| 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.7673473_7673539dup | CA2535386204 | TP53 | c.991_993+64dup c.595_597+64dup c.712_714+64dup c.970_972+64dup c.782+644_782+710dup (n.782+644_782+710dup) c.51_53+64dup c.874_876+64dup c.514_516+64dup c.958_960+64dup | gnomAD v4 |
| 17 | g.7673528_7673536del | CA2573154624 | TP53 | c.992_993+7del c.596_597+7del c.713_714+7del c.971_972+7del c.782+645_782+653del (n.782+645_782+653del) c.52_53+7del c.875_876+7del c.515_516+7del c.959_960+7del | dbSNP |
| 17 | g.7673529_7673541del | CA645587337 | TP53 | c.987_993+6del c.591_597+6del c.708_714+6del c.966_972+6del c.782+640_782+652del (n.782+640_782+652del) c.47_53+6del c.870_876+6del c.510_516+6del c.954_960+6del | COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673532_7673541del | CA645587338 | TP53 | c.988_993+4del c.592_597+4del c.709_714+4del c.967_972+4del c.782+641_782+650del (n.782+641_782+650del) c.48_53+4del c.871_876+4del c.511_516+4del c.955_960+4del | COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673533_7673541delinsTA | CA2580094895 | TP53 | c.987_993+2delinsTA c.591_597+2delinsTA c.708_714+2delinsTA c.966_972+2delinsTA c.782+640_782+648delinsTA (n.782+640_782+648delinsTA) c.47_53+2delinsTA c.870_876+2delinsTA c.510_516+2delinsTA c.954_960+2delinsTA | ClinVar |
| 17 | g.7673535del | CA645369685 | TP53 | c.993+1del c.597+1del c.714+1del c.972+1del c.782+647del (n.782+647del) c.53+1del c.876+1del c.516+1del c.960+1del | ClinVar dbSNP |
| 17 | g.7673534_7673538delinsCCTGA | CA2245947390 | TP53 | c.990_993+1delinsTCAGG c.594_597+1delinsTCAGG c.711_714+1delinsTCAGG c.969_972+1delinsTCAGG c.782+643_782+647delinsTCAGG (n.782+643_782+647delinsTCAGG) c.50_53+1delinsTCAGG c.873_876+1delinsTCAGG c.513_516+1delinsTCAGG c.957_960+1delinsTCAGG | |
| 17 | g.7673535C>A | CA287486501 | TP53 | c.993G>T (p.Gln331His) c.597G>T (p.Gln199His) c.714G>T (p.Gln238His) c.972G>T (p.Gln324His) c.782+646G>T (n.782+646G>T) c.53G>T c.876G>T (p.Gln292His) c.516G>T (p.Gln172His) c.960G>T (p.Gln320His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673535C= | CA2245947419 | TP53 | c.993G= (p.Gln331=) c.597G= (p.Gln199=) c.714G= (p.Gln238=) c.972G= (p.Gln324=) c.782+646G= (n.782+646G=) c.53G= c.876G= (p.Gln292=) c.516G= (p.Gln172=) c.960G= (p.Gln320=) | |
| 17 | g.7673535C>G | CA397835662 | TP53 | c.993G>C (p.Gln331His) c.597G>C (p.Gln199His) c.714G>C (p.Gln238His) c.972G>C (p.Gln324His) c.782+646G>C (n.782+646G>C) c.53G>C c.876G>C (p.Gln292His) c.516G>C (p.Gln172His) c.960G>C (p.Gln320His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673535C>T | CA10590137 | TP53 | c.993G>A (p.Gln331=) c.597G>A (p.Gln199=) c.714G>A (p.Gln238=) c.972G>A (p.Gln324=) c.782+646G>A (n.782+646G>A) c.53G>A c.876G>A (p.Gln292=) c.516G>A (p.Gln172=) c.960G>A (p.Gln320=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673535_7673536del | CA645587344 | TP53 | c.992_993del (p.Gln331HisfsTer5) c.596_597del (p.Gln199HisfsTer5) c.713_714del (p.Gln238HisfsTer5) c.971_972del (p.Gln324HisfsTer5) c.992_993del (p.Lys332AsnfsTer?) c.782+645_782+646del (n.782+645_782+646del) c.992_993del (p.Gln331ArgfsTer15) c.992_993del (p.Gln331HisfsTer4) c.596_597del (p.Gln199HisfsTer4) c.596_597del (p.Gln199=) c.596_597del (p.Gln199ArgfsTer15) c.52_53del c.875_876del (p.Gln292HisfsTer5) c.875_876del (p.Gln292HisfsTer4) c.515_516del (p.Gln172HisfsTer4) c.959_960del (p.Gln320HisfsTer5) c.515_516del (p.Gln172ArgfsTer15) c.515_516del (p.Gln172HisfsTer5) c.875_876del (p.Gln292ArgfsTer15) | COSMIC |
| 17 | g.7673535_7673536delinsTG | CA645587342 | TP53 | c.992_993delinsCA (p.Gln331Pro) c.596_597delinsCA (p.Gln199Pro) c.713_714delinsCA (p.Gln238Pro) c.971_972delinsCA (p.Gln324Pro) c.782+645_782+646delinsCA (n.782+645_782+646delinsCA) c.52_53delinsCA c.875_876delinsCA (p.Gln292Pro) c.515_516delinsCA (p.Gln172Pro) c.959_960delinsCA (p.Gln320Pro) | COSMIC |
| 17 | g.7673535_7673538del | CA658656523 | TP53 | c.990_993del (p.Gln331SerfsTer13) c.594_597del (p.Gln199SerfsTer13) c.711_714del (p.Gln238SerfsTer13) c.969_972del (p.Gln324SerfsTer13) c.990_993del (p.Gln331LysfsTer20) c.782+643_782+646del (n.782+643_782+646del) c.990_993del (p.Gln331ThrfsTer19) c.990_993del (p.Gln331CysfsTer11) c.594_597del (p.Gln199CysfsTer11) c.594_597del (p.Leu198=) c.594_597del (p.Gln199ThrfsTer19) c.50_53del c.873_876del (p.Gln292SerfsTer13) c.873_876del (p.Gln292CysfsTer11) c.513_516del (p.Gln172CysfsTer11) c.957_960del (p.Gln320SerfsTer13) c.513_516del (p.Gln172ThrfsTer19) c.513_516del (p.Gln172SerfsTer13) c.873_876del (p.Gln292ThrfsTer19) | ClinVar dbSNP |
| 17 | g.7673536T>A | CA397835673 | TP53 | c.992A>T (p.Gln331Leu) c.596A>T (p.Gln199Leu) c.713A>T (p.Gln238Leu) c.971A>T (p.Gln324Leu) c.782+645A>T (n.782+645A>T) c.52A>T c.875A>T (p.Gln292Leu) c.515A>T (p.Gln172Leu) c.959A>T (p.Gln320Leu) | |
| 17 | g.7673536T>C | CA16620611 | TP53 | c.992A>G (p.Gln331Arg) c.596A>G (p.Gln199Arg) c.713A>G (p.Gln238Arg) c.971A>G (p.Gln324Arg) c.782+645A>G (n.782+645A>G) c.52A>G c.875A>G (p.Gln292Arg) c.515A>G (p.Gln172Arg) c.959A>G (p.Gln320Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673536T>G | CA397835672 | TP53 | c.992A>C (p.Gln331Pro) c.596A>C (p.Gln199Pro) c.713A>C (p.Gln238Pro) c.971A>C (p.Gln324Pro) c.782+645A>C (n.782+645A>C) c.52A>C c.875A>C (p.Gln292Pro) c.515A>C (p.Gln172Pro) c.959A>C (p.Gln320Pro) | COSMIC |
| 17 | g.7673536T= | CA2245947430 | TP53 | c.992A= (p.Gln331=) c.596A= (p.Gln199=) c.713A= (p.Gln238=) c.971A= (p.Gln324=) c.782+645A= (n.782+645A=) c.52A= c.875A= (p.Gln292=) c.515A= (p.Gln172=) c.959A= (p.Gln320=) | |
| 17 | g.7673536_7673594dup | CA2499224956 | TP53 | c.934_992dup (p.Ile332ProfsTer33) c.538_596dup (p.Ile200ProfsTer33) c.655_713dup (p.Ile239ProfsTer33) c.913_971dup (p.Ile325ProfsTer33) c.934_992dup (p.Lys332ProfsTer40) c.782+587_782+645dup (n.782+587_782+645dup) c.934_992dup (p.Asp332ProfsTer39) c.934_992dup (p.Met332ProfsTer31) c.538_596dup (p.Met200ProfsTer31) c.538_596dup (p.Gln199=) c.538_596dup (p.Asp200ProfsTer39) c.817_875dup (p.Ile293ProfsTer33) c.817_875dup (p.Met293ProfsTer31) c.457_515dup (p.Met173ProfsTer31) c.901_959dup (p.Ile321ProfsTer33) c.457_515dup (p.Asp173ProfsTer39) c.457_515dup (p.Ile173ProfsTer33) c.817_875dup (p.Asp293ProfsTer39) | ClinVar dbSNP |
| 17 | g.7673537G>A | CA397835674 | TP53 | c.991C>T (p.Gln331Ter) c.595C>T (p.Gln199Ter) c.712C>T (p.Gln238Ter) c.970C>T (p.Gln324Ter) c.782+644C>T (n.782+644C>T) c.51C>T c.874C>T (p.Gln292Ter) c.514C>T (p.Gln172Ter) c.958C>T (p.Gln320Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673537G>C | CA397835677 | TP53 | c.991C>G (p.Gln331Glu) c.595C>G (p.Gln199Glu) c.712C>G (p.Gln238Glu) c.970C>G (p.Gln324Glu) c.782+644C>G (n.782+644C>G) c.51C>G c.874C>G (p.Gln292Glu) c.514C>G (p.Gln172Glu) c.958C>G (p.Gln320Glu) | ClinVar |
| 17 | g.7673537G= | CA2245947449 | TP53 | c.991C= (p.Gln331=) c.595C= (p.Gln199=) c.712C= (p.Gln238=) c.970C= (p.Gln324=) c.782+644C= (n.782+644C=) c.51C= c.874C= (p.Gln292=) c.514C= (p.Gln172=) c.958C= (p.Gln320=) | |
| 17 | g.7673537G>T | CA397835679 | TP53 | c.991C>A (p.Gln331Lys) c.595C>A (p.Gln199Lys) c.712C>A (p.Gln238Lys) c.970C>A (p.Gln324Lys) c.782+644C>A (n.782+644C>A) c.51C>A c.874C>A (p.Gln292Lys) c.514C>A (p.Gln172Lys) c.958C>A (p.Gln320Lys) | ClinVar dbSNP |
| 17 | g.7673538A>C | CA497713725 | TP53 | c.990T>G (p.Leu330=) c.594T>G (p.Leu198=) c.711T>G (p.Leu237=) c.969T>G (p.Leu323=) c.782+643T>G (n.782+643T>G) c.50T>G c.873T>G (p.Leu291=) c.513T>G (p.Leu171=) c.957T>G (p.Leu319=) | dbSNP |
| 17 | g.7673538A>G | CA497713729 | TP53 | c.990T>C (p.Leu330=) c.594T>C (p.Leu198=) c.711T>C (p.Leu237=) c.969T>C (p.Leu323=) c.782+643T>C (n.782+643T>C) c.50T>C c.873T>C (p.Leu291=) c.513T>C (p.Leu171=) c.957T>C (p.Leu319=) | dbSNP |
| 17 | g.7673538A>T | CA497713734 | TP53 | c.990T>A (p.Leu330=) c.594T>A (p.Leu198=) c.711T>A (p.Leu237=) c.969T>A (p.Leu323=) c.782+643T>A (n.782+643T>A) c.50T>A c.873T>A (p.Leu291=) c.513T>A (p.Leu171=) c.957T>A (p.Leu319=) | dbSNP |
| 17 | g.7673539dup | CA645587345 | TP53 | c.990dup (p.Gln331SerfsTer6) c.594dup (p.Gln199SerfsTer6) c.711dup (p.Gln238SerfsTer6) c.969dup (p.Gln324SerfsTer6) c.990dup (p.Gln331SerfsTer?) c.782+643dup (n.782+643dup) c.990dup (p.Gln331SerfsTer16) c.990dup (p.Gln331SerfsTer5) c.594dup (p.Gln199SerfsTer5) c.594dup (p.Gln199SerfsTer?) c.594dup (p.Gln199SerfsTer16) c.50dup c.873dup (p.Gln292SerfsTer6) c.873dup (p.Gln292SerfsTer5) c.513dup (p.Gln172SerfsTer5) c.957dup (p.Gln320SerfsTer6) c.513dup (p.Gln172SerfsTer16) c.513dup (p.Gln172SerfsTer6) c.873dup (p.Gln292SerfsTer16) | COSMIC COSMIC |
| 17 | g.7673539del | CA497713744 | TP53 | c.990del (p.Gln331ArgfsTer14) c.594del (p.Gln199ArgfsTer14) c.711del (p.Gln238ArgfsTer14) c.969del (p.Gln324ArgfsTer14) c.990del (p.Gln331ArgfsTer21) c.782+643del (n.782+643del) c.990del (p.Gln331ArgfsTer20) c.990del (p.Gln331ArgfsTer12) c.594del (p.Gln199ArgfsTer12) c.594del (p.Leu198=) c.594del (p.Gln199ArgfsTer20) c.50del c.873del (p.Gln292ArgfsTer14) c.873del (p.Gln292ArgfsTer12) c.513del (p.Gln172ArgfsTer12) c.957del (p.Gln320ArgfsTer14) c.513del (p.Gln172ArgfsTer20) c.513del (p.Gln172ArgfsTer14) c.873del (p.Gln292ArgfsTer20) | ClinVar dbSNP COSMIC |
| 17 | g.7673538_7673539insT | CA497713747 | TP53 | c.989_990insA (p.Gln331SerfsTer6) c.593_594insA (p.Gln199SerfsTer6) c.710_711insA (p.Gln238SerfsTer6) c.968_969insA (p.Gln324SerfsTer6) c.989_990insA (p.Gln331SerfsTer?) c.782+642_782+643insA (n.782+642_782+643insA) c.989_990insA (p.Gln331SerfsTer16) c.989_990insA (p.Gln331SerfsTer5) c.593_594insA (p.Gln199SerfsTer5) c.593_594insA (p.Gln199SerfsTer?) c.593_594insA (p.Gln199SerfsTer16) c.49_50insA c.872_873insA (p.Gln292SerfsTer6) c.872_873insA (p.Gln292SerfsTer5) c.512_513insA (p.Gln172SerfsTer5) c.956_957insA (p.Gln320SerfsTer6) c.512_513insA (p.Gln172SerfsTer16) c.512_513insA (p.Gln172SerfsTer6) c.872_873insA (p.Gln292SerfsTer16) | |
| 17 | g.7673539A= | CA2245947462 | TP53 | c.989T= (p.Leu330=) c.593T= (p.Leu198=) c.710T= (p.Leu237=) c.968T= (p.Leu323=) c.782+642T= (n.782+642T=) c.49T= c.872T= (p.Leu291=) c.512T= (p.Leu171=) c.956T= (p.Leu319=) | |
| 17 | g.7673539A>C | CA397835702 | TP53 | c.989T>G (p.Leu330Arg) c.593T>G (p.Leu198Arg) c.710T>G (p.Leu237Arg) c.968T>G (p.Leu323Arg) c.782+642T>G (n.782+642T>G) c.49T>G c.872T>G (p.Leu291Arg) c.512T>G (p.Leu171Arg) c.956T>G (p.Leu319Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673539A>G | CA397835704 | TP53 | c.989T>C (p.Leu330Pro) c.593T>C (p.Leu198Pro) c.710T>C (p.Leu237Pro) c.968T>C (p.Leu323Pro) c.782+642T>C (n.782+642T>C) c.49T>C c.872T>C (p.Leu291Pro) c.512T>C (p.Leu171Pro) c.956T>C (p.Leu319Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673539A>T | CA397835707 | TP53 | c.989T>A (p.Leu330His) c.593T>A (p.Leu198His) c.710T>A (p.Leu237His) c.968T>A (p.Leu323His) c.782+642T>A (n.782+642T>A) c.49T>A c.872T>A (p.Leu291His) c.512T>A (p.Leu171His) c.956T>A (p.Leu319His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673539_7673540delinsAG | CA2245947468 | TP53 | c.988_989delinsCT (p.Leu330=) c.592_593delinsCT (p.Leu198=) c.709_710delinsCT (p.Leu237=) c.967_968delinsCT (p.Leu323=) c.782+641_782+642delinsCT (n.782+641_782+642delinsCT) c.48_49delinsCT c.871_872delinsCT (p.Leu291=) c.511_512delinsCT (p.Leu171=) c.955_956delinsCT (p.Leu319=) | |
| 17 | g.7673540G>A | CA397835712 | TP53 | c.988C>T (p.Leu330Phe) c.592C>T (p.Leu198Phe) c.709C>T (p.Leu237Phe) c.967C>T (p.Leu323Phe) c.782+641C>T (n.782+641C>T) c.48C>T c.871C>T (p.Leu291Phe) c.511C>T (p.Leu171Phe) c.955C>T (p.Leu319Phe) | ClinVar dbSNP |
| 17 | g.7673540G>C | CA397835714 | TP53 | c.988C>G (p.Leu330Val) c.592C>G (p.Leu198Val) c.709C>G (p.Leu237Val) c.967C>G (p.Leu323Val) c.782+641C>G (n.782+641C>G) c.48C>G c.871C>G (p.Leu291Val) c.511C>G (p.Leu171Val) c.955C>G (p.Leu319Val) | dbSNP |
| 17 | g.7673540G= | CA2245947485 | TP53 | c.988C= (p.Leu330=) c.592C= (p.Leu198=) c.709C= (p.Leu237=) c.967C= (p.Leu323=) c.782+641C= (n.782+641C=) c.48C= c.871C= (p.Leu291=) c.511C= (p.Leu171=) c.955C= (p.Leu319=) | |
| 17 | g.7673540G>T | CA397835718 | TP53 | c.988C>A (p.Leu330Ile) c.592C>A (p.Leu198Ile) c.709C>A (p.Leu237Ile) c.967C>A (p.Leu323Ile) c.782+641C>A (n.782+641C>A) c.48C>A c.871C>A (p.Leu291Ile) c.511C>A (p.Leu171Ile) c.955C>A (p.Leu319Ile) | dbSNP |
| 17 | g.7673542del | CA497713751 | TP53 | c.988del (p.Leu330PhefsTer15) c.592del (p.Leu198PhefsTer15) c.709del (p.Leu237PhefsTer15) c.967del (p.Leu323PhefsTer15) c.988del (p.Leu330PhefsTer22) c.782+641del (n.782+641del) c.988del (p.Leu330PhefsTer21) c.988del (p.Leu330PhefsTer13) c.592del (p.Leu198PhefsTer13) c.592del (p.Leu198PhefsTer?) c.592del (p.Leu198PhefsTer21) c.48del c.871del (p.Leu291PhefsTer15) c.871del (p.Leu291PhefsTer13) c.511del (p.Leu171PhefsTer13) c.955del (p.Leu319PhefsTer15) c.511del (p.Leu171PhefsTer21) c.511del (p.Leu171PhefsTer15) c.871del (p.Leu291PhefsTer21) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673541G>A | CA497713763 | TP53 | c.987C>T (p.Thr329=) c.591C>T (p.Thr197=) c.708C>T (p.Thr236=) c.966C>T (p.Thr322=) c.782+640C>T (n.782+640C>T) c.47C>T c.870C>T (p.Thr290=) c.510C>T (p.Thr170=) c.954C>T (p.Thr318=) | ClinVar dbSNP gnomAD v4 COSMIC |
| 17 | g.7673541G>C | CA497713766 | TP53 | c.987C>G (p.Thr329=) c.591C>G (p.Thr197=) c.708C>G (p.Thr236=) c.966C>G (p.Thr322=) c.782+640C>G (n.782+640C>G) c.47C>G c.870C>G (p.Thr290=) c.510C>G (p.Thr170=) c.954C>G (p.Thr318=) | dbSNP |
| 17 | g.7673541G>T | CA497713769 | TP53 | c.987C>A (p.Thr329=) c.591C>A (p.Thr197=) c.708C>A (p.Thr236=) c.966C>A (p.Thr322=) c.782+640C>A (n.782+640C>A) c.47C>A c.870C>A (p.Thr290=) c.510C>A (p.Thr170=) c.954C>A (p.Thr318=) | ClinVar dbSNP COSMIC |
| 17 | g.7673541_7673542delinsAA | CA645587346 | TP53 | c.986_987delinsTT (p.Thr329Ile) c.590_591delinsTT (p.Thr197Ile) c.707_708delinsTT (p.Thr236Ile) c.965_966delinsTT (p.Thr322Ile) c.782+639_782+640delinsTT (n.782+639_782+640delinsTT) c.46_47delinsTT c.869_870delinsTT (p.Thr290Ile) c.509_510delinsTT (p.Thr170Ile) c.953_954delinsTT (p.Thr318Ile) | COSMIC COSMIC |
| 17 | g.7673541_7673560delinsGGTGAAATATTCTCCATCCA | CA2245947495 | TP53 | c.968_987delinsTGGATGGAGAATATTTCACC (p.Leu323=) c.572_591delinsTGGATGGAGAATATTTCACC (p.Leu191=) c.689_708delinsTGGATGGAGAATATTTCACC (p.Leu230=) c.947_966delinsTGGATGGAGAATATTTCACC (p.Leu316=) c.782+621_782+640delinsTGGATGGAGAATATTTCACC (n.782+621_782+640delinsTGGATGGAGAATATTTCACC) c.28_47delinsTGGATGGAGAATATTTCACC c.851_870delinsTGGATGGAGAATATTTCACC (p.Leu284=) c.491_510delinsTGGATGGAGAATATTTCACC (p.Leu164=) c.935_954delinsTGGATGGAGAATATTTCACC (p.Leu312=) | |
| 17 | g.7673542G>A | CA287486504 | TP53 | c.986C>T (p.Thr329Ile) c.590C>T (p.Thr197Ile) c.707C>T (p.Thr236Ile) c.965C>T (p.Thr322Ile) c.782+639C>T (n.782+639C>T) c.46C>T c.869C>T (p.Thr290Ile) c.509C>T (p.Thr170Ile) c.953C>T (p.Thr318Ile) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 17 | g.7673542G>C | CA397835725 | TP53 | c.986C>G (p.Thr329Ser) c.590C>G (p.Thr197Ser) c.707C>G (p.Thr236Ser) c.965C>G (p.Thr322Ser) c.782+639C>G (n.782+639C>G) c.46C>G c.869C>G (p.Thr290Ser) c.509C>G (p.Thr170Ser) c.953C>G (p.Thr318Ser) | dbSNP |
| 17 | g.7673542G= | CA2245947503 | TP53 | c.986C= (p.Thr329=) c.590C= (p.Thr197=) c.707C= (p.Thr236=) c.965C= (p.Thr322=) c.782+639C= (n.782+639C=) c.46C= c.869C= (p.Thr290=) c.509C= (p.Thr170=) c.953C= (p.Thr318=) | |
| 17 | g.7673542G>T | CA397835730 | TP53 | c.986C>A (p.Thr329Asn) c.590C>A (p.Thr197Asn) c.707C>A (p.Thr236Asn) c.965C>A (p.Thr322Asn) c.782+639C>A (n.782+639C>A) c.46C>A c.869C>A (p.Thr290Asn) c.509C>A (p.Thr170Asn) c.953C>A (p.Thr318Asn) | dbSNP |