Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.15445625A= | CA1155328532 | CTRC | c.668A= (p.Gln223=) c.*122A= (n.*122A=) n.432A= c.522A= (p.Pro174=) | |
1 | g.15445625A>C | CA338567728 | CTRC | c.668A>C (p.Gln223Pro) c.*122A>C (n.*122A>C) n.432A>C c.522A>C (p.Pro174=) | |
1 | g.15445625A>G | CA338567729 | CTRC | c.668A>G (p.Gln223Arg) c.*122A>G (n.*122A>G) n.432A>G c.522A>G (p.Pro174=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445625A>T | CA338567730 | CTRC | c.668A>T (p.Gln223Leu) c.*122A>T (n.*122A>T) n.432A>T c.522A>T (p.Pro174=) | |
1 | g.15445626G>A | CA416207356 | CTRC | c.669G>A (p.Gln223=) c.*123G>A (n.*123G>A) n.433G>A c.523G>A (p.Val175Ile) | ClinVar gnomAD v4 |
1 | g.15445626G>C | CA613438 | CTRC | c.669G>C (p.Gln223His) c.*123G>C (n.*123G>C) n.433G>C c.523G>C (p.Val175Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445626G= | CA1155328538 | CTRC | c.669G= (p.Gln223=) c.*123G= (n.*123G=) n.433G= c.523G= (p.Val175=) | |
1 | g.15445626G>T | CA338567731 | CTRC | c.669G>T (p.Gln223His) c.*123G>T (n.*123G>T) n.433G>T c.523G>T (p.Val175Phe) | gnomAD v4 |
1 | g.15445627T>A | CA338567732 | CTRC | c.670T>A (p.Leu224Met) c.*124T>A (n.*124T>A) n.434T>A c.524T>A (p.Val175Asp) | |
1 | g.15445627T>C | CA416207357 | CTRC | c.670T>C (p.Leu224=) c.*124T>C (n.*124T>C) n.434T>C c.524T>C (p.Val175Ala) | ClinVar |
1 | g.15445627T>G | CA338567733 | CTRC | c.670T>G (p.Leu224Val) c.*124T>G (n.*124T>G) n.434T>G c.524T>G (p.Val175Gly) | |
1 | g.15445628T>A | CA338567734 | CTRC | c.671T>A (p.Leu224Ter) c.*125T>A (n.*125T>A) n.435T>A c.525T>A (p.Val175=) | |
1 | g.15445628T>C | CA338567736 | CTRC | c.671T>C (p.Leu224Ser) c.*125T>C (n.*125T>C) n.435T>C c.525T>C (p.Val175=) | |
1 | g.15445628T>G | CA338567735 | CTRC | c.671T>G (p.Leu224Trp) c.*125T>G (n.*125T>G) n.435T>G c.525T>G (p.Val175=) | |
1 | g.15445629G>A | CA416207358 | CTRC | c.672G>A (p.Leu224=) c.*126G>A (n.*126G>A) n.436G>A c.526G>A (p.Gly176Arg) | ClinVar dbSNP |
1 | g.15445629G>C | CA338567737 | CTRC | c.672G>C (p.Leu224Phe) c.*126G>C (n.*126G>C) n.436G>C c.526G>C (p.Gly176Arg) | |
1 | g.15445629G>T | CA338567738 | CTRC | c.672G>T (p.Leu224Phe) c.*126G>T (n.*126G>T) n.436G>T c.526G>T (p.Gly176Ter) | ClinVar |
1 | g.15445630G>A | CA338567739 | CTRC | c.673G>A (p.Glu225Lys) c.*127G>A (n.*127G>A) n.437G>A c.527G>A (p.Gly176Glu) | dbSNP |
1 | g.15445630G>C | CA338567740 | CTRC | c.673G>C (p.Glu225Gln) c.*127G>C (n.*127G>C) n.437G>C c.527G>C (p.Gly176Ala) | |
1 | g.15445630G>T | CA338567741 | CTRC | c.673G>T (p.Glu225Ter) c.*127G>T (n.*127G>T) n.437G>T c.527G>T (p.Gly176Val) | |
1 | g.15445631A= | CA1143485616 | CTRC | c.674A= (p.Glu225=) c.*128A= (n.*128A=) n.438A= c.528A= (p.Gly176=) | |
1 | g.15445631A>C | CA613439 | CTRC | c.674A>C (p.Glu225Ala) c.*128A>C (n.*128A>C) n.438A>C c.528A>C (p.Gly176=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445631A>G | CA338567742 | CTRC | c.674A>G (p.Glu225Gly) c.*128A>G (n.*128A>G) n.438A>G c.528A>G (p.Gly176=) | |
1 | g.15445631A>T | CA338567743 | CTRC | c.674A>T (p.Glu225Val) c.*128A>T (n.*128A>T) n.438A>T c.528A>T (p.Gly176=) | |
1 | g.15445632G>A | CA416207359 | CTRC | c.675G>A (p.Glu225=) c.*129G>A (n.*129G>A) n.439G>A c.529G>A (p.Glu177Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445632G>C | CA338567744 | CTRC | c.675G>C (p.Glu225Asp) c.*129G>C (n.*129G>C) n.439G>C c.529G>C (p.Glu177Gln) | |
1 | g.15445632G= | CA1155328550 | CTRC | c.675G= (p.Glu225=) c.*129G= (n.*129G=) n.439G= c.529G= (p.Glu177=) | |
1 | g.15445632G>T | CA338567745 | CTRC | c.675G>T (p.Glu225Asp) c.*129G>T (n.*129G>T) n.439G>T c.529G>T (p.Glu177Ter) | |
1 | g.15445633A= | CA1155328552 | CTRC | c.676A= (p.Asn226=) c.*130A= (n.*130A=) n.440A= c.530A= (p.Glu177=) | |
1 | g.15445633A>C | CA338567746 | CTRC | c.676A>C (p.Asn226His) c.*130A>C (n.*130A>C) n.440A>C c.530A>C (p.Glu177Ala) | |
1 | g.15445633A>G | CA338567747 | CTRC | c.676A>G (p.Asn226Asp) c.*130A>G (n.*130A>G) n.440A>G c.530A>G (p.Glu177Gly) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.15445633A>T | CA338567748 | CTRC | c.676A>T (p.Asn226Tyr) c.*130A>T (n.*130A>T) n.440A>T c.530A>T (p.Glu177Val) | |
1 | g.15445634A>C | CA338567751 | CTRC | c.677A>C (p.Asn226Thr) c.*131A>C (n.*131A>C) n.441A>C c.531A>C (p.Glu177Asp) | |
1 | g.15445634A>G | CA338567749 | CTRC | c.677A>G (p.Asn226Ser) c.*131A>G (n.*131A>G) n.441A>G c.531A>G (p.Glu177=) | |
1 | g.15445634A>T | CA338567750 | CTRC | c.677A>T (p.Asn226Ile) c.*131A>T (n.*131A>T) n.441A>T c.531A>T (p.Glu177Asp) | |
1 | g.15445635C>A | CA18253735 | CTRC | c.678C>A (p.Asn226Lys) c.*132C>A (n.*132C>A) n.442C>A c.532C>A (p.Arg178=) | dbSNP |
1 | g.15445635C= | CA1155328558 | CTRC | c.678C= (p.Asn226=) c.*132C= (n.*132C=) n.442C= c.532C= (p.Arg178=) | |
1 | g.15445635C>G | CA338567752 | CTRC | c.678C>G (p.Asn226Lys) c.*132C>G (n.*132C>G) n.442C>G c.532C>G (p.Arg178Gly) | |
1 | g.15445635C>T | CA613440 | CTRC | c.678C>T (p.Asn226=) c.*132C>T (n.*132C>T) n.442C>T c.532C>T (p.Arg178Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.15445636G>A | CA613441 | CTRC | c.679G>A (p.Gly227Ser) c.*133G>A (n.*133G>A) n.443G>A c.533G>A (p.Arg178Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445636G>C | CA338567753 | CTRC | c.679G>C (p.Gly227Arg) c.*133G>C (n.*133G>C) n.443G>C c.533G>C (p.Arg178Pro) | |
1 | g.15445636G= | CA1147320399 | CTRC | c.679G= (p.Gly227=) c.*133G= (n.*133G=) n.443G= c.533G= (p.Arg178=) | |
1 | g.15445636G>T | CA338567754 | CTRC | c.679G>T (p.Gly227Cys) c.*133G>T (n.*133G>T) n.443G>T c.533G>T (p.Arg178Leu) | |
1 | g.15445637G>A | CA613442 | CTRC | c.680G>A (p.Gly227Asp) c.*134G>A (n.*134G>A) n.444G>A c.534G>A (p.Arg178=) | dbSNP ExAC gnomAD v2 COSMIC |
1 | g.15445637G>C | CA338567755 | CTRC | c.680G>C (p.Gly227Ala) c.*134G>C (n.*134G>C) n.444G>C c.534G>C (p.Arg178=) | |
1 | g.15445637G= | CA1141841631 | CTRC | c.680G= (p.Gly227=) c.*134G= (n.*134G=) n.444G= c.534G= (p.Arg178=) | |
1 | g.15445637G>T | CA338567756 | CTRC | c.680G>T (p.Gly227Val) c.*134G>T (n.*134G>T) n.444G>T c.534G>T (p.Arg178=) | |
1 | g.15445638T>A | CA416207360 | CTRC | c.681T>A (p.Gly227=) c.*135T>A (n.*135T>A) n.445T>A c.535T>A (p.Phe179Ile) | ClinVar dbSNP gnomAD v4 |
1 | g.15445638T>C | CA416207361 | CTRC | c.681T>C (p.Gly227=) c.*135T>C (n.*135T>C) n.445T>C c.535T>C (p.Phe179Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445638T>G | CA416207362 | CTRC | c.681T>G (p.Gly227=) c.*135T>G (n.*135T>G) n.445T>G c.535T>G (p.Phe179Val) | |
1 | g.15445638T= | CA1155328572 | CTRC | c.681T= (p.Gly227=) c.*135T= (n.*135T=) n.445T= c.535T= (p.Phe179=) | |
1 | g.15445639dup | CA2840709548 | CTRC | c.682dup (p.Ser228PhefsTer?) c.*136dup (n.*136dup) n.446dup c.536dup (p.Leu180ProfsTer23) | |
1 | g.15445639T>A | CA338567757 | CTRC | c.682T>A (p.Ser228Thr) c.*136T>A (n.*136T>A) n.446T>A c.536T>A (p.Phe179Tyr) | |
1 | g.15445639T>C | CA338567758 | CTRC | c.682T>C (p.Ser228Pro) c.*136T>C (n.*136T>C) n.446T>C c.536T>C (p.Phe179Ser) | |
1 | g.15445639T>G | CA338567759 | CTRC | c.682T>G (p.Ser228Ala) c.*136T>G (n.*136T>G) n.446T>G c.536T>G (p.Phe179Cys) | |
1 | g.15445640C>A | CA338567760 | CTRC | c.683C>A (p.Ser228Tyr) c.*137C>A (n.*137C>A) n.447C>A c.537C>A (p.Phe179Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.15445640C= | CA1155328576 | CTRC | c.683C= (p.Ser228=) c.*137C= (n.*137C=) n.447C= c.537C= (p.Phe179=) | |
1 | g.15445640C>G | CA613443 | CTRC | c.683C>G (p.Ser228Cys) c.*137C>G (n.*137C>G) n.447C>G c.537C>G (p.Phe179Leu) | dbSNP ExAC gnomAD v2 |
1 | g.15445640C>T | CA18253754 | CTRC | c.683C>T (p.Ser228Phe) c.*137C>T (n.*137C>T) n.447C>T c.537C>T (p.Phe179=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.15445641C>A | CA416207363 | CTRC | c.684C>A (p.Ser228=) c.*138C>A (n.*138C>A) n.448C>A c.538C>A (p.Leu180Met) | |
1 | g.15445641C>G | CA416207364 | CTRC | c.684C>G (p.Ser228=) c.*138C>G (n.*138C>G) n.448C>G c.538C>G (p.Leu180Val) | |
1 | g.15445641C>T | CA416207365 | CTRC | c.684C>T (p.Ser228=) c.*138C>T (n.*138C>T) n.448C>T c.538C>T (p.Leu180=) | COSMIC |
1 | g.15445642T>A | CA338567761 | CTRC | c.685T>A (p.Trp229Arg) c.*139T>A (n.*139T>A) n.449T>A c.539T>A (p.Leu180Gln) | |
1 | g.15445642T>C | CA338567763 | CTRC | c.685T>C (p.Trp229Arg) c.*139T>C (n.*139T>C) n.449T>C c.539T>C (p.Leu180Pro) | dbSNP gnomAD v4 |
1 | g.15445642T>G | CA338567762 | CTRC | c.685T>G (p.Trp229Gly) c.*139T>G (n.*139T>G) n.449T>G c.539T>G (p.Leu180Arg) | |
1 | g.15445642T= | CA1155328579 | CTRC | c.685T= (p.Trp229=) c.*139T= (n.*139T=) n.449T= c.539T= (p.Leu180=) | |
1 | g.15445643G>A | CA338567764 | CTRC | c.686G>A (p.Trp229Ter) c.*140G>A (n.*140G>A) n.450G>A c.540G>A (p.Leu180=) | |
1 | g.15445643G>C | CA338567765 | CTRC | c.686G>C (p.Trp229Ser) c.*140G>C (n.*140G>C) n.450G>C c.540G>C (p.Leu180=) | |
1 | g.15445643G>T | CA338567766 | CTRC | c.686G>T (p.Trp229Leu) c.*140G>T (n.*140G>T) n.450G>T c.540G>T (p.Leu180=) | |
1 | g.15445644G>A | CA338567767 | CTRC | c.687G>A (p.Trp229Ter) c.*141G>A (n.*141G>A) n.451G>A c.541G>A (p.Gly181Arg) | gnomAD v4 |
1 | g.15445644G>C | CA338567768 | CTRC | c.687G>C (p.Trp229Cys) c.*141G>C (n.*141G>C) n.451G>C c.541G>C (p.Gly181Arg) | |
1 | g.15445644G>T | CA338567769 | CTRC | c.687G>T (p.Trp229Cys) c.*141G>T (n.*141G>T) n.451G>T c.541G>T (p.Gly181Ter) | |
1 | g.15445645G>A | CA338567770 | CTRC | c.688G>A (p.Glu230Lys) c.*142G>A (n.*142G>A) n.452G>A c.542G>A (p.Gly181Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445645G>C | CA338567771 | CTRC | c.688G>C (p.Glu230Gln) c.*142G>C (n.*142G>C) n.452G>C c.542G>C (p.Gly181Ala) | |
1 | g.15445645G= | CA1155328584 | CTRC | c.688G= (p.Glu230=) c.*142G= (n.*142G=) n.452G= c.542G= (p.Gly181=) | |
1 | g.15445645G>T | CA338567772 | CTRC | c.688G>T (p.Glu230Ter) c.*142G>T (n.*142G>T) n.452G>T c.542G>T (p.Gly181Val) | |
1 | g.15445646A>C | CA338567773 | CTRC | c.689A>C (p.Glu230Ala) c.*143A>C (n.*143A>C) n.453A>C c.543A>C (p.Gly181=) | |
1 | g.15445646A>G | CA338567774 | CTRC | c.689A>G (p.Glu230Gly) c.*143A>G (n.*143A>G) n.453A>G c.543A>G (p.Gly181=) | |
1 | g.15445646A>T | CA338567775 | CTRC | c.689A>T (p.Glu230Val) c.*143A>T (n.*143A>T) n.453A>T c.543A>T (p.Gly181=) | |
1 | g.15445647G>A | CA613444 | CTRC | c.690G>A (p.Glu230=) c.*144G>A (n.*144G>A) n.454G>A c.544G>A (p.Gly182Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445647G>C | CA338567776 | CTRC | c.690G>C (p.Glu230Asp) c.*144G>C (n.*144G>C) n.454G>C c.544G>C (p.Gly182Arg) | |
1 | g.15445647G= | CA1140968875 | CTRC | c.690G= (p.Glu230=) c.*144G= (n.*144G=) n.454G= c.544G= (p.Gly182=) | |
1 | g.15445647G>T | CA338567777 | CTRC | c.690G>T (p.Glu230Asp) c.*144G>T (n.*144G>T) n.454G>T c.544G>T (p.Gly182Cys) | |
1 | g.15445648G>A | CA338567778 | CTRC | c.691G>A (p.Val231Met) c.*145G>A (n.*145G>A) n.455G>A c.545G>A (p.Gly182Asp) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.15445648G>C | CA338567779 | CTRC | c.691G>C (p.Val231Leu) c.*145G>C (n.*145G>C) n.455G>C c.545G>C (p.Gly182Ala) | |
1 | g.15445648G= | CA1155328592 | CTRC | c.691G= (p.Val231=) c.*145G= (n.*145G=) n.455G= c.545G= (p.Gly182=) | |
1 | g.15445648G>T | CA338567780 | CTRC | c.691G>T (p.Val231Leu) c.*145G>T (n.*145G>T) n.455G>T c.545G>T (p.Gly182Val) | |
1 | g.15445649T>A | CA338567781 | CTRC | c.692T>A (p.Val231Glu) c.*146T>A (n.*146T>A) n.456T>A c.546T>A (p.Gly182=) | |
1 | g.15445649T>C | CA338567782 | CTRC | c.692T>C (p.Val231Ala) c.*146T>C (n.*146T>C) n.456T>C c.546T>C (p.Gly182=) | |
1 | g.15445649T>G | CA338567783 | CTRC | c.692T>G (p.Val231Gly) c.*146T>G (n.*146T>G) n.456T>G c.546T>G (p.Gly182=) | |
1 | g.15445650G>A | CA416207368 | CTRC | c.693G>A (p.Val231=) c.*147G>A (n.*147G>A) n.457G>A c.547G>A (p.Val183Ile) | |
1 | g.15445650G>C | CA416207366 | CTRC | c.693G>C (p.Val231=) c.*147G>C (n.*147G>C) n.457G>C c.547G>C (p.Val183Leu) | |
1 | g.15445650G>T | CA416207367 | CTRC | c.693G>T (p.Val231=) c.*147G>T (n.*147G>T) n.457G>T c.547G>T (p.Val183Phe) | |
1 | g.15445651T>A | CA338567784 | CTRC | c.694T>A (p.Phe232Ile) c.*148T>A (n.*148T>A) n.458T>A c.548T>A (p.Val183Asp) | |
1 | g.15445651T>C | CA338567785 | CTRC | c.694T>C (p.Phe232Leu) c.*148T>C (n.*148T>C) n.458T>C c.548T>C (p.Val183Ala) | |
1 | g.15445651T>G | CA338567786 | CTRC | c.694T>G (p.Phe232Val) c.*148T>G (n.*148T>G) n.458T>G c.548T>G (p.Val183Gly) | |
1 | g.15445653dup | CA2840709549 | CTRC | c.696dup (p.Gly233TrpfsTer?) c.*150dup (n.*150dup) n.460dup c.550dup (p.Trp184LeufsTer19) | |
1 | g.15445652T>A | CA338567787 | CTRC | c.695T>A (p.Phe232Tyr) c.*149T>A (n.*149T>A) n.459T>A c.549T>A (p.Val183=) | |
1 | g.15445652T>C | CA338567788 | CTRC | c.695T>C (p.Phe232Ser) c.*149T>C (n.*149T>C) n.459T>C c.549T>C (p.Val183=) | ClinVar |
1 | g.15445652T>G | CA338567789 | CTRC | c.695T>G (p.Phe232Cys) c.*149T>G (n.*149T>G) n.459T>G c.549T>G (p.Val183=) | |
1 | g.15445653T>A | CA338567791 | CTRC | c.696T>A (p.Phe232Leu) c.*150T>A (n.*150T>A) n.460T>A c.550T>A (p.Trp184Arg) | |
1 | g.15445653T>C | CA416207369 | CTRC | c.696T>C (p.Phe232=) c.*150T>C (n.*150T>C) n.460T>C c.550T>C (p.Trp184Arg) | ClinVar dbSNP |
1 | g.15445653T>G | CA338567790 | CTRC | c.696T>G (p.Phe232Leu) c.*150T>G (n.*150T>G) n.460T>G c.550T>G (p.Trp184Gly) | |
1 | g.15445653T= | CA1155328597 | CTRC | c.696T= (p.Phe232=) c.*150T= (n.*150T=) n.460T= c.550T= (p.Trp184=) | |
1 | g.15445654G>A | CA338567792 | CTRC | c.697G>A (p.Gly233Ser) c.*151G>A (n.*151G>A) n.461G>A c.551G>A (p.Trp184Ter) | gnomAD v4 |
1 | g.15445654G>C | CA338567793 | CTRC | c.697G>C (p.Gly233Arg) c.*151G>C (n.*151G>C) n.461G>C c.551G>C (p.Trp184Ser) | |
1 | g.15445654G>T | CA338567794 | CTRC | c.697G>T (p.Gly233Cys) c.*151G>T (n.*151G>T) n.461G>T c.551G>T (p.Trp184Leu) | |
1 | g.15445654_15445659delinsGGCATC | CA1155328600 | CTRC | c.697_702delinsGGCATC (p.Gly233=) c.*151_*156delinsGGCATC (n.*151_*156delinsGGCATC) n.461_466delinsGGCATC c.551_556delinsGGCATC (p.Trp184=) | |
1 | g.15445655G>A | CA338567795 | CTRC | c.698G>A (p.Gly233Asp) c.*152G>A (n.*152G>A) n.462G>A c.552G>A (p.Trp184Ter) | ClinVar |
1 | g.15445655G>C | CA338567796 | CTRC | c.698G>C (p.Gly233Ala) c.*152G>C (n.*152G>C) n.462G>C c.552G>C (p.Trp184Cys) | |
1 | g.15445655G= | CA1155328605 | CTRC | c.698G= (p.Gly233=) c.*152G= (n.*152G=) n.462G= c.552G= (p.Trp184=) | |
1 | g.15445655G>T | CA338567797 | CTRC | c.698G>T (p.Gly233Val) c.*152G>T (n.*152G>T) n.462G>T c.552G>T (p.Trp184Cys) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445656_15445660del | CA658795400 | CTRC | c.699_703del (p.Ile234GlnfsTer?) c.*153_*157del (n.*153_*157del) n.463_467del c.553_557del (p.His185SerfsTer16) | ClinVar dbSNP |
1 | g.15445656C>A | CA416207370 | CTRC | c.699C>A (p.Gly233=) c.*153C>A (n.*153C>A) n.463C>A c.553C>A (p.His185Asn) | |
1 | g.15445656C= | CA1155328608 | CTRC | c.699C= (p.Gly233=) c.*153C= (n.*153C=) n.463C= c.553C= (p.His185=) | |
1 | g.15445656C>G | CA416207371 | CTRC | c.699C>G (p.Gly233=) c.*153C>G (n.*153C>G) n.463C>G c.553C>G (p.His185Asp) | |
1 | g.15445656C>T | CA613445 | CTRC | c.699C>T (p.Gly233=) c.*153C>T (n.*153C>T) n.463C>T c.553C>T (p.His185Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445657A>C | CA338567800 | CTRC | c.700A>C (p.Ile234Leu) c.*154A>C (n.*154A>C) n.464A>C c.554A>C (p.His185Pro) | |
1 | g.15445657A>G | CA338567798 | CTRC | c.700A>G (p.Ile234Val) c.*154A>G (n.*154A>G) n.464A>G c.554A>G (p.His185Arg) | ClinVar gnomAD v4 |
1 | g.15445657A>T | CA338567799 | CTRC | c.700A>T (p.Ile234Phe) c.*154A>T (n.*154A>T) n.464A>T c.554A>T (p.His185Leu) | |
1 | g.15445658T>A | CA338567801 | CTRC | c.701T>A (p.Ile234Asn) c.*155T>A (n.*155T>A) n.465T>A c.555T>A (p.His185Gln) | |
1 | g.15445658T>C | CA338567802 | CTRC | c.701T>C (p.Ile234Thr) c.*155T>C (n.*155T>C) n.465T>C c.555T>C (p.His185=) | |
1 | g.15445658T>G | CA338567803 | CTRC | c.701T>G (p.Ile234Ser) c.*155T>G (n.*155T>G) n.465T>G c.555T>G (p.His185Gln) | |
1 | g.15445659C>A | CA416207372 | CTRC | c.702C>A (p.Ile234=) c.*156C>A (n.*156C>A) n.466C>A c.556C>A (p.Arg186Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445659C= | CA1155328613 | CTRC | c.702C= (p.Ile234=) c.*156C= (n.*156C=) n.466C= c.556C= (p.Arg186=) | |
1 | g.15445659C>G | CA338567804 | CTRC | c.702C>G (p.Ile234Met) c.*156C>G (n.*156C>G) n.466C>G c.556C>G (p.Arg186Gly) | |
1 | g.15445659C>T | CA613446 | CTRC | c.702C>T (p.Ile234=) c.*156C>T (n.*156C>T) n.466C>T c.556C>T (p.Arg186Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.15445660G>A | CA613447 | CTRC | c.703G>A (p.Val235Ile) c.*157G>A (n.*157G>A) n.467G>A c.557G>A (p.Arg186His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.15445660G>C | CA338567806 | CTRC | c.703G>C (p.Val235Leu) c.*157G>C (n.*157G>C) n.467G>C c.557G>C (p.Arg186Pro) | gnomAD v4 |
1 | g.15445660G= | CA1141777103 | CTRC | c.703G= (p.Val235=) c.*157G= (n.*157G=) n.467G= c.557G= (p.Arg186=) | |
1 | g.15445660G>T | CA338567805 | CTRC | c.703G>T (p.Val235Phe) c.*157G>T (n.*157G>T) n.467G>T c.557G>T (p.Arg186Leu) | |
1 | g.15445661T>A | CA338567807 | CTRC | c.704T>A (p.Val235Asp) c.*158T>A (n.*158T>A) n.468T>A c.558T>A (p.Arg186=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445661T>C | CA338567808 | CTRC | c.704T>C (p.Val235Ala) c.*158T>C (n.*158T>C) n.468T>C c.558T>C (p.Arg186=) | |
1 | g.15445661T>G | CA613448 | CTRC | c.704T>G (p.Val235Gly) c.*158T>G (n.*158T>G) n.468T>G c.558T>G (p.Arg186=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445661T= | CA1155328618 | CTRC | c.704T= (p.Val235=) c.*158T= (n.*158T=) n.468T= c.558T= (p.Arg186=) | |
1 | g.15445662C>A | CA416207373 | CTRC | c.705C>A (p.Val235=) c.*159C>A (n.*159C>A) n.469C>A c.559C>A (p.Gln187Lys) | |
1 | g.15445662C>G | CA416207374 | CTRC | c.705C>G (p.Val235=) c.*159C>G (n.*159C>G) n.469C>G c.559C>G (p.Gln187Glu) | |
1 | g.15445662C>T | CA416207375 | CTRC | c.705C>T (p.Val235=) c.*159C>T (n.*159C>T) n.469C>T c.559C>T (p.Gln187Ter) | ClinVar gnomAD v4 |
1 | g.15445663A>C | CA338567809 | CTRC | c.706A>C (p.Ser236Arg) c.*160A>C (n.*160A>C) n.470A>C c.560A>C (p.Gln187Pro) | |
1 | g.15445663A>G | CA338567810 | CTRC | c.706A>G (p.Ser236Gly) c.*160A>G (n.*160A>G) n.470A>G c.560A>G (p.Gln187Arg) | |
1 | g.15445663A>T | CA338567811 | CTRC | c.706A>T (p.Ser236Cys) c.*160A>T (n.*160A>T) n.470A>T c.560A>T (p.Gln187Leu) | |
1 | g.15445664G>A | CA338567812 | CTRC | c.707G>A (p.Ser236Asn) c.*161G>A (n.*161G>A) n.471G>A c.561G>A (p.Gln187=) | |
1 | g.15445664G>C | CA338567813 | CTRC | c.707G>C (p.Ser236Thr) c.*161G>C (n.*161G>C) n.471G>C c.561G>C (p.Gln187His) | ClinVar |
1 | g.15445664G>T | CA338567814 | CTRC | c.707G>T (p.Ser236Ile) c.*161G>T (n.*161G>T) n.471G>T c.561G>T (p.Gln187His) | |
1 | g.15445665C>A | CA338567815 | CTRC | c.708C>A (p.Ser236Arg) c.*162C>A (n.*162C>A) n.472C>A c.562C>A (p.Leu188Ile) | |
1 | g.15445665C>G | CA338567816 | CTRC | c.708C>G (p.Ser236Arg) c.*162C>G (n.*162C>G) n.472C>G c.562C>G (p.Leu188Val) | |
1 | g.15445665C>T | CA416207376 | CTRC | c.708C>T (p.Ser236=) c.*162C>T (n.*162C>T) n.472C>T c.562C>T (p.Leu188Phe) | |
1 | g.15445666T>A | CA338567819 | CTRC | c.709T>A (p.Phe237Ile) c.*163T>A (n.*163T>A) n.473T>A c.563T>A (p.Leu188His) | |
1 | g.15445666T>C | CA338567817 | CTRC | c.709T>C (p.Phe237Leu) c.*163T>C (n.*163T>C) n.473T>C c.563T>C (p.Leu188Pro) | |
1 | g.15445666T>G | CA338567818 | CTRC | c.709T>G (p.Phe237Val) c.*163T>G (n.*163T>G) n.473T>G c.563T>G (p.Leu188Arg) | |
1 | g.15445667T>A | CA338567820 | CTRC | c.710T>A (p.Phe237Tyr) c.*164T>A (n.*164T>A) n.474T>A c.564T>A (p.Leu188=) | |
1 | g.15445667T>C | CA338567822 | CTRC | c.710T>C (p.Phe237Ser) c.*164T>C (n.*164T>C) n.474T>C c.564T>C (p.Leu188=) | |
1 | g.15445667T>G | CA338567821 | CTRC | c.710T>G (p.Phe237Cys) c.*164T>G (n.*164T>G) n.474T>G c.564T>G (p.Leu188=) | |
1 | g.15445668T>A | CA338567823 | CTRC | c.711T>A (p.Phe237Leu) c.*165T>A (n.*165T>A) n.475T>A c.565T>A (p.Trp189Arg) | |
1 | g.15445668T>C | CA416207377 | CTRC | c.711T>C (p.Phe237=) c.*165T>C (n.*165T>C) n.475T>C c.565T>C (p.Trp189Arg) | |
1 | g.15445668T>G | CA338567824 | CTRC | c.711T>G (p.Phe237Leu) c.*165T>G (n.*165T>G) n.475T>G c.565T>G (p.Trp189Gly) | |
1 | g.15445669G>A | CA338567825 | CTRC | c.712G>A (p.Gly238Ser) c.*166G>A (n.*166G>A) n.476G>A c.566G>A (p.Trp189Ter) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445669G>C | CA338567826 | CTRC | c.712G>C (p.Gly238Arg) c.*166G>C (n.*166G>C) n.476G>C c.566G>C (p.Trp189Ser) | |
1 | g.15445669G= | CA1155328620 | CTRC | c.712G= (p.Gly238=) c.*166G= (n.*166G=) n.476G= c.566G= (p.Trp189=) | |
1 | g.15445669G>T | CA338567827 | CTRC | c.712G>T (p.Gly238Cys) c.*166G>T (n.*166G>T) n.476G>T c.566G>T (p.Trp189Leu) | |
1 | g.15445670G>A | CA338567828 | CTRC | c.713G>A (p.Gly238Asp) c.*167G>A (n.*167G>A) n.477G>A c.567G>A (p.Trp189Ter) | |
1 | g.15445670G>C | CA338567829 | CTRC | c.713G>C (p.Gly238Ala) c.*167G>C (n.*167G>C) n.477G>C c.567G>C (p.Trp189Cys) | |
1 | g.15445670G>T | CA338567830 | CTRC | c.713G>T (p.Gly238Val) c.*167G>T (n.*167G>T) n.477G>T c.567G>T (p.Trp189Cys) | |
1 | g.15445671del | CA2643487263 | CTRC | c.714del (p.Ser239ProfsTer12) c.*168del (n.*168del) n.478del c.568del (p.Leu190SerfsTer?) | gnomAD v4 |
1 | g.15445671C>A | CA416207378 | CTRC | c.714C>A (p.Gly238=) c.*168C>A (n.*168C>A) n.478C>A c.568C>A (p.Leu190Ile) | |
1 | g.15445671C>G | CA416207379 | CTRC | c.714C>G (p.Gly238=) c.*168C>G (n.*168C>G) n.478C>G c.568C>G (p.Leu190Val) | ClinVar gnomAD v4 |
1 | g.15445671C>T | CA416207380 | CTRC | c.714C>T (p.Gly238=) c.*168C>T (n.*168C>T) n.478C>T c.568C>T (p.Leu190Phe) | |
1 | g.15445672T>A | CA338567831 | CTRC | c.715T>A (p.Ser239Thr) c.*169T>A (n.*169T>A) n.479T>A c.569T>A (p.Leu190His) | |
1 | g.15445672T>C | CA338567832 | CTRC | c.715T>C (p.Ser239Pro) c.*169T>C (n.*169T>C) n.479T>C c.569T>C (p.Leu190Pro) | |
1 | g.15445672T>G | CA338567833 | CTRC | c.715T>G (p.Ser239Ala) c.*169T>G (n.*169T>G) n.479T>G c.569T>G (p.Leu190Arg) | |
1 | g.15445673C>A | CA338567836 | CTRC | c.716C>A (p.Ser239Tyr) c.*170C>A (n.*170C>A) n.480C>A c.570C>A (p.Leu190=) | |
1 | g.15445673C= | CA1155328624 | CTRC | c.716C= (p.Ser239=) c.*170C= (n.*170C=) n.480C= c.570C= (p.Leu190=) | |
1 | g.15445673C>G | CA338567834 | CTRC | c.716C>G (p.Ser239Cys) c.*170C>G (n.*170C>G) n.480C>G c.570C>G (p.Leu190=) | dbSNP gnomAD v4 |
1 | g.15445673C>T | CA338567835 | CTRC | c.716C>T (p.Ser239Phe) c.*170C>T (n.*170C>T) n.480C>T c.570C>T (p.Leu190=) | ClinVar dbSNP |
1 | g.15445674C>A | CA416207381 | CTRC | c.717C>A (p.Ser239=) c.*171C>A (n.*171C>A) n.481C>A c.571C>A (p.Pro191Thr) | |
1 | g.15445674C>G | CA416207382 | CTRC | c.717C>G (p.Ser239=) c.*171C>G (n.*171C>G) n.481C>G c.571C>G (p.Pro191Ala) | |
1 | g.15445674C>T | CA416207383 | CTRC | c.717C>T (p.Ser239=) c.*171C>T (n.*171C>T) n.481C>T c.571C>T (p.Pro191Ser) | ClinVar gnomAD v4 |
1 | g.15445675C>A | CA416207384 | CTRC | c.718C>A (p.Arg240=) c.*172C>A (n.*172C>A) n.482C>A c.572C>A (p.Pro191Gln) | |
1 | g.15445675C= | CA1143546641 | CTRC | c.718C= (p.Arg240=) c.*172C= (n.*172C=) n.482C= c.572C= (p.Pro191=) | |
1 | g.15445675C>G | CA338567837 | CTRC | c.718C>G (p.Arg240Gly) c.*172C>G (n.*172C>G) n.482C>G c.572C>G (p.Pro191Arg) | |
1 | g.15445675C>T | CA613449 | CTRC | c.718C>T (p.Arg240Trp) c.*172C>T (n.*172C>T) n.482C>T c.572C>T (p.Pro191Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445676G>A | CA613450 | CTRC | c.719G>A (p.Arg240Gln) c.*173G>A (n.*173G>A) n.483G>A c.573G>A (p.Pro191=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445676G>C | CA338567838 | CTRC | c.719G>C (p.Arg240Pro) c.*173G>C (n.*173G>C) n.483G>C c.573G>C (p.Pro191=) | dbSNP gnomAD v2 |
1 | g.15445676G= | CA1155328633 | CTRC | c.719G= (p.Arg240=) c.*173G= (n.*173G=) n.483G= c.573G= (p.Pro191=) | |
1 | g.15445676G>T | CA338567839 | CTRC | c.719G>T (p.Arg240Leu) c.*173G>T (n.*173G>T) n.483G>T c.573G>T (p.Pro191=) | |
1 | g.15445677G>A | CA416207385 | CTRC | c.720G>A (p.Arg240=) c.*174G>A (n.*174G>A) n.484G>A c.574G>A (p.Ala192Thr) | |
1 | g.15445677G>C | CA416207386 | CTRC | c.720G>C (p.Arg240=) c.*174G>C (n.*174G>C) n.484G>C c.574G>C (p.Ala192Pro) | |
1 | g.15445677G>T | CA416207387 | CTRC | c.720G>T (p.Arg240=) c.*174G>T (n.*174G>T) n.484G>T c.574G>T (p.Ala192Ser) | |
1 | g.15445679_15445686dup | CA2643487264 | CTRC | c.722_729dup (p.Asn244GlyfsTer10) c.*176_*183dup (n.*176_*183dup) n.486_493dup c.576_583dup (p.Gln195ArgfsTer29) | gnomAD v4 |
1 | g.15445678C>A | CA613451 | CTRC | c.721C>A (p.Arg241=) c.*175C>A (n.*175C>A) n.485C>A c.575C>A (p.Ala192Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445678C= | CA1155328642 | CTRC | c.721C= (p.Arg241=) c.*175C= (n.*175C=) n.485C= c.575C= (p.Ala192=) | |
1 | g.15445678C>G | CA338567840 | CTRC | c.721C>G (p.Arg241Gly) c.*175C>G (n.*175C>G) n.485C>G c.575C>G (p.Ala192Gly) | ClinVar |
1 | g.15445678C>T | CA613453 | CTRC | c.721C>T (p.Arg241Trp) c.*175C>T (n.*175C>T) n.485C>T c.575C>T (p.Ala192Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.15445678_15445679delinsCG | CA1155328643 | CTRC | c.721_722delinsCG (p.Arg241=) c.*175_*176delinsCG (n.*175_*176delinsCG) n.485_486delinsCG c.575_576delinsCG (p.Ala192=) | |
1 | g.15445679G>A | CA613454 | CTRC | c.722G>A (p.Arg241Gln) c.*176G>A (n.*176G>A) n.486G>A c.576G>A (p.Ala192=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445679G>C | CA338567841 | CTRC | c.722G>C (p.Arg241Pro) c.*176G>C (n.*176G>C) n.486G>C c.576G>C (p.Ala192=) | |
1 | g.15445679G= | CA1155328654 | CTRC | c.722G= (p.Arg241=) c.*176G= (n.*176G=) n.486G= c.576G= (p.Ala192=) | |
1 | g.15445679G>T | CA338567842 | CTRC | c.722G>T (p.Arg241Leu) c.*176G>T (n.*176G>T) n.486G>T c.576G>T (p.Ala192=) | ClinVar |
1 | g.15445682dup | CA1155328652 | CTRC | c.725dup (p.Cys243LeufsTer?) c.*179dup (n.*179dup) n.489dup c.579dup (p.Leu194AlafsTer9) | dbSNP gnomAD v4 |
1 | g.15445682del | CA613452 | CTRC | c.725del (p.Gly242AlafsTer9) c.*179del (n.*179del) n.489del c.579del (p.Leu194CysfsTer27) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445680G>A | CA416207388 | CTRC | c.723G>A (p.Arg241=) c.*177G>A (n.*177G>A) n.487G>A c.577G>A (p.Gly193Arg) | |
1 | g.15445680G>C | CA416207389 | CTRC | c.723G>C (p.Arg241=) c.*177G>C (n.*177G>C) n.487G>C c.577G>C (p.Gly193Arg) | |
1 | g.15445680G>T | CA416207390 | CTRC | c.723G>T (p.Arg241=) c.*177G>T (n.*177G>T) n.487G>T c.577G>T (p.Gly193Trp) | |
1 | g.15445681G>A | CA338567844 | CTRC | c.724G>A (p.Gly242Ser) c.*178G>A (n.*178G>A) n.488G>A c.578G>A (p.Gly193Glu) | COSMIC |
1 | g.15445681G>C | CA338567845 | CTRC | c.724G>C (p.Gly242Arg) c.*178G>C (n.*178G>C) n.488G>C c.578G>C (p.Gly193Ala) | |
1 | g.15445681G>T | CA338567843 | CTRC | c.724G>T (p.Gly242Cys) c.*178G>T (n.*178G>T) n.488G>T c.578G>T (p.Gly193Val) | |
1 | g.15445682G>A | CA338567846 | CTRC | c.725G>A (p.Gly242Asp) c.*179G>A (n.*179G>A) n.489G>A c.579G>A (p.Gly193=) | ClinVar |
1 | g.15445682G>C | CA338567847 | CTRC | c.725G>C (p.Gly242Ala) c.*179G>C (n.*179G>C) n.489G>C c.579G>C (p.Gly193=) | |
1 | g.15445682G>T | CA338567848 | CTRC | c.725G>T (p.Gly242Val) c.*179G>T (n.*179G>T) n.489G>T c.579G>T (p.Gly193=) | |
1 | g.15445683C>A | CA416207391 | CTRC | c.726C>A (p.Gly242=) c.*180C>A (n.*180C>A) n.490C>A c.580C>A (p.Leu194Met) | |
1 | g.15445683C>G | CA416207392 | CTRC | c.726C>G (p.Gly242=) c.*180C>G (n.*180C>G) n.490C>G c.580C>G (p.Leu194Val) | |
1 | g.15445683C>T | CA416207393 | CTRC | c.726C>T (p.Gly242=) c.*180C>T (n.*180C>T) n.490C>T c.580C>T (p.Leu194=) | |
1 | g.15445684T>A | CA338567849 | CTRC | c.727T>A (p.Cys243Ser) c.*181T>A (n.*181T>A) n.491T>A c.581T>A (p.Leu194Gln) | |
1 | g.15445684T>C | CA338567850 | CTRC | c.727T>C (p.Cys243Arg) c.*181T>C (n.*181T>C) n.491T>C c.581T>C (p.Leu194Pro) | |
1 | g.15445684T>G | CA338567851 | CTRC | c.727T>G (p.Cys243Gly) c.*181T>G (n.*181T>G) n.491T>G c.581T>G (p.Leu194Arg) | |
1 | g.15445685G>A | CA338567854 | CTRC | c.728G>A (p.Cys243Tyr) c.*182G>A (n.*182G>A) n.492G>A c.582G>A (p.Leu194=) | |
1 | g.15445685G>C | CA338567852 | CTRC | c.728G>C (p.Cys243Ser) c.*182G>C (n.*182G>C) n.492G>C c.582G>C (p.Leu194=) | |
1 | g.15445685G>T | CA338567853 | CTRC | c.728G>T (p.Cys243Phe) c.*182G>T (n.*182G>T) n.492G>T c.582G>T (p.Leu194=) | |
1 | g.15445686C>A | CA338567855 | CTRC | c.729C>A (p.Cys243Ter) c.*183C>A (n.*183C>A) n.493C>A c.583C>A (p.Gln195Lys) | |
1 | g.15445686C>G | CA338567856 | CTRC | c.729C>G (p.Cys243Trp) c.*183C>G (n.*183C>G) n.493C>G c.583C>G (p.Gln195Glu) | |
1 | g.15445686C>T | CA416207394 | CTRC | c.729C>T (p.Cys243=) c.*183C>T (n.*183C>T) n.493C>T c.583C>T (p.Gln195Ter) | |
1 | g.15445687A= | CA1155328658 | CTRC | c.730A= (p.Asn244=) c.*184A= (n.*184A=) n.494A= c.584A= (p.Gln195=) | |
1 | g.15445687A>C | CA338567857 | CTRC | c.730A>C (p.Asn244His) c.*184A>C (n.*184A>C) n.494A>C c.584A>C (p.Gln195Pro) | ClinVar dbSNP gnomAD v4 |
1 | g.15445687A>G | CA338567858 | CTRC | c.730A>G (p.Asn244Asp) c.*184A>G (n.*184A>G) n.494A>G c.584A>G (p.Gln195Arg) | |
1 | g.15445687A>T | CA338567859 | CTRC | c.730A>T (p.Asn244Tyr) c.*184A>T (n.*184A>T) n.494A>T c.584A>T (p.Gln195Leu) | |
1 | g.15445687_15445711delinsAACACCCGCAAGAAGCCGGTAGTCT | CA1155328657 | CTRC | c.730_754delinsAACACCCGCAAGAAGCCGGTAGTCT (p.Asn244=) c.*184_*208delinsAACACCCGCAAGAAGCCGGTAGTCT (n.*184_*208delinsAACACCCGCAAGAAGCCGGTAGTCT) n.494_518delinsAACACCCGCAAGAAGCCGGTAGTCT c.584_608delinsAACACCCGCAAGAAGCCGGTAGTCT (p.Gln195=) | |
1 | g.15445688A= | CA1155328666 | CTRC | c.731A= (p.Asn244=) c.*185A= (n.*185A=) n.495A= c.585A= (p.Gln195=) | |
1 | g.15445688A>C | CA338567860 | CTRC | c.731A>C (p.Asn244Thr) c.*185A>C (n.*185A>C) n.495A>C c.585A>C (p.Gln195His) | |
1 | g.15445688A>G | CA338567861 | CTRC | c.731A>G (p.Asn244Ser) c.*185A>G (n.*185A>G) n.495A>G c.585A>G (p.Gln195=) | gnomAD v4 |
1 | g.15445688A>T | CA613455 | CTRC | c.731A>T (p.Asn244Ile) c.*185A>T (n.*185A>T) n.495A>T c.585A>T (p.Gln195His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445688_15445718delinsACACCCGCAAGAAGCCGGTAGTCTACACCCG | CA1144232719 | CTRC | c.731_761delinsACACCCGCAAGAAGCCGGTAGTCTACACCCG (p.Asn244=) c.*185_*215delinsACACCCGCAAGAAGCCGGTAGTCTACACCCG (n.*185_*215delinsACACCCGCAAGAAGCCGGTAGTCTACACCCG) n.495_525delinsACACCCGCAAGAAGCCGGTAGTCTACACCCG c.585_615delinsACACCCGCAAGAAGCCGGTAGTCTACACCCG (p.Gln195=) | |
1 | g.15445695_15445718del | CA345648 | CTRC | c.738_761del (p.Lys247_Arg254del) c.*192_*215del (n.*192_*215del) n.502_525del c.592_615del (p.Gln198_Pro205del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445689C>A | CA338567862 | CTRC | c.732C>A (p.Asn244Lys) c.*186C>A (n.*186C>A) n.496C>A c.586C>A (p.His196Asn) | |
1 | g.15445689C>G | CA338567863 | CTRC | c.732C>G (p.Asn244Lys) c.*186C>G (n.*186C>G) n.496C>G c.586C>G (p.His196Asp) | |
1 | g.15445689C>T | CA416207395 | CTRC | c.732C>T (p.Asn244=) c.*186C>T (n.*186C>T) n.496C>T c.586C>T (p.His196Tyr) | |
1 | g.15445690A>C | CA338567864 | CTRC | c.733A>C (p.Thr245Pro) c.*187A>C (n.*187A>C) n.497A>C c.587A>C (p.His196Pro) | |
1 | g.15445690A>G | CA338567865 | CTRC | c.733A>G (p.Thr245Ala) c.*187A>G (n.*187A>G) n.497A>G c.587A>G (p.His196Arg) | |
1 | g.15445690A>T | CA338567866 | CTRC | c.733A>T (p.Thr245Ser) c.*187A>T (n.*187A>T) n.497A>T c.587A>T (p.His196Leu) | |
1 | g.15445691C>A | CA338567867 | CTRC | c.734C>A (p.Thr245Asn) c.*188C>A (n.*188C>A) n.498C>A c.588C>A (p.His196Gln) | gnomAD v4 |
1 | g.15445691C= | CA1155328673 | CTRC | c.734C= (p.Thr245=) c.*188C= (n.*188C=) n.498C= c.588C= (p.His196=) | |
1 | g.15445691C>G | CA338567868 | CTRC | c.734C>G (p.Thr245Ser) c.*188C>G (n.*188C>G) n.498C>G c.588C>G (p.His196Gln) | |
1 | g.15445691C>T | CA338567869 | CTRC | c.734C>T (p.Thr245Ile) c.*188C>T (n.*188C>T) n.498C>T c.588C>T (p.His196=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
1 | g.15445692C>A | CA416207398 | CTRC | c.735C>A (p.Thr245=) c.*189C>A (n.*189C>A) n.499C>A c.589C>A (p.Pro197Thr) | |
1 | g.15445692C>G | CA416207397 | CTRC | c.735C>G (p.Thr245=) c.*189C>G (n.*189C>G) n.499C>G c.589C>G (p.Pro197Ala) | |
1 | g.15445692C>T | CA416207396 | CTRC | c.735C>T (p.Thr245=) c.*189C>T (n.*189C>T) n.499C>T c.589C>T (p.Pro197Ser) | ClinVar |
1 | g.15445693C>A | CA338567870 | CTRC | c.736C>A (p.Arg246Ser) c.*190C>A (n.*190C>A) n.500C>A c.590C>A (p.Pro197Gln) | |
1 | g.15445693C= | CA1143415653 | CTRC | c.736C= (p.Arg246=) c.*190C= (n.*190C=) n.500C= c.590C= (p.Pro197=) | |
1 | g.15445693C>G | CA338567871 | CTRC | c.736C>G (p.Arg246Gly) c.*190C>G (n.*190C>G) n.500C>G c.590C>G (p.Pro197Arg) | ClinVar dbSNP gnomAD v4 |
1 | g.15445693C>T | CA613456 | CTRC | c.736C>T (p.Arg246Cys) c.*190C>T (n.*190C>T) n.500C>T c.590C>T (p.Pro197Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445694G>A | CA613457 | CTRC | c.737G>A (p.Arg246His) c.*191G>A (n.*191G>A) n.501G>A c.591G>A (p.Pro197=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445694G>C | CA338567872 | CTRC | c.737G>C (p.Arg246Pro) c.*191G>C (n.*191G>C) n.501G>C c.591G>C (p.Pro197=) | dbSNP |
1 | g.15445694G= | CA1142207989 | CTRC | c.737G= (p.Arg246=) c.*191G= (n.*191G=) n.501G= c.591G= (p.Pro197=) | |
1 | g.15445694G>T | CA613458 | CTRC | c.737G>T (p.Arg246Leu) c.*191G>T (n.*191G>T) n.501G>T c.591G>T (p.Pro197=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445695C>A | CA416207399 | CTRC | c.738C>A (p.Arg246=) c.*192C>A (n.*192C>A) n.502C>A c.592C>A (p.Gln198Lys) | ClinVar |
1 | g.15445695C>G | CA416207400 | CTRC | c.738C>G (p.Arg246=) c.*192C>G (n.*192C>G) n.502C>G c.592C>G (p.Gln198Glu) | |
1 | g.15445695C>T | CA416207401 | CTRC | c.738C>T (p.Arg246=) c.*192C>T (n.*192C>T) n.502C>T c.592C>T (p.Gln198Ter) | |
1 | g.15445696A= | CA1155328694 | CTRC | c.739A= (p.Lys247=) c.*193A= (n.*193A=) n.503A= c.593A= (p.Gln198=) | |
1 | g.15445696A>C | CA338567874 | CTRC | c.739A>C (p.Lys247Gln) c.*193A>C (n.*193A>C) n.503A>C c.593A>C (p.Gln198Pro) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.15445696A>G | CA338567873 | CTRC | c.739A>G (p.Lys247Glu) c.*193A>G (n.*193A>G) n.503A>G c.593A>G (p.Gln198Arg) | gnomAD v4 |
1 | g.15445696A>T | CA338567875 | CTRC | c.739A>T (p.Lys247Ter) c.*193A>T (n.*193A>T) n.503A>T c.593A>T (p.Gln198Leu) | |
1 | g.15445697A= | CA1155328697 | CTRC | c.740A= (p.Lys247=) c.*194A= (n.*194A=) n.504A= c.594A= (p.Gln198=) | |
1 | g.15445697A>C | CA338567876 | CTRC | c.740A>C (p.Lys247Thr) c.*194A>C (n.*194A>C) n.504A>C c.594A>C (p.Gln198His) | |
1 | g.15445697A>G | CA18253809 | CTRC | c.740A>G (p.Lys247Arg) c.*194A>G (n.*194A>G) n.504A>G c.594A>G (p.Gln198=) | dbSNP |
1 | g.15445697A>T | CA338567877 | CTRC | c.740A>T (p.Lys247Met) c.*194A>T (n.*194A>T) n.504A>T c.594A>T (p.Gln198His) | |
1 | g.15445698G>A | CA416207403 | CTRC | c.741G>A (p.Lys247=) c.*195G>A (n.*195G>A) n.505G>A c.595G>A (p.Glu199Lys) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445698G>C | CA338567878 | CTRC | c.741G>C (p.Lys247Asn) c.*195G>C (n.*195G>C) n.505G>C c.595G>C (p.Glu199Gln) | |
1 | g.15445698G= | CA1155328701 | CTRC | c.741G= (p.Lys247=) c.*195G= (n.*195G=) n.505G= c.595G= (p.Glu199=) | |
1 | g.15445698G>T | CA338567879 | CTRC | c.741G>T (p.Lys247Asn) c.*195G>T (n.*195G>T) n.505G>T c.595G>T (p.Glu199Ter) | |
1 | g.15445699A>C | CA338567880 | CTRC | c.742A>C (p.Lys248Gln) c.*196A>C (n.*196A>C) n.506A>C c.596A>C (p.Glu199Ala) | |
1 | g.15445699A>G | CA338567881 | CTRC | c.742A>G (p.Lys248Glu) c.*196A>G (n.*196A>G) n.506A>G c.596A>G (p.Glu199Gly) | ClinVar |
1 | g.15445699A>T | CA338567882 | CTRC | c.742A>T (p.Lys248Ter) c.*196A>T (n.*196A>T) n.506A>T c.596A>T (p.Glu199Val) | |
1 | g.15445700A>C | CA338567883 | CTRC | c.743A>C (p.Lys248Thr) c.*197A>C (n.*197A>C) n.507A>C c.597A>C (p.Glu199Asp) | |
1 | g.15445700A>G | CA338567884 | CTRC | c.743A>G (p.Lys248Arg) c.*197A>G (n.*197A>G) n.507A>G c.597A>G (p.Glu199=) | ClinVar gnomAD v4 |
1 | g.15445700A>T | CA338567885 | CTRC | c.743A>T (p.Lys248Met) c.*197A>T (n.*197A>T) n.507A>T c.597A>T (p.Glu199Asp) | |
1 | g.15445701G>A | CA416207406 | CTRC | c.744G>A (p.Lys248=) c.*198G>A (n.*198G>A) n.508G>A c.598G>A (p.Ala200Thr) | ClinVar gnomAD v4 |
1 | g.15445701G>C | CA338567886 | CTRC | c.744G>C (p.Lys248Asn) c.*198G>C (n.*198G>C) n.508G>C c.598G>C (p.Ala200Pro) | |
1 | g.15445701G>T | CA338567887 | CTRC | c.744G>T (p.Lys248Asn) c.*198G>T (n.*198G>T) n.508G>T c.598G>T (p.Ala200Ser) | |
1 | g.15445702C>A | CA338567890 | CTRC | c.745C>A (p.Pro249Thr) c.*199C>A (n.*199C>A) n.509C>A c.599C>A (p.Ala200Asp) | |
1 | g.15445702C>G | CA338567889 | CTRC | c.745C>G (p.Pro249Ala) c.*199C>G (n.*199C>G) n.509C>G c.599C>G (p.Ala200Gly) | |
1 | g.15445702C>T | CA338567888 | CTRC | c.745C>T (p.Pro249Ser) c.*199C>T (n.*199C>T) n.509C>T c.599C>T (p.Ala200Val) | ClinVar gnomAD v4 |
1 | g.15445703C>A | CA338567891 | CTRC | c.746C>A (p.Pro249Gln) c.*200C>A (n.*200C>A) n.510C>A c.600C>A (p.Ala200=) | |
1 | g.15445703C= | CA1141874374 | CTRC | c.746C= (p.Pro249=) c.*200C= (n.*200C=) n.510C= c.600C= (p.Ala200=) | |
1 | g.15445703C>G | CA338567892 | CTRC | c.746C>G (p.Pro249Arg) c.*200C>G (n.*200C>G) n.510C>G c.600C>G (p.Ala200=) | gnomAD v4 |
1 | g.15445703C>T | CA613459 | CTRC | c.746C>T (p.Pro249Leu) c.*200C>T (n.*200C>T) n.510C>T c.600C>T (p.Ala200=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445704G>A | CA613460 | CTRC | c.747G>A (p.Pro249=) c.*201G>A (n.*201G>A) n.511G>A c.601G>A (p.Gly201Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445704G>C | CA416207410 | CTRC | c.747G>C (p.Pro249=) c.*201G>C (n.*201G>C) n.511G>C c.601G>C (p.Gly201Arg) | |
1 | g.15445704G= | CA1142342038 | CTRC | c.747G= (p.Pro249=) c.*201G= (n.*201G=) n.511G= c.601G= (p.Gly201=) | |
1 | g.15445704G>T | CA416207412 | CTRC | c.747G>T (p.Pro249=) c.*201G>T (n.*201G>T) n.511G>T c.601G>T (p.Gly201Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445705G>A | CA338567893 | CTRC | c.748G>A (p.Val250Ile) c.*202G>A (n.*202G>A) n.512G>A c.602G>A (p.Gly201Asp) | |
1 | g.15445705G>C | CA338567894 | CTRC | c.748G>C (p.Val250Leu) c.*202G>C (n.*202G>C) n.512G>C c.602G>C (p.Gly201Ala) | |
1 | g.15445705G>T | CA338567895 | CTRC | c.748G>T (p.Val250Leu) c.*202G>T (n.*202G>T) n.512G>T c.602G>T (p.Gly201Val) | COSMIC |
1 | g.15445706T>A | CA338567896 | CTRC | c.749T>A (p.Val250Glu) c.*203T>A (n.*203T>A) n.513T>A c.603T>A (p.Gly201=) | |
1 | g.15445706T>C | CA338567897 | CTRC | c.749T>C (p.Val250Ala) c.*203T>C (n.*203T>C) n.513T>C c.603T>C (p.Gly201=) | |
1 | g.15445706T>G | CA338567898 | CTRC | c.749T>G (p.Val250Gly) c.*203T>G (n.*203T>G) n.513T>G c.603T>G (p.Gly201=) | |
1 | g.15445707A>C | CA416207414 | CTRC | c.750A>C (p.Val250=) c.*204A>C (n.*204A>C) n.514A>C c.604A>C (p.Ser202Arg) | |
1 | g.15445707A>G | CA416207415 | CTRC | c.750A>G (p.Val250=) c.*204A>G (n.*204A>G) n.514A>G c.604A>G (p.Ser202Gly) | ClinVar |
1 | g.15445707A>T | CA416207416 | CTRC | c.750A>T (p.Val250=) c.*204A>T (n.*204A>T) n.514A>T c.604A>T (p.Ser202Cys) | ClinVar |
1 | g.15445708G>A | CA338567899 | CTRC | c.751G>A (p.Val251Ile) c.*205G>A (n.*205G>A) n.515G>A c.605G>A (p.Ser202Asn) | |
1 | g.15445708G>C | CA338567900 | CTRC | c.751G>C (p.Val251Leu) c.*205G>C (n.*205G>C) n.515G>C c.605G>C (p.Ser202Thr) | dbSNP |
1 | g.15445708G= | CA1155328716 | CTRC | c.751G= (p.Val251=) c.*205G= (n.*205G=) n.515G= c.605G= (p.Ser202=) | |
1 | g.15445708G>T | CA338567901 | CTRC | c.751G>T (p.Val251Phe) c.*205G>T (n.*205G>T) n.515G>T c.605G>T (p.Ser202Ile) | |
1 | g.15445709T>A | CA338567903 | CTRC | c.752T>A (p.Val251Asp) c.*206T>A (n.*206T>A) n.516T>A c.606T>A (p.Ser202Arg) | |
1 | g.15445709T>C | CA338567904 | CTRC | c.752T>C (p.Val251Ala) c.*206T>C (n.*206T>C) n.516T>C c.606T>C (p.Ser202=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445709T>G | CA338567902 | CTRC | c.752T>G (p.Val251Gly) c.*206T>G (n.*206T>G) n.516T>G c.606T>G (p.Ser202Arg) | |
1 | g.15445709T= | CA1155328726 | CTRC | c.752T= (p.Val251=) c.*206T= (n.*206T=) n.516T= c.606T= (p.Ser202=) | |
1 | g.15445710_15445711insAACACCCGCAAGAAGCCGGTACTC | CA521458357 | CTRC | c.753_754insAACACCCGCAAGAAGCCGGTACTC (p.Val251_Tyr252insAsnThrArgLysLysProValLeu) c.*207_*208insAACACCCGCAAGAAGCCGGTACTC (n.*207_*208insAACACCCGCAAGAAGCCGGTACTC) n.517_518insAACACCCGCAAGAAGCCGGTACTC c.607_608insAACACCCGCAAGAAGCCGGTACTC (p.Ser202_Leu203insGlnHisProGlnGluAlaGlyThr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445710C>A | CA416207418 | CTRC | c.753C>A (p.Val251=) c.*207C>A (n.*207C>A) n.517C>A c.607C>A (p.Leu203Ile) | ClinVar |
1 | g.15445710C= | CA1155328731 | CTRC | c.753C= (p.Val251=) c.*207C= (n.*207C=) n.517C= c.607C= (p.Leu203=) | |
1 | g.15445710C>G | CA416207419 | CTRC | c.753C>G (p.Val251=) c.*207C>G (n.*207C>G) n.517C>G c.607C>G (p.Leu203Val) | ClinVar dbSNP |
1 | g.15445710C>T | CA416207420 | CTRC | c.753C>T (p.Val251=) c.*207C>T (n.*207C>T) n.517C>T c.607C>T (p.Leu203=) | |
1 | g.15445711T>A | CA338567905 | CTRC | c.754T>A (p.Tyr252Asn) c.*208T>A (n.*208T>A) n.518T>A c.608T>A (p.Leu203Gln) | dbSNP |
1 | g.15445711T>C | CA338567906 | CTRC | c.754T>C (p.Tyr252His) c.*208T>C (n.*208T>C) n.518T>C c.608T>C (p.Leu203Pro) | |
1 | g.15445711T>G | CA338567907 | CTRC | c.754T>G (p.Tyr252Asp) c.*208T>G (n.*208T>G) n.518T>G c.608T>G (p.Leu203Arg) | |
1 | g.15445711T= | CA1155328734 | CTRC | c.754T= (p.Tyr252=) c.*208T= (n.*208T=) n.518T= c.608T= (p.Leu203=) | |
1 | g.15445712A= | CA1141324183 | CTRC | c.755A= (p.Tyr252=) c.*209A= (n.*209A=) n.519A= c.609A= (p.Leu203=) | |
1 | g.15445712A>C | CA338567908 | CTRC | c.755A>C (p.Tyr252Ser) c.*209A>C (n.*209A>C) n.519A>C c.609A>C (p.Leu203=) | |
1 | g.15445712A>G | CA338567909 | CTRC | c.755A>G (p.Tyr252Cys) c.*209A>G (n.*209A>G) n.519A>G c.609A>G (p.Leu203=) | |
1 | g.15445712A>T | CA18253817 | CTRC | c.755A>T (p.Tyr252Phe) c.*209A>T (n.*209A>T) n.519A>T c.609A>T (p.Leu203=) | dbSNP |
1 | g.15445713C>A | CA338567910 | CTRC | c.756C>A (p.Tyr252Ter) c.*210C>A (n.*210C>A) n.520C>A c.610C>A (p.His204Asn) | |
1 | g.15445713C>G | CA338567911 | CTRC | c.756C>G (p.Tyr252Ter) c.*210C>G (n.*210C>G) n.520C>G c.610C>G (p.His204Asp) | |
1 | g.15445713C>T | CA416207422 | CTRC | c.756C>T (p.Tyr252=) c.*210C>T (n.*210C>T) n.520C>T c.610C>T (p.His204Tyr) | ClinVar |
1 | g.15445714A= | CA1155328737 | CTRC | c.757A= (p.Thr253=) c.*211A= (n.*211A=) n.521A= c.611A= (p.His204=) | |
1 | g.15445714A>C | CA338567912 | CTRC | c.757A>C (p.Thr253Pro) c.*211A>C (n.*211A>C) n.521A>C c.611A>C (p.His204Pro) | dbSNP |
1 | g.15445714A>G | CA613461 | CTRC | c.757A>G (p.Thr253Ala) c.*211A>G (n.*211A>G) n.521A>G c.611A>G (p.His204Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445714A>T | CA338567913 | CTRC | c.757A>T (p.Thr253Ser) c.*211A>T (n.*211A>T) n.521A>T c.611A>T (p.His204Leu) | |
1 | g.15445715C>A | CA338567918 | CTRC | c.758C>A (p.Thr253Asn) c.*212C>A (n.*212C>A) n.522C>A c.612C>A (p.His204Gln) | ClinVar gnomAD v4 |
1 | g.15445715C= | CA1155328740 | CTRC | c.758C= (p.Thr253=) c.*212C= (n.*212C=) n.522C= c.612C= (p.His204=) | |
1 | g.15445715C>G | CA338567915 | CTRC | c.758C>G (p.Thr253Ser) c.*212C>G (n.*212C>G) n.522C>G c.612C>G (p.His204Gln) | |
1 | g.15445715C>T | CA613462 | CTRC | c.758C>T (p.Thr253Ile) c.*212C>T (n.*212C>T) n.522C>T c.612C>T (p.His204=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445716C>A | CA416207423 | CTRC | c.759C>A (p.Thr253=) c.*213C>A (n.*213C>A) n.523C>A c.613C>A (p.Pro205Thr) | |
1 | g.15445716C= | CA1155328746 | CTRC | c.759C= (p.Thr253=) c.*213C= (n.*213C=) n.523C= c.613C= (p.Pro205=) | |
1 | g.15445716C>G | CA416207424 | CTRC | c.759C>G (p.Thr253=) c.*213C>G (n.*213C>G) n.523C>G c.613C>G (p.Pro205Ala) | |
1 | g.15445716C>T | CA416207425 | CTRC | c.759C>T (p.Thr253=) c.*213C>T (n.*213C>T) n.523C>T c.613C>T (p.Pro205Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.15445717C>A | CA416207426 | CTRC | c.760C>A (p.Arg254=) c.*214C>A (n.*214C>A) n.524C>A c.614C>A (p.Pro205Gln) | |
1 | g.15445717C= | CA1141580597 | CTRC | c.760C= (p.Arg254=) c.*214C= (n.*214C=) n.524C= c.614C= (p.Pro205=) | |
1 | g.15445717C>G | CA338567920 | CTRC | c.760C>G (p.Arg254Gly) c.*214C>G (n.*214C>G) n.524C>G c.614C>G (p.Pro205Arg) | |
1 | g.15445717C>T | CA119351 | CTRC | c.760C>T (p.Arg254Trp) c.*214C>T (n.*214C>T) n.524C>T c.614C>T (p.Pro205Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445718G>A | CA613463 | CTRC | c.761G>A (p.Arg254Gln) c.*215G>A (n.*215G>A) n.525G>A c.615G>A (p.Pro205=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445718G>C | CA613464 | CTRC | c.761G>C (p.Arg254Pro) c.*215G>C (n.*215G>C) n.525G>C c.615G>C (p.Pro205=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445718G= | CA1155328764 | CTRC | c.761G= (p.Arg254=) c.*215G= (n.*215G=) n.525G= c.615G= (p.Pro205=) | |
1 | g.15445718G>T | CA338567926 | CTRC | c.761G>T (p.Arg254Leu) c.*215G>T (n.*215G>T) n.525G>T c.615G>T (p.Pro205=) | |
1 | g.15445720del | CA2500775821 | CTRC | c.763del (p.Val255CysfsTer?) c.*217del (n.*217del) n.527del c.617del (p.Gly206ValfsTer15) | gnomAD v4 |
1 | g.15445719G>A | CA416207430 | CTRC | c.762G>A (p.Arg254=) c.*216G>A (n.*216G>A) n.526G>A c.616G>A (p.Gly206Ser) | ClinVar |
1 | g.15445719G>C | CA416207431 | CTRC | c.762G>C (p.Arg254=) c.*216G>C (n.*216G>C) n.526G>C c.616G>C (p.Gly206Arg) | ClinVar |
1 | g.15445719G= | CA1149038692 | CTRC | c.762G= (p.Arg254=) c.*216G= (n.*216G=) n.526G= c.616G= (p.Gly206=) | |
1 | g.15445719G>T | CA613465 | CTRC | c.762G>T (p.Arg254=) c.*216G>T (n.*216G>T) n.526G>T c.616G>T (p.Gly206Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445720G>A | CA18253843 | CTRC | c.763G>A (p.Val255Met) c.*217G>A (n.*217G>A) n.527G>A c.617G>A (p.Gly206Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.15445720G>C | CA338567934 | CTRC | c.763G>C (p.Val255Leu) c.*217G>C (n.*217G>C) n.527G>C c.617G>C (p.Gly206Ala) | ClinVar |
1 | g.15445720G= | CA1141199444 | CTRC | c.763G= (p.Val255=) c.*217G= (n.*217G=) n.527G= c.617G= (p.Gly206=) | |
1 | g.15445720G>T | CA338567935 | CTRC | c.763G>T (p.Val255Leu) c.*217G>T (n.*217G>T) n.527G>T c.617G>T (p.Gly206Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.15445721T>A | CA338567938 | CTRC | c.764T>A (p.Val255Glu) c.*218T>A (n.*218T>A) n.528T>A c.618T>A (p.Gly206=) | ClinVar dbSNP gnomAD v4 |
1 | g.15445721T>C | CA338567939 | CTRC | c.764T>C (p.Val255Ala) c.*218T>C (n.*218T>C) n.528T>C c.618T>C (p.Gly206=) | |
1 | g.15445721T>G | CA338567942 | CTRC | c.764T>G (p.Val255Gly) c.*218T>G (n.*218T>G) n.528T>G c.618T>G (p.Gly206=) | ClinVar dbSNP |
1 | g.15445721T= | CA1155328779 | CTRC | c.764T= (p.Val255=) c.*218T= (n.*218T=) n.528T= c.618T= (p.Gly206=) | |
1 | g.15445722G>A | CA416207433 | CTRC | c.765G>A (p.Val255=) c.*219G>A (n.*219G>A) n.529G>A c.619G>A (p.Val207Ile) | ClinVar dbSNP gnomAD v4 |
1 | g.15445722G>C | CA416207435 | CTRC | c.765G>C (p.Val255=) c.*219G>C (n.*219G>C) n.529G>C c.619G>C (p.Val207Leu) | |
1 | g.15445722G= | CA1155328781 | CTRC | c.765G= (p.Val255=) c.*219G= (n.*219G=) n.529G= c.619G= (p.Val207=) | |
1 | g.15445722G>T | CA416207434 | CTRC | c.765G>T (p.Val255=) c.*219G>T (n.*219G>T) n.529G>T c.619G>T (p.Val207Phe) | |
1 | g.15445723T>A | CA338567950 | CTRC | c.766T>A (p.Ser256Thr) c.*220T>A (n.*220T>A) n.530T>A c.620T>A (p.Val207Asp) | |
1 | g.15445723T>C | CA338567948 | CTRC | c.766T>C (p.Ser256Pro) c.*220T>C (n.*220T>C) n.530T>C c.620T>C (p.Val207Ala) | |
1 | g.15445723T>G | CA338567947 | CTRC | c.766T>G (p.Ser256Ala) c.*220T>G (n.*220T>G) n.530T>G c.620T>G (p.Val207Gly) | |
1 | g.15445724C>A | CA338567953 | CTRC | c.767C>A (p.Ser256Tyr) c.*221C>A (n.*221C>A) n.531C>A c.621C>A (p.Val207=) | |
1 | g.15445724C= | CA1155328787 | CTRC | c.767C= (p.Ser256=) c.*221C= (n.*221C=) n.531C= c.621C= (p.Val207=) | |
1 | g.15445724C>G | CA613466 | CTRC | c.767C>G (p.Ser256Cys) c.*221C>G (n.*221C>G) n.531C>G c.621C>G (p.Val207=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.15445724C>T | CA338567956 | CTRC | c.767C>T (p.Ser256Phe) c.*221C>T (n.*221C>T) n.531C>T c.621C>T (p.Val207=) | |
1 | g.15445725C>A | CA416207440 | CTRC | c.768C>A (p.Ser256=) c.*222C>A (n.*222C>A) n.532C>A c.622C>A (p.Arg208Ser) | |
1 | g.15445725C= | CA1155328792 | CTRC | c.768C= (p.Ser256=) c.*222C= (n.*222C=) n.532C= c.622C= (p.Arg208=) | |
1 | g.15445725C>G | CA416207438 | CTRC | c.768C>G (p.Ser256=) c.*222C>G (n.*222C>G) n.532C>G c.622C>G (p.Arg208Gly) | |
1 | g.15445725C>T | CA613467 | CTRC | c.768C>T (p.Ser256=) c.*222C>T (n.*222C>T) n.532C>T c.622C>T (p.Arg208Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |