10g.129766892C>GCA471816575MGMTc.612C>G (p.Gly204=)
c.519C>G (p.Gly173=)
c.342C>G (p.Gly114=)
c.528C>G (p.Gly176=)
10g.129766892C>TCA471816576MGMTc.612C>T (p.Gly204=)
c.519C>T (p.Gly173=)
c.342C>T (p.Gly114=)
c.528C>T (p.Gly176=)
10g.129766893C>ACA378713144MGMTc.613C>A (p.His205Asn)
c.520C>A (p.His174Asn)
c.343C>A (p.His115Asn)
c.529C>A (p.His177Asn)
10g.129766893C=CA1944891141MGMTc.613C= (p.His205=)
c.520C= (p.His174=)
c.343C= (p.His115=)
c.529C= (p.His177=)
10g.129766893C>GCA378713142MGMTc.613C>G (p.His205Asp)
c.520C>G (p.His174Asp)
c.343C>G (p.His115Asp)
c.529C>G (p.His177Asp)
10g.129766893C>TCA378713143MGMTc.613C>T (p.His205Tyr)
c.520C>T (p.His174Tyr)
c.343C>T (p.His115Tyr)
c.529C>T (p.His177Tyr)
 dbSNP gnomAD v2 gnomAD v4
10g.129766894A>CCA378713145MGMTc.614A>C (p.His205Pro)
c.521A>C (p.His174Pro)
c.344A>C (p.His115Pro)
c.530A>C (p.His177Pro)
10g.129766894A>GCA378713146MGMTc.614A>G (p.His205Arg)
c.521A>G (p.His174Arg)
c.344A>G (p.His115Arg)
c.530A>G (p.His177Arg)
10g.129766894A>TCA378713147MGMTc.614A>T (p.His205Leu)
c.521A>T (p.His174Leu)
c.344A>T (p.His115Leu)
c.530A>T (p.His177Leu)
10g.129766895C>ACA378713148MGMTc.615C>A (p.His205Gln)
c.522C>A (p.His174Gln)
c.345C>A (p.His115Gln)
c.531C>A (p.His177Gln)
10g.129766895C>GCA378713149MGMTc.615C>G (p.His205Gln)
c.522C>G (p.His174Gln)
c.345C>G (p.His115Gln)
c.531C>G (p.His177Gln)
10g.129766895C>TCA471816577MGMTc.615C>T (p.His205=)
c.522C>T (p.His174=)
c.345C>T (p.His115=)
c.531C>T (p.His177=)
10g.129766896C>ACA471816578MGMTc.616C>A (p.Arg206=)
c.523C>A (p.Arg175=)
c.346C>A (p.Arg116=)
c.532C>A (p.Arg178=)
10g.129766896C=CA1944891150MGMTc.616C= (p.Arg206=)
c.523C= (p.Arg175=)
c.346C= (p.Arg116=)
c.532C= (p.Arg178=)
10g.129766896C>GCA5748146MGMTc.616C>G (p.Arg206Gly)
c.523C>G (p.Arg175Gly)
c.346C>G (p.Arg116Gly)
c.532C>G (p.Arg178Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766896C>TCA5748145MGMTc.616C>T (p.Arg206Trp)
c.523C>T (p.Arg175Trp)
c.346C>T (p.Arg116Trp)
c.532C>T (p.Arg178Trp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766897G>ACA5748147MGMTc.617G>A (p.Arg206Gln)
c.524G>A (p.Arg175Gln)
c.347G>A (p.Arg116Gln)
c.533G>A (p.Arg178Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766897G>CCA378713150MGMTc.617G>C (p.Arg206Pro)
c.524G>C (p.Arg175Pro)
c.347G>C (p.Arg116Pro)
c.533G>C (p.Arg178Pro)
 dbSNP gnomAD v3 gnomAD v4
10g.129766897G=CA1944891157MGMTc.617G= (p.Arg206=)
c.524G= (p.Arg175=)
c.347G= (p.Arg116=)
c.533G= (p.Arg178=)
10g.129766897G>TCA378713151MGMTc.617G>T (p.Arg206Leu)
c.524G>T (p.Arg175Leu)
c.347G>T (p.Arg116Leu)
c.533G>T (p.Arg178Leu)
 dbSNP
10g.129766898G>ACA471816584MGMTc.618G>A (p.Arg206=)
c.525G>A (p.Arg175=)
c.348G>A (p.Arg116=)
c.534G>A (p.Arg178=)
 gnomAD v4
10g.129766898G>CCA471816583MGMTc.618G>C (p.Arg206=)
c.525G>C (p.Arg175=)
c.348G>C (p.Arg116=)
c.534G>C (p.Arg178=)
10g.129766898G>TCA471816582MGMTc.618G>T (p.Arg206=)
c.525G>T (p.Arg175=)
c.348G>T (p.Arg116=)
c.534G>T (p.Arg178=)
10g.129766899T>ACA378713152MGMTc.619T>A (p.Leu207Met)
c.526T>A (p.Leu176Met)
c.349T>A (p.Leu117Met)
c.535T>A (p.Leu179Met)
 dbSNP gnomAD v3 gnomAD v4
10g.129766899T>CCA5748148MGMTc.619T>C (p.Leu207=)
c.526T>C (p.Leu176=)
c.349T>C (p.Leu117=)
c.535T>C (p.Leu179=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766899T>GCA378713153MGMTc.619T>G (p.Leu207Val)
c.526T>G (p.Leu176Val)
c.349T>G (p.Leu117Val)
c.535T>G (p.Leu179Val)
 dbSNP gnomAD v2 gnomAD v4
10g.129766899T=CA1944891163MGMTc.619T= (p.Leu207=)
c.526T= (p.Leu176=)
c.349T= (p.Leu117=)
c.535T= (p.Leu179=)
10g.129766900T>ACA378713154MGMTc.620T>A (p.Leu207Ter)
c.527T>A (p.Leu176Ter)
c.350T>A (p.Leu117Ter)
c.536T>A (p.Leu179Ter)
10g.129766900T>CCA378713156MGMTc.620T>C (p.Leu207Ser)
c.527T>C (p.Leu176Ser)
c.350T>C (p.Leu117Ser)
c.536T>C (p.Leu179Ser)
10g.129766900T>GCA378713155MGMTc.620T>G (p.Leu207Trp)
c.527T>G (p.Leu176Trp)
c.350T>G (p.Leu117Trp)
c.536T>G (p.Leu179Trp)
10g.129766901G>ACA471816588MGMTc.621G>A (p.Leu207=)
c.528G>A (p.Leu176=)
c.351G>A (p.Leu117=)
c.537G>A (p.Leu179=)
10g.129766901G>CCA378713157MGMTc.621G>C (p.Leu207Phe)
c.528G>C (p.Leu176Phe)
c.351G>C (p.Leu117Phe)
c.537G>C (p.Leu179Phe)
10g.129766901G>TCA378713158MGMTc.621G>T (p.Leu207Phe)
c.528G>T (p.Leu176Phe)
c.351G>T (p.Leu117Phe)
c.537G>T (p.Leu179Phe)
 gnomAD v4
10g.129766902G>ACA5748149MGMTc.622G>A (p.Gly208Arg)
c.529G>A (p.Gly177Arg)
c.352G>A (p.Gly118Arg)
c.538G>A (p.Gly180Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766902G>CCA5748150MGMTc.622G>C (p.Gly208Arg)
c.529G>C (p.Gly177Arg)
c.352G>C (p.Gly118Arg)
c.538G>C (p.Gly180Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766902G=CA1944891169MGMTc.622G= (p.Gly208=)
c.529G= (p.Gly177=)
c.352G= (p.Gly118=)
c.538G= (p.Gly180=)
10g.129766902G>TCA378713159MGMTc.622G>T (p.Gly208Trp)
c.529G>T (p.Gly177Trp)
c.352G>T (p.Gly118Trp)
c.538G>T (p.Gly180Trp)
 dbSNP gnomAD v2 gnomAD v4
10g.129766903G>ACA5748151MGMTc.623G>A (p.Gly208Glu)
c.530G>A (p.Gly177Glu)
c.353G>A (p.Gly118Glu)
c.539G>A (p.Gly180Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766903G>CCA378713160MGMTc.623G>C (p.Gly208Ala)
c.530G>C (p.Gly177Ala)
c.353G>C (p.Gly118Ala)
c.539G>C (p.Gly180Ala)
10g.129766903G=CA1944891180MGMTc.623G= (p.Gly208=)
c.530G= (p.Gly177=)
c.353G= (p.Gly118=)
c.539G= (p.Gly180=)
10g.129766903G>TCA378713161MGMTc.623G>T (p.Gly208Val)
c.530G>T (p.Gly177Val)
c.353G>T (p.Gly118Val)
c.539G>T (p.Gly180Val)
10g.129766904G>ACA471816590MGMTc.624G>A (p.Gly208=)
c.531G>A (p.Gly177=)
c.354G>A (p.Gly118=)
c.540G>A (p.Gly180=)
 dbSNP gnomAD v2 gnomAD v4
10g.129766904G>CCA471816591MGMTc.624G>C (p.Gly208=)
c.531G>C (p.Gly177=)
c.354G>C (p.Gly118=)
c.540G>C (p.Gly180=)
10g.129766904G=CA1944891181MGMTc.624G= (p.Gly208=)
c.531G= (p.Gly177=)
c.354G= (p.Gly118=)
c.540G= (p.Gly180=)
10g.129766904G>TCA471816592MGMTc.624G>T (p.Gly208=)
c.531G>T (p.Gly177=)
c.354G>T (p.Gly118=)
c.540G>T (p.Gly180=)
10g.129766905A>CCA378713162MGMTc.625A>C (p.Lys209Gln)
c.532A>C (p.Lys178Gln)
c.355A>C (p.Lys119Gln)
c.541A>C (p.Lys181Gln)
10g.129766905A>GCA378713163MGMTc.625A>G (p.Lys209Glu)
c.532A>G (p.Lys178Glu)
c.355A>G (p.Lys119Glu)
c.541A>G (p.Lys181Glu)
10g.129766905A>TCA378713164MGMTc.625A>T (p.Lys209Ter)
c.532A>T (p.Lys178Ter)
c.355A>T (p.Lys119Ter)
c.541A>T (p.Lys181Ter)
10g.129766906A=CA1944891186MGMTc.626A= (p.Lys209=)
c.533A= (p.Lys178=)
c.356A= (p.Lys119=)
c.542A= (p.Lys181=)
10g.129766906A>CCA378713165MGMTc.626A>C (p.Lys209Thr)
c.533A>C (p.Lys178Thr)
c.356A>C (p.Lys119Thr)
c.542A>C (p.Lys181Thr)
10g.129766906A>GCA5748152MGMTc.626A>G (p.Lys209Arg)
c.533A>G (p.Lys178Arg)
c.356A>G (p.Lys119Arg)
c.542A>G (p.Lys181Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.129766906A>TCA378713166MGMTc.626A>T (p.Lys209Met)
c.533A>T (p.Lys178Met)
c.356A>T (p.Lys119Met)
c.542A>T (p.Lys181Met)
10g.129766907G>ACA471816594MGMTc.627G>A (p.Lys209=)
c.534G>A (p.Lys178=)
c.357G>A (p.Lys119=)
c.543G>A (p.Lys181=)
10g.129766907G>CCA378713167MGMTc.627G>C (p.Lys209Asn)
c.534G>C (p.Lys178Asn)
c.357G>C (p.Lys119Asn)
c.543G>C (p.Lys181Asn)
10g.129766907G=CA1944891191MGMTc.627G= (p.Lys209=)
c.534G= (p.Lys178=)
c.357G= (p.Lys119=)
c.543G= (p.Lys181=)
10g.129766907G>TCA378713168MGMTc.627G>T (p.Lys209Asn)
c.534G>T (p.Lys178Asn)
c.357G>T (p.Lys119Asn)
c.543G>T (p.Lys181Asn)
 dbSNP
10g.129766908C>ACA378713169MGMTc.628C>A (p.Pro210Thr)
c.535C>A (p.Pro179Thr)
c.358C>A (p.Pro120Thr)
c.544C>A (p.Pro182Thr)
10g.129766908C>GCA378713170MGMTc.628C>G (p.Pro210Ala)
c.535C>G (p.Pro179Ala)
c.358C>G (p.Pro120Ala)
c.544C>G (p.Pro182Ala)
10g.129766908C>TCA378713171MGMTc.628C>T (p.Pro210Ser)
c.535C>T (p.Pro179Ser)
c.358C>T (p.Pro120Ser)
c.544C>T (p.Pro182Ser)
10g.129766909C>ACA378713172MGMTc.629C>A (p.Pro210Gln)
c.536C>A (p.Pro179Gln)
c.359C>A (p.Pro120Gln)
c.545C>A (p.Pro182Gln)
10g.129766909C>GCA378713173MGMTc.629C>G (p.Pro210Arg)
c.536C>G (p.Pro179Arg)
c.359C>G (p.Pro120Arg)
c.545C>G (p.Pro182Arg)
10g.129766909C>TCA378713174MGMTc.629C>T (p.Pro210Leu)
c.536C>T (p.Pro179Leu)
c.359C>T (p.Pro120Leu)
c.545C>T (p.Pro182Leu)
10g.129766910A>CCA471816596MGMTc.630A>C (p.Pro210=)
c.537A>C (p.Pro179=)
c.360A>C (p.Pro120=)
c.546A>C (p.Pro182=)
10g.129766910A>GCA471816597MGMTc.630A>G (p.Pro210=)
c.537A>G (p.Pro179=)
c.360A>G (p.Pro120=)
c.546A>G (p.Pro182=)
10g.129766910A>TCA471816598MGMTc.630A>T (p.Pro210=)
c.537A>T (p.Pro179=)
c.360A>T (p.Pro120=)
c.546A>T (p.Pro182=)
10g.129766911G>ACA5748153MGMTc.631G>A (p.Gly211Ser)
c.538G>A (p.Gly180Ser)
c.361G>A (p.Gly121Ser)
c.547G>A (p.Gly183Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.129766911G>CCA378713175MGMTc.631G>C (p.Gly211Arg)
c.538G>C (p.Gly180Arg)
c.361G>C (p.Gly121Arg)
c.547G>C (p.Gly183Arg)
10g.129766911G=CA1944891196MGMTc.631G= (p.Gly211=)
c.538G= (p.Gly180=)
c.361G= (p.Gly121=)
c.547G= (p.Gly183=)
10g.129766911G>TCA378713176MGMTc.631G>T (p.Gly211Cys)
c.538G>T (p.Gly180Cys)
c.361G>T (p.Gly121Cys)
c.547G>T (p.Gly183Cys)

Number of alleles fetched