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.7673705_7673827del | CA645587414 | TP53 | c.794_916del (p.Leu265_Lys305del) c.398_520del (p.Leu133_Lys173del) c.515_637del (p.Leu172_Lys212del) c.773_895del (p.Leu258_Lys298del) c.782+355_782+477del (n.782+355_782+477del) c.677_799del (p.Leu226_Lys266del) c.317_439del (p.Leu106_Lys146del) c.761_883del (p.Leu254_Lys294del) | COSMIC |
17 | g.7673788_7673827del | CA645588390 | TP53 | c.799_838del (p.Arg267GlufsTer?) c.403_442del (p.Arg135GlufsTer?) c.520_559del (p.Arg174GlufsTer?) c.778_817del (p.Arg260GlufsTer?) c.782+360_782+399del (n.782+360_782+399del) c.682_721del (p.Arg228GlufsTer?) c.322_361del (p.Arg108GlufsTer?) c.766_805del (p.Arg256GlufsTer?) | 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.7673808_7673825del | CA645588426 | TP53 | c.797_814del (p.Gly266_Glu271del) c.401_418del (p.Gly134_Glu139del) c.518_535del (p.Gly173_Glu178del) c.776_793del (p.Gly259_Glu264del) c.782+358_782+375del (n.782+358_782+375del) c.680_697del (p.Gly227_Glu232del) c.320_337del (p.Gly107_Glu112del) c.764_781del (p.Gly255_Glu260del) | COSMIC 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.7673811_7673824delinsAAGCTGTTCCGTCC | CA2245950037 | TP53 | c.796_809delinsGGACGGAACAGCTT (p.Gly266=) c.400_413delinsGGACGGAACAGCTT (p.Gly134=) c.517_530delinsGGACGGAACAGCTT (p.Gly173=) c.775_788delinsGGACGGAACAGCTT (p.Gly259=) c.782+357_782+370delinsGGACGGAACAGCTT (n.782+357_782+370delinsGGACGGAACAGCTT) c.679_692delinsGGACGGAACAGCTT (p.Gly227=) c.319_332delinsGGACGGAACAGCTT (p.Gly107=) c.763_776delinsGGACGGAACAGCTT (p.Gly255=) | |
17 | g.7673812_7673824del | CA10590112 | TP53 | c.796_808del (p.Gly266LeufsTer?) c.400_412del (p.Gly134LeufsTer?) c.517_529del (p.Gly173LeufsTer?) c.775_787del (p.Gly259LeufsTer?) c.782+357_782+369del (n.782+357_782+369del) c.679_691del (p.Gly227LeufsTer?) c.319_331del (p.Gly107LeufsTer?) c.763_775del (p.Gly255LeufsTer?) | ClinVar dbSNP |
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.7673816_7673824del | CA645588438 | TP53 | c.796_804del (p.Gly266_Asn268del) c.400_408del (p.Gly134_Asn136del) c.517_525del (p.Gly173_Asn175del) c.775_783del (p.Gly259_Asn261del) c.782+357_782+365del (n.782+357_782+365del) c.679_687del (p.Gly227_Asn229del) c.319_327del (p.Gly107_Asn109del) c.763_771del (p.Gly255_Asn257del) | 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.7673821_7673825del | CA645588443 | TP53 | c.797_801del (p.Gly266GlufsTer4) c.401_405del (p.Gly134GlufsTer4) c.518_522del (p.Gly173GlufsTer4) c.776_780del (p.Gly259GlufsTer4) c.782+358_782+362del (n.782+358_782+362del) c.680_684del (p.Gly227GlufsTer4) c.320_324del (p.Gly107GlufsTer4) c.764_768del (p.Gly255GlufsTer4) | COSMIC |
17 | g.7673819_7673827del | CA645588442 | TP53 | c.793_801del (p.Leu265_Arg267del) c.397_405del (p.Leu133_Arg135del) c.514_522del (p.Leu172_Arg174del) c.772_780del (p.Leu258_Arg260del) c.782+354_782+362del (n.782+354_782+362del) c.676_684del (p.Leu226_Arg228del) c.316_324del (p.Leu106_Arg108del) c.760_768del (p.Leu254_Arg256del) | 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.7673822_7673823delinsTC | CA2245950168 | TP53 | c.797_798delinsGA (p.Gly266=) c.401_402delinsGA (p.Gly134=) c.518_519delinsGA (p.Gly173=) c.776_777delinsGA (p.Gly259=) c.782+358_782+359delinsGA (n.782+358_782+359delinsGA) c.680_681delinsGA (p.Gly227=) c.320_321delinsGA (p.Gly107=) c.764_765delinsGA (p.Gly255=) | |
17 | g.7673822_7673826dup | CA287486647 | TP53 | c.794_798dup (p.Arg267TrpfsTer?) c.398_402dup (p.Arg135TrpfsTer?) c.515_519dup (p.Arg174TrpfsTer?) c.773_777dup (p.Arg260TrpfsTer?) c.782+355_782+359dup (n.782+355_782+359dup) c.677_681dup (p.Arg228TrpfsTer?) c.317_321dup (p.Arg108TrpfsTer?) c.761_765dup (p.Arg256TrpfsTer?) | dbSNP |
17 | g.7673823C>A | CA10580919 | TP53 | c.797G>T (p.Gly266Val) c.401G>T (p.Gly134Val) c.518G>T (p.Gly173Val) c.776G>T (p.Gly259Val) c.782+358G>T (n.782+358G>T) c.680G>T (p.Gly227Val) c.320G>T (p.Gly107Val) c.764G>T (p.Gly255Val) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673823C= | CA2245950187 | TP53 | c.797G= (p.Gly266=) c.401G= (p.Gly134=) c.518G= (p.Gly173=) c.776G= (p.Gly259=) c.782+358G= (n.782+358G=) c.680G= (p.Gly227=) c.320G= (p.Gly107=) c.764G= (p.Gly255=) | |
17 | g.7673823C>G | CA397837134 | TP53 | c.797G>C (p.Gly266Ala) c.401G>C (p.Gly134Ala) c.518G>C (p.Gly173Ala) c.776G>C (p.Gly259Ala) c.782+358G>C (n.782+358G>C) c.680G>C (p.Gly227Ala) c.320G>C (p.Gly107Ala) c.764G>C (p.Gly255Ala) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673823C>T | CA000421 | TP53 | c.797G>A (p.Gly266Glu) c.401G>A (p.Gly134Glu) c.518G>A (p.Gly173Glu) c.776G>A (p.Gly259Glu) c.782+358G>A (n.782+358G>A) c.680G>A (p.Gly227Glu) c.320G>A (p.Gly107Glu) c.764G>A (p.Gly255Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673823_7673824delinsGT | CA645588446 | TP53 | c.796_797delinsAC (p.Gly266Thr) c.400_401delinsAC (p.Gly134Thr) c.517_518delinsAC (p.Gly173Thr) c.775_776delinsAC (p.Gly259Thr) c.782+357_782+358delinsAC (n.782+357_782+358delinsAC) c.679_680delinsAC (p.Gly227Thr) c.319_320delinsAC (p.Gly107Thr) c.763_764delinsAC (p.Gly255Thr) | COSMIC |
17 | g.7673823_7673824delinsTT | CA645588447 | TP53 | c.796_797delinsAA (p.Gly266Lys) c.400_401delinsAA (p.Gly134Lys) c.517_518delinsAA (p.Gly173Lys) c.775_776delinsAA (p.Gly259Lys) c.782+357_782+358delinsAA (n.782+357_782+358delinsAA) c.679_680delinsAA (p.Gly227Lys) c.319_320delinsAA (p.Gly107Lys) c.763_764delinsAA (p.Gly255Lys) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673825del | CA497716419 | TP53 | c.797del (p.Gly266AspfsTer?) c.401del (p.Gly134AspfsTer?) c.518del (p.Gly173AspfsTer?) c.776del (p.Gly259AspfsTer?) c.782+358del (n.782+358del) c.680del (p.Gly227AspfsTer?) c.320del (p.Gly107AspfsTer?) c.764del (p.Gly255AspfsTer?) | ClinVar dbSNP COSMIC COSMIC |
17 | g.7673824C>A | CA397837139 | TP53 | c.796G>T (p.Gly266Ter) c.400G>T (p.Gly134Ter) c.517G>T (p.Gly173Ter) c.775G>T (p.Gly259Ter) c.782+357G>T (n.782+357G>T) c.679G>T (p.Gly227Ter) c.319G>T (p.Gly107Ter) c.763G>T (p.Gly255Ter) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673824C= | CA2245950210 | TP53 | c.796G= (p.Gly266=) c.400G= (p.Gly134=) c.517G= (p.Gly173=) c.775G= (p.Gly259=) c.782+357G= (n.782+357G=) c.679G= (p.Gly227=) c.319G= (p.Gly107=) c.763G= (p.Gly255=) | |
17 | g.7673824C>G | CA16603026 | TP53 | c.796G>C (p.Gly266Arg) c.400G>C (p.Gly134Arg) c.517G>C (p.Gly173Arg) c.775G>C (p.Gly259Arg) c.782+357G>C (n.782+357G>C) c.679G>C (p.Gly227Arg) c.319G>C (p.Gly107Arg) c.763G>C (p.Gly255Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673824C>T | CA397837142 | TP53 | c.796G>A (p.Gly266Arg) c.400G>A (p.Gly134Arg) c.517G>A (p.Gly173Arg) c.775G>A (p.Gly259Arg) c.782+357G>A (n.782+357G>A) c.679G>A (p.Gly227Arg) c.319G>A (p.Gly107Arg) c.763G>A (p.Gly255Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673824_7673825delinsAG | CA658683981 | TP53 | c.795_796delinsCT (p.Leu266Ter) c.399_400delinsCT (p.Leu134Ter) c.516_517delinsCT (p.Leu173Ter) c.774_775delinsCT (p.Leu259Ter) c.782+356_782+357delinsCT (n.782+356_782+357delinsCT) c.678_679delinsCT (p.Leu227Ter) c.318_319delinsCT (p.Leu107Ter) c.762_763delinsCT (p.Leu255Ter) | ClinVar dbSNP |
17 | g.7673824_7673825delinsCC | CA2245950229 | TP53 | c.795_796delinsGG (p.Leu265=) c.399_400delinsGG (p.Leu133=) c.516_517delinsGG (p.Leu172=) c.774_775delinsGG (p.Leu258=) c.782+356_782+357delinsGG (n.782+356_782+357delinsGG) c.678_679delinsGG (p.Leu226=) c.318_319delinsGG (p.Leu106=) c.762_763delinsGG (p.Leu254=) | |
17 | g.7673824_7673825delinsTT | CA645588448 | TP53 | c.795_796delinsAA (p.Gly266Arg) c.399_400delinsAA (p.Gly134Arg) c.516_517delinsAA (p.Gly173Arg) c.774_775delinsAA (p.Gly259Arg) c.782+356_782+357delinsAA (n.782+356_782+357delinsAA) c.678_679delinsAA (p.Gly227Arg) c.318_319delinsAA (p.Gly107Arg) c.762_763delinsAA (p.Gly255Arg) | COSMIC |
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) | ClinVar COSMIC |
17 | g.7673825C>A | CA497716431 | TP53 | c.795G>T (p.Leu265=) c.399G>T (p.Leu133=) c.516G>T (p.Leu172=) c.774G>T (p.Leu258=) c.782+356G>T (n.782+356G>T) c.678G>T (p.Leu226=) c.318G>T (p.Leu106=) c.762G>T (p.Leu254=) | ClinVar dbSNP |
17 | g.7673825C= | CA2245950248 | TP53 | c.795G= (p.Leu265=) c.399G= (p.Leu133=) c.516G= (p.Leu172=) c.774G= (p.Leu258=) c.782+356G= (n.782+356G=) c.678G= (p.Leu226=) c.318G= (p.Leu106=) c.762G= (p.Leu254=) | |
17 | g.7673825C>G | CA497716433 | TP53 | c.795G>C (p.Leu265=) c.399G>C (p.Leu133=) c.516G>C (p.Leu172=) c.774G>C (p.Leu258=) c.782+356G>C (n.782+356G>C) c.678G>C (p.Leu226=) c.318G>C (p.Leu106=) c.762G>C (p.Leu254=) | dbSNP COSMIC |
17 | g.7673825C>T | CA497716435 | TP53 | c.795G>A (p.Leu265=) c.399G>A (p.Leu133=) c.516G>A (p.Leu172=) c.774G>A (p.Leu258=) c.782+356G>A (n.782+356G>A) c.678G>A (p.Leu226=) c.318G>A (p.Leu106=) c.762G>A (p.Leu254=) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673825_7673826delinsAG | CA645588450 | TP53 | c.794_795delinsCT (p.Leu265Pro) c.398_399delinsCT (p.Leu133Pro) c.515_516delinsCT (p.Leu172Pro) c.773_774delinsCT (p.Leu258Pro) c.782+355_782+356delinsCT (n.782+355_782+356delinsCT) c.677_678delinsCT (p.Leu226Pro) c.317_318delinsCT (p.Leu106Pro) c.761_762delinsCT (p.Leu254Pro) | COSMIC |
17 | g.7673826A= | CA2245950260 | TP53 | c.794T= (p.Leu265=) c.398T= (p.Leu133=) c.515T= (p.Leu172=) c.773T= (p.Leu258=) c.782+355T= (n.782+355T=) c.677T= (p.Leu226=) c.317T= (p.Leu106=) c.761T= (p.Leu254=) | |
17 | g.7673826A>C | CA397837160 | TP53 | c.794T>G (p.Leu265Arg) c.398T>G (p.Leu133Arg) c.515T>G (p.Leu172Arg) c.773T>G (p.Leu258Arg) c.782+355T>G (n.782+355T>G) c.677T>G (p.Leu226Arg) c.317T>G (p.Leu106Arg) c.761T>G (p.Leu254Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673826A>G | CA10584586 | TP53 | c.794T>C (p.Leu265Pro) c.398T>C (p.Leu133Pro) c.515T>C (p.Leu172Pro) c.773T>C (p.Leu258Pro) c.782+355T>C (n.782+355T>C) c.677T>C (p.Leu226Pro) c.317T>C (p.Leu106Pro) c.761T>C (p.Leu254Pro) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673826A>T | CA397837169 | TP53 | c.794T>A (p.Leu265Gln) c.398T>A (p.Leu133Gln) c.515T>A (p.Leu172Gln) c.773T>A (p.Leu258Gln) c.782+355T>A (n.782+355T>A) c.677T>A (p.Leu226Gln) c.317T>A (p.Leu106Gln) c.761T>A (p.Leu254Gln) | ClinVar dbSNP 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.7673827del | CA497716459 | TP53 | c.793del (p.Leu265TrpfsTer?) c.397del (p.Leu133TrpfsTer?) c.514del (p.Leu172TrpfsTer?) c.772del (p.Leu258TrpfsTer?) c.782+354del (n.782+354del) c.676del (p.Leu226TrpfsTer?) c.316del (p.Leu106TrpfsTer?) c.760del (p.Leu254TrpfsTer?) | COSMIC |
17 | g.7673827G>A | CA497716445 | TP53 | c.793C>T (p.Leu265=) c.397C>T (p.Leu133=) c.514C>T (p.Leu172=) c.772C>T (p.Leu258=) c.782+354C>T (n.782+354C>T) c.676C>T (p.Leu226=) c.316C>T (p.Leu106=) c.760C>T (p.Leu254=) | dbSNP COSMIC |
17 | g.7673827G>C | CA397837177 | TP53 | c.793C>G (p.Leu265Val) c.397C>G (p.Leu133Val) c.514C>G (p.Leu172Val) c.772C>G (p.Leu258Val) c.782+354C>G (n.782+354C>G) c.676C>G (p.Leu226Val) c.316C>G (p.Leu106Val) c.760C>G (p.Leu254Val) | dbSNP |
17 | g.7673827G>T | CA397837180 | TP53 | c.793C>A (p.Leu265Met) c.397C>A (p.Leu133Met) c.514C>A (p.Leu172Met) c.772C>A (p.Leu258Met) c.782+354C>A (n.782+354C>A) c.676C>A (p.Leu226Met) c.316C>A (p.Leu106Met) c.760C>A (p.Leu254Met) | COSMIC COSMIC COSMIC COSMIC |