Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112477664G>ACA481887639PTPN11c.867G>A (p.Arg289=)
c.753G>A (p.Arg251=)
c.864G>A (p.Arg288=)
 dbSNP gnomAD v3 gnomAD v4
12g.112477664G>CCA386790485PTPN11c.867G>C (p.Arg289Ser)
c.753G>C (p.Arg251Ser)
c.864G>C (p.Arg288Ser)
 ClinVar dbSNP gnomAD v4
12g.112477664G=CA2063775689PTPN11c.867G= (p.Arg289=)
c.753G= (p.Arg251=)
c.864G= (p.Arg288=)
12g.112477664G>TCA386790488PTPN11c.867G>T (p.Arg289Ser)
c.753G>T (p.Arg251Ser)
c.864G>T (p.Arg288Ser)
 dbSNP gnomAD v4
12g.112477665G>ACA386790490PTPN11c.868G>A (p.Val290Ile)
c.754G>A (p.Val252Ile)
c.865G>A (p.Val289Ile)
 ClinVar dbSNP
12g.112477665G>CCA386790492PTPN11c.868G>C (p.Val290Leu)
c.754G>C (p.Val252Leu)
c.865G>C (p.Val289Leu)
 ClinVar dbSNP
12g.112477665G=CA2063775693PTPN11c.868G= (p.Val290=)
c.754G= (p.Val252=)
c.865G= (p.Val289=)
12g.112477665G>TCA386790495PTPN11c.868G>T (p.Val290Phe)
c.754G>T (p.Val252Phe)
c.865G>T (p.Val289Phe)
 dbSNP
12g.112477666T>ACA386790505PTPN11c.869T>A (p.Val290Asp)
c.755T>A (p.Val252Asp)
c.866T>A (p.Val289Asp)
 dbSNP
12g.112477666T>CCA386790498PTPN11c.869T>C (p.Val290Ala)
c.755T>C (p.Val252Ala)
c.866T>C (p.Val289Ala)
 dbSNP gnomAD v2 gnomAD v4
12g.112477666T>GCA386790502PTPN11c.869T>G (p.Val290Gly)
c.755T>G (p.Val252Gly)
c.866T>G (p.Val289Gly)
12g.112477666T=CA2063775697PTPN11c.869T= (p.Val290=)
c.755T= (p.Val252=)
c.866T= (p.Val289=)
12g.112477667T>ACA481887641PTPN11c.870T>A (p.Val290=)
c.756T>A (p.Val252=)
c.867T>A (p.Val289=)
12g.112477667T>CCA481887642PTPN11c.870T>C (p.Val290=)
c.756T>C (p.Val252=)
c.867T>C (p.Val289=)
 dbSNP gnomAD v2 gnomAD v4
12g.112477667T>GCA481887643PTPN11c.870T>G (p.Val290=)
c.756T>G (p.Val252=)
c.867T>G (p.Val289=)
12g.112477667T=CA2063775701PTPN11c.870T= (p.Val290=)
c.756T= (p.Val252=)
c.867T= (p.Val289=)
12g.112477668G>ACA386790508PTPN11c.871G>A (p.Val291Ile)
c.757G>A (p.Val253Ile)
c.868G>A (p.Val290Ile)
 dbSNP
12g.112477668G>CCA386790511PTPN11c.871G>C (p.Val291Leu)
c.757G>C (p.Val253Leu)
c.868G>C (p.Val290Leu)
 dbSNP
12g.112477668G>TCA386790512PTPN11c.871G>T (p.Val291Phe)
c.757G>T (p.Val253Phe)
c.868G>T (p.Val290Phe)
12g.112477669T>ACA386790517PTPN11c.872T>A (p.Val291Asp)
c.758T>A (p.Val253Asp)
c.869T>A (p.Val290Asp)
 dbSNP
12g.112477669T>CCA386790520PTPN11c.872T>C (p.Val291Ala)
c.758T>C (p.Val253Ala)
c.869T>C (p.Val290Ala)
12g.112477669T>GCA386790522PTPN11c.872T>G (p.Val291Gly)
c.758T>G (p.Val253Gly)
c.869T>G (p.Val290Gly)
12g.112477670C>ACA481887644PTPN11c.873C>A (p.Val291=)
c.759C>A (p.Val253=)
c.870C>A (p.Val290=)
12g.112477670C>GCA481887645PTPN11c.873C>G (p.Val291=)
c.759C>G (p.Val253=)
c.870C>G (p.Val290=)
 dbSNP
12g.112477670C>TCA481887646PTPN11c.873C>T (p.Val291=)
c.759C>T (p.Val253=)
c.870C>T (p.Val290=)
 dbSNP
12g.112477671C>ACA386790525PTPN11c.874C>A (p.Leu292Ile)
c.760C>A (p.Leu254Ile)
c.871C>A (p.Leu291Ile)
 dbSNP
12g.112477671C=CA2063775707PTPN11c.874C= (p.Leu292=)
c.760C= (p.Leu254=)
c.871C= (p.Leu291=)
12g.112477671C>GCA386790528PTPN11c.874C>G (p.Leu292Val)
c.760C>G (p.Leu254Val)
c.871C>G (p.Leu291Val)
12g.112477671C>TCA243711914PTPN11c.874C>T (p.Leu292=)
c.760C>T (p.Leu254=)
c.871C>T (p.Leu291=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
12g.112477672T>ACA386790531PTPN11c.875T>A (p.Leu292Gln)
c.761T>A (p.Leu254Gln)
c.872T>A (p.Leu291Gln)
12g.112477672T>CCA386790533PTPN11c.875T>C (p.Leu292Pro)
c.761T>C (p.Leu254Pro)
c.872T>C (p.Leu291Pro)
 gnomAD v4
12g.112477672T>GCA386790534PTPN11c.875T>G (p.Leu292Arg)
c.761T>G (p.Leu254Arg)
c.872T>G (p.Leu291Arg)
12g.112477673A>CCA481887647PTPN11c.876A>C (p.Leu292=)
c.762A>C (p.Leu254=)
c.873A>C (p.Leu291=)
 dbSNP
12g.112477673A>GCA481887648PTPN11c.876A>G (p.Leu292=)
c.762A>G (p.Leu254=)
c.873A>G (p.Leu291=)
 gnomAD v4
12g.112477673A>TCA481887649PTPN11c.876A>T (p.Leu292=)
c.762A>T (p.Leu254=)
c.873A>T (p.Leu291=)
 dbSNP
12g.112477674C>ACA386790543PTPN11c.877C>A (p.His293Asn)
c.763C>A (p.His255Asn)
c.874C>A (p.His292Asn)
 dbSNP
12g.112477674C=CA2063775714PTPN11c.877C= (p.His293=)
c.763C= (p.His255=)
c.874C= (p.His292=)
12g.112477674C>GCA386790539PTPN11c.877C>G (p.His293Asp)
c.763C>G (p.His255Asp)
c.874C>G (p.His292Asp)
 dbSNP
12g.112477674C>TCA386790541PTPN11c.877C>T (p.His293Tyr)
c.763C>T (p.His255Tyr)
c.874C>T (p.His292Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.112477675A>CCA386790547PTPN11c.878A>C (p.His293Pro)
c.764A>C (p.His255Pro)
c.875A>C (p.His292Pro)
12g.112477675A>GCA386790550PTPN11c.878A>G (p.His293Arg)
c.764A>G (p.His255Arg)
c.875A>G (p.His292Arg)
12g.112477675A>TCA386790549PTPN11c.878A>T (p.His293Leu)
c.764A>T (p.His255Leu)
c.875A>T (p.His292Leu)
 dbSNP
12g.112477676C>ACA386790553PTPN11c.879C>A (p.His293Gln)
c.765C>A (p.His255Gln)
c.876C>A (p.His292Gln)
 ClinVar dbSNP gnomAD v4
12g.112477676C=CA2063775718PTPN11c.879C= (p.His293=)
c.765C= (p.His255=)
c.876C= (p.His292=)
12g.112477676C>GCA6798673PTPN11c.879C>G (p.His293Gln)
c.765C>G (p.His255Gln)
c.876C>G (p.His292Gln)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
12g.112477676C>TCA282101PTPN11c.879C>T (p.His293=)
c.765C>T (p.His255=)
c.876C>T (p.His292=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.112477677G>ACA243711916PTPN11c.880G>A (p.Asp294Asn)
c.766G>A (p.Asp256Asn)
c.877G>A (p.Asp293Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.112477677G>CCA386790562PTPN11c.880G>C (p.Asp294His)
c.766G>C (p.Asp256His)
c.877G>C (p.Asp293His)
 dbSNP
12g.112477677G=CA2063775726PTPN11c.880G= (p.Asp294=)
c.766G= (p.Asp256=)
c.877G= (p.Asp293=)
12g.112477677G>TCA243711919PTPN11c.880G>T (p.Asp294Tyr)
c.766G>T (p.Asp256Tyr)
c.877G>T (p.Asp293Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.112477678A=CA2063775731PTPN11c.881A= (p.Asp294=)
c.767A= (p.Asp256=)
c.878A= (p.Asp293=)
12g.112477678A>CCA386790568PTPN11c.881A>C (p.Asp294Ala)
c.767A>C (p.Asp256Ala)
c.878A>C (p.Asp293Ala)
12g.112477678A>GCA6798674PTPN11c.881A>G (p.Asp294Gly)
c.767A>G (p.Asp256Gly)
c.878A>G (p.Asp293Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.112477678A>TCA386790571PTPN11c.881A>T (p.Asp294Val)
c.767A>T (p.Asp256Val)
c.878A>T (p.Asp293Val)
 dbSNP
12g.112477679T>ACA386790577PTPN11c.882T>A (p.Asp294Glu)
c.768T>A (p.Asp256Glu)
c.879T>A (p.Asp293Glu)
12g.112477679T>CCA481887652PTPN11c.882T>C (p.Asp294=)
c.768T>C (p.Asp256=)
c.879T>C (p.Asp293=)
 ClinVar dbSNP gnomAD v4
12g.112477679T>GCA386790574PTPN11c.882T>G (p.Asp294Glu)
c.768T>G (p.Asp256Glu)
c.879T>G (p.Asp293Glu)
 gnomAD v4
12g.112477679T=CA2063775734PTPN11c.882T= (p.Asp294=)
c.768T= (p.Asp256=)
c.879T= (p.Asp293=)
12g.112477680G>ACA386790578PTPN11c.883G>A (p.Gly295Ser)
c.769G>A (p.Gly257Ser)
c.880G>A (p.Gly294Ser)
 dbSNP
12g.112477680G>CCA386790579PTPN11c.883G>C (p.Gly295Arg)
c.769G>C (p.Gly257Arg)
c.880G>C (p.Gly294Arg)
 dbSNP
12g.112477680G>TCA386790580PTPN11c.883G>T (p.Gly295Cys)
c.769G>T (p.Gly257Cys)
c.880G>T (p.Gly294Cys)
12g.112477681G>ACA386790582PTPN11c.884G>A (p.Gly295Asp)
c.770G>A (p.Gly257Asp)
c.881G>A (p.Gly294Asp)
 dbSNP
12g.112477681G>CCA386790583PTPN11c.884G>C (p.Gly295Ala)
c.770G>C (p.Gly257Ala)
c.881G>C (p.Gly294Ala)
 dbSNP
12g.112477681G>TCA386790585PTPN11c.884G>T (p.Gly295Val)
c.770G>T (p.Gly257Val)
c.881G>T (p.Gly294Val)
 dbSNP
12g.112477682T>ACA481887656PTPN11c.885T>A (p.Gly295=)
c.771T>A (p.Gly257=)
c.882T>A (p.Gly294=)
 dbSNP
12g.112477682T>CCA481887657PTPN11c.885T>C (p.Gly295=)
c.771T>C (p.Gly257=)
c.882T>C (p.Gly294=)
12g.112477682T>GCA481887658PTPN11c.885T>G (p.Gly295=)
c.771T>G (p.Gly257=)
c.882T>G (p.Gly294=)
12g.112477683G>ACA386790588PTPN11c.886G>A (p.Asp296Asn)
c.772G>A (p.Asp258Asn)
c.883G>A (p.Asp295Asn)
 dbSNP
12g.112477683G>CCA386790591PTPN11c.886G>C (p.Asp296His)
c.772G>C (p.Asp258His)
c.883G>C (p.Asp295His)
 dbSNP
12g.112477683G>TCA386790590PTPN11c.886G>T (p.Asp296Tyr)
c.772G>T (p.Asp258Tyr)
c.883G>T (p.Asp295Tyr)
12g.112477684A>CCA386790594PTPN11c.887A>C (p.Asp296Ala)
c.773A>C (p.Asp258Ala)
c.884A>C (p.Asp295Ala)
12g.112477684A>GCA386790597PTPN11c.887A>G (p.Asp296Gly)
c.773A>G (p.Asp258Gly)
c.884A>G (p.Asp295Gly)
 dbSNP
12g.112477684A>TCA386790599PTPN11c.887A>T (p.Asp296Val)
c.773A>T (p.Asp258Val)
c.884A>T (p.Asp295Val)
 dbSNP
12g.112477685T>ACA386790604PTPN11c.888T>A (p.Asp296Glu)
c.774T>A (p.Asp258Glu)
c.885T>A (p.Asp295Glu)
12g.112477685T>CCA481887659PTPN11c.888T>C (p.Asp296=)
c.774T>C (p.Asp258=)
c.885T>C (p.Asp295=)
 COSMIC
12g.112477685T>GCA386790606PTPN11c.888T>G (p.Asp296Glu)
c.774T>G (p.Asp258Glu)
c.885T>G (p.Asp295Glu)
12g.112477686C>ACA386790609PTPN11c.889C>A (p.Pro297Thr)
c.775C>A (p.Pro259Thr)
c.886C>A (p.Pro296Thr)
 dbSNP
12g.112477686C=CA2063775736PTPN11c.889C= (p.Pro297=)
c.775C= (p.Pro259=)
c.886C= (p.Pro296=)
12g.112477686C>GCA386790612PTPN11c.889C>G (p.Pro297Ala)
c.775C>G (p.Pro259Ala)
c.886C>G (p.Pro296Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v4
12g.112477686C>TCA386790615PTPN11c.889C>T (p.Pro297Ser)
c.775C>T (p.Pro259Ser)
c.886C>T (p.Pro296Ser)
 dbSNP
12g.112477687C>ACA386790619PTPN11c.890C>A (p.Pro297His)
c.776C>A (p.Pro259His)
c.887C>A (p.Pro296His)
 dbSNP
12g.112477687C>GCA386790621PTPN11c.890C>G (p.Pro297Arg)
c.776C>G (p.Pro259Arg)
c.887C>G (p.Pro296Arg)
 dbSNP
12g.112477687C>TCA386790624PTPN11c.890C>T (p.Pro297Leu)
c.776C>T (p.Pro259Leu)
c.887C>T (p.Pro296Leu)
 dbSNP
12g.112477688C>ACA481887660PTPN11c.891C>A (p.Pro297=)
c.777C>A (p.Pro259=)
c.888C>A (p.Pro296=)
 dbSNP
12g.112477688C>GCA481887662PTPN11c.891C>G (p.Pro297=)
c.777C>G (p.Pro259=)
c.888C>G (p.Pro296=)
 dbSNP
12g.112477688C>TCA481887664PTPN11c.891C>T (p.Pro297=)
c.777C>T (p.Pro259=)
c.888C>T (p.Pro296=)
 dbSNP
12g.112477689A=CA2063775738PTPN11c.892A= (p.Asn298=)
c.778A= (p.Asn260=)
c.889A= (p.Asn297=)
12g.112477689A>CCA386790627PTPN11c.892A>C (p.Asn298His)
c.778A>C (p.Asn260His)
c.889A>C (p.Asn297His)
12g.112477689A>GCA243711925PTPN11c.892A>G (p.Asn298Asp)
c.778A>G (p.Asn260Asp)
c.889A>G (p.Asn297Asp)
 dbSNP gnomAD v4
12g.112477689A>TCA386790631PTPN11c.892A>T (p.Asn298Tyr)
c.778A>T (p.Asn260Tyr)
c.889A>T (p.Asn297Tyr)
12g.112477690A=CA2063775743PTPN11c.893A= (p.Asn298=)
c.779A= (p.Asn260=)
c.890A= (p.Asn297=)
12g.112477690A>CCA386790637PTPN11c.893A>C (p.Asn298Thr)
c.779A>C (p.Asn260Thr)
c.890A>C (p.Asn297Thr)
 dbSNP
12g.112477690A>GCA297088PTPN11c.893A>G (p.Asn298Ser)
c.779A>G (p.Asn260Ser)
c.890A>G (p.Asn297Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.112477690A>TCA386790639PTPN11c.893A>T (p.Asn298Ile)
c.779A>T (p.Asn260Ile)
c.890A>T (p.Asn297Ile)
12g.112477691T>ACA386790642PTPN11c.894T>A (p.Asn298Lys)
c.780T>A (p.Asn260Lys)
c.891T>A (p.Asn297Lys)
 dbSNP
12g.112477691T>CCA481887671PTPN11c.894T>C (p.Asn298=)
c.780T>C (p.Asn260=)
c.891T>C (p.Asn297=)
 dbSNP COSMIC
12g.112477691T>GCA386790645PTPN11c.894T>G (p.Asn298Lys)
c.780T>G (p.Asn260Lys)
c.891T>G (p.Asn297Lys)
12g.112477691T=CA2063775749PTPN11c.894T= (p.Asn298=)
c.780T= (p.Asn260=)
c.891T= (p.Asn297=)
12g.112477692G>ACA386790649PTPN11c.895G>A (p.Glu299Lys)
c.781G>A (p.Glu261Lys)
c.892G>A (p.Glu298Lys)
 dbSNP
12g.112477692G>CCA386790650PTPN11c.895G>C (p.Glu299Gln)
c.781G>C (p.Glu261Gln)
c.892G>C (p.Glu298Gln)
 dbSNP
12g.112477692G>TCA386790652PTPN11c.895G>T (p.Glu299Ter)
c.781G>T (p.Glu261Ter)
c.892G>T (p.Glu298Ter)
12g.112477693A>CCA386790656PTPN11c.896A>C (p.Glu299Ala)
c.782A>C (p.Glu261Ala)
c.893A>C (p.Glu298Ala)
12g.112477693A>GCA386790659PTPN11c.896A>G (p.Glu299Gly)
c.782A>G (p.Glu261Gly)
c.893A>G (p.Glu298Gly)
12g.112477693A>TCA386790661PTPN11c.896A>T (p.Glu299Val)
c.782A>T (p.Glu261Val)
c.893A>T (p.Glu298Val)
 dbSNP
12g.112477694G>ACA6798675PTPN11c.897G>A (p.Glu299=)
c.783G>A (p.Glu261=)
c.894G>A (p.Glu298=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477694G>CCA386790667PTPN11c.897G>C (p.Glu299Asp)
c.783G>C (p.Glu261Asp)
c.894G>C (p.Glu298Asp)
 dbSNP
12g.112477694G=CA2063775751PTPN11c.897G= (p.Glu299=)
c.783G= (p.Glu261=)
c.894G= (p.Glu298=)
12g.112477694G>TCA386790666PTPN11c.897G>T (p.Glu299Asp)
c.783G>T (p.Glu261Asp)
c.894G>T (p.Glu298Asp)
 dbSNP
12g.112477695C>ACA243711930PTPN11c.898C>A (p.Pro300Thr)
c.784C>A (p.Pro262Thr)
c.895C>A (p.Pro299Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.112477695C=CA2063775754PTPN11c.898C= (p.Pro300=)
c.784C= (p.Pro262=)
c.895C= (p.Pro299=)
12g.112477695C>GCA386790673PTPN11c.898C>G (p.Pro300Ala)
c.784C>G (p.Pro262Ala)
c.895C>G (p.Pro299Ala)
 dbSNP
12g.112477695C>TCA386790676PTPN11c.898C>T (p.Pro300Ser)
c.784C>T (p.Pro262Ser)
c.895C>T (p.Pro299Ser)
 dbSNP gnomAD v4
12g.112477696C>ACA386790679PTPN11c.899C>A (p.Pro300His)
c.785C>A (p.Pro262His)
c.896C>A (p.Pro299His)
 dbSNP
12g.112477696C>GCA386790682PTPN11c.899C>G (p.Pro300Arg)
c.785C>G (p.Pro262Arg)
c.896C>G (p.Pro299Arg)
 dbSNP
12g.112477696C>TCA386790683PTPN11c.899C>T (p.Pro300Leu)
c.785C>T (p.Pro262Leu)
c.896C>T (p.Pro299Leu)
 dbSNP
12g.112477697T>ACA243711932PTPN11c.900T>A (p.Pro300=)
c.786T>A (p.Pro262=)
c.897T>A (p.Pro299=)
 dbSNP
12g.112477697T>CCA481887679PTPN11c.900T>C (p.Pro300=)
c.786T>C (p.Pro262=)
c.897T>C (p.Pro299=)
 dbSNP
12g.112477697T>GCA481887678PTPN11c.900T>G (p.Pro300=)
c.786T>G (p.Pro262=)
c.897T>G (p.Pro299=)
12g.112477697T=CA2063775755PTPN11c.900T= (p.Pro300=)
c.786T= (p.Pro262=)
c.897T= (p.Pro299=)
12g.112477698G>ACA386790686PTPN11c.901G>A (p.Val301Ile)
c.787G>A (p.Val263Ile)
c.898G>A (p.Val300Ile)
 dbSNP
12g.112477698G>CCA386790688PTPN11c.901G>C (p.Val301Leu)
c.787G>C (p.Val263Leu)
c.898G>C (p.Val300Leu)
 dbSNP
12g.112477698G>TCA386790691PTPN11c.901G>T (p.Val301Phe)
c.787G>T (p.Val263Phe)
c.898G>T (p.Val300Phe)
12g.112477699T>ACA386790693PTPN11c.902T>A (p.Val301Asp)
c.788T>A (p.Val263Asp)
c.899T>A (p.Val300Asp)
 dbSNP
12g.112477699T>CCA386790696PTPN11c.902T>C (p.Val301Ala)
c.788T>C (p.Val263Ala)
c.899T>C (p.Val300Ala)
 dbSNP
12g.112477699T>GCA386790698PTPN11c.902T>G (p.Val301Gly)
c.788T>G (p.Val263Gly)
c.899T>G (p.Val300Gly)
12g.112477700T>ACA481887684PTPN11c.903T>A (p.Val301=)
c.789T>A (p.Val263=)
c.900T>A (p.Val300=)
12g.112477700T>CCA481887686PTPN11c.903T>C (p.Val301=)
c.789T>C (p.Val263=)
c.900T>C (p.Val300=)
12g.112477700T>GCA481887688PTPN11c.903T>G (p.Val301=)
c.789T>G (p.Val263=)
c.900T>G (p.Val300=)
 gnomAD v4
12g.112477701T>ACA386790704PTPN11c.904T>A (p.Ser302Thr)
c.790T>A (p.Ser264Thr)
c.901T>A (p.Ser301Thr)
 dbSNP
12g.112477701T>CCA386790708PTPN11c.904T>C (p.Ser302Pro)
c.790T>C (p.Ser264Pro)
c.901T>C (p.Ser301Pro)
 gnomAD v4
12g.112477701T>GCA386790702PTPN11c.904T>G (p.Ser302Ala)
c.790T>G (p.Ser264Ala)
c.901T>G (p.Ser301Ala)
12g.112477702C>ACA386790716PTPN11c.905C>A (p.Ser302Ter)
c.791C>A (p.Ser264Ter)
c.902C>A (p.Ser301Ter)
 dbSNP
12g.112477702C>GCA386790711PTPN11c.905C>G (p.Ser302Ter)
c.791C>G (p.Ser264Ter)
c.902C>G (p.Ser301Ter)
 dbSNP
12g.112477702C>TCA386790713PTPN11c.905C>T (p.Ser302Leu)
c.791C>T (p.Ser264Leu)
c.902C>T (p.Ser301Leu)
 dbSNP
12g.112477703A>CCA481887690PTPN11c.906A>C (p.Ser302=)
c.792A>C (p.Ser264=)
c.903A>C (p.Ser301=)
12g.112477703A>GCA481887692PTPN11c.906A>G (p.Ser302=)
c.792A>G (p.Ser264=)
c.903A>G (p.Ser301=)
 ClinVar dbSNP gnomAD v4 COSMIC
12g.112477703A>TCA481887694PTPN11c.906A>T (p.Ser302=)
c.792A>T (p.Ser264=)
c.903A>T (p.Ser301=)
12g.112477704G>ACA386790720PTPN11c.907G>A (p.Asp303Asn)
c.793G>A (p.Asp265Asn)
c.904G>A (p.Asp302Asn)
 dbSNP
12g.112477704G>CCA386790721PTPN11c.907G>C (p.Asp303His)
c.793G>C (p.Asp265His)
c.904G>C (p.Asp302His)
 dbSNP
12g.112477704G>TCA386790724PTPN11c.907G>T (p.Asp303Tyr)
c.793G>T (p.Asp265Tyr)
c.904G>T (p.Asp302Tyr)
 dbSNP
12g.112477705A=CA2063775757PTPN11c.908A= (p.Asp303=)
c.794A= (p.Asp265=)
c.905A= (p.Asp302=)
12g.112477705A>CCA386790728PTPN11c.908A>C (p.Asp303Ala)
c.794A>C (p.Asp265Ala)
c.905A>C (p.Asp302Ala)
12g.112477705A>GCA386790730PTPN11c.908A>G (p.Asp303Gly)
c.794A>G (p.Asp265Gly)
c.905A>G (p.Asp302Gly)
 dbSNP
12g.112477705A>TCA386790732PTPN11c.908A>T (p.Asp303Val)
c.794A>T (p.Asp265Val)
c.905A>T (p.Asp302Val)
12g.112477706T>ACA386790735PTPN11c.909T>A (p.Asp303Glu)
c.795T>A (p.Asp265Glu)
c.906T>A (p.Asp302Glu)
12g.112477706T>CCA481887696PTPN11c.909T>C (p.Asp303=)
c.795T>C (p.Asp265=)
c.906T>C (p.Asp302=)
12g.112477706T>GCA386790737PTPN11c.909T>G (p.Asp303Glu)
c.795T>G (p.Asp265Glu)
c.906T>G (p.Asp302Glu)
12g.112477707T>ACA386790739PTPN11c.910T>A (p.Tyr304Asn)
c.796T>A (p.Tyr266Asn)
c.907T>A (p.Tyr303Asn)
 dbSNP
12g.112477707T>CCA386790740PTPN11c.910T>C (p.Tyr304His)
c.796T>C (p.Tyr266His)
c.907T>C (p.Tyr303His)
 dbSNP
12g.112477707T>GCA243711935PTPN11c.910T>G (p.Tyr304Asp)
c.796T>G (p.Tyr266Asp)
c.907T>G (p.Tyr303Asp)
 dbSNP
12g.112477707T=CA2063775758PTPN11c.910T= (p.Tyr304=)
c.796T= (p.Tyr266=)
c.907T= (p.Tyr303=)
12g.112477708A>CCA386790743PTPN11c.911A>C (p.Tyr304Ser)
c.797A>C (p.Tyr266Ser)
c.908A>C (p.Tyr303Ser)
12g.112477708A>GCA386790741PTPN11c.911A>G (p.Tyr304Cys)
c.797A>G (p.Tyr266Cys)
c.908A>G (p.Tyr303Cys)
12g.112477708A>TCA386790742PTPN11c.911A>T (p.Tyr304Phe)
c.797A>T (p.Tyr266Phe)
c.908A>T (p.Tyr303Phe)
 dbSNP
12g.112477709C>ACA386790745PTPN11c.912C>A (p.Tyr304Ter)
c.798C>A (p.Tyr266Ter)
c.909C>A (p.Tyr303Ter)
12g.112477709C=CA2063775760PTPN11c.912C= (p.Tyr304=)
c.798C= (p.Tyr266=)
c.909C= (p.Tyr303=)
12g.112477709C>GCA386790751PTPN11c.912C>G (p.Tyr304Ter)
c.798C>G (p.Tyr266Ter)
c.909C>G (p.Tyr303Ter)
 dbSNP
12g.112477709C>TCA481887700PTPN11c.912C>T (p.Tyr304=)
c.798C>T (p.Tyr266=)
c.909C>T (p.Tyr303=)
 ClinVar dbSNP gnomAD v4
12g.112477710A=CA2063775763PTPN11c.913A= (p.Ile305=)
c.799A= (p.Ile267=)
c.910A= (p.Ile304=)
12g.112477710A>CCA386790755PTPN11c.913A>C (p.Ile305Leu)
c.799A>C (p.Ile267Leu)
c.910A>C (p.Ile304Leu)
12g.112477710A>GCA297100PTPN11c.913A>G (p.Ile305Val)
c.799A>G (p.Ile267Val)
c.910A>G (p.Ile304Val)
 ClinVar dbSNP gnomAD v4
12g.112477710A>TCA386790757PTPN11c.913A>T (p.Ile305Phe)
c.799A>T (p.Ile267Phe)
c.910A>T (p.Ile304Phe)
 dbSNP
12g.112477711T>ACA386790760PTPN11c.914T>A (p.Ile305Asn)
c.800T>A (p.Ile267Asn)
c.911T>A (p.Ile304Asn)
 dbSNP
12g.112477711T>CCA386790763PTPN11c.914T>C (p.Ile305Thr)
c.800T>C (p.Ile267Thr)
c.911T>C (p.Ile304Thr)
12g.112477711T>GCA386790765PTPN11c.914T>G (p.Ile305Ser)
c.800T>G (p.Ile267Ser)
c.911T>G (p.Ile304Ser)
12g.112477712C>ACA481887706PTPN11c.915C>A (p.Ile305=)
c.801C>A (p.Ile267=)
c.912C>A (p.Ile304=)
12g.112477712C=CA2063775765PTPN11c.915C= (p.Ile305=)
c.801C= (p.Ile267=)
c.912C= (p.Ile304=)
12g.112477712C>GCA386790766PTPN11c.915C>G (p.Ile305Met)
c.801C>G (p.Ile267Met)
c.912C>G (p.Ile304Met)
 dbSNP
12g.112477712C>TCA481887708PTPN11c.915C>T (p.Ile305=)
c.801C>T (p.Ile267=)
c.912C>T (p.Ile304=)
 ClinVar dbSNP
12g.112477713A>CCA386790769PTPN11c.916A>C (p.Asn306His)
c.802A>C (p.Asn268His)
c.913A>C (p.Asn305His)
12g.112477713A>GCA386790772PTPN11c.916A>G (p.Asn306Asp)
c.802A>G (p.Asn268Asp)
c.913A>G (p.Asn305Asp)
12g.112477713A>TCA386790773PTPN11c.916A>T (p.Asn306Tyr)
c.802A>T (p.Asn268Tyr)
c.913A>T (p.Asn305Tyr)
12g.112477714A>CCA386790779PTPN11c.917A>C (p.Asn306Thr)
c.803A>C (p.Asn268Thr)
c.914A>C (p.Asn305Thr)
12g.112477714A>GCA386790776PTPN11c.917A>G (p.Asn306Ser)
c.803A>G (p.Asn268Ser)
c.914A>G (p.Asn305Ser)
 COSMIC
12g.112477714A>TCA386790775PTPN11c.917A>T (p.Asn306Ile)
c.803A>T (p.Asn268Ile)
c.914A>T (p.Asn305Ile)
 dbSNP
12g.112477715T>ACA386790784PTPN11c.918T>A (p.Asn306Lys)
c.804T>A (p.Asn268Lys)
c.915T>A (p.Asn305Lys)
 dbSNP
12g.112477715T>CCA481887715PTPN11c.918T>C (p.Asn306=)
c.804T>C (p.Asn268=)
c.915T>C (p.Asn305=)
12g.112477715T>GCA386790785PTPN11c.918T>G (p.Asn306Lys)
c.804T>G (p.Asn268Lys)
c.915T>G (p.Asn305Lys)
12g.112477718_112477741delCA2695199174PTPN11c.921_933+11del
c.807_819+11del
c.918_930+11del
 ClinVar
12g.112477716G>ACA386790787PTPN11c.919G>A (p.Ala307Thr)
c.805G>A (p.Ala269Thr)
c.916G>A (p.Ala306Thr)
 dbSNP
12g.112477716G>CCA386790789PTPN11c.919G>C (p.Ala307Pro)
c.805G>C (p.Ala269Pro)
c.916G>C (p.Ala306Pro)
 dbSNP
12g.112477716G>TCA386790791PTPN11c.919G>T (p.Ala307Ser)
c.805G>T (p.Ala269Ser)
c.916G>T (p.Ala306Ser)
 gnomAD v4
12g.112477717C>ACA386790793PTPN11c.920C>A (p.Ala307Glu)
c.806C>A (p.Ala269Glu)
c.917C>A (p.Ala306Glu)
 COSMIC
12g.112477717C>GCA386790796PTPN11c.920C>G (p.Ala307Gly)
c.806C>G (p.Ala269Gly)
c.917C>G (p.Ala306Gly)
12g.112477717C>TCA386790797PTPN11c.920C>T (p.Ala307Val)
c.806C>T (p.Ala269Val)
c.917C>T (p.Ala306Val)
12g.112477718A=CA2063775769PTPN11c.921A= (p.Ala307=)
c.807A= (p.Ala269=)
c.918A= (p.Ala306=)
12g.112477718A>CCA481887719PTPN11c.921A>C (p.Ala307=)
c.807A>C (p.Ala269=)
c.918A>C (p.Ala306=)
12g.112477718A>GCA243711940PTPN11c.921A>G (p.Ala307=)
c.807A>G (p.Ala269=)
c.918A>G (p.Ala306=)
 dbSNP
12g.112477718A>TCA481887724PTPN11c.921A>T (p.Ala307=)
c.807A>T (p.Ala269=)
c.918A>T (p.Ala306=)
 dbSNP
12g.112477719A=CA2063775772PTPN11c.922A= (p.Asn308=)
c.808A= (p.Asn270=)
c.919A= (p.Asn307=)
12g.112477719A>CCA386790803PTPN11c.922A>C (p.Asn308His)
c.808A>C (p.Asn270His)
c.919A>C (p.Asn307His)
12g.112477719A>GCA220158PTPN11c.922A>G (p.Asn308Asp)
c.808A>G (p.Asn270Asp)
c.919A>G (p.Asn307Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.112477719A>TCA386790812PTPN11c.922A>T (p.Asn308Tyr)
c.808A>T (p.Asn270Tyr)
c.919A>T (p.Asn307Tyr)
12g.112477720A=CA2063775782PTPN11c.923A= (p.Asn308=)
c.809A= (p.Asn270=)
c.920A= (p.Asn307=)
12g.112477720A>CCA261607PTPN11c.923A>C (p.Asn308Thr)
c.809A>C (p.Asn270Thr)
c.920A>C (p.Asn307Thr)
 ClinVar dbSNP COSMIC
12g.112477720A>GCA235328PTPN11c.923A>G (p.Asn308Ser)
c.809A>G (p.Asn270Ser)
c.920A>G (p.Asn307Ser)
 ClinVar dbSNP COSMIC
12g.112477720A>TCA386790819PTPN11c.923A>T (p.Asn308Ile)
c.809A>T (p.Asn270Ile)
c.920A>T (p.Asn307Ile)
12g.112477721T>ACA386790823PTPN11c.924T>A (p.Asn308Lys)
c.810T>A (p.Asn270Lys)
c.921T>A (p.Asn307Lys)
 dbSNP
12g.112477721T>CCA481887726PTPN11c.924T>C (p.Asn308=)
c.810T>C (p.Asn270=)
c.921T>C (p.Asn307=)
12g.112477721T>GCA386790829PTPN11c.924T>G (p.Asn308Lys)
c.810T>G (p.Asn270Lys)
c.921T>G (p.Asn307Lys)
12g.112477722A=CA2063775795PTPN11c.925A= (p.Ile309=)
c.811A= (p.Ile271=)
c.922A= (p.Ile308=)
12g.112477722A>CCA386790833PTPN11c.925A>C (p.Ile309Leu)
c.811A>C (p.Ile271Leu)
c.922A>C (p.Ile308Leu)
12g.112477722A>GCA177674PTPN11c.925A>G (p.Ile309Val)
c.811A>G (p.Ile271Val)
c.922A>G (p.Ile308Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477722A>TCA386790836PTPN11c.925A>T (p.Ile309Phe)
c.811A>T (p.Ile271Phe)
c.922A>T (p.Ile308Phe)
12g.112477723T>ACA386790838PTPN11c.926T>A (p.Ile309Asn)
c.812T>A (p.Ile271Asn)
c.923T>A (p.Ile308Asn)
12g.112477723T>CCA386790840PTPN11c.926T>C (p.Ile309Thr)
c.812T>C (p.Ile271Thr)
c.923T>C (p.Ile308Thr)
12g.112477723T>GCA386790843PTPN11c.926T>G (p.Ile309Ser)
c.812T>G (p.Ile271Ser)
c.923T>G (p.Ile308Ser)
12g.112477724C>ACA481887731PTPN11c.927C>A (p.Ile309=)
c.813C>A (p.Ile271=)
c.924C>A (p.Ile308=)
12g.112477724C>GCA386790848PTPN11c.927C>G (p.Ile309Met)
c.813C>G (p.Ile271Met)
c.924C>G (p.Ile308Met)
 dbSNP
12g.112477724C>TCA481887736PTPN11c.927C>T (p.Ile309=)
c.813C>T (p.Ile271=)
c.924C>T (p.Ile308=)
 dbSNP
12g.112477725A>CCA386790852PTPN11c.928A>C (p.Ile310Leu)
c.814A>C (p.Ile272Leu)
c.925A>C (p.Ile309Leu)
 gnomAD v4
12g.112477725A>GCA386790856PTPN11c.928A>G (p.Ile310Val)
c.814A>G (p.Ile272Val)
c.925A>G (p.Ile309Val)
12g.112477725A>TCA386790859PTPN11c.928A>T (p.Ile310Phe)
c.814A>T (p.Ile272Phe)
c.925A>T (p.Ile309Phe)
12g.112477726T>ACA386790864PTPN11c.929T>A (p.Ile310Asn)
c.815T>A (p.Ile272Asn)
c.926T>A (p.Ile309Asn)
12g.112477726T>CCA386790866PTPN11c.929T>C (p.Ile310Thr)
c.815T>C (p.Ile272Thr)
c.926T>C (p.Ile309Thr)
12g.112477726T>GCA386790868PTPN11c.929T>G (p.Ile310Ser)
c.815T>G (p.Ile272Ser)
c.926T>G (p.Ile309Ser)
12g.112477727C>ACA481887738PTPN11c.930C>A (p.Ile310=)
c.816C>A (p.Ile272=)
c.927C>A (p.Ile309=)
12g.112477727C>GCA386790872PTPN11c.930C>G (p.Ile310Met)
c.816C>G (p.Ile272Met)
c.927C>G (p.Ile309Met)
 dbSNP
12g.112477727C>TCA481887739PTPN11c.930C>T (p.Ile310=)
c.816C>T (p.Ile272=)
c.927C>T (p.Ile309=)
 dbSNP
12g.112477728A=CA2063775801PTPN11c.931A= (p.Met311=)
c.817A= (p.Met273=)
c.928A= (p.Met310=)
12g.112477728A>CCA386790874PTPN11c.931A>C (p.Met311Leu)
c.817A>C (p.Met273Leu)
c.928A>C (p.Met310Leu)
12g.112477728A>GCA6798676PTPN11c.931A>G (p.Met311Val)
c.817A>G (p.Met273Val)
c.928A>G (p.Met310Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.112477728A>TCA386790875PTPN11c.931A>T (p.Met311Leu)
c.817A>T (p.Met273Leu)
c.928A>T (p.Met310Leu)
 gnomAD v4
12g.112477729T>ACA386790877PTPN11c.932T>A (p.Met311Lys)
c.818T>A (p.Met273Lys)
c.929T>A (p.Met310Lys)
 dbSNP
12g.112477729T>CCA6798677PTPN11c.932T>C (p.Met311Thr)
c.818T>C (p.Met273Thr)
c.929T>C (p.Met310Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477729T>GCA386790883PTPN11c.932T>G (p.Met311Arg)
c.818T>G (p.Met273Arg)
c.929T>G (p.Met310Arg)
12g.112477729T=CA2063775805PTPN11c.932T= (p.Met311=)
c.818T= (p.Met273=)
c.929T= (p.Met310=)
12g.112477730G>ACA386790886PTPN11c.933G>A (p.Met311Ile)
c.819G>A (p.Met273Ile)
c.930G>A (p.Met310Ile)
 dbSNP
12g.112477730G>CCA386790888PTPN11c.933G>C (p.Met311Ile)
c.819G>C (p.Met273Ile)
c.930G>C (p.Met310Ile)
 dbSNP
12g.112477730G>TCA386790889PTPN11c.933G>T (p.Met311Ile)
c.819G>T (p.Met273Ile)
c.930G>T (p.Met310Ile)
12g.112477731G>ACA386790890PTPN11c.933+1G>A (n.933+1G>A)
c.819+1G>A (n.819+1G>A)
c.930+1G>A (n.930+1G>A)
 dbSNP
12g.112477731G>CCA386790893PTPN11c.933+1G>C (n.933+1G>C)
c.819+1G>C (n.819+1G>C)
c.930+1G>C (n.930+1G>C)
 dbSNP
12g.112477731G>TCA386790895PTPN11c.933+1G>T (n.933+1G>T)
c.819+1G>T (n.819+1G>T)
c.930+1G>T (n.930+1G>T)
12g.112477732T>ACA386790899PTPN11c.933+2T>A (n.933+2T>A)
c.819+2T>A (n.819+2T>A)
c.930+2T>A (n.930+2T>A)
 dbSNP
12g.112477732T>CCA386790903PTPN11c.933+2T>C (n.933+2T>C)
c.819+2T>C (n.819+2T>C)
c.930+2T>C (n.930+2T>C)
12g.112477732T>GCA386790906PTPN11c.933+2T>G (n.933+2T>G)
c.819+2T>G (n.819+2T>G)
c.930+2T>G (n.930+2T>G)
12g.112477734A=CA2063775808PTPN11c.933+4A= (n.933+4A=)
c.819+4A= (n.819+4A=)
c.930+4A= (n.930+4A=)
12g.112477734A>TCA913190493PTPN11c.933+4A>T (n.933+4A>T)
c.819+4A>T (n.819+4A>T)
c.930+4A>T (n.930+4A>T)
 ClinVar dbSNP
12g.112477735G>ACA2621024626PTPN11c.933+5G>A (n.933+5G>A)
c.819+5G>A (n.819+5G>A)
c.930+5G>A (n.930+5G>A)
 gnomAD v4
12g.112477735G>CCA2727224594PTPN11c.933+5G>C (n.933+5G>C)
c.819+5G>C (n.819+5G>C)
c.930+5G>C (n.930+5G>C)
 dbSNP
12g.112477736C>ACA2727224628PTPN11c.933+6C>A (n.933+6C>A)
c.819+6C>A (n.819+6C>A)
c.930+6C>A (n.930+6C>A)
 dbSNP
12g.112477736C>GCA2727224633PTPN11c.933+6C>G (n.933+6C>G)
c.819+6C>G (n.819+6C>G)
c.930+6C>G (n.930+6C>G)
 dbSNP
12g.112477736C>TCA2727224634PTPN11c.933+6C>T (n.933+6C>T)
c.819+6C>T (n.819+6C>T)
c.930+6C>T (n.930+6C>T)
 dbSNP
12g.112477737T>ACA2727224636PTPN11c.933+7T>A (n.933+7T>A)
c.819+7T>A (n.819+7T>A)
c.930+7T>A (n.930+7T>A)
 dbSNP
12g.112477737T>GCA2575298959PTPN11c.933+7T>G (n.933+7T>G)
c.819+7T>G (n.819+7T>G)
c.930+7T>G (n.930+7T>G)
 ClinVar
12g.112477738T>CCA2580085812PTPN11c.933+8T>C (n.933+8T>C)
c.819+8T>C (n.819+8T>C)
c.930+8T>C (n.930+8T>C)
 ClinVar
12g.112477739T>CCA2621024627PTPN11c.933+9T>C (n.933+9T>C)
c.819+9T>C (n.819+9T>C)
c.930+9T>C (n.930+9T>C)
 gnomAD v4
12g.112477739T>GCA2063775813PTPN11c.933+9T>G (n.933+9T>G)
c.819+9T>G (n.819+9T>G)
c.930+9T>G (n.930+9T>G)
 dbSNP
12g.112477739T=CA2063775811PTPN11c.933+9T= (n.933+9T=)
c.819+9T= (n.819+9T=)
c.930+9T= (n.930+9T=)
12g.112477740G>ACA2727224660PTPN11c.933+10G>A (n.933+10G>A)
c.819+10G>A (n.819+10G>A)
c.930+10G>A (n.930+10G>A)
 dbSNP
12g.112477740G>CCA2727224747PTPN11c.933+10G>C (n.933+10G>C)
c.819+10G>C (n.819+10G>C)
c.930+10G>C (n.930+10G>C)
 dbSNP
12g.112477741C>ACA2727053171PTPN11c.933+11C>A (n.933+11C>A)
c.819+11C>A (n.819+11C>A)
c.930+11C>A (n.930+11C>A)
 dbSNP
12g.112477741C=CA2063775815PTPN11c.933+11C= (n.933+11C=)
c.819+11C= (n.819+11C=)
c.930+11C= (n.930+11C=)
12g.112477741C>GCA2727053172PTPN11c.933+11C>G (n.933+11C>G)
c.819+11C>G (n.819+11C>G)
c.930+11C>G (n.930+11C>G)
 dbSNP
12g.112477741C>TCA282104PTPN11c.933+11C>T (n.933+11C>T)
c.819+11C>T (n.819+11C>T)
c.930+11C>T (n.930+11C>T)
 ClinVar dbSNP
12g.112477742T>ACA2727224752PTPN11c.933+12T>A (n.933+12T>A)
c.819+12T>A (n.819+12T>A)
c.930+12T>A (n.930+12T>A)
 dbSNP
12g.112477745dupCA2621024628PTPN11c.933+15dup (n.933+15dup)
c.819+15dup (n.819+15dup)
c.930+15dup (n.930+15dup)
 gnomAD v4
12g.112477743T>ACA2727224927PTPN11c.933+13T>A (n.933+13T>A)
c.819+13T>A (n.819+13T>A)
c.930+13T>A (n.930+13T>A)
 dbSNP
12g.112477744_112477750delinsTTCACAGCA2063775817PTPN11c.933+14_933+20delinsTTCACAG (n.933+14_933+20delinsTTCACAG)
c.819+14_819+20delinsTTCACAG (n.819+14_819+20delinsTTCACAG)
c.930+14_930+20delinsTTCACAG (n.930+14_930+20delinsTTCACAG)
12g.112477746_112477751delCA6798678PTPN11c.933+16_933+21del (n.933+16_933+21del)
c.819+16_819+21del (n.819+16_819+21del)
c.930+16_930+21del (n.930+16_930+21del)
 dbSNP ExAC gnomAD v2
12g.112477747A>CCA2727224958PTPN11c.933+17A>C (n.933+17A>C)
c.819+17A>C (n.819+17A>C)
c.930+17A>C (n.930+17A>C)
 dbSNP
12g.112477747A>TCA2727224937PTPN11c.933+17A>T (n.933+17A>T)
c.819+17A>T (n.819+17A>T)
c.930+17A>T (n.930+17A>T)
 dbSNP
12g.112477748C>GCA2727225052PTPN11c.933+18C>G (n.933+18C>G)
c.819+18C>G (n.819+18C>G)
c.930+18C>G (n.930+18C>G)
 dbSNP
12g.112477748C>TCA2727225050PTPN11c.933+18C>T (n.933+18C>T)
c.819+18C>T (n.819+18C>T)
c.930+18C>T (n.930+18C>T)
 dbSNP
12g.112477749A=CA2063775820PTPN11c.933+19A= (n.933+19A=)
c.819+19A= (n.819+19A=)
c.930+19A= (n.930+19A=)
12g.112477749A>CCA2063775819PTPN11c.933+19A>C (n.933+19A>C)
c.819+19A>C (n.819+19A>C)
c.930+19A>C (n.930+19A>C)
 dbSNP
12g.112477750G>ACA2727225061PTPN11c.933+20G>A (n.933+20G>A)
c.819+20G>A (n.819+20G>A)
c.930+20G>A (n.930+20G>A)
 dbSNP
12g.112477750G>CCA2727225062PTPN11c.933+20G>C (n.933+20G>C)
c.819+20G>C (n.819+20G>C)
c.930+20G>C (n.930+20G>C)
 dbSNP
12g.112477751T>CCA2727058503PTPN11c.933+21T>C (n.933+21T>C)
c.819+21T>C (n.819+21T>C)
c.930+21T>C (n.930+21T>C)
 dbSNP
12g.112477751T>GCA6798679PTPN11c.933+21T>G (n.933+21T>G)
c.819+21T>G (n.819+21T>G)
c.930+21T>G (n.930+21T>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.112477751T=CA2063775823PTPN11c.933+21T= (n.933+21T=)
c.819+21T= (n.819+21T=)
c.930+21T= (n.930+21T=)
12g.112477752G>ACA243711967PTPN11c.933+22G>A (n.933+22G>A)
c.819+22G>A (n.819+22G>A)
c.930+22G>A (n.930+22G>A)
 dbSNP
12g.112477752G>CCA607604974PTPN11c.933+22G>C (n.933+22G>C)
c.819+22G>C (n.819+22G>C)
c.930+22G>C (n.930+22G>C)
 dbSNP gnomAD v2 gnomAD v4
12g.112477752G=CA2063775825PTPN11c.933+22G= (n.933+22G=)
c.819+22G= (n.819+22G=)
c.930+22G= (n.930+22G=)
12g.112477753T>ACA2575298961PTPN11c.933+23T>A (n.933+23T>A)
c.819+23T>A (n.819+23T>A)
c.930+23T>A (n.930+23T>A)
12g.112477756dupCA2621024629PTPN11c.933+26dup (n.933+26dup)
c.819+26dup (n.819+26dup)
c.930+26dup (n.930+26dup)
 gnomAD v4
12g.112477755T>ACA2727056255PTPN11c.933+25T>A (n.933+25T>A)
c.819+25T>A (n.819+25T>A)
c.930+25T>A (n.930+25T>A)
 dbSNP
12g.112477755T>CCA273708PTPN11c.933+25T>C (n.933+25T>C)
c.819+25T>C (n.819+25T>C)
c.930+25T>C (n.930+25T>C)
 ClinVar dbSNP
12g.112477755T>GCA2621024630PTPN11c.933+25T>G (n.933+25T>G)
c.819+25T>G (n.819+25T>G)
c.930+25T>G (n.930+25T>G)
 gnomAD v4
12g.112477755T=CA2063775829PTPN11c.933+25T= (n.933+25T=)
c.819+25T= (n.819+25T=)
c.930+25T= (n.930+25T=)
12g.112477756T>ACA2063775832PTPN11c.933+26T>A (n.933+26T>A)
c.819+26T>A (n.819+26T>A)
c.930+26T>A (n.930+26T>A)
 dbSNP
12g.112477756T=CA2063775831PTPN11c.933+26T= (n.933+26T=)
c.819+26T= (n.819+26T=)
c.930+26T= (n.930+26T=)
12g.112477757C>ACA2727225118PTPN11c.933+27C>A (n.933+27C>A)
c.819+27C>A (n.819+27C>A)
c.930+27C>A (n.930+27C>A)
 dbSNP
12g.112477757C>GCA2727225115PTPN11c.933+27C>G (n.933+27C>G)
c.819+27C>G (n.819+27C>G)
c.930+27C>G (n.930+27C>G)
 dbSNP
12g.112477758T>ACA2621024631PTPN11c.933+28T>A (n.933+28T>A)
c.819+28T>A (n.819+28T>A)
c.930+28T>A (n.930+28T>A)
 dbSNP gnomAD v4
12g.112477759G>ACA2727225387PTPN11c.933+29G>A (n.933+29G>A)
c.819+29G>A (n.819+29G>A)
c.930+29G>A (n.930+29G>A)
 dbSNP
12g.112477759G>CCA2727225385PTPN11c.933+29G>C (n.933+29G>C)
c.819+29G>C (n.819+29G>C)
c.930+29G>C (n.930+29G>C)
 dbSNP
12g.112477759G>TCA2621024632PTPN11c.933+29G>T (n.933+29G>T)
c.819+29G>T (n.819+29G>T)
c.930+29G>T (n.930+29G>T)
 gnomAD v4
12g.112477760A>GCA2575298963PTPN11c.933+30A>G (n.933+30A>G)
c.819+30A>G (n.819+30A>G)
c.930+30A>G (n.930+30A>G)
12g.112477761C>ACA2727174341PTPN11c.933+31C>A (n.933+31C>A)
c.819+31C>A (n.819+31C>A)
c.930+31C>A (n.930+31C>A)
 dbSNP
12g.112477761C=CA2063775835PTPN11c.933+31C= (n.933+31C=)
c.819+31C= (n.819+31C=)
c.930+31C= (n.930+31C=)
12g.112477761C>GCA2621024633PTPN11c.933+31C>G (n.933+31C>G)
c.819+31C>G (n.819+31C>G)
c.930+31C>G (n.930+31C>G)
 dbSNP gnomAD v4
12g.112477761C>TCA2063775834PTPN11c.933+31C>T (n.933+31C>T)
c.819+31C>T (n.819+31C>T)
c.930+31C>T (n.930+31C>T)
 dbSNP gnomAD v4
12g.112477762C>ACA2727225428PTPN11c.933+32C>A (n.933+32C>A)
c.819+32C>A (n.819+32C>A)
c.930+32C>A (n.930+32C>A)
 dbSNP
12g.112477762C>GCA2727225429PTPN11c.933+32C>G (n.933+32C>G)
c.819+32C>G (n.819+32C>G)
c.930+32C>G (n.930+32C>G)
 dbSNP
12g.112477762C>TCA2727225430PTPN11c.933+32C>T (n.933+32C>T)
c.819+32C>T (n.819+32C>T)
c.930+32C>T (n.930+32C>T)
 dbSNP
12g.112477763A=CA2063775837PTPN11c.933+33A= (n.933+33A=)
c.819+33A= (n.819+33A=)
c.930+33A= (n.930+33A=)
12g.112477763A>CCA6798680PTPN11c.933+33A>C (n.933+33A>C)
c.819+33A>C (n.819+33A>C)
c.930+33A>C (n.930+33A>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477763A>GCA243711970PTPN11c.933+33A>G (n.933+33A>G)
c.819+33A>G (n.819+33A>G)
c.930+33A>G (n.930+33A>G)
 dbSNP gnomAD v4
12g.112477764T>CCA6798681PTPN11c.933+34T>C (n.933+34T>C)
c.819+34T>C (n.819+34T>C)
c.930+34T>C (n.930+34T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.112477764T=CA2063775842PTPN11c.933+34T= (n.933+34T=)
c.819+34T= (n.819+34T=)
c.930+34T= (n.930+34T=)

Number of alleles fetched