Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.53889889G>A | CA407414341 | PRKCG | c.401G>A (p.Cys134Tyr) n.699G>A n.703G>A c.17G>A (p.Cys6Tyr) | dbSNP gnomAD v4 |
19 | g.53889889G>C | CA407414342 | PRKCG | c.401G>C (p.Cys134Ser) n.699G>C n.703G>C c.17G>C (p.Cys6Ser) | |
19 | g.53889889G>T | CA407414343 | PRKCG | c.401G>T (p.Cys134Phe) n.699G>T n.703G>T c.17G>T (p.Cys6Phe) | gnomAD v4 |
19 | g.53889889_53889890delinsGC | CA2342579372 | PRKCG | c.401_402delinsGC (p.Cys134=) n.699_700delinsGC n.703_704delinsGC c.17_18delinsGC (p.Cys6=) | |
19 | g.53889889_53889890delinsTT | CA1139666580 | PRKCG | c.401_402delinsTT (p.Cys134Phe) n.699_700delinsTT n.703_704delinsTT c.17_18delinsTT (p.Cys6Phe) | ClinVar dbSNP |
19 | g.53889890C>A | CA407414344 | PRKCG | c.402C>A (p.Cys134Ter) n.700C>A n.704C>A c.18C>A (p.Cys6Ter) | gnomAD v4 |
19 | g.53889890C= | CA2342579373 | PRKCG | c.402C= (p.Cys134=) n.700C= n.704C= c.18C= (p.Cys6=) | |
19 | g.53889890C>G | CA407414345 | PRKCG | c.402C>G (p.Cys134Trp) n.700C>G n.704C>G c.18C>G (p.Cys6Trp) | dbSNP |
19 | g.53889890C>T | CA508787620 | PRKCG | c.402C>T (p.Cys134=) n.700C>T n.704C>T c.18C>T (p.Cys6=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889891G>A | CA407414346 | PRKCG | c.403G>A (p.Glu135Lys) n.701G>A n.705G>A c.19G>A (p.Glu7Lys) | gnomAD v4 |
19 | g.53889891G>C | CA407414347 | PRKCG | c.403G>C (p.Glu135Gln) n.701G>C n.705G>C c.19G>C (p.Glu7Gln) | gnomAD v4 |
19 | g.53889891G>T | CA407414348 | PRKCG | c.403G>T (p.Glu135Ter) n.701G>T n.705G>T c.19G>T (p.Glu7Ter) | gnomAD v4 |
19 | g.53889892A>C | CA407414349 | PRKCG | c.404A>C (p.Glu135Ala) n.702A>C n.706A>C c.20A>C (p.Glu7Ala) | |
19 | g.53889892A>G | CA407414350 | PRKCG | c.404A>G (p.Glu135Gly) n.702A>G n.706A>G c.20A>G (p.Glu7Gly) | dbSNP gnomAD v4 |
19 | g.53889892A>T | CA407414351 | PRKCG | c.404A>T (p.Glu135Val) n.702A>T n.706A>T c.20A>T (p.Glu7Val) | dbSNP gnomAD v4 |
19 | g.53889893G>A | CA508787635 | PRKCG | c.405G>A (p.Glu135=) n.703G>A n.707G>A c.21G>A (p.Glu7=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889893G>C | CA407414352 | PRKCG | c.405G>C (p.Glu135Asp) n.703G>C n.707G>C c.21G>C (p.Glu7Asp) | gnomAD v4 |
19 | g.53889893G= | CA2342579374 | PRKCG | c.405G= (p.Glu135=) n.703G= n.707G= c.21G= (p.Glu7=) | |
19 | g.53889893G>T | CA407414353 | PRKCG | c.405G>T (p.Glu135Asp) n.703G>T n.707G>T c.21G>T (p.Glu7Asp) | gnomAD v4 |
19 | g.53889894A>C | CA407414356 | PRKCG | c.406A>C (p.Met136Leu) n.704A>C n.708A>C c.22A>C (p.Met8Leu) | |
19 | g.53889894A>G | CA407414354 | PRKCG | c.406A>G (p.Met136Val) n.704A>G n.708A>G c.22A>G (p.Met8Val) | dbSNP |
19 | g.53889894A>T | CA407414355 | PRKCG | c.406A>T (p.Met136Leu) n.704A>T n.708A>T c.22A>T (p.Met8Leu) | |
19 | g.53889895T>A | CA407414357 | PRKCG | c.407T>A (p.Met136Lys) n.705T>A n.709T>A c.23T>A (p.Met8Lys) | |
19 | g.53889895T>C | CA407414358 | PRKCG | c.407T>C (p.Met136Thr) n.705T>C n.709T>C c.23T>C (p.Met8Thr) | gnomAD v4 |
19 | g.53889895T>G | CA407414359 | PRKCG | c.407T>G (p.Met136Arg) n.705T>G n.709T>G c.23T>G (p.Met8Arg) | |
19 | g.53889896G>A | CA407414360 | PRKCG | c.408G>A (p.Met136Ile) n.706G>A n.710G>A c.24G>A (p.Met8Ile) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889896G>C | CA407414361 | PRKCG | c.408G>C (p.Met136Ile) n.706G>C n.710G>C c.24G>C (p.Met8Ile) | |
19 | g.53889896G= | CA2342579375 | PRKCG | c.408G= (p.Met136=) n.706G= n.710G= c.24G= (p.Met8=) | |
19 | g.53889896G>T | CA407414362 | PRKCG | c.408G>T (p.Met136Ile) n.706G>T n.710G>T c.24G>T (p.Met8Ile) | gnomAD v4 |
19 | g.53889897A= | CA2342579376 | PRKCG | c.409A= (p.Asn137=) n.707A= n.711A= c.25A= (p.Asn9=) | |
19 | g.53889897A>C | CA407414363 | PRKCG | c.409A>C (p.Asn137His) n.707A>C n.711A>C c.25A>C (p.Asn9His) | |
19 | g.53889897A>G | CA407414364 | PRKCG | c.409A>G (p.Asn137Asp) n.707A>G n.711A>G c.25A>G (p.Asn9Asp) | gnomAD v4 |
19 | g.53889897A>T | CA407414365 | PRKCG | c.409A>T (p.Asn137Tyr) n.707A>T n.711A>T c.25A>T (p.Asn9Tyr) | ClinVar dbSNP |
19 | g.53889898A>C | CA407414366 | PRKCG | c.410A>C (p.Asn137Thr) n.708A>C n.712A>C c.26A>C (p.Asn9Thr) | |
19 | g.53889898A>G | CA407414367 | PRKCG | c.410A>G (p.Asn137Ser) n.708A>G n.712A>G c.26A>G (p.Asn9Ser) | gnomAD v4 |
19 | g.53889898A>T | CA407414368 | PRKCG | c.410A>T (p.Asn137Ile) n.708A>T n.712A>T c.26A>T (p.Asn9Ile) | |
19 | g.53889899C>A | CA407414369 | PRKCG | c.411C>A (p.Asn137Lys) n.709C>A n.713C>A c.27C>A (p.Asn9Lys) | gnomAD v4 |
19 | g.53889899C>G | CA407414370 | PRKCG | c.411C>G (p.Asn137Lys) n.709C>G n.713C>G c.27C>G (p.Asn9Lys) | |
19 | g.53889899C>T | CA508787705 | PRKCG | c.411C>T (p.Asn137=) n.709C>T n.713C>T c.27C>T (p.Asn9=) | gnomAD v4 |
19 | g.53889900G>A | CA407414371 | PRKCG | c.412G>A (p.Val138Met) n.710G>A n.714G>A c.28G>A (p.Val10Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889900G>C | CA407414372 | PRKCG | c.412G>C (p.Val138Leu) n.710G>C n.714G>C c.28G>C (p.Val10Leu) | |
19 | g.53889900G= | CA2342579377 | PRKCG | c.412G= (p.Val138=) n.710G= n.714G= c.28G= (p.Val10=) | |
19 | g.53889900G>T | CA407414373 | PRKCG | c.412G>T (p.Val138Leu) n.710G>T n.714G>T c.28G>T (p.Val10Leu) | gnomAD v4 |
19 | g.53889901T>A | CA344640 | PRKCG | c.413T>A (p.Val138Glu) n.711T>A n.715T>A c.29T>A (p.Val10Glu) | ClinVar dbSNP |
19 | g.53889901T>C | CA9640291 | PRKCG | c.413T>C (p.Val138Ala) n.711T>C n.715T>C c.29T>C (p.Val10Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889901T>G | CA407414374 | PRKCG | c.413T>G (p.Val138Gly) n.711T>G n.715T>G c.29T>G (p.Val10Gly) | |
19 | g.53889901T= | CA2342579378 | PRKCG | c.413T= (p.Val138=) n.711T= n.715T= c.29T= (p.Val10=) | |
19 | g.53889902G>A | CA508787733 | PRKCG | c.414G>A (p.Val138=) n.712G>A n.716G>A c.30G>A (p.Val10=) | gnomAD v4 |
19 | g.53889902G>C | CA508787737 | PRKCG | c.414G>C (p.Val138=) n.712G>C n.716G>C c.30G>C (p.Val10=) | |
19 | g.53889902G>T | CA508787740 | PRKCG | c.414G>T (p.Val138=) n.712G>T n.716G>T c.30G>T (p.Val10=) | gnomAD v4 |
19 | g.53889903C>A | CA407414375 | PRKCG | c.415C>A (p.His139Asn) n.713C>A n.717C>A c.31C>A (p.His11Asn) | ClinVar dbSNP gnomAD v4 |
19 | g.53889903C= | CA2342579379 | PRKCG | c.415C= (p.His139=) n.713C= n.717C= c.31C= (p.His11=) | |
19 | g.53889903C>G | CA407414376 | PRKCG | c.415C>G (p.His139Asp) n.713C>G n.717C>G c.31C>G (p.His11Asp) | |
19 | g.53889903C>T | CA407414377 | PRKCG | c.415C>T (p.His139Tyr) n.713C>T n.717C>T c.31C>T (p.His11Tyr) | gnomAD v4 |
19 | g.53889904A>C | CA407414378 | PRKCG | c.416A>C (p.His139Pro) n.714A>C n.718A>C c.32A>C (p.His11Pro) | |
19 | g.53889904A>G | CA407414379 | PRKCG | c.416A>G (p.His139Arg) n.714A>G n.718A>G c.32A>G (p.His11Arg) | gnomAD v4 |
19 | g.53889904A>T | CA407414380 | PRKCG | c.416A>T (p.His139Leu) n.714A>T n.718A>T c.32A>T (p.His11Leu) | |
19 | g.53889905C>A | CA344646 | PRKCG | c.417C>A (p.His139Gln) n.715C>A n.719C>A c.33C>A (p.His11Gln) | ClinVar dbSNP gnomAD v4 |
19 | g.53889905C= | CA2342579380 | PRKCG | c.417C= (p.His139=) n.715C= n.719C= c.33C= (p.His11=) | |
19 | g.53889905C>G | CA407414381 | PRKCG | c.417C>G (p.His139Gln) n.715C>G n.719C>G c.33C>G (p.His11Gln) | |
19 | g.53889905C>T | CA508787766 | PRKCG | c.417C>T (p.His139=) n.715C>T n.719C>T c.33C>T (p.His11=) | gnomAD v4 |
19 | g.53889906C>A | CA508787772 | PRKCG | c.418C>A (p.Arg140=) n.716C>A n.720C>A c.34C>A (p.Arg12=) | gnomAD v4 |
19 | g.53889906C= | CA2342579381 | PRKCG | c.418C= (p.Arg140=) n.716C= n.720C= c.34C= (p.Arg12=) | |
19 | g.53889906C>G | CA407414382 | PRKCG | c.418C>G (p.Arg140Gly) n.716C>G n.720C>G c.34C>G (p.Arg12Gly) | |
19 | g.53889906C>T | CA407414383 | PRKCG | c.418C>T (p.Arg140Trp) n.716C>T n.720C>T c.34C>T (p.Arg12Trp) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889907G>A | CA9640292 | PRKCG | c.419G>A (p.Arg140Gln) n.717G>A n.721G>A c.35G>A (p.Arg12Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889907G>C | CA407414384 | PRKCG | c.419G>C (p.Arg140Pro) n.717G>C n.721G>C c.35G>C (p.Arg12Pro) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889907G= | CA2342579382 | PRKCG | c.419G= (p.Arg140=) n.717G= n.721G= c.35G= (p.Arg12=) | |
19 | g.53889907G>T | CA407414385 | PRKCG | c.419G>T (p.Arg140Leu) n.717G>T n.721G>T c.35G>T (p.Arg12Leu) | gnomAD v4 |
19 | g.53889908G>A | CA508787798 | PRKCG | c.420G>A (p.Arg140=) n.718G>A n.722G>A c.36G>A (p.Arg12=) | gnomAD v4 |
19 | g.53889908G>C | CA508787790 | PRKCG | c.420G>C (p.Arg140=) n.718G>C n.722G>C c.36G>C (p.Arg12=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889908G= | CA2342579383 | PRKCG | c.420G= (p.Arg140=) n.718G= n.722G= c.36G= (p.Arg12=) | |
19 | g.53889908G>T | CA508787794 | PRKCG | c.420G>T (p.Arg140=) n.718G>T n.722G>T c.36G>T (p.Arg12=) | gnomAD v4 |
19 | g.53889909C>A | CA407414386 | PRKCG | c.421C>A (p.Arg141Ser) n.719C>A n.723C>A c.37C>A (p.Arg13Ser) | gnomAD v4 |
19 | g.53889909C>G | CA407414387 | PRKCG | c.421C>G (p.Arg141Gly) n.719C>G n.723C>G c.37C>G (p.Arg13Gly) | |
19 | g.53889909C>T | CA407414388 | PRKCG | c.421C>T (p.Arg141Cys) n.719C>T n.723C>T c.37C>T (p.Arg13Cys) | gnomAD v4 |
19 | g.53889910G>A | CA407414389 | PRKCG | c.422G>A (p.Arg141His) n.720G>A n.724G>A c.38G>A (p.Arg13His) | gnomAD v4 |
19 | g.53889910G>C | CA407414390 | PRKCG | c.422G>C (p.Arg141Pro) n.720G>C n.724G>C c.38G>C (p.Arg13Pro) | |
19 | g.53889910G>T | CA407414391 | PRKCG | c.422G>T (p.Arg141Leu) n.720G>T n.724G>T c.38G>T (p.Arg13Leu) | gnomAD v4 |
19 | g.53889911C>A | CA508787821 | PRKCG | c.423C>A (p.Arg141=) n.721C>A n.725C>A c.39C>A (p.Arg13=) | gnomAD v4 COSMIC COSMIC |
19 | g.53889911C>G | CA508787823 | PRKCG | c.423C>G (p.Arg141=) n.721C>G n.725C>G c.39C>G (p.Arg13=) | |
19 | g.53889911C>T | CA508787827 | PRKCG | c.423C>T (p.Arg141=) n.721C>T n.725C>T c.39C>T (p.Arg13=) | gnomAD v4 |
19 | g.53889912T>A | CA407414392 | PRKCG | c.424T>A (p.Cys142Ser) n.722T>A n.726T>A c.40T>A (p.Cys14Ser) | gnomAD v4 |
19 | g.53889912T>C | CA407414393 | PRKCG | c.424T>C (p.Cys142Arg) n.722T>C n.726T>C c.40T>C (p.Cys14Arg) | gnomAD v4 |
19 | g.53889912T>G | CA407414394 | PRKCG | c.424T>G (p.Cys142Gly) n.722T>G n.726T>G c.40T>G (p.Cys14Gly) | |
19 | g.53889913G>A | CA407414395 | PRKCG | c.425G>A (p.Cys142Tyr) n.723G>A n.727G>A c.41G>A (p.Cys14Tyr) | ClinVar gnomAD v4 |
19 | g.53889913G>C | CA407414397 | PRKCG | c.425G>C (p.Cys142Ser) n.723G>C n.727G>C c.41G>C (p.Cys14Ser) | |
19 | g.53889913G>T | CA407414396 | PRKCG | c.425G>T (p.Cys142Phe) n.723G>T n.727G>T c.41G>T (p.Cys14Phe) | gnomAD v4 |
19 | g.53889914T>A | CA407414398 | PRKCG | c.426T>A (p.Cys142Ter) n.724T>A n.728T>A c.42T>A (p.Cys14Ter) | |
19 | g.53889914T>C | CA508787853 | PRKCG | c.426T>C (p.Cys142=) n.724T>C n.728T>C c.42T>C (p.Cys14=) | COSMIC COSMIC |
19 | g.53889914T>G | CA407414399 | PRKCG | c.426T>G (p.Cys142Trp) n.724T>G n.728T>G c.42T>G (p.Cys14Trp) | gnomAD v4 |
19 | g.53889915G>A | CA407414400 | PRKCG | c.427G>A (p.Val143Met) n.725G>A n.729G>A c.43G>A (p.Val15Met) | dbSNP gnomAD v4 |
19 | g.53889915G>C | CA407414401 | PRKCG | c.427G>C (p.Val143Leu) n.725G>C n.729G>C c.43G>C (p.Val15Leu) | |
19 | g.53889915G= | CA2342579384 | PRKCG | c.427G= (p.Val143=) n.725G= n.729G= c.43G= (p.Val15=) | |
19 | g.53889915G>T | CA407414402 | PRKCG | c.427G>T (p.Val143Leu) n.725G>T n.729G>T c.43G>T (p.Val15Leu) | gnomAD v4 |
19 | g.53889916T>A | CA407414403 | PRKCG | c.428T>A (p.Val143Glu) n.726T>A n.730T>A c.44T>A (p.Val15Glu) | |
19 | g.53889916T>C | CA407414404 | PRKCG | c.428T>C (p.Val143Ala) n.726T>C n.730T>C c.44T>C (p.Val15Ala) | gnomAD v4 |
19 | g.53889916T>G | CA407414405 | PRKCG | c.428T>G (p.Val143Gly) n.726T>G n.730T>G c.44T>G (p.Val15Gly) | |
19 | g.53889917G>A | CA508787885 | PRKCG | c.429G>A (p.Val143=) n.727G>A n.731G>A c.45G>A (p.Val15=) | gnomAD v4 |
19 | g.53889917G>C | CA9640293 | PRKCG | c.429G>C (p.Val143=) n.727G>C n.731G>C c.45G>C (p.Val15=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.53889917G= | CA2342579385 | PRKCG | c.429G= (p.Val143=) n.727G= n.731G= c.45G= (p.Val15=) | |
19 | g.53889917G>T | CA508787890 | PRKCG | c.429G>T (p.Val143=) n.727G>T n.731G>T c.45G>T (p.Val15=) | gnomAD v4 |
19 | g.53889918C>A | CA407414406 | PRKCG | c.430C>A (p.Arg144Ser) n.728C>A n.732C>A c.46C>A (p.Arg16Ser) | gnomAD v4 |
19 | g.53889918C>G | CA407414407 | PRKCG | c.430C>G (p.Arg144Gly) n.728C>G n.732C>G c.46C>G (p.Arg16Gly) | |
19 | g.53889918C>T | CA407414408 | PRKCG | c.430C>T (p.Arg144Cys) n.728C>T n.732C>T c.46C>T (p.Arg16Cys) | gnomAD v4 |
19 | g.53889919G>A | CA407414411 | PRKCG | c.431G>A (p.Arg144His) n.729G>A n.733G>A c.47G>A (p.Arg16His) | gnomAD v4 |
19 | g.53889919G>C | CA407414410 | PRKCG | c.431G>C (p.Arg144Pro) n.729G>C n.733G>C c.47G>C (p.Arg16Pro) | |
19 | g.53889919G>T | CA407414409 | PRKCG | c.431G>T (p.Arg144Leu) n.729G>T n.733G>T c.47G>T (p.Arg16Leu) | gnomAD v4 |
19 | g.53889920T>A | CA508787914 | PRKCG | c.432T>A (p.Arg144=) n.730T>A n.734T>A c.48T>A (p.Arg16=) | |
19 | g.53889920T>C | CA9640294 | PRKCG | c.432T>C (p.Arg144=) n.730T>C n.734T>C c.48T>C (p.Arg16=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.53889920T>G | CA508787920 | PRKCG | c.432T>G (p.Arg144=) n.730T>G n.734T>G c.48T>G (p.Arg16=) | |
19 | g.53889920T= | CA2342579386 | PRKCG | c.432T= (p.Arg144=) n.730T= n.734T= c.48T= (p.Arg16=) | |
19 | g.53889921A>C | CA407414412 | PRKCG | c.433A>C (p.Ser145Arg) n.731A>C n.735A>C c.49A>C (p.Ser17Arg) | |
19 | g.53889921A>G | CA407414413 | PRKCG | c.433A>G (p.Ser145Gly) n.731A>G n.735A>G c.49A>G (p.Ser17Gly) | gnomAD v4 |
19 | g.53889921A>T | CA407414414 | PRKCG | c.433A>T (p.Ser145Cys) n.731A>T n.735A>T c.49A>T (p.Ser17Cys) | |
19 | g.53889922G>A | CA407414415 | PRKCG | c.434G>A (p.Ser145Asn) n.732G>A n.736G>A c.50G>A (p.Ser17Asn) | |
19 | g.53889922G>C | CA407414416 | PRKCG | c.434G>C (p.Ser145Thr) n.732G>C n.736G>C c.50G>C (p.Ser17Thr) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889922G= | CA2342579387 | PRKCG | c.434G= (p.Ser145=) n.732G= n.736G= c.50G= (p.Ser17=) | |
19 | g.53889922G>T | CA407414417 | PRKCG | c.434G>T (p.Ser145Ile) n.732G>T n.736G>T c.50G>T (p.Ser17Ile) | gnomAD v4 |
19 | g.53889923C>A | CA407414418 | PRKCG | c.435C>A (p.Ser145Arg) n.733C>A n.737C>A c.51C>A (p.Ser17Arg) | gnomAD v4 |
19 | g.53889923C= | CA2342579388 | PRKCG | c.435C= (p.Ser145=) n.733C= n.737C= c.51C= (p.Ser17=) | |
19 | g.53889923C>G | CA407414419 | PRKCG | c.435C>G (p.Ser145Arg) n.733C>G n.737C>G c.51C>G (p.Ser17Arg) | |
19 | g.53889923C>T | CA310082642 | PRKCG | c.435C>T (p.Ser145=) n.733C>T n.737C>T c.51C>T (p.Ser17=) | dbSNP gnomAD v4 |
19 | g.53889924G>A | CA407414420 | PRKCG | c.436G>A (p.Val146Met) n.734G>A n.738G>A c.52G>A (p.Val18Met) | dbSNP gnomAD v4 |
19 | g.53889924G>C | CA407414421 | PRKCG | c.436G>C (p.Val146Leu) n.734G>C n.738G>C c.52G>C (p.Val18Leu) | |
19 | g.53889924G= | CA2342579389 | PRKCG | c.436G= (p.Val146=) n.734G= n.738G= c.52G= (p.Val18=) | |
19 | g.53889924G>T | CA407414422 | PRKCG | c.436G>T (p.Val146Leu) n.734G>T n.738G>T c.52G>T (p.Val18Leu) | |
19 | g.53889925T>A | CA407414424 | PRKCG | c.437T>A (p.Val146Glu) n.735T>A n.739T>A c.53T>A (p.Val18Glu) | |
19 | g.53889925T>C | CA407414425 | PRKCG | c.437T>C (p.Val146Ala) n.735T>C n.739T>C c.53T>C (p.Val18Ala) | |
19 | g.53889925T>G | CA407414423 | PRKCG | c.437T>G (p.Val146Gly) n.735T>G n.739T>G c.53T>G (p.Val18Gly) | |
19 | g.53889926G>A | CA508787978 | PRKCG | c.438G>A (p.Val146=) n.736G>A n.740G>A c.54G>A (p.Val18=) | gnomAD v4 |
19 | g.53889926G>C | CA508787984 | PRKCG | c.438G>C (p.Val146=) n.736G>C n.740G>C c.54G>C (p.Val18=) | gnomAD v4 |
19 | g.53889926G>T | CA508787988 | PRKCG | c.438G>T (p.Val146=) n.736G>T n.740G>T c.54G>T (p.Val18=) | gnomAD v4 |
19 | g.53889927C>A | CA407414426 | PRKCG | c.439C>A (p.Pro147Thr) n.737C>A n.741C>A c.55C>A (p.Pro19Thr) | |
19 | g.53889927C= | CA2342579390 | PRKCG | c.439C= (p.Pro147=) n.737C= n.741C= c.55C= (p.Pro19=) | |
19 | g.53889927C>G | CA407414427 | PRKCG | c.439C>G (p.Pro147Ala) n.737C>G n.741C>G c.55C>G (p.Pro19Ala) | |
19 | g.53889927C>T | CA310082644 | PRKCG | c.439C>T (p.Pro147Ser) n.737C>T n.741C>T c.55C>T (p.Pro19Ser) | dbSNP gnomAD v4 |
19 | g.53889928C>A | CA407414428 | PRKCG | c.440C>A (p.Pro147His) n.738C>A n.742C>A c.56C>A (p.Pro19His) | gnomAD v4 |
19 | g.53889928C>G | CA407414429 | PRKCG | c.440C>G (p.Pro147Arg) n.738C>G n.742C>G c.56C>G (p.Pro19Arg) | |
19 | g.53889928C>T | CA407414430 | PRKCG | c.440C>T (p.Pro147Leu) n.738C>T n.742C>T c.56C>T (p.Pro19Leu) | |
19 | g.53889929C>A | CA508788018 | PRKCG | c.441C>A (p.Pro147=) n.739C>A n.743C>A c.57C>A (p.Pro19=) | gnomAD v4 |
19 | g.53889929C= | CA2342579391 | PRKCG | c.441C= (p.Pro147=) n.739C= n.743C= c.57C= (p.Pro19=) | |
19 | g.53889929C>G | CA508788011 | PRKCG | c.441C>G (p.Pro147=) n.739C>G n.743C>G c.57C>G (p.Pro19=) | |
19 | g.53889929C>T | CA9640295 | PRKCG | c.441C>T (p.Pro147=) n.739C>T n.743C>T c.57C>T (p.Pro19=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889930T>A | CA407414431 | PRKCG | c.442T>A (p.Ser148Thr) n.740T>A n.744T>A c.58T>A (p.Ser20Thr) c.58T>A | |
19 | g.53889930T>C | CA407414432 | PRKCG | c.442T>C (p.Ser148Pro) n.740T>C n.744T>C c.58T>C (p.Ser20Pro) c.58T>C | gnomAD v4 |
19 | g.53889930T>G | CA407414433 | PRKCG | c.442T>G (p.Ser148Ala) n.740T>G n.744T>G c.58T>G (p.Ser20Ala) c.58T>G | |
19 | g.53889931C>A | CA407414434 | PRKCG | c.443C>A (p.Ser148Tyr) n.741C>A n.745C>A c.59C>A (p.Ser20Tyr) | gnomAD v4 |
19 | g.53889931C>G | CA407414435 | PRKCG | c.443C>G (p.Ser148Cys) n.741C>G n.745C>G c.59C>G (p.Ser20Cys) | dbSNP |
19 | g.53889931C>T | CA407414436 | PRKCG | c.443C>T (p.Ser148Phe) n.741C>T n.745C>T c.59C>T (p.Ser20Phe) | gnomAD v4 |
19 | g.53889933del | CA2586963390 | PRKCG | c.445del (p.Leu149CysfsTer27) n.743del n.747del c.61del (p.Leu21CysfsTer?) c.61del (p.Leu21CysfsTer27) | gnomAD v4 |
19 | g.53889932C>A | CA508788034 | PRKCG | c.444C>A (p.Ser148=) n.742C>A n.746C>A c.60C>A (p.Ser20=) | gnomAD v4 |
19 | g.53889932C= | CA2342579392 | PRKCG | c.444C= (p.Ser148=) n.742C= n.746C= c.60C= (p.Ser20=) | |
19 | g.53889932C>G | CA508788036 | PRKCG | c.444C>G (p.Ser148=) n.742C>G n.746C>G c.60C>G (p.Ser20=) | |
19 | g.53889932C>T | CA508788038 | PRKCG | c.444C>T (p.Ser148=) n.742C>T n.746C>T c.60C>T (p.Ser20=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889933C>A | CA407414437 | PRKCG | c.445C>A (p.Leu149Met) n.743C>A n.747C>A c.61C>A (p.Leu21Met) | gnomAD v4 |
19 | g.53889933C>G | CA407414438 | PRKCG | c.445C>G (p.Leu149Val) n.743C>G n.747C>G c.61C>G (p.Leu21Val) | gnomAD v4 |
19 | g.53889933C>T | CA508788045 | PRKCG | c.445C>T (p.Leu149=) n.743C>T n.747C>T c.61C>T (p.Leu21=) | gnomAD v4 |
19 | g.53889934T>A | CA407414439 | PRKCG | c.446T>A (p.Leu149Gln) n.744T>A n.748T>A c.62T>A (p.Leu21Gln) | |
19 | g.53889934T>C | CA407414440 | PRKCG | c.446T>C (p.Leu149Pro) n.744T>C n.748T>C c.62T>C (p.Leu21Pro) | gnomAD v4 |
19 | g.53889934T>G | CA407414441 | PRKCG | c.446T>G (p.Leu149Arg) n.744T>G n.748T>G c.62T>G (p.Leu21Arg) | |
19 | g.53889935G>A | CA508788054 | PRKCG | c.447G>A (p.Leu149=) n.745G>A n.749G>A c.63G>A (p.Leu21=) | gnomAD v4 |
19 | g.53889935G>C | CA508788056 | PRKCG | c.447G>C (p.Leu149=) n.745G>C n.749G>C c.63G>C (p.Leu21=) | gnomAD v4 |
19 | g.53889935G>T | CA508788058 | PRKCG | c.447G>T (p.Leu149=) n.745G>T n.749G>T c.63G>T (p.Leu21=) | gnomAD v4 |
19 | g.53889936T>A | CA407414442 | PRKCG | c.448T>A (p.Cys150Ser) n.746T>A n.750T>A c.64T>A (p.Cys22Ser) | |
19 | g.53889936T>C | CA407414443 | PRKCG | c.448T>C (p.Cys150Arg) n.746T>C n.750T>C c.64T>C (p.Cys22Arg) | ClinVar dbSNP |
19 | g.53889936T>G | CA407414444 | PRKCG | c.448T>G (p.Cys150Gly) n.746T>G n.750T>G c.64T>G (p.Cys22Gly) | |
19 | g.53889936T= | CA2342579393 | PRKCG | c.448T= (p.Cys150=) n.746T= n.750T= c.64T= (p.Cys22=) | |
19 | g.53889936_53889948del | CA2586963391 | PRKCG | c.448_460del (p.Cys150ThrfsTer22) n.746_758del n.750_762del c.64_76del (p.Cys22ThrfsTer?) c.64_76del (p.Cys22ThrfsTer22) | gnomAD v4 |
19 | g.53889937G>A | CA407414445 | PRKCG | c.449G>A (p.Cys150Tyr) n.747G>A n.751G>A c.65G>A (p.Cys22Tyr) | |
19 | g.53889937G>C | CA407414446 | PRKCG | c.449G>C (p.Cys150Ser) n.747G>C n.751G>C c.65G>C (p.Cys22Ser) | |
19 | g.53889937G>T | CA407414447 | PRKCG | c.449G>T (p.Cys150Phe) n.747G>T n.751G>T c.65G>T (p.Cys22Phe) | gnomAD v4 |
19 | g.53889937_53889938delinsGC | CA2342579394 | PRKCG | c.449_450delinsGC (p.Cys150=) n.747_748delinsGC n.751_752delinsGC c.65_66delinsGC (p.Cys22=) | |
19 | g.53889937_53889938delinsTT | CA344643 | PRKCG | c.449_450delinsTT (p.Cys150Phe) n.747_748delinsTT n.751_752delinsTT c.65_66delinsTT (p.Cys22Phe) | ClinVar dbSNP |
19 | g.53889938C>A | CA407414448 | PRKCG | c.450C>A (p.Cys150Ter) n.748C>A n.752C>A c.66C>A (p.Cys22Ter) | gnomAD v4 |
19 | g.53889938C= | CA2342579395 | PRKCG | c.450C= (p.Cys150=) n.748C= n.752C= c.66C= (p.Cys22=) | |
19 | g.53889938C>G | CA407414449 | PRKCG | c.450C>G (p.Cys150Trp) n.748C>G n.752C>G c.66C>G (p.Cys22Trp) | ClinVar dbSNP |
19 | g.53889938C>T | CA508788079 | PRKCG | c.450C>T (p.Cys150=) n.748C>T n.752C>T c.66C>T (p.Cys22=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889939G>A | CA407414452 | PRKCG | c.451G>A (p.Gly151Ser) n.749G>A n.753G>A c.67G>A (p.Gly23Ser) | dbSNP gnomAD v2 |
19 | g.53889939G>C | CA407414451 | PRKCG | c.451G>C (p.Gly151Arg) n.749G>C n.753G>C c.67G>C (p.Gly23Arg) | gnomAD v4 |
19 | g.53889939G= | CA2342579396 | PRKCG | c.451G= (p.Gly151=) n.749G= n.753G= c.67G= (p.Gly23=) | |
19 | g.53889939G>T | CA407414450 | PRKCG | c.451G>T (p.Gly151Cys) n.749G>T n.753G>T c.67G>T (p.Gly23Cys) | gnomAD v4 |
19 | g.53889940G>A | CA9640296 | PRKCG | c.452G>A (p.Gly151Asp) n.750G>A n.754G>A c.68G>A (p.Gly23Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889940G>C | CA407414454 | PRKCG | c.452G>C (p.Gly151Ala) n.750G>C n.754G>C c.68G>C (p.Gly23Ala) | |
19 | g.53889940G= | CA2342579397 | PRKCG | c.452G= (p.Gly151=) n.750G= n.754G= c.68G= (p.Gly23=) | |
19 | g.53889940G>T | CA407414453 | PRKCG | c.452G>T (p.Gly151Val) n.750G>T n.754G>T c.68G>T (p.Gly23Val) | gnomAD v4 |
19 | g.53889943_53889944dup | CA2736007018 | PRKCG | c.455_456dup (p.Asp153TrpfsTer24) n.753_754dup n.757_758dup c.71_72dup (p.Asp25TrpfsTer?) c.71_72dup (p.Asp25TrpfsTer24) | dbSNP |
19 | g.53889941T>A | CA508788108 | PRKCG | c.453T>A (p.Gly151=) n.751T>A n.755T>A c.69T>A (p.Gly23=) | |
19 | g.53889941T>C | CA508788110 | PRKCG | c.453T>C (p.Gly151=) n.751T>C n.755T>C c.69T>C (p.Gly23=) | gnomAD v4 |
19 | g.53889941T>G | CA508788112 | PRKCG | c.453T>G (p.Gly151=) n.751T>G n.755T>G c.69T>G (p.Gly23=) | |
19 | g.53889942G>A | CA407414455 | PRKCG | c.454G>A (p.Val152Met) n.752G>A n.756G>A c.70G>A (p.Val24Met) | dbSNP gnomAD v4 |
19 | g.53889942G>C | CA407414456 | PRKCG | c.454G>C (p.Val152Leu) n.752G>C n.756G>C c.70G>C (p.Val24Leu) | |
19 | g.53889942G= | CA2342579398 | PRKCG | c.454G= (p.Val152=) n.752G= n.756G= c.70G= (p.Val24=) | |
19 | g.53889942G>T | CA407414457 | PRKCG | c.454G>T (p.Val152Leu) n.752G>T n.756G>T c.70G>T (p.Val24Leu) | gnomAD v4 |
19 | g.53889942_53889952del | CA2586963392 | PRKCG | c.454_464del (p.Val152ArgfsTer17) n.752_762del n.756_766del c.70_80del (p.Val24ArgfsTer?) c.70_80del (p.Val24ArgfsTer17) | gnomAD v4 |
19 | g.53889943T>A | CA407414458 | PRKCG | c.455T>A (p.Val152Glu) n.753T>A n.757T>A c.71T>A (p.Val24Glu) | gnomAD v4 |
19 | g.53889943T>C | CA407414459 | PRKCG | c.455T>C (p.Val152Ala) n.753T>C n.757T>C c.71T>C (p.Val24Ala) | gnomAD v4 |
19 | g.53889943T>G | CA407414460 | PRKCG | c.455T>G (p.Val152Gly) n.753T>G n.757T>G c.71T>G (p.Val24Gly) | |
19 | g.53889944G>A | CA508788123 | PRKCG | c.456G>A (p.Val152=) n.754G>A n.758G>A c.72G>A (p.Val24=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889944G>C | CA508788124 | PRKCG | c.456G>C (p.Val152=) n.754G>C n.758G>C c.72G>C (p.Val24=) | |
19 | g.53889944G= | CA2342579399 | PRKCG | c.456G= (p.Val152=) n.754G= n.758G= c.72G= (p.Val24=) | |
19 | g.53889944G>T | CA508788125 | PRKCG | c.456G>T (p.Val152=) n.754G>T n.758G>T c.72G>T (p.Val24=) | gnomAD v4 |
19 | g.53889946_53889964del | CA2586963393 | PRKCG | c.458_476del (p.Asp153GlyfsTer17) n.756_774del n.760_778del c.74_92del (p.Asp25GlyfsTer?) c.74_92del (p.Asp25GlyfsTer17) | gnomAD v4 |
19 | g.53889945G>A | CA407414461 | PRKCG | c.457G>A (p.Asp153Asn) n.755G>A n.759G>A c.73G>A (p.Asp25Asn) | gnomAD v4 |
19 | g.53889945G>C | CA407414462 | PRKCG | c.457G>C (p.Asp153His) n.755G>C n.759G>C c.73G>C (p.Asp25His) | gnomAD v4 |
19 | g.53889945G>T | CA407414463 | PRKCG | c.457G>T (p.Asp153Tyr) n.755G>T n.759G>T c.73G>T (p.Asp25Tyr) | gnomAD v4 |
19 | g.53889946A>C | CA407414464 | PRKCG | c.458A>C (p.Asp153Ala) n.756A>C n.760A>C c.74A>C (p.Asp25Ala) | |
19 | g.53889946A>G | CA407414465 | PRKCG | c.458A>G (p.Asp153Gly) n.756A>G n.760A>G c.74A>G (p.Asp25Gly) | |
19 | g.53889946A>T | CA407414466 | PRKCG | c.458A>T (p.Asp153Val) n.756A>T n.760A>T c.74A>T (p.Asp25Val) | |
19 | g.53889947C>A | CA407414468 | PRKCG | c.459C>A (p.Asp153Glu) n.757C>A n.761C>A c.75C>A (p.Asp25Glu) | gnomAD v4 |
19 | g.53889947C= | CA2342579400 | PRKCG | c.459C= (p.Asp153=) n.757C= n.761C= c.75C= (p.Asp25=) | |
19 | g.53889947C>G | CA407414467 | PRKCG | c.459C>G (p.Asp153Glu) n.757C>G n.761C>G c.75C>G (p.Asp25Glu) | gnomAD v4 |
19 | g.53889947C>T | CA310082651 | PRKCG | c.459C>T (p.Asp153=) n.757C>T n.761C>T c.75C>T (p.Asp25=) | dbSNP gnomAD v4 |
19 | g.53889948C>A | CA407414469 | PRKCG | c.460C>A (p.His154Asn) n.758C>A n.762C>A c.76C>A (p.His26Asn) | gnomAD v4 |
19 | g.53889948C>G | CA407414470 | PRKCG | c.460C>G (p.His154Asp) n.758C>G n.762C>G c.76C>G (p.His26Asp) | |
19 | g.53889948C>T | CA407414471 | PRKCG | c.460C>T (p.His154Tyr) n.758C>T n.762C>T c.76C>T (p.His26Tyr) | gnomAD v4 |
19 | g.53889949A>C | CA407414472 | PRKCG | c.461A>C (p.His154Pro) n.759A>C n.763A>C c.77A>C (p.His26Pro) | |
19 | g.53889949A>G | CA407414473 | PRKCG | c.461A>G (p.His154Arg) n.759A>G n.763A>G c.77A>G (p.His26Arg) | gnomAD v4 |
19 | g.53889949A>T | CA407414474 | PRKCG | c.461A>T (p.His154Leu) n.759A>T n.763A>T c.77A>T (p.His26Leu) | |
19 | g.53889950C>A | CA407414476 | PRKCG | c.462C>A (p.His154Gln) n.760C>A n.764C>A c.78C>A (p.His26Gln) | |
19 | g.53889950C>G | CA407414475 | PRKCG | c.462C>G (p.His154Gln) n.760C>G n.764C>G c.78C>G (p.His26Gln) | |
19 | g.53889950C>T | CA508788155 | PRKCG | c.462C>T (p.His154=) n.760C>T n.764C>T c.78C>T (p.His26=) | gnomAD v4 |
19 | g.53889951del | CA2586963394 | PRKCG | c.463del (p.Thr155ProfsTer21) n.761del n.765del c.79del (p.Thr27ProfsTer?) c.79del (p.Thr27ProfsTer21) | gnomAD v4 |
19 | g.53889951A>C | CA407414477 | PRKCG | c.463A>C (p.Thr155Pro) n.761A>C n.765A>C c.79A>C (p.Thr27Pro) | |
19 | g.53889951A>G | CA407414478 | PRKCG | c.463A>G (p.Thr155Ala) n.761A>G n.765A>G c.79A>G (p.Thr27Ala) | |
19 | g.53889951A>T | CA407414479 | PRKCG | c.463A>T (p.Thr155Ser) n.761A>T n.765A>T c.79A>T (p.Thr27Ser) | |
19 | g.53889952C>A | CA407414480 | PRKCG | c.464C>A (p.Thr155Asn) n.762C>A n.766C>A c.80C>A (p.Thr27Asn) | gnomAD v4 |
19 | g.53889952C>G | CA407414481 | PRKCG | c.464C>G (p.Thr155Ser) n.762C>G n.766C>G c.80C>G (p.Thr27Ser) | gnomAD v4 |
19 | g.53889952C>T | CA407414482 | PRKCG | c.464C>T (p.Thr155Ile) n.762C>T n.766C>T c.80C>T (p.Thr27Ile) | gnomAD v4 |
19 | g.53889953C>A | CA508788172 | PRKCG | c.465C>A (p.Thr155=) n.763C>A n.767C>A c.81C>A (p.Thr27=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889953C= | CA2342579401 | PRKCG | c.465C= (p.Thr155=) n.763C= n.767C= c.81C= (p.Thr27=) | |
19 | g.53889953C>G | CA508788175 | PRKCG | c.465C>G (p.Thr155=) n.763C>G n.767C>G c.81C>G (p.Thr27=) | |
19 | g.53889953C>T | CA508788177 | PRKCG | c.465C>T (p.Thr155=) n.763C>T n.767C>T c.81C>T (p.Thr27=) | gnomAD v4 |
19 | g.53889953_53889973del | CA2586963395 | PRKCG | c.465_485del (p.Glu156_Gln162del) n.763_783del n.767_787del c.81_101del (p.Glu28_Gln34del) | gnomAD v4 |
19 | g.53889954G>A | CA407414483 | PRKCG | c.466G>A (p.Glu156Lys) n.764G>A n.768G>A c.82G>A (p.Glu28Lys) | ClinVar dbSNP gnomAD v4 |
19 | g.53889954G>C | CA407414485 | PRKCG | c.466G>C (p.Glu156Gln) n.764G>C n.768G>C c.82G>C (p.Glu28Gln) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889954G= | CA2342579402 | PRKCG | c.466G= (p.Glu156=) n.764G= n.768G= c.82G= (p.Glu28=) | |
19 | g.53889954G>T | CA407414484 | PRKCG | c.466G>T (p.Glu156Ter) n.764G>T n.768G>T c.82G>T (p.Glu28Ter) | gnomAD v4 |
19 | g.53889954_53889955insCAC | CA2741640839 | PRKCG | c.466_467insCAC (p.Glu156delinsAlaGln) n.764_765insCAC n.768_769insCAC c.82_83insCAC (p.Glu28delinsAlaGln) | |
19 | g.53889955A= | CA2342579403 | PRKCG | c.467A= (p.Glu156=) n.765A= n.769A= c.83A= (p.Glu28=) | |
19 | g.53889955A>C | CA407414486 | PRKCG | c.467A>C (p.Glu156Ala) n.765A>C n.769A>C c.83A>C (p.Glu28Ala) | |
19 | g.53889955A>G | CA407414487 | PRKCG | c.467A>G (p.Glu156Gly) n.765A>G n.769A>G c.83A>G (p.Glu28Gly) | dbSNP |
19 | g.53889955A>T | CA407414488 | PRKCG | c.467A>T (p.Glu156Val) n.765A>T n.769A>T c.83A>T (p.Glu28Val) | |
19 | g.53889956G>A | CA9640297 | PRKCG | c.468G>A (p.Glu156=) n.766G>A n.770G>A c.84G>A (p.Glu28=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.53889956G>C | CA407414489 | PRKCG | c.468G>C (p.Glu156Asp) n.766G>C n.770G>C c.84G>C (p.Glu28Asp) | |
19 | g.53889956G= | CA2342579404 | PRKCG | c.468G= (p.Glu156=) n.766G= n.770G= c.84G= (p.Glu28=) | |
19 | g.53889956G>T | CA407414490 | PRKCG | c.468G>T (p.Glu156Asp) n.766G>T n.770G>T c.84G>T (p.Glu28Asp) | gnomAD v4 |
19 | g.53889957C>A | CA407414491 | PRKCG | c.469C>A (p.Arg157Ser) n.767C>A n.771C>A c.85C>A (p.Arg29Ser) | gnomAD v4 |
19 | g.53889957C>G | CA407414492 | PRKCG | c.469C>G (p.Arg157Gly) n.767C>G n.771C>G c.85C>G (p.Arg29Gly) | gnomAD v4 |
19 | g.53889957C>T | CA407414493 | PRKCG | c.469C>T (p.Arg157Cys) n.767C>T n.771C>T c.85C>T (p.Arg29Cys) | gnomAD v4 |
19 | g.53889958G>A | CA407414494 | PRKCG | c.470G>A (p.Arg157His) n.768G>A n.772G>A c.86G>A (p.Arg29His) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889958G>C | CA407414495 | PRKCG | c.470G>C (p.Arg157Pro) n.768G>C n.772G>C c.86G>C (p.Arg29Pro) | |
19 | g.53889958G= | CA2342579405 | PRKCG | c.470G= (p.Arg157=) n.768G= n.772G= c.86G= (p.Arg29=) | |
19 | g.53889958G>T | CA407414496 | PRKCG | c.470G>T (p.Arg157Leu) n.768G>T n.772G>T c.86G>T (p.Arg29Leu) | gnomAD v4 |
19 | g.53889959C>A | CA508788222 | PRKCG | c.471C>A (p.Arg157=) n.769C>A n.773C>A c.87C>A (p.Arg29=) | |
19 | g.53889959C>G | CA508788225 | PRKCG | c.471C>G (p.Arg157=) n.769C>G n.773C>G c.87C>G (p.Arg29=) | |
19 | g.53889959C>T | CA508788227 | PRKCG | c.471C>T (p.Arg157=) n.769C>T n.773C>T c.87C>T (p.Arg29=) | |
19 | g.53889960C>A | CA407414499 | PRKCG | c.472C>A (p.Arg158Ser) n.770C>A n.774C>A c.88C>A (p.Arg30Ser) | |
19 | g.53889960C>G | CA407414498 | PRKCG | c.472C>G (p.Arg158Gly) n.770C>G n.774C>G c.88C>G (p.Arg30Gly) | |
19 | g.53889960C>T | CA407414497 | PRKCG | c.472C>T (p.Arg158Cys) n.770C>T n.774C>T c.88C>T (p.Arg30Cys) | gnomAD v4 COSMIC COSMIC |
19 | g.53889961G>A | CA407414500 | PRKCG | c.473G>A (p.Arg158His) n.771G>A n.775G>A c.89G>A (p.Arg30His) | gnomAD v4 |
19 | g.53889961G>C | CA407414501 | PRKCG | c.473G>C (p.Arg158Pro) n.771G>C n.775G>C c.89G>C (p.Arg30Pro) | |
19 | g.53889961G>T | CA407414502 | PRKCG | c.473G>T (p.Arg158Leu) n.771G>T n.775G>T c.89G>T (p.Arg30Leu) | gnomAD v4 |
19 | g.53889962C>A | CA508788249 | PRKCG | c.474C>A (p.Arg158=) n.772C>A n.776C>A c.90C>A (p.Arg30=) | gnomAD v4 |
19 | g.53889962C>G | CA508788250 | PRKCG | c.474C>G (p.Arg158=) n.772C>G n.776C>G c.90C>G (p.Arg30=) | |
19 | g.53889962C>T | CA508788251 | PRKCG | c.474C>T (p.Arg158=) n.772C>T n.776C>T c.90C>T (p.Arg30=) | gnomAD v4 |
19 | g.53889963G>A | CA407414503 | PRKCG | c.475G>A (p.Gly159Arg) n.773G>A n.777G>A c.91G>A (p.Gly31Arg) | ClinVar dbSNP gnomAD v4 |
19 | g.53889963G>C | CA407414504 | PRKCG | c.475G>C (p.Gly159Arg) n.773G>C n.777G>C c.91G>C (p.Gly31Arg) | ClinVar |
19 | g.53889963G= | CA2342579406 | PRKCG | c.475G= (p.Gly159=) n.773G= n.777G= c.91G= (p.Gly31=) | |
19 | g.53889963G>T | CA310082655 | PRKCG | c.475G>T (p.Gly159Trp) n.773G>T n.777G>T c.91G>T (p.Gly31Trp) | dbSNP gnomAD v4 |
19 | g.53889964G>A | CA407414505 | PRKCG | c.476G>A (p.Gly159Glu) n.774G>A n.778G>A c.92G>A (p.Gly31Glu) | ClinVar dbSNP gnomAD v4 |
19 | g.53889964G>C | CA407414506 | PRKCG | c.476G>C (p.Gly159Ala) n.774G>C n.778G>C c.92G>C (p.Gly31Ala) | |
19 | g.53889964G= | CA2342579407 | PRKCG | c.476G= (p.Gly159=) n.774G= n.778G= c.92G= (p.Gly31=) | |
19 | g.53889964G>T | CA407414507 | PRKCG | c.476G>T (p.Gly159Val) n.774G>T n.778G>T c.92G>T (p.Gly31Val) | |
19 | g.53889965G>A | CA508788266 | PRKCG | c.477G>A (p.Gly159=) n.775G>A n.779G>A c.93G>A (p.Gly31=) | dbSNP gnomAD v4 |
19 | g.53889965G>C | CA508788268 | PRKCG | c.477G>C (p.Gly159=) n.775G>C n.779G>C c.93G>C (p.Gly31=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889965G= | CA2342579408 | PRKCG | c.477G= (p.Gly159=) n.775G= n.779G= c.93G= (p.Gly31=) | |
19 | g.53889965G>T | CA508788271 | PRKCG | c.477G>T (p.Gly159=) n.775G>T n.779G>T c.93G>T (p.Gly31=) | |
19 | g.53889966C>A | CA407414508 | PRKCG | c.478C>A (p.Arg160Ser) n.776C>A n.780C>A c.94C>A (p.Arg32Ser) | gnomAD v4 |
19 | g.53889966C>G | CA407414509 | PRKCG | c.478C>G (p.Arg160Gly) n.776C>G n.780C>G c.94C>G (p.Arg32Gly) | |
19 | g.53889966C>T | CA407414510 | PRKCG | c.478C>T (p.Arg160Cys) n.776C>T n.780C>T c.94C>T (p.Arg32Cys) | gnomAD v4 |
19 | g.53889967G>A | CA407414511 | PRKCG | c.479G>A (p.Arg160His) n.777G>A n.781G>A c.95G>A (p.Arg32His) | gnomAD v4 |
19 | g.53889967G>C | CA407414513 | PRKCG | c.479G>C (p.Arg160Pro) n.777G>C n.781G>C c.95G>C (p.Arg32Pro) | dbSNP |
19 | g.53889967G= | CA2342579409 | PRKCG | c.479G= (p.Arg160=) n.777G= n.781G= c.95G= (p.Arg32=) | |
19 | g.53889967G>T | CA407414512 | PRKCG | c.479G>T (p.Arg160Leu) n.777G>T n.781G>T c.95G>T (p.Arg32Leu) | ClinVar dbSNP gnomAD v4 |
19 | g.53889968C>A | CA508788287 | PRKCG | c.480C>A (p.Arg160=) n.778C>A n.782C>A c.96C>A (p.Arg32=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889968C= | CA2342579410 | PRKCG | c.480C= (p.Arg160=) n.778C= n.782C= c.96C= (p.Arg32=) | |
19 | g.53889968C>G | CA508788289 | PRKCG | c.480C>G (p.Arg160=) n.778C>G n.782C>G c.96C>G (p.Arg32=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889968C>T | CA9640298 | PRKCG | c.480C>T (p.Arg160=) n.778C>T n.782C>T c.96C>T (p.Arg32=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.53889969C>A | CA407414515 | PRKCG | c.481C>A (p.Leu161Met) n.779C>A n.783C>A c.97C>A (p.Leu33Met) | gnomAD v4 |
19 | g.53889969C>G | CA407414514 | PRKCG | c.481C>G (p.Leu161Val) n.779C>G n.783C>G c.97C>G (p.Leu33Val) | gnomAD v4 |
19 | g.53889969C>T | CA508788302 | PRKCG | c.481C>T (p.Leu161=) n.779C>T n.783C>T c.97C>T (p.Leu33=) | gnomAD v4 |
19 | g.53889970T>A | CA407414516 | PRKCG | c.482T>A (p.Leu161Gln) n.780T>A n.784T>A c.98T>A (p.Leu33Gln) | |
19 | g.53889970T>C | CA407414517 | PRKCG | c.482T>C (p.Leu161Pro) n.780T>C n.784T>C c.98T>C (p.Leu33Pro) | gnomAD v4 |
19 | g.53889970T>G | CA407414518 | PRKCG | c.482T>G (p.Leu161Arg) n.780T>G n.784T>G c.98T>G (p.Leu33Arg) | gnomAD v4 |
19 | g.53889971G>A | CA508788324 | PRKCG | c.483G>A (p.Leu161=) n.781G>A n.785G>A c.99G>A (p.Leu33=) | gnomAD v4 |
19 | g.53889971G>C | CA508788320 | PRKCG | c.483G>C (p.Leu161=) n.781G>C n.785G>C c.99G>C (p.Leu33=) | |
19 | g.53889971G>T | CA508788317 | PRKCG | c.483G>T (p.Leu161=) n.781G>T n.785G>T c.99G>T (p.Leu33=) | |
19 | g.53889972C>A | CA407414519 | PRKCG | c.484C>A (p.Gln162Lys) n.782C>A n.786C>A c.100C>A (p.Gln34Lys) | gnomAD v4 |
19 | g.53889972C>G | CA407414520 | PRKCG | c.484C>G (p.Gln162Glu) n.782C>G n.786C>G c.100C>G (p.Gln34Glu) | |
19 | g.53889972C>T | CA407414521 | PRKCG | c.484C>T (p.Gln162Ter) n.782C>T n.786C>T c.100C>T (p.Gln34Ter) | gnomAD v4 |
19 | g.53889973A>C | CA407414522 | PRKCG | c.485A>C (p.Gln162Pro) n.783A>C n.787A>C c.101A>C (p.Gln34Pro) | |
19 | g.53889973A>G | CA407414523 | PRKCG | c.485A>G (p.Gln162Arg) n.783A>G n.787A>G c.101A>G (p.Gln34Arg) | |
19 | g.53889973A>T | CA407414524 | PRKCG | c.485A>T (p.Gln162Leu) n.783A>T n.787A>T c.101A>T (p.Gln34Leu) | |
19 | g.53889974G>A | CA508788347 | PRKCG | c.486G>A (p.Gln162=) n.784G>A n.788G>A c.102G>A (p.Gln34=) | gnomAD v4 |
19 | g.53889974G>C | CA407414525 | PRKCG | c.486G>C (p.Gln162His) n.784G>C n.788G>C c.102G>C (p.Gln34His) | gnomAD v4 |
19 | g.53889974G>T | CA407414526 | PRKCG | c.486G>T (p.Gln162His) n.784G>T n.788G>T c.102G>T (p.Gln34His) | gnomAD v4 |
19 | g.53889975C>A | CA407414528 | PRKCG | c.487C>A (p.Leu163Met) n.785C>A n.789C>A c.103C>A (p.Leu35Met) | gnomAD v4 |
19 | g.53889975C= | CA2342579411 | PRKCG | c.487C= (p.Leu163=) n.785C= n.789C= c.103C= (p.Leu35=) | |
19 | g.53889975C>G | CA407414527 | PRKCG | c.487C>G (p.Leu163Val) n.785C>G n.789C>G c.103C>G (p.Leu35Val) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889975C>T | CA508788359 | PRKCG | c.487C>T (p.Leu163=) n.785C>T n.789C>T c.103C>T (p.Leu35=) | gnomAD v4 |
19 | g.53889976T>A | CA407414529 | PRKCG | c.488T>A (p.Leu163Gln) n.786T>A n.790T>A c.104T>A (p.Leu35Gln) | |
19 | g.53889976T>C | CA407414530 | PRKCG | c.488T>C (p.Leu163Pro) n.786T>C n.790T>C c.104T>C (p.Leu35Pro) | gnomAD v4 |
19 | g.53889976T>G | CA407414531 | PRKCG | c.488T>G (p.Leu163Arg) n.786T>G n.790T>G c.104T>G (p.Leu35Arg) | gnomAD v4 |
19 | g.53889977G>A | CA9640299 | PRKCG | c.489G>A (p.Leu163=) n.787G>A n.791G>A c.105G>A (p.Leu35=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.53889977G>C | CA508788373 | PRKCG | c.489G>C (p.Leu163=) n.787G>C n.791G>C c.105G>C (p.Leu35=) | |
19 | g.53889977G= | CA2342579412 | PRKCG | c.489G= (p.Leu163=) n.787G= n.791G= c.105G= (p.Leu35=) | |
19 | g.53889977G>T | CA508788374 | PRKCG | c.489G>T (p.Leu163=) n.787G>T n.791G>T c.105G>T (p.Leu35=) | gnomAD v4 |
19 | g.53889978G>A | CA407414532 | PRKCG | c.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 |
19 | g.53889978G>C | CA407414533 | PRKCG | c.490G>C (p.Glu164Gln) n.788G>C n.792G>C c.106G>C c.106G>C (p.Glu36Gln) | gnomAD v4 |
19 | g.53889978G= | CA2342579413 | PRKCG | c.490G= (p.Glu164=) n.788G= n.792G= c.106G= c.106G= (p.Glu36=) | |
19 | g.53889978G>T | CA407414534 | PRKCG | c.490G>T (p.Glu164Ter) n.788G>T n.792G>T c.106G>T c.106G>T (p.Glu36Ter) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889979A= | CA2342579414 | PRKCG | c.491A= (p.Glu164=) n.789A= n.793A= c.107A= c.107A= (p.Glu36=) | |
19 | g.53889979A>C | CA407414535 | PRKCG | c.491A>C (p.Glu164Ala) n.789A>C n.793A>C c.107A>C c.107A>C (p.Glu36Ala) | |
19 | g.53889979A>G | CA407414536 | PRKCG | c.491A>G (p.Glu164Gly) n.789A>G n.793A>G c.107A>G c.107A>G (p.Glu36Gly) | gnomAD v4 |
19 | g.53889979A>T | CA407414537 | PRKCG | c.491A>T (p.Glu164Val) n.789A>T n.793A>T c.107A>T c.107A>T (p.Glu36Val) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889980G>A | CA508788392 | PRKCG | c.492G>A (p.Glu164=) n.790G>A n.794G>A c.108G>A (p.Glu36=) | |
19 | g.53889980G>C | CA407414538 | PRKCG | c.492G>C (p.Glu164Asp) n.790G>C n.794G>C c.108G>C (p.Glu36Asp) | |
19 | g.53889980G= | CA2342579415 | PRKCG | c.492G= (p.Glu164=) n.790G= n.794G= c.108G= (p.Glu36=) | |
19 | g.53889980G>T | CA407414539 | PRKCG | c.492G>T (p.Glu164Asp) n.790G>T n.794G>T c.108G>T (p.Glu36Asp) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889981A>C | CA407414542 | PRKCG | c.493A>C (p.Ile165Leu) n.791A>C n.795A>C c.109A>C (p.Ile37Leu) | |
19 | g.53889981A>G | CA407414541 | PRKCG | c.493A>G (p.Ile165Val) n.791A>G n.795A>G c.109A>G (p.Ile37Val) | gnomAD v4 |
19 | g.53889981A>T | CA407414540 | PRKCG | c.493A>T (p.Ile165Phe) n.791A>T n.795A>T c.109A>T (p.Ile37Phe) | |
19 | g.53889982T>A | CA407414543 | PRKCG | c.494T>A (p.Ile165Asn) n.792T>A n.796T>A c.110T>A (p.Ile37Asn) | gnomAD v4 |
19 | g.53889982T>C | CA407414544 | PRKCG | c.494T>C (p.Ile165Thr) n.792T>C n.796T>C c.110T>C (p.Ile37Thr) | gnomAD v4 |
19 | g.53889982T>G | CA310082660 | PRKCG | c.494T>G (p.Ile165Ser) n.792T>G n.796T>G c.110T>G (p.Ile37Ser) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.53889982T= | CA2342579416 | PRKCG | c.494T= (p.Ile165=) n.792T= n.796T= c.110T= (p.Ile37=) | |
19 | g.53889983C>A | CA508788422 | PRKCG | c.495C>A (p.Ile165=) n.793C>A n.797C>A c.111C>A (p.Ile37=) | gnomAD v4 |
19 | g.53889983C= | CA2342579417 | PRKCG | c.495C= (p.Ile165=) n.793C= n.797C= c.111C= (p.Ile37=) | |
19 | g.53889983C>G | CA407414545 | PRKCG | c.495C>G (p.Ile165Met) n.793C>G n.797C>G c.111C>G (p.Ile37Met) | ClinVar dbSNP |
19 | g.53889983C>T | CA508788431 | PRKCG | c.495C>T (p.Ile165=) n.793C>T n.797C>T c.111C>T (p.Ile37=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889984C>A | CA508788437 | PRKCG | c.496C>A (p.Arg166=) n.794C>A n.798C>A c.112C>A (p.Arg38=) | gnomAD v4 |
19 | g.53889984C>G | CA407414546 | PRKCG | c.496C>G (p.Arg166Gly) n.794C>G n.798C>G c.112C>G (p.Arg38Gly) | |
19 | g.53889984C>T | CA407414547 | PRKCG | c.496C>T (p.Arg166Trp) n.794C>T n.798C>T c.112C>T (p.Arg38Trp) | gnomAD v4 |
19 | g.53889985G>A | CA407414548 | PRKCG | c.497G>A (p.Arg166Gln) n.795G>A n.799G>A c.113G>A (p.Arg38Gln) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889985G>C | CA407414549 | PRKCG | c.497G>C (p.Arg166Pro) n.795G>C n.799G>C c.113G>C (p.Arg38Pro) | gnomAD v4 |
19 | g.53889985G= | CA2342579418 | PRKCG | c.497G= (p.Arg166=) n.795G= n.799G= c.113G= (p.Arg38=) | |
19 | g.53889985G>T | CA310082662 | PRKCG | c.497G>T (p.Arg166Leu) n.795G>T n.799G>T c.113G>T (p.Arg38Leu) | dbSNP gnomAD v4 |
19 | g.53889986G>A | CA508788447 | PRKCG | c.498G>A (p.Arg166=) n.796G>A n.800G>A c.114G>A (p.Arg38=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889986G>C | CA508788449 | PRKCG | c.498G>C (p.Arg166=) n.796G>C n.800G>C c.114G>C (p.Arg38=) | |
19 | g.53889986G= | CA2342579419 | PRKCG | c.498G= (p.Arg166=) n.796G= n.800G= c.114G= (p.Arg38=) | |
19 | g.53889986G>T | CA9640300 | PRKCG | c.498G>T (p.Arg166=) n.796G>T n.800G>T c.114G>T (p.Arg38=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889987G>A | CA407414550 | PRKCG | c.499G>A (p.Ala167Thr) n.797G>A n.801G>A c.115G>A (p.Ala39Thr) | gnomAD v4 |
19 | g.53889987G>C | CA407414551 | PRKCG | c.499G>C (p.Ala167Pro) n.797G>C n.801G>C c.115G>C (p.Ala39Pro) | |
19 | g.53889987G>T | CA407414552 | PRKCG | c.499G>T (p.Ala167Ser) n.797G>T n.801G>T c.115G>T (p.Ala39Ser) | gnomAD v4 |
19 | g.53889988C>A | CA407414554 | PRKCG | c.500C>A (p.Ala167Asp) n.798C>A n.802C>A c.116C>A (p.Ala39Asp) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.53889988C= | CA2342579420 | PRKCG | c.500C= (p.Ala167=) n.798C= n.802C= c.116C= (p.Ala39=) | |
19 | g.53889988C>G | CA407414553 | PRKCG | c.500C>G (p.Ala167Gly) n.798C>G n.802C>G c.116C>G (p.Ala39Gly) | |
19 | g.53889988C>T | CA9640301 | PRKCG | c.500C>T (p.Ala167Val) n.798C>T n.802C>T c.116C>T (p.Ala39Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.53889989T>A | CA508788478 | PRKCG | c.501T>A (p.Ala167=) n.799T>A n.803T>A c.117T>A (p.Ala39=) | |
19 | g.53889989T>C | CA508788481 | PRKCG | c.501T>C (p.Ala167=) n.799T>C n.803T>C c.117T>C (p.Ala39=) | gnomAD v4 |
19 | g.53889989T>G | CA508788485 | PRKCG | c.501T>G (p.Ala167=) n.799T>G n.803T>G c.117T>G (p.Ala39=) |