Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7669589_7676614del | CA2499224945 | TP53 | c.-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 |
17 | g.7669609_7676594del | CA2581463470 | TP53 | c.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 | |
17 | g.7673635_7673845del | CA645587395 | TP53 | c.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 |
17 | g.7673799_7673834dup | CA891842234 | TP53 | c.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) | |
17 | g.7673802_7674193del | CA645588414 | TP53 | c.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 |
17 | g.7673811_7673837del | CA645588432 | TP53 | c.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 |
17 | g.7673813_7673836del | CA645588435 | TP53 | c.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 |
17 | g.7673814_7673836del | CA645588437 | TP53 | c.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 |
17 | g.7673816_7673839del | CA645588436 | TP53 | c.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 |
17 | g.7673818_7673848del | CA645588440 | TP53 | c.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 |
17 | g.7673822_7673845del | CA2576230624 | TP53 | c.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 | |
17 | g.7673827_7673837del | CA645588449 | TP53 | c.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 |
17 | g.7673828_7673830del | CA645588451 | TP53 | c.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 |
17 | g.7673830_7673834del | CA645588456 | TP53 | c.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 |
17 | g.7673830_7673840del | CA645588457 | TP53 | c.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 |
17 | g.7673829_7673842del | CA2580094808 | TP53 | c.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 |
17 | g.7673829_7673830delinsAG | CA2245950279 | TP53 | c.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=) | |
17 | g.7673829_7673837del | CA645588460 | TP53 | c.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 |
17 | g.7673831_7673845dup | CA645588459 | TP53 | c.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 |
17 | g.7673830_7673847del | CA891842237 | TP53 | c.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 | |
17 | g.7673830del | CA16615995 | TP53 | c.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 |
17 | g.7673830G>A | CA497716496 | TP53 | c.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 |
17 | g.7673830G>C | CA397837206 | TP53 | c.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 |
17 | g.7673830G= | CA2245950306 | TP53 | c.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=) | |
17 | g.7673830G>T | CA397837207 | TP53 | c.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 |
17 | g.7673831del | CA645588462 | TP53 | c.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 |
17 | g.7673831A= | CA2245950323 | TP53 | c.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=) | |
17 | g.7673831A>C | CA397837208 | TP53 | c.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 |
17 | g.7673831A>G | CA001572 | TP53 | c.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 |
17 | g.7673831A>T | CA397837212 | TP53 | c.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 |
17 | g.7673831_7673832delinsAT | CA2245950318 | TP53 | c.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=) | |
17 | g.7673832T>A | CA397837220 | TP53 | c.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 |
17 | g.7673832T>C | CA397837224 | TP53 | c.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 |
17 | g.7673832T>G | CA397837226 | TP53 | c.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 |
17 | g.7673832T= | CA2245950333 | TP53 | c.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=) | |
17 | g.7673833del | CA497716507 | TP53 | c.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 |
17 | g.7673833_7673842dup | CA2635875226 | TP53 | c.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 |
17 | g.7673833T>A | CA397837239 | TP53 | c.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 |
17 | g.7673833T>C | CA000419 | TP53 | c.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 |
17 | g.7673833T>G | CA397837248 | TP53 | c.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 |
17 | g.7673833T= | CA2245950345 | TP53 | c.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=) | |
17 | g.7673833_7673834delinsGT | CA645588463 | TP53 | c.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 |
17 | g.7673833_7673836delinsTACC | CA2245950351 | TP53 | c.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=) | |
17 | g.7673834del | CA2573154644 | TP53 | c.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 |
17 | g.7673834A>C | CA497716530 | TP53 | c.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=) | |
17 | g.7673834A>G | CA497716528 | TP53 | c.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 |
17 | g.7673834A>T | CA497716533 | TP53 | c.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=) | |
17 | g.7673834_7673835delinsAC | CA2245950361 | TP53 | c.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=) | |
17 | g.7673836_7673838del | CA645588464 | TP53 | c.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 |
17 | g.7673835C>A | CA397837253 | TP53 | c.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 |