Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.4110576G>ACA9091012MAP2K2n.822C>T
c.383C>T (p.Pro128Leu)
c.92C>T (p.Pro31Leu)
n.580C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.4110576G>CCA180731MAP2K2n.822C>G
c.383C>G (p.Pro128Arg)
c.92C>G (p.Pro31Arg)
n.580C>G
 ClinVar dbSNP
19g.4110576G=CA2319230228MAP2K2n.822C=
c.383C= (p.Pro128=)
c.92C= (p.Pro31=)
n.580C=
19g.4110576G>TCA279962MAP2K2n.822C>A
c.383C>A (p.Pro128Gln)
c.92C>A (p.Pro31Gln)
n.580C>A
 ClinVar dbSNP
19g.4110577delCA2585249275MAP2K2n.822del
c.383del (p.Pro128ArgfsTer?)
c.92del (p.Pro31ArgfsTer?)
n.580del
 gnomAD v4
19g.4110577G>ACA403391477MAP2K2n.821C>T
c.382C>T (p.Pro128Ser)
c.91C>T (p.Pro31Ser)
n.579C>T
 dbSNP gnomAD v4
19g.4110577G>CCA403391479MAP2K2n.821C>G
c.382C>G (p.Pro128Ala)
c.91C>G (p.Pro31Ala)
n.579C>G
 dbSNP
19g.4110577G>TCA403391481MAP2K2n.821C>A
c.382C>A (p.Pro128Thr)
c.91C>A (p.Pro31Thr)
n.579C>A
19g.4110578C>ACA9091014MAP2K2n.820G>T
c.381G>T (p.Ser127=)
c.90G>T (p.Ser30=)
n.578G>T
 dbSNP ExAC
19g.4110578C=CA2319230238MAP2K2n.820G=
c.381G= (p.Ser127=)
c.90G= (p.Ser30=)
n.578G=
19g.4110578C>GCA504987500MAP2K2n.820G>C
c.381G>C (p.Ser127=)
c.90G>C (p.Ser30=)
n.578G>C
 dbSNP
19g.4110578C>TCA9091013MAP2K2n.820G>A
c.381G>A (p.Ser127=)
c.90G>A (p.Ser30=)
n.578G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110579G>ACA403391488MAP2K2n.819C>T
c.380C>T (p.Ser127Leu)
c.89C>T (p.Ser30Leu)
n.577C>T
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
19g.4110579G>CCA403391490MAP2K2n.819C>G
c.380C>G (p.Ser127Trp)
c.89C>G (p.Ser30Trp)
n.577C>G
 dbSNP
19g.4110579G=CA2319230243MAP2K2n.819C=
c.380C= (p.Ser127=)
c.89C= (p.Ser30=)
n.577C=
19g.4110579G>TCA403391486MAP2K2n.819C>A
c.380C>A (p.Ser127Ter)
c.89C>A (p.Ser30Ter)
n.577C>A
 dbSNP gnomAD v4
19g.4110580A>CCA403391493MAP2K2n.818T>G
c.379T>G (p.Ser127Ala)
c.88T>G (p.Ser30Ala)
n.576T>G
19g.4110580A>GCA403391495MAP2K2n.818T>C
c.379T>C (p.Ser127Pro)
c.88T>C (p.Ser30Pro)
n.576T>C
 dbSNP
19g.4110580A>TCA403391497MAP2K2n.818T>A
c.379T>A (p.Ser127Thr)
c.88T>A (p.Ser30Thr)
n.576T>A
 dbSNP gnomAD v4
19g.4110581G>ACA504987502MAP2K2n.817C>T
c.378C>T (p.Asn126=)
c.87C>T (p.Asn29=)
n.575C>T
 dbSNP gnomAD v3 gnomAD v4
19g.4110581G>CCA403391499MAP2K2n.817C>G
c.378C>G (p.Asn126Lys)
c.87C>G (p.Asn29Lys)
n.575C>G
 dbSNP
19g.4110581G=CA2319230248MAP2K2n.817C=
c.378C= (p.Asn126=)
c.87C= (p.Asn29=)
n.575C=
19g.4110581G>TCA403391500MAP2K2n.817C>A
c.378C>A (p.Asn126Lys)
c.87C>A (p.Asn29Lys)
n.575C>A
19g.4110582T>ACA403391503MAP2K2n.816A>T
c.377A>T (p.Asn126Ile)
c.86A>T (p.Asn29Ile)
n.574A>T
 dbSNP
19g.4110582T>CCA403391504MAP2K2n.816A>G
c.377A>G (p.Asn126Ser)
c.86A>G (p.Asn29Ser)
n.574A>G
 ClinVar gnomAD v4
19g.4110582T>GCA403391506MAP2K2n.816A>C
c.377A>C (p.Asn126Thr)
c.86A>C (p.Asn29Thr)
n.574A>C
 dbSNP
19g.4110583T>ACA403391508MAP2K2n.815A>T
c.376A>T (p.Asn126Tyr)
c.85A>T (p.Asn29Tyr)
n.573A>T
19g.4110583T>CCA16602631MAP2K2n.815A>G
c.376A>G (p.Asn126Asp)
c.85A>G (p.Asn29Asp)
n.573A>G
 ClinVar dbSNP COSMIC COSMIC
19g.4110583T>GCA403391510MAP2K2n.815A>C
c.376A>C (p.Asn126His)
c.85A>C (p.Asn29His)
n.573A>C
 ClinVar dbSNP gnomAD v4
19g.4110583T=CA2319230252MAP2K2n.815A=
c.376A= (p.Asn126=)
c.85A= (p.Asn29=)
n.573A=
19g.4110584G>ACA504987503MAP2K2n.814C>T
c.375C>T (p.Cys125=)
c.84C>T (p.Cys28=)
n.572C>T
 dbSNP COSMIC COSMIC
19g.4110584G>CCA403391512MAP2K2n.814C>G
c.375C>G (p.Cys125Trp)
c.84C>G (p.Cys28Trp)
n.572C>G
 dbSNP
19g.4110584G>TCA403391514MAP2K2n.814C>A
c.375C>A (p.Cys125Ter)
c.84C>A (p.Cys28Ter)
n.572C>A
19g.4110585C>ACA403391521MAP2K2n.813G>T
c.374G>T (p.Cys125Phe)
c.83G>T (p.Cys28Phe)
n.571G>T
19g.4110585C>GCA403391519MAP2K2n.813G>C
c.374G>C (p.Cys125Ser)
c.83G>C (p.Cys28Ser)
n.571G>C
 COSMIC
19g.4110585C>TCA403391517MAP2K2n.813G>A
c.374G>A (p.Cys125Tyr)
c.83G>A (p.Cys28Tyr)
n.571G>A
19g.4110586A=CA2319230261MAP2K2n.812T=
c.373T= (p.Cys125=)
c.82T= (p.Cys28=)
n.570T=
19g.4110586A>CCA403391522MAP2K2n.812T>G
c.373T>G (p.Cys125Gly)
c.82T>G (p.Cys28Gly)
n.570T>G
 dbSNP
19g.4110586A>GCA403391525MAP2K2n.812T>C
c.373T>C (p.Cys125Arg)
c.82T>C (p.Cys28Arg)
n.570T>C
19g.4110586A>TCA16602632MAP2K2n.812T>A
c.373T>A (p.Cys125Ser)
c.82T>A (p.Cys28Ser)
n.570T>A
 ClinVar dbSNP COSMIC COSMIC
19g.4110587T>ACA403391528MAP2K2n.811A>T
c.372A>T (p.Glu124Asp)
c.81A>T (p.Glu27Asp)
n.569A>T
 dbSNP gnomAD v2 gnomAD v4
19g.4110587T>CCA504987504MAP2K2n.811A>G
c.372A>G (p.Glu124=)
c.81A>G (p.Glu27=)
n.569A>G
19g.4110587T>GCA403391529MAP2K2n.811A>C
c.372A>C (p.Glu124Asp)
c.81A>C (p.Glu27Asp)
n.569A>C
 dbSNP
19g.4110587T=CA2319230269MAP2K2n.811A=
c.372A= (p.Glu124=)
c.81A= (p.Glu27=)
n.569A=
19g.4110588T>ACA403391531MAP2K2n.810A>T
c.371A>T (p.Glu124Val)
c.80A>T (p.Glu27Val)
n.568A>T
19g.4110588T>CCA9091015MAP2K2n.810A>G
c.371A>G (p.Glu124Gly)
c.80A>G (p.Glu27Gly)
n.568A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110588T>GCA403391534MAP2K2n.810A>C
c.371A>C (p.Glu124Ala)
c.80A>C (p.Glu27Ala)
n.568A>C
19g.4110588T=CA2319230272MAP2K2n.810A=
c.371A= (p.Glu124=)
c.80A= (p.Glu27=)
n.568A=
19g.4110589C>ACA403391536MAP2K2n.809G>T
c.370G>T (p.Glu124Ter)
c.79G>T (p.Glu27Ter)
n.567G>T
 dbSNP
19g.4110589C=CA2319230275MAP2K2n.809G=
c.370G= (p.Glu124=)
c.79G= (p.Glu27=)
n.567G=
19g.4110589C>GCA403391538MAP2K2n.809G>C
c.370G>C (p.Glu124Gln)
c.79G>C (p.Glu27Gln)
n.567G>C
 dbSNP
19g.4110589C>TCA304453891MAP2K2n.809G>A
c.370G>A (p.Glu124Lys)
c.79G>A (p.Glu27Lys)
n.567G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110590G>ACA9091016MAP2K2n.808C>T
c.369C>T (p.His123=)
c.78C>T (p.His26=)
n.566C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110590G>CCA403391541MAP2K2n.808C>G
c.369C>G (p.His123Gln)
c.78C>G (p.His26Gln)
n.566C>G
 dbSNP
19g.4110590G=CA2319230277MAP2K2n.808C=
c.369C= (p.His123=)
c.78C= (p.His26=)
n.566C=
19g.4110590G>TCA403391543MAP2K2n.808C>A
c.369C>A (p.His123Gln)
c.78C>A (p.His26Gln)
n.566C>A
19g.4110591T>ACA403391547MAP2K2n.807A>T
c.368A>T (p.His123Leu)
c.77A>T (p.His26Leu)
n.565A>T
 dbSNP
19g.4110591T>CCA403391549MAP2K2n.807A>G
c.368A>G (p.His123Arg)
c.77A>G (p.His26Arg)
n.565A>G
 dbSNP
19g.4110591T>GCA403391545MAP2K2n.807A>C
c.368A>C (p.His123Pro)
c.77A>C (p.His26Pro)
n.565A>C
 dbSNP
19g.4110592G>ACA403391551MAP2K2n.806C>T
c.367C>T (p.His123Tyr)
c.76C>T (p.His26Tyr)
n.564C>T
 dbSNP
19g.4110592G>CCA403391553MAP2K2n.806C>G
c.367C>G (p.His123Asp)
c.76C>G (p.His26Asp)
n.564C>G
 dbSNP
19g.4110592G>TCA403391552MAP2K2n.806C>A
c.367C>A (p.His123Asn)
c.76C>A (p.His26Asn)
n.564C>A
19g.4110593C>ACA504987506MAP2K2n.805G>T
c.366G>T (p.Leu122=)
c.75G>T (p.Leu25=)
n.563G>T
 dbSNP
19g.4110593C=CA2319230281MAP2K2n.805G=
c.366G= (p.Leu122=)
c.75G= (p.Leu25=)
n.563G=
19g.4110593C>GCA504987507MAP2K2n.805G>C
c.366G>C (p.Leu122=)
c.75G>C (p.Leu25=)
n.563G>C
 dbSNP
19g.4110593C>TCA504987508MAP2K2n.805G>A
c.366G>A (p.Leu122=)
c.75G>A (p.Leu25=)
n.563G>A
 dbSNP
19g.4110594A>CCA403391555MAP2K2n.804T>G
c.365T>G (p.Leu122Arg)
c.74T>G (p.Leu25Arg)
n.562T>G
19g.4110594A>GCA403391557MAP2K2n.804T>C
c.365T>C (p.Leu122Pro)
c.74T>C (p.Leu25Pro)
n.562T>C
 dbSNP
19g.4110594A>TCA403391562MAP2K2n.804T>A
c.365T>A (p.Leu122Gln)
c.74T>A (p.Leu25Gln)
n.562T>A
 dbSNP
19g.4110595G>ACA504987509MAP2K2n.803C>T
c.364C>T (p.Leu122=)
c.73C>T (p.Leu25=)
n.561C>T
 dbSNP gnomAD v4
19g.4110595G>CCA403391563MAP2K2n.803C>G
c.364C>G (p.Leu122Val)
c.73C>G (p.Leu25Val)
n.561C>G
 dbSNP
19g.4110595G>TCA403391565MAP2K2n.803C>A
c.364C>A (p.Leu122Met)
c.73C>A (p.Leu25Met)
n.561C>A
 gnomAD v4
19g.4110596G>ACA504987510MAP2K2n.802C>T
c.363C>T (p.Val121=)
c.72C>T (p.Val24=)
n.560C>T
 ClinVar dbSNP
19g.4110596G>CCA504987511MAP2K2n.802C>G
c.363C>G (p.Val121=)
c.72C>G (p.Val24=)
n.560C>G
 ClinVar dbSNP gnomAD v4
19g.4110596G=CA2319230285MAP2K2n.802C=
c.363C= (p.Val121=)
c.72C= (p.Val24=)
n.560C=
19g.4110596G>TCA504987512MAP2K2n.802C>A
c.363C>A (p.Val121=)
c.72C>A (p.Val24=)
n.560C>A
 ClinVar dbSNP COSMIC COSMIC
19g.4110597A>CCA403391568MAP2K2n.801T>G
c.362T>G (p.Val121Gly)
c.71T>G (p.Val24Gly)
n.559T>G
 dbSNP
19g.4110597A>GCA403391569MAP2K2n.801T>C
c.362T>C (p.Val121Ala)
c.71T>C (p.Val24Ala)
n.559T>C
 dbSNP
19g.4110597A>TCA403391572MAP2K2n.801T>A
c.362T>A (p.Val121Asp)
c.71T>A (p.Val24Asp)
n.559T>A
 dbSNP
19g.4110598C>ACA403391574MAP2K2n.800G>T
c.361G>T (p.Val121Phe)
c.70G>T (p.Val24Phe)
n.558G>T
19g.4110598C>GCA403391575MAP2K2n.800G>C
c.361G>C (p.Val121Leu)
c.70G>C (p.Val24Leu)
n.558G>C
 dbSNP
19g.4110598C>TCA403391576MAP2K2n.800G>A
c.361G>A (p.Val121Ile)
c.70G>A (p.Val24Ile)
n.558G>A
 dbSNP
19g.4110599C>ACA403391578MAP2K2n.799G>T
c.360G>T (p.Gln120His)
c.69G>T (p.Gln23His)
n.557G>T
 ClinVar dbSNP
19g.4110599C>GCA403391580MAP2K2n.799G>C
c.360G>C (p.Gln120His)
c.69G>C (p.Gln23His)
n.557G>C
19g.4110599C>TCA504987513MAP2K2n.799G>A
c.360G>A (p.Gln120=)
c.69G>A (p.Gln23=)
n.557G>A
 dbSNP
19g.4110600T>ACA403391585MAP2K2n.798A>T
c.359A>T (p.Gln120Leu)
c.68A>T (p.Gln23Leu)
n.556A>T
 dbSNP
19g.4110600T>CCA403391583MAP2K2n.798A>G
c.359A>G (p.Gln120Arg)
c.68A>G (p.Gln23Arg)
n.556A>G
 dbSNP
19g.4110600T>GCA403391581MAP2K2n.798A>C
c.359A>C (p.Gln120Pro)
c.68A>C (p.Gln23Pro)
n.556A>C
19g.4110600T=CA2319230770MAP2K2n.798A=
c.359A= (p.Gln120=)
c.68A= (p.Gln23=)
n.556A=
19g.4110601G>ACA403391586MAP2K2n.797C>T
c.358C>T (p.Gln120Ter)
c.67C>T (p.Gln23Ter)
n.555C>T
 dbSNP
19g.4110601G>CCA403391587MAP2K2n.797C>G
c.358C>G (p.Gln120Glu)
c.67C>G (p.Gln23Glu)
n.555C>G
 ClinVar dbSNP
19g.4110601G=CA2319230771MAP2K2n.797C=
c.358C= (p.Gln120=)
c.67C= (p.Gln23=)
n.555C=
19g.4110601G>TCA403391589MAP2K2n.797C>A
c.358C>A (p.Gln120Lys)
c.67C>A (p.Gln23Lys)
n.555C>A
19g.4110602C>ACA504987516MAP2K2n.796G>T
c.357G>T (p.Leu119=)
c.66G>T (p.Leu22=)
n.554G>T
19g.4110602C=CA2319230772MAP2K2n.796G=
c.357G= (p.Leu119=)
c.66G= (p.Leu22=)
n.554G=
19g.4110602C>GCA504987515MAP2K2n.796G>C
c.357G>C (p.Leu119=)
c.66G>C (p.Leu22=)
n.554G>C
 dbSNP
19g.4110602C>TCA504987514MAP2K2n.796G>A
c.357G>A (p.Leu119=)
c.66G>A (p.Leu22=)
n.554G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.4110603A>CCA403391591MAP2K2n.795T>G
c.356T>G (p.Leu119Arg)
c.65T>G (p.Leu22Arg)
n.553T>G
19g.4110603A>GCA403391593MAP2K2n.795T>C
c.356T>C (p.Leu119Pro)
c.65T>C (p.Leu22Pro)
n.553T>C
 ClinVar dbSNP
19g.4110603A>TCA403391595MAP2K2n.795T>A
c.356T>A (p.Leu119Gln)
c.65T>A (p.Leu22Gln)
n.553T>A
 dbSNP
19g.4110604G>ACA504987517MAP2K2n.794C>T
c.355C>T (p.Leu119=)
c.64C>T (p.Leu22=)
n.552C>T
 dbSNP
19g.4110604G>CCA403391597MAP2K2n.794C>G
c.355C>G (p.Leu119Val)
c.64C>G (p.Leu22Val)
n.552C>G
 dbSNP gnomAD v4
19g.4110604G>TCA403391599MAP2K2n.794C>A
c.355C>A (p.Leu119Met)
c.64C>A (p.Leu22Met)
n.552C>A
19g.4110605C>ACA403391601MAP2K2n.793G>T
c.354G>T (p.Glu118Asp)
c.63G>T (p.Glu21Asp)
n.551G>T
 dbSNP
19g.4110605C>GCA403391603MAP2K2n.793G>C
c.354G>C (p.Glu118Asp)
c.63G>C (p.Glu21Asp)
n.551G>C
 dbSNP
19g.4110605C>TCA504987518MAP2K2n.793G>A
c.354G>A (p.Glu118=)
c.63G>A (p.Glu21=)
n.551G>A
 dbSNP gnomAD v4
19g.4110606T>ACA403391605MAP2K2n.792A>T
c.353A>T (p.Glu118Val)
c.62A>T (p.Glu21Val)
n.550A>T
 dbSNP
19g.4110606T>CCA403391607MAP2K2n.792A>G
c.353A>G (p.Glu118Gly)
c.62A>G (p.Glu21Gly)
n.550A>G
19g.4110606T>GCA403391609MAP2K2n.792A>C
c.353A>C (p.Glu118Ala)
c.62A>C (p.Glu21Ala)
n.550A>C
19g.4110607C>ACA403391612MAP2K2n.791G>T
c.352G>T (p.Glu118Ter)
c.61G>T (p.Glu21Ter)
n.549G>T
 dbSNP
19g.4110607C=CA2319230773MAP2K2n.791G=
c.352G= (p.Glu118=)
c.61G= (p.Glu21=)
n.549G=
19g.4110607C>GCA403391613MAP2K2n.791G>C
c.352G>C (p.Glu118Gln)
c.61G>C (p.Glu21Gln)
n.549G>C
 dbSNP
19g.4110607C>TCA9091017MAP2K2n.791G>A
c.352G>A (p.Glu118Lys)
c.61G>A (p.Glu21Lys)
n.549G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.4110608G>ACA504987520MAP2K2n.790C>T
c.351C>T (p.Arg117=)
c.60C>T (p.Arg20=)
n.548C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110608G>CCA9091018MAP2K2n.790C>G
c.351C>G (p.Arg117=)
c.60C>G (p.Arg20=)
n.548C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110608G=CA2319230774MAP2K2n.790C=
c.351C= (p.Arg117=)
c.60C= (p.Arg20=)
n.548C=
19g.4110608G>TCA504987521MAP2K2n.790C>A
c.351C>A (p.Arg117=)
c.60C>A (p.Arg20=)
n.548C>A
 dbSNP
19g.4110609C>ACA403391616MAP2K2n.789G>T
c.350G>T (p.Arg117Leu)
c.59G>T (p.Arg20Leu)
n.547G>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110609C=CA2319230775MAP2K2n.789G=
c.350G= (p.Arg117=)
c.59G= (p.Arg20=)
n.547G=
19g.4110609C>GCA403391617MAP2K2n.789G>C
c.350G>C (p.Arg117Pro)
c.59G>C (p.Arg20Pro)
n.547G>C
19g.4110609C>TCA403391619MAP2K2n.789G>A
c.350G>A (p.Arg117His)
c.59G>A (p.Arg20His)
n.547G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.4110610G>ACA9091019MAP2K2n.788C>T
c.349C>T (p.Arg117Cys)
c.58C>T (p.Arg20Cys)
n.546C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110610G>CCA403391622MAP2K2n.788C>G
c.349C>G (p.Arg117Gly)
c.58C>G (p.Arg20Gly)
n.546C>G
 dbSNP
19g.4110610G=CA2319230776MAP2K2n.788C=
c.349C= (p.Arg117=)
c.58C= (p.Arg20=)
n.546C=
19g.4110610G>TCA403391624MAP2K2n.788C>A
c.349C>A (p.Arg117Ser)
c.58C>A (p.Arg20Ser)
n.546C>A
 dbSNP
19g.4110611G>ACA504987522MAP2K2n.787C>T
c.348C>T (p.Ile116=)
c.57C>T (p.Ile19=)
n.545C>T
 dbSNP
19g.4110611G>CCA403391626MAP2K2n.787C>G
c.348C>G (p.Ile116Met)
c.57C>G (p.Ile19Met)
n.545C>G
 dbSNP
19g.4110611G>TCA504987523MAP2K2n.787C>A
c.348C>A (p.Ile116=)
c.57C>A (p.Ile19=)
n.545C>A
 dbSNP
19g.4110612A>CCA403391628MAP2K2n.786T>G
c.347T>G (p.Ile116Ser)
c.56T>G (p.Ile19Ser)
n.544T>G
19g.4110612A>GCA403391630MAP2K2n.786T>C
c.347T>C (p.Ile116Thr)
c.56T>C (p.Ile19Thr)
n.544T>C
 dbSNP
19g.4110612A>TCA403391632MAP2K2n.786T>A
c.347T>A (p.Ile116Asn)
c.56T>A (p.Ile19Asn)
n.544T>A
 dbSNP
19g.4110613T>ACA403391638MAP2K2n.785A>T
c.346A>T (p.Ile116Phe)
c.55A>T (p.Ile19Phe)
n.543A>T
 dbSNP
19g.4110613T>CCA403391637MAP2K2n.785A>G
c.346A>G (p.Ile116Val)
c.55A>G (p.Ile19Val)
n.543A>G
 ClinVar gnomAD v4
19g.4110613T>GCA403391635MAP2K2n.785A>C
c.346A>C (p.Ile116Leu)
c.55A>C (p.Ile19Leu)
n.543A>C
 dbSNP
19g.4110614G>ACA9091020MAP2K2n.784C>T
c.345C>T (p.Ile115=)
c.54C>T (p.Ile18=)
n.542C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.4110614G>CCA403391642MAP2K2n.784C>G
c.345C>G (p.Ile115Met)
c.54C>G (p.Ile18Met)
n.542C>G
 dbSNP
19g.4110614G=CA2319230777MAP2K2n.784C=
c.345C= (p.Ile115=)
c.54C= (p.Ile18=)
n.542C=
19g.4110614G>TCA504987524MAP2K2n.784C>A
c.345C>A (p.Ile115=)
c.54C>A (p.Ile18=)
n.542C>A
19g.4110615A>CCA403391644MAP2K2n.783T>G
c.344T>G (p.Ile115Ser)
c.53T>G (p.Ile18Ser)
n.541T>G
 dbSNP
19g.4110615A>GCA403391646MAP2K2n.783T>C
c.344T>C (p.Ile115Thr)
c.53T>C (p.Ile18Thr)
n.541T>C
 dbSNP
19g.4110615A>TCA403391648MAP2K2n.783T>A
c.344T>A (p.Ile115Asn)
c.53T>A (p.Ile18Asn)
n.541T>A
 dbSNP
19g.4110615_4110643delinsATCTGGTTCCGGATGGCCGGCTTGATCTCCA2319230778MAP2K2n.755_783delinsGAGATCAAGCCGGCCATCCGGAACCAGAT
c.316_344delinsGAGATCAAGCCGGCCATCCGGAACCAGAT (p.Glu106=)
c.25_53delinsGAGATCAAGCCGGCCATCCGGAACCAGAT (p.Glu9=)
n.513_541delinsGAGATCAAGCCGGCCATCCGGAACCAGAT
19g.4110616T>ACA403391651MAP2K2n.782A>T
c.343A>T (p.Ile115Phe)
c.52A>T (p.Ile18Phe)
n.540A>T
19g.4110616T>CCA403391653MAP2K2n.782A>G
c.343A>G (p.Ile115Val)
c.52A>G (p.Ile18Val)
n.540A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110616T>GCA403391654MAP2K2n.782A>C
c.343A>C (p.Ile115Leu)
c.52A>C (p.Ile18Leu)
n.540A>C
 dbSNP
19g.4110616T=CA2319230779MAP2K2n.782A=
c.343A= (p.Ile115=)
c.52A= (p.Ile18=)
n.540A=
19g.4110616_4110643delCA9091021MAP2K2n.755_782del
c.316_343del (p.Glu106SerfsTer?)
c.25_52del (p.Glu9SerfsTer?)
n.513_540del
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110617C>ACA403391655MAP2K2n.781G>T
c.342G>T (p.Gln114His)
c.51G>T (p.Gln17His)
n.539G>T
 dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.4110617C=CA2319230780MAP2K2n.781G=
c.342G= (p.Gln114=)
c.51G= (p.Gln17=)
n.539G=
19g.4110617C>GCA403391658MAP2K2n.781G>C
c.342G>C (p.Gln114His)
c.51G>C (p.Gln17His)
n.539G>C
 dbSNP gnomAD v4
19g.4110617C>TCA504987525MAP2K2n.781G>A
c.342G>A (p.Gln114=)
c.51G>A (p.Gln17=)
n.539G>A
 dbSNP gnomAD v4
19g.4110618T>ACA403391664MAP2K2n.780A>T
c.341A>T (p.Gln114Leu)
c.50A>T (p.Gln17Leu)
n.538A>T
19g.4110618T>CCA403391662MAP2K2n.780A>G
c.341A>G (p.Gln114Arg)
c.50A>G (p.Gln17Arg)
n.538A>G
19g.4110618T>GCA403391660MAP2K2n.780A>C
c.341A>C (p.Gln114Pro)
c.50A>C (p.Gln17Pro)
n.538A>C
19g.4110619G>ACA403391666MAP2K2n.779C>T
c.340C>T (p.Gln114Ter)
c.49C>T (p.Gln17Ter)
n.537C>T
 COSMIC COSMIC
19g.4110619G>CCA403391670MAP2K2n.779C>G
c.340C>G (p.Gln114Glu)
c.49C>G (p.Gln17Glu)
n.537C>G
19g.4110619G>TCA403391668MAP2K2n.779C>A
c.340C>A (p.Gln114Lys)
c.49C>A (p.Gln17Lys)
n.537C>A
19g.4110620G>ACA504987526MAP2K2n.778C>T
c.339C>T (p.Asn113=)
c.48C>T (p.Asn16=)
n.536C>T
 ClinVar dbSNP
19g.4110620G>CCA403391672MAP2K2n.778C>G
c.339C>G (p.Asn113Lys)
c.48C>G (p.Asn16Lys)
n.536C>G
 dbSNP
19g.4110620G=CA2319230781MAP2K2n.778C=
c.339C= (p.Asn113=)
c.48C= (p.Asn16=)
n.536C=
19g.4110620G>TCA403391674MAP2K2n.778C>A
c.339C>A (p.Asn113Lys)
c.48C>A (p.Asn16Lys)
n.536C>A
19g.4110621T>ACA403391676MAP2K2n.777A>T
c.338A>T (p.Asn113Ile)
c.47A>T (p.Asn16Ile)
n.535A>T
 dbSNP
19g.4110621T>CCA403391678MAP2K2n.777A>G
c.338A>G (p.Asn113Ser)
c.47A>G (p.Asn16Ser)
n.535A>G
 dbSNP
19g.4110621T>GCA403391680MAP2K2n.777A>C
c.338A>C (p.Asn113Thr)
c.47A>C (p.Asn16Thr)
n.535A>C
 dbSNP
19g.4110621T=CA2319230782MAP2K2n.777A=
c.338A= (p.Asn113=)
c.47A= (p.Asn16=)
n.535A=
19g.4110622T>ACA403391682MAP2K2n.776A>T
c.337A>T (p.Asn113Tyr)
c.46A>T (p.Asn16Tyr)
n.534A>T
 dbSNP
19g.4110622T>CCA403391684MAP2K2n.776A>G
c.337A>G (p.Asn113Asp)
c.46A>G (p.Asn16Asp)
n.534A>G
19g.4110622T>GCA403391686MAP2K2n.776A>C
c.337A>C (p.Asn113His)
c.46A>C (p.Asn16His)
n.534A>C
19g.4110623C>ACA504987527MAP2K2n.775G>T
c.336G>T (p.Arg112=)
c.45G>T (p.Arg15=)
n.533G>T
19g.4110623C=CA2319230783MAP2K2n.775G=
c.336G= (p.Arg112=)
c.45G= (p.Arg15=)
n.533G=
19g.4110623C>GCA9091022MAP2K2n.775G>C
c.336G>C (p.Arg112=)
c.45G>C (p.Arg15=)
n.533G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.4110623C>TCA504987528MAP2K2n.775G>A
c.336G>A (p.Arg112=)
c.45G>A (p.Arg15=)
n.533G>A
 dbSNP
19g.4110624C>ACA403391689MAP2K2n.774G>T
c.335G>T (p.Arg112Leu)
c.44G>T (p.Arg15Leu)
n.532G>T
 ClinVar dbSNP
19g.4110624C=CA2319230784MAP2K2n.774G=
c.335G= (p.Arg112=)
c.44G= (p.Arg15=)
n.532G=
19g.4110624C>GCA403391691MAP2K2n.774G>C
c.335G>C (p.Arg112Pro)
c.44G>C (p.Arg15Pro)
n.532G>C
 dbSNP
19g.4110624C>TCA403391693MAP2K2n.774G>A
c.335G>A (p.Arg112Gln)
c.44G>A (p.Arg15Gln)
n.532G>A
 ClinVar dbSNP gnomAD v4
19g.4110625G>ACA304453904MAP2K2n.773C>T
c.334C>T (p.Arg112Trp)
c.43C>T (p.Arg15Trp)
n.531C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110625G>CCA403391695MAP2K2n.773C>G
c.334C>G (p.Arg112Gly)
c.43C>G (p.Arg15Gly)
n.531C>G
 dbSNP
19g.4110625G=CA2319230785MAP2K2n.773C=
c.334C= (p.Arg112=)
c.43C= (p.Arg15=)
n.531C=
19g.4110625G>TCA504987529MAP2K2n.773C>A
c.334C>A (p.Arg112=)
c.43C>A (p.Arg15=)
n.531C>A
 dbSNP COSMIC COSMIC
19g.4110626G>ACA504987530MAP2K2n.772C>T
c.333C>T (p.Ile111=)
c.42C>T (p.Ile14=)
n.530C>T
 dbSNP gnomAD v4
19g.4110626G>CCA403391696MAP2K2n.772C>G
c.333C>G (p.Ile111Met)
c.42C>G (p.Ile14Met)
n.530C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.4110626G=CA2319230786MAP2K2n.772C=
c.333C= (p.Ile111=)
c.42C= (p.Ile14=)
n.530C=
19g.4110626G>TCA504987531MAP2K2n.772C>A
c.333C>A (p.Ile111=)
c.42C>A (p.Ile14=)
n.530C>A
 dbSNP
19g.4110627A>CCA403391697MAP2K2n.771T>G
c.332T>G (p.Ile111Ser)
c.41T>G (p.Ile14Ser)
n.529T>G
19g.4110627A>GCA403391698MAP2K2n.771T>C
c.332T>C (p.Ile111Thr)
c.41T>C (p.Ile14Thr)
n.529T>C
 dbSNP gnomAD v4
19g.4110627A>TCA403391701MAP2K2n.771T>A
c.332T>A (p.Ile111Asn)
c.41T>A (p.Ile14Asn)
n.529T>A
 dbSNP
19g.4110628T>ACA403391703MAP2K2n.770A>T
c.331A>T (p.Ile111Phe)
c.40A>T (p.Ile14Phe)
n.528A>T
 ClinVar dbSNP
19g.4110628T>CCA403391705MAP2K2n.770A>G
c.331A>G (p.Ile111Val)
c.40A>G (p.Ile14Val)
n.528A>G
 gnomAD v4
19g.4110628T>GCA403391707MAP2K2n.770A>C
c.331A>C (p.Ile111Leu)
c.40A>C (p.Ile14Leu)
n.528A>C
19g.4110628T=CA2319230787MAP2K2n.770A=
c.331A= (p.Ile111=)
c.40A= (p.Ile14=)
n.528A=
19g.4110629G>ACA504987532MAP2K2n.769C>T
c.330C>T (p.Ala110=)
c.39C>T (p.Ala13=)
n.527C>T
 dbSNP gnomAD v2 gnomAD v4
19g.4110629G>CCA504987533MAP2K2n.769C>G
c.330C>G (p.Ala110=)
c.39C>G (p.Ala13=)
n.527C>G
19g.4110629G=CA2319230788MAP2K2n.769C=
c.330C= (p.Ala110=)
c.39C= (p.Ala13=)
n.527C=
19g.4110629G>TCA504987534MAP2K2n.769C>A
c.330C>A (p.Ala110=)
c.39C>A (p.Ala13=)
n.527C>A
19g.4110630G>ACA9091023MAP2K2n.768C>T
c.329C>T (p.Ala110Val)
c.38C>T (p.Ala13Val)
n.526C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.4110630G>CCA403391710MAP2K2n.768C>G
c.329C>G (p.Ala110Gly)
c.38C>G (p.Ala13Gly)
n.526C>G
 dbSNP
19g.4110630G=CA2319230789MAP2K2n.768C=
c.329C= (p.Ala110=)
c.38C= (p.Ala13=)
n.526C=
19g.4110630G>TCA403391711MAP2K2n.768C>A
c.329C>A (p.Ala110Asp)
c.38C>A (p.Ala13Asp)
n.526C>A
 dbSNP
19g.4110631C>ACA403391714MAP2K2n.767G>T
c.328G>T (p.Ala110Ser)
c.37G>T (p.Ala13Ser)
n.525G>T
 dbSNP
19g.4110631C>GCA403391716MAP2K2n.767G>C
c.328G>C (p.Ala110Pro)
c.37G>C (p.Ala13Pro)
n.525G>C
 dbSNP
19g.4110631C>TCA403391718MAP2K2n.767G>A
c.328G>A (p.Ala110Thr)
c.37G>A (p.Ala13Thr)
n.525G>A
 dbSNP
19g.4110632C>ACA504987535MAP2K2n.766G>T
c.327G>T (p.Pro109=)
c.36G>T (p.Pro12=)
n.524G>T
 dbSNP COSMIC COSMIC
19g.4110632C=CA2319230790MAP2K2n.766G=
c.327G= (p.Pro109=)
c.36G= (p.Pro12=)
n.524G=
19g.4110632C>GCA504987536MAP2K2n.766G>C
c.327G>C (p.Pro109=)
c.36G>C (p.Pro12=)
n.524G>C
 dbSNP gnomAD v4
19g.4110632C>TCA9091024MAP2K2n.766G>A
c.327G>A (p.Pro109=)
c.36G>A (p.Pro12=)
n.524G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110633G>ACA9091025MAP2K2n.765C>T
c.326C>T (p.Pro109Leu)
c.35C>T (p.Pro12Leu)
n.523C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110633G>CCA403391721MAP2K2n.765C>G
c.326C>G (p.Pro109Arg)
c.35C>G (p.Pro12Arg)
n.523C>G
 dbSNP
19g.4110633G=CA2319230791MAP2K2n.765C=
c.326C= (p.Pro109=)
c.35C= (p.Pro12=)
n.523C=
19g.4110633G>TCA403391722MAP2K2n.765C>A
c.326C>A (p.Pro109Gln)
c.35C>A (p.Pro12Gln)
n.523C>A
19g.4110634G>ACA403391725MAP2K2n.764C>T
c.325C>T (p.Pro109Ser)
c.34C>T (p.Pro12Ser)
n.522C>T
 dbSNP gnomAD v4
19g.4110634G>CCA16616268MAP2K2n.764C>G
c.325C>G (p.Pro109Ala)
c.34C>G (p.Pro12Ala)
n.522C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.4110634G=CA2319230792MAP2K2n.764C=
c.325C= (p.Pro109=)
c.34C= (p.Pro12=)
n.522C=
19g.4110634G>TCA403391728MAP2K2n.764C>A
c.325C>A (p.Pro109Thr)
c.34C>A (p.Pro12Thr)
n.522C>A
 dbSNP
19g.4110635C>ACA403391733MAP2K2n.763G>T
c.324G>T (p.Lys108Asn)
c.33G>T (p.Lys11Asn)
n.521G>T
 dbSNP
19g.4110635C>GCA403391735MAP2K2n.763G>C
c.324G>C (p.Lys108Asn)
c.33G>C (p.Lys11Asn)
n.521G>C
 dbSNP
19g.4110635C>TCA504987537MAP2K2n.763G>A
c.324G>A (p.Lys108=)
c.33G>A (p.Lys11=)
n.521G>A
 dbSNP
19g.4110636T>ACA403391738MAP2K2n.762A>T
c.323A>T (p.Lys108Met)
c.32A>T (p.Lys11Met)
n.520A>T
 dbSNP
19g.4110636T>CCA403391741MAP2K2n.762A>G
c.323A>G (p.Lys108Arg)
c.32A>G (p.Lys11Arg)
n.520A>G
 dbSNP
19g.4110636T>GCA403391739MAP2K2n.762A>C
c.323A>C (p.Lys108Thr)
c.32A>C (p.Lys11Thr)
n.520A>C
 dbSNP
19g.4110637T>ACA403391744MAP2K2n.761A>T
c.322A>T (p.Lys108Ter)
c.31A>T (p.Lys11Ter)
n.519A>T
 dbSNP gnomAD v4
19g.4110637T>CCA403391745MAP2K2n.761A>G
c.322A>G (p.Lys108Glu)
c.31A>G (p.Lys11Glu)
n.519A>G
 dbSNP
19g.4110637T>GCA403391746MAP2K2n.761A>C
c.322A>C (p.Lys108Gln)
c.31A>C (p.Lys11Gln)
n.519A>C
19g.4110638G>ACA504987538MAP2K2n.760C>T
c.321C>T (p.Ile107=)
c.30C>T (p.Ile10=)
n.518C>T
 dbSNP gnomAD v4
19g.4110638G>CCA403391747MAP2K2n.760C>G
c.321C>G (p.Ile107Met)
c.30C>G (p.Ile10Met)
n.518C>G
 dbSNP gnomAD v4
19g.4110638G>TCA504987539MAP2K2n.760C>A
c.321C>A (p.Ile107=)
c.30C>A (p.Ile10=)
n.518C>A
 dbSNP
19g.4110639A=CA2319230793MAP2K2n.759T=
c.320T= (p.Ile107=)
c.29T= (p.Ile10=)
n.517T=
19g.4110639A>CCA403391748MAP2K2n.759T>G
c.320T>G (p.Ile107Ser)
c.29T>G (p.Ile10Ser)
n.517T>G
 dbSNP
19g.4110639A>GCA403391750MAP2K2n.759T>C
c.320T>C (p.Ile107Thr)
c.29T>C (p.Ile10Thr)
n.517T>C
 dbSNP
19g.4110639A>TCA403391749MAP2K2n.759T>A
c.320T>A (p.Ile107Asn)
c.29T>A (p.Ile10Asn)
n.517T>A
 ClinVar dbSNP
19g.4110640T>ACA403391751MAP2K2n.758A>T
c.319A>T (p.Ile107Phe)
c.28A>T (p.Ile10Phe)
n.516A>T
 dbSNP
19g.4110640T>CCA403391752MAP2K2n.758A>G
c.319A>G (p.Ile107Val)
c.28A>G (p.Ile10Val)
n.516A>G
 dbSNP
19g.4110640T>GCA403391753MAP2K2n.758A>C
c.319A>C (p.Ile107Leu)
c.28A>C (p.Ile10Leu)
n.516A>C
19g.4110641C>ACA403391754MAP2K2n.757G>T
c.318G>T (p.Glu106Asp)
c.27G>T (p.Glu9Asp)
n.515G>T
19g.4110641C>GCA403391755MAP2K2n.757G>C
c.318G>C (p.Glu106Asp)
c.27G>C (p.Glu9Asp)
n.515G>C
 dbSNP
19g.4110641C>TCA504987540MAP2K2n.757G>A
c.318G>A (p.Glu106=)
c.27G>A (p.Glu9=)
n.515G>A
 dbSNP
19g.4110642T>ACA403391756MAP2K2n.756A>T
c.317A>T (p.Glu106Val)
c.26A>T (p.Glu9Val)
n.514A>T
 dbSNP
19g.4110642T>CCA403391757MAP2K2n.756A>G
c.317A>G (p.Glu106Gly)
c.26A>G (p.Glu9Gly)
n.514A>G
 dbSNP
19g.4110642T>GCA403391758MAP2K2n.756A>C
c.317A>C (p.Glu106Ala)
c.26A>C (p.Glu9Ala)
n.514A>C
 ClinVar
19g.4110642T=CA2319230794MAP2K2n.756A=
c.317A= (p.Glu106=)
c.26A= (p.Glu9=)
n.514A=
19g.4110643C>ACA403391759MAP2K2n.755G>T
c.316G>T (p.Glu106Ter)
c.25G>T (p.Glu9Ter)
n.513G>T
19g.4110643C>GCA403391760MAP2K2n.755G>C
c.316G>C (p.Glu106Gln)
c.25G>C (p.Glu9Gln)
n.513G>C
19g.4110643C>TCA403391761MAP2K2n.755G>A
c.316G>A (p.Glu106Lys)
c.25G>A (p.Glu9Lys)
n.513G>A
 COSMIC COSMIC
19g.4110644A=CA2319230795MAP2K2n.754T=
c.315T= (p.Leu105=)
c.24T= (p.Leu8=)
n.512T=
19g.4110644A>CCA9091026MAP2K2n.754T>G
c.315T>G (p.Leu105=)
c.24T>G (p.Leu8=)
n.512T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110644A>GCA504987541MAP2K2n.754T>C
c.315T>C (p.Leu105=)
c.24T>C (p.Leu8=)
n.512T>C
 dbSNP gnomAD v4
19g.4110644A>TCA504987542MAP2K2n.754T>A
c.315T>A (p.Leu105=)
c.24T>A (p.Leu8=)
n.512T>A
19g.4110645A>CCA403391763MAP2K2n.753T>G
c.314T>G (p.Leu105Arg)
c.23T>G (p.Leu8Arg)
n.511T>G
19g.4110645A>GCA403391762MAP2K2n.753T>C
c.314T>C (p.Leu105Pro)
c.23T>C (p.Leu8Pro)
n.511T>C
 dbSNP
19g.4110645A>TCA403391764MAP2K2n.753T>A
c.314T>A (p.Leu105His)
c.23T>A (p.Leu8His)
n.511T>A
 dbSNP
19g.4110646G>ACA403391765MAP2K2n.752C>T
c.313C>T (p.Leu105Phe)
c.22C>T (p.Leu8Phe)
n.510C>T
 dbSNP
19g.4110646G>CCA296179MAP2K2n.752C>G
c.313C>G (p.Leu105Val)
c.22C>G (p.Leu8Val)
n.510C>G
 ClinVar dbSNP gnomAD v4
19g.4110646G=CA2319230796MAP2K2n.752C=
c.313C= (p.Leu105=)
c.22C= (p.Leu8=)
n.510C=
19g.4110646G>TCA403391766MAP2K2n.752C>A
c.313C>A (p.Leu105Ile)
c.22C>A (p.Leu8Ile)
n.510C>A
 dbSNP
19g.4110647G>ACA504987543MAP2K2n.751C>T
c.312C>T (p.His104=)
c.21C>T (p.His7=)
n.509C>T
 dbSNP
19g.4110647G>CCA403391767MAP2K2n.751C>G
c.312C>G (p.His104Gln)
c.21C>G (p.His7Gln)
n.509C>G
 dbSNP
19g.4110647G>TCA403391768MAP2K2n.751C>A
c.312C>A (p.His104Gln)
c.21C>A (p.His7Gln)
n.509C>A
19g.4110648T>ACA403391769MAP2K2n.750A>T
c.311A>T (p.His104Leu)
c.20A>T (p.His7Leu)
n.508A>T
19g.4110648T>CCA403391771MAP2K2n.750A>G
c.311A>G (p.His104Arg)
c.20A>G (p.His7Arg)
n.508A>G
19g.4110648T>GCA403391770MAP2K2n.750A>C
c.311A>C (p.His104Pro)
c.20A>C (p.His7Pro)
n.508A>C
 dbSNP
19g.4110648T=CA2319230797MAP2K2n.750A=
c.311A= (p.His104=)
c.20A= (p.His7=)
n.508A=
19g.4110649G>ACA403391772MAP2K2n.749C>T
c.310C>T (p.His104Tyr)
c.19C>T (p.His7Tyr)
n.507C>T
19g.4110649G>CCA403391774MAP2K2n.749C>G
c.310C>G (p.His104Asp)
c.19C>G (p.His7Asp)
n.507C>G
19g.4110649G>TCA403391773MAP2K2n.749C>A
c.310C>A (p.His104Asn)
c.19C>A (p.His7Asn)
n.507C>A
19g.4110650G>ACA504987544MAP2K2n.748C>T
c.309C>T (p.Ile103=)
c.18C>T (p.Ile6=)
n.506C>T
 dbSNP
19g.4110650G>CCA403391775MAP2K2n.748C>G
c.309C>G (p.Ile103Met)
c.18C>G (p.Ile6Met)
n.506C>G
 dbSNP
19g.4110650G=CA2319230798MAP2K2n.748C=
c.309C= (p.Ile103=)
c.18C= (p.Ile6=)
n.506C=
19g.4110650G>TCA504987545MAP2K2n.748C>A
c.309C>A (p.Ile103=)
c.18C>A (p.Ile6=)
n.506C>A
 dbSNP gnomAD v2 gnomAD v4
19g.4110651A>CCA403391776MAP2K2n.747T>G
c.308T>G (p.Ile103Ser)
c.17T>G (p.Ile6Ser)
n.505T>G
 dbSNP
19g.4110651A>GCA403391777MAP2K2n.747T>C
c.308T>C (p.Ile103Thr)
c.17T>C (p.Ile6Thr)
n.505T>C
 dbSNP
19g.4110651A>TCA403391778MAP2K2n.747T>A
c.308T>A (p.Ile103Asn)
c.17T>A (p.Ile6Asn)
n.505T>A
 dbSNP
19g.4110652T>ACA403391779MAP2K2n.746A>T
c.307A>T (p.Ile103Phe)
c.16A>T (p.Ile6Phe)
n.504A>T
 dbSNP
19g.4110652T>CCA403391780MAP2K2n.746A>G
c.307A>G (p.Ile103Val)
c.16A>G (p.Ile6Val)
n.504A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110652T>GCA403391781MAP2K2n.746A>C
c.307A>C (p.Ile103Leu)
c.16A>C (p.Ile6Leu)
n.504A>C
 dbSNP
19g.4110652T=CA2319230799MAP2K2n.746A=
c.307A= (p.Ile103=)
c.16A= (p.Ile6=)
n.504A=
19g.4110653C>ACA504987546MAP2K2n.745G>T
c.306G>T (p.Leu102=)
c.15G>T (p.Leu5=)
n.503G>T
 gnomAD v4
19g.4110653C>GCA504987547MAP2K2n.745G>C
c.306G>C (p.Leu102=)
c.15G>C (p.Leu5=)
n.503G>C
 dbSNP
19g.4110653C>TCA504987548MAP2K2n.745G>A
c.306G>A (p.Leu102=)
c.15G>A (p.Leu5=)
n.503G>A
 dbSNP gnomAD v4
19g.4110654A=CA2319230800MAP2K2n.744T=
c.305T= (p.Leu102=)
c.14T= (p.Leu5=)
n.502T=
19g.4110654A>CCA403391782MAP2K2n.744T>G
c.305T>G (p.Leu102Arg)
c.14T>G (p.Leu5Arg)
n.502T>G
19g.4110654A>GCA403391783MAP2K2n.744T>C
c.305T>C (p.Leu102Pro)
c.14T>C (p.Leu5Pro)
n.502T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.4110654A>TCA403391784MAP2K2n.744T>A
c.305T>A (p.Leu102Gln)
c.14T>A (p.Leu5Gln)
n.502T>A
 dbSNP
19g.4110655G>ACA504987549MAP2K2n.743C>T
c.304C>T (p.Leu102=)
c.13C>T (p.Leu5=)
n.501C>T
 dbSNP
19g.4110655G>CCA403391785MAP2K2n.743C>G
c.304C>G (p.Leu102Val)
c.13C>G (p.Leu5Val)
n.501C>G
 gnomAD v4
19g.4110655G>TCA403391786MAP2K2n.743C>A
c.304C>A (p.Leu102Met)
c.13C>A (p.Leu5Met)
n.501C>A
19g.4110656C>ACA403391789MAP2K2n.743-1G>T
c.304-1G>T (n.304-1G>T)
c.13-1G>T (n.13-1G>T)
n.501-1G>T
 dbSNP
19g.4110656C>GCA403391787MAP2K2n.743-1G>C
c.304-1G>C (n.304-1G>C)
c.13-1G>C (n.13-1G>C)
n.501-1G>C
 dbSNP
19g.4110656C>TCA403391788MAP2K2n.743-1G>A
c.304-1G>A (n.304-1G>A)
c.13-1G>A (n.13-1G>A)
n.501-1G>A
 dbSNP
19g.4110657T>ACA403391790MAP2K2n.743-2A>T
c.304-2A>T (n.304-2A>T)
c.13-2A>T (n.13-2A>T)
n.501-2A>T
 dbSNP
19g.4110657T>CCA403391791MAP2K2n.743-2A>G
c.304-2A>G (n.304-2A>G)
c.13-2A>G (n.13-2A>G)
n.501-2A>G
 gnomAD v4
19g.4110657T>GCA403391792MAP2K2n.743-2A>C
c.304-2A>C (n.304-2A>C)
c.13-2A>C (n.13-2A>C)
n.501-2A>C
19g.4110658G>ACA2319230801MAP2K2n.743-3C>T
c.304-3C>T (n.304-3C>T)
c.13-3C>T (n.13-3C>T)
n.501-3C>T
 dbSNP gnomAD v4
19g.4110658G>CCA2735392566MAP2K2n.743-3C>G
c.304-3C>G (n.304-3C>G)
c.13-3C>G (n.13-3C>G)
n.501-3C>G
 dbSNP
19g.4110658G=CA2319230802MAP2K2n.743-3C=
c.304-3C= (n.304-3C=)
c.13-3C= (n.13-3C=)
n.501-3C=
19g.4110658G>TCA2585249276MAP2K2n.743-3C>A
c.304-3C>A (n.304-3C>A)
c.13-3C>A (n.13-3C>A)
n.501-3C>A
 gnomAD v4
19g.4110659C>ACA2319230804MAP2K2n.743-4G>T
c.304-4G>T (n.304-4G>T)
c.13-4G>T (n.13-4G>T)
n.501-4G>T
 dbSNP
19g.4110659C=CA2319230803MAP2K2n.743-4G=
c.304-4G= (n.304-4G=)
c.13-4G= (n.13-4G=)
n.501-4G=
19g.4110659C>GCA2735392567MAP2K2n.743-4G>C
c.304-4G>C (n.304-4G>C)
c.13-4G>C (n.13-4G>C)
n.501-4G>C
 dbSNP
19g.4110659C>TCA2585249277MAP2K2n.743-4G>A
c.304-4G>A (n.304-4G>A)
c.13-4G>A (n.13-4G>A)
n.501-4G>A
 ClinVar gnomAD v4
19g.4110660A=CA2319230805MAP2K2n.743-5T=
c.304-5T= (n.304-5T=)
c.13-5T= (n.13-5T=)
n.501-5T=
19g.4110660A>GCA9091027MAP2K2n.743-5T>C
c.304-5T>C (n.304-5T>C)
c.13-5T>C (n.13-5T>C)
n.501-5T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.4110661A>GCA2735505114MAP2K2n.743-6T>C
c.304-6T>C (n.304-6T>C)
c.13-6T>C (n.13-6T>C)
n.501-6T>C
 dbSNP
19g.4110661A>TCA2735505151MAP2K2n.743-6T>A
c.304-6T>A (n.304-6T>A)
c.13-6T>A (n.13-6T>A)
n.501-6T>A
 dbSNP
19g.4110662G>ACA9091028MAP2K2n.743-7C>T
c.304-7C>T (n.304-7C>T)
c.13-7C>T (n.13-7C>T)
n.501-7C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110662G>CCA2585249278MAP2K2n.743-7C>G
c.304-7C>G (n.304-7C>G)
c.13-7C>G (n.13-7C>G)
n.501-7C>G
 gnomAD v4
19g.4110662G=CA2319230806MAP2K2n.743-7C=
c.304-7C= (n.304-7C=)
c.13-7C= (n.13-7C=)
n.501-7C=
19g.4110663G>ACA631541606MAP2K2n.743-8C>T
c.304-8C>T (n.304-8C>T)
c.13-8C>T (n.13-8C>T)
n.501-8C>T
 dbSNP gnomAD v2 gnomAD v4
19g.4110663G>CCA2735373131MAP2K2n.743-8C>G
c.304-8C>G (n.304-8C>G)
c.13-8C>G (n.13-8C>G)
n.501-8C>G
 dbSNP
19g.4110663G=CA2319230807MAP2K2n.743-8C=
c.304-8C= (n.304-8C=)
c.13-8C= (n.13-8C=)
n.501-8C=
19g.4110664G>ACA2735505154MAP2K2n.743-9C>T
c.304-9C>T (n.304-9C>T)
c.13-9C>T (n.13-9C>T)
n.501-9C>T
 dbSNP
19g.4110664G>CCA2735505175MAP2K2n.743-9C>G
c.304-9C>G (n.304-9C>G)
c.13-9C>G (n.13-9C>G)
n.501-9C>G
 dbSNP
19g.4110664G>TCA2735505193MAP2K2n.743-9C>A
c.304-9C>A (n.304-9C>A)
c.13-9C>A (n.13-9C>A)
n.501-9C>A
 dbSNP
19g.4110665G>ACA631541607MAP2K2n.743-10C>T
c.304-10C>T (n.304-10C>T)
c.13-10C>T (n.13-10C>T)
n.501-10C>T
 dbSNP gnomAD v2 gnomAD v4
19g.4110665G>CCA2735358214MAP2K2n.743-10C>G
c.304-10C>G (n.304-10C>G)
c.13-10C>G (n.13-10C>G)
n.501-10C>G
 dbSNP
19g.4110665G=CA2319230808MAP2K2n.743-10C=
c.304-10C= (n.304-10C=)
c.13-10C= (n.13-10C=)
n.501-10C=
19g.4110665G>TCA882251706MAP2K2n.743-10C>A
c.304-10C>A (n.304-10C>A)
c.13-10C>A (n.13-10C>A)
n.501-10C>A
 ClinVar dbSNP gnomAD v4
19g.4110666A>GCA2585249279MAP2K2n.743-11T>C
c.304-11T>C (n.304-11T>C)
c.13-11T>C (n.13-11T>C)
n.501-11T>C
 ClinVar dbSNP gnomAD v4
19g.4110666A>TCA2735505258MAP2K2n.743-11T>A
c.304-11T>A (n.304-11T>A)
c.13-11T>A (n.13-11T>A)
n.501-11T>A
 dbSNP
19g.4110667G>ACA2585249280MAP2K2n.743-12C>T
c.304-12C>T (n.304-12C>T)
c.13-12C>T (n.13-12C>T)
n.501-12C>T
 dbSNP gnomAD v4
19g.4110667G>CCA9091029MAP2K2n.743-12C>G
c.304-12C>G (n.304-12C>G)
c.13-12C>G (n.13-12C>G)
n.501-12C>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110667G=CA2319230809MAP2K2n.743-12C=
c.304-12C= (n.304-12C=)
c.13-12C= (n.13-12C=)
n.501-12C=
19g.4110667G>TCA2735342229MAP2K2n.743-12C>A
c.304-12C>A (n.304-12C>A)
c.13-12C>A (n.13-12C>A)
n.501-12C>A
 dbSNP
19g.4110668A>GCA2735505277MAP2K2n.743-13T>C
c.304-13T>C (n.304-13T>C)
c.13-13T>C (n.13-13T>C)
n.501-13T>C
 dbSNP
19g.4110668A>TCA2735505318MAP2K2n.743-13T>A
c.304-13T>A (n.304-13T>A)
c.13-13T>A (n.13-13T>A)
n.501-13T>A
 dbSNP
19g.4110669G>ACA2585249282MAP2K2n.743-14C>T
c.304-14C>T (n.304-14C>T)
c.13-14C>T (n.13-14C>T)
n.501-14C>T
 dbSNP gnomAD v4
19g.4110669G>TCA2585249283MAP2K2n.743-14C>A
c.304-14C>A (n.304-14C>A)
c.13-14C>A (n.13-14C>A)
n.501-14C>A
 dbSNP gnomAD v4
19g.4110672delCA2585249281MAP2K2n.743-14del
c.304-14del (n.304-14del)
c.13-14del (n.13-14del)
n.501-14del
 gnomAD v4
19g.4110670G>ACA2576573334MAP2K2n.743-15C>T
c.304-15C>T (n.304-15C>T)
c.13-15C>T (n.13-15C>T)
n.501-15C>T
19g.4110670G>CCA2573155875MAP2K2n.743-15C>G
c.304-15C>G (n.304-15C>G)
c.13-15C>G (n.13-15C>G)
n.501-15C>G
 ClinVar dbSNP
19g.4110670G>TCA2571948668MAP2K2n.743-15C>A
c.304-15C>A (n.304-15C>A)
c.13-15C>A (n.13-15C>A)
n.501-15C>A
19g.4110671G>ACA2735505393MAP2K2n.743-16C>T
c.304-16C>T (n.304-16C>T)
c.13-16C>T (n.13-16C>T)
n.501-16C>T
 dbSNP
19g.4110671G>CCA2735505389MAP2K2n.743-16C>G
c.304-16C>G (n.304-16C>G)
c.13-16C>G (n.13-16C>G)
n.501-16C>G
 dbSNP
19g.4110672G>ACA2585249284MAP2K2n.743-17C>T
c.304-17C>T (n.304-17C>T)
c.13-17C>T (n.13-17C>T)
n.501-17C>T
 dbSNP gnomAD v4
19g.4110672G>CCA2735505416MAP2K2n.743-17C>G
c.304-17C>G (n.304-17C>G)
c.13-17C>G (n.13-17C>G)
n.501-17C>G
 dbSNP
19g.4110672G>TCA2585249285MAP2K2n.743-17C>A
c.304-17C>A (n.304-17C>A)
c.13-17C>A (n.13-17C>A)
n.501-17C>A
 dbSNP gnomAD v4
19g.4110673C>ACA9091031MAP2K2n.743-18G>T
c.304-18G>T (n.304-18G>T)
c.13-18G>T (n.13-18G>T)
n.501-18G>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110673C=CA2319230810MAP2K2n.743-18G=
c.304-18G= (n.304-18G=)
c.13-18G= (n.13-18G=)
n.501-18G=
19g.4110673C>TCA9091030MAP2K2n.743-18G>A
c.304-18G>A (n.304-18G>A)
c.13-18G>A (n.13-18G>A)
n.501-18G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110674G>ACA9091032MAP2K2n.743-19C>T
c.304-19C>T (n.304-19C>T)
c.13-19C>T (n.13-19C>T)
n.501-19C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110674G>CCA2319230812MAP2K2n.743-19C>G
c.304-19C>G (n.304-19C>G)
c.13-19C>G (n.13-19C>G)
n.501-19C>G
 dbSNP
19g.4110674G=CA2319230811MAP2K2n.743-19C=
c.304-19C= (n.304-19C=)
c.13-19C= (n.13-19C=)
n.501-19C=
19g.4110674G>TCA2585249286MAP2K2n.743-19C>A
c.304-19C>A (n.304-19C>A)
c.13-19C>A (n.13-19C>A)
n.501-19C>A
 gnomAD v4
19g.4110675A>GCA2735505455MAP2K2n.743-20T>C
c.304-20T>C (n.304-20T>C)
c.13-20T>C (n.13-20T>C)
n.501-20T>C
 dbSNP
19g.4110675A>TCA2735505475MAP2K2n.743-20T>A
c.304-20T>A (n.304-20T>A)
c.13-20T>A (n.13-20T>A)
n.501-20T>A
 dbSNP
19g.4110676G>ACA2735505479MAP2K2n.743-21C>T
c.304-21C>T (n.304-21C>T)
c.13-21C>T (n.13-21C>T)
n.501-21C>T
 dbSNP
19g.4110676G>CCA2735505478MAP2K2n.743-21C>G
c.304-21C>G (n.304-21C>G)
c.13-21C>G (n.13-21C>G)
n.501-21C>G
 dbSNP

Number of alleles fetched