Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7669589_7676614delCA2499224945TP53c.-19_*21del
c.-21-1377_*21del
c.-19_*310del
c.-19_*222del
c.-253_*21del
c.-136_*222del
c.-136_*21del
c.-136_*310del
c.-136_983+1021del
ClinVar
17g.7669609_7676594delCA2581463470TP53c.1_1182del
c.-21-1358_786del
c.1_903del
c.1_1161del
c.1_994-3365del
c.1_782+4572del
c.1_*289del
c.1_*201del
c.-234_1065del
c.-117_*201del
c.1_1149del
c.-117_1065del
c.-117_*289del
c.-117_983+1000del
17g.7673635_7673845delCA645587395TP53c.783-8_920-27del
c.387-8_524-27del
c.504-8_641-27del
c.762-8_899-27del
c.782+336_782+546del (n.782+336_782+546del)
c.666-8_803-27del
c.306-8_443-27del
c.750-8_887-27del
COSMIC
17g.7673799_7673834dupCA891842234TP53c.787_822dup (p.Val274_Cys275insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
c.391_426dup (p.Val142_Cys143insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
c.508_543dup (p.Val181_Cys182insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
c.766_801dup (p.Val267_Cys268insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
c.782+348_782+383dup (n.782+348_782+383dup)
c.670_705dup (p.Val235_Cys236insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
c.310_345dup (p.Val115_Cys116insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
c.754_789dup (p.Val263_Cys264insAsnLeuLeuGlyArgAsnSerPheGluValArgVal)
17g.7673802_7674193delCA645588414TP53c.772_820del
c.376_424del
c.493_541del
c.751_799del
c.772_782+381del
c.655_703del
c.295_343del
c.739_787del
COSMIC
17g.7673811_7673837delCA645588432TP53c.785_811del (p.Gly262_Phe270del)
c.389_415del (p.Gly130_Phe138del)
c.506_532del (p.Gly169_Phe177del)
c.764_790del (p.Gly255_Phe263del)
c.782+346_782+372del (n.782+346_782+372del)
c.668_694del (p.Gly223_Phe231del)
c.308_334del (p.Gly103_Phe111del)
c.752_778del (p.Gly251_Phe259del)
COSMIC
17g.7673813_7673836delCA645588435TP53c.784_807del (p.Gly262_Ser269del)
c.388_411del (p.Gly130_Ser137del)
c.505_528del (p.Gly169_Ser176del)
c.763_786del (p.Gly255_Ser262del)
c.782+345_782+368del (n.782+345_782+368del)
c.667_690del (p.Gly223_Ser230del)
c.307_330del (p.Gly103_Ser110del)
c.751_774del (p.Gly251_Ser258del)
COSMIC
17g.7673814_7673836delCA645588437TP53c.784_806del (p.Gly262LeufsTer2)
c.388_410del (p.Gly130LeufsTer2)
c.505_527del (p.Gly169LeufsTer2)
c.763_785del (p.Gly255LeufsTer2)
c.782+345_782+367del (n.782+345_782+367del)
c.667_689del (p.Gly223LeufsTer2)
c.307_329del (p.Gly103LeufsTer2)
c.751_773del (p.Gly251LeufsTer2)
COSMIC
17g.7673816_7673839delCA645588436TP53c.783_806del
c.387_410del
c.504_527del
c.762_785del
c.782+344_782+367del (n.782+344_782+367del)
c.666_689del
c.306_329del
c.750_773del
COSMIC
17g.7673818_7673848delCA645588440TP53c.783-10_803del
c.387-10_407del
c.504-10_524del
c.762-10_782del
c.782+334_782+364del (n.782+334_782+364del)
c.666-10_686del
c.306-10_326del
c.750-10_770del
COSMIC
17g.7673822_7673845delCA2576230624TP53c.783-7_799del
c.387-7_403del
c.504-7_520del
c.762-7_778del
c.782+337_782+360del (n.782+337_782+360del)
c.666-7_682del
c.306-7_322del
c.750-7_766del
17g.7673827_7673837delCA645588449TP53c.786_796del (p.Asn263ThrfsTer5)
c.390_400del (p.Asn131ThrfsTer5)
c.507_517del (p.Asn170ThrfsTer5)
c.765_775del (p.Asn256ThrfsTer5)
c.782+347_782+357del (n.782+347_782+357del)
c.669_679del (p.Asn224ThrfsTer5)
c.309_319del (p.Asn104ThrfsTer5)
c.753_763del (p.Asn252ThrfsTer5)
COSMIC
17g.7673828_7673830delCA645588451TP53c.792_794del (p.Leu265del)
c.396_398del (p.Leu133del)
c.513_515del (p.Leu172del)
c.771_773del (p.Leu258del)
c.782+353_782+355del (n.782+353_782+355del)
c.675_677del (p.Leu226del)
c.315_317del (p.Leu106del)
c.759_761del (p.Leu254del)
gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7673830_7673834delCA645588456TP53c.788_792del (p.Asn263ThrfsTer7)
c.392_396del (p.Asn131ThrfsTer7)
c.509_513del (p.Asn170ThrfsTer7)
c.767_771del (p.Asn256ThrfsTer7)
c.782+349_782+353del (n.782+349_782+353del)
c.671_675del (p.Asn224ThrfsTer7)
c.311_315del (p.Asn104ThrfsTer7)
c.755_759del (p.Asn252ThrfsTer7)
COSMIC COSMIC COSMIC COSMIC
17g.7673830_7673840delCA645588457TP53c.783-1_792del
c.387-1_396del
c.504-1_513del
c.762-1_771del
c.782+343_782+353del (n.782+343_782+353del)
c.666-1_675del
c.306-1_315del
c.750-1_759del
COSMIC COSMIC
17g.7673829_7673842delCA2580094808TP53c.783-4_792del
c.387-4_396del
c.504-4_513del
c.762-4_771del
c.782+340_782+353del (n.782+340_782+353del)
c.666-4_675del
c.306-4_315del
c.750-4_759del
ClinVar
17g.7673829_7673830delinsAGCA2245950279TP53c.790_791delinsCT (p.Leu264=)
c.394_395delinsCT (p.Leu132=)
c.511_512delinsCT (p.Leu171=)
c.769_770delinsCT (p.Leu257=)
c.782+351_782+352delinsCT (n.782+351_782+352delinsCT)
c.673_674delinsCT (p.Leu225=)
c.313_314delinsCT (p.Leu105=)
c.757_758delinsCT (p.Leu253=)
17g.7673829_7673837delCA645588460TP53c.783_791del (p.Ser261_Leu264delinsArg)
c.387_395del (p.Ser129_Leu132delinsArg)
c.504_512del (p.Ser168_Leu171delinsArg)
c.762_770del (p.Ser254_Leu257delinsArg)
c.782+344_782+352del (n.782+344_782+352del)
c.666_674del (p.Ser222_Leu225delinsArg)
c.306_314del (p.Ser102_Leu105delinsArg)
c.750_758del (p.Ser250_Leu253delinsArg)
COSMIC
17g.7673831_7673845dupCA645588459TP53c.783-6_791dup
c.387-6_395dup
c.504-6_512dup
c.762-6_770dup
c.782+338_782+352dup (n.782+338_782+352dup)
c.666-6_674dup
c.306-6_314dup
c.750-6_758dup
COSMIC
17g.7673830_7673847delCA891842237TP53c.783-9_791del
c.387-9_395del
c.504-9_512del
c.762-9_770del
c.782+335_782+352del (n.782+335_782+352del)
c.666-9_674del
c.306-9_314del
c.750-9_758del
17g.7673830delCA16615995TP53c.790del (p.Leu264TyrfsTer?)
c.394del (p.Leu132TyrfsTer?)
c.511del (p.Leu171TyrfsTer?)
c.769del (p.Leu257TyrfsTer?)
c.782+351del (n.782+351del)
c.673del (p.Leu225TyrfsTer?)
c.313del (p.Leu105TyrfsTer?)
c.757del (p.Leu253TyrfsTer?)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673830G>ACA497716496TP53c.790C>T (p.Leu264=)
c.394C>T (p.Leu132=)
c.511C>T (p.Leu171=)
c.769C>T (p.Leu257=)
c.782+351C>T (n.782+351C>T)
c.673C>T (p.Leu225=)
c.313C>T (p.Leu105=)
c.757C>T (p.Leu253=)
ClinVar dbSNP gnomAD v4 COSMIC
17g.7673830G>CCA397837206TP53c.790C>G (p.Leu264Val)
c.394C>G (p.Leu132Val)
c.511C>G (p.Leu171Val)
c.769C>G (p.Leu257Val)
c.782+351C>G (n.782+351C>G)
c.673C>G (p.Leu225Val)
c.313C>G (p.Leu105Val)
c.757C>G (p.Leu253Val)
dbSNP COSMIC
17g.7673830G=CA2245950306TP53c.790C= (p.Leu264=)
c.394C= (p.Leu132=)
c.511C= (p.Leu171=)
c.769C= (p.Leu257=)
c.782+351C= (n.782+351C=)
c.673C= (p.Leu225=)
c.313C= (p.Leu105=)
c.757C= (p.Leu253=)
17g.7673830G>TCA397837207TP53c.790C>A (p.Leu264Ile)
c.394C>A (p.Leu132Ile)
c.511C>A (p.Leu171Ile)
c.769C>A (p.Leu257Ile)
c.782+351C>A (n.782+351C>A)
c.673C>A (p.Leu225Ile)
c.313C>A (p.Leu105Ile)
c.757C>A (p.Leu253Ile)
ClinVar dbSNP COSMIC
17g.7673831delCA645588462TP53c.789del (p.Leu264TyrfsTer?)
c.393del (p.Leu132TyrfsTer?)
c.510del (p.Leu171TyrfsTer?)
c.768del (p.Leu257TyrfsTer?)
c.782+350del (n.782+350del)
c.672del (p.Leu225TyrfsTer?)
c.312del (p.Leu105TyrfsTer?)
c.756del (p.Leu253TyrfsTer?)
COSMIC COSMIC COSMIC COSMIC
17g.7673831A=CA2245950323TP53c.789T= (p.Asn263=)
c.393T= (p.Asn131=)
c.510T= (p.Asn170=)
c.768T= (p.Asn256=)
c.782+350T= (n.782+350T=)
c.672T= (p.Asn224=)
c.312T= (p.Asn104=)
c.756T= (p.Asn252=)
17g.7673831A>CCA397837208TP53c.789T>G (p.Asn263Lys)
c.393T>G (p.Asn131Lys)
c.510T>G (p.Asn170Lys)
c.768T>G (p.Asn256Lys)
c.782+350T>G (n.782+350T>G)
c.672T>G (p.Asn224Lys)
c.312T>G (p.Asn104Lys)
c.756T>G (p.Asn252Lys)
COSMIC
17g.7673831A>GCA001572TP53c.789T>C (p.Asn263=)
c.393T>C (p.Asn131=)
c.510T>C (p.Asn170=)
c.768T>C (p.Asn256=)
c.782+350T>C (n.782+350T>C)
c.672T>C (p.Asn224=)
c.312T>C (p.Asn104=)
c.756T>C (p.Asn252=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673831A>TCA397837212TP53c.789T>A (p.Asn263Lys)
c.393T>A (p.Asn131Lys)
c.510T>A (p.Asn170Lys)
c.768T>A (p.Asn256Lys)
c.782+350T>A (n.782+350T>A)
c.672T>A (p.Asn224Lys)
c.312T>A (p.Asn104Lys)
c.756T>A (p.Asn252Lys)
ClinVar dbSNP
17g.7673831_7673832delinsATCA2245950318TP53c.788_789delinsAT (p.Asn263=)
c.392_393delinsAT (p.Asn131=)
c.509_510delinsAT (p.Asn170=)
c.767_768delinsAT (p.Asn256=)
c.782+349_782+350delinsAT (n.782+349_782+350delinsAT)
c.671_672delinsAT (p.Asn224=)
c.311_312delinsAT (p.Asn104=)
c.755_756delinsAT (p.Asn252=)
17g.7673832T>ACA397837220TP53c.788A>T (p.Asn263Ile)
c.392A>T (p.Asn131Ile)
c.509A>T (p.Asn170Ile)
c.767A>T (p.Asn256Ile)
c.782+349A>T (n.782+349A>T)
c.671A>T (p.Asn224Ile)
c.311A>T (p.Asn104Ile)
c.755A>T (p.Asn252Ile)
dbSNP COSMIC
17g.7673832T>CCA397837224TP53c.788A>G (p.Asn263Ser)
c.392A>G (p.Asn131Ser)
c.509A>G (p.Asn170Ser)
c.767A>G (p.Asn256Ser)
c.782+349A>G (n.782+349A>G)
c.671A>G (p.Asn224Ser)
c.311A>G (p.Asn104Ser)
c.755A>G (p.Asn252Ser)
ClinVar dbSNP
17g.7673832T>GCA397837226TP53c.788A>C (p.Asn263Thr)
c.392A>C (p.Asn131Thr)
c.509A>C (p.Asn170Thr)
c.767A>C (p.Asn256Thr)
c.782+349A>C (n.782+349A>C)
c.671A>C (p.Asn224Thr)
c.311A>C (p.Asn104Thr)
c.755A>C (p.Asn252Thr)
dbSNP
17g.7673832T=CA2245950333TP53c.788A= (p.Asn263=)
c.392A= (p.Asn131=)
c.509A= (p.Asn170=)
c.767A= (p.Asn256=)
c.782+349A= (n.782+349A=)
c.671A= (p.Asn224=)
c.311A= (p.Asn104=)
c.755A= (p.Asn252=)
17g.7673833delCA497716507TP53c.788del (p.Asn263IlefsTer?)
c.392del (p.Asn131IlefsTer?)
c.509del (p.Asn170IlefsTer?)
c.767del (p.Asn256IlefsTer?)
c.782+349del (n.782+349del)
c.671del (p.Asn224IlefsTer?)
c.311del (p.Asn104IlefsTer?)
c.755del (p.Asn252IlefsTer?)
ClinVar dbSNP COSMIC
17g.7673833_7673842dupCA2635875226TP53c.783-4_788dup
c.387-4_392dup
c.504-4_509dup
c.762-4_767dup
c.782+340_782+349dup (n.782+340_782+349dup)
c.666-4_671dup
c.306-4_311dup
c.750-4_755dup
gnomAD v4
17g.7673833T>ACA397837239TP53c.787A>T (p.Asn263Tyr)
c.391A>T (p.Asn131Tyr)
c.508A>T (p.Asn170Tyr)
c.766A>T (p.Asn256Tyr)
c.782+348A>T (n.782+348A>T)
c.670A>T (p.Asn224Tyr)
c.310A>T (p.Asn104Tyr)
c.754A>T (p.Asn252Tyr)
ClinVar dbSNP
17g.7673833T>CCA000419TP53c.787A>G (p.Asn263Asp)
c.391A>G (p.Asn131Asp)
c.508A>G (p.Asn170Asp)
c.766A>G (p.Asn256Asp)
c.782+348A>G (n.782+348A>G)
c.670A>G (p.Asn224Asp)
c.310A>G (p.Asn104Asp)
c.754A>G (p.Asn252Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673833T>GCA397837248TP53c.787A>C (p.Asn263His)
c.391A>C (p.Asn131His)
c.508A>C (p.Asn170His)
c.766A>C (p.Asn256His)
c.782+348A>C (n.782+348A>C)
c.670A>C (p.Asn224His)
c.310A>C (p.Asn104His)
c.754A>C (p.Asn252His)
ClinVar dbSNP COSMIC
17g.7673833T=CA2245950345TP53c.787A= (p.Asn263=)
c.391A= (p.Asn131=)
c.508A= (p.Asn170=)
c.766A= (p.Asn256=)
c.782+348A= (n.782+348A=)
c.670A= (p.Asn224=)
c.310A= (p.Asn104=)
c.754A= (p.Asn252=)
17g.7673833_7673834delinsGTCA645588463TP53c.786_787delinsAC (p.Asn263His)
c.390_391delinsAC (p.Asn131His)
c.507_508delinsAC (p.Asn170His)
c.765_766delinsAC (p.Asn256His)
c.782+347_782+348delinsAC (n.782+347_782+348delinsAC)
c.669_670delinsAC (p.Asn224His)
c.309_310delinsAC (p.Asn104His)
c.753_754delinsAC (p.Asn252His)
COSMIC
17g.7673833_7673836delinsTACCCA2245950351TP53c.784_787delinsGGTA (p.Gly262=)
c.388_391delinsGGTA (p.Gly130=)
c.505_508delinsGGTA (p.Gly169=)
c.763_766delinsGGTA (p.Gly255=)
c.782+345_782+348delinsGGTA (n.782+345_782+348delinsGGTA)
c.667_670delinsGGTA (p.Gly223=)
c.307_310delinsGGTA (p.Gly103=)
c.751_754delinsGGTA (p.Gly251=)
17g.7673834delCA2573154644TP53c.786del (p.Asn263IlefsTer?)
c.390del (p.Asn131IlefsTer?)
c.507del (p.Asn170IlefsTer?)
c.765del (p.Asn256IlefsTer?)
c.782+347del (n.782+347del)
c.669del (p.Asn224IlefsTer?)
c.309del (p.Asn104IlefsTer?)
c.753del (p.Asn252IlefsTer?)
ClinVar dbSNP
17g.7673834A>CCA497716530TP53c.786T>G (p.Gly262=)
c.390T>G (p.Gly130=)
c.507T>G (p.Gly169=)
c.765T>G (p.Gly255=)
c.782+347T>G (n.782+347T>G)
c.669T>G (p.Gly223=)
c.309T>G (p.Gly103=)
c.753T>G (p.Gly251=)
17g.7673834A>GCA497716528TP53c.786T>C (p.Gly262=)
c.390T>C (p.Gly130=)
c.507T>C (p.Gly169=)
c.765T>C (p.Gly255=)
c.782+347T>C (n.782+347T>C)
c.669T>C (p.Gly223=)
c.309T>C (p.Gly103=)
c.753T>C (p.Gly251=)
COSMIC
17g.7673834A>TCA497716533TP53c.786T>A (p.Gly262=)
c.390T>A (p.Gly130=)
c.507T>A (p.Gly169=)
c.765T>A (p.Gly255=)
c.782+347T>A (n.782+347T>A)
c.669T>A (p.Gly223=)
c.309T>A (p.Gly103=)
c.753T>A (p.Gly251=)
17g.7673834_7673835delinsACCA2245950361TP53c.785_786delinsGT (p.Gly262=)
c.389_390delinsGT (p.Gly130=)
c.506_507delinsGT (p.Gly169=)
c.764_765delinsGT (p.Gly255=)
c.782+346_782+347delinsGT (n.782+346_782+347delinsGT)
c.668_669delinsGT (p.Gly223=)
c.308_309delinsGT (p.Gly103=)
c.752_753delinsGT (p.Gly251=)
17g.7673836_7673838delCA645588464TP53c.784_786del
c.388_390del
c.505_507del
c.763_765del
c.782+345_782+347del (n.782+345_782+347del)
c.667_669del
c.307_309del
c.751_753del
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673835C>ACA397837253TP53c.785G>T (p.Gly262Val)
c.389G>T (p.Gly130Val)
c.506G>T (p.Gly169Val)
c.764G>T (p.Gly255Val)
c.782+346G>T (n.782+346G>T)
c.668G>T (p.Gly223Val)
c.308G>T (p.Gly103Val)
c.752G>T (p.Gly251Val)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched