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.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.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.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 |
17 | g.7673545_7673563del | CA913188778 | TP53 | c.968_986del (p.Leu323ProfsTer16) c.572_590del (p.Leu191ProfsTer16) c.689_707del (p.Leu230ProfsTer16) c.947_965del (p.Leu316ProfsTer16) c.968_986del (p.Leu323ProfsTer23) c.782+621_782+639del (n.782+621_782+639del) c.968_986del (p.Leu323ProfsTer22) c.968_986del (p.Leu323ProfsTer14) c.572_590del (p.Leu191ProfsTer14) c.572_590del (p.Leu191ProfsTer?) c.572_590del (p.Leu191ProfsTer22) c.28_46del c.851_869del (p.Leu284ProfsTer16) c.851_869del (p.Leu284ProfsTer14) c.491_509del (p.Leu164ProfsTer14) c.935_953del (p.Leu312ProfsTer16) c.491_509del (p.Leu164ProfsTer22) c.491_509del (p.Leu164ProfsTer16) c.851_869del (p.Leu284ProfsTer22) | ClinVar dbSNP |
17 | g.7673543T>A | CA397835737 | TP53 | c.985A>T (p.Thr329Ser) c.589A>T (p.Thr197Ser) c.706A>T (p.Thr236Ser) c.964A>T (p.Thr322Ser) c.782+638A>T (n.782+638A>T) c.45A>T c.868A>T (p.Thr290Ser) c.508A>T (p.Thr170Ser) c.952A>T (p.Thr318Ser) | dbSNP |
17 | g.7673543T>C | CA397835735 | TP53 | c.985A>G (p.Thr329Ala) c.589A>G (p.Thr197Ala) c.706A>G (p.Thr236Ala) c.964A>G (p.Thr322Ala) c.782+638A>G (n.782+638A>G) c.45A>G c.868A>G (p.Thr290Ala) c.508A>G (p.Thr170Ala) c.952A>G (p.Thr318Ala) | ClinVar dbSNP gnomAD v4 |
17 | g.7673543T>G | CA397835733 | TP53 | c.985A>C (p.Thr329Pro) c.589A>C (p.Thr197Pro) c.706A>C (p.Thr236Pro) c.964A>C (p.Thr322Pro) c.782+638A>C (n.782+638A>C) c.45A>C c.868A>C (p.Thr290Pro) c.508A>C (p.Thr170Pro) c.952A>C (p.Thr318Pro) | dbSNP |
17 | g.7673543T= | CA2245947510 | TP53 | c.985A= (p.Thr329=) c.589A= (p.Thr197=) c.706A= (p.Thr236=) c.964A= (p.Thr322=) c.782+638A= (n.782+638A=) c.45A= c.868A= (p.Thr290=) c.508A= (p.Thr170=) c.952A= (p.Thr318=) | |
17 | g.7673543_7673546dup | CA2825002630 | TP53 | c.982_985dup (p.Thr329IlefsTer9) c.586_589dup (p.Thr197IlefsTer9) c.703_706dup (p.Thr236IlefsTer9) c.961_964dup (p.Thr322IlefsTer9) c.982_985dup (p.Thr329IlefsTer?) c.782+635_782+638dup (n.782+635_782+638dup) c.982_985dup (p.Thr329IlefsTer19) c.982_985dup (p.Thr329IlefsTer8) c.586_589dup (p.Thr197IlefsTer8) c.586_589dup (p.Thr197IlefsTer?) c.586_589dup (p.Thr197IlefsTer19) c.42_45dup c.865_868dup (p.Thr290IlefsTer9) c.865_868dup (p.Thr290IlefsTer8) c.505_508dup (p.Thr170IlefsTer8) c.949_952dup (p.Thr318IlefsTer9) c.505_508dup (p.Thr170IlefsTer19) c.505_508dup (p.Thr170IlefsTer9) c.865_868dup (p.Thr290IlefsTer19) | ClinVar |
17 | g.7673544G>A | CA16608656 | TP53 | c.984C>T (p.Phe328=) c.588C>T (p.Phe196=) c.705C>T (p.Phe235=) c.963C>T (p.Phe321=) c.782+637C>T (n.782+637C>T) c.44C>T c.867C>T (p.Phe289=) c.507C>T (p.Phe169=) c.951C>T (p.Phe317=) | ClinVar dbSNP COSMIC |
17 | g.7673544G>C | CA397835743 | TP53 | c.984C>G (p.Phe328Leu) c.588C>G (p.Phe196Leu) c.705C>G (p.Phe235Leu) c.963C>G (p.Phe321Leu) c.782+637C>G (n.782+637C>G) c.44C>G c.867C>G (p.Phe289Leu) c.507C>G (p.Phe169Leu) c.951C>G (p.Phe317Leu) | dbSNP |
17 | g.7673544G= | CA2245947520 | TP53 | c.984C= (p.Phe328=) c.588C= (p.Phe196=) c.705C= (p.Phe235=) c.963C= (p.Phe321=) c.782+637C= (n.782+637C=) c.44C= c.867C= (p.Phe289=) c.507C= (p.Phe169=) c.951C= (p.Phe317=) | |
17 | g.7673544G>T | CA397835745 | TP53 | c.984C>A (p.Phe328Leu) c.588C>A (p.Phe196Leu) c.705C>A (p.Phe235Leu) c.963C>A (p.Phe321Leu) c.782+637C>A (n.782+637C>A) c.44C>A c.867C>A (p.Phe289Leu) c.507C>A (p.Phe169Leu) c.951C>A (p.Phe317Leu) | dbSNP |
17 | g.7673544_7673545insT | CA645587347 | TP53 | c.983_984insA (p.Phe328LeufsTer9) c.587_588insA (p.Phe196LeufsTer9) c.704_705insA (p.Phe235LeufsTer9) c.962_963insA (p.Phe321LeufsTer9) c.983_984insA (p.Phe328LeufsTer?) c.782+636_782+637insA (n.782+636_782+637insA) c.983_984insA (p.Phe328LeufsTer19) c.983_984insA (p.Phe328LeufsTer8) c.587_588insA (p.Phe196LeufsTer8) c.587_588insA (p.Phe196LeufsTer?) c.587_588insA (p.Phe196LeufsTer19) c.43_44insA c.866_867insA (p.Phe289LeufsTer9) c.866_867insA (p.Phe289LeufsTer8) c.506_507insA (p.Phe169LeufsTer8) c.950_951insA (p.Phe317LeufsTer9) c.506_507insA (p.Phe169LeufsTer19) c.506_507insA (p.Phe169LeufsTer9) c.866_867insA (p.Phe289LeufsTer19) | COSMIC |
17 | g.7673545A= | CA2245947539 | TP53 | c.983T= (p.Phe328=) c.587T= (p.Phe196=) c.704T= (p.Phe235=) c.962T= (p.Phe321=) c.782+636T= (n.782+636T=) c.43T= c.866T= (p.Phe289=) c.506T= (p.Phe169=) c.950T= (p.Phe317=) | |
17 | g.7673545A>C | CA397835749 | TP53 | c.983T>G (p.Phe328Cys) c.587T>G (p.Phe196Cys) c.704T>G (p.Phe235Cys) c.962T>G (p.Phe321Cys) c.782+636T>G (n.782+636T>G) c.43T>G c.866T>G (p.Phe289Cys) c.506T>G (p.Phe169Cys) c.950T>G (p.Phe317Cys) | |
17 | g.7673545A>G | CA397835751 | TP53 | c.983T>C (p.Phe328Ser) c.587T>C (p.Phe196Ser) c.704T>C (p.Phe235Ser) c.962T>C (p.Phe321Ser) c.782+636T>C (n.782+636T>C) c.43T>C c.866T>C (p.Phe289Ser) c.506T>C (p.Phe169Ser) c.950T>C (p.Phe317Ser) | ClinVar dbSNP COSMIC |
17 | g.7673545A>T | CA397835754 | TP53 | c.983T>A (p.Phe328Tyr) c.587T>A (p.Phe196Tyr) c.704T>A (p.Phe235Tyr) c.962T>A (p.Phe321Tyr) c.782+636T>A (n.782+636T>A) c.43T>A c.866T>A (p.Phe289Tyr) c.506T>A (p.Phe169Tyr) c.950T>A (p.Phe317Tyr) | dbSNP |
17 | g.7673547dup | CA10603410 | TP53 | c.983dup (p.Thr329HisfsTer8) c.587dup (p.Thr197HisfsTer8) c.704dup (p.Thr236HisfsTer8) c.962dup (p.Thr322HisfsTer8) c.983dup (p.Thr329HisfsTer?) c.782+636dup (n.782+636dup) c.983dup (p.Thr329HisfsTer18) c.983dup (p.Thr329HisfsTer7) c.587dup (p.Thr197HisfsTer7) c.587dup (p.Thr197HisfsTer?) c.587dup (p.Thr197HisfsTer18) c.43dup c.866dup (p.Thr290HisfsTer8) c.866dup (p.Thr290HisfsTer7) c.506dup (p.Thr170HisfsTer7) c.950dup (p.Thr318HisfsTer8) c.506dup (p.Thr170HisfsTer18) c.506dup (p.Thr170HisfsTer8) c.866dup (p.Thr290HisfsTer18) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673546_7673547dup | CA2573154629 | TP53 | c.982_983dup (p.Thr329SerfsTer17) c.586_587dup (p.Thr197SerfsTer17) c.703_704dup (p.Thr236SerfsTer17) c.961_962dup (p.Thr322SerfsTer17) c.982_983dup (p.Thr329SerfsTer24) c.782+635_782+636dup (n.782+635_782+636dup) c.982_983dup (p.Thr329SerfsTer23) c.982_983dup (p.Thr329SerfsTer15) c.586_587dup (p.Thr197SerfsTer15) c.586_587dup (p.Thr197SerfsTer?) c.586_587dup (p.Thr197SerfsTer23) c.42_43dup c.865_866dup (p.Thr290SerfsTer17) c.865_866dup (p.Thr290SerfsTer15) c.505_506dup (p.Thr170SerfsTer15) c.949_950dup (p.Thr318SerfsTer17) c.505_506dup (p.Thr170SerfsTer23) c.505_506dup (p.Thr170SerfsTer17) c.865_866dup (p.Thr290SerfsTer23) | ClinVar dbSNP |
17 | g.7673547del | CA497713799 | TP53 | c.983del (p.Phe328SerfsTer17) c.587del (p.Phe196SerfsTer17) c.704del (p.Phe235SerfsTer17) c.962del (p.Phe321SerfsTer17) c.983del (p.Phe328SerfsTer24) c.782+636del (n.782+636del) c.983del (p.Phe328SerfsTer23) c.983del (p.Phe328SerfsTer15) c.587del (p.Phe196SerfsTer15) c.587del (p.Phe196SerfsTer?) c.587del (p.Phe196SerfsTer23) c.43del c.866del (p.Phe289SerfsTer17) c.866del (p.Phe289SerfsTer15) c.506del (p.Phe169SerfsTer15) c.950del (p.Phe317SerfsTer17) c.506del (p.Phe169SerfsTer23) c.506del (p.Phe169SerfsTer17) c.866del (p.Phe289SerfsTer23) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673545_7673546insT | CA497713806 | TP53 | c.982_983insA (p.Phe328TyrfsTer9) c.586_587insA (p.Phe196TyrfsTer9) c.703_704insA (p.Phe235TyrfsTer9) c.961_962insA (p.Phe321TyrfsTer9) c.982_983insA (p.Phe328TyrfsTer?) c.782+635_782+636insA (n.782+635_782+636insA) c.982_983insA (p.Phe328TyrfsTer19) c.982_983insA (p.Phe328TyrfsTer8) c.586_587insA (p.Phe196TyrfsTer8) c.586_587insA (p.Phe196TyrfsTer?) c.586_587insA (p.Phe196TyrfsTer19) c.42_43insA c.865_866insA (p.Phe289TyrfsTer9) c.865_866insA (p.Phe289TyrfsTer8) c.505_506insA (p.Phe169TyrfsTer8) c.949_950insA (p.Phe317TyrfsTer9) c.505_506insA (p.Phe169TyrfsTer19) c.505_506insA (p.Phe169TyrfsTer9) c.865_866insA (p.Phe289TyrfsTer19) | |
17 | g.7673546A>C | CA397835758 | TP53 | c.982T>G (p.Phe328Val) c.586T>G (p.Phe196Val) c.703T>G (p.Phe235Val) c.961T>G (p.Phe321Val) c.782+635T>G (n.782+635T>G) c.42T>G c.865T>G (p.Phe289Val) c.505T>G (p.Phe169Val) c.949T>G (p.Phe317Val) | COSMIC |
17 | g.7673546A>G | CA397835759 | TP53 | c.982T>C (p.Phe328Leu) c.586T>C (p.Phe196Leu) c.703T>C (p.Phe235Leu) c.961T>C (p.Phe321Leu) c.782+635T>C (n.782+635T>C) c.42T>C c.865T>C (p.Phe289Leu) c.505T>C (p.Phe169Leu) c.949T>C (p.Phe317Leu) | |
17 | g.7673546A>T | CA397835761 | TP53 | c.982T>A (p.Phe328Ile) c.586T>A (p.Phe196Ile) c.703T>A (p.Phe235Ile) c.961T>A (p.Phe321Ile) c.782+635T>A (n.782+635T>A) c.42T>A c.865T>A (p.Phe289Ile) c.505T>A (p.Phe169Ile) c.949T>A (p.Phe317Ile) | dbSNP |
17 | g.7673546_7673548delinsAAT | CA2245947548 | TP53 | c.980_982delinsATT (p.Tyr327=) c.584_586delinsATT (p.Tyr195=) c.701_703delinsATT (p.Tyr234=) c.959_961delinsATT (p.Tyr320=) c.782+633_782+635delinsATT (n.782+633_782+635delinsATT) c.40_42delinsATT c.863_865delinsATT (p.Tyr288=) c.503_505delinsATT (p.Tyr168=) c.947_949delinsATT (p.Tyr316=) | |
17 | g.7673547A= | CA2245947559 | TP53 | c.981T= (p.Tyr327=) c.585T= (p.Tyr195=) c.702T= (p.Tyr234=) c.960T= (p.Tyr320=) c.782+634T= (n.782+634T=) c.41T= c.864T= (p.Tyr288=) c.504T= (p.Tyr168=) c.948T= (p.Tyr316=) | |
17 | g.7673547A>C | CA10584585 | TP53 | c.981T>G (p.Tyr327Ter) c.585T>G (p.Tyr195Ter) c.702T>G (p.Tyr234Ter) c.960T>G (p.Tyr320Ter) c.782+634T>G (n.782+634T>G) c.41T>G c.864T>G (p.Tyr288Ter) c.504T>G (p.Tyr168Ter) c.948T>G (p.Tyr316Ter) | ClinVar dbSNP COSMIC COSMIC |
17 | g.7673547A>G | CA497713821 | TP53 | c.981T>C (p.Tyr327=) c.585T>C (p.Tyr195=) c.702T>C (p.Tyr234=) c.960T>C (p.Tyr320=) c.782+634T>C (n.782+634T>C) c.41T>C c.864T>C (p.Tyr288=) c.504T>C (p.Tyr168=) c.948T>C (p.Tyr316=) | dbSNP |
17 | g.7673547A>T | CA397835766 | TP53 | c.981T>A (p.Tyr327Ter) c.585T>A (p.Tyr195Ter) c.702T>A (p.Tyr234Ter) c.960T>A (p.Tyr320Ter) c.782+634T>A (n.782+634T>A) c.41T>A c.864T>A (p.Tyr288Ter) c.504T>A (p.Tyr168Ter) c.948T>A (p.Tyr316Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673549_7673550del | CA645587348 | TP53 | c.980_981del (p.Tyr327PhefsTer9) c.584_585del (p.Tyr195PhefsTer9) c.701_702del (p.Tyr234PhefsTer9) c.959_960del (p.Tyr320PhefsTer9) c.980_981del (p.Tyr327PhefsTer?) c.782+633_782+634del (n.782+633_782+634del) c.980_981del (p.Tyr327PhefsTer19) c.980_981del (p.Tyr327PhefsTer8) c.584_585del (p.Tyr195PhefsTer8) c.584_585del (p.Tyr195PhefsTer?) c.584_585del (p.Tyr195PhefsTer19) c.40_41del c.863_864del (p.Tyr288PhefsTer9) c.863_864del (p.Tyr288PhefsTer8) c.503_504del (p.Tyr168PhefsTer8) c.947_948del (p.Tyr316PhefsTer9) c.503_504del (p.Tyr168PhefsTer19) c.503_504del (p.Tyr168PhefsTer9) c.863_864del (p.Tyr288PhefsTer19) | ClinVar dbSNP COSMIC |
17 | g.7673548T>A | CA397835768 | TP53 | c.980A>T (p.Tyr327Phe) c.584A>T (p.Tyr195Phe) c.701A>T (p.Tyr234Phe) c.959A>T (p.Tyr320Phe) c.782+633A>T (n.782+633A>T) c.40A>T c.863A>T (p.Tyr288Phe) c.503A>T (p.Tyr168Phe) c.947A>T (p.Tyr316Phe) | dbSNP |
17 | g.7673548T>C | CA397835771 | TP53 | c.980A>G (p.Tyr327Cys) c.584A>G (p.Tyr195Cys) c.701A>G (p.Tyr234Cys) c.959A>G (p.Tyr320Cys) c.782+633A>G (n.782+633A>G) c.40A>G c.863A>G (p.Tyr288Cys) c.503A>G (p.Tyr168Cys) c.947A>G (p.Tyr316Cys) | ClinVar dbSNP |
17 | g.7673548T>G | CA397835778 | TP53 | c.980A>C (p.Tyr327Ser) c.584A>C (p.Tyr195Ser) c.701A>C (p.Tyr234Ser) c.959A>C (p.Tyr320Ser) c.782+633A>C (n.782+633A>C) c.40A>C c.863A>C (p.Tyr288Ser) c.503A>C (p.Tyr168Ser) c.947A>C (p.Tyr316Ser) | dbSNP |
17 | g.7673548_7673549insTT | CA645587349 | TP53 | c.980_981insAA (p.Tyr327Ter) c.584_585insAA (p.Tyr195Ter) c.701_702insAA (p.Tyr234Ter) c.959_960insAA (p.Tyr320Ter) c.782+633_782+634insAA (n.782+633_782+634insAA) c.40_41insAA c.863_864insAA (p.Tyr288Ter) c.503_504insAA (p.Tyr168Ter) c.947_948insAA (p.Tyr316Ter) | COSMIC |
17 | g.7673549A>C | CA397835781 | TP53 | c.979T>G (p.Tyr327Asp) c.583T>G (p.Tyr195Asp) c.700T>G (p.Tyr234Asp) c.958T>G (p.Tyr320Asp) c.782+632T>G (n.782+632T>G) c.39T>G c.862T>G (p.Tyr288Asp) c.502T>G (p.Tyr168Asp) c.946T>G (p.Tyr316Asp) | dbSNP COSMIC |
17 | g.7673549A>G | CA397835786 | TP53 | c.979T>C (p.Tyr327His) c.583T>C (p.Tyr195His) c.700T>C (p.Tyr234His) c.958T>C (p.Tyr320His) c.782+632T>C (n.782+632T>C) c.39T>C c.862T>C (p.Tyr288His) c.502T>C (p.Tyr168His) c.946T>C (p.Tyr316His) | |
17 | g.7673549A>T | CA397835783 | TP53 | c.979T>A (p.Tyr327Asn) c.583T>A (p.Tyr195Asn) c.700T>A (p.Tyr234Asn) c.958T>A (p.Tyr320Asn) c.782+632T>A (n.782+632T>A) c.39T>A c.862T>A (p.Tyr288Asn) c.502T>A (p.Tyr168Asn) c.946T>A (p.Tyr316Asn) | dbSNP |
17 | g.7673550T>A | CA287486513 | TP53 | c.978A>T (p.Glu326Asp) c.582A>T (p.Glu194Asp) c.699A>T (p.Glu233Asp) c.957A>T (p.Glu319Asp) c.782+631A>T (n.782+631A>T) c.38A>T c.861A>T (p.Glu287Asp) c.501A>T (p.Glu167Asp) c.945A>T (p.Glu315Asp) | ClinVar dbSNP gnomAD v4 |
17 | g.7673550T>C | CA497713840 | TP53 | c.978A>G (p.Glu326=) c.582A>G (p.Glu194=) c.699A>G (p.Glu233=) c.957A>G (p.Glu319=) c.782+631A>G (n.782+631A>G) c.38A>G c.861A>G (p.Glu287=) c.501A>G (p.Glu167=) c.945A>G (p.Glu315=) | ClinVar dbSNP |
17 | g.7673550T>G | CA397835791 | TP53 | c.978A>C (p.Glu326Asp) c.582A>C (p.Glu194Asp) c.699A>C (p.Glu233Asp) c.957A>C (p.Glu319Asp) c.782+631A>C (n.782+631A>C) c.38A>C c.861A>C (p.Glu287Asp) c.501A>C (p.Glu167Asp) c.945A>C (p.Glu315Asp) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673550T= | CA2245947569 | TP53 | c.978A= (p.Glu326=) c.582A= (p.Glu194=) c.699A= (p.Glu233=) c.957A= (p.Glu319=) c.782+631A= (n.782+631A=) c.38A= c.861A= (p.Glu287=) c.501A= (p.Glu167=) c.945A= (p.Glu315=) | |
17 | g.7673551_7673553del | CA2635874179 | TP53 | c.976_978del (p.Glu326del) c.580_582del (p.Glu194del) c.697_699del (p.Glu233del) c.955_957del (p.Glu319del) c.782+629_782+631del (n.782+629_782+631del) c.36_38del c.859_861del (p.Glu287del) c.499_501del (p.Glu167del) c.943_945del (p.Glu315del) | gnomAD v4 |
17 | g.7673551T>A | CA397835794 | TP53 | c.977A>T (p.Glu326Val) c.581A>T (p.Glu194Val) c.698A>T (p.Glu233Val) c.956A>T (p.Glu319Val) c.782+630A>T (n.782+630A>T) c.37A>T c.860A>T (p.Glu287Val) c.500A>T (p.Glu167Val) c.944A>T (p.Glu315Val) | ClinVar dbSNP |
17 | g.7673551T>C | CA397835798 | TP53 | c.977A>G (p.Glu326Gly) c.581A>G (p.Glu194Gly) c.698A>G (p.Glu233Gly) c.956A>G (p.Glu319Gly) c.782+630A>G (n.782+630A>G) c.37A>G c.860A>G (p.Glu287Gly) c.500A>G (p.Glu167Gly) c.944A>G (p.Glu315Gly) | dbSNP |
17 | g.7673551T>G | CA397835801 | TP53 | c.977A>C (p.Glu326Ala) c.581A>C (p.Glu194Ala) c.698A>C (p.Glu233Ala) c.956A>C (p.Glu319Ala) c.782+630A>C (n.782+630A>C) c.37A>C c.860A>C (p.Glu287Ala) c.500A>C (p.Glu167Ala) c.944A>C (p.Glu315Ala) | dbSNP |
17 | g.7673553_7673554dup | CA915949514 | TP53 | c.976_977dup (p.Tyr327AsnfsTer19) c.580_581dup (p.Tyr195AsnfsTer19) c.697_698dup (p.Tyr234AsnfsTer19) c.955_956dup (p.Tyr320AsnfsTer19) c.976_977dup (p.Tyr327AsnfsTer26) c.782+629_782+630dup (n.782+629_782+630dup) c.976_977dup (p.Tyr327AsnfsTer25) c.976_977dup (p.Tyr327AsnfsTer17) c.580_581dup (p.Tyr195AsnfsTer17) c.580_581dup (p.Tyr195AsnfsTer?) c.580_581dup (p.Tyr195AsnfsTer25) c.36_37dup c.859_860dup (p.Tyr288AsnfsTer19) c.859_860dup (p.Tyr288AsnfsTer17) c.499_500dup (p.Tyr168AsnfsTer17) c.943_944dup (p.Tyr316AsnfsTer19) c.499_500dup (p.Tyr168AsnfsTer25) c.499_500dup (p.Tyr168AsnfsTer19) c.859_860dup (p.Tyr288AsnfsTer25) | ClinVar dbSNP |
17 | g.7673552C>A | CA10580908 | TP53 | c.976G>T (p.Glu326Ter) c.580G>T (p.Glu194Ter) c.697G>T (p.Glu233Ter) c.955G>T (p.Glu319Ter) c.782+629G>T (n.782+629G>T) c.36G>T c.859G>T (p.Glu287Ter) c.499G>T (p.Glu167Ter) c.943G>T (p.Glu315Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673552C= | CA2245947579 | TP53 | c.976G= (p.Glu326=) c.580G= (p.Glu194=) c.697G= (p.Glu233=) c.955G= (p.Glu319=) c.782+629G= (n.782+629G=) c.36G= c.859G= (p.Glu287=) c.499G= (p.Glu167=) c.943G= (p.Glu315=) | |
17 | g.7673552C>G | CA397835806 | TP53 | c.976G>C (p.Glu326Gln) c.580G>C (p.Glu194Gln) c.697G>C (p.Glu233Gln) c.955G>C (p.Glu319Gln) c.782+629G>C (n.782+629G>C) c.36G>C c.859G>C (p.Glu287Gln) c.499G>C (p.Glu167Gln) c.943G>C (p.Glu315Gln) | dbSNP |
17 | g.7673552C>T | CA397835809 | TP53 | c.976G>A (p.Glu326Lys) c.580G>A (p.Glu194Lys) c.697G>A (p.Glu233Lys) c.955G>A (p.Glu319Lys) c.782+629G>A (n.782+629G>A) c.36G>A c.859G>A (p.Glu287Lys) c.499G>A (p.Glu167Lys) c.943G>A (p.Glu315Lys) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673553T>A | CA497713884 | TP53 | c.975A>T (p.Gly325=) c.579A>T (p.Gly193=) c.696A>T (p.Gly232=) c.954A>T (p.Gly318=) c.782+628A>T (n.782+628A>T) c.35A>T c.858A>T (p.Gly286=) c.498A>T (p.Gly166=) c.942A>T (p.Gly314=) | |
17 | g.7673553T>C | CA497713893 | TP53 | c.975A>G (p.Gly325=) c.579A>G (p.Gly193=) c.696A>G (p.Gly232=) c.954A>G (p.Gly318=) c.782+628A>G (n.782+628A>G) c.35A>G c.858A>G (p.Gly286=) c.498A>G (p.Gly166=) c.942A>G (p.Gly314=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673553T>G | CA497713894 | TP53 | c.975A>C (p.Gly325=) c.579A>C (p.Gly193=) c.696A>C (p.Gly232=) c.954A>C (p.Gly318=) c.782+628A>C (n.782+628A>C) c.35A>C c.858A>C (p.Gly286=) c.498A>C (p.Gly166=) c.942A>C (p.Gly314=) | |
17 | g.7673553T= | CA2245947582 | TP53 | c.975A= (p.Gly325=) c.579A= (p.Gly193=) c.696A= (p.Gly232=) c.954A= (p.Gly318=) c.782+628A= (n.782+628A=) c.35A= c.858A= (p.Gly286=) c.498A= (p.Gly166=) c.942A= (p.Gly314=) | |
17 | g.7673554C>A | CA000516 | TP53 | c.974G>T (p.Gly325Val) c.578G>T (p.Gly193Val) c.695G>T (p.Gly232Val) c.953G>T (p.Gly318Val) c.782+627G>T (n.782+627G>T) c.34G>T c.857G>T (p.Gly286Val) c.497G>T (p.Gly166Val) c.941G>T (p.Gly314Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673554C= | CA2245947593 | TP53 | c.974G= (p.Gly325=) c.578G= (p.Gly193=) c.695G= (p.Gly232=) c.953G= (p.Gly318=) c.782+627G= (n.782+627G=) c.34G= c.857G= (p.Gly286=) c.497G= (p.Gly166=) c.941G= (p.Gly314=) | |
17 | g.7673554C>G | CA397835813 | TP53 | c.974G>C (p.Gly325Ala) c.578G>C (p.Gly193Ala) c.695G>C (p.Gly232Ala) c.953G>C (p.Gly318Ala) c.782+627G>C (n.782+627G>C) c.34G>C c.857G>C (p.Gly286Ala) c.497G>C (p.Gly166Ala) c.941G>C (p.Gly314Ala) | dbSNP COSMIC |
17 | g.7673554C>T | CA397835817 | TP53 | c.974G>A (p.Gly325Glu) c.578G>A (p.Gly193Glu) c.695G>A (p.Gly232Glu) c.953G>A (p.Gly318Glu) c.782+627G>A (n.782+627G>A) c.34G>A c.857G>A (p.Gly286Glu) c.497G>A (p.Gly166Glu) c.941G>A (p.Gly314Glu) | ClinVar dbSNP COSMIC |
17 | g.7673555C>A | CA335679 | TP53 | c.973G>T (p.Gly325Ter) c.577G>T (p.Gly193Ter) c.694G>T (p.Gly232Ter) c.952G>T (p.Gly318Ter) c.782+626G>T (n.782+626G>T) c.33G>T c.856G>T (p.Gly286Ter) c.496G>T (p.Gly166Ter) c.940G>T (p.Gly314Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673555C= | CA2245947602 | TP53 | c.973G= (p.Gly325=) c.577G= (p.Gly193=) c.694G= (p.Gly232=) c.952G= (p.Gly318=) c.782+626G= (n.782+626G=) c.33G= c.856G= (p.Gly286=) c.496G= (p.Gly166=) c.940G= (p.Gly314=) | |
17 | g.7673555C>G | CA397835825 | TP53 | c.973G>C (p.Gly325Arg) c.577G>C (p.Gly193Arg) c.694G>C (p.Gly232Arg) c.952G>C (p.Gly318Arg) c.782+626G>C (n.782+626G>C) c.33G>C c.856G>C (p.Gly286Arg) c.496G>C (p.Gly166Arg) c.940G>C (p.Gly314Arg) | dbSNP |
17 | g.7673555C>T | CA397835820 | TP53 | c.973G>A (p.Gly325Arg) c.577G>A (p.Gly193Arg) c.694G>A (p.Gly232Arg) c.952G>A (p.Gly318Arg) c.782+626G>A (n.782+626G>A) c.33G>A c.856G>A (p.Gly286Arg) c.496G>A (p.Gly166Arg) c.940G>A (p.Gly314Arg) | ClinVar dbSNP |
17 | g.7673556A>C | CA397835833 | TP53 | c.972T>G (p.Asp324Glu) c.576T>G (p.Asp192Glu) c.693T>G (p.Asp231Glu) c.951T>G (p.Asp317Glu) c.782+625T>G (n.782+625T>G) c.32T>G c.855T>G (p.Asp285Glu) c.495T>G (p.Asp165Glu) c.939T>G (p.Asp313Glu) | dbSNP COSMIC |
17 | g.7673556A>G | CA497713910 | TP53 | c.972T>C (p.Asp324=) c.576T>C (p.Asp192=) c.693T>C (p.Asp231=) c.951T>C (p.Asp317=) c.782+625T>C (n.782+625T>C) c.32T>C c.855T>C (p.Asp285=) c.495T>C (p.Asp165=) c.939T>C (p.Asp313=) | dbSNP COSMIC |
17 | g.7673556A>T | CA397835829 | TP53 | c.972T>A (p.Asp324Glu) c.576T>A (p.Asp192Glu) c.693T>A (p.Asp231Glu) c.951T>A (p.Asp317Glu) c.782+625T>A (n.782+625T>A) c.32T>A c.855T>A (p.Asp285Glu) c.495T>A (p.Asp165Glu) c.939T>A (p.Asp313Glu) | ClinVar dbSNP COSMIC |
17 | g.7673557del | CA497713915 | TP53 | c.971del (p.Asp324ValfsTer21) c.575del (p.Asp192ValfsTer21) c.692del (p.Asp231ValfsTer21) c.950del (p.Asp317ValfsTer21) c.971del (p.Asp324ValfsTer28) c.782+624del (n.782+624del) c.971del (p.Asp324ValfsTer27) c.971del (p.Asp324ValfsTer19) c.575del (p.Asp192ValfsTer19) c.575del (p.Asp192ValfsTer?) c.575del (p.Asp192ValfsTer27) c.31del c.854del (p.Asp285ValfsTer21) c.854del (p.Asp285ValfsTer19) c.494del (p.Asp165ValfsTer19) c.938del (p.Asp313ValfsTer21) c.494del (p.Asp165ValfsTer27) c.494del (p.Asp165ValfsTer21) c.854del (p.Asp285ValfsTer27) | COSMIC |
17 | g.7673557T>A | CA397835834 | TP53 | c.971A>T (p.Asp324Val) c.575A>T (p.Asp192Val) c.692A>T (p.Asp231Val) c.950A>T (p.Asp317Val) c.782+624A>T (n.782+624A>T) c.31A>T c.854A>T (p.Asp285Val) c.494A>T (p.Asp165Val) c.938A>T (p.Asp313Val) | |
17 | g.7673557T>C | CA397835837 | TP53 | c.971A>G (p.Asp324Gly) c.575A>G (p.Asp192Gly) c.692A>G (p.Asp231Gly) c.950A>G (p.Asp317Gly) c.782+624A>G (n.782+624A>G) c.31A>G c.854A>G (p.Asp285Gly) c.494A>G (p.Asp165Gly) c.938A>G (p.Asp313Gly) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673557T>G | CA397835840 | TP53 | c.971A>C (p.Asp324Ala) c.575A>C (p.Asp192Ala) c.692A>C (p.Asp231Ala) c.950A>C (p.Asp317Ala) c.782+624A>C (n.782+624A>C) c.31A>C c.854A>C (p.Asp285Ala) c.494A>C (p.Asp165Ala) c.938A>C (p.Asp313Ala) | dbSNP |
17 | g.7673557T= | CA2245947614 | TP53 | c.971A= (p.Asp324=) c.575A= (p.Asp192=) c.692A= (p.Asp231=) c.950A= (p.Asp317=) c.782+624A= (n.782+624A=) c.31A= c.854A= (p.Asp285=) c.494A= (p.Asp165=) c.938A= (p.Asp313=) | |
17 | g.7673557_7673558delinsCT | CA645587350 | TP53 | c.970_971delinsAG (p.Asp324Ser) c.574_575delinsAG (p.Asp192Ser) c.691_692delinsAG (p.Asp231Ser) c.949_950delinsAG (p.Asp317Ser) c.782+623_782+624delinsAG (n.782+623_782+624delinsAG) c.30_31delinsAG c.853_854delinsAG (p.Asp285Ser) c.493_494delinsAG (p.Asp165Ser) c.937_938delinsAG (p.Asp313Ser) | COSMIC |
17 | g.7673557_7673558delinsTC | CA2245947611 | TP53 | c.970_971delinsGA (p.Asp324=) c.574_575delinsGA (p.Asp192=) c.691_692delinsGA (p.Asp231=) c.949_950delinsGA (p.Asp317=) c.782+623_782+624delinsGA (n.782+623_782+624delinsGA) c.30_31delinsGA c.853_854delinsGA (p.Asp285=) c.493_494delinsGA (p.Asp165=) c.937_938delinsGA (p.Asp313=) | |
17 | g.7673558C>A | CA397835843 | TP53 | c.970G>T (p.Asp324Tyr) c.574G>T (p.Asp192Tyr) c.691G>T (p.Asp231Tyr) c.949G>T (p.Asp317Tyr) c.782+623G>T (n.782+623G>T) c.30G>T c.853G>T (p.Asp285Tyr) c.493G>T (p.Asp165Tyr) c.937G>T (p.Asp313Tyr) | ClinVar dbSNP |
17 | g.7673558C= | CA2245947625 | TP53 | c.970G= (p.Asp324=) c.574G= (p.Asp192=) c.691G= (p.Asp231=) c.949G= (p.Asp317=) c.782+623G= (n.782+623G=) c.30G= c.853G= (p.Asp285=) c.493G= (p.Asp165=) c.937G= (p.Asp313=) | |
17 | g.7673558C>G | CA16620612 | TP53 | c.970G>C (p.Asp324His) c.574G>C (p.Asp192His) c.691G>C (p.Asp231His) c.949G>C (p.Asp317His) c.782+623G>C (n.782+623G>C) c.30G>C c.853G>C (p.Asp285His) c.493G>C (p.Asp165His) c.937G>C (p.Asp313His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673558C>T | CA397835847 | TP53 | c.970G>A (p.Asp324Asn) c.574G>A (p.Asp192Asn) c.691G>A (p.Asp231Asn) c.949G>A (p.Asp317Asn) c.782+623G>A (n.782+623G>A) c.30G>A c.853G>A (p.Asp285Asn) c.493G>A (p.Asp165Asn) c.937G>A (p.Asp313Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673559del | CA658683980 | TP53 | c.970del (p.Asp324MetfsTer21) c.574del (p.Asp192MetfsTer21) c.691del (p.Asp231MetfsTer21) c.949del (p.Asp317MetfsTer21) c.970del (p.Asp324MetfsTer28) c.782+623del (n.782+623del) c.970del (p.Asp324MetfsTer27) c.970del (p.Asp324MetfsTer19) c.574del (p.Asp192MetfsTer19) c.574del (p.Asp192MetfsTer?) c.574del (p.Asp192MetfsTer27) c.30del c.853del (p.Asp285MetfsTer21) c.853del (p.Asp285MetfsTer19) c.493del (p.Asp165MetfsTer19) c.937del (p.Asp313MetfsTer21) c.493del (p.Asp165MetfsTer27) c.493del (p.Asp165MetfsTer21) c.853del (p.Asp285MetfsTer27) | ClinVar dbSNP |
17 | g.7673558_7673580dup | CA645587351 | TP53 | c.948_970dup (p.Asp324AlafsTer29) c.552_574dup (p.Asp192AlafsTer29) c.669_691dup (p.Asp231AlafsTer29) c.927_949dup (p.Asp317AlafsTer29) c.948_970dup (p.Asp324AlafsTer36) c.782+601_782+623dup (n.782+601_782+623dup) c.948_970dup (p.Asp324AlafsTer35) c.948_970dup (p.Asp324AlafsTer27) c.552_574dup (p.Asp192AlafsTer27) c.552_574dup (p.Asp192AlafsTer?) c.552_574dup (p.Asp192AlafsTer35) c.8_30dup c.831_853dup (p.Asp285AlafsTer29) c.831_853dup (p.Asp285AlafsTer27) c.471_493dup (p.Asp165AlafsTer27) c.915_937dup (p.Asp313AlafsTer29) c.471_493dup (p.Asp165AlafsTer35) c.471_493dup (p.Asp165AlafsTer29) c.831_853dup (p.Asp285AlafsTer35) | COSMIC |
17 | g.7673559C>A | CA497713919 | TP53 | c.969G>T (p.Leu323=) c.573G>T (p.Leu191=) c.690G>T (p.Leu230=) c.948G>T (p.Leu316=) c.782+622G>T (n.782+622G>T) c.29G>T c.852G>T (p.Leu284=) c.492G>T (p.Leu164=) c.936G>T (p.Leu312=) | dbSNP |
17 | g.7673559C= | CA2245947634 | TP53 | c.969G= (p.Leu323=) c.573G= (p.Leu191=) c.690G= (p.Leu230=) c.948G= (p.Leu316=) c.782+622G= (n.782+622G=) c.29G= c.852G= (p.Leu284=) c.492G= (p.Leu164=) c.936G= (p.Leu312=) | |
17 | g.7673559C>G | CA497713923 | TP53 | c.969G>C (p.Leu323=) c.573G>C (p.Leu191=) c.690G>C (p.Leu230=) c.948G>C (p.Leu316=) c.782+622G>C (n.782+622G>C) c.29G>C c.852G>C (p.Leu284=) c.492G>C (p.Leu164=) c.936G>C (p.Leu312=) | ClinVar dbSNP |
17 | g.7673559C>T | CA000512 | TP53 | c.969G>A (p.Leu323=) c.573G>A (p.Leu191=) c.690G>A (p.Leu230=) c.948G>A (p.Leu316=) c.782+622G>A (n.782+622G>A) c.29G>A c.852G>A (p.Leu284=) c.492G>A (p.Leu164=) c.936G>A (p.Leu312=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7673560A= | CA2245947643 | TP53 | c.968T= (p.Leu323=) c.572T= (p.Leu191=) c.689T= (p.Leu230=) c.947T= (p.Leu316=) c.782+621T= (n.782+621T=) c.28T= c.851T= (p.Leu284=) c.491T= (p.Leu164=) c.935T= (p.Leu312=) | |
17 | g.7673560A>C | CA397835852 | TP53 | c.968T>G (p.Leu323Arg) c.572T>G (p.Leu191Arg) c.689T>G (p.Leu230Arg) c.947T>G (p.Leu316Arg) c.782+621T>G (n.782+621T>G) c.28T>G c.851T>G (p.Leu284Arg) c.491T>G (p.Leu164Arg) c.935T>G (p.Leu312Arg) | COSMIC |
17 | g.7673560A>G | CA397835853 | TP53 | c.968T>C (p.Leu323Pro) c.572T>C (p.Leu191Pro) c.689T>C (p.Leu230Pro) c.947T>C (p.Leu316Pro) c.782+621T>C (n.782+621T>C) c.28T>C c.851T>C (p.Leu284Pro) c.491T>C (p.Leu164Pro) c.935T>C (p.Leu312Pro) | ClinVar dbSNP COSMIC |
17 | g.7673560A>T | CA397835857 | TP53 | c.968T>A (p.Leu323Gln) c.572T>A (p.Leu191Gln) c.689T>A (p.Leu230Gln) c.947T>A (p.Leu316Gln) c.782+621T>A (n.782+621T>A) c.28T>A c.851T>A (p.Leu284Gln) c.491T>A (p.Leu164Gln) c.935T>A (p.Leu312Gln) | dbSNP |
17 | g.7673560_7673561delinsCC | CA645587352 | TP53 | c.967_968delinsGG (p.Leu323Gly) c.571_572delinsGG (p.Leu191Gly) c.688_689delinsGG (p.Leu230Gly) c.946_947delinsGG (p.Leu316Gly) c.782+620_782+621delinsGG (n.782+620_782+621delinsGG) c.27_28delinsGG c.850_851delinsGG (p.Leu284Gly) c.490_491delinsGG (p.Leu164Gly) c.934_935delinsGG (p.Leu312Gly) | COSMIC |
17 | g.7673562_7673586del | CA645587353 | TP53 | c.944_968del (p.Ser315TrpfsTer22) c.548_572del (p.Ser183TrpfsTer22) c.665_689del (p.Ser222TrpfsTer22) c.923_947del (p.Ser308TrpfsTer22) c.944_968del (p.Ser315TrpfsTer29) c.782+597_782+621del (n.782+597_782+621del) c.944_968del (p.Ser315TrpfsTer28) c.944_968del (p.Ser315TrpfsTer20) c.548_572del (p.Ser183TrpfsTer20) c.548_572del (p.Ser183TrpfsTer?) c.548_572del (p.Ser183TrpfsTer28) c.4_28del c.827_851del (p.Ser276TrpfsTer22) c.827_851del (p.Ser276TrpfsTer20) c.467_491del (p.Ser156TrpfsTer20) c.911_935del (p.Ser304TrpfsTer22) c.467_491del (p.Ser156TrpfsTer28) c.467_491del (p.Ser156TrpfsTer22) c.827_851del (p.Ser276TrpfsTer28) | COSMIC |
17 | g.7673561del | CA497713940 | TP53 | c.967del (p.Leu323TrpfsTer22) c.571del (p.Leu191TrpfsTer22) c.688del (p.Leu230TrpfsTer22) c.946del (p.Leu316TrpfsTer22) c.967del (p.Leu323TrpfsTer29) c.782+620del (n.782+620del) c.967del (p.Leu323TrpfsTer28) c.967del (p.Leu323TrpfsTer20) c.571del (p.Leu191TrpfsTer20) c.571del (p.Leu191TrpfsTer?) c.571del (p.Leu191TrpfsTer28) c.27del c.850del (p.Leu284TrpfsTer22) c.850del (p.Leu284TrpfsTer20) c.490del (p.Leu164TrpfsTer20) c.934del (p.Leu312TrpfsTer22) c.490del (p.Leu164TrpfsTer28) c.490del (p.Leu164TrpfsTer22) c.850del (p.Leu284TrpfsTer28) | COSMIC |
17 | g.7673561G>A | CA497713934 | TP53 | c.967C>T (p.Leu323=) c.571C>T (p.Leu191=) c.688C>T (p.Leu230=) c.946C>T (p.Leu316=) c.782+620C>T (n.782+620C>T) c.27C>T c.850C>T (p.Leu284=) c.490C>T (p.Leu164=) c.934C>T (p.Leu312=) | dbSNP |
17 | g.7673561G>C | CA397835860 | TP53 | c.967C>G (p.Leu323Val) c.571C>G (p.Leu191Val) c.688C>G (p.Leu230Val) c.946C>G (p.Leu316Val) c.782+620C>G (n.782+620C>G) c.27C>G c.850C>G (p.Leu284Val) c.490C>G (p.Leu164Val) c.934C>G (p.Leu312Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673561G= | CA2245947652 | TP53 | c.967C= (p.Leu323=) c.571C= (p.Leu191=) c.688C= (p.Leu230=) c.946C= (p.Leu316=) c.782+620C= (n.782+620C=) c.27C= c.850C= (p.Leu284=) c.490C= (p.Leu164=) c.934C= (p.Leu312=) | |
17 | g.7673561G>T | CA397835867 | TP53 | c.967C>A (p.Leu323Met) c.571C>A (p.Leu191Met) c.688C>A (p.Leu230Met) c.946C>A (p.Leu316Met) c.782+620C>A (n.782+620C>A) c.27C>A c.850C>A (p.Leu284Met) c.490C>A (p.Leu164Met) c.934C>A (p.Leu312Met) | dbSNP COSMIC |
17 | g.7673562T>A | CA497713943 | TP53 | c.966A>T (p.Pro322=) c.570A>T (p.Pro190=) c.687A>T (p.Pro229=) c.945A>T (p.Pro315=) c.782+619A>T (n.782+619A>T) c.26A>T c.849A>T (p.Pro283=) c.489A>T (p.Pro163=) c.933A>T (p.Pro311=) | |
17 | g.7673562T>C | CA497713945 | TP53 | c.966A>G (p.Pro322=) c.570A>G (p.Pro190=) c.687A>G (p.Pro229=) c.945A>G (p.Pro315=) c.782+619A>G (n.782+619A>G) c.26A>G c.849A>G (p.Pro283=) c.489A>G (p.Pro163=) c.933A>G (p.Pro311=) | ClinVar |
17 | g.7673562T>G | CA497713950 | TP53 | c.966A>C (p.Pro322=) c.570A>C (p.Pro190=) c.687A>C (p.Pro229=) c.945A>C (p.Pro315=) c.782+619A>C (n.782+619A>C) c.26A>C c.849A>C (p.Pro283=) c.489A>C (p.Pro163=) c.933A>C (p.Pro311=) | ClinVar |
17 | g.7673562dup | CA2245947657 | TP53 | c.966dup (p.Leu323ThrfsTer14) c.570dup (p.Leu191ThrfsTer14) c.687dup (p.Leu230ThrfsTer14) c.945dup (p.Leu316ThrfsTer14) c.966dup (p.Leu323ThrfsTer?) c.782+619dup (n.782+619dup) c.966dup (p.Leu323ThrfsTer24) c.966dup (p.Leu323ThrfsTer13) c.570dup (p.Leu191ThrfsTer13) c.570dup (p.Leu191ThrfsTer?) c.570dup (p.Leu191ThrfsTer24) c.26dup c.849dup (p.Leu284ThrfsTer14) c.849dup (p.Leu284ThrfsTer13) c.489dup (p.Leu164ThrfsTer13) c.933dup (p.Leu312ThrfsTer14) c.489dup (p.Leu164ThrfsTer24) c.489dup (p.Leu164ThrfsTer14) c.849dup (p.Leu284ThrfsTer24) | dbSNP |
17 | g.7673563G>A | CA397835873 | TP53 | c.965C>T (p.Pro322Leu) c.569C>T (p.Pro190Leu) c.686C>T (p.Pro229Leu) c.944C>T (p.Pro315Leu) c.782+618C>T (n.782+618C>T) c.25C>T c.848C>T (p.Pro283Leu) c.488C>T (p.Pro163Leu) c.932C>T (p.Pro311Leu) | dbSNP COSMIC |
17 | g.7673563G>C | CA397835872 | TP53 | c.965C>G (p.Pro322Arg) c.569C>G (p.Pro190Arg) c.686C>G (p.Pro229Arg) c.944C>G (p.Pro315Arg) c.782+618C>G (n.782+618C>G) c.25C>G c.848C>G (p.Pro283Arg) c.488C>G (p.Pro163Arg) c.932C>G (p.Pro311Arg) | ClinVar dbSNP COSMIC |
17 | g.7673563G>T | CA397835870 | TP53 | c.965C>A (p.Pro322Gln) c.569C>A (p.Pro190Gln) c.686C>A (p.Pro229Gln) c.944C>A (p.Pro315Gln) c.782+618C>A (n.782+618C>A) c.25C>A c.848C>A (p.Pro283Gln) c.488C>A (p.Pro163Gln) c.932C>A (p.Pro311Gln) | dbSNP |
17 | g.7673564del | CA497713957 | TP53 | c.965del (p.Pro322HisfsTer23) c.569del (p.Pro190HisfsTer23) c.686del (p.Pro229HisfsTer23) c.944del (p.Pro315HisfsTer23) c.965del (p.Pro322HisfsTer30) c.782+618del (n.782+618del) c.965del (p.Pro322HisfsTer29) c.965del (p.Pro322HisfsTer21) c.569del (p.Pro190HisfsTer21) c.569del (p.Pro190HisfsTer?) c.569del (p.Pro190HisfsTer29) c.25del c.848del (p.Pro283HisfsTer23) c.848del (p.Pro283HisfsTer21) c.488del (p.Pro163HisfsTer21) c.932del (p.Pro311HisfsTer23) c.488del (p.Pro163HisfsTer29) c.488del (p.Pro163HisfsTer23) c.848del (p.Pro283HisfsTer29) | ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7673564G>A | CA336073 | TP53 | c.964C>T (p.Pro322Ser) c.568C>T (p.Pro190Ser) c.685C>T (p.Pro229Ser) c.943C>T (p.Pro315Ser) c.782+617C>T (n.782+617C>T) c.24C>T c.847C>T (p.Pro283Ser) c.487C>T (p.Pro163Ser) c.931C>T (p.Pro311Ser) | ClinVar dbSNP gnomAD v4 |
17 | g.7673564G>C | CA397835876 | TP53 | c.964C>G (p.Pro322Ala) c.568C>G (p.Pro190Ala) c.685C>G (p.Pro229Ala) c.943C>G (p.Pro315Ala) c.782+617C>G (n.782+617C>G) c.24C>G c.847C>G (p.Pro283Ala) c.487C>G (p.Pro163Ala) c.931C>G (p.Pro311Ala) | ClinVar dbSNP |
17 | g.7673564G= | CA2245947670 | TP53 | c.964C= (p.Pro322=) c.568C= (p.Pro190=) c.685C= (p.Pro229=) c.943C= (p.Pro315=) c.782+617C= (n.782+617C=) c.24C= c.847C= (p.Pro283=) c.487C= (p.Pro163=) c.931C= (p.Pro311=) | |
17 | g.7673564G>T | CA10580909 | TP53 | c.964C>A (p.Pro322Thr) c.568C>A (p.Pro190Thr) c.685C>A (p.Pro229Thr) c.943C>A (p.Pro315Thr) c.782+617C>A (n.782+617C>A) c.24C>A c.847C>A (p.Pro283Thr) c.487C>A (p.Pro163Thr) c.931C>A (p.Pro311Thr) | ClinVar dbSNP |
17 | g.7673565T>A | CA397835878 | TP53 | c.963A>T (p.Lys321Asn) c.567A>T (p.Lys189Asn) c.684A>T (p.Lys228Asn) c.942A>T (p.Lys314Asn) c.782+616A>T (n.782+616A>T) c.23A>T c.846A>T (p.Lys282Asn) c.486A>T (p.Lys162Asn) c.930A>T (p.Lys310Asn) | dbSNP |
17 | g.7673565T>C | CA497713967 | TP53 | c.963A>G (p.Lys321=) c.567A>G (p.Lys189=) c.684A>G (p.Lys228=) c.942A>G (p.Lys314=) c.782+616A>G (n.782+616A>G) c.23A>G c.846A>G (p.Lys282=) c.486A>G (p.Lys162=) c.930A>G (p.Lys310=) | ClinVar dbSNP COSMIC |
17 | g.7673565T>G | CA397835879 | TP53 | c.963A>C (p.Lys321Asn) c.567A>C (p.Lys189Asn) c.684A>C (p.Lys228Asn) c.942A>C (p.Lys314Asn) c.782+616A>C (n.782+616A>C) c.23A>C c.846A>C (p.Lys282Asn) c.486A>C (p.Lys162Asn) c.930A>C (p.Lys310Asn) | dbSNP |
17 | g.7673567dup | CA645587355 | TP53 | c.963dup (p.Pro322ThrfsTer15) c.567dup (p.Pro190ThrfsTer15) c.684dup (p.Pro229ThrfsTer15) c.942dup (p.Pro315ThrfsTer15) c.963dup (p.Pro322ThrfsTer?) c.782+616dup (n.782+616dup) c.963dup (p.Pro322ThrfsTer25) c.963dup (p.Pro322ThrfsTer14) c.567dup (p.Pro190ThrfsTer14) c.567dup (p.Pro190ThrfsTer?) c.567dup (p.Pro190ThrfsTer25) c.23dup c.846dup (p.Pro283ThrfsTer15) c.846dup (p.Pro283ThrfsTer14) c.486dup (p.Pro163ThrfsTer14) c.930dup (p.Pro311ThrfsTer15) c.486dup (p.Pro163ThrfsTer25) c.486dup (p.Pro163ThrfsTer15) c.846dup (p.Pro283ThrfsTer25) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673567del | CA497713971 | TP53 | c.963del (p.Lys321AsnfsTer24) c.567del (p.Lys189AsnfsTer24) c.684del (p.Lys228AsnfsTer24) c.942del (p.Lys314AsnfsTer24) c.963del (p.Lys321AsnfsTer?) c.782+616del (n.782+616del) c.963del (p.Lys321AsnfsTer30) c.963del (p.Lys321AsnfsTer22) c.567del (p.Lys189AsnfsTer22) c.567del (p.Lys189AsnfsTer?) c.567del (p.Lys189AsnfsTer30) c.23del c.846del (p.Lys282AsnfsTer24) c.846del (p.Lys282AsnfsTer22) c.486del (p.Lys162AsnfsTer22) c.930del (p.Lys310AsnfsTer24) c.486del (p.Lys162AsnfsTer30) c.486del (p.Lys162AsnfsTer24) c.846del (p.Lys282AsnfsTer30) | COSMIC |
17 | g.7673565_7673568delinsTTTC | CA2245947676 | TP53 | c.960_963delinsGAAA (p.Lys320=) c.564_567delinsGAAA (p.Lys188=) c.681_684delinsGAAA (p.Lys227=) c.939_942delinsGAAA (p.Lys313=) c.782+613_782+616delinsGAAA (n.782+613_782+616delinsGAAA) c.20_23delinsGAAA c.843_846delinsGAAA (p.Lys281=) c.483_486delinsGAAA (p.Lys161=) c.927_930delinsGAAA (p.Lys309=) | |
17 | g.7673565_7673605del | CA645587356 | TP53 | c.923_963del (p.Leu308ProfsTer15) c.527_567del (p.Leu176ProfsTer15) c.644_684del (p.Leu215ProfsTer15) c.902_942del (p.Leu301ProfsTer15) c.923_963del (p.Leu308ProfsTer?) c.782+576_782+616del (n.782+576_782+616del) c.923_963del (p.Leu308ProfsTer25) c.923_963del (p.Leu308ProfsTer14) c.527_567del (p.Leu176ProfsTer14) c.527_567del (p.Leu176ProfsTer?) c.527_567del (p.Leu176ProfsTer25) c.806_846del (p.Leu269ProfsTer15) c.806_846del (p.Leu269ProfsTer14) c.446_486del (p.Leu149ProfsTer14) c.890_930del (p.Leu297ProfsTer15) c.446_486del (p.Leu149ProfsTer25) c.446_486del (p.Leu149ProfsTer15) c.806_846del (p.Leu269ProfsTer25) | COSMIC |
17 | g.7673566T>A | CA397835881 | TP53 | c.962A>T (p.Lys321Ile) c.566A>T (p.Lys189Ile) c.683A>T (p.Lys228Ile) c.941A>T (p.Lys314Ile) c.782+615A>T (n.782+615A>T) c.22A>T c.845A>T (p.Lys282Ile) c.485A>T (p.Lys162Ile) c.929A>T (p.Lys310Ile) | dbSNP |
17 | g.7673566T>C | CA397835882 | TP53 | c.962A>G (p.Lys321Arg) c.566A>G (p.Lys189Arg) c.683A>G (p.Lys228Arg) c.941A>G (p.Lys314Arg) c.782+615A>G (n.782+615A>G) c.22A>G c.845A>G (p.Lys282Arg) c.485A>G (p.Lys162Arg) c.929A>G (p.Lys310Arg) | dbSNP |
17 | g.7673566T>G | CA397835886 | TP53 | c.962A>C (p.Lys321Thr) c.566A>C (p.Lys189Thr) c.683A>C (p.Lys228Thr) c.941A>C (p.Lys314Thr) c.782+615A>C (n.782+615A>C) c.22A>C c.845A>C (p.Lys282Thr) c.485A>C (p.Lys162Thr) c.929A>C (p.Lys310Thr) | dbSNP |
17 | g.7673571_7673573dup | CA645587357 | TP53 | c.960_962dup (p.Lys321_Pro322insLys) c.564_566dup (p.Lys189_Pro190insLys) c.681_683dup (p.Lys228_Pro229insLys) c.939_941dup (p.Lys314_Pro315insLys) c.782+613_782+615dup (n.782+613_782+615dup) c.20_22dup c.843_845dup (p.Lys282_Pro283insLys) c.483_485dup (p.Lys162_Pro163insLys) c.927_929dup (p.Lys310_Pro311insLys) | COSMIC COSMIC |
17 | g.7673571_7673573del | CA891844039 | TP53 | c.960_962del (p.Lys321del) c.564_566del (p.Lys189del) c.681_683del (p.Lys228del) c.939_941del (p.Lys314del) c.782+613_782+615del (n.782+613_782+615del) c.20_22del c.843_845del (p.Lys282del) c.483_485del (p.Lys162del) c.927_929del (p.Lys310del) | ClinVar dbSNP |
17 | g.7673567T>A | CA397835889 | TP53 | c.961A>T (p.Lys321Ter) c.565A>T (p.Lys189Ter) c.682A>T (p.Lys228Ter) c.940A>T (p.Lys314Ter) c.782+614A>T (n.782+614A>T) c.21A>T c.844A>T (p.Lys282Ter) c.484A>T (p.Lys162Ter) c.928A>T (p.Lys310Ter) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673567T>C | CA397835893 | TP53 | c.961A>G (p.Lys321Glu) c.565A>G (p.Lys189Glu) c.682A>G (p.Lys228Glu) c.940A>G (p.Lys314Glu) c.782+614A>G (n.782+614A>G) c.21A>G c.844A>G (p.Lys282Glu) c.484A>G (p.Lys162Glu) c.928A>G (p.Lys310Glu) | |
17 | g.7673567T>G | CA397835894 | TP53 | c.961A>C (p.Lys321Gln) c.565A>C (p.Lys189Gln) c.682A>C (p.Lys228Gln) c.940A>C (p.Lys314Gln) c.782+614A>C (n.782+614A>C) c.21A>C c.844A>C (p.Lys282Gln) c.484A>C (p.Lys162Gln) c.928A>C (p.Lys310Gln) | |
17 | g.7673567T= | CA2245947687 | TP53 | c.961A= (p.Lys321=) c.565A= (p.Lys189=) c.682A= (p.Lys228=) c.940A= (p.Lys314=) c.782+614A= (n.782+614A=) c.21A= c.844A= (p.Lys282=) c.484A= (p.Lys162=) c.928A= (p.Lys310=) | |
17 | g.7673568del | CA645587358 | TP53 | c.960del (p.Lys321AsnfsTer24) c.564del (p.Lys189AsnfsTer24) c.681del (p.Lys228AsnfsTer24) c.939del (p.Lys314AsnfsTer24) c.960del (p.Lys321AsnfsTer?) c.782+613del (n.782+613del) c.960del (p.Lys321AsnfsTer22) c.564del (p.Lys189AsnfsTer22) c.564del (p.Lys189AsnfsTer?) c.20del c.843del (p.Lys282AsnfsTer24) c.843del (p.Lys282AsnfsTer22) c.483del (p.Lys162AsnfsTer22) c.927del (p.Lys310AsnfsTer24) c.483del (p.Lys162AsnfsTer?) c.483del (p.Lys162AsnfsTer24) c.843del (p.Lys282AsnfsTer?) | ClinVar COSMIC COSMIC COSMIC COSMIC |
17 | g.7673568C>A | CA397835895 | TP53 | c.960G>T (p.Lys320Asn) c.564G>T (p.Lys188Asn) c.681G>T (p.Lys227Asn) c.939G>T (p.Lys313Asn) c.782+613G>T (n.782+613G>T) c.20G>T c.843G>T (p.Lys281Asn) c.483G>T (p.Lys161Asn) c.927G>T (p.Lys309Asn) | dbSNP |
17 | g.7673568C>G | CA397835897 | TP53 | c.960G>C (p.Lys320Asn) c.564G>C (p.Lys188Asn) c.681G>C (p.Lys227Asn) c.939G>C (p.Lys313Asn) c.782+613G>C (n.782+613G>C) c.20G>C c.843G>C (p.Lys281Asn) c.483G>C (p.Lys161Asn) c.927G>C (p.Lys309Asn) | dbSNP COSMIC |
17 | g.7673568C>T | CA497713987 | TP53 | c.960G>A (p.Lys320=) c.564G>A (p.Lys188=) c.681G>A (p.Lys227=) c.939G>A (p.Lys313=) c.782+613G>A (n.782+613G>A) c.20G>A c.843G>A (p.Lys281=) c.483G>A (p.Lys161=) c.927G>A (p.Lys309=) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673569T>A | CA397835903 | TP53 | c.959A>T (p.Lys320Met) c.563A>T (p.Lys188Met) c.680A>T (p.Lys227Met) c.938A>T (p.Lys313Met) c.782+612A>T (n.782+612A>T) c.19A>T c.842A>T (p.Lys281Met) c.482A>T (p.Lys161Met) c.926A>T (p.Lys309Met) | dbSNP |
17 | g.7673569T>C | CA397835905 | TP53 | c.959A>G (p.Lys320Arg) c.563A>G (p.Lys188Arg) c.680A>G (p.Lys227Arg) c.938A>G (p.Lys313Arg) c.782+612A>G (n.782+612A>G) c.19A>G c.842A>G (p.Lys281Arg) c.482A>G (p.Lys161Arg) c.926A>G (p.Lys309Arg) | dbSNP |
17 | g.7673569T>G | CA397835900 | TP53 | c.959A>C (p.Lys320Thr) c.563A>C (p.Lys188Thr) c.680A>C (p.Lys227Thr) c.938A>C (p.Lys313Thr) c.782+612A>C (n.782+612A>C) c.19A>C c.842A>C (p.Lys281Thr) c.482A>C (p.Lys161Thr) c.926A>C (p.Lys309Thr) | ClinVar |
17 | g.7673570del | CA497714003 | TP53 | c.959del (p.Lys320ArgfsTer25) c.563del (p.Lys188ArgfsTer25) c.680del (p.Lys227ArgfsTer25) c.938del (p.Lys313ArgfsTer25) c.959del (p.Lys320ArgfsTer?) c.782+612del (n.782+612del) c.959del (p.Lys320ArgfsTer23) c.563del (p.Lys188ArgfsTer23) c.563del (p.Lys188ArgfsTer?) c.19del c.842del (p.Lys281ArgfsTer25) c.842del (p.Lys281ArgfsTer23) c.482del (p.Lys161ArgfsTer23) c.926del (p.Lys309ArgfsTer25) c.482del (p.Lys161ArgfsTer?) c.482del (p.Lys161ArgfsTer25) c.842del (p.Lys281ArgfsTer?) | COSMIC |
17 | g.7673570T>A | CA397835908 | TP53 | c.958A>T (p.Lys320Ter) c.562A>T (p.Lys188Ter) c.679A>T (p.Lys227Ter) c.937A>T (p.Lys313Ter) c.782+611A>T (n.782+611A>T) c.18A>T c.841A>T (p.Lys281Ter) c.481A>T (p.Lys161Ter) c.925A>T (p.Lys309Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673570T>C | CA397835912 | TP53 | c.958A>G (p.Lys320Glu) c.562A>G (p.Lys188Glu) c.679A>G (p.Lys227Glu) c.937A>G (p.Lys313Glu) c.782+611A>G (n.782+611A>G) c.18A>G c.841A>G (p.Lys281Glu) c.481A>G (p.Lys161Glu) c.925A>G (p.Lys309Glu) | dbSNP |
17 | g.7673570T>G | CA397835915 | TP53 | c.958A>C (p.Lys320Gln) c.562A>C (p.Lys188Gln) c.679A>C (p.Lys227Gln) c.937A>C (p.Lys313Gln) c.782+611A>C (n.782+611A>C) c.18A>C c.841A>C (p.Lys281Gln) c.481A>C (p.Lys161Gln) c.925A>C (p.Lys309Gln) | |
17 | g.7673570_7673587del | CA645587360 | TP53 | c.941_958del (p.Ser314Ter) c.545_562del (p.Ser182Ter) c.662_679del (p.Ser221Ter) c.920_937del (p.Ser307Ter) c.782+594_782+611del (n.782+594_782+611del) c.1_18del c.824_841del (p.Ser275Ter) c.464_481del (p.Ser155Ter) c.908_925del (p.Ser303Ter) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673570_7673588del | CA645587363 | TP53 | c.940_958del (p.Ser314ArgfsTer25) c.544_562del (p.Ser182ArgfsTer25) c.661_679del (p.Ser221ArgfsTer25) c.919_937del (p.Ser307ArgfsTer25) c.940_958del (p.Ser314ArgfsTer?) c.782+593_782+611del (n.782+593_782+611del) c.940_958del (p.Ser314ArgfsTer23) c.544_562del (p.Ser182ArgfsTer23) c.544_562del (p.Ser182ArgfsTer?) c.823_841del (p.Ser275ArgfsTer25) c.823_841del (p.Ser275ArgfsTer23) c.463_481del (p.Ser155ArgfsTer23) c.907_925del (p.Ser303ArgfsTer25) c.463_481del (p.Ser155ArgfsTer?) c.463_481del (p.Ser155ArgfsTer25) c.823_841del (p.Ser275ArgfsTer?) | COSMIC |
17 | g.7673571del | CA645587364 | TP53 | c.957del (p.Lys320ArgfsTer25) c.561del (p.Lys188ArgfsTer25) c.678del (p.Lys227ArgfsTer25) c.936del (p.Lys313ArgfsTer25) c.957del (p.Lys320ArgfsTer?) c.782+610del (n.782+610del) c.957del (p.Lys320ArgfsTer23) c.561del (p.Lys188ArgfsTer23) c.561del (p.Lys188ArgfsTer?) c.17del c.840del (p.Lys281ArgfsTer25) c.840del (p.Lys281ArgfsTer23) c.480del (p.Lys161ArgfsTer23) c.924del (p.Lys309ArgfsTer25) c.480del (p.Lys161ArgfsTer?) c.480del (p.Lys161ArgfsTer25) c.840del (p.Lys281ArgfsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673571C>A | CA397835919 | TP53 | c.957G>T (p.Lys319Asn) c.561G>T (p.Lys187Asn) c.678G>T (p.Lys226Asn) c.936G>T (p.Lys312Asn) c.782+610G>T (n.782+610G>T) c.17G>T c.840G>T (p.Lys280Asn) c.480G>T (p.Lys160Asn) c.924G>T (p.Lys308Asn) | dbSNP COSMIC |
17 | g.7673571C>G | CA397835921 | TP53 | c.957G>C (p.Lys319Asn) c.561G>C (p.Lys187Asn) c.678G>C (p.Lys226Asn) c.936G>C (p.Lys312Asn) c.782+610G>C (n.782+610G>C) c.17G>C c.840G>C (p.Lys280Asn) c.480G>C (p.Lys160Asn) c.924G>C (p.Lys308Asn) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673571C>T | CA497714016 | TP53 | c.957G>A (p.Lys319=) c.561G>A (p.Lys187=) c.678G>A (p.Lys226=) c.936G>A (p.Lys312=) c.782+610G>A (n.782+610G>A) c.17G>A c.840G>A (p.Lys280=) c.480G>A (p.Lys160=) c.924G>A (p.Lys308=) | dbSNP COSMIC |
17 | g.7673572T>A | CA397835924 | TP53 | c.956A>T (p.Lys319Met) c.560A>T (p.Lys187Met) c.677A>T (p.Lys226Met) c.935A>T (p.Lys312Met) c.782+609A>T (n.782+609A>T) c.16A>T c.839A>T (p.Lys280Met) c.479A>T (p.Lys160Met) c.923A>T (p.Lys308Met) | dbSNP |
17 | g.7673572T>C | CA397835927 | TP53 | c.956A>G (p.Lys319Arg) c.560A>G (p.Lys187Arg) c.677A>G (p.Lys226Arg) c.935A>G (p.Lys312Arg) c.782+609A>G (n.782+609A>G) c.16A>G c.839A>G (p.Lys280Arg) c.479A>G (p.Lys160Arg) c.923A>G (p.Lys308Arg) | dbSNP COSMIC |
17 | g.7673572T>G | CA397835930 | TP53 | c.956A>C (p.Lys319Thr) c.560A>C (p.Lys187Thr) c.677A>C (p.Lys226Thr) c.935A>C (p.Lys312Thr) c.782+609A>C (n.782+609A>C) c.16A>C c.839A>C (p.Lys280Thr) c.479A>C (p.Lys160Thr) c.923A>C (p.Lys308Thr) | |
17 | g.7673573T>A | CA397835934 | TP53 | c.955A>T (p.Lys319Ter) c.559A>T (p.Lys187Ter) c.676A>T (p.Lys226Ter) c.934A>T (p.Lys312Ter) c.782+608A>T (n.782+608A>T) c.15A>T c.838A>T (p.Lys280Ter) c.478A>T (p.Lys160Ter) c.922A>T (p.Lys308Ter) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673573T>C | CA397835937 | TP53 | c.955A>G (p.Lys319Glu) c.559A>G (p.Lys187Glu) c.676A>G (p.Lys226Glu) c.934A>G (p.Lys312Glu) c.782+608A>G (n.782+608A>G) c.15A>G c.838A>G (p.Lys280Glu) c.478A>G (p.Lys160Glu) c.922A>G (p.Lys308Glu) | COSMIC |
17 | g.7673573T>G | CA397835940 | TP53 | c.955A>C (p.Lys319Gln) c.559A>C (p.Lys187Gln) c.676A>C (p.Lys226Gln) c.934A>C (p.Lys312Gln) c.782+608A>C (n.782+608A>C) c.15A>C c.838A>C (p.Lys280Gln) c.478A>C (p.Lys160Gln) c.922A>C (p.Lys308Gln) | |
17 | g.7673573_7673577delinsTTGGC | CA2245947690 | TP53 | c.951_955delinsGCCAA (p.Gln317=) c.555_559delinsGCCAA (p.Gln185=) c.672_676delinsGCCAA (p.Gln224=) c.930_934delinsGCCAA (p.Gln310=) c.782+604_782+608delinsGCCAA (n.782+604_782+608delinsGCCAA) c.11_15delinsGCCAA c.834_838delinsGCCAA (p.Gln278=) c.474_478delinsGCCAA (p.Gln158=) c.918_922delinsGCCAA (p.Gln306=) | |
17 | g.7673574T>A | CA497714040 | TP53 | c.954A>T (p.Pro318=) c.558A>T (p.Pro186=) c.675A>T (p.Pro225=) c.933A>T (p.Pro311=) c.782+607A>T (n.782+607A>T) c.14A>T c.837A>T (p.Pro279=) c.477A>T (p.Pro159=) c.921A>T (p.Pro307=) | ClinVar |
17 | g.7673574T>C | CA497714031 | TP53 | c.954A>G (p.Pro318=) c.558A>G (p.Pro186=) c.675A>G (p.Pro225=) c.933A>G (p.Pro311=) c.782+607A>G (n.782+607A>G) c.14A>G c.837A>G (p.Pro279=) c.477A>G (p.Pro159=) c.921A>G (p.Pro307=) | ClinVar dbSNP |
17 | g.7673574T>G | CA001195 | TP53 | c.954A>C (p.Pro318=) c.558A>C (p.Pro186=) c.675A>C (p.Pro225=) c.933A>C (p.Pro311=) c.782+607A>C (n.782+607A>C) c.14A>C c.837A>C (p.Pro279=) c.477A>C (p.Pro159=) c.921A>C (p.Pro307=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673574T= | CA2245947701 | TP53 | c.954A= (p.Pro318=) c.558A= (p.Pro186=) c.675A= (p.Pro225=) c.933A= (p.Pro311=) c.782+607A= (n.782+607A=) c.14A= c.837A= (p.Pro279=) c.477A= (p.Pro159=) c.921A= (p.Pro307=) | |
17 | g.7673577_7673580dup | CA645587367 | TP53 | c.951_954dup (p.Lys319AlafsTer19) c.555_558dup (p.Lys187AlafsTer19) c.672_675dup (p.Lys226AlafsTer19) c.930_933dup (p.Lys312AlafsTer19) c.951_954dup (p.Lys319AlafsTer?) c.782+604_782+607dup (n.782+604_782+607dup) c.951_954dup (p.Lys319AlafsTer29) c.951_954dup (p.Lys319AlafsTer18) c.555_558dup (p.Lys187AlafsTer18) c.555_558dup (p.Lys187AlafsTer?) c.555_558dup (p.Lys187AlafsTer29) c.11_14dup c.834_837dup (p.Lys280AlafsTer19) c.834_837dup (p.Lys280AlafsTer18) c.474_477dup (p.Lys160AlafsTer18) c.918_921dup (p.Lys308AlafsTer19) c.474_477dup (p.Lys160AlafsTer29) c.474_477dup (p.Lys160AlafsTer19) c.834_837dup (p.Lys280AlafsTer29) | COSMIC COSMIC |
17 | g.7673577_7673580del | CA915949515 | TP53 | c.951_954del (p.Pro318ArgfsTer26) c.555_558del (p.Pro186ArgfsTer26) c.672_675del (p.Pro225ArgfsTer26) c.930_933del (p.Pro311ArgfsTer26) c.951_954del (p.Pro318ArgfsTer?) c.782+604_782+607del (n.782+604_782+607del) c.951_954del (p.Pro318ArgfsTer24) c.555_558del (p.Pro186ArgfsTer24) c.555_558del (p.Pro186ArgfsTer?) c.11_14del c.834_837del (p.Pro279ArgfsTer26) c.834_837del (p.Pro279ArgfsTer24) c.474_477del (p.Pro159ArgfsTer24) c.918_921del (p.Pro307ArgfsTer26) c.474_477del (p.Pro159ArgfsTer?) c.474_477del (p.Pro159ArgfsTer26) c.834_837del (p.Pro279ArgfsTer?) | ClinVar dbSNP |
17 | g.7673575G>A | CA397835952 | TP53 | c.953C>T (p.Pro318Leu) c.557C>T (p.Pro186Leu) c.674C>T (p.Pro225Leu) c.932C>T (p.Pro311Leu) c.782+606C>T (n.782+606C>T) c.13C>T c.836C>T (p.Pro279Leu) c.476C>T (p.Pro159Leu) c.920C>T (p.Pro307Leu) | ClinVar dbSNP gnomAD v4 |
17 | g.7673575G>C | CA397835946 | TP53 | c.953C>G (p.Pro318Arg) c.557C>G (p.Pro186Arg) c.674C>G (p.Pro225Arg) c.932C>G (p.Pro311Arg) c.782+606C>G (n.782+606C>G) c.13C>G c.836C>G (p.Pro279Arg) c.476C>G (p.Pro159Arg) c.920C>G (p.Pro307Arg) | ClinVar dbSNP |
17 | g.7673575G= | CA2245947708 | TP53 | c.953C= (p.Pro318=) c.557C= (p.Pro186=) c.674C= (p.Pro225=) c.932C= (p.Pro311=) c.782+606C= (n.782+606C=) c.13C= c.836C= (p.Pro279=) c.476C= (p.Pro159=) c.920C= (p.Pro307=) | |
17 | g.7673575G>T | CA397835949 | TP53 | c.953C>A (p.Pro318Gln) c.557C>A (p.Pro186Gln) c.674C>A (p.Pro225Gln) c.932C>A (p.Pro311Gln) c.782+606C>A (n.782+606C>A) c.13C>A c.836C>A (p.Pro279Gln) c.476C>A (p.Pro159Gln) c.920C>A (p.Pro307Gln) | dbSNP |
17 | g.7673576G>A | CA397835955 | TP53 | c.952C>T (p.Pro318Ser) c.556C>T (p.Pro186Ser) c.673C>T (p.Pro225Ser) c.931C>T (p.Pro311Ser) c.782+605C>T (n.782+605C>T) c.12C>T c.835C>T (p.Pro279Ser) c.475C>T (p.Pro159Ser) c.919C>T (p.Pro307Ser) | ClinVar dbSNP |
17 | g.7673576G>C | CA397835958 | TP53 | c.952C>G (p.Pro318Ala) c.556C>G (p.Pro186Ala) c.673C>G (p.Pro225Ala) c.931C>G (p.Pro311Ala) c.782+605C>G (n.782+605C>G) c.12C>G c.835C>G (p.Pro279Ala) c.475C>G (p.Pro159Ala) c.919C>G (p.Pro307Ala) | dbSNP COSMIC |
17 | g.7673576G>T | CA397835961 | TP53 | c.952C>A (p.Pro318Thr) c.556C>A (p.Pro186Thr) c.673C>A (p.Pro225Thr) c.931C>A (p.Pro311Thr) c.782+605C>A (n.782+605C>A) c.12C>A c.835C>A (p.Pro279Thr) c.475C>A (p.Pro159Thr) c.919C>A (p.Pro307Thr) | dbSNP |
17 | g.7673577del | CA645587368 | TP53 | c.951del (p.Gln317HisfsTer28) c.555del (p.Gln185HisfsTer28) c.672del (p.Gln224HisfsTer28) c.930del (p.Gln310HisfsTer28) c.951del (p.Gln317HisfsTer?) c.782+604del (n.782+604del) c.951del (p.Gln317HisfsTer26) c.555del (p.Gln185HisfsTer26) c.555del (p.Gln185HisfsTer?) c.11del c.834del (p.Gln278HisfsTer28) c.834del (p.Gln278HisfsTer26) c.474del (p.Gln158HisfsTer26) c.918del (p.Gln306HisfsTer28) c.474del (p.Gln158HisfsTer?) c.474del (p.Gln158HisfsTer28) c.834del (p.Gln278HisfsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673577C>A | CA16615689 | TP53 | c.951G>T (p.Gln317His) c.555G>T (p.Gln185His) c.672G>T (p.Gln224His) c.930G>T (p.Gln310His) c.782+604G>T (n.782+604G>T) c.11G>T c.834G>T (p.Gln278His) c.474G>T (p.Gln158His) c.918G>T (p.Gln306His) | ClinVar dbSNP |
17 | g.7673577C= | CA2245947719 | TP53 | c.951G= (p.Gln317=) c.555G= (p.Gln185=) c.672G= (p.Gln224=) c.930G= (p.Gln310=) c.782+604G= (n.782+604G=) c.11G= c.834G= (p.Gln278=) c.474G= (p.Gln158=) c.918G= (p.Gln306=) | |
17 | g.7673577C>G | CA397835964 | TP53 | c.951G>C (p.Gln317His) c.555G>C (p.Gln185His) c.672G>C (p.Gln224His) c.930G>C (p.Gln310His) c.782+604G>C (n.782+604G>C) c.11G>C c.834G>C (p.Gln278His) c.474G>C (p.Gln158His) c.918G>C (p.Gln306His) | dbSNP |
17 | g.7673577C>T | CA497714069 | TP53 | c.951G>A (p.Gln317=) c.555G>A (p.Gln185=) c.672G>A (p.Gln224=) c.930G>A (p.Gln310=) c.782+604G>A (n.782+604G>A) c.11G>A c.834G>A (p.Gln278=) c.474G>A (p.Gln158=) c.918G>A (p.Gln306=) | ClinVar dbSNP |
17 | g.7673577_7673578delinsCT | CA2245947725 | TP53 | c.950_951delinsAG (p.Gln317=) c.554_555delinsAG (p.Gln185=) c.671_672delinsAG (p.Gln224=) c.929_930delinsAG (p.Gln310=) c.782+603_782+604delinsAG (n.782+603_782+604delinsAG) c.10_11delinsAG c.833_834delinsAG (p.Gln278=) c.473_474delinsAG (p.Gln158=) c.917_918delinsAG (p.Gln306=) | |
17 | g.7673578del | CA645587369 | TP53 | c.950del (p.Gln317ArgfsTer28) c.554del (p.Gln185ArgfsTer28) c.671del (p.Gln224ArgfsTer28) c.929del (p.Gln310ArgfsTer28) c.950del (p.Gln317ArgfsTer?) c.782+603del (n.782+603del) c.950del (p.Gln317ArgfsTer26) c.554del (p.Gln185ArgfsTer26) c.554del (p.Gln185ArgfsTer?) c.10del c.833del (p.Gln278ArgfsTer28) c.833del (p.Gln278ArgfsTer26) c.473del (p.Gln158ArgfsTer26) c.917del (p.Gln306ArgfsTer28) c.473del (p.Gln158ArgfsTer?) c.473del (p.Gln158ArgfsTer28) c.833del (p.Gln278ArgfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673578T>A | CA397835969 | TP53 | c.950A>T (p.Gln317Leu) c.554A>T (p.Gln185Leu) c.671A>T (p.Gln224Leu) c.929A>T (p.Gln310Leu) c.782+603A>T (n.782+603A>T) c.10A>T c.833A>T (p.Gln278Leu) c.473A>T (p.Gln158Leu) c.917A>T (p.Gln306Leu) | ClinVar dbSNP |
17 | g.7673578T>C | CA397835971 | TP53 | c.950A>G (p.Gln317Arg) c.554A>G (p.Gln185Arg) c.671A>G (p.Gln224Arg) c.929A>G (p.Gln310Arg) c.782+603A>G (n.782+603A>G) c.10A>G c.833A>G (p.Gln278Arg) c.473A>G (p.Gln158Arg) c.917A>G (p.Gln306Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673578T>G | CA397835972 | TP53 | c.950A>C (p.Gln317Pro) c.554A>C (p.Gln185Pro) c.671A>C (p.Gln224Pro) c.929A>C (p.Gln310Pro) c.782+603A>C (n.782+603A>C) c.10A>C c.833A>C (p.Gln278Pro) c.473A>C (p.Gln158Pro) c.917A>C (p.Gln306Pro) | COSMIC |
17 | g.7673578T= | CA2245947747 | TP53 | c.950A= (p.Gln317=) c.554A= (p.Gln185=) c.671A= (p.Gln224=) c.929A= (p.Gln310=) c.782+603A= (n.782+603A=) c.10A= c.833A= (p.Gln278=) c.473A= (p.Gln158=) c.917A= (p.Gln306=) | |
17 | g.7673578_7673579delinsTG | CA2245947741 | TP53 | c.949_950delinsCA (p.Gln317=) c.553_554delinsCA (p.Gln185=) c.670_671delinsCA (p.Gln224=) c.928_929delinsCA (p.Gln310=) c.782+602_782+603delinsCA (n.782+602_782+603delinsCA) c.9_10delinsCA c.832_833delinsCA (p.Gln278=) c.472_473delinsCA (p.Gln158=) c.916_917delinsCA (p.Gln306=) | |
17 | g.7673578_7673582del | CA645587370 | TP53 | c.946_950del (p.Pro316AlafsTer19) c.550_554del (p.Pro184AlafsTer19) c.667_671del (p.Pro223AlafsTer19) c.925_929del (p.Pro309AlafsTer19) c.946_950del (p.Pro316AlafsTer?) c.782+599_782+603del (n.782+599_782+603del) c.946_950del (p.Pro316AlafsTer29) c.946_950del (p.Pro316AlafsTer18) c.550_554del (p.Pro184AlafsTer18) c.550_554del (p.Pro184AlafsTer?) c.550_554del (p.Pro184AlafsTer29) c.6_10del c.829_833del (p.Pro277AlafsTer19) c.829_833del (p.Pro277AlafsTer18) c.469_473del (p.Pro157AlafsTer18) c.913_917del (p.Pro305AlafsTer19) c.469_473del (p.Pro157AlafsTer29) c.469_473del (p.Pro157AlafsTer19) c.829_833del (p.Pro277AlafsTer29) | COSMIC |
17 | g.7673579G>A | CA397835973 | TP53 | c.949C>T (p.Gln317Ter) c.553C>T (p.Gln185Ter) c.670C>T (p.Gln224Ter) c.928C>T (p.Gln310Ter) c.782+602C>T (n.782+602C>T) c.9C>T c.832C>T (p.Gln278Ter) c.472C>T (p.Gln158Ter) c.916C>T (p.Gln306Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673579G>C | CA397835975 | TP53 | c.949C>G (p.Gln317Glu) c.553C>G (p.Gln185Glu) c.670C>G (p.Gln224Glu) c.928C>G (p.Gln310Glu) c.782+602C>G (n.782+602C>G) c.9C>G c.832C>G (p.Gln278Glu) c.472C>G (p.Gln158Glu) c.916C>G (p.Gln306Glu) | dbSNP |
17 | g.7673579G= | CA2245947768 | TP53 | c.949C= (p.Gln317=) c.553C= (p.Gln185=) c.670C= (p.Gln224=) c.928C= (p.Gln310=) c.782+602C= (n.782+602C=) c.9C= c.832C= (p.Gln278=) c.472C= (p.Gln158=) c.916C= (p.Gln306=) | |
17 | g.7673579G>T | CA001204 | TP53 | c.949C>A (p.Gln317Lys) c.553C>A (p.Gln185Lys) c.670C>A (p.Gln224Lys) c.928C>A (p.Gln310Lys) c.782+602C>A (n.782+602C>A) c.9C>A c.832C>A (p.Gln278Lys) c.472C>A (p.Gln158Lys) c.916C>A (p.Gln306Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673579_7673580delinsAA | CA645587373 | TP53 | c.948_949delinsTT (p.Pro317Ter) c.552_553delinsTT (p.Pro185Ter) c.669_670delinsTT (p.Pro224Ter) c.927_928delinsTT (p.Pro310Ter) c.782+601_782+602delinsTT (n.782+601_782+602delinsTT) c.8_9delinsTT c.831_832delinsTT (p.Pro278Ter) c.471_472delinsTT (p.Pro158Ter) c.915_916delinsTT (p.Pro306Ter) | COSMIC |
17 | g.7673582dup | CA645587372 | TP53 | c.949dup (p.Gln317ProfsTer20) c.553dup (p.Gln185ProfsTer20) c.670dup (p.Gln224ProfsTer20) c.928dup (p.Gln310ProfsTer20) c.949dup (p.Gln317ProfsTer?) c.782+602dup (n.782+602dup) c.949dup (p.Gln317ProfsTer30) c.949dup (p.Gln317ProfsTer19) c.553dup (p.Gln185ProfsTer19) c.553dup (p.Gln185ProfsTer?) c.553dup (p.Gln185ProfsTer30) c.9dup c.832dup (p.Gln278ProfsTer20) c.832dup (p.Gln278ProfsTer19) c.472dup (p.Gln158ProfsTer19) c.916dup (p.Gln306ProfsTer20) c.472dup (p.Gln158ProfsTer30) c.472dup (p.Gln158ProfsTer20) c.832dup (p.Gln278ProfsTer30) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673582del | CA497714083 | TP53 | c.949del (p.Gln317SerfsTer28) c.553del (p.Gln185SerfsTer28) c.670del (p.Gln224SerfsTer28) c.928del (p.Gln310SerfsTer28) c.949del (p.Gln317SerfsTer?) c.782+602del (n.782+602del) c.949del (p.Gln317SerfsTer26) c.553del (p.Gln185SerfsTer26) c.553del (p.Gln185SerfsTer?) c.9del c.832del (p.Gln278SerfsTer28) c.832del (p.Gln278SerfsTer26) c.472del (p.Gln158SerfsTer26) c.916del (p.Gln306SerfsTer28) c.472del (p.Gln158SerfsTer?) c.472del (p.Gln158SerfsTer28) c.832del (p.Gln278SerfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC |
17 | g.7673581_7673582del | CA645587371 | TP53 | c.948_949del (p.Gln317AlafsTer19) c.552_553del (p.Gln185AlafsTer19) c.669_670del (p.Gln224AlafsTer19) c.927_928del (p.Gln310AlafsTer19) c.948_949del (p.Gln317AlafsTer?) c.782+601_782+602del (n.782+601_782+602del) c.948_949del (p.Gln317AlafsTer29) c.948_949del (p.Gln317AlafsTer18) c.552_553del (p.Gln185AlafsTer18) c.552_553del (p.Gln185AlafsTer?) c.552_553del (p.Gln185AlafsTer29) c.8_9del c.831_832del (p.Gln278AlafsTer19) c.831_832del (p.Gln278AlafsTer18) c.471_472del (p.Gln158AlafsTer18) c.915_916del (p.Gln306AlafsTer19) c.471_472del (p.Gln158AlafsTer29) c.471_472del (p.Gln158AlafsTer19) c.831_832del (p.Gln278AlafsTer29) | COSMIC |
17 | g.7673580G>A | CA497714095 | TP53 | c.948C>T (p.Pro316=) c.552C>T (p.Pro184=) c.669C>T (p.Pro223=) c.927C>T (p.Pro309=) c.782+601C>T (n.782+601C>T) c.8C>T c.831C>T (p.Pro277=) c.471C>T (p.Pro157=) c.915C>T (p.Pro305=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673580G>C | CA497714109 | TP53 | c.948C>G (p.Pro316=) c.552C>G (p.Pro184=) c.669C>G (p.Pro223=) c.927C>G (p.Pro309=) c.782+601C>G (n.782+601C>G) c.8C>G c.831C>G (p.Pro277=) c.471C>G (p.Pro157=) c.915C>G (p.Pro305=) | ClinVar dbSNP |
17 | g.7673580G= | CA2245947794 | TP53 | c.948C= (p.Pro316=) c.552C= (p.Pro184=) c.669C= (p.Pro223=) c.927C= (p.Pro309=) c.782+601C= (n.782+601C=) c.8C= c.831C= (p.Pro277=) c.471C= (p.Pro157=) c.915C= (p.Pro305=) | |
17 | g.7673580G>T | CA497714113 | TP53 | c.948C>A (p.Pro316=) c.552C>A (p.Pro184=) c.669C>A (p.Pro223=) c.927C>A (p.Pro309=) c.782+601C>A (n.782+601C>A) c.8C>A c.831C>A (p.Pro277=) c.471C>A (p.Pro157=) c.915C>A (p.Pro305=) | |
17 | g.7673581G>A | CA397835981 | TP53 | c.947C>T (p.Pro316Leu) c.551C>T (p.Pro184Leu) c.668C>T (p.Pro223Leu) c.926C>T (p.Pro309Leu) c.782+600C>T (n.782+600C>T) c.7C>T c.830C>T (p.Pro277Leu) c.470C>T (p.Pro157Leu) c.914C>T (p.Pro305Leu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673581G>C | CA397835984 | TP53 | c.947C>G (p.Pro316Arg) c.551C>G (p.Pro184Arg) c.668C>G (p.Pro223Arg) c.926C>G (p.Pro309Arg) c.782+600C>G (n.782+600C>G) c.7C>G c.830C>G (p.Pro277Arg) c.470C>G (p.Pro157Arg) c.914C>G (p.Pro305Arg) | |
17 | g.7673581G= | CA2245947801 | TP53 | c.947C= (p.Pro316=) c.551C= (p.Pro184=) c.668C= (p.Pro223=) c.926C= (p.Pro309=) c.782+600C= (n.782+600C=) c.7C= c.830C= (p.Pro277=) c.470C= (p.Pro157=) c.914C= (p.Pro305=) | |
17 | g.7673581G>T | CA397835980 | TP53 | c.947C>A (p.Pro316His) c.551C>A (p.Pro184His) c.668C>A (p.Pro223His) c.926C>A (p.Pro309His) c.782+600C>A (n.782+600C>A) c.7C>A c.830C>A (p.Pro277His) c.470C>A (p.Pro157His) c.914C>A (p.Pro305His) | dbSNP |
17 | g.7673585_7673589del | CA2838032359 | TP53 | c.943_947del (p.Ser315ProfsTer20) c.547_551del (p.Ser183ProfsTer20) c.664_668del (p.Ser222ProfsTer20) c.922_926del (p.Ser308ProfsTer20) c.943_947del (p.Ser315ProfsTer?) c.782+596_782+600del (n.782+596_782+600del) c.943_947del (p.Ser315ProfsTer30) c.943_947del (p.Ser315ProfsTer19) c.547_551del (p.Ser183ProfsTer19) c.547_551del (p.Ser183ProfsTer?) c.547_551del (p.Ser183ProfsTer30) c.826_830del (p.Ser276ProfsTer20) c.826_830del (p.Ser276ProfsTer19) c.466_470del (p.Ser156ProfsTer19) c.910_914del (p.Ser304ProfsTer20) c.466_470del (p.Ser156ProfsTer30) c.466_470del (p.Ser156ProfsTer20) c.826_830del (p.Ser276ProfsTer30) | |
17 | g.7673581_7673591delinsGGAGAGGAGCT | CA2245947806 | TP53 | c.937_947delinsAGCTCCTCTCC (p.Ser313=) c.541_551delinsAGCTCCTCTCC (p.Ser181=) c.658_668delinsAGCTCCTCTCC (p.Ser220=) c.916_926delinsAGCTCCTCTCC (p.Ser306=) c.782+590_782+600delinsAGCTCCTCTCC (n.782+590_782+600delinsAGCTCCTCTCC) c.820_830delinsAGCTCCTCTCC (p.Ser274=) c.460_470delinsAGCTCCTCTCC (p.Ser154=) c.904_914delinsAGCTCCTCTCC (p.Ser302=) | |
17 | g.7673582G>A | CA397835996 | TP53 | c.946C>T (p.Pro316Ser) c.550C>T (p.Pro184Ser) c.667C>T (p.Pro223Ser) c.925C>T (p.Pro309Ser) c.782+599C>T (n.782+599C>T) c.6C>T c.829C>T (p.Pro277Ser) c.469C>T (p.Pro157Ser) c.913C>T (p.Pro305Ser) | ClinVar dbSNP |
17 | g.7673582G>C | CA397835999 | TP53 | c.946C>G (p.Pro316Ala) c.550C>G (p.Pro184Ala) c.667C>G (p.Pro223Ala) c.925C>G (p.Pro309Ala) c.782+599C>G (n.782+599C>G) c.6C>G c.829C>G (p.Pro277Ala) c.469C>G (p.Pro157Ala) c.913C>G (p.Pro305Ala) | dbSNP |
17 | g.7673582G= | CA2245947821 | TP53 | c.946C= (p.Pro316=) c.550C= (p.Pro184=) c.667C= (p.Pro223=) c.925C= (p.Pro309=) c.782+599C= (n.782+599C=) c.6C= c.829C= (p.Pro277=) c.469C= (p.Pro157=) c.913C= (p.Pro305=) | |
17 | g.7673582G>T | CA001212 | TP53 | c.946C>A (p.Pro316Thr) c.550C>A (p.Pro184Thr) c.667C>A (p.Pro223Thr) c.925C>A (p.Pro309Thr) c.782+599C>A (n.782+599C>A) c.6C>A c.829C>A (p.Pro277Thr) c.469C>A (p.Pro157Thr) c.913C>A (p.Pro305Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673582_7673583delinsGA | CA2245947828 | TP53 | c.945_946delinsTC (p.Ser315=) c.549_550delinsTC (p.Ser183=) c.666_667delinsTC (p.Ser222=) c.924_925delinsTC (p.Ser308=) c.782+598_782+599delinsTC (n.782+598_782+599delinsTC) c.5_6delinsTC c.828_829delinsTC (p.Ser276=) c.468_469delinsTC (p.Ser156=) c.912_913delinsTC (p.Ser304=) | |
17 | g.7673585_7673586dup | CA2573102338 | TP53 | c.945_946dup (p.Pro316LeufsTer30) c.549_550dup (p.Pro184LeufsTer30) c.666_667dup (p.Pro223LeufsTer30) c.924_925dup (p.Pro309LeufsTer30) c.945_946dup (p.Pro316LeufsTer?) c.782+598_782+599dup (n.782+598_782+599dup) c.945_946dup (p.Pro316LeufsTer28) c.549_550dup (p.Pro184LeufsTer28) c.549_550dup (p.Pro184LeufsTer?) c.5_6dup c.828_829dup (p.Pro277LeufsTer30) c.828_829dup (p.Pro277LeufsTer28) c.468_469dup (p.Pro157LeufsTer28) c.912_913dup (p.Pro305LeufsTer30) c.468_469dup (p.Pro157LeufsTer?) c.468_469dup (p.Pro157LeufsTer30) c.828_829dup (p.Pro277LeufsTer?) | |
17 | g.7673585_7673586del | CA645587374 | TP53 | c.945_946del (p.Gln317AlafsTer19) c.549_550del (p.Gln185AlafsTer19) c.666_667del (p.Gln224AlafsTer19) c.924_925del (p.Gln310AlafsTer19) c.945_946del (p.Gln317AlafsTer?) c.782+598_782+599del (n.782+598_782+599del) c.945_946del (p.Gln317AlafsTer18) c.549_550del (p.Gln185AlafsTer18) c.549_550del (p.Gln185AlafsTer?) c.5_6del c.828_829del (p.Gln278AlafsTer19) c.828_829del (p.Gln278AlafsTer18) c.468_469del (p.Gln158AlafsTer18) c.912_913del (p.Gln306AlafsTer19) c.468_469del (p.Gln158AlafsTer?) c.468_469del (p.Gln158AlafsTer19) c.828_829del (p.Gln278AlafsTer?) | ClinVar dbSNP COSMIC COSMIC |
17 | g.7673583_7673592del | CA913190577 | TP53 | c.937_946del (p.Ser313ProfsTer29) c.541_550del (p.Ser181ProfsTer29) c.658_667del (p.Ser220ProfsTer29) c.916_925del (p.Ser306ProfsTer29) c.937_946del (p.Ser313ProfsTer?) c.782+590_782+599del (n.782+590_782+599del) c.937_946del (p.Ser313ProfsTer27) c.541_550del (p.Ser181ProfsTer27) c.541_550del (p.Ser181ProfsTer?) c.820_829del (p.Ser274ProfsTer29) c.820_829del (p.Ser274ProfsTer27) c.460_469del (p.Ser154ProfsTer27) c.904_913del (p.Ser302ProfsTer29) c.460_469del (p.Ser154ProfsTer?) c.460_469del (p.Ser154ProfsTer29) c.820_829del (p.Ser274ProfsTer?) | ClinVar dbSNP |
17 | g.7673583del | CA915949516 | TP53 | c.945del (p.Gln317SerfsTer28) c.549del (p.Gln185SerfsTer28) c.666del (p.Gln224SerfsTer28) c.924del (p.Gln310SerfsTer28) c.945del (p.Gln317SerfsTer?) c.782+598del (n.782+598del) c.945del (p.Gln317SerfsTer26) c.549del (p.Gln185SerfsTer26) c.549del (p.Gln185SerfsTer?) c.5del c.828del (p.Gln278SerfsTer28) c.828del (p.Gln278SerfsTer26) c.468del (p.Gln158SerfsTer26) c.912del (p.Gln306SerfsTer28) c.468del (p.Gln158SerfsTer?) c.468del (p.Gln158SerfsTer28) c.828del (p.Gln278SerfsTer?) | ClinVar dbSNP |
17 | g.7673583A>C | CA497714137 | TP53 | c.945T>G (p.Ser315=) c.549T>G (p.Ser183=) c.666T>G (p.Ser222=) c.924T>G (p.Ser308=) c.782+598T>G (n.782+598T>G) c.5T>G c.828T>G (p.Ser276=) c.468T>G (p.Ser156=) c.912T>G (p.Ser304=) | COSMIC |
17 | g.7673583A>G | CA497714150 | TP53 | c.945T>C (p.Ser315=) c.549T>C (p.Ser183=) c.666T>C (p.Ser222=) c.924T>C (p.Ser308=) c.782+598T>C (n.782+598T>C) c.5T>C c.828T>C (p.Ser276=) c.468T>C (p.Ser156=) c.912T>C (p.Ser304=) | dbSNP |
17 | g.7673583A>T | CA497714154 | TP53 | c.945T>A (p.Ser315=) c.549T>A (p.Ser183=) c.666T>A (p.Ser222=) c.924T>A (p.Ser308=) c.782+598T>A (n.782+598T>A) c.5T>A c.828T>A (p.Ser276=) c.468T>A (p.Ser156=) c.912T>A (p.Ser304=) | dbSNP |
17 | g.7673583dup | CA645587375 | TP53 | c.945dup (p.Pro316SerfsTer21) c.549dup (p.Pro184SerfsTer21) c.666dup (p.Pro223SerfsTer21) c.924dup (p.Pro309SerfsTer21) c.945dup (p.Pro316SerfsTer?) c.782+598dup (n.782+598dup) c.945dup (p.Pro316SerfsTer20) c.549dup (p.Pro184SerfsTer20) c.549dup (p.Pro184SerfsTer?) c.5dup c.828dup (p.Pro277SerfsTer21) c.828dup (p.Pro277SerfsTer20) c.468dup (p.Pro157SerfsTer20) c.912dup (p.Pro305SerfsTer21) c.468dup (p.Pro157SerfsTer?) c.468dup (p.Pro157SerfsTer21) c.828dup (p.Pro277SerfsTer?) | ClinVar dbSNP COSMIC |
17 | g.7673583_7673584insT | CA497714157 | TP53 | c.944_945insA (p.Pro316SerfsTer21) c.548_549insA (p.Pro184SerfsTer21) c.665_666insA (p.Pro223SerfsTer21) c.923_924insA (p.Pro309SerfsTer21) c.944_945insA (p.Pro316SerfsTer?) c.782+597_782+598insA (n.782+597_782+598insA) c.944_945insA (p.Pro316SerfsTer20) c.548_549insA (p.Pro184SerfsTer20) c.548_549insA (p.Pro184SerfsTer?) c.4_5insA c.827_828insA (p.Pro277SerfsTer21) c.827_828insA (p.Pro277SerfsTer20) c.467_468insA (p.Pro157SerfsTer20) c.911_912insA (p.Pro305SerfsTer21) c.467_468insA (p.Pro157SerfsTer?) c.467_468insA (p.Pro157SerfsTer21) c.827_828insA (p.Pro277SerfsTer?) | |
17 | g.7673584G>A | CA397836004 | TP53 | c.944C>T (p.Ser315Phe) c.548C>T (p.Ser183Phe) c.665C>T (p.Ser222Phe) c.923C>T (p.Ser308Phe) c.782+597C>T (n.782+597C>T) c.4C>T c.827C>T (p.Ser276Phe) c.467C>T (p.Ser156Phe) c.911C>T (p.Ser304Phe) | ClinVar dbSNP |
17 | g.7673584G>C | CA397836006 | TP53 | c.944C>G (p.Ser315Cys) c.548C>G (p.Ser183Cys) c.665C>G (p.Ser222Cys) c.923C>G (p.Ser308Cys) c.782+597C>G (n.782+597C>G) c.4C>G c.827C>G (p.Ser276Cys) c.467C>G (p.Ser156Cys) c.911C>G (p.Ser304Cys) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673584G= | CA2245947848 | TP53 | c.944C= (p.Ser315=) c.548C= (p.Ser183=) c.665C= (p.Ser222=) c.923C= (p.Ser308=) c.782+597C= (n.782+597C=) c.4C= c.827C= (p.Ser276=) c.467C= (p.Ser156=) c.911C= (p.Ser304=) | |
17 | g.7673584G>T | CA397836013 | TP53 | c.944C>A (p.Ser315Tyr) c.548C>A (p.Ser183Tyr) c.665C>A (p.Ser222Tyr) c.923C>A (p.Ser308Tyr) c.782+597C>A (n.782+597C>A) c.4C>A c.827C>A (p.Ser276Tyr) c.467C>A (p.Ser156Tyr) c.911C>A (p.Ser304Tyr) | dbSNP |
17 | g.7673585A= | CA2245947858 | TP53 | c.943T= (p.Ser315=) c.547T= (p.Ser183=) c.664T= (p.Ser222=) c.922T= (p.Ser308=) c.782+596T= (n.782+596T=) c.3T= c.826T= (p.Ser276=) c.466T= (p.Ser156=) c.910T= (p.Ser304=) | |
17 | g.7673585A>C | CA397836018 | TP53 | c.943T>G (p.Ser315Ala) c.547T>G (p.Ser183Ala) c.664T>G (p.Ser222Ala) c.922T>G (p.Ser308Ala) c.782+596T>G (n.782+596T>G) c.3T>G c.826T>G (p.Ser276Ala) c.466T>G (p.Ser156Ala) c.910T>G (p.Ser304Ala) | |
17 | g.7673585A>G | CA397836023 | TP53 | c.943T>C (p.Ser315Pro) c.547T>C (p.Ser183Pro) c.664T>C (p.Ser222Pro) c.922T>C (p.Ser308Pro) c.782+596T>C (n.782+596T>C) c.3T>C c.826T>C (p.Ser276Pro) c.466T>C (p.Ser156Pro) c.910T>C (p.Ser304Pro) | ClinVar dbSNP COSMIC |
17 | g.7673585A>T | CA000506 | TP53 | c.943T>A (p.Ser315Thr) c.547T>A (p.Ser183Thr) c.664T>A (p.Ser222Thr) c.922T>A (p.Ser308Thr) c.782+596T>A (n.782+596T>A) c.3T>A c.826T>A (p.Ser276Thr) c.466T>A (p.Ser156Thr) c.910T>A (p.Ser304Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673586G>A | CA497714190 | TP53 | c.942C>T (p.Ser314=) c.546C>T (p.Ser182=) c.663C>T (p.Ser221=) c.921C>T (p.Ser307=) c.782+595C>T (n.782+595C>T) c.2C>T c.825C>T (p.Ser275=) c.465C>T (p.Ser155=) c.909C>T (p.Ser303=) | dbSNP |
17 | g.7673586G>C | CA497714198 | TP53 | c.942C>G (p.Ser314=) c.546C>G (p.Ser182=) c.663C>G (p.Ser221=) c.921C>G (p.Ser307=) c.782+595C>G (n.782+595C>G) c.2C>G c.825C>G (p.Ser275=) c.465C>G (p.Ser155=) c.909C>G (p.Ser303=) | ClinVar dbSNP |
17 | g.7673586G= | CA2245947870 | TP53 | c.942C= (p.Ser314=) c.546C= (p.Ser182=) c.663C= (p.Ser221=) c.921C= (p.Ser307=) c.782+595C= (n.782+595C=) c.2C= c.825C= (p.Ser275=) c.465C= (p.Ser155=) c.909C= (p.Ser303=) | |
17 | g.7673586G>T | CA001225 | TP53 | c.942C>A (p.Ser314=) c.546C>A (p.Ser182=) c.663C>A (p.Ser221=) c.921C>A (p.Ser307=) c.782+595C>A (n.782+595C>A) c.2C>A c.825C>A (p.Ser275=) c.465C>A (p.Ser155=) c.909C>A (p.Ser303=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673587G>A | CA001234 | TP53 | c.941C>T (p.Ser314Phe) c.545C>T (p.Ser182Phe) c.662C>T (p.Ser221Phe) c.920C>T (p.Ser307Phe) c.782+594C>T (n.782+594C>T) c.1C>T c.824C>T (p.Ser275Phe) c.464C>T (p.Ser155Phe) c.908C>T (p.Ser303Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
17 | g.7673587G>C | CA397836031 | TP53 | c.941C>G (p.Ser314Cys) c.545C>G (p.Ser182Cys) c.662C>G (p.Ser221Cys) c.920C>G (p.Ser307Cys) c.782+594C>G (n.782+594C>G) c.1C>G c.824C>G (p.Ser275Cys) c.464C>G (p.Ser155Cys) c.908C>G (p.Ser303Cys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673587G= | CA2245947882 | TP53 | c.941C= (p.Ser314=) c.545C= (p.Ser182=) c.662C= (p.Ser221=) c.920C= (p.Ser307=) c.782+594C= (n.782+594C=) c.1C= c.824C= (p.Ser275=) c.464C= (p.Ser155=) c.908C= (p.Ser303=) | |
17 | g.7673587G>T | CA397836036 | TP53 | c.941C>A (p.Ser314Tyr) c.545C>A (p.Ser182Tyr) c.662C>A (p.Ser221Tyr) c.920C>A (p.Ser307Tyr) c.782+594C>A (n.782+594C>A) c.1C>A c.824C>A (p.Ser275Tyr) c.464C>A (p.Ser155Tyr) c.908C>A (p.Ser303Tyr) | dbSNP |
17 | g.7673588A>C | CA397836044 | TP53 | c.940T>G (p.Ser314Ala) c.544T>G (p.Ser182Ala) c.661T>G (p.Ser221Ala) c.919T>G (p.Ser307Ala) c.782+593T>G (n.782+593T>G) c.823T>G (p.Ser275Ala) c.463T>G (p.Ser155Ala) c.907T>G (p.Ser303Ala) | |
17 | g.7673588A>G | CA397836042 | TP53 | c.940T>C (p.Ser314Pro) c.544T>C (p.Ser182Pro) c.661T>C (p.Ser221Pro) c.919T>C (p.Ser307Pro) c.782+593T>C (n.782+593T>C) c.823T>C (p.Ser275Pro) c.463T>C (p.Ser155Pro) c.907T>C (p.Ser303Pro) | |
17 | g.7673588A>T | CA397836039 | TP53 | c.940T>A (p.Ser314Thr) c.544T>A (p.Ser182Thr) c.661T>A (p.Ser221Thr) c.919T>A (p.Ser307Thr) c.782+593T>A (n.782+593T>A) c.823T>A (p.Ser275Thr) c.463T>A (p.Ser155Thr) c.907T>A (p.Ser303Thr) | dbSNP |
17 | g.7673589G>A | CA497714209 | TP53 | c.939C>T (p.Ser313=) c.543C>T (p.Ser181=) c.660C>T (p.Ser220=) c.918C>T (p.Ser306=) c.782+592C>T (n.782+592C>T) c.822C>T (p.Ser274=) c.462C>T (p.Ser154=) c.906C>T (p.Ser302=) | dbSNP |
17 | g.7673589G>C | CA397836048 | TP53 | c.939C>G (p.Ser313Arg) c.543C>G (p.Ser181Arg) c.660C>G (p.Ser220Arg) c.918C>G (p.Ser306Arg) c.782+592C>G (n.782+592C>G) c.822C>G (p.Ser274Arg) c.462C>G (p.Ser154Arg) c.906C>G (p.Ser302Arg) | dbSNP |
17 | g.7673589G= | CA2245947895 | TP53 | c.939C= (p.Ser313=) c.543C= (p.Ser181=) c.660C= (p.Ser220=) c.918C= (p.Ser306=) c.782+592C= (n.782+592C=) c.822C= (p.Ser274=) c.462C= (p.Ser154=) c.906C= (p.Ser302=) | |
17 | g.7673589G>T | CA397836050 | TP53 | c.939C>A (p.Ser313Arg) c.543C>A (p.Ser181Arg) c.660C>A (p.Ser220Arg) c.918C>A (p.Ser306Arg) c.782+592C>A (n.782+592C>A) c.822C>A (p.Ser274Arg) c.462C>A (p.Ser154Arg) c.906C>A (p.Ser302Arg) | dbSNP |
17 | g.7673592_7673610del | CA645587376 | TP53 | c.921_939del c.525_543del c.642_660del c.900_918del c.782+574_782+592del (n.782+574_782+592del) c.804_822del c.444_462del c.888_906del | COSMIC |
17 | g.7673590del | CA891842223 | TP53 | c.938del (p.Ser313ThrfsTer?) c.542del (p.Ser181ThrfsTer?) c.659del (p.Ser220ThrfsTer?) c.917del (p.Ser306ThrfsTer?) c.782+591del (n.782+591del) c.938del (p.Ser313ThrfsTer30) c.542del (p.Ser181ThrfsTer30) c.821del (p.Ser274ThrfsTer?) c.821del (p.Ser274ThrfsTer30) c.461del (p.Ser154ThrfsTer30) c.905del (p.Ser302ThrfsTer?) c.461del (p.Ser154ThrfsTer?) | |
17 | g.7673590C>A | CA397836053 | TP53 | c.938G>T (p.Ser313Ile) c.542G>T (p.Ser181Ile) c.659G>T (p.Ser220Ile) c.917G>T (p.Ser306Ile) c.782+591G>T (n.782+591G>T) c.821G>T (p.Ser274Ile) c.461G>T (p.Ser154Ile) c.905G>T (p.Ser302Ile) | dbSNP |
17 | g.7673590C>G | CA397836056 | TP53 | c.938G>C (p.Ser313Thr) c.542G>C (p.Ser181Thr) c.659G>C (p.Ser220Thr) c.917G>C (p.Ser306Thr) c.782+591G>C (n.782+591G>C) c.821G>C (p.Ser274Thr) c.461G>C (p.Ser154Thr) c.905G>C (p.Ser302Thr) | dbSNP |
17 | g.7673590C>T | CA397836058 | TP53 | c.938G>A (p.Ser313Asn) c.542G>A (p.Ser181Asn) c.659G>A (p.Ser220Asn) c.917G>A (p.Ser306Asn) c.782+591G>A (n.782+591G>A) c.821G>A (p.Ser274Asn) c.461G>A (p.Ser154Asn) c.905G>A (p.Ser302Asn) | ClinVar dbSNP COSMIC |
17 | g.7673592_7673702del | CA645587377 | TP53 | c.919+1_938del c.523+1_542del c.640+1_659del c.898+1_917del c.782+481_782+591del (n.782+481_782+591del) c.802+1_821del c.442+1_461del c.886+1_905del | COSMIC |
17 | g.7673591T>A | CA397836061 | TP53 | c.937A>T (p.Ser313Cys) c.541A>T (p.Ser181Cys) c.658A>T (p.Ser220Cys) c.916A>T (p.Ser306Cys) c.782+590A>T (n.782+590A>T) c.820A>T (p.Ser274Cys) c.460A>T (p.Ser154Cys) c.904A>T (p.Ser302Cys) | COSMIC |
17 | g.7673591T>C | CA397836063 | TP53 | c.937A>G (p.Ser313Gly) c.541A>G (p.Ser181Gly) c.658A>G (p.Ser220Gly) c.916A>G (p.Ser306Gly) c.782+590A>G (n.782+590A>G) c.820A>G (p.Ser274Gly) c.460A>G (p.Ser154Gly) c.904A>G (p.Ser302Gly) | |
17 | g.7673591T>G | CA397836065 | TP53 | c.937A>C (p.Ser313Arg) c.541A>C (p.Ser181Arg) c.658A>C (p.Ser220Arg) c.916A>C (p.Ser306Arg) c.782+590A>C (n.782+590A>C) c.820A>C (p.Ser274Arg) c.460A>C (p.Ser154Arg) c.904A>C (p.Ser302Arg) | |
17 | g.7673592G>A | CA497714260 | TP53 | c.936C>T (p.Thr312=) c.540C>T (p.Thr180=) c.657C>T (p.Thr219=) c.915C>T (p.Thr305=) c.782+589C>T (n.782+589C>T) c.819C>T (p.Thr273=) c.459C>T (p.Thr153=) c.903C>T (p.Thr301=) | COSMIC |
17 | g.7673592G>C | CA497714258 | TP53 | c.936C>G (p.Thr312=) c.540C>G (p.Thr180=) c.657C>G (p.Thr219=) c.915C>G (p.Thr305=) c.782+589C>G (n.782+589C>G) c.819C>G (p.Thr273=) c.459C>G (p.Thr153=) c.903C>G (p.Thr301=) | ClinVar dbSNP gnomAD v4 |
17 | g.7673592G= | CA2245947902 | TP53 | c.936C= (p.Thr312=) c.540C= (p.Thr180=) c.657C= (p.Thr219=) c.915C= (p.Thr305=) c.782+589C= (n.782+589C=) c.819C= (p.Thr273=) c.459C= (p.Thr153=) c.903C= (p.Thr301=) | |
17 | g.7673592G>T | CA497714264 | TP53 | c.936C>A (p.Thr312=) c.540C>A (p.Thr180=) c.657C>A (p.Thr219=) c.915C>A (p.Thr305=) c.782+589C>A (n.782+589C>A) c.819C>A (p.Thr273=) c.459C>A (p.Thr153=) c.903C>A (p.Thr301=) | ClinVar dbSNP COSMIC |
17 | g.7673593del | CA497714256 | TP53 | c.936del (p.Ser313AlafsTer?) c.540del (p.Ser181AlafsTer?) c.657del (p.Ser220AlafsTer?) c.915del (p.Ser306AlafsTer?) c.782+589del (n.782+589del) c.819del (p.Ser274AlafsTer?) c.459del (p.Ser154AlafsTer?) c.903del (p.Ser302AlafsTer?) | COSMIC COSMIC COSMIC |
17 | g.7673593G>A | CA397836069 | TP53 | c.935C>T (p.Thr312Ile) c.539C>T (p.Thr180Ile) c.656C>T (p.Thr219Ile) c.914C>T (p.Thr305Ile) c.782+588C>T (n.782+588C>T) c.818C>T (p.Thr273Ile) c.458C>T (p.Thr153Ile) c.902C>T (p.Thr301Ile) | ClinVar dbSNP COSMIC |
17 | g.7673593G>C | CA000505 | TP53 | c.935C>G (p.Thr312Ser) c.539C>G (p.Thr180Ser) c.656C>G (p.Thr219Ser) c.914C>G (p.Thr305Ser) c.782+588C>G (n.782+588C>G) c.818C>G (p.Thr273Ser) c.458C>G (p.Thr153Ser) c.902C>G (p.Thr301Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673593G= | CA2245947910 | TP53 | c.935C= (p.Thr312=) c.539C= (p.Thr180=) c.656C= (p.Thr219=) c.914C= (p.Thr305=) c.782+588C= (n.782+588C=) c.818C= (p.Thr273=) c.458C= (p.Thr153=) c.902C= (p.Thr301=) | |
17 | g.7673593G>T | CA397836074 | TP53 | c.935C>A (p.Thr312Asn) c.539C>A (p.Thr180Asn) c.656C>A (p.Thr219Asn) c.914C>A (p.Thr305Asn) c.782+588C>A (n.782+588C>A) c.818C>A (p.Thr273Asn) c.458C>A (p.Thr153Asn) c.902C>A (p.Thr301Asn) | ClinVar dbSNP |
17 | g.7673593_7673594insACTTAGTACCTGAAGGGTGAAATATTCTCCATCCAGTG | CA645587378 | TP53 | c.935_936insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser313LeufsTer?) c.539_540insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser181LeufsTer?) c.656_657insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser220LeufsTer?) c.914_915insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser306LeufsTer?) c.782+588_782+589insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (n.782+588_782+589insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC) c.818_819insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser274LeufsTer?) c.458_459insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser154LeufsTer?) c.902_903insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser302LeufsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673594del | CA497714281 | TP53 | c.934del (p.Thr312ProfsTer?) c.538del (p.Thr180ProfsTer?) c.655del (p.Thr219ProfsTer?) c.913del (p.Thr305ProfsTer?) c.782+587del (n.782+587del) c.817del (p.Thr273ProfsTer?) c.457del (p.Thr153ProfsTer?) c.901del (p.Thr301ProfsTer?) | COSMIC |
17 | g.7673594T>A | CA397836079 | TP53 | c.934A>T (p.Thr312Ser) c.538A>T (p.Thr180Ser) c.655A>T (p.Thr219Ser) c.913A>T (p.Thr305Ser) c.782+587A>T (n.782+587A>T) c.817A>T (p.Thr273Ser) c.457A>T (p.Thr153Ser) c.901A>T (p.Thr301Ser) | dbSNP COSMIC |
17 | g.7673594T>C | CA397836082 | TP53 | c.934A>G (p.Thr312Ala) c.538A>G (p.Thr180Ala) c.655A>G (p.Thr219Ala) c.913A>G (p.Thr305Ala) c.782+587A>G (n.782+587A>G) c.817A>G (p.Thr273Ala) c.457A>G (p.Thr153Ala) c.901A>G (p.Thr301Ala) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673594T>G | CA397836085 | TP53 | c.934A>C (p.Thr312Pro) c.538A>C (p.Thr180Pro) c.655A>C (p.Thr219Pro) c.913A>C (p.Thr305Pro) c.782+587A>C (n.782+587A>C) c.817A>C (p.Thr273Pro) c.457A>C (p.Thr153Pro) c.901A>C (p.Thr301Pro) | dbSNP |
17 | g.7673594dup | CA645587379 | TP53 | c.934dup (p.Thr312AsnfsTer25) c.538dup (p.Thr180AsnfsTer25) c.655dup (p.Thr219AsnfsTer25) c.913dup (p.Thr305AsnfsTer25) c.934dup (p.Thr312AsnfsTer?) c.782+587dup (n.782+587dup) c.934dup (p.Thr312AsnfsTer24) c.538dup (p.Thr180AsnfsTer24) c.538dup (p.Thr180AsnfsTer?) c.817dup (p.Thr273AsnfsTer25) c.817dup (p.Thr273AsnfsTer24) c.457dup (p.Thr153AsnfsTer24) c.901dup (p.Thr301AsnfsTer25) c.457dup (p.Thr153AsnfsTer?) c.457dup (p.Thr153AsnfsTer25) c.817dup (p.Thr273AsnfsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673594_7673595delinsTG | CA2245947916 | TP53 | c.933_934delinsCA (p.Asn311=) c.537_538delinsCA (p.Asn179=) c.654_655delinsCA (p.Asn218=) c.912_913delinsCA (p.Asn304=) c.782+586_782+587delinsCA (n.782+586_782+587delinsCA) c.816_817delinsCA (p.Asn272=) c.456_457delinsCA (p.Asn152=) c.900_901delinsCA (p.Asn300=) | |
17 | g.7673595del | CA497714310 | TP53 | c.933del (p.Asn311LysfsTer?) c.537del (p.Asn179LysfsTer?) c.654del (p.Asn218LysfsTer?) c.912del (p.Asn304LysfsTer?) c.782+586del (n.782+586del) c.816del (p.Asn272LysfsTer?) c.456del (p.Asn152LysfsTer?) c.900del (p.Asn300LysfsTer?) | ClinVar dbSNP COSMIC |
17 | g.7673595G>A | CA16607849 | TP53 | c.933C>T (p.Asn311=) c.537C>T (p.Asn179=) c.654C>T (p.Asn218=) c.912C>T (p.Asn304=) c.782+586C>T (n.782+586C>T) c.816C>T (p.Asn272=) c.456C>T (p.Asn152=) c.900C>T (p.Asn300=) | ClinVar dbSNP |
17 | g.7673595G>C | CA397836091 | TP53 | c.933C>G (p.Asn311Lys) c.537C>G (p.Asn179Lys) c.654C>G (p.Asn218Lys) c.912C>G (p.Asn304Lys) c.782+586C>G (n.782+586C>G) c.816C>G (p.Asn272Lys) c.456C>G (p.Asn152Lys) c.900C>G (p.Asn300Lys) | dbSNP COSMIC |
17 | g.7673595G= | CA2245947932 | TP53 | c.933C= (p.Asn311=) c.537C= (p.Asn179=) c.654C= (p.Asn218=) c.912C= (p.Asn304=) c.782+586C= (n.782+586C=) c.816C= (p.Asn272=) c.456C= (p.Asn152=) c.900C= (p.Asn300=) | |
17 | g.7673595G>T | CA397836089 | TP53 | c.933C>A (p.Asn311Lys) c.537C>A (p.Asn179Lys) c.654C>A (p.Asn218Lys) c.912C>A (p.Asn304Lys) c.782+586C>A (n.782+586C>A) c.816C>A (p.Asn272Lys) c.456C>A (p.Asn152Lys) c.900C>A (p.Asn300Lys) | |
17 | g.7673596T>A | CA397836095 | TP53 | c.932A>T (p.Asn311Ile) c.536A>T (p.Asn179Ile) c.653A>T (p.Asn218Ile) c.911A>T (p.Asn304Ile) c.782+585A>T (n.782+585A>T) c.815A>T (p.Asn272Ile) c.455A>T (p.Asn152Ile) c.899A>T (p.Asn300Ile) | dbSNP |
17 | g.7673596T>C | CA16615690 | TP53 | c.932A>G (p.Asn311Ser) c.536A>G (p.Asn179Ser) c.653A>G (p.Asn218Ser) c.911A>G (p.Asn304Ser) c.782+585A>G (n.782+585A>G) c.815A>G (p.Asn272Ser) c.455A>G (p.Asn152Ser) c.899A>G (p.Asn300Ser) | ClinVar dbSNP gnomAD v4 |
17 | g.7673596T>G | CA349248 | TP53 | c.932A>C (p.Asn311Thr) c.536A>C (p.Asn179Thr) c.653A>C (p.Asn218Thr) c.911A>C (p.Asn304Thr) c.782+585A>C (n.782+585A>C) c.815A>C (p.Asn272Thr) c.455A>C (p.Asn152Thr) c.899A>C (p.Asn300Thr) | ClinVar dbSNP gnomAD v4 |
17 | g.7673596T= | CA2245947945 | TP53 | c.932A= (p.Asn311=) c.536A= (p.Asn179=) c.653A= (p.Asn218=) c.911A= (p.Asn304=) c.782+585A= (n.782+585A=) c.815A= (p.Asn272=) c.455A= (p.Asn152=) c.899A= (p.Asn300=) | |
17 | g.7673597dup | CA891842224 | TP53 | c.932dup (p.Asn311LysfsTer26) c.536dup (p.Asn179LysfsTer26) c.653dup (p.Asn218LysfsTer26) c.911dup (p.Asn304LysfsTer26) c.932dup (p.Asn311LysfsTer?) c.782+585dup (n.782+585dup) c.932dup (p.Asn311LysfsTer25) c.536dup (p.Asn179LysfsTer25) c.536dup (p.Asn179LysfsTer?) c.815dup (p.Asn272LysfsTer26) c.815dup (p.Asn272LysfsTer25) c.455dup (p.Asn152LysfsTer25) c.899dup (p.Asn300LysfsTer26) c.455dup (p.Asn152LysfsTer?) c.455dup (p.Asn152LysfsTer26) c.815dup (p.Asn272LysfsTer?) | ClinVar |
17 | g.7673597T>A | CA397836102 | TP53 | c.931A>T (p.Asn311Tyr) c.535A>T (p.Asn179Tyr) c.652A>T (p.Asn218Tyr) c.910A>T (p.Asn304Tyr) c.782+584A>T (n.782+584A>T) c.814A>T (p.Asn272Tyr) c.454A>T (p.Asn152Tyr) c.898A>T (p.Asn300Tyr) | dbSNP COSMIC |
17 | g.7673597T>C | CA397836104 | TP53 | c.931A>G (p.Asn311Asp) c.535A>G (p.Asn179Asp) c.652A>G (p.Asn218Asp) c.910A>G (p.Asn304Asp) c.782+584A>G (n.782+584A>G) c.814A>G (p.Asn272Asp) c.454A>G (p.Asn152Asp) c.898A>G (p.Asn300Asp) | |
17 | g.7673597T>G | CA397836105 | TP53 | c.931A>C (p.Asn311His) c.535A>C (p.Asn179His) c.652A>C (p.Asn218His) c.910A>C (p.Asn304His) c.782+584A>C (n.782+584A>C) c.814A>C (p.Asn272His) c.454A>C (p.Asn152His) c.898A>C (p.Asn300His) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673597T= | CA2245947959 | TP53 | c.931A= (p.Asn311=) c.535A= (p.Asn179=) c.652A= (p.Asn218=) c.910A= (p.Asn304=) c.782+584A= (n.782+584A=) c.814A= (p.Asn272=) c.454A= (p.Asn152=) c.898A= (p.Asn300=) | |
17 | g.7673598_7673702del | CA645587380 | TP53 | c.919_931del c.523_535del c.640_652del c.898_910del c.782+480_782+584del (n.782+480_782+584del) c.802_814del c.442_454del c.886_898del | COSMIC |
17 | g.7673598G>A | CA497714331 | TP53 | c.930C>T (p.Asn310=) c.534C>T (p.Asn178=) c.651C>T (p.Asn217=) c.909C>T (p.Asn303=) c.782+583C>T (n.782+583C>T) c.813C>T (p.Asn271=) c.453C>T (p.Asn151=) c.897C>T (p.Asn299=) | ClinVar dbSNP |
17 | g.7673598G>C | CA397836109 | TP53 | c.930C>G (p.Asn310Lys) c.534C>G (p.Asn178Lys) c.651C>G (p.Asn217Lys) c.909C>G (p.Asn303Lys) c.782+583C>G (n.782+583C>G) c.813C>G (p.Asn271Lys) c.453C>G (p.Asn151Lys) c.897C>G (p.Asn299Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673598G= | CA2245947967 | TP53 | c.930C= (p.Asn310=) c.534C= (p.Asn178=) c.651C= (p.Asn217=) c.909C= (p.Asn303=) c.782+583C= (n.782+583C=) c.813C= (p.Asn271=) c.453C= (p.Asn151=) c.897C= (p.Asn299=) | |
17 | g.7673598G>T | CA10580910 | TP53 | c.930C>A (p.Asn310Lys) c.534C>A (p.Asn178Lys) c.651C>A (p.Asn217Lys) c.909C>A (p.Asn303Lys) c.782+583C>A (n.782+583C>A) c.813C>A (p.Asn271Lys) c.453C>A (p.Asn151Lys) c.897C>A (p.Asn299Lys) | ClinVar dbSNP |
17 | g.7673598_7673600delinsCAA | CA645587381 | TP53 | c.928_930delinsTTG (p.Asn310Leu) c.532_534delinsTTG (p.Asn178Leu) c.649_651delinsTTG (p.Asn217Leu) c.907_909delinsTTG (p.Asn303Leu) c.782+581_782+583delinsTTG (n.782+581_782+583delinsTTG) c.811_813delinsTTG (p.Asn271Leu) c.451_453delinsTTG (p.Asn151Leu) c.895_897delinsTTG (p.Asn299Leu) | COSMIC |
17 | g.7673598_7673599insA | CA645587383 | TP53 | c.929_930insT (p.Asn311GlnfsTer26) c.533_534insT (p.Asn179GlnfsTer26) c.650_651insT (p.Asn218GlnfsTer26) c.908_909insT (p.Asn304GlnfsTer26) c.929_930insT (p.Asn311GlnfsTer?) c.782+582_782+583insT (n.782+582_782+583insT) c.929_930insT (p.Asn311GlnfsTer25) c.533_534insT (p.Asn179GlnfsTer25) c.533_534insT (p.Asn179GlnfsTer?) c.812_813insT (p.Asn272GlnfsTer26) c.812_813insT (p.Asn272GlnfsTer25) c.452_453insT (p.Asn152GlnfsTer25) c.896_897insT (p.Asn300GlnfsTer26) c.452_453insT (p.Asn152GlnfsTer?) c.452_453insT (p.Asn152GlnfsTer26) c.812_813insT (p.Asn272GlnfsTer?) | COSMIC |
17 | g.7673599T>A | CA397836112 | TP53 | c.929A>T (p.Asn310Ile) c.533A>T (p.Asn178Ile) c.650A>T (p.Asn217Ile) c.908A>T (p.Asn303Ile) c.782+582A>T (n.782+582A>T) c.812A>T (p.Asn271Ile) c.452A>T (p.Asn151Ile) c.896A>T (p.Asn299Ile) | ClinVar dbSNP |
17 | g.7673599T>C | CA397836116 | TP53 | c.929A>G (p.Asn310Ser) c.533A>G (p.Asn178Ser) c.650A>G (p.Asn217Ser) c.908A>G (p.Asn303Ser) c.782+582A>G (n.782+582A>G) c.812A>G (p.Asn271Ser) c.452A>G (p.Asn151Ser) c.896A>G (p.Asn299Ser) | ClinVar dbSNP |
17 | g.7673599T>G | CA397836117 | TP53 | c.929A>C (p.Asn310Thr) c.533A>C (p.Asn178Thr) c.650A>C (p.Asn217Thr) c.908A>C (p.Asn303Thr) c.782+582A>C (n.782+582A>C) c.812A>C (p.Asn271Thr) c.452A>C (p.Asn151Thr) c.896A>C (p.Asn299Thr) | dbSNP COSMIC |
17 | g.7673600dup | CA497714339 | TP53 | c.929dup (p.Asn310LysfsTer27) c.533dup (p.Asn178LysfsTer27) c.650dup (p.Asn217LysfsTer27) c.908dup (p.Asn303LysfsTer27) c.929dup (p.Asn310LysfsTer?) c.782+582dup (n.782+582dup) c.929dup (p.Asn310LysfsTer26) c.533dup (p.Asn178LysfsTer26) c.533dup (p.Asn178LysfsTer?) c.812dup (p.Asn271LysfsTer27) c.812dup (p.Asn271LysfsTer26) c.452dup (p.Asn151LysfsTer26) c.896dup (p.Asn299LysfsTer27) c.452dup (p.Asn151LysfsTer?) c.452dup (p.Asn151LysfsTer27) c.812dup (p.Asn271LysfsTer?) | |
17 | g.7673600T>A | CA397836121 | TP53 | c.928A>T (p.Asn310Tyr) c.532A>T (p.Asn178Tyr) c.649A>T (p.Asn217Tyr) c.907A>T (p.Asn303Tyr) c.782+581A>T (n.782+581A>T) c.811A>T (p.Asn271Tyr) c.451A>T (p.Asn151Tyr) c.895A>T (p.Asn299Tyr) | |
17 | g.7673600T>C | CA397836124 | TP53 | c.928A>G (p.Asn310Asp) c.532A>G (p.Asn178Asp) c.649A>G (p.Asn217Asp) c.907A>G (p.Asn303Asp) c.782+581A>G (n.782+581A>G) c.811A>G (p.Asn271Asp) c.451A>G (p.Asn151Asp) c.895A>G (p.Asn299Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673600T>G | CA397836126 | TP53 | c.928A>C (p.Asn310His) c.532A>C (p.Asn178His) c.649A>C (p.Asn217His) c.907A>C (p.Asn303His) c.782+581A>C (n.782+581A>C) c.811A>C (p.Asn271His) c.451A>C (p.Asn151His) c.895A>C (p.Asn299His) | ClinVar COSMIC COSMIC COSMIC COSMIC |
17 | g.7673600T= | CA2245947978 | TP53 | c.928A= (p.Asn310=) c.532A= (p.Asn178=) c.649A= (p.Asn217=) c.907A= (p.Asn303=) c.782+581A= (n.782+581A=) c.811A= (p.Asn271=) c.451A= (p.Asn151=) c.895A= (p.Asn299=) | |
17 | g.7673600_7673601delinsTG | CA2245947981 | TP53 | c.927_928delinsCA (p.Pro309=) c.531_532delinsCA (p.Pro177=) c.648_649delinsCA (p.Pro216=) c.906_907delinsCA (p.Pro302=) c.782+580_782+581delinsCA (n.782+580_782+581delinsCA) c.810_811delinsCA (p.Pro270=) c.450_451delinsCA (p.Pro150=) c.894_895delinsCA (p.Pro298=) | |
17 | g.7673600_7673604del | CA645587385 | TP53 | c.924_928del (p.Pro309GlnfsTer26) c.528_532del (p.Pro177GlnfsTer26) c.645_649del (p.Pro216GlnfsTer26) c.903_907del (p.Pro302GlnfsTer26) c.924_928del (p.Pro309GlnfsTer?) c.782+577_782+581del (n.782+577_782+581del) c.924_928del (p.Pro309GlnfsTer25) c.528_532del (p.Pro177GlnfsTer25) c.528_532del (p.Pro177GlnfsTer?) c.807_811del (p.Pro270GlnfsTer26) c.807_811del (p.Pro270GlnfsTer25) c.447_451del (p.Pro150GlnfsTer25) c.891_895del (p.Pro298GlnfsTer26) c.447_451del (p.Pro150GlnfsTer?) c.447_451del (p.Pro150GlnfsTer26) c.807_811del (p.Pro270GlnfsTer?) | COSMIC |
17 | g.7673600_7673614del | CA645587386 | TP53 | c.920-6_928del c.524-6_532del c.641-6_649del c.899-6_907del c.782+567_782+581del (n.782+567_782+581del) c.803-6_811del c.443-6_451del c.887-6_895del | COSMIC |
17 | g.7673601G>A | CA497714349 | TP53 | c.927C>T (p.Pro309=) c.531C>T (p.Pro177=) c.648C>T (p.Pro216=) c.906C>T (p.Pro302=) c.782+580C>T (n.782+580C>T) c.810C>T (p.Pro270=) c.450C>T (p.Pro150=) c.894C>T (p.Pro298=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673601G>C | CA497714350 | TP53 | c.927C>G (p.Pro309=) c.531C>G (p.Pro177=) c.648C>G (p.Pro216=) c.906C>G (p.Pro302=) c.782+580C>G (n.782+580C>G) c.810C>G (p.Pro270=) c.450C>G (p.Pro150=) c.894C>G (p.Pro298=) | dbSNP |
17 | g.7673601G= | CA2245947993 | TP53 | c.927C= (p.Pro309=) c.531C= (p.Pro177=) c.648C= (p.Pro216=) c.906C= (p.Pro302=) c.782+580C= (n.782+580C=) c.810C= (p.Pro270=) c.450C= (p.Pro150=) c.894C= (p.Pro298=) | |
17 | g.7673601G>T | CA497714352 | TP53 | c.927C>A (p.Pro309=) c.531C>A (p.Pro177=) c.648C>A (p.Pro216=) c.906C>A (p.Pro302=) c.782+580C>A (n.782+580C>A) c.810C>A (p.Pro270=) c.450C>A (p.Pro150=) c.894C>A (p.Pro298=) | ClinVar dbSNP COSMIC |
17 | g.7673603del | CA497714355 | TP53 | c.927del (p.Asn310ThrfsTer?) c.531del (p.Asn178ThrfsTer?) c.648del (p.Asn217ThrfsTer?) c.906del (p.Asn303ThrfsTer?) c.782+580del (n.782+580del) c.810del (p.Asn271ThrfsTer?) c.450del (p.Asn151ThrfsTer?) c.894del (p.Asn299ThrfsTer?) | ClinVar dbSNP COSMIC COSMIC |
17 | g.7673602G>A | CA397836130 | TP53 | c.926C>T (p.Pro309Leu) c.530C>T (p.Pro177Leu) c.647C>T (p.Pro216Leu) c.905C>T (p.Pro302Leu) c.782+579C>T (n.782+579C>T) c.809C>T (p.Pro270Leu) c.449C>T (p.Pro150Leu) c.893C>T (p.Pro298Leu) | ClinVar dbSNP |
17 | g.7673602G>C | CA397836137 | TP53 | c.926C>G (p.Pro309Arg) c.530C>G (p.Pro177Arg) c.647C>G (p.Pro216Arg) c.905C>G (p.Pro302Arg) c.782+579C>G (n.782+579C>G) c.809C>G (p.Pro270Arg) c.449C>G (p.Pro150Arg) c.893C>G (p.Pro298Arg) | dbSNP COSMIC |
17 | g.7673602G>T | CA397836134 | TP53 | c.926C>A (p.Pro309His) c.530C>A (p.Pro177His) c.647C>A (p.Pro216His) c.905C>A (p.Pro302His) c.782+579C>A (n.782+579C>A) c.809C>A (p.Pro270His) c.449C>A (p.Pro150His) c.893C>A (p.Pro298His) | dbSNP |
17 | g.7673606_7673622del | CA645587387 | TP53 | c.920-10_926del c.524-10_530del c.641-10_647del c.899-10_905del c.782+563_782+579del (n.782+563_782+579del) c.803-10_809del c.443-10_449del c.887-10_893del | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673603G>A | CA397836140 | TP53 | c.925C>T (p.Pro309Ser) c.529C>T (p.Pro177Ser) c.646C>T (p.Pro216Ser) c.904C>T (p.Pro302Ser) c.782+578C>T (n.782+578C>T) c.808C>T (p.Pro270Ser) c.448C>T (p.Pro150Ser) c.892C>T (p.Pro298Ser) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673603G>C | CA397836142 | TP53 | c.925C>G (p.Pro309Ala) c.529C>G (p.Pro177Ala) c.646C>G (p.Pro216Ala) c.904C>G (p.Pro302Ala) c.782+578C>G (n.782+578C>G) c.808C>G (p.Pro270Ala) c.448C>G (p.Pro150Ala) c.892C>G (p.Pro298Ala) | dbSNP |
17 | g.7673603G= | CA2245948005 | TP53 | c.925C= (p.Pro309=) c.529C= (p.Pro177=) c.646C= (p.Pro216=) c.904C= (p.Pro302=) c.782+578C= (n.782+578C=) c.808C= (p.Pro270=) c.448C= (p.Pro150=) c.892C= (p.Pro298=) | |
17 | g.7673603G>T | CA397836145 | TP53 | c.925C>A (p.Pro309Thr) c.529C>A (p.Pro177Thr) c.646C>A (p.Pro216Thr) c.904C>A (p.Pro302Thr) c.782+578C>A (n.782+578C>A) c.808C>A (p.Pro270Thr) c.448C>A (p.Pro150Thr) c.892C>A (p.Pro298Thr) | dbSNP |
17 | g.7673604C>A | CA497714384 | TP53 | c.924G>T (p.Leu308=) c.528G>T (p.Leu176=) c.645G>T (p.Leu215=) c.903G>T (p.Leu301=) c.782+577G>T (n.782+577G>T) c.807G>T (p.Leu269=) c.447G>T (p.Leu149=) c.891G>T (p.Leu297=) | ClinVar |
17 | g.7673604C= | CA2245948012 | TP53 | c.924G= (p.Leu308=) c.528G= (p.Leu176=) c.645G= (p.Leu215=) c.903G= (p.Leu301=) c.782+577G= (n.782+577G=) c.807G= (p.Leu269=) c.447G= (p.Leu149=) c.891G= (p.Leu297=) | |
17 | g.7673604C>G | CA16615992 | TP53 | c.924G>C (p.Leu308=) c.528G>C (p.Leu176=) c.645G>C (p.Leu215=) c.903G>C (p.Leu301=) c.782+577G>C (n.782+577G>C) c.807G>C (p.Leu269=) c.447G>C (p.Leu149=) c.891G>C (p.Leu297=) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673604C>T | CA000503 | TP53 | c.924G>A (p.Leu308=) c.528G>A (p.Leu176=) c.645G>A (p.Leu215=) c.903G>A (p.Leu301=) c.782+577G>A (n.782+577G>A) c.807G>A (p.Leu269=) c.447G>A (p.Leu149=) c.891G>A (p.Leu297=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.7673610_7673611insCAACAGTGCT | CA645587389 | TP53 | c.924_925insTTGAGCACTG c.528_529insTTGAGCACTG c.645_646insTTGAGCACTG c.903_904insTTGAGCACTG c.782+577_782+578insTTGAGCACTG (n.782+577_782+578insTTGAGCACTG) c.807_808insTTGAGCACTG c.447_448insTTGAGCACTG c.891_892insTTGAGCACTG | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673605A>C | CA397836151 | TP53 | c.923T>G (p.Leu308Arg) c.527T>G (p.Leu176Arg) c.644T>G (p.Leu215Arg) c.902T>G (p.Leu301Arg) c.782+576T>G (n.782+576T>G) c.806T>G (p.Leu269Arg) c.446T>G (p.Leu149Arg) c.890T>G (p.Leu297Arg) | |
17 | g.7673605A>G | CA397836154 | TP53 | c.923T>C (p.Leu308Pro) c.527T>C (p.Leu176Pro) c.644T>C (p.Leu215Pro) c.902T>C (p.Leu301Pro) c.782+576T>C (n.782+576T>C) c.806T>C (p.Leu269Pro) c.446T>C (p.Leu149Pro) c.890T>C (p.Leu297Pro) | dbSNP |
17 | g.7673605A>T | CA397836155 | TP53 | c.923T>A (p.Leu308Gln) c.527T>A (p.Leu176Gln) c.644T>A (p.Leu215Gln) c.902T>A (p.Leu301Gln) c.782+576T>A (n.782+576T>A) c.806T>A (p.Leu269Gln) c.446T>A (p.Leu149Gln) c.890T>A (p.Leu297Gln) | dbSNP |
17 | g.7673605_7673611del | CA2580094903 | TP53 | c.920-3_923del c.524-3_527del c.641-3_644del c.899-3_902del c.782+570_782+576del (n.782+570_782+576del) c.803-3_806del c.443-3_446del c.887-3_890del | ClinVar |
17 | g.7673606G>A | CA497714399 | TP53 | c.922C>T (p.Leu308=) c.526C>T (p.Leu176=) c.643C>T (p.Leu215=) c.901C>T (p.Leu301=) c.782+575C>T (n.782+575C>T) c.805C>T (p.Leu269=) c.445C>T (p.Leu149=) c.889C>T (p.Leu297=) | ClinVar dbSNP gnomAD v4 |
17 | g.7673606G>C | CA397836159 | TP53 | c.922C>G (p.Leu308Val) c.526C>G (p.Leu176Val) c.643C>G (p.Leu215Val) c.901C>G (p.Leu301Val) c.782+575C>G (n.782+575C>G) c.805C>G (p.Leu269Val) c.445C>G (p.Leu149Val) c.889C>G (p.Leu297Val) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673606G= | CA2245948029 | TP53 | c.922C= (p.Leu308=) c.526C= (p.Leu176=) c.643C= (p.Leu215=) c.901C= (p.Leu301=) c.782+575C= (n.782+575C=) c.805C= (p.Leu269=) c.445C= (p.Leu149=) c.889C= (p.Leu297=) | |
17 | g.7673606G>T | CA397836161 | TP53 | c.922C>A (p.Leu308Met) c.526C>A (p.Leu176Met) c.643C>A (p.Leu215Met) c.901C>A (p.Leu301Met) c.782+575C>A (n.782+575C>A) c.805C>A (p.Leu269Met) c.445C>A (p.Leu149Met) c.889C>A (p.Leu297Met) | COSMIC |
17 | g.7673607_7673608del | CA645587390 | TP53 | c.921_922del (p.Leu308AlafsTer28) c.525_526del (p.Leu176AlafsTer28) c.642_643del (p.Leu215AlafsTer28) c.900_901del (p.Leu301AlafsTer28) c.921_922del (p.Leu308AlafsTer?) c.782+574_782+575del (n.782+574_782+575del) c.921_922del (p.Leu308AlafsTer27) c.525_526del (p.Leu176AlafsTer27) c.525_526del (p.Leu176AlafsTer?) c.804_805del (p.Leu269AlafsTer28) c.804_805del (p.Leu269AlafsTer27) c.444_445del (p.Leu149AlafsTer27) c.888_889del (p.Leu297AlafsTer28) c.444_445del (p.Leu149AlafsTer?) c.444_445del (p.Leu149AlafsTer28) c.804_805del (p.Leu269AlafsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673607T>A | CA497714414 | TP53 | c.921A>T (p.Ala307=) c.525A>T (p.Ala175=) c.642A>T (p.Ala214=) c.900A>T (p.Ala300=) c.782+574A>T (n.782+574A>T) c.804A>T (p.Ala268=) c.444A>T (p.Ala148=) c.888A>T (p.Ala296=) | dbSNP |
17 | g.7673607T>C | CA497714418 | TP53 | c.921A>G (p.Ala307=) c.525A>G (p.Ala175=) c.642A>G (p.Ala214=) c.900A>G (p.Ala300=) c.782+574A>G (n.782+574A>G) c.804A>G (p.Ala268=) c.444A>G (p.Ala148=) c.888A>G (p.Ala296=) | ClinVar dbSNP COSMIC |
17 | g.7673607T>G | CA497714421 | TP53 | c.921A>C (p.Ala307=) c.525A>C (p.Ala175=) c.642A>C (p.Ala214=) c.900A>C (p.Ala300=) c.782+574A>C (n.782+574A>C) c.804A>C (p.Ala268=) c.444A>C (p.Ala148=) c.888A>C (p.Ala296=) | dbSNP |
17 | g.7673607T= | CA2245948035 | TP53 | c.921A= (p.Ala307=) c.525A= (p.Ala175=) c.642A= (p.Ala214=) c.900A= (p.Ala300=) c.782+574A= (n.782+574A=) c.804A= (p.Ala268=) c.444A= (p.Ala148=) c.888A= (p.Ala296=) | |
17 | g.7673608del | CA2697559393 | TP53 | c.920del (p.Ala307AspfsTer?) c.524del (p.Ala175AspfsTer?) c.641del (p.Ala214AspfsTer?) c.899del (p.Ala300AspfsTer?) c.782+573del (n.782+573del) c.803del (p.Ala268AspfsTer?) c.443del (p.Ala148AspfsTer?) c.887del (p.Ala296AspfsTer?) | ClinVar |
17 | g.7673608G>A | CA397836165 | TP53 | c.920C>T (p.Ala307Val) c.524C>T (p.Ala175Val) c.641C>T (p.Ala214Val) c.899C>T (p.Ala300Val) c.782+573C>T (n.782+573C>T) c.803C>T (p.Ala268Val) c.443C>T (p.Ala148Val) c.887C>T (p.Ala296Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673608G>C | CA397836168 | TP53 | c.920C>G (p.Ala307Gly) c.524C>G (p.Ala175Gly) c.641C>G (p.Ala214Gly) c.899C>G (p.Ala300Gly) c.782+573C>G (n.782+573C>G) c.803C>G (p.Ala268Gly) c.443C>G (p.Ala148Gly) c.887C>G (p.Ala296Gly) | ClinVar dbSNP gnomAD v4 |
17 | g.7673608G= | CA2245948041 | TP53 | c.920C= (p.Ala307=) c.524C= (p.Ala175=) c.641C= (p.Ala214=) c.899C= (p.Ala300=) c.782+573C= (n.782+573C=) c.803C= (p.Ala268=) c.443C= (p.Ala148=) c.887C= (p.Ala296=) | |
17 | g.7673608G>T | CA397836170 | TP53 | c.920C>A (p.Ala307Glu) c.524C>A (p.Ala175Glu) c.641C>A (p.Ala214Glu) c.899C>A (p.Ala300Glu) c.782+573C>A (n.782+573C>A) c.803C>A (p.Ala268Glu) c.443C>A (p.Ala148Glu) c.887C>A (p.Ala296Glu) | dbSNP |
17 | g.7673609_7673613del | CA2573154631 | TP53 | c.920-4_920del c.524-4_524del c.641-4_641del c.899-4_899del c.782+569_782+573del (n.782+569_782+573del) c.803-4_803del c.443-4_443del c.887-4_887del | ClinVar dbSNP |
17 | g.7673609C>A | CA397836174 | TP53 | c.920-1G>T (n.920-1G>T) c.524-1G>T (n.524-1G>T) c.641-1G>T (n.641-1G>T) c.899-1G>T (n.899-1G>T) c.782+572G>T (n.782+572G>T) c.803-1G>T (n.803-1G>T) c.443-1G>T (n.443-1G>T) c.887-1G>T (n.887-1G>T) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673609C= | CA2245948059 | TP53 | c.920-1G= (n.920-1G=) c.524-1G= (n.524-1G=) c.641-1G= (n.641-1G=) c.899-1G= (n.899-1G=) c.782+572G= (n.782+572G=) c.803-1G= (n.803-1G=) c.443-1G= (n.443-1G=) c.887-1G= (n.887-1G=) | |
17 | g.7673609C>G | CA16615686 | TP53 | c.920-1G>C (n.920-1G>C) c.524-1G>C (n.524-1G>C) c.641-1G>C (n.641-1G>C) c.899-1G>C (n.899-1G>C) c.782+572G>C (n.782+572G>C) c.803-1G>C (n.803-1G>C) c.443-1G>C (n.443-1G>C) c.887-1G>C (n.887-1G>C) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673609C>T | CA000499 | TP53 | c.920-1G>A (n.920-1G>A) c.524-1G>A (n.524-1G>A) c.641-1G>A (n.641-1G>A) c.899-1G>A (n.899-1G>A) c.782+572G>A (n.782+572G>A) c.803-1G>A (n.803-1G>A) c.443-1G>A (n.443-1G>A) c.887-1G>A (n.887-1G>A) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673609_7673611delinsGAAAGGTGCAAGTGGAAAGAGGCAGT | CA2825002631 | TP53 | c.920-3_920-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.920-3_920-1delinsACTGCCTCTTTCCACTTGCACCTTTC) c.524-3_524-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.524-3_524-1delinsACTGCCTCTTTCCACTTGCACCTTTC) c.641-3_641-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.641-3_641-1delinsACTGCCTCTTTCCACTTGCACCTTTC) c.899-3_899-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.899-3_899-1delinsACTGCCTCTTTCCACTTGCACCTTTC) c.782+570_782+572delinsACTGCCTCTTTCCACTTGCACCTTTC (n.782+570_782+572delinsACTGCCTCTTTCCACTTGCACCTTTC) c.803-3_803-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.803-3_803-1delinsACTGCCTCTTTCCACTTGCACCTTTC) c.443-3_443-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.443-3_443-1delinsACTGCCTCTTTCCACTTGCACCTTTC) c.887-3_887-1delinsACTGCCTCTTTCCACTTGCACCTTTC (n.887-3_887-1delinsACTGCCTCTTTCCACTTGCACCTTTC) | ClinVar |
17 | g.7673611_7673702del | CA2556749014 | TP53 | c.919+1_920-1del c.523+1_524-1del c.640+1_641-1del c.898+1_899-1del c.782+481_782+572del (n.782+481_782+572del) c.802+1_803-1del c.442+1_443-1del c.886+1_887-1del | |
17 | g.7673610T>A | CA397836180 | TP53 | c.920-2A>T (n.920-2A>T) c.524-2A>T (n.524-2A>T) c.641-2A>T (n.641-2A>T) c.899-2A>T (n.899-2A>T) c.782+571A>T (n.782+571A>T) c.803-2A>T (n.803-2A>T) c.443-2A>T (n.443-2A>T) c.887-2A>T (n.887-2A>T) | ClinVar COSMIC COSMIC COSMIC COSMIC |
17 | g.7673610T>C | CA000500 | TP53 | c.920-2A>G (n.920-2A>G) c.524-2A>G (n.524-2A>G) c.641-2A>G (n.641-2A>G) c.899-2A>G (n.899-2A>G) c.782+571A>G (n.782+571A>G) c.803-2A>G (n.803-2A>G) c.443-2A>G (n.443-2A>G) c.887-2A>G (n.887-2A>G) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673610T>G | CA397836182 | TP53 | c.920-2A>C (n.920-2A>C) c.524-2A>C (n.524-2A>C) c.641-2A>C (n.641-2A>C) c.899-2A>C (n.899-2A>C) c.782+571A>C (n.782+571A>C) c.803-2A>C (n.803-2A>C) c.443-2A>C (n.443-2A>C) c.887-2A>C (n.887-2A>C) | ClinVar COSMIC |
17 | g.7673610T= | CA2245948085 | TP53 | c.920-2A= (n.920-2A=) c.524-2A= (n.524-2A=) c.641-2A= (n.641-2A=) c.899-2A= (n.899-2A=) c.782+571A= (n.782+571A=) c.803-2A= (n.803-2A=) c.443-2A= (n.443-2A=) c.887-2A= (n.887-2A=) | |
17 | g.7673610_7673622delinsTAGGAAAGAGGCA | CA2245948075 | TP53 | c.920-14_920-2delinsTGCCTCTTTCCTA (n.920-14_920-2delinsTGCCTCTTTCCTA) c.524-14_524-2delinsTGCCTCTTTCCTA (n.524-14_524-2delinsTGCCTCTTTCCTA) c.641-14_641-2delinsTGCCTCTTTCCTA (n.641-14_641-2delinsTGCCTCTTTCCTA) c.899-14_899-2delinsTGCCTCTTTCCTA (n.899-14_899-2delinsTGCCTCTTTCCTA) c.782+559_782+571delinsTGCCTCTTTCCTA (n.782+559_782+571delinsTGCCTCTTTCCTA) c.803-14_803-2delinsTGCCTCTTTCCTA (n.803-14_803-2delinsTGCCTCTTTCCTA) c.443-14_443-2delinsTGCCTCTTTCCTA (n.443-14_443-2delinsTGCCTCTTTCCTA) c.887-14_887-2delinsTGCCTCTTTCCTA (n.887-14_887-2delinsTGCCTCTTTCCTA) | |
17 | g.7673611A= | CA2245948094 | TP53 | c.920-3T= (n.920-3T=) c.524-3T= (n.524-3T=) c.641-3T= (n.641-3T=) c.899-3T= (n.899-3T=) c.782+570T= (n.782+570T=) c.803-3T= (n.803-3T=) c.443-3T= (n.443-3T=) c.887-3T= (n.887-3T=) | |
17 | g.7673611A>G | CA658656531 | TP53 | c.920-3T>C (n.920-3T>C) c.524-3T>C (n.524-3T>C) c.641-3T>C (n.641-3T>C) c.899-3T>C (n.899-3T>C) c.782+570T>C (n.782+570T>C) c.803-3T>C (n.803-3T>C) c.443-3T>C (n.443-3T>C) c.887-3T>C (n.887-3T>C) | ClinVar dbSNP gnomAD v4 |
17 | g.7673611A>T | CA2732956179 | TP53 | c.920-3T>A (n.920-3T>A) c.524-3T>A (n.524-3T>A) c.641-3T>A (n.641-3T>A) c.899-3T>A (n.899-3T>A) c.782+570T>A (n.782+570T>A) c.803-3T>A (n.803-3T>A) c.443-3T>A (n.443-3T>A) c.887-3T>A (n.887-3T>A) | dbSNP |
17 | g.7673618_7673629del | CA001246 | TP53 | c.920-14_920-3del (n.920-14_920-3del) c.524-14_524-3del (n.524-14_524-3del) c.641-14_641-3del (n.641-14_641-3del) c.899-14_899-3del (n.899-14_899-3del) c.782+559_782+570del (n.782+559_782+570del) c.803-14_803-3del (n.803-14_803-3del) c.443-14_443-3del (n.443-14_443-3del) c.887-14_887-3del (n.887-14_887-3del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673611_7673649del | CA645587393 | TP53 | c.920-41_920-3del (n.920-41_920-3del) c.524-41_524-3del (n.524-41_524-3del) c.641-41_641-3del (n.641-41_641-3del) c.899-41_899-3del (n.899-41_899-3del) c.782+532_782+570del (n.782+532_782+570del) c.803-41_803-3del (n.803-41_803-3del) c.443-41_443-3del (n.443-41_443-3del) c.887-41_887-3del (n.887-41_887-3del) | COSMIC COSMIC COSMIC |
17 | g.7673612G>A | CA915949517 | TP53 | c.920-4C>T (n.920-4C>T) c.524-4C>T (n.524-4C>T) c.641-4C>T (n.641-4C>T) c.899-4C>T (n.899-4C>T) c.782+569C>T (n.782+569C>T) c.803-4C>T (n.803-4C>T) c.443-4C>T (n.443-4C>T) c.887-4C>T (n.887-4C>T) | ClinVar dbSNP |
17 | g.7673612G>C | CA658798696 | TP53 | c.920-4C>G (n.920-4C>G) c.524-4C>G (n.524-4C>G) c.641-4C>G (n.641-4C>G) c.899-4C>G (n.899-4C>G) c.782+569C>G (n.782+569C>G) c.803-4C>G (n.803-4C>G) c.443-4C>G (n.443-4C>G) c.887-4C>G (n.887-4C>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7673612G= | CA2245948100 | TP53 | c.920-4C= (n.920-4C=) c.524-4C= (n.524-4C=) c.641-4C= (n.641-4C=) c.899-4C= (n.899-4C=) c.782+569C= (n.782+569C=) c.803-4C= (n.803-4C=) c.443-4C= (n.443-4C=) c.887-4C= (n.887-4C=) | |
17 | g.7673612G>T | CA2732963323 | TP53 | c.920-4C>A (n.920-4C>A) c.524-4C>A (n.524-4C>A) c.641-4C>A (n.641-4C>A) c.899-4C>A (n.899-4C>A) c.782+569C>A (n.782+569C>A) c.803-4C>A (n.803-4C>A) c.443-4C>A (n.443-4C>A) c.887-4C>A (n.887-4C>A) | dbSNP |
17 | g.7673613G>A | CA000502 | TP53 | c.920-5C>T (n.920-5C>T) c.524-5C>T (n.524-5C>T) c.641-5C>T (n.641-5C>T) c.899-5C>T (n.899-5C>T) c.782+568C>T (n.782+568C>T) c.803-5C>T (n.803-5C>T) c.443-5C>T (n.443-5C>T) c.887-5C>T (n.887-5C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673613G>C | CA2732923356 | TP53 | c.920-5C>G (n.920-5C>G) c.524-5C>G (n.524-5C>G) c.641-5C>G (n.641-5C>G) c.899-5C>G (n.899-5C>G) c.782+568C>G (n.782+568C>G) c.803-5C>G (n.803-5C>G) c.443-5C>G (n.443-5C>G) c.887-5C>G (n.887-5C>G) | dbSNP |
17 | g.7673613G= | CA2245948104 | TP53 | c.920-5C= (n.920-5C=) c.524-5C= (n.524-5C=) c.641-5C= (n.641-5C=) c.899-5C= (n.899-5C=) c.782+568C= (n.782+568C=) c.803-5C= (n.803-5C=) c.443-5C= (n.443-5C=) c.887-5C= (n.887-5C=) | |
17 | g.7673613G>T | CA16615935 | TP53 | c.920-5C>A (n.920-5C>A) c.524-5C>A (n.524-5C>A) c.641-5C>A (n.641-5C>A) c.899-5C>A (n.899-5C>A) c.782+568C>A (n.782+568C>A) c.803-5C>A (n.803-5C>A) c.443-5C>A (n.443-5C>A) c.887-5C>A (n.887-5C>A) | ClinVar dbSNP |
17 | g.7673614A>C | CA2825002632 | TP53 | c.920-6T>G (n.920-6T>G) c.524-6T>G (n.524-6T>G) c.641-6T>G (n.641-6T>G) c.899-6T>G (n.899-6T>G) c.782+567T>G (n.782+567T>G) c.803-6T>G (n.803-6T>G) c.443-6T>G (n.443-6T>G) c.887-6T>G (n.887-6T>G) | ClinVar |
17 | g.7673614A>G | CA2739265578 | TP53 | c.920-6T>C (n.920-6T>C) c.524-6T>C (n.524-6T>C) c.641-6T>C (n.641-6T>C) c.899-6T>C (n.899-6T>C) c.782+567T>C (n.782+567T>C) c.803-6T>C (n.803-6T>C) c.443-6T>C (n.443-6T>C) c.887-6T>C (n.887-6T>C) | ClinVar |
17 | g.7673614A>T | CA2733128278 | TP53 | c.920-6T>A (n.920-6T>A) c.524-6T>A (n.524-6T>A) c.641-6T>A (n.641-6T>A) c.899-6T>A (n.899-6T>A) c.782+567T>A (n.782+567T>A) c.803-6T>A (n.803-6T>A) c.443-6T>A (n.443-6T>A) c.887-6T>A (n.887-6T>A) | dbSNP |
17 | g.7673615A= | CA2245948109 | TP53 | c.920-7T= (n.920-7T=) c.524-7T= (n.524-7T=) c.641-7T= (n.641-7T=) c.899-7T= (n.899-7T=) c.782+566T= (n.782+566T=) c.803-7T= (n.803-7T=) c.443-7T= (n.443-7T=) c.887-7T= (n.887-7T=) | |
17 | g.7673615A>C | CA2245948110 | TP53 | c.920-7T>G (n.920-7T>G) c.524-7T>G (n.524-7T>G) c.641-7T>G (n.641-7T>G) c.899-7T>G (n.899-7T>G) c.782+566T>G (n.782+566T>G) c.803-7T>G (n.803-7T>G) c.443-7T>G (n.443-7T>G) c.887-7T>G (n.887-7T>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7673615A>T | CA497714457 | TP53 | c.920-7T>A (n.920-7T>A) c.524-7T>A (n.524-7T>A) c.641-7T>A (n.641-7T>A) c.899-7T>A (n.899-7T>A) c.782+566T>A (n.782+566T>A) c.803-7T>A (n.803-7T>A) c.443-7T>A (n.443-7T>A) c.887-7T>A (n.887-7T>A) | dbSNP COSMIC |
17 | g.7673616A= | CA2245948112 | TP53 | c.920-8T= (n.920-8T=) c.524-8T= (n.524-8T=) c.641-8T= (n.641-8T=) c.899-8T= (n.899-8T=) c.782+565T= (n.782+565T=) c.803-8T= (n.803-8T=) c.443-8T= (n.443-8T=) c.887-8T= (n.887-8T=) | |
17 | g.7673616A>G | CA658798698 | TP53 | c.920-8T>C (n.920-8T>C) c.524-8T>C (n.524-8T>C) c.641-8T>C (n.641-8T>C) c.899-8T>C (n.899-8T>C) c.782+565T>C (n.782+565T>C) c.803-8T>C (n.803-8T>C) c.443-8T>C (n.443-8T>C) c.887-8T>C (n.887-8T>C) | ClinVar dbSNP |
17 | g.7673616A>T | CA2732963324 | TP53 | c.920-8T>A (n.920-8T>A) c.524-8T>A (n.524-8T>A) c.641-8T>A (n.641-8T>A) c.899-8T>A (n.899-8T>A) c.782+565T>A (n.782+565T>A) c.803-8T>A (n.803-8T>A) c.443-8T>A (n.443-8T>A) c.887-8T>A (n.887-8T>A) | dbSNP |
17 | g.7673617G>A | CA624865101 | TP53 | c.920-9C>T (n.920-9C>T) c.524-9C>T (n.524-9C>T) c.641-9C>T (n.641-9C>T) c.899-9C>T (n.899-9C>T) c.782+564C>T (n.782+564C>T) c.803-9C>T (n.803-9C>T) c.443-9C>T (n.443-9C>T) c.887-9C>T (n.887-9C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673617G>C | CA2732949794 | TP53 | c.920-9C>G (n.920-9C>G) c.524-9C>G (n.524-9C>G) c.641-9C>G (n.641-9C>G) c.899-9C>G (n.899-9C>G) c.782+564C>G (n.782+564C>G) c.803-9C>G (n.803-9C>G) c.443-9C>G (n.443-9C>G) c.887-9C>G (n.887-9C>G) | dbSNP |
17 | g.7673617G= | CA2245948120 | TP53 | c.920-9C= (n.920-9C=) c.524-9C= (n.524-9C=) c.641-9C= (n.641-9C=) c.899-9C= (n.899-9C=) c.782+564C= (n.782+564C=) c.803-9C= (n.803-9C=) c.443-9C= (n.443-9C=) c.887-9C= (n.887-9C=) | |
17 | g.7673617G>T | CA916081890 | TP53 | c.920-9C>A (n.920-9C>A) c.524-9C>A (n.524-9C>A) c.641-9C>A (n.641-9C>A) c.899-9C>A (n.899-9C>A) c.782+564C>A (n.782+564C>A) c.803-9C>A (n.803-9C>A) c.443-9C>A (n.443-9C>A) c.887-9C>A (n.887-9C>A) | ClinVar dbSNP |
17 | g.7673618A= | CA2245948122 | TP53 | c.920-10T= (n.920-10T=) c.524-10T= (n.524-10T=) c.641-10T= (n.641-10T=) c.899-10T= (n.899-10T=) c.782+563T= (n.782+563T=) c.803-10T= (n.803-10T=) c.443-10T= (n.443-10T=) c.887-10T= (n.887-10T=) | |
17 | g.7673618A>G | CA915949518 | TP53 | c.920-10T>C (n.920-10T>C) c.524-10T>C (n.524-10T>C) c.641-10T>C (n.641-10T>C) c.899-10T>C (n.899-10T>C) c.782+563T>C (n.782+563T>C) c.803-10T>C (n.803-10T>C) c.443-10T>C (n.443-10T>C) c.887-10T>C (n.887-10T>C) | ClinVar dbSNP |
17 | g.7673618A>T | CA2580094907 | TP53 | c.920-10T>A (n.920-10T>A) c.524-10T>A (n.524-10T>A) c.641-10T>A (n.641-10T>A) c.899-10T>A (n.899-10T>A) c.782+563T>A (n.782+563T>A) c.803-10T>A (n.803-10T>A) c.443-10T>A (n.443-10T>A) c.887-10T>A (n.887-10T>A) | ClinVar dbSNP |
17 | g.7673619G>A | CA16608659 | TP53 | c.920-11C>T (n.920-11C>T) c.524-11C>T (n.524-11C>T) c.641-11C>T (n.641-11C>T) c.899-11C>T (n.899-11C>T) c.782+562C>T (n.782+562C>T) c.803-11C>T (n.803-11C>T) c.443-11C>T (n.443-11C>T) c.887-11C>T (n.887-11C>T) | ClinVar dbSNP gnomAD v4 |
17 | g.7673619G>C | CA2732943610 | TP53 | c.920-11C>G (n.920-11C>G) c.524-11C>G (n.524-11C>G) c.641-11C>G (n.641-11C>G) c.899-11C>G (n.899-11C>G) c.782+562C>G (n.782+562C>G) c.803-11C>G (n.803-11C>G) c.443-11C>G (n.443-11C>G) c.887-11C>G (n.887-11C>G) | dbSNP |
17 | g.7673619G= | CA2245948123 | TP53 | c.920-11C= (n.920-11C=) c.524-11C= (n.524-11C=) c.641-11C= (n.641-11C=) c.899-11C= (n.899-11C=) c.782+562C= (n.782+562C=) c.803-11C= (n.803-11C=) c.443-11C= (n.443-11C=) c.887-11C= (n.887-11C=) | |
17 | g.7673619G>T | CA2732943609 | TP53 | c.920-11C>A (n.920-11C>A) c.524-11C>A (n.524-11C>A) c.641-11C>A (n.641-11C>A) c.899-11C>A (n.899-11C>A) c.782+562C>A (n.782+562C>A) c.803-11C>A (n.803-11C>A) c.443-11C>A (n.443-11C>A) c.887-11C>A (n.887-11C>A) | dbSNP |
17 | g.7673620G>A | CA2697559394 | TP53 | c.920-12C>T (n.920-12C>T) c.524-12C>T (n.524-12C>T) c.641-12C>T (n.641-12C>T) c.899-12C>T (n.899-12C>T) c.782+561C>T (n.782+561C>T) c.803-12C>T (n.803-12C>T) c.443-12C>T (n.443-12C>T) c.887-12C>T (n.887-12C>T) | ClinVar dbSNP |
17 | g.7673621C>A | CA775168943 | TP53 | c.920-13G>T (n.920-13G>T) c.524-13G>T (n.524-13G>T) c.641-13G>T (n.641-13G>T) c.899-13G>T (n.899-13G>T) c.782+560G>T (n.782+560G>T) c.803-13G>T (n.803-13G>T) c.443-13G>T (n.443-13G>T) c.887-13G>T (n.887-13G>T) | ClinVar dbSNP gnomAD v4 |
17 | g.7673621C= | CA2245948130 | TP53 | c.920-13G= (n.920-13G=) c.524-13G= (n.524-13G=) c.641-13G= (n.641-13G=) c.899-13G= (n.899-13G=) c.782+560G= (n.782+560G=) c.803-13G= (n.803-13G=) c.443-13G= (n.443-13G=) c.887-13G= (n.887-13G=) | |
17 | g.7673621C>G | CA16607880 | TP53 | c.920-13G>C (n.920-13G>C) c.524-13G>C (n.524-13G>C) c.641-13G>C (n.641-13G>C) c.899-13G>C (n.899-13G>C) c.782+560G>C (n.782+560G>C) c.803-13G>C (n.803-13G>C) c.443-13G>C (n.443-13G>C) c.887-13G>C (n.887-13G>C) | ClinVar dbSNP |
17 | g.7673621C>T | CA624865102 | TP53 | c.920-13G>A (n.920-13G>A) c.524-13G>A (n.524-13G>A) c.641-13G>A (n.641-13G>A) c.899-13G>A (n.899-13G>A) c.782+560G>A (n.782+560G>A) c.803-13G>A (n.803-13G>A) c.443-13G>A (n.443-13G>A) c.887-13G>A (n.887-13G>A) | ClinVar dbSNP gnomAD v2 |
17 | g.7673622A= | CA2245948137 | TP53 | c.920-14T= (n.920-14T=) c.524-14T= (n.524-14T=) c.641-14T= (n.641-14T=) c.899-14T= (n.899-14T=) c.782+559T= (n.782+559T=) c.803-14T= (n.803-14T=) c.443-14T= (n.443-14T=) c.887-14T= (n.887-14T=) | |
17 | g.7673622A>G | CA001258 | TP53 | c.920-14T>C (n.920-14T>C) c.524-14T>C (n.524-14T>C) c.641-14T>C (n.641-14T>C) c.899-14T>C (n.899-14T>C) c.782+559T>C (n.782+559T>C) c.803-14T>C (n.803-14T>C) c.443-14T>C (n.443-14T>C) c.887-14T>C (n.887-14T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673622A>T | CA2732929496 | TP53 | c.920-14T>A (n.920-14T>A) c.524-14T>A (n.524-14T>A) c.641-14T>A (n.641-14T>A) c.899-14T>A (n.899-14T>A) c.782+559T>A (n.782+559T>A) c.803-14T>A (n.803-14T>A) c.443-14T>A (n.443-14T>A) c.887-14T>A (n.887-14T>A) | dbSNP |
17 | g.7673623A>G | CA2697559395 | TP53 | c.920-15T>C (n.920-15T>C) c.524-15T>C (n.524-15T>C) c.641-15T>C (n.641-15T>C) c.899-15T>C (n.899-15T>C) c.782+558T>C (n.782+558T>C) c.803-15T>C (n.803-15T>C) c.443-15T>C (n.443-15T>C) c.887-15T>C (n.887-15T>C) | ClinVar dbSNP |
17 | g.7673623A>T | CA2733128381 | TP53 | c.920-15T>A (n.920-15T>A) c.524-15T>A (n.524-15T>A) c.641-15T>A (n.641-15T>A) c.899-15T>A (n.899-15T>A) c.782+558T>A (n.782+558T>A) c.803-15T>A (n.803-15T>A) c.443-15T>A (n.443-15T>A) c.887-15T>A (n.887-15T>A) | dbSNP |
17 | g.7673624G>A | CA2739265581 | TP53 | c.920-16C>T (n.920-16C>T) c.524-16C>T (n.524-16C>T) c.641-16C>T (n.641-16C>T) c.899-16C>T (n.899-16C>T) c.782+557C>T (n.782+557C>T) c.803-16C>T (n.803-16C>T) c.443-16C>T (n.443-16C>T) c.887-16C>T (n.887-16C>T) | ClinVar |
17 | g.7673625G= | CA2245948141 | TP53 | c.920-17C= (n.920-17C=) c.524-17C= (n.524-17C=) c.641-17C= (n.641-17C=) c.899-17C= (n.899-17C=) c.782+556C= (n.782+556C=) c.803-17C= (n.803-17C=) c.443-17C= (n.443-17C=) c.887-17C= (n.887-17C=) | |
17 | g.7673625G>T | CA287486535 | TP53 | c.920-17C>A (n.920-17C>A) c.524-17C>A (n.524-17C>A) c.641-17C>A (n.641-17C>A) c.899-17C>A (n.899-17C>A) c.782+556C>A (n.782+556C>A) c.803-17C>A (n.803-17C>A) c.443-17C>A (n.443-17C>A) c.887-17C>A (n.887-17C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673626A>C | CA2733128625 | TP53 | c.920-18T>G (n.920-18T>G) c.524-18T>G (n.524-18T>G) c.641-18T>G (n.641-18T>G) c.899-18T>G (n.899-18T>G) c.782+555T>G (n.782+555T>G) c.803-18T>G (n.803-18T>G) c.443-18T>G (n.443-18T>G) c.887-18T>G (n.887-18T>G) | dbSNP |
17 | g.7673626A>G | CA2733128490 | TP53 | c.920-18T>C (n.920-18T>C) c.524-18T>C (n.524-18T>C) c.641-18T>C (n.641-18T>C) c.899-18T>C (n.899-18T>C) c.782+555T>C (n.782+555T>C) c.803-18T>C (n.803-18T>C) c.443-18T>C (n.443-18T>C) c.887-18T>C (n.887-18T>C) | dbSNP |
17 | g.7673626A>T | CA2733128656 | TP53 | c.920-18T>A (n.920-18T>A) c.524-18T>A (n.524-18T>A) c.641-18T>A (n.641-18T>A) c.899-18T>A (n.899-18T>A) c.782+555T>A (n.782+555T>A) c.803-18T>A (n.803-18T>A) c.443-18T>A (n.443-18T>A) c.887-18T>A (n.887-18T>A) | dbSNP |
17 | g.7673628A>C | CA2733129134 | TP53 | c.920-20T>G (n.920-20T>G) c.524-20T>G (n.524-20T>G) c.641-20T>G (n.641-20T>G) c.899-20T>G (n.899-20T>G) c.782+553T>G (n.782+553T>G) c.803-20T>G (n.803-20T>G) c.443-20T>G (n.443-20T>G) c.887-20T>G (n.887-20T>G) | dbSNP |
17 | g.7673628A>G | CA2733129135 | TP53 | c.920-20T>C (n.920-20T>C) c.524-20T>C (n.524-20T>C) c.641-20T>C (n.641-20T>C) c.899-20T>C (n.899-20T>C) c.782+553T>C (n.782+553T>C) c.803-20T>C (n.803-20T>C) c.443-20T>C (n.443-20T>C) c.887-20T>C (n.887-20T>C) | dbSNP |
17 | g.7673628A>T | CA2733129136 | TP53 | c.920-20T>A (n.920-20T>A) c.524-20T>A (n.524-20T>A) c.641-20T>A (n.641-20T>A) c.899-20T>A (n.899-20T>A) c.782+553T>A (n.782+553T>A) c.803-20T>A (n.803-20T>A) c.443-20T>A (n.443-20T>A) c.887-20T>A (n.887-20T>A) | dbSNP |
17 | g.7673629G>A | CA645587394 | TP53 | c.920-21C>T (n.920-21C>T) c.524-21C>T (n.524-21C>T) c.641-21C>T (n.641-21C>T) c.899-21C>T (n.899-21C>T) c.782+552C>T (n.782+552C>T) c.803-21C>T (n.803-21C>T) c.443-21C>T (n.443-21C>T) c.887-21C>T (n.887-21C>T) | COSMIC |
17 | g.7673629G>T | CA2635874421 | TP53 | c.920-21C>A (n.920-21C>A) c.524-21C>A (n.524-21C>A) c.641-21C>A (n.641-21C>A) c.899-21C>A (n.899-21C>A) c.782+552C>A (n.782+552C>A) c.803-21C>A (n.803-21C>A) c.443-21C>A (n.443-21C>A) c.887-21C>A (n.887-21C>A) | gnomAD v4 |
17 | g.7673630G>A | CA001264 | TP53 | c.920-22C>T (n.920-22C>T) c.524-22C>T (n.524-22C>T) c.641-22C>T (n.641-22C>T) c.899-22C>T (n.899-22C>T) c.782+551C>T (n.782+551C>T) c.803-22C>T (n.803-22C>T) c.443-22C>T (n.443-22C>T) c.887-22C>T (n.887-22C>T) | dbSNP ExAC gnomAD v3 gnomAD v4 |
17 | g.7673630G= | CA2245948147 | TP53 | c.920-22C= (n.920-22C=) c.524-22C= (n.524-22C=) c.641-22C= (n.641-22C=) c.899-22C= (n.899-22C=) c.782+551C= (n.782+551C=) c.803-22C= (n.803-22C=) c.443-22C= (n.443-22C=) c.887-22C= (n.887-22C=) | |
17 | g.7673630G>T | CA624865103 | TP53 | c.920-22C>A (n.920-22C>A) c.524-22C>A (n.524-22C>A) c.641-22C>A (n.641-22C>A) c.899-22C>A (n.899-22C>A) c.782+551C>A (n.782+551C>A) c.803-22C>A (n.803-22C>A) c.443-22C>A (n.443-22C>A) c.887-22C>A (n.887-22C>A) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673631T>A | CA2732965381 | TP53 | c.920-23A>T (n.920-23A>T) c.524-23A>T (n.524-23A>T) c.641-23A>T (n.641-23A>T) c.899-23A>T (n.899-23A>T) c.782+550A>T (n.782+550A>T) c.803-23A>T (n.803-23A>T) c.443-23A>T (n.443-23A>T) c.887-23A>T (n.887-23A>T) | dbSNP |
17 | g.7673631T>G | CA2245948151 | TP53 | c.920-23A>C (n.920-23A>C) c.524-23A>C (n.524-23A>C) c.641-23A>C (n.641-23A>C) c.899-23A>C (n.899-23A>C) c.782+550A>C (n.782+550A>C) c.803-23A>C (n.803-23A>C) c.443-23A>C (n.443-23A>C) c.887-23A>C (n.887-23A>C) | dbSNP |
17 | g.7673631T= | CA2245948152 | TP53 | c.920-23A= (n.920-23A=) c.524-23A= (n.524-23A=) c.641-23A= (n.641-23A=) c.899-23A= (n.899-23A=) c.782+550A= (n.782+550A=) c.803-23A= (n.803-23A=) c.443-23A= (n.443-23A=) c.887-23A= (n.887-23A=) | |
17 | g.7673632G>A | CA2635874450 | TP53 | c.920-24C>T (n.920-24C>T) c.524-24C>T (n.524-24C>T) c.641-24C>T (n.641-24C>T) c.899-24C>T (n.899-24C>T) c.782+549C>T (n.782+549C>T) c.803-24C>T (n.803-24C>T) c.443-24C>T (n.443-24C>T) c.887-24C>T (n.887-24C>T) | dbSNP gnomAD v4 |
17 | g.7673632G>C | CA2635874453 | TP53 | c.920-24C>G (n.920-24C>G) c.524-24C>G (n.524-24C>G) c.641-24C>G (n.641-24C>G) c.899-24C>G (n.899-24C>G) c.782+549C>G (n.782+549C>G) c.803-24C>G (n.803-24C>G) c.443-24C>G (n.443-24C>G) c.887-24C>G (n.887-24C>G) | dbSNP gnomAD v4 |
17 | g.7673633A>G | CA2733129137 | TP53 | c.920-25T>C (n.920-25T>C) c.524-25T>C (n.524-25T>C) c.641-25T>C (n.641-25T>C) c.899-25T>C (n.899-25T>C) c.782+548T>C (n.782+548T>C) c.803-25T>C (n.803-25T>C) c.443-25T>C (n.443-25T>C) c.887-25T>C (n.887-25T>C) | dbSNP |
17 | g.7673633A>T | CA2733129138 | TP53 | c.920-25T>A (n.920-25T>A) c.524-25T>A (n.524-25T>A) c.641-25T>A (n.641-25T>A) c.899-25T>A (n.899-25T>A) c.782+548T>A (n.782+548T>A) c.803-25T>A (n.803-25T>A) c.443-25T>A (n.443-25T>A) c.887-25T>A (n.887-25T>A) | dbSNP |
17 | g.7673634T>A | CA2733129140 | TP53 | c.920-26A>T (n.920-26A>T) c.524-26A>T (n.524-26A>T) c.641-26A>T (n.641-26A>T) c.899-26A>T (n.899-26A>T) c.782+547A>T (n.782+547A>T) c.803-26A>T (n.803-26A>T) c.443-26A>T (n.443-26A>T) c.887-26A>T (n.887-26A>T) | dbSNP |
17 | g.7673634T>G | CA2733129139 | TP53 | c.920-26A>C (n.920-26A>C) c.524-26A>C (n.524-26A>C) c.641-26A>C (n.641-26A>C) c.899-26A>C (n.899-26A>C) c.782+547A>C (n.782+547A>C) c.803-26A>C (n.803-26A>C) c.443-26A>C (n.443-26A>C) c.887-26A>C (n.887-26A>C) | dbSNP |
17 | g.7673635A= | CA2245948158 | TP53 | c.920-27T= (n.920-27T=) c.524-27T= (n.524-27T=) c.641-27T= (n.641-27T=) c.899-27T= (n.899-27T=) c.782+546T= (n.782+546T=) c.803-27T= (n.803-27T=) c.443-27T= (n.443-27T=) c.887-27T= (n.887-27T=) | |
17 | g.7673635A>G | CA624865104 | TP53 | c.920-27T>C (n.920-27T>C) c.524-27T>C (n.524-27T>C) c.641-27T>C (n.641-27T>C) c.899-27T>C (n.899-27T>C) c.782+546T>C (n.782+546T>C) c.803-27T>C (n.803-27T>C) c.443-27T>C (n.443-27T>C) c.887-27T>C (n.887-27T>C) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673635A>T | CA2732944968 | TP53 | c.920-27T>A (n.920-27T>A) c.524-27T>A (n.524-27T>A) c.641-27T>A (n.641-27T>A) c.899-27T>A (n.899-27T>A) c.782+546T>A (n.782+546T>A) c.803-27T>A (n.803-27T>A) c.443-27T>A (n.443-27T>A) c.887-27T>A (n.887-27T>A) | dbSNP |
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.7673636A>T | CA2733129141 | TP53 | c.920-28T>A (n.920-28T>A) c.524-28T>A (n.524-28T>A) c.641-28T>A (n.641-28T>A) c.899-28T>A (n.899-28T>A) c.782+545T>A (n.782+545T>A) c.803-28T>A (n.803-28T>A) c.443-28T>A (n.443-28T>A) c.887-28T>A (n.887-28T>A) | dbSNP |
17 | g.7673637A>G | CA2733129142 | TP53 | c.920-29T>C (n.920-29T>C) c.524-29T>C (n.524-29T>C) c.641-29T>C (n.641-29T>C) c.899-29T>C (n.899-29T>C) c.782+544T>C (n.782+544T>C) c.803-29T>C (n.803-29T>C) c.443-29T>C (n.443-29T>C) c.887-29T>C (n.887-29T>C) | dbSNP |
17 | g.7673637A>T | CA2733129143 | TP53 | c.920-29T>A (n.920-29T>A) c.524-29T>A (n.524-29T>A) c.641-29T>A (n.641-29T>A) c.899-29T>A (n.899-29T>A) c.782+544T>A (n.782+544T>A) c.803-29T>A (n.803-29T>A) c.443-29T>A (n.443-29T>A) c.887-29T>A (n.887-29T>A) | dbSNP |
17 | g.7673638A>C | CA2733129144 | TP53 | c.920-30T>G (n.920-30T>G) c.524-30T>G (n.524-30T>G) c.641-30T>G (n.641-30T>G) c.899-30T>G (n.899-30T>G) c.782+543T>G (n.782+543T>G) c.803-30T>G (n.803-30T>G) c.443-30T>G (n.443-30T>G) c.887-30T>G (n.887-30T>G) | dbSNP |
17 | g.7673638A>G | CA2733129146 | TP53 | c.920-30T>C (n.920-30T>C) c.524-30T>C (n.524-30T>C) c.641-30T>C (n.641-30T>C) c.899-30T>C (n.899-30T>C) c.782+543T>C (n.782+543T>C) c.803-30T>C (n.803-30T>C) c.443-30T>C (n.443-30T>C) c.887-30T>C (n.887-30T>C) | dbSNP |
17 | g.7673638A>T | CA2733129147 | TP53 | c.920-30T>A (n.920-30T>A) c.524-30T>A (n.524-30T>A) c.641-30T>A (n.641-30T>A) c.899-30T>A (n.899-30T>A) c.782+543T>A (n.782+543T>A) c.803-30T>A (n.803-30T>A) c.443-30T>A (n.443-30T>A) c.887-30T>A (n.887-30T>A) | dbSNP |
17 | g.7673639G>A | CA2733129149 | TP53 | c.920-31C>T (n.920-31C>T) c.524-31C>T (n.524-31C>T) c.641-31C>T (n.641-31C>T) c.899-31C>T (n.899-31C>T) c.782+542C>T (n.782+542C>T) c.803-31C>T (n.803-31C>T) c.443-31C>T (n.443-31C>T) c.887-31C>T (n.887-31C>T) | dbSNP |
17 | g.7673639G>C | CA2733129304 | TP53 | c.920-31C>G (n.920-31C>G) c.524-31C>G (n.524-31C>G) c.641-31C>G (n.641-31C>G) c.899-31C>G (n.899-31C>G) c.782+542C>G (n.782+542C>G) c.803-31C>G (n.803-31C>G) c.443-31C>G (n.443-31C>G) c.887-31C>G (n.887-31C>G) | dbSNP |
17 | g.7673639_7673640delinsGT | CA2245948162 | TP53 | c.920-32_920-31delinsAC (n.920-32_920-31delinsAC) c.524-32_524-31delinsAC (n.524-32_524-31delinsAC) c.641-32_641-31delinsAC (n.641-32_641-31delinsAC) c.899-32_899-31delinsAC (n.899-32_899-31delinsAC) c.782+541_782+542delinsAC (n.782+541_782+542delinsAC) c.803-32_803-31delinsAC (n.803-32_803-31delinsAC) c.443-32_443-31delinsAC (n.443-32_443-31delinsAC) c.887-32_887-31delinsAC (n.887-32_887-31delinsAC) | |
17 | g.7673640del | CA624865105 | TP53 | c.920-32del (n.920-32del) c.524-32del (n.524-32del) c.641-32del (n.641-32del) c.899-32del (n.899-32del) c.782+541del (n.782+541del) c.803-32del (n.803-32del) c.443-32del (n.443-32del) c.887-32del (n.887-32del) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673640T>A | CA2635874460 | TP53 | c.920-32A>T (n.920-32A>T) c.524-32A>T (n.524-32A>T) c.641-32A>T (n.641-32A>T) c.899-32A>T (n.899-32A>T) c.782+541A>T (n.782+541A>T) c.803-32A>T (n.803-32A>T) c.443-32A>T (n.443-32A>T) c.887-32A>T (n.887-32A>T) | dbSNP gnomAD v4 |
17 | g.7673640T>C | CA2733129680 | TP53 | c.920-32A>G (n.920-32A>G) c.524-32A>G (n.524-32A>G) c.641-32A>G (n.641-32A>G) c.899-32A>G (n.899-32A>G) c.782+541A>G (n.782+541A>G) c.803-32A>G (n.803-32A>G) c.443-32A>G (n.443-32A>G) c.887-32A>G (n.887-32A>G) | dbSNP |
17 | g.7673640T>G | CA2733129779 | TP53 | c.920-32A>C (n.920-32A>C) c.524-32A>C (n.524-32A>C) c.641-32A>C (n.641-32A>C) c.899-32A>C (n.899-32A>C) c.782+541A>C (n.782+541A>C) c.803-32A>C (n.803-32A>C) c.443-32A>C (n.443-32A>C) c.887-32A>C (n.887-32A>C) | dbSNP |