Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.53889888T>ACA407414338PRKCGc.400T>A (p.Cys134Ser)
n.698T>A
n.702T>A
c.16T>A (p.Cys6Ser)
dbSNP gnomAD v4
19g.53889888T>CCA407414340PRKCGc.400T>C (p.Cys134Arg)
n.698T>C
n.702T>C
c.16T>C (p.Cys6Arg)
gnomAD v4
19g.53889888T>GCA407414339PRKCGc.400T>G (p.Cys134Gly)
n.698T>G
n.702T>G
c.16T>G (p.Cys6Gly)
19g.53889889G>ACA407414341PRKCGc.401G>A (p.Cys134Tyr)
n.699G>A
n.703G>A
c.17G>A (p.Cys6Tyr)
dbSNP gnomAD v4
19g.53889889G>CCA407414342PRKCGc.401G>C (p.Cys134Ser)
n.699G>C
n.703G>C
c.17G>C (p.Cys6Ser)
19g.53889889G>TCA407414343PRKCGc.401G>T (p.Cys134Phe)
n.699G>T
n.703G>T
c.17G>T (p.Cys6Phe)
gnomAD v4
19g.53889889_53889890delinsGCCA2342579372PRKCGc.401_402delinsGC (p.Cys134=)
n.699_700delinsGC
n.703_704delinsGC
c.17_18delinsGC (p.Cys6=)
19g.53889889_53889890delinsTTCA1139666580PRKCGc.401_402delinsTT (p.Cys134Phe)
n.699_700delinsTT
n.703_704delinsTT
c.17_18delinsTT (p.Cys6Phe)
ClinVar dbSNP
19g.53889890C>ACA407414344PRKCGc.402C>A (p.Cys134Ter)
n.700C>A
n.704C>A
c.18C>A (p.Cys6Ter)
gnomAD v4
19g.53889890C=CA2342579373PRKCGc.402C= (p.Cys134=)
n.700C=
n.704C=
c.18C= (p.Cys6=)
19g.53889890C>GCA407414345PRKCGc.402C>G (p.Cys134Trp)
n.700C>G
n.704C>G
c.18C>G (p.Cys6Trp)
dbSNP
19g.53889890C>TCA508787620PRKCGc.402C>T (p.Cys134=)
n.700C>T
n.704C>T
c.18C>T (p.Cys6=)
dbSNP gnomAD v2 gnomAD v4
19g.53889891G>ACA407414346PRKCGc.403G>A (p.Glu135Lys)
n.701G>A
n.705G>A
c.19G>A (p.Glu7Lys)
gnomAD v4
19g.53889891G>CCA407414347PRKCGc.403G>C (p.Glu135Gln)
n.701G>C
n.705G>C
c.19G>C (p.Glu7Gln)
gnomAD v4
19g.53889891G>TCA407414348PRKCGc.403G>T (p.Glu135Ter)
n.701G>T
n.705G>T
c.19G>T (p.Glu7Ter)
gnomAD v4
19g.53889892A>CCA407414349PRKCGc.404A>C (p.Glu135Ala)
n.702A>C
n.706A>C
c.20A>C (p.Glu7Ala)
19g.53889892A>GCA407414350PRKCGc.404A>G (p.Glu135Gly)
n.702A>G
n.706A>G
c.20A>G (p.Glu7Gly)
dbSNP gnomAD v4
19g.53889892A>TCA407414351PRKCGc.404A>T (p.Glu135Val)
n.702A>T
n.706A>T
c.20A>T (p.Glu7Val)
dbSNP gnomAD v4
19g.53889893G>ACA508787635PRKCGc.405G>A (p.Glu135=)
n.703G>A
n.707G>A
c.21G>A (p.Glu7=)
dbSNP gnomAD v3 gnomAD v4
19g.53889893G>CCA407414352PRKCGc.405G>C (p.Glu135Asp)
n.703G>C
n.707G>C
c.21G>C (p.Glu7Asp)
gnomAD v4
19g.53889893G=CA2342579374PRKCGc.405G= (p.Glu135=)
n.703G=
n.707G=
c.21G= (p.Glu7=)
19g.53889893G>TCA407414353PRKCGc.405G>T (p.Glu135Asp)
n.703G>T
n.707G>T
c.21G>T (p.Glu7Asp)
gnomAD v4
19g.53889894A>CCA407414356PRKCGc.406A>C (p.Met136Leu)
n.704A>C
n.708A>C
c.22A>C (p.Met8Leu)
19g.53889894A>GCA407414354PRKCGc.406A>G (p.Met136Val)
n.704A>G
n.708A>G
c.22A>G (p.Met8Val)
dbSNP
19g.53889894A>TCA407414355PRKCGc.406A>T (p.Met136Leu)
n.704A>T
n.708A>T
c.22A>T (p.Met8Leu)
19g.53889895T>ACA407414357PRKCGc.407T>A (p.Met136Lys)
n.705T>A
n.709T>A
c.23T>A (p.Met8Lys)
19g.53889895T>CCA407414358PRKCGc.407T>C (p.Met136Thr)
n.705T>C
n.709T>C
c.23T>C (p.Met8Thr)
gnomAD v4
19g.53889895T>GCA407414359PRKCGc.407T>G (p.Met136Arg)
n.705T>G
n.709T>G
c.23T>G (p.Met8Arg)
19g.53889896G>ACA407414360PRKCGc.408G>A (p.Met136Ile)
n.706G>A
n.710G>A
c.24G>A (p.Met8Ile)
dbSNP gnomAD v2 gnomAD v4
19g.53889896G>CCA407414361PRKCGc.408G>C (p.Met136Ile)
n.706G>C
n.710G>C
c.24G>C (p.Met8Ile)
19g.53889896G=CA2342579375PRKCGc.408G= (p.Met136=)
n.706G=
n.710G=
c.24G= (p.Met8=)
19g.53889896G>TCA407414362PRKCGc.408G>T (p.Met136Ile)
n.706G>T
n.710G>T
c.24G>T (p.Met8Ile)
gnomAD v4
19g.53889897A=CA2342579376PRKCGc.409A= (p.Asn137=)
n.707A=
n.711A=
c.25A= (p.Asn9=)
19g.53889897A>CCA407414363PRKCGc.409A>C (p.Asn137His)
n.707A>C
n.711A>C
c.25A>C (p.Asn9His)
19g.53889897A>GCA407414364PRKCGc.409A>G (p.Asn137Asp)
n.707A>G
n.711A>G
c.25A>G (p.Asn9Asp)
gnomAD v4
19g.53889897A>TCA407414365PRKCGc.409A>T (p.Asn137Tyr)
n.707A>T
n.711A>T
c.25A>T (p.Asn9Tyr)
ClinVar dbSNP
19g.53889898A>CCA407414366PRKCGc.410A>C (p.Asn137Thr)
n.708A>C
n.712A>C
c.26A>C (p.Asn9Thr)
19g.53889898A>GCA407414367PRKCGc.410A>G (p.Asn137Ser)
n.708A>G
n.712A>G
c.26A>G (p.Asn9Ser)
gnomAD v4
19g.53889898A>TCA407414368PRKCGc.410A>T (p.Asn137Ile)
n.708A>T
n.712A>T
c.26A>T (p.Asn9Ile)
19g.53889899C>ACA407414369PRKCGc.411C>A (p.Asn137Lys)
n.709C>A
n.713C>A
c.27C>A (p.Asn9Lys)
gnomAD v4
19g.53889899C>GCA407414370PRKCGc.411C>G (p.Asn137Lys)
n.709C>G
n.713C>G
c.27C>G (p.Asn9Lys)
19g.53889899C>TCA508787705PRKCGc.411C>T (p.Asn137=)
n.709C>T
n.713C>T
c.27C>T (p.Asn9=)
gnomAD v4
19g.53889900G>ACA407414371PRKCGc.412G>A (p.Val138Met)
n.710G>A
n.714G>A
c.28G>A (p.Val10Met)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.53889900G>CCA407414372PRKCGc.412G>C (p.Val138Leu)
n.710G>C
n.714G>C
c.28G>C (p.Val10Leu)
19g.53889900G=CA2342579377PRKCGc.412G= (p.Val138=)
n.710G=
n.714G=
c.28G= (p.Val10=)
19g.53889900G>TCA407414373PRKCGc.412G>T (p.Val138Leu)
n.710G>T
n.714G>T
c.28G>T (p.Val10Leu)
gnomAD v4
19g.53889901T>ACA344640PRKCGc.413T>A (p.Val138Glu)
n.711T>A
n.715T>A
c.29T>A (p.Val10Glu)
ClinVar dbSNP
19g.53889901T>CCA9640291PRKCGc.413T>C (p.Val138Ala)
n.711T>C
n.715T>C
c.29T>C (p.Val10Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53889901T>GCA407414374PRKCGc.413T>G (p.Val138Gly)
n.711T>G
n.715T>G
c.29T>G (p.Val10Gly)
19g.53889901T=CA2342579378PRKCGc.413T= (p.Val138=)
n.711T=
n.715T=
c.29T= (p.Val10=)
19g.53889902G>ACA508787733PRKCGc.414G>A (p.Val138=)
n.712G>A
n.716G>A
c.30G>A (p.Val10=)
gnomAD v4
19g.53889902G>CCA508787737PRKCGc.414G>C (p.Val138=)
n.712G>C
n.716G>C
c.30G>C (p.Val10=)
19g.53889902G>TCA508787740PRKCGc.414G>T (p.Val138=)
n.712G>T
n.716G>T
c.30G>T (p.Val10=)
gnomAD v4
19g.53889903C>ACA407414375PRKCGc.415C>A (p.His139Asn)
n.713C>A
n.717C>A
c.31C>A (p.His11Asn)
ClinVar dbSNP gnomAD v4
19g.53889903C=CA2342579379PRKCGc.415C= (p.His139=)
n.713C=
n.717C=
c.31C= (p.His11=)
19g.53889903C>GCA407414376PRKCGc.415C>G (p.His139Asp)
n.713C>G
n.717C>G
c.31C>G (p.His11Asp)
19g.53889903C>TCA407414377PRKCGc.415C>T (p.His139Tyr)
n.713C>T
n.717C>T
c.31C>T (p.His11Tyr)
gnomAD v4
19g.53889904A>CCA407414378PRKCGc.416A>C (p.His139Pro)
n.714A>C
n.718A>C
c.32A>C (p.His11Pro)
19g.53889904A>GCA407414379PRKCGc.416A>G (p.His139Arg)
n.714A>G
n.718A>G
c.32A>G (p.His11Arg)
gnomAD v4
19g.53889904A>TCA407414380PRKCGc.416A>T (p.His139Leu)
n.714A>T
n.718A>T
c.32A>T (p.His11Leu)
19g.53889905C>ACA344646PRKCGc.417C>A (p.His139Gln)
n.715C>A
n.719C>A
c.33C>A (p.His11Gln)
ClinVar dbSNP gnomAD v4
19g.53889905C=CA2342579380PRKCGc.417C= (p.His139=)
n.715C=
n.719C=
c.33C= (p.His11=)
19g.53889905C>GCA407414381PRKCGc.417C>G (p.His139Gln)
n.715C>G
n.719C>G
c.33C>G (p.His11Gln)
19g.53889905C>TCA508787766PRKCGc.417C>T (p.His139=)
n.715C>T
n.719C>T
c.33C>T (p.His11=)
gnomAD v4
19g.53889906C>ACA508787772PRKCGc.418C>A (p.Arg140=)
n.716C>A
n.720C>A
c.34C>A (p.Arg12=)
gnomAD v4
19g.53889906C=CA2342579381PRKCGc.418C= (p.Arg140=)
n.716C=
n.720C=
c.34C= (p.Arg12=)
19g.53889906C>GCA407414382PRKCGc.418C>G (p.Arg140Gly)
n.716C>G
n.720C>G
c.34C>G (p.Arg12Gly)
19g.53889906C>TCA407414383PRKCGc.418C>T (p.Arg140Trp)
n.716C>T
n.720C>T
c.34C>T (p.Arg12Trp)
dbSNP gnomAD v2 gnomAD v4
19g.53889907G>ACA9640292PRKCGc.419G>A (p.Arg140Gln)
n.717G>A
n.721G>A
c.35G>A (p.Arg12Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53889907G>CCA407414384PRKCGc.419G>C (p.Arg140Pro)
n.717G>C
n.721G>C
c.35G>C (p.Arg12Pro)
dbSNP gnomAD v2 gnomAD v4
19g.53889907G=CA2342579382PRKCGc.419G= (p.Arg140=)
n.717G=
n.721G=
c.35G= (p.Arg12=)
19g.53889907G>TCA407414385PRKCGc.419G>T (p.Arg140Leu)
n.717G>T
n.721G>T
c.35G>T (p.Arg12Leu)
gnomAD v4
19g.53889908G>ACA508787798PRKCGc.420G>A (p.Arg140=)
n.718G>A
n.722G>A
c.36G>A (p.Arg12=)
gnomAD v4
19g.53889908G>CCA508787790PRKCGc.420G>C (p.Arg140=)
n.718G>C
n.722G>C
c.36G>C (p.Arg12=)
dbSNP gnomAD v3 gnomAD v4
19g.53889908G=CA2342579383PRKCGc.420G= (p.Arg140=)
n.718G=
n.722G=
c.36G= (p.Arg12=)
19g.53889908G>TCA508787794PRKCGc.420G>T (p.Arg140=)
n.718G>T
n.722G>T
c.36G>T (p.Arg12=)
gnomAD v4
19g.53889909C>ACA407414386PRKCGc.421C>A (p.Arg141Ser)
n.719C>A
n.723C>A
c.37C>A (p.Arg13Ser)
gnomAD v4
19g.53889909C>GCA407414387PRKCGc.421C>G (p.Arg141Gly)
n.719C>G
n.723C>G
c.37C>G (p.Arg13Gly)
19g.53889909C>TCA407414388PRKCGc.421C>T (p.Arg141Cys)
n.719C>T
n.723C>T
c.37C>T (p.Arg13Cys)
gnomAD v4
19g.53889910G>ACA407414389PRKCGc.422G>A (p.Arg141His)
n.720G>A
n.724G>A
c.38G>A (p.Arg13His)
gnomAD v4
19g.53889910G>CCA407414390PRKCGc.422G>C (p.Arg141Pro)
n.720G>C
n.724G>C
c.38G>C (p.Arg13Pro)
19g.53889910G>TCA407414391PRKCGc.422G>T (p.Arg141Leu)
n.720G>T
n.724G>T
c.38G>T (p.Arg13Leu)
gnomAD v4
19g.53889911C>ACA508787821PRKCGc.423C>A (p.Arg141=)
n.721C>A
n.725C>A
c.39C>A (p.Arg13=)
gnomAD v4 COSMIC COSMIC
19g.53889911C>GCA508787823PRKCGc.423C>G (p.Arg141=)
n.721C>G
n.725C>G
c.39C>G (p.Arg13=)
19g.53889911C>TCA508787827PRKCGc.423C>T (p.Arg141=)
n.721C>T
n.725C>T
c.39C>T (p.Arg13=)
gnomAD v4
19g.53889912T>ACA407414392PRKCGc.424T>A (p.Cys142Ser)
n.722T>A
n.726T>A
c.40T>A (p.Cys14Ser)
gnomAD v4
19g.53889912T>CCA407414393PRKCGc.424T>C (p.Cys142Arg)
n.722T>C
n.726T>C
c.40T>C (p.Cys14Arg)
gnomAD v4
19g.53889912T>GCA407414394PRKCGc.424T>G (p.Cys142Gly)
n.722T>G
n.726T>G
c.40T>G (p.Cys14Gly)
19g.53889913G>ACA407414395PRKCGc.425G>A (p.Cys142Tyr)
n.723G>A
n.727G>A
c.41G>A (p.Cys14Tyr)
ClinVar gnomAD v4
19g.53889913G>CCA407414397PRKCGc.425G>C (p.Cys142Ser)
n.723G>C
n.727G>C
c.41G>C (p.Cys14Ser)
19g.53889913G>TCA407414396PRKCGc.425G>T (p.Cys142Phe)
n.723G>T
n.727G>T
c.41G>T (p.Cys14Phe)
gnomAD v4
19g.53889914T>ACA407414398PRKCGc.426T>A (p.Cys142Ter)
n.724T>A
n.728T>A
c.42T>A (p.Cys14Ter)
19g.53889914T>CCA508787853PRKCGc.426T>C (p.Cys142=)
n.724T>C
n.728T>C
c.42T>C (p.Cys14=)
COSMIC COSMIC
19g.53889914T>GCA407414399PRKCGc.426T>G (p.Cys142Trp)
n.724T>G
n.728T>G
c.42T>G (p.Cys14Trp)
gnomAD v4
19g.53889915G>ACA407414400PRKCGc.427G>A (p.Val143Met)
n.725G>A
n.729G>A
c.43G>A (p.Val15Met)
dbSNP gnomAD v4
19g.53889915G>CCA407414401PRKCGc.427G>C (p.Val143Leu)
n.725G>C
n.729G>C
c.43G>C (p.Val15Leu)
19g.53889915G=CA2342579384PRKCGc.427G= (p.Val143=)
n.725G=
n.729G=
c.43G= (p.Val15=)
19g.53889915G>TCA407414402PRKCGc.427G>T (p.Val143Leu)
n.725G>T
n.729G>T
c.43G>T (p.Val15Leu)
gnomAD v4
19g.53889916T>ACA407414403PRKCGc.428T>A (p.Val143Glu)
n.726T>A
n.730T>A
c.44T>A (p.Val15Glu)
19g.53889916T>CCA407414404PRKCGc.428T>C (p.Val143Ala)
n.726T>C
n.730T>C
c.44T>C (p.Val15Ala)
gnomAD v4
19g.53889916T>GCA407414405PRKCGc.428T>G (p.Val143Gly)
n.726T>G
n.730T>G
c.44T>G (p.Val15Gly)
19g.53889917G>ACA508787885PRKCGc.429G>A (p.Val143=)
n.727G>A
n.731G>A
c.45G>A (p.Val15=)
gnomAD v4
19g.53889917G>CCA9640293PRKCGc.429G>C (p.Val143=)
n.727G>C
n.731G>C
c.45G>C (p.Val15=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.53889917G=CA2342579385PRKCGc.429G= (p.Val143=)
n.727G=
n.731G=
c.45G= (p.Val15=)
19g.53889917G>TCA508787890PRKCGc.429G>T (p.Val143=)
n.727G>T
n.731G>T
c.45G>T (p.Val15=)
gnomAD v4
19g.53889918C>ACA407414406PRKCGc.430C>A (p.Arg144Ser)
n.728C>A
n.732C>A
c.46C>A (p.Arg16Ser)
gnomAD v4
19g.53889918C>GCA407414407PRKCGc.430C>G (p.Arg144Gly)
n.728C>G
n.732C>G
c.46C>G (p.Arg16Gly)
19g.53889918C>TCA407414408PRKCGc.430C>T (p.Arg144Cys)
n.728C>T
n.732C>T
c.46C>T (p.Arg16Cys)
gnomAD v4
19g.53889919G>ACA407414411PRKCGc.431G>A (p.Arg144His)
n.729G>A
n.733G>A
c.47G>A (p.Arg16His)
gnomAD v4
19g.53889919G>CCA407414410PRKCGc.431G>C (p.Arg144Pro)
n.729G>C
n.733G>C
c.47G>C (p.Arg16Pro)
19g.53889919G>TCA407414409PRKCGc.431G>T (p.Arg144Leu)
n.729G>T
n.733G>T
c.47G>T (p.Arg16Leu)
gnomAD v4
19g.53889920T>ACA508787914PRKCGc.432T>A (p.Arg144=)
n.730T>A
n.734T>A
c.48T>A (p.Arg16=)
19g.53889920T>CCA9640294PRKCGc.432T>C (p.Arg144=)
n.730T>C
n.734T>C
c.48T>C (p.Arg16=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.53889920T>GCA508787920PRKCGc.432T>G (p.Arg144=)
n.730T>G
n.734T>G
c.48T>G (p.Arg16=)
19g.53889920T=CA2342579386PRKCGc.432T= (p.Arg144=)
n.730T=
n.734T=
c.48T= (p.Arg16=)
19g.53889921A>CCA407414412PRKCGc.433A>C (p.Ser145Arg)
n.731A>C
n.735A>C
c.49A>C (p.Ser17Arg)
19g.53889921A>GCA407414413PRKCGc.433A>G (p.Ser145Gly)
n.731A>G
n.735A>G
c.49A>G (p.Ser17Gly)
gnomAD v4
19g.53889921A>TCA407414414PRKCGc.433A>T (p.Ser145Cys)
n.731A>T
n.735A>T
c.49A>T (p.Ser17Cys)
19g.53889922G>ACA407414415PRKCGc.434G>A (p.Ser145Asn)
n.732G>A
n.736G>A
c.50G>A (p.Ser17Asn)
19g.53889922G>CCA407414416PRKCGc.434G>C (p.Ser145Thr)
n.732G>C
n.736G>C
c.50G>C (p.Ser17Thr)
dbSNP gnomAD v3 gnomAD v4
19g.53889922G=CA2342579387PRKCGc.434G= (p.Ser145=)
n.732G=
n.736G=
c.50G= (p.Ser17=)
19g.53889922G>TCA407414417PRKCGc.434G>T (p.Ser145Ile)
n.732G>T
n.736G>T
c.50G>T (p.Ser17Ile)
gnomAD v4
19g.53889923C>ACA407414418PRKCGc.435C>A (p.Ser145Arg)
n.733C>A
n.737C>A
c.51C>A (p.Ser17Arg)
gnomAD v4
19g.53889923C=CA2342579388PRKCGc.435C= (p.Ser145=)
n.733C=
n.737C=
c.51C= (p.Ser17=)
19g.53889923C>GCA407414419PRKCGc.435C>G (p.Ser145Arg)
n.733C>G
n.737C>G
c.51C>G (p.Ser17Arg)
19g.53889923C>TCA310082642PRKCGc.435C>T (p.Ser145=)
n.733C>T
n.737C>T
c.51C>T (p.Ser17=)
dbSNP gnomAD v4
19g.53889924G>ACA407414420PRKCGc.436G>A (p.Val146Met)
n.734G>A
n.738G>A
c.52G>A (p.Val18Met)
dbSNP gnomAD v4
19g.53889924G>CCA407414421PRKCGc.436G>C (p.Val146Leu)
n.734G>C
n.738G>C
c.52G>C (p.Val18Leu)
19g.53889924G=CA2342579389PRKCGc.436G= (p.Val146=)
n.734G=
n.738G=
c.52G= (p.Val18=)
19g.53889924G>TCA407414422PRKCGc.436G>T (p.Val146Leu)
n.734G>T
n.738G>T
c.52G>T (p.Val18Leu)
19g.53889925T>ACA407414424PRKCGc.437T>A (p.Val146Glu)
n.735T>A
n.739T>A
c.53T>A (p.Val18Glu)
19g.53889925T>CCA407414425PRKCGc.437T>C (p.Val146Ala)
n.735T>C
n.739T>C
c.53T>C (p.Val18Ala)
19g.53889925T>GCA407414423PRKCGc.437T>G (p.Val146Gly)
n.735T>G
n.739T>G
c.53T>G (p.Val18Gly)
19g.53889926G>ACA508787978PRKCGc.438G>A (p.Val146=)
n.736G>A
n.740G>A
c.54G>A (p.Val18=)
gnomAD v4
19g.53889926G>CCA508787984PRKCGc.438G>C (p.Val146=)
n.736G>C
n.740G>C
c.54G>C (p.Val18=)
gnomAD v4
19g.53889926G>TCA508787988PRKCGc.438G>T (p.Val146=)
n.736G>T
n.740G>T
c.54G>T (p.Val18=)
gnomAD v4
19g.53889927C>ACA407414426PRKCGc.439C>A (p.Pro147Thr)
n.737C>A
n.741C>A
c.55C>A (p.Pro19Thr)
19g.53889927C=CA2342579390PRKCGc.439C= (p.Pro147=)
n.737C=
n.741C=
c.55C= (p.Pro19=)
19g.53889927C>GCA407414427PRKCGc.439C>G (p.Pro147Ala)
n.737C>G
n.741C>G
c.55C>G (p.Pro19Ala)
19g.53889927C>TCA310082644PRKCGc.439C>T (p.Pro147Ser)
n.737C>T
n.741C>T
c.55C>T (p.Pro19Ser)
dbSNP gnomAD v4
19g.53889928C>ACA407414428PRKCGc.440C>A (p.Pro147His)
n.738C>A
n.742C>A
c.56C>A (p.Pro19His)
gnomAD v4
19g.53889928C>GCA407414429PRKCGc.440C>G (p.Pro147Arg)
n.738C>G
n.742C>G
c.56C>G (p.Pro19Arg)
19g.53889928C>TCA407414430PRKCGc.440C>T (p.Pro147Leu)
n.738C>T
n.742C>T
c.56C>T (p.Pro19Leu)
19g.53889929C>ACA508788018PRKCGc.441C>A (p.Pro147=)
n.739C>A
n.743C>A
c.57C>A (p.Pro19=)
gnomAD v4
19g.53889929C=CA2342579391PRKCGc.441C= (p.Pro147=)
n.739C=
n.743C=
c.57C= (p.Pro19=)
19g.53889929C>GCA508788011PRKCGc.441C>G (p.Pro147=)
n.739C>G
n.743C>G
c.57C>G (p.Pro19=)
19g.53889929C>TCA9640295PRKCGc.441C>T (p.Pro147=)
n.739C>T
n.743C>T
c.57C>T (p.Pro19=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53889930T>ACA407414431PRKCGc.442T>A (p.Ser148Thr)
n.740T>A
n.744T>A
c.58T>A (p.Ser20Thr)
c.58T>A
19g.53889930T>CCA407414432PRKCGc.442T>C (p.Ser148Pro)
n.740T>C
n.744T>C
c.58T>C (p.Ser20Pro)
c.58T>C
gnomAD v4
19g.53889930T>GCA407414433PRKCGc.442T>G (p.Ser148Ala)
n.740T>G
n.744T>G
c.58T>G (p.Ser20Ala)
c.58T>G
19g.53889931C>ACA407414434PRKCGc.443C>A (p.Ser148Tyr)
n.741C>A
n.745C>A
c.59C>A (p.Ser20Tyr)
gnomAD v4
19g.53889931C>GCA407414435PRKCGc.443C>G (p.Ser148Cys)
n.741C>G
n.745C>G
c.59C>G (p.Ser20Cys)
dbSNP
19g.53889931C>TCA407414436PRKCGc.443C>T (p.Ser148Phe)
n.741C>T
n.745C>T
c.59C>T (p.Ser20Phe)
gnomAD v4
19g.53889933delCA2586963390PRKCGc.445del (p.Leu149CysfsTer27)
n.743del
n.747del
c.61del (p.Leu21CysfsTer?)
c.61del (p.Leu21CysfsTer27)
gnomAD v4
19g.53889932C>ACA508788034PRKCGc.444C>A (p.Ser148=)
n.742C>A
n.746C>A
c.60C>A (p.Ser20=)
gnomAD v4
19g.53889932C=CA2342579392PRKCGc.444C= (p.Ser148=)
n.742C=
n.746C=
c.60C= (p.Ser20=)
19g.53889932C>GCA508788036PRKCGc.444C>G (p.Ser148=)
n.742C>G
n.746C>G
c.60C>G (p.Ser20=)
19g.53889932C>TCA508788038PRKCGc.444C>T (p.Ser148=)
n.742C>T
n.746C>T
c.60C>T (p.Ser20=)
dbSNP gnomAD v3 gnomAD v4
19g.53889933C>ACA407414437PRKCGc.445C>A (p.Leu149Met)
n.743C>A
n.747C>A
c.61C>A (p.Leu21Met)
gnomAD v4
19g.53889933C>GCA407414438PRKCGc.445C>G (p.Leu149Val)
n.743C>G
n.747C>G
c.61C>G (p.Leu21Val)
gnomAD v4
19g.53889933C>TCA508788045PRKCGc.445C>T (p.Leu149=)
n.743C>T
n.747C>T
c.61C>T (p.Leu21=)
gnomAD v4
19g.53889934T>ACA407414439PRKCGc.446T>A (p.Leu149Gln)
n.744T>A
n.748T>A
c.62T>A (p.Leu21Gln)
19g.53889934T>CCA407414440PRKCGc.446T>C (p.Leu149Pro)
n.744T>C
n.748T>C
c.62T>C (p.Leu21Pro)
gnomAD v4
19g.53889934T>GCA407414441PRKCGc.446T>G (p.Leu149Arg)
n.744T>G
n.748T>G
c.62T>G (p.Leu21Arg)
19g.53889935G>ACA508788054PRKCGc.447G>A (p.Leu149=)
n.745G>A
n.749G>A
c.63G>A (p.Leu21=)
gnomAD v4
19g.53889935G>CCA508788056PRKCGc.447G>C (p.Leu149=)
n.745G>C
n.749G>C
c.63G>C (p.Leu21=)
gnomAD v4
19g.53889935G>TCA508788058PRKCGc.447G>T (p.Leu149=)
n.745G>T
n.749G>T
c.63G>T (p.Leu21=)
gnomAD v4
19g.53889936T>ACA407414442PRKCGc.448T>A (p.Cys150Ser)
n.746T>A
n.750T>A
c.64T>A (p.Cys22Ser)
19g.53889936T>CCA407414443PRKCGc.448T>C (p.Cys150Arg)
n.746T>C
n.750T>C
c.64T>C (p.Cys22Arg)
ClinVar dbSNP
19g.53889936T>GCA407414444PRKCGc.448T>G (p.Cys150Gly)
n.746T>G
n.750T>G
c.64T>G (p.Cys22Gly)
19g.53889936T=CA2342579393PRKCGc.448T= (p.Cys150=)
n.746T=
n.750T=
c.64T= (p.Cys22=)
19g.53889936_53889948delCA2586963391PRKCGc.448_460del (p.Cys150ThrfsTer22)
n.746_758del
n.750_762del
c.64_76del (p.Cys22ThrfsTer?)
c.64_76del (p.Cys22ThrfsTer22)
gnomAD v4
19g.53889937G>ACA407414445PRKCGc.449G>A (p.Cys150Tyr)
n.747G>A
n.751G>A
c.65G>A (p.Cys22Tyr)
19g.53889937G>CCA407414446PRKCGc.449G>C (p.Cys150Ser)
n.747G>C
n.751G>C
c.65G>C (p.Cys22Ser)
19g.53889937G>TCA407414447PRKCGc.449G>T (p.Cys150Phe)
n.747G>T
n.751G>T
c.65G>T (p.Cys22Phe)
gnomAD v4
19g.53889937_53889938delinsGCCA2342579394PRKCGc.449_450delinsGC (p.Cys150=)
n.747_748delinsGC
n.751_752delinsGC
c.65_66delinsGC (p.Cys22=)
19g.53889937_53889938delinsTTCA344643PRKCGc.449_450delinsTT (p.Cys150Phe)
n.747_748delinsTT
n.751_752delinsTT
c.65_66delinsTT (p.Cys22Phe)
ClinVar dbSNP
19g.53889938C>ACA407414448PRKCGc.450C>A (p.Cys150Ter)
n.748C>A
n.752C>A
c.66C>A (p.Cys22Ter)
gnomAD v4
19g.53889938C=CA2342579395PRKCGc.450C= (p.Cys150=)
n.748C=
n.752C=
c.66C= (p.Cys22=)
19g.53889938C>GCA407414449PRKCGc.450C>G (p.Cys150Trp)
n.748C>G
n.752C>G
c.66C>G (p.Cys22Trp)
ClinVar dbSNP
19g.53889938C>TCA508788079PRKCGc.450C>T (p.Cys150=)
n.748C>T
n.752C>T
c.66C>T (p.Cys22=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.53889939G>ACA407414452PRKCGc.451G>A (p.Gly151Ser)
n.749G>A
n.753G>A
c.67G>A (p.Gly23Ser)
dbSNP gnomAD v2
19g.53889939G>CCA407414451PRKCGc.451G>C (p.Gly151Arg)
n.749G>C
n.753G>C
c.67G>C (p.Gly23Arg)
gnomAD v4
19g.53889939G=CA2342579396PRKCGc.451G= (p.Gly151=)
n.749G=
n.753G=
c.67G= (p.Gly23=)
19g.53889939G>TCA407414450PRKCGc.451G>T (p.Gly151Cys)
n.749G>T
n.753G>T
c.67G>T (p.Gly23Cys)
gnomAD v4
19g.53889940G>ACA9640296PRKCGc.452G>A (p.Gly151Asp)
n.750G>A
n.754G>A
c.68G>A (p.Gly23Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53889940G>CCA407414454PRKCGc.452G>C (p.Gly151Ala)
n.750G>C
n.754G>C
c.68G>C (p.Gly23Ala)
19g.53889940G=CA2342579397PRKCGc.452G= (p.Gly151=)
n.750G=
n.754G=
c.68G= (p.Gly23=)
19g.53889940G>TCA407414453PRKCGc.452G>T (p.Gly151Val)
n.750G>T
n.754G>T
c.68G>T (p.Gly23Val)
gnomAD v4
19g.53889943_53889944dupCA2736007018PRKCGc.455_456dup (p.Asp153TrpfsTer24)
n.753_754dup
n.757_758dup
c.71_72dup (p.Asp25TrpfsTer?)
c.71_72dup (p.Asp25TrpfsTer24)
dbSNP
19g.53889941T>ACA508788108PRKCGc.453T>A (p.Gly151=)
n.751T>A
n.755T>A
c.69T>A (p.Gly23=)
19g.53889941T>CCA508788110PRKCGc.453T>C (p.Gly151=)
n.751T>C
n.755T>C
c.69T>C (p.Gly23=)
gnomAD v4
19g.53889941T>GCA508788112PRKCGc.453T>G (p.Gly151=)
n.751T>G
n.755T>G
c.69T>G (p.Gly23=)
19g.53889942G>ACA407414455PRKCGc.454G>A (p.Val152Met)
n.752G>A
n.756G>A
c.70G>A (p.Val24Met)
dbSNP gnomAD v4
19g.53889942G>CCA407414456PRKCGc.454G>C (p.Val152Leu)
n.752G>C
n.756G>C
c.70G>C (p.Val24Leu)
19g.53889942G=CA2342579398PRKCGc.454G= (p.Val152=)
n.752G=
n.756G=
c.70G= (p.Val24=)
19g.53889942G>TCA407414457PRKCGc.454G>T (p.Val152Leu)
n.752G>T
n.756G>T
c.70G>T (p.Val24Leu)
gnomAD v4
19g.53889942_53889952delCA2586963392PRKCGc.454_464del (p.Val152ArgfsTer17)
n.752_762del
n.756_766del
c.70_80del (p.Val24ArgfsTer?)
c.70_80del (p.Val24ArgfsTer17)
gnomAD v4
19g.53889943T>ACA407414458PRKCGc.455T>A (p.Val152Glu)
n.753T>A
n.757T>A
c.71T>A (p.Val24Glu)
gnomAD v4
19g.53889943T>CCA407414459PRKCGc.455T>C (p.Val152Ala)
n.753T>C
n.757T>C
c.71T>C (p.Val24Ala)
gnomAD v4
19g.53889943T>GCA407414460PRKCGc.455T>G (p.Val152Gly)
n.753T>G
n.757T>G
c.71T>G (p.Val24Gly)
19g.53889944G>ACA508788123PRKCGc.456G>A (p.Val152=)
n.754G>A
n.758G>A
c.72G>A (p.Val24=)
dbSNP gnomAD v2 gnomAD v4
19g.53889944G>CCA508788124PRKCGc.456G>C (p.Val152=)
n.754G>C
n.758G>C
c.72G>C (p.Val24=)
19g.53889944G=CA2342579399PRKCGc.456G= (p.Val152=)
n.754G=
n.758G=
c.72G= (p.Val24=)
19g.53889944G>TCA508788125PRKCGc.456G>T (p.Val152=)
n.754G>T
n.758G>T
c.72G>T (p.Val24=)
gnomAD v4
19g.53889946_53889964delCA2586963393PRKCGc.458_476del (p.Asp153GlyfsTer17)
n.756_774del
n.760_778del
c.74_92del (p.Asp25GlyfsTer?)
c.74_92del (p.Asp25GlyfsTer17)
gnomAD v4
19g.53889945G>ACA407414461PRKCGc.457G>A (p.Asp153Asn)
n.755G>A
n.759G>A
c.73G>A (p.Asp25Asn)
gnomAD v4
19g.53889945G>CCA407414462PRKCGc.457G>C (p.Asp153His)
n.755G>C
n.759G>C
c.73G>C (p.Asp25His)
gnomAD v4
19g.53889945G>TCA407414463PRKCGc.457G>T (p.Asp153Tyr)
n.755G>T
n.759G>T
c.73G>T (p.Asp25Tyr)
gnomAD v4
19g.53889946A>CCA407414464PRKCGc.458A>C (p.Asp153Ala)
n.756A>C
n.760A>C
c.74A>C (p.Asp25Ala)
19g.53889946A>GCA407414465PRKCGc.458A>G (p.Asp153Gly)
n.756A>G
n.760A>G
c.74A>G (p.Asp25Gly)
19g.53889946A>TCA407414466PRKCGc.458A>T (p.Asp153Val)
n.756A>T
n.760A>T
c.74A>T (p.Asp25Val)
19g.53889947C>ACA407414468PRKCGc.459C>A (p.Asp153Glu)
n.757C>A
n.761C>A
c.75C>A (p.Asp25Glu)
gnomAD v4
19g.53889947C=CA2342579400PRKCGc.459C= (p.Asp153=)
n.757C=
n.761C=
c.75C= (p.Asp25=)
19g.53889947C>GCA407414467PRKCGc.459C>G (p.Asp153Glu)
n.757C>G
n.761C>G
c.75C>G (p.Asp25Glu)
gnomAD v4
19g.53889947C>TCA310082651PRKCGc.459C>T (p.Asp153=)
n.757C>T
n.761C>T
c.75C>T (p.Asp25=)
dbSNP gnomAD v4
19g.53889948C>ACA407414469PRKCGc.460C>A (p.His154Asn)
n.758C>A
n.762C>A
c.76C>A (p.His26Asn)
gnomAD v4
19g.53889948C>GCA407414470PRKCGc.460C>G (p.His154Asp)
n.758C>G
n.762C>G
c.76C>G (p.His26Asp)
19g.53889948C>TCA407414471PRKCGc.460C>T (p.His154Tyr)
n.758C>T
n.762C>T
c.76C>T (p.His26Tyr)
gnomAD v4
19g.53889949A>CCA407414472PRKCGc.461A>C (p.His154Pro)
n.759A>C
n.763A>C
c.77A>C (p.His26Pro)
19g.53889949A>GCA407414473PRKCGc.461A>G (p.His154Arg)
n.759A>G
n.763A>G
c.77A>G (p.His26Arg)
gnomAD v4
19g.53889949A>TCA407414474PRKCGc.461A>T (p.His154Leu)
n.759A>T
n.763A>T
c.77A>T (p.His26Leu)
19g.53889950C>ACA407414476PRKCGc.462C>A (p.His154Gln)
n.760C>A
n.764C>A
c.78C>A (p.His26Gln)
19g.53889950C>GCA407414475PRKCGc.462C>G (p.His154Gln)
n.760C>G
n.764C>G
c.78C>G (p.His26Gln)
19g.53889950C>TCA508788155PRKCGc.462C>T (p.His154=)
n.760C>T
n.764C>T
c.78C>T (p.His26=)
gnomAD v4
19g.53889951delCA2586963394PRKCGc.463del (p.Thr155ProfsTer21)
n.761del
n.765del
c.79del (p.Thr27ProfsTer?)
c.79del (p.Thr27ProfsTer21)
gnomAD v4
19g.53889951A>CCA407414477PRKCGc.463A>C (p.Thr155Pro)
n.761A>C
n.765A>C
c.79A>C (p.Thr27Pro)
19g.53889951A>GCA407414478PRKCGc.463A>G (p.Thr155Ala)
n.761A>G
n.765A>G
c.79A>G (p.Thr27Ala)
19g.53889951A>TCA407414479PRKCGc.463A>T (p.Thr155Ser)
n.761A>T
n.765A>T
c.79A>T (p.Thr27Ser)
19g.53889952C>ACA407414480PRKCGc.464C>A (p.Thr155Asn)
n.762C>A
n.766C>A
c.80C>A (p.Thr27Asn)
gnomAD v4
19g.53889952C>GCA407414481PRKCGc.464C>G (p.Thr155Ser)
n.762C>G
n.766C>G
c.80C>G (p.Thr27Ser)
gnomAD v4
19g.53889952C>TCA407414482PRKCGc.464C>T (p.Thr155Ile)
n.762C>T
n.766C>T
c.80C>T (p.Thr27Ile)
gnomAD v4
19g.53889953C>ACA508788172PRKCGc.465C>A (p.Thr155=)
n.763C>A
n.767C>A
c.81C>A (p.Thr27=)
dbSNP gnomAD v2 gnomAD v4
19g.53889953C=CA2342579401PRKCGc.465C= (p.Thr155=)
n.763C=
n.767C=
c.81C= (p.Thr27=)
19g.53889953C>GCA508788175PRKCGc.465C>G (p.Thr155=)
n.763C>G
n.767C>G
c.81C>G (p.Thr27=)
19g.53889953C>TCA508788177PRKCGc.465C>T (p.Thr155=)
n.763C>T
n.767C>T
c.81C>T (p.Thr27=)
gnomAD v4
19g.53889953_53889973delCA2586963395PRKCGc.465_485del (p.Glu156_Gln162del)
n.763_783del
n.767_787del
c.81_101del (p.Glu28_Gln34del)
gnomAD v4
19g.53889954G>ACA407414483PRKCGc.466G>A (p.Glu156Lys)
n.764G>A
n.768G>A
c.82G>A (p.Glu28Lys)
ClinVar dbSNP gnomAD v4
19g.53889954G>CCA407414485PRKCGc.466G>C (p.Glu156Gln)
n.764G>C
n.768G>C
c.82G>C (p.Glu28Gln)
dbSNP gnomAD v2 gnomAD v4
19g.53889954G=CA2342579402PRKCGc.466G= (p.Glu156=)
n.764G=
n.768G=
c.82G= (p.Glu28=)
19g.53889954G>TCA407414484PRKCGc.466G>T (p.Glu156Ter)
n.764G>T
n.768G>T
c.82G>T (p.Glu28Ter)
gnomAD v4
19g.53889954_53889955insCACCA2741640839PRKCGc.466_467insCAC (p.Glu156delinsAlaGln)
n.764_765insCAC
n.768_769insCAC
c.82_83insCAC (p.Glu28delinsAlaGln)
19g.53889955A=CA2342579403PRKCGc.467A= (p.Glu156=)
n.765A=
n.769A=
c.83A= (p.Glu28=)
19g.53889955A>CCA407414486PRKCGc.467A>C (p.Glu156Ala)
n.765A>C
n.769A>C
c.83A>C (p.Glu28Ala)
19g.53889955A>GCA407414487PRKCGc.467A>G (p.Glu156Gly)
n.765A>G
n.769A>G
c.83A>G (p.Glu28Gly)
dbSNP
19g.53889955A>TCA407414488PRKCGc.467A>T (p.Glu156Val)
n.765A>T
n.769A>T
c.83A>T (p.Glu28Val)
19g.53889956G>ACA9640297PRKCGc.468G>A (p.Glu156=)
n.766G>A
n.770G>A
c.84G>A (p.Glu28=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.53889956G>CCA407414489PRKCGc.468G>C (p.Glu156Asp)
n.766G>C
n.770G>C
c.84G>C (p.Glu28Asp)
19g.53889956G=CA2342579404PRKCGc.468G= (p.Glu156=)
n.766G=
n.770G=
c.84G= (p.Glu28=)
19g.53889956G>TCA407414490PRKCGc.468G>T (p.Glu156Asp)
n.766G>T
n.770G>T
c.84G>T (p.Glu28Asp)
gnomAD v4
19g.53889957C>ACA407414491PRKCGc.469C>A (p.Arg157Ser)
n.767C>A
n.771C>A
c.85C>A (p.Arg29Ser)
gnomAD v4
19g.53889957C>GCA407414492PRKCGc.469C>G (p.Arg157Gly)
n.767C>G
n.771C>G
c.85C>G (p.Arg29Gly)
gnomAD v4
19g.53889957C>TCA407414493PRKCGc.469C>T (p.Arg157Cys)
n.767C>T
n.771C>T
c.85C>T (p.Arg29Cys)
gnomAD v4
19g.53889958G>ACA407414494PRKCGc.470G>A (p.Arg157His)
n.768G>A
n.772G>A
c.86G>A (p.Arg29His)
dbSNP gnomAD v2 gnomAD v4
19g.53889958G>CCA407414495PRKCGc.470G>C (p.Arg157Pro)
n.768G>C
n.772G>C
c.86G>C (p.Arg29Pro)
19g.53889958G=CA2342579405PRKCGc.470G= (p.Arg157=)
n.768G=
n.772G=
c.86G= (p.Arg29=)
19g.53889958G>TCA407414496PRKCGc.470G>T (p.Arg157Leu)
n.768G>T
n.772G>T
c.86G>T (p.Arg29Leu)
gnomAD v4
19g.53889959C>ACA508788222PRKCGc.471C>A (p.Arg157=)
n.769C>A
n.773C>A
c.87C>A (p.Arg29=)
19g.53889959C>GCA508788225PRKCGc.471C>G (p.Arg157=)
n.769C>G
n.773C>G
c.87C>G (p.Arg29=)
19g.53889959C>TCA508788227PRKCGc.471C>T (p.Arg157=)
n.769C>T
n.773C>T
c.87C>T (p.Arg29=)
19g.53889960C>ACA407414499PRKCGc.472C>A (p.Arg158Ser)
n.770C>A
n.774C>A
c.88C>A (p.Arg30Ser)
19g.53889960C>GCA407414498PRKCGc.472C>G (p.Arg158Gly)
n.770C>G
n.774C>G
c.88C>G (p.Arg30Gly)
19g.53889960C>TCA407414497PRKCGc.472C>T (p.Arg158Cys)
n.770C>T
n.774C>T
c.88C>T (p.Arg30Cys)
gnomAD v4 COSMIC COSMIC
19g.53889961G>ACA407414500PRKCGc.473G>A (p.Arg158His)
n.771G>A
n.775G>A
c.89G>A (p.Arg30His)
gnomAD v4
19g.53889961G>CCA407414501PRKCGc.473G>C (p.Arg158Pro)
n.771G>C
n.775G>C
c.89G>C (p.Arg30Pro)
19g.53889961G>TCA407414502PRKCGc.473G>T (p.Arg158Leu)
n.771G>T
n.775G>T
c.89G>T (p.Arg30Leu)
gnomAD v4
19g.53889962C>ACA508788249PRKCGc.474C>A (p.Arg158=)
n.772C>A
n.776C>A
c.90C>A (p.Arg30=)
gnomAD v4
19g.53889962C>GCA508788250PRKCGc.474C>G (p.Arg158=)
n.772C>G
n.776C>G
c.90C>G (p.Arg30=)
19g.53889962C>TCA508788251PRKCGc.474C>T (p.Arg158=)
n.772C>T
n.776C>T
c.90C>T (p.Arg30=)
gnomAD v4
19g.53889963G>ACA407414503PRKCGc.475G>A (p.Gly159Arg)
n.773G>A
n.777G>A
c.91G>A (p.Gly31Arg)
ClinVar dbSNP gnomAD v4
19g.53889963G>CCA407414504PRKCGc.475G>C (p.Gly159Arg)
n.773G>C
n.777G>C
c.91G>C (p.Gly31Arg)
ClinVar
19g.53889963G=CA2342579406PRKCGc.475G= (p.Gly159=)
n.773G=
n.777G=
c.91G= (p.Gly31=)
19g.53889963G>TCA310082655PRKCGc.475G>T (p.Gly159Trp)
n.773G>T
n.777G>T
c.91G>T (p.Gly31Trp)
dbSNP gnomAD v4
19g.53889964G>ACA407414505PRKCGc.476G>A (p.Gly159Glu)
n.774G>A
n.778G>A
c.92G>A (p.Gly31Glu)
ClinVar dbSNP gnomAD v4
19g.53889964G>CCA407414506PRKCGc.476G>C (p.Gly159Ala)
n.774G>C
n.778G>C
c.92G>C (p.Gly31Ala)
19g.53889964G=CA2342579407PRKCGc.476G= (p.Gly159=)
n.774G=
n.778G=
c.92G= (p.Gly31=)
19g.53889964G>TCA407414507PRKCGc.476G>T (p.Gly159Val)
n.774G>T
n.778G>T
c.92G>T (p.Gly31Val)
19g.53889965G>ACA508788266PRKCGc.477G>A (p.Gly159=)
n.775G>A
n.779G>A
c.93G>A (p.Gly31=)
dbSNP gnomAD v4
19g.53889965G>CCA508788268PRKCGc.477G>C (p.Gly159=)
n.775G>C
n.779G>C
c.93G>C (p.Gly31=)
dbSNP gnomAD v3 gnomAD v4
19g.53889965G=CA2342579408PRKCGc.477G= (p.Gly159=)
n.775G=
n.779G=
c.93G= (p.Gly31=)
19g.53889965G>TCA508788271PRKCGc.477G>T (p.Gly159=)
n.775G>T
n.779G>T
c.93G>T (p.Gly31=)
19g.53889966C>ACA407414508PRKCGc.478C>A (p.Arg160Ser)
n.776C>A
n.780C>A
c.94C>A (p.Arg32Ser)
gnomAD v4
19g.53889966C>GCA407414509PRKCGc.478C>G (p.Arg160Gly)
n.776C>G
n.780C>G
c.94C>G (p.Arg32Gly)
19g.53889966C>TCA407414510PRKCGc.478C>T (p.Arg160Cys)
n.776C>T
n.780C>T
c.94C>T (p.Arg32Cys)
gnomAD v4
19g.53889967G>ACA407414511PRKCGc.479G>A (p.Arg160His)
n.777G>A
n.781G>A
c.95G>A (p.Arg32His)
gnomAD v4
19g.53889967G>CCA407414513PRKCGc.479G>C (p.Arg160Pro)
n.777G>C
n.781G>C
c.95G>C (p.Arg32Pro)
dbSNP
19g.53889967G=CA2342579409PRKCGc.479G= (p.Arg160=)
n.777G=
n.781G=
c.95G= (p.Arg32=)
19g.53889967G>TCA407414512PRKCGc.479G>T (p.Arg160Leu)
n.777G>T
n.781G>T
c.95G>T (p.Arg32Leu)
ClinVar dbSNP gnomAD v4
19g.53889968C>ACA508788287PRKCGc.480C>A (p.Arg160=)
n.778C>A
n.782C>A
c.96C>A (p.Arg32=)
dbSNP gnomAD v3 gnomAD v4
19g.53889968C=CA2342579410PRKCGc.480C= (p.Arg160=)
n.778C=
n.782C=
c.96C= (p.Arg32=)
19g.53889968C>GCA508788289PRKCGc.480C>G (p.Arg160=)
n.778C>G
n.782C>G
c.96C>G (p.Arg32=)
dbSNP gnomAD v2 gnomAD v4
19g.53889968C>TCA9640298PRKCGc.480C>T (p.Arg160=)
n.778C>T
n.782C>T
c.96C>T (p.Arg32=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.53889969C>ACA407414515PRKCGc.481C>A (p.Leu161Met)
n.779C>A
n.783C>A
c.97C>A (p.Leu33Met)
gnomAD v4
19g.53889969C>GCA407414514PRKCGc.481C>G (p.Leu161Val)
n.779C>G
n.783C>G
c.97C>G (p.Leu33Val)
gnomAD v4
19g.53889969C>TCA508788302PRKCGc.481C>T (p.Leu161=)
n.779C>T
n.783C>T
c.97C>T (p.Leu33=)
gnomAD v4
19g.53889970T>ACA407414516PRKCGc.482T>A (p.Leu161Gln)
n.780T>A
n.784T>A
c.98T>A (p.Leu33Gln)
19g.53889970T>CCA407414517PRKCGc.482T>C (p.Leu161Pro)
n.780T>C
n.784T>C
c.98T>C (p.Leu33Pro)
gnomAD v4
19g.53889970T>GCA407414518PRKCGc.482T>G (p.Leu161Arg)
n.780T>G
n.784T>G
c.98T>G (p.Leu33Arg)
gnomAD v4
19g.53889971G>ACA508788324PRKCGc.483G>A (p.Leu161=)
n.781G>A
n.785G>A
c.99G>A (p.Leu33=)
gnomAD v4
19g.53889971G>CCA508788320PRKCGc.483G>C (p.Leu161=)
n.781G>C
n.785G>C
c.99G>C (p.Leu33=)
19g.53889971G>TCA508788317PRKCGc.483G>T (p.Leu161=)
n.781G>T
n.785G>T
c.99G>T (p.Leu33=)
19g.53889972C>ACA407414519PRKCGc.484C>A (p.Gln162Lys)
n.782C>A
n.786C>A
c.100C>A (p.Gln34Lys)
gnomAD v4
19g.53889972C>GCA407414520PRKCGc.484C>G (p.Gln162Glu)
n.782C>G
n.786C>G
c.100C>G (p.Gln34Glu)
19g.53889972C>TCA407414521PRKCGc.484C>T (p.Gln162Ter)
n.782C>T
n.786C>T
c.100C>T (p.Gln34Ter)
gnomAD v4
19g.53889973A>CCA407414522PRKCGc.485A>C (p.Gln162Pro)
n.783A>C
n.787A>C
c.101A>C (p.Gln34Pro)
19g.53889973A>GCA407414523PRKCGc.485A>G (p.Gln162Arg)
n.783A>G
n.787A>G
c.101A>G (p.Gln34Arg)
19g.53889973A>TCA407414524PRKCGc.485A>T (p.Gln162Leu)
n.783A>T
n.787A>T
c.101A>T (p.Gln34Leu)
19g.53889974G>ACA508788347PRKCGc.486G>A (p.Gln162=)
n.784G>A
n.788G>A
c.102G>A (p.Gln34=)
gnomAD v4
19g.53889974G>CCA407414525PRKCGc.486G>C (p.Gln162His)
n.784G>C
n.788G>C
c.102G>C (p.Gln34His)
gnomAD v4
19g.53889974G>TCA407414526PRKCGc.486G>T (p.Gln162His)
n.784G>T
n.788G>T
c.102G>T (p.Gln34His)
gnomAD v4
19g.53889975C>ACA407414528PRKCGc.487C>A (p.Leu163Met)
n.785C>A
n.789C>A
c.103C>A (p.Leu35Met)
gnomAD v4
19g.53889975C=CA2342579411PRKCGc.487C= (p.Leu163=)
n.785C=
n.789C=
c.103C= (p.Leu35=)
19g.53889975C>GCA407414527PRKCGc.487C>G (p.Leu163Val)
n.785C>G
n.789C>G
c.103C>G (p.Leu35Val)
dbSNP gnomAD v2 gnomAD v4
19g.53889975C>TCA508788359PRKCGc.487C>T (p.Leu163=)
n.785C>T
n.789C>T
c.103C>T (p.Leu35=)
gnomAD v4
19g.53889976T>ACA407414529PRKCGc.488T>A (p.Leu163Gln)
n.786T>A
n.790T>A
c.104T>A (p.Leu35Gln)
19g.53889976T>CCA407414530PRKCGc.488T>C (p.Leu163Pro)
n.786T>C
n.790T>C
c.104T>C (p.Leu35Pro)
gnomAD v4
19g.53889976T>GCA407414531PRKCGc.488T>G (p.Leu163Arg)
n.786T>G
n.790T>G
c.104T>G (p.Leu35Arg)
gnomAD v4
19g.53889977G>ACA9640299PRKCGc.489G>A (p.Leu163=)
n.787G>A
n.791G>A
c.105G>A (p.Leu35=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.53889977G>CCA508788373PRKCGc.489G>C (p.Leu163=)
n.787G>C
n.791G>C
c.105G>C (p.Leu35=)
19g.53889977G=CA2342579412PRKCGc.489G= (p.Leu163=)
n.787G=
n.791G=
c.105G= (p.Leu35=)
19g.53889977G>TCA508788374PRKCGc.489G>T (p.Leu163=)
n.787G>T
n.791G>T
c.105G>T (p.Leu35=)
gnomAD v4
19g.53889978G>ACA407414532PRKCGc.490G>A (p.Glu164Lys)
n.788G>A
n.792G>A
c.106G>A
c.106G>A (p.Glu36Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.53889978G>CCA407414533PRKCGc.490G>C (p.Glu164Gln)
n.788G>C
n.792G>C
c.106G>C
c.106G>C (p.Glu36Gln)
gnomAD v4
19g.53889978G=CA2342579413PRKCGc.490G= (p.Glu164=)
n.788G=
n.792G=
c.106G=
c.106G= (p.Glu36=)
19g.53889978G>TCA407414534PRKCGc.490G>T (p.Glu164Ter)
n.788G>T
n.792G>T
c.106G>T
c.106G>T (p.Glu36Ter)
dbSNP gnomAD v2 gnomAD v4
19g.53889979A=CA2342579414PRKCGc.491A= (p.Glu164=)
n.789A=
n.793A=
c.107A=
c.107A= (p.Glu36=)
19g.53889979A>CCA407414535PRKCGc.491A>C (p.Glu164Ala)
n.789A>C
n.793A>C
c.107A>C
c.107A>C (p.Glu36Ala)
19g.53889979A>GCA407414536PRKCGc.491A>G (p.Glu164Gly)
n.789A>G
n.793A>G
c.107A>G
c.107A>G (p.Glu36Gly)
gnomAD v4
19g.53889979A>TCA407414537PRKCGc.491A>T (p.Glu164Val)
n.789A>T
n.793A>T
c.107A>T
c.107A>T (p.Glu36Val)
dbSNP gnomAD v2 gnomAD v4
19g.53889980G>ACA508788392PRKCGc.492G>A (p.Glu164=)
n.790G>A
n.794G>A
c.108G>A (p.Glu36=)
19g.53889980G>CCA407414538PRKCGc.492G>C (p.Glu164Asp)
n.790G>C
n.794G>C
c.108G>C (p.Glu36Asp)
19g.53889980G=CA2342579415PRKCGc.492G= (p.Glu164=)
n.790G=
n.794G=
c.108G= (p.Glu36=)
19g.53889980G>TCA407414539PRKCGc.492G>T (p.Glu164Asp)
n.790G>T
n.794G>T
c.108G>T (p.Glu36Asp)
dbSNP gnomAD v2 gnomAD v4
19g.53889981A>CCA407414542PRKCGc.493A>C (p.Ile165Leu)
n.791A>C
n.795A>C
c.109A>C (p.Ile37Leu)
19g.53889981A>GCA407414541PRKCGc.493A>G (p.Ile165Val)
n.791A>G
n.795A>G
c.109A>G (p.Ile37Val)
gnomAD v4
19g.53889981A>TCA407414540PRKCGc.493A>T (p.Ile165Phe)
n.791A>T
n.795A>T
c.109A>T (p.Ile37Phe)
19g.53889982T>ACA407414543PRKCGc.494T>A (p.Ile165Asn)
n.792T>A
n.796T>A
c.110T>A (p.Ile37Asn)
gnomAD v4
19g.53889982T>CCA407414544PRKCGc.494T>C (p.Ile165Thr)
n.792T>C
n.796T>C
c.110T>C (p.Ile37Thr)
gnomAD v4
19g.53889982T>GCA310082660PRKCGc.494T>G (p.Ile165Ser)
n.792T>G
n.796T>G
c.110T>G (p.Ile37Ser)
dbSNP gnomAD v3 gnomAD v4
19g.53889982T=CA2342579416PRKCGc.494T= (p.Ile165=)
n.792T=
n.796T=
c.110T= (p.Ile37=)
19g.53889983C>ACA508788422PRKCGc.495C>A (p.Ile165=)
n.793C>A
n.797C>A
c.111C>A (p.Ile37=)
gnomAD v4
19g.53889983C=CA2342579417PRKCGc.495C= (p.Ile165=)
n.793C=
n.797C=
c.111C= (p.Ile37=)
19g.53889983C>GCA407414545PRKCGc.495C>G (p.Ile165Met)
n.793C>G
n.797C>G
c.111C>G (p.Ile37Met)
ClinVar dbSNP
19g.53889983C>TCA508788431PRKCGc.495C>T (p.Ile165=)
n.793C>T
n.797C>T
c.111C>T (p.Ile37=)
dbSNP gnomAD v2 gnomAD v4
19g.53889984C>ACA508788437PRKCGc.496C>A (p.Arg166=)
n.794C>A
n.798C>A
c.112C>A (p.Arg38=)
gnomAD v4
19g.53889984C>GCA407414546PRKCGc.496C>G (p.Arg166Gly)
n.794C>G
n.798C>G
c.112C>G (p.Arg38Gly)
19g.53889984C>TCA407414547PRKCGc.496C>T (p.Arg166Trp)
n.794C>T
n.798C>T
c.112C>T (p.Arg38Trp)
gnomAD v4
19g.53889985G>ACA407414548PRKCGc.497G>A (p.Arg166Gln)
n.795G>A
n.799G>A
c.113G>A (p.Arg38Gln)
dbSNP gnomAD v2 gnomAD v4
19g.53889985G>CCA407414549PRKCGc.497G>C (p.Arg166Pro)
n.795G>C
n.799G>C
c.113G>C (p.Arg38Pro)
gnomAD v4
19g.53889985G=CA2342579418PRKCGc.497G= (p.Arg166=)
n.795G=
n.799G=
c.113G= (p.Arg38=)
19g.53889985G>TCA310082662PRKCGc.497G>T (p.Arg166Leu)
n.795G>T
n.799G>T
c.113G>T (p.Arg38Leu)
dbSNP gnomAD v4
19g.53889986G>ACA508788447PRKCGc.498G>A (p.Arg166=)
n.796G>A
n.800G>A
c.114G>A (p.Arg38=)
dbSNP gnomAD v2 gnomAD v4
19g.53889986G>CCA508788449PRKCGc.498G>C (p.Arg166=)
n.796G>C
n.800G>C
c.114G>C (p.Arg38=)
19g.53889986G=CA2342579419PRKCGc.498G= (p.Arg166=)
n.796G=
n.800G=
c.114G= (p.Arg38=)
19g.53889986G>TCA9640300PRKCGc.498G>T (p.Arg166=)
n.796G>T
n.800G>T
c.114G>T (p.Arg38=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53889987G>ACA407414550PRKCGc.499G>A (p.Ala167Thr)
n.797G>A
n.801G>A
c.115G>A (p.Ala39Thr)
gnomAD v4
19g.53889987G>CCA407414551PRKCGc.499G>C (p.Ala167Pro)
n.797G>C
n.801G>C
c.115G>C (p.Ala39Pro)
19g.53889987G>TCA407414552PRKCGc.499G>T (p.Ala167Ser)
n.797G>T
n.801G>T
c.115G>T (p.Ala39Ser)
gnomAD v4
19g.53889988C>ACA407414554PRKCGc.500C>A (p.Ala167Asp)
n.798C>A
n.802C>A
c.116C>A (p.Ala39Asp)
dbSNP gnomAD v2 gnomAD v4
19g.53889988C=CA2342579420PRKCGc.500C= (p.Ala167=)
n.798C=
n.802C=
c.116C= (p.Ala39=)
19g.53889988C>GCA407414553PRKCGc.500C>G (p.Ala167Gly)
n.798C>G
n.802C>G
c.116C>G (p.Ala39Gly)
19g.53889988C>TCA9640301PRKCGc.500C>T (p.Ala167Val)
n.798C>T
n.802C>T
c.116C>T (p.Ala39Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched