| 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.7674218_7674967del | CA645588534 | TP53 | c.569_750del c.173_354del c.290_471del c.548_729del c.452_633del c.92_273del c.536_717del | COSMIC COSMIC COSMIC |
| 17 | g.7674838_7674882del | CA645588698 | TP53 | c.649_672+21del c.253_276+21del c.370_393+21del c.628_651+21del n.905_949del n.67+171_67+215del c.532_555+21del c.172_195+21del c.616_639+21del | COSMIC |
| 17 | g.7674856_7674884del | CA645588704 | TP53 | c.651_672+7del c.255_276+7del c.372_393+7del c.630_651+7del n.907_935del n.67+173_67+201del c.534_555+7del c.174_195+7del c.618_639+7del | COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674860_7674880dup | CA1139665121 | TP53 | c.654_672+2dup c.258_276+2dup c.375_393+2dup c.633_651+2dup n.910_930dup n.67+176_67+196dup c.537_555+2dup c.177_195+2dup c.621_639+2dup | ClinVar dbSNP |
| 17 | g.7674860_7674880del | CA645588706 | TP53 | c.654_672+2del c.258_276+2del c.375_393+2del c.633_651+2del n.910_930del n.67+176_67+196del c.537_555+2del c.177_195+2del c.621_639+2del | COSMIC |
| 17 | g.7674860_7674870del | CA645588709 | TP53 | c.662_672del (p.Glu221GlyfsTer4) c.266_276del (p.Glu89GlyfsTer4) c.383_393del (p.Glu128GlyfsTer4) c.641_651del (p.Glu214GlyfsTer4) n.918_928del n.67+184_67+194del c.545_555del (p.Glu182GlyfsTer4) c.185_195del (p.Glu62GlyfsTer4) c.629_639del (p.Glu210GlyfsTer4) | COSMIC |
| 17 | g.7674861_7676624dup | CA2573130640 | TP53 | c.-28_672dup c.-21-1386_276dup c.-28_393dup c.-28_651dup c.-25-3_672dup n.112_928dup c.-262_555dup c.-145_555dup c.-142-3_555dup | ClinVar |
| 17 | g.7674860_7674876delinsTCAGGCGGCTCATAGGG | CA2245953899 | TP53 | c.655_671delinsCCCTATGAGCCGCCTGA (p.Pro219=) c.259_275delinsCCCTATGAGCCGCCTGA (p.Pro87=) c.376_392delinsCCCTATGAGCCGCCTGA (p.Pro126=) c.634_650delinsCCCTATGAGCCGCCTGA (p.Pro212=) n.911_927delinsCCCTATGAGCCGCCTGA n.67+177_67+193delinsCCCTATGAGCCGCCTGA c.538_554delinsCCCTATGAGCCGCCTGA (p.Pro180=) c.178_194delinsCCCTATGAGCCGCCTGA (p.Pro60=) c.622_638delinsCCCTATGAGCCGCCTGA (p.Pro208=) | |
| 17 | g.7674861_7674868del | CA645588711 | TP53 | c.663_670del (p.Pro222GlyfsTer4) c.267_274del (p.Pro90GlyfsTer4) c.384_391del (p.Pro129GlyfsTer4) c.642_649del (p.Pro215GlyfsTer4) n.919_926del n.67+185_67+192del c.546_553del (p.Pro183GlyfsTer4) c.186_193del (p.Pro63GlyfsTer4) c.630_637del (p.Pro211GlyfsTer4) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674863_7674878del | CA658656530 | TP53 | c.655_670del (p.Pro219ArgfsTer23) c.259_274del (p.Pro87ArgfsTer23) c.376_391del (p.Pro126ArgfsTer23) c.634_649del (p.Pro212ArgfsTer23) n.911_926del n.67+177_67+192del c.538_553del (p.Pro180ArgfsTer23) c.178_193del (p.Pro60ArgfsTer23) c.622_637del (p.Pro208ArgfsTer23) | ClinVar dbSNP |
| 17 | g.7674862_7674874delinsAGGCGGCTCATAG | CA2245953922 | TP53 | c.657_669delinsCTATGAGCCGCCT (p.Pro219=) c.261_273delinsCTATGAGCCGCCT (p.Pro87=) c.378_390delinsCTATGAGCCGCCT (p.Pro126=) c.636_648delinsCTATGAGCCGCCT (p.Pro212=) n.913_925delinsCTATGAGCCGCCT n.67+179_67+191delinsCTATGAGCCGCCT c.540_552delinsCTATGAGCCGCCT (p.Pro180=) c.180_192delinsCTATGAGCCGCCT (p.Pro60=) c.624_636delinsCTATGAGCCGCCT (p.Pro208=) | |
| 17 | g.7674864_7674867del | CA645588714 | TP53 | c.665_668del (p.Pro222LeufsTer24) c.269_272del (p.Pro90LeufsTer24) c.386_389del (p.Pro129LeufsTer24) c.644_647del (p.Pro215LeufsTer24) n.921_924del n.67+187_67+190del c.548_551del (p.Pro183LeufsTer24) c.188_191del (p.Pro63LeufsTer24) c.632_635del (p.Pro211LeufsTer24) | COSMIC |
| 17 | g.7674866_7674877del | CA10580929 | TP53 | c.657_668del (p.Tyr220_Pro223del) c.261_272del (p.Tyr88_Pro91del) c.378_389del (p.Tyr127_Pro130del) c.636_647del (p.Tyr213_Pro216del) n.913_924del n.67+179_67+190del c.540_551del (p.Tyr181_Pro184del) c.180_191del (p.Tyr61_Pro64del) c.624_635del (p.Tyr209_Pro212del) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674865_7674866del | CA645588716 | TP53 | c.666_667del (p.Pro223Ter) c.270_271del (p.Pro91Ter) c.387_388del (p.Pro130Ter) c.645_646del (p.Pro216Ter) n.922_923del n.67+188_67+189del c.549_550del (p.Pro184Ter) c.189_190del (p.Pro64Ter) c.633_634del (p.Pro212Ter) | COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674864_7674870dup | CA645588715 | TP53 | c.661_667dup (p.Pro223ArgfsTer4) c.265_271dup (p.Pro91ArgfsTer4) c.382_388dup (p.Pro130ArgfsTer4) c.640_646dup (p.Pro216ArgfsTer4) n.917_923dup n.67+183_67+189dup c.544_550dup (p.Pro184ArgfsTer4) c.184_190dup (p.Pro64ArgfsTer4) c.628_634dup (p.Pro212ArgfsTer4) | COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674864_7674880delinsGCGGCTCATAGGGCACC | CA2245953948 | TP53 | c.651_667delinsGGTGCCCTATGAGCCGC (p.Val217=) c.255_271delinsGGTGCCCTATGAGCCGC (p.Val85=) c.372_388delinsGGTGCCCTATGAGCCGC (p.Val124=) c.630_646delinsGGTGCCCTATGAGCCGC (p.Val210=) n.907_923delinsGGTGCCCTATGAGCCGC n.67+173_67+189delinsGGTGCCCTATGAGCCGC c.534_550delinsGGTGCCCTATGAGCCGC (p.Val178=) c.174_190delinsGGTGCCCTATGAGCCGC (p.Val58=) c.618_634delinsGGTGCCCTATGAGCCGC (p.Val206=) | |
| 17 | g.7674865C>A | CA000321 | TP53 | c.666G>T (p.Pro222=) c.270G>T (p.Pro90=) c.387G>T (p.Pro129=) c.645G>T (p.Pro215=) n.922G>T n.67+188G>T c.549G>T (p.Pro183=) c.189G>T (p.Pro63=) c.633G>T (p.Pro211=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.7674865C= | CA2245953968 | TP53 | c.666G= (p.Pro222=) c.270G= (p.Pro90=) c.387G= (p.Pro129=) c.645G= (p.Pro215=) n.922G= n.67+188G= c.549G= (p.Pro183=) c.189G= (p.Pro63=) c.633G= (p.Pro211=) | |
| 17 | g.7674865C>G | CA497925280 | TP53 | c.666G>C (p.Pro222=) c.270G>C (p.Pro90=) c.387G>C (p.Pro129=) c.645G>C (p.Pro215=) n.922G>C n.67+188G>C c.549G>C (p.Pro183=) c.189G>C (p.Pro63=) c.633G>C (p.Pro211=) | dbSNP gnomAD v4 COSMIC |
| 17 | g.7674865C>T | CA000319 | TP53 | c.666G>A (p.Pro222=) c.270G>A (p.Pro90=) c.387G>A (p.Pro129=) c.645G>A (p.Pro215=) n.922G>A n.67+188G>A c.549G>A (p.Pro183=) c.189G>A (p.Pro63=) c.633G>A (p.Pro211=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.7674865_7674866delinsCG | CA2245953962 | TP53 | c.665_666delinsCG (p.Pro222=) c.269_270delinsCG (p.Pro90=) c.386_387delinsCG (p.Pro129=) c.644_645delinsCG (p.Pro215=) n.921_922delinsCG n.67+187_67+188delinsCG c.548_549delinsCG (p.Pro183=) c.188_189delinsCG (p.Pro63=) c.632_633delinsCG (p.Pro211=) | |
| 17 | g.7674866_7674870del | CA645588717 | TP53 | c.662_666del (p.Glu221AlafsTer2) c.266_270del (p.Glu89AlafsTer2) c.383_387del (p.Glu128AlafsTer2) c.641_645del (p.Glu214AlafsTer2) n.918_922del n.67+184_67+188del c.545_549del (p.Glu182AlafsTer2) c.185_189del (p.Glu62AlafsTer2) c.629_633del (p.Glu210AlafsTer2) | ClinVar dbSNP COSMIC |
| 17 | g.7674865_7674874delinsCGGCTCATAG | CA2245953964 | TP53 | c.657_666delinsCTATGAGCCG (p.Pro219=) c.261_270delinsCTATGAGCCG (p.Pro87=) c.378_387delinsCTATGAGCCG (p.Pro126=) c.636_645delinsCTATGAGCCG (p.Pro212=) n.913_922delinsCTATGAGCCG n.67+179_67+188delinsCTATGAGCCG c.540_549delinsCTATGAGCCG (p.Pro180=) c.180_189delinsCTATGAGCCG (p.Pro60=) c.624_633delinsCTATGAGCCG (p.Pro208=) | |
| 17 | g.7674865_7674880del | CA000310 | TP53 | c.651_666del (p.Val218LeufsTer24) c.255_270del (p.Val86LeufsTer24) c.372_387del (p.Val125LeufsTer24) c.630_645del (p.Val211LeufsTer24) n.907_922del n.67+173_67+188del c.534_549del (p.Val179LeufsTer24) c.174_189del (p.Val59LeufsTer24) c.618_633del (p.Val207LeufsTer24) | ClinVar dbSNP |
| 17 | g.7674866G>A | CA000317 | TP53 | c.665C>T (p.Pro222Leu) c.269C>T (p.Pro90Leu) c.386C>T (p.Pro129Leu) c.644C>T (p.Pro215Leu) n.921C>T n.67+187C>T c.548C>T (p.Pro183Leu) c.188C>T (p.Pro63Leu) c.632C>T (p.Pro211Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.7674866G>C | CA397839834 | TP53 | c.665C>G (p.Pro222Arg) c.269C>G (p.Pro90Arg) c.386C>G (p.Pro129Arg) c.644C>G (p.Pro215Arg) n.921C>G n.67+187C>G c.548C>G (p.Pro183Arg) c.188C>G (p.Pro63Arg) c.632C>G (p.Pro211Arg) | dbSNP |
| 17 | g.7674866G= | CA2245953991 | TP53 | c.665C= (p.Pro222=) c.269C= (p.Pro90=) c.386C= (p.Pro129=) c.644C= (p.Pro215=) n.921C= n.67+187C= c.548C= (p.Pro183=) c.188C= (p.Pro63=) c.632C= (p.Pro211=) | |
| 17 | g.7674866G>T | CA397839839 | TP53 | c.665C>A (p.Pro222Gln) c.269C>A (p.Pro90Gln) c.386C>A (p.Pro129Gln) c.644C>A (p.Pro215Gln) n.921C>A n.67+187C>A c.548C>A (p.Pro183Gln) c.188C>A (p.Pro63Gln) c.632C>A (p.Pro211Gln) | ClinVar dbSNP COSMIC |
| 17 | g.7674866_7674867delinsAA | CA645588718 | TP53 | c.664_665delinsTT (p.Pro222Leu) c.268_269delinsTT (p.Pro90Leu) c.385_386delinsTT (p.Pro129Leu) c.643_644delinsTT (p.Pro215Leu) n.920_921delinsTT n.67+186_67+187delinsTT c.547_548delinsTT (p.Pro183Leu) c.187_188delinsTT (p.Pro63Leu) c.631_632delinsTT (p.Pro211Leu) | COSMIC |
| 17 | g.7674867dup | CA2499224965 | TP53 | c.665dup (p.Pro223AlafsTer2) c.269dup (p.Pro91AlafsTer2) c.386dup (p.Pro130AlafsTer2) c.644dup (p.Pro216AlafsTer2) n.921dup n.67+187dup c.548dup (p.Pro184AlafsTer2) c.188dup (p.Pro64AlafsTer2) c.632dup (p.Pro212AlafsTer2) | ClinVar dbSNP |
| 17 | g.7674867del | CA497925281 | TP53 | c.665del (p.Pro222ArgfsTer25) c.269del (p.Pro90ArgfsTer25) c.386del (p.Pro129ArgfsTer25) c.644del (p.Pro215ArgfsTer25) n.921del n.67+187del c.548del (p.Pro183ArgfsTer25) c.188del (p.Pro63ArgfsTer25) c.632del (p.Pro211ArgfsTer25) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674869_7674877del | CA10580930 | TP53 | c.657_665del (p.Tyr220_Pro222del) c.261_269del (p.Tyr88_Pro90del) c.378_386del (p.Tyr127_Pro129del) c.636_644del (p.Tyr213_Pro215del) n.913_921del n.67+179_67+187del c.540_548del (p.Tyr181_Pro183del) c.180_188del (p.Tyr61_Pro63del) c.624_632del (p.Tyr209_Pro211del) | ClinVar dbSNP |
| 17 | g.7674867G>A | CA16615720 | TP53 | c.664C>T (p.Pro222Ser) c.268C>T (p.Pro90Ser) c.385C>T (p.Pro129Ser) c.643C>T (p.Pro215Ser) n.920C>T n.67+186C>T c.547C>T (p.Pro183Ser) c.187C>T (p.Pro63Ser) c.631C>T (p.Pro211Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
| 17 | g.7674867G>C | CA397839848 | TP53 | c.664C>G (p.Pro222Ala) c.268C>G (p.Pro90Ala) c.385C>G (p.Pro129Ala) c.643C>G (p.Pro215Ala) n.920C>G n.67+186C>G c.547C>G (p.Pro183Ala) c.187C>G (p.Pro63Ala) c.631C>G (p.Pro211Ala) | dbSNP COSMIC |
| 17 | g.7674867G= | CA2245954000 | TP53 | c.664C= (p.Pro222=) c.268C= (p.Pro90=) c.385C= (p.Pro129=) c.643C= (p.Pro215=) n.920C= n.67+186C= c.547C= (p.Pro183=) c.187C= (p.Pro63=) c.631C= (p.Pro211=) | |
| 17 | g.7674867G>T | CA397839851 | TP53 | c.664C>A (p.Pro222Thr) c.268C>A (p.Pro90Thr) c.385C>A (p.Pro129Thr) c.643C>A (p.Pro215Thr) n.920C>A n.67+186C>A c.547C>A (p.Pro183Thr) c.187C>A (p.Pro63Thr) c.631C>A (p.Pro211Thr) | dbSNP COSMIC |
| 17 | g.7674868_7674874del | CA645588719 | TP53 | c.658_664del (p.Tyr220ArgfsTer25) c.262_268del (p.Tyr88ArgfsTer25) c.379_385del (p.Tyr127ArgfsTer25) c.637_643del (p.Tyr213ArgfsTer25) n.914_920del n.67+180_67+186del c.541_547del (p.Tyr181ArgfsTer25) c.181_187del (p.Tyr61ArgfsTer25) c.625_631del (p.Tyr209ArgfsTer25) | gnomAD v4 COSMIC |
| 17 | g.7674868C>A | CA397839856 | TP53 | c.663G>T (p.Glu221Asp) c.267G>T (p.Glu89Asp) c.384G>T (p.Glu128Asp) c.642G>T (p.Glu214Asp) n.919G>T n.67+185G>T c.546G>T (p.Glu182Asp) c.186G>T (p.Glu62Asp) c.630G>T (p.Glu210Asp) | dbSNP COSMIC |
| 17 | g.7674868C= | CA2245954006 | TP53 | c.663G= (p.Glu221=) c.267G= (p.Glu89=) c.384G= (p.Glu128=) c.642G= (p.Glu214=) n.919G= n.67+185G= c.546G= (p.Glu182=) c.186G= (p.Glu62=) c.630G= (p.Glu210=) | |
| 17 | g.7674868C>G | CA397839857 | TP53 | c.663G>C (p.Glu221Asp) c.267G>C (p.Glu89Asp) c.384G>C (p.Glu128Asp) c.642G>C (p.Glu214Asp) n.919G>C n.67+185G>C c.546G>C (p.Glu182Asp) c.186G>C (p.Glu62Asp) c.630G>C (p.Glu210Asp) | dbSNP COSMIC |
| 17 | g.7674868C>T | CA16615692 | TP53 | c.663G>A (p.Glu221=) c.267G>A (p.Glu89=) c.384G>A (p.Glu128=) c.642G>A (p.Glu214=) n.919G>A n.67+185G>A c.546G>A (p.Glu182=) c.186G>A (p.Glu62=) c.630G>A (p.Glu210=) | ClinVar dbSNP COSMIC |
| 17 | g.7674868_7674869delinsCT | CA2245954005 | TP53 | c.662_663delinsAG (p.Glu221=) c.266_267delinsAG (p.Glu89=) c.383_384delinsAG (p.Glu128=) c.641_642delinsAG (p.Glu214=) n.918_919delinsAG n.67+184_67+185delinsAG c.545_546delinsAG (p.Glu182=) c.185_186delinsAG (p.Glu62=) c.629_630delinsAG (p.Glu210=) | |
| 17 | g.7674869_7674880dup | CA2580094935 | TP53 | c.652_663dup (p.Glu221_Pro222insValProTyrGlu) c.256_267dup (p.Glu89_Pro90insValProTyrGlu) c.373_384dup (p.Glu128_Pro129insValProTyrGlu) c.631_642dup (p.Glu214_Pro215insValProTyrGlu) n.908_919dup n.67+174_67+185dup c.535_546dup (p.Glu182_Pro183insValProTyrGlu) c.175_186dup (p.Glu62_Pro63insValProTyrGlu) c.619_630dup (p.Glu210_Pro211insValProTyrGlu) | ClinVar |
| 17 | g.7674869_7674880del | CA645588720 | TP53 | c.652_663del (p.Val218_Glu221del) c.256_267del (p.Val86_Glu89del) c.373_384del (p.Val125_Glu128del) c.631_642del (p.Val211_Glu214del) n.908_919del n.67+174_67+185del c.535_546del (p.Val179_Glu182del) c.175_186del (p.Val59_Glu62del) c.619_630del (p.Val207_Glu210del) | ClinVar COSMIC |
| 17 | g.7674869del | CA10583678 | TP53 | c.662del (p.Glu221GlyfsTer26) c.266del (p.Glu89GlyfsTer26) c.383del (p.Glu128GlyfsTer26) c.641del (p.Glu214GlyfsTer26) n.918del n.67+184del c.545del (p.Glu182GlyfsTer26) c.185del (p.Glu62GlyfsTer26) c.629del (p.Glu210GlyfsTer26) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674869T>A | CA397839864 | TP53 | c.662A>T (p.Glu221Val) c.266A>T (p.Glu89Val) c.383A>T (p.Glu128Val) c.641A>T (p.Glu214Val) n.918A>T n.67+184A>T c.545A>T (p.Glu182Val) c.185A>T (p.Glu62Val) c.629A>T (p.Glu210Val) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7674869T>C | CA397839867 | TP53 | c.662A>G (p.Glu221Gly) c.266A>G (p.Glu89Gly) c.383A>G (p.Glu128Gly) c.641A>G (p.Glu214Gly) n.918A>G n.67+184A>G c.545A>G (p.Glu182Gly) c.185A>G (p.Glu62Gly) c.629A>G (p.Glu210Gly) | dbSNP COSMIC |
| 17 | g.7674869T>G | CA397839870 | TP53 | c.662A>C (p.Glu221Ala) c.266A>C (p.Glu89Ala) c.383A>C (p.Glu128Ala) c.641A>C (p.Glu214Ala) n.918A>C n.67+184A>C c.545A>C (p.Glu182Ala) c.185A>C (p.Glu62Ala) c.629A>C (p.Glu210Ala) | ClinVar dbSNP |