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.7674861_7676624dup | CA2573130640 | TP53 | c.-28_672dup c.-21-1386_276dup c.-28_393dup c.-28_651dup c.-25-3_672dup n.112_928dup c.-262_555dup c.-145_555dup c.-142-3_555dup | |
17 | g.7675197_7676153del | CA645589160 | TP53 | c.216_415del c.-21-917_19del c.96+229_136del c.216_394del n.472_671del c.99_298del c.216_382del | COSMIC |
17 | g.7675226_7676561del | CA645589205 | TP53 | c.36_388del c.-21-1323_-9del c.36_109del c.36_376-9del n.175_644del c.-199_271del c.-82_271del c.36_355del | COSMIC |
17 | g.7675995_7676194del | CA645589234 | TP53 | c.179_375+3del c.-21-954_-21-755del (n.-21-954_-21-755del) c.96+192_96+391del (n.96+192_96+391del) n.435_631+3del c.62_258+3del c.179_340+34del | COSMIC |
17 | g.7675995_7676272del | CA645589239 | TP53 | c.97_374del (p.Ser33ValfsTer23) c.-21-1036_-21-759del (n.-21-1036_-21-759del) c.96+110_96+387del (n.96+110_96+387del) c.97_374del (p.Ser33AspfsTer16) c.97_374del (p.Ser33ValfsTer?) n.353_630del c.-21_257del c.97_340+30del | COSMIC |
17 | g.7676099_7676151del | CA645369690 | TP53 | c.227_279del (p.Ala76ValfsTer?) c.-21-906_-21-854del (n.-21-906_-21-854del) c.96+240_96+292del (n.96+240_96+292del) n.483_535del c.110_162del (p.Ala37ValfsTer?) | ClinVar dbSNP |
17 | g.7676096_7676232del | CA645589328 | TP53 | c.141_277del (p.Asp48ValfsTer?) c.-21-992_-21-856del (n.-21-992_-21-856del) c.96+154_96+290del (n.96+154_96+290del) n.397_533del c.24_160del (p.Asp9ValfsTer?) | COSMIC |
17 | g.7676121_7676150del | CA002925 | TP53 | c.234_263del (p.Ala79_Ala88del) c.-21-899_-21-870del (n.-21-899_-21-870del) c.96+247_96+276del (n.96+247_96+276del) n.490_519del c.117_146del (p.Ala40_Ala49del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676119_7676179del | CA645589349 | TP53 | c.193_253del (p.Arg65LeufsTer?) c.-21-940_-21-880del (n.-21-940_-21-880del) c.96+206_96+266del (n.96+206_96+266del) n.449_509del c.76_136del (p.Arg26LeufsTer?) | COSMIC |
17 | g.7676128_7676156del | CA891842282 | TP53 | c.214_242del (p.Pro72ThrfsTer?) c.-21-919_-21-891del (n.-21-919_-21-891del) c.96+227_96+255del (n.96+227_96+255del) n.470_498del c.97_125del (p.Pro33ThrfsTer?) | |
17 | g.7676133_7676151del | CA2580095105 | TP53 | c.219_237del (p.Ala74LeufsTer?) c.-21-914_-21-896del (n.-21-914_-21-896del) c.96+232_96+250del (n.96+232_96+250del) n.475_493del c.102_120del (p.Ala35LeufsTer?) | ClinVar |
17 | g.7676136_7676184delinsGCTGGTGCAGGGGCCACGGGGGGAGCAGCCTCTGGCATTCTGGGAGCTT | CA2245934518 | TP53 | c.185_233delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (p.Glu62=) c.-21-948_-21-900delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (n.-21-948_-21-900delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC) c.96+198_96+246delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (n.96+198_96+246delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC) n.441_489delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC c.68_116delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (p.Glu23=) | |
17 | g.7676138_7676185del | CA913191061 | TP53 | c.185_232del (p.Glu62_Pro77del) c.-21-948_-21-901del (n.-21-948_-21-901del) c.96+198_96+245del (n.96+198_96+245del) n.441_488del c.68_115del (p.Glu23_Pro38del) | ClinVar dbSNP |
17 | g.7676139_7676149del | CA645589363 | TP53 | c.220_230del (p.Ala74SerfsTer?) c.-21-913_-21-903del (n.-21-913_-21-903del) c.96+233_96+243del (n.96+233_96+243del) n.476_486del c.103_113del (p.Ala35SerfsTer?) | COSMIC |
17 | g.7676142_7676201del | CA645589366 | TP53 | c.169_228del (p.Asp57_Ala76del) c.-21-964_-21-905del (n.-21-964_-21-905del) c.96+182_96+241del (n.96+182_96+241del) n.425_484del c.52_111del (p.Asp18_Ala37del) | COSMIC |
17 | g.7676143_7676171del | CA2580574333 | TP53 | c.198_226del (p.Met66IlefsTer?) c.-21-935_-21-907del (n.-21-935_-21-907del) c.96+211_96+239del (n.96+211_96+239del) n.454_482del c.81_109del (p.Met27IlefsTer?) | |
17 | g.7676149_7676153dup | CA2697552149 | TP53 | c.217_221dup (p.Pro75TrpfsTer?) c.-21-916_-21-912dup (n.-21-916_-21-912dup) c.96+230_96+234dup (n.96+230_96+234dup) n.473_477dup c.100_104dup (p.Pro36TrpfsTer?) | ClinVar |
17 | g.7676148_7676166delinsCTCCC | CA645589367 | TP53 | c.203_221delinsGGGAG (p.Glu68GlyfsTer?) c.-21-930_-21-912delinsGGGAG (n.-21-930_-21-912delinsGGGAG) c.96+216_96+234delinsGGGAG (n.96+216_96+234delinsGGGAG) n.459_477delinsGGGAG c.86_104delinsGGGAG (p.Glu29GlyfsTer?) | COSMIC |
17 | g.7676149C>A | CA397845695 | TP53 | c.220G>T (p.Ala74Ser) c.-21-913G>T (n.-21-913G>T) c.96+233G>T (n.96+233G>T) n.476G>T c.103G>T (p.Ala35Ser) | ClinVar dbSNP gnomAD v4 |
17 | g.7676149C>G | CA397845699 | TP53 | c.220G>C (p.Ala74Pro) c.-21-913G>C (n.-21-913G>C) c.96+233G>C (n.96+233G>C) n.476G>C c.103G>C (p.Ala35Pro) | |
17 | g.7676149C>T | CA397845701 | TP53 | c.220G>A (p.Ala74Thr) c.-21-913G>A (n.-21-913G>A) c.96+233G>A (n.96+233G>A) n.476G>A c.103G>A (p.Ala35Thr) | dbSNP |
17 | g.7676150del | CA497925983 | TP53 | c.220del (p.Ala74ProfsTer?) c.-21-913del (n.-21-913del) c.96+233del (n.96+233del) n.476del c.103del (p.Ala35ProfsTer?) | COSMIC |
17 | g.7676150C>A | CA497925985 | TP53 | c.219G>T (p.Val73=) c.-21-914G>T (n.-21-914G>T) c.96+232G>T (n.96+232G>T) n.475G>T c.102G>T (p.Val34=) | ClinVar dbSNP |
17 | g.7676150C= | CA2245934617 | TP53 | c.219G= (p.Val73=) c.-21-914G= (n.-21-914G=) c.96+232G= (n.96+232G=) n.475G= c.102G= (p.Val34=) | |
17 | g.7676150C>G | CA497925986 | TP53 | c.219G>C (p.Val73=) c.-21-914G>C (n.-21-914G>C) c.96+232G>C (n.96+232G>C) n.475G>C c.102G>C (p.Val34=) | dbSNP |
17 | g.7676150C>T | CA497925984 | TP53 | c.219G>A (p.Val73=) c.-21-914G>A (n.-21-914G>A) c.96+232G>A (n.96+232G>A) n.475G>A c.102G>A (p.Val34=) | ClinVar dbSNP |
17 | g.7676150_7676151insCG | CA645589368 | TP53 | c.218_219insCG (p.Ala74GlyfsTer?) c.-21-915_-21-914insCG (n.-21-915_-21-914insCG) c.96+231_96+232insCG (n.96+231_96+232insCG) n.474_475insCG c.101_102insCG (p.Ala35GlyfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676151del | CA497925987 | TP53 | c.218del (p.Val73GlyfsTer?) c.-21-915del (n.-21-915del) c.96+231del (n.96+231del) n.474del c.101del (p.Val34GlyfsTer?) | COSMIC |
17 | g.7676151A>C | CA397845706 | TP53 | c.218T>G (p.Val73Gly) c.-21-915T>G (n.-21-915T>G) c.96+231T>G (n.96+231T>G) n.474T>G c.101T>G (p.Val34Gly) | |
17 | g.7676151A>G | CA397845710 | TP53 | c.218T>C (p.Val73Ala) c.-21-915T>C (n.-21-915T>C) c.96+231T>C (n.96+231T>C) n.474T>C c.101T>C (p.Val34Ala) | ClinVar dbSNP |
17 | g.7676151A>T | CA397845712 | TP53 | c.218T>A (p.Val73Glu) c.-21-915T>A (n.-21-915T>A) c.96+231T>A (n.96+231T>A) n.474T>A c.101T>A (p.Val34Glu) | dbSNP COSMIC |
17 | g.7676151_7676152insG | CA645589369 | TP53 | c.217_218insC (p.Val73AlafsTer?) c.-21-916_-21-915insC (n.-21-916_-21-915insC) c.96+230_96+231insC (n.96+230_96+231insC) n.473_474insC c.100_101insC (p.Val34AlafsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676152del | CA2695223137 | TP53 | c.217del (p.Val73TrpfsTer?) c.-21-916del (n.-21-916del) c.96+230del (n.96+230del) n.473del c.100del (p.Val34TrpfsTer?) | |
17 | g.7676152C>A | CA397845729 | TP53 | c.217G>T (p.Val73Leu) c.-21-916G>T (n.-21-916G>T) c.96+230G>T (n.96+230G>T) n.473G>T c.100G>T (p.Val34Leu) | COSMIC |
17 | g.7676152C= | CA2245934642 | TP53 | c.217G= (p.Val73=) c.-21-916G= (n.-21-916G=) c.96+230G= (n.96+230G=) n.473G= c.100G= (p.Val34=) | |
17 | g.7676152C>G | CA397845718 | TP53 | c.217G>C (p.Val73Leu) c.-21-916G>C (n.-21-916G>C) c.96+230G>C (n.96+230G>C) n.473G>C c.100G>C (p.Val34Leu) | dbSNP gnomAD v4 COSMIC |
17 | g.7676152C>T | CA000075 | TP53 | c.217G>A (p.Val73Met) c.-21-916G>A (n.-21-916G>A) c.96+230G>A (n.96+230G>A) n.473G>A c.100G>A (p.Val34Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7676152_7676153delinsCG | CA2245934651 | TP53 | c.216_217delinsCG (p.Pro72=) c.-21-917_-21-916delinsCG (n.-21-917_-21-916delinsCG) c.96+229_96+230delinsCG (n.96+229_96+230delinsCG) n.472_473delinsCG c.99_100delinsCG (p.Pro33=) | |
17 | g.7676152_7676154delinsTGC | CA913187840 | TP53 | c.215_217delinsGCA (p.Pro72_Val73delinsArgMet) c.-21-918_-21-916delinsGCA (n.-21-918_-21-916delinsGCA) c.96+228_96+230delinsGCA (n.96+228_96+230delinsGCA) n.471_473delinsGCA c.98_100delinsGCA (p.Pro33_Val34delinsArgMet) | ClinVar |
17 | g.7676153G>A | CA000074 | TP53 | c.216C>T (p.Pro72=) c.-21-917C>T (n.-21-917C>T) c.96+229C>T (n.96+229C>T) n.472C>T c.99C>T (p.Pro33=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676153G>C | CA287489091 | TP53 | c.216C>G (p.Pro72=) c.-21-917C>G (n.-21-917C>G) c.96+229C>G (n.96+229C>G) n.472C>G c.99C>G (p.Pro33=) | ClinVar dbSNP gnomAD v4 |
17 | g.7676153G= | CA2245934701 | TP53 | c.216C= (p.Pro72=) c.-21-917C= (n.-21-917C=) c.96+229C= (n.96+229C=) n.472C= c.99C= (p.Pro33=) | |
17 | g.7676153G>T | CA497925989 | TP53 | c.216C>A (p.Pro72=) c.-21-917C>A (n.-21-917C>A) c.96+229C>A (n.96+229C>A) n.472C>A c.99C>A (p.Pro33=) | gnomAD v4 |
17 | g.7676153_7676154delinsA | CA645589371 | TP53 | c.215_216delinsT (p.Pro72LeufsTer?) c.-21-918_-21-917delinsT (n.-21-918_-21-917delinsT) c.96+228_96+229delinsT (n.96+228_96+229delinsT) n.471_472delinsT c.98_99delinsT (p.Pro33LeufsTer?) | COSMIC |
17 | g.7676153_7676154delinsAC | CA10583683 | TP53 | c.215_216delinsGT (p.Pro72Arg) c.-21-918_-21-917delinsGT (n.-21-918_-21-917delinsGT) c.96+228_96+229delinsGT (n.96+228_96+229delinsGT) n.471_472delinsGT c.98_99delinsGT (p.Pro33Arg) | ClinVar dbSNP |
17 | g.7676153_7676154delinsGG | CA2245934705 | TP53 | c.215_216delinsCC (p.Pro72=) c.-21-918_-21-917delinsCC (n.-21-918_-21-917delinsCC) c.96+228_96+229delinsCC (n.96+228_96+229delinsCC) n.471_472delinsCC c.98_99delinsCC (p.Pro33=) | |
17 | g.7676153_7676155delinsCC | CA645589370 | TP53 | c.214_216delinsGG (p.Pro72GlyfsTer?) c.-21-919_-21-917delinsGG (n.-21-919_-21-917delinsGG) c.96+227_96+229delinsGG (n.96+227_96+229delinsGG) n.470_472delinsGG c.97_99delinsGG (p.Pro33GlyfsTer?) | COSMIC |
17 | g.7676158dup | CA000073 | TP53 | c.216dup (p.Val73ArgfsTer?) c.-21-917dup (n.-21-917dup) c.96+229dup (n.96+229dup) n.472dup c.99dup (p.Val34ArgfsTer?) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676158del | CA497925988 | TP53 | c.216del (p.Val73TrpfsTer?) c.-21-917del (n.-21-917del) c.96+229del (n.96+229del) n.472del c.99del (p.Val34TrpfsTer?) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676153_7676154insC | CA497925990 | TP53 | c.215_216insG (p.Val73ArgfsTer?) c.-21-918_-21-917insG (n.-21-918_-21-917insG) c.96+228_96+229insG (n.96+228_96+229insG) n.471_472insG c.98_99insG (p.Val34ArgfsTer?) | dbSNP |
17 | g.7676154G>A | CA397845758 | TP53 | c.215C>T (p.Pro72Leu) c.-21-918C>T (n.-21-918C>T) c.96+228C>T (n.96+228C>T) n.471C>T c.98C>T (p.Pro33Leu) | ClinVar dbSNP gnomAD v4 |
17 | g.7676154G>C | CA000072 | TP53 | c.215C>G (p.Pro72Arg) c.-21-918C>G (n.-21-918C>G) c.96+228C>G (n.96+228C>G) n.471C>G c.98C>G (p.Pro33Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676154G= | CA178298 | TP53 | c.215C= (p.Pro72=) c.-21-918C= (n.-21-918C=) c.96+228C= (n.96+228C=) n.471C= c.98C= (p.Pro33=) | |
17 | g.7676154G>T | CA000071 | TP53 | c.215C>A (p.Pro72His) c.-21-918C>A (n.-21-918C>A) c.96+228C>A (n.96+228C>A) n.471C>A c.98C>A (p.Pro33His) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7676154_7676155delinsCA | CA000069 | TP53 | c.214_215delinsTG (p.Pro72Cys) c.-21-919_-21-918delinsTG (n.-21-919_-21-918delinsTG) c.96+227_96+228delinsTG (n.96+227_96+228delinsTG) n.470_471delinsTG c.97_98delinsTG (p.Pro33Cys) | ClinVar dbSNP |
17 | g.7676154_7676155delinsCC | CA2580095108 | TP53 | c.214_215delinsGG (p.Pro72Gly) c.-21-919_-21-918delinsGG (n.-21-919_-21-918delinsGG) c.96+227_96+228delinsGG (n.96+227_96+228delinsGG) n.470_471delinsGG c.97_98delinsGG (p.Pro33Gly) | ClinVar |
17 | g.7676154_7676155delinsCT | CA2838032368 | TP53 | c.214_215delinsAG (p.Pro72Ser) c.-21-919_-21-918delinsAG (n.-21-919_-21-918delinsAG) c.96+227_96+228delinsAG (n.96+227_96+228delinsAG) n.470_471delinsAG c.97_98delinsAG (p.Pro33Ser) | |
17 | g.7676154_7676155delinsGG | CA2245934737 | TP53 | c.214_215delinsCC (p.Pro72=) c.-21-919_-21-918delinsCC (n.-21-919_-21-918delinsCC) c.96+227_96+228delinsCC (n.96+227_96+228delinsCC) n.470_471delinsCC c.97_98delinsCC (p.Pro33=) | |
17 | g.7676154_7676160delinsCCT | CA891842284 | TP53 | c.209_215delinsAGG (p.Ala70GlufsTer?) c.-21-924_-21-918delinsAGG (n.-21-924_-21-918delinsAGG) c.96+222_96+228delinsAGG (n.96+222_96+228delinsAGG) n.465_471delinsAGG c.92_98delinsAGG (p.Ala31GlufsTer?) | |
17 | g.7676154_7676155insC | CA645369692 | TP53 | c.214_215insG (p.Pro72ArgfsTer?) c.-21-919_-21-918insG (n.-21-919_-21-918insG) c.96+227_96+228insG (n.96+227_96+228insG) n.470_471insG c.97_98insG (p.Pro33ArgfsTer?) | ClinVar dbSNP |
17 | g.7676155G>A | CA003069 | TP53 | c.214C>T (p.Pro72Ser) c.-21-919C>T (n.-21-919C>T) c.96+227C>T (n.96+227C>T) n.470C>T c.97C>T (p.Pro33Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676155G>C | CA000070 | TP53 | c.214C>G (p.Pro72Ala) c.-21-919C>G (n.-21-919C>G) c.96+227C>G (n.96+227C>G) n.470C>G c.97C>G (p.Pro33Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676155G= | CA2245934766 | TP53 | c.214C= (p.Pro72=) c.-21-919C= (n.-21-919C=) c.96+227C= (n.96+227C=) n.470C= c.97C= (p.Pro33=) | |
17 | g.7676155G>T | CA003071 | TP53 | c.214C>A (p.Pro72Thr) c.-21-919C>A (n.-21-919C>A) c.96+227C>A (n.96+227C>A) n.470C>A c.97C>A (p.Pro33Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676156G>A | CA497925991 | TP53 | c.213C>T (p.Pro71=) c.-21-920C>T (n.-21-920C>T) c.96+226C>T (n.96+226C>T) n.469C>T c.96C>T (p.Pro32=) | ClinVar dbSNP |
17 | g.7676156G>C | CA497925992 | TP53 | c.213C>G (p.Pro71=) c.-21-920C>G (n.-21-920C>G) c.96+226C>G (n.96+226C>G) n.469C>G c.96C>G (p.Pro32=) | |
17 | g.7676156G= | CA2245934780 | TP53 | c.213C= (p.Pro71=) c.-21-920C= (n.-21-920C=) c.96+226C= (n.96+226C=) n.469C= c.96C= (p.Pro32=) | |
17 | g.7676156G>T | CA497925993 | TP53 | c.213C>A (p.Pro71=) c.-21-920C>A (n.-21-920C>A) c.96+226C>A (n.96+226C>A) n.469C>A c.96C>A (p.Pro32=) | dbSNP |
17 | g.7676162_7676182del | CA645589372 | TP53 | c.193_213del (p.Arg65_Pro71del) c.-21-940_-21-920del (n.-21-940_-21-920del) c.96+206_96+226del (n.96+206_96+226del) n.449_469del c.76_96del (p.Arg26_Pro32del) | COSMIC |
17 | g.7676157G>A | CA397845812 | TP53 | c.212C>T (p.Pro71Leu) c.-21-921C>T (n.-21-921C>T) c.96+225C>T (n.96+225C>T) n.468C>T c.95C>T (p.Pro32Leu) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676157G>C | CA10583684 | TP53 | c.212C>G (p.Pro71Arg) c.-21-921C>G (n.-21-921C>G) c.96+225C>G (n.96+225C>G) n.468C>G c.95C>G (p.Pro32Arg) | ClinVar dbSNP |
17 | g.7676157G= | CA2245934796 | TP53 | c.212C= (p.Pro71=) c.-21-921C= (n.-21-921C=) c.96+225C= (n.96+225C=) n.468C= c.95C= (p.Pro32=) | |
17 | g.7676157G>T | CA397845819 | TP53 | c.212C>A (p.Pro71His) c.-21-921C>A (n.-21-921C>A) c.96+225C>A (n.96+225C>A) n.468C>A c.95C>A (p.Pro32His) | |
17 | g.7676158G>A | CA397845838 | TP53 | c.211C>T (p.Pro71Ser) c.-21-922C>T (n.-21-922C>T) c.96+224C>T (n.96+224C>T) n.467C>T c.94C>T (p.Pro32Ser) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676158G>C | CA397845842 | TP53 | c.211C>G (p.Pro71Ala) c.-21-922C>G (n.-21-922C>G) c.96+224C>G (n.96+224C>G) n.467C>G c.94C>G (p.Pro32Ala) | ClinVar dbSNP |
17 | g.7676158G= | CA2245934811 | TP53 | c.211C= (p.Pro71=) c.-21-922C= (n.-21-922C=) c.96+224C= (n.96+224C=) n.467C= c.94C= (p.Pro32=) | |
17 | g.7676158G>T | CA397845843 | TP53 | c.211C>A (p.Pro71Thr) c.-21-922C>A (n.-21-922C>A) c.96+224C>A (n.96+224C>A) n.467C>A c.94C>A (p.Pro32Thr) | |
17 | g.7676159_7676160del | CA645589373 | TP53 | c.210_211del (p.Pro72ArgfsTer?) c.-21-923_-21-922del (n.-21-923_-21-922del) c.96+223_96+224del (n.96+223_96+224del) n.466_467del c.93_94del (p.Pro33ArgfsTer?) | COSMIC COSMIC COSMIC |
17 | g.7676159A= | CA2245934844 | TP53 | c.210T= (p.Ala70=) c.-21-923T= (n.-21-923T=) c.96+223T= (n.96+223T=) n.466T= c.93T= (p.Ala31=) | |
17 | g.7676159A>C | CA497925994 | TP53 | c.210T>G (p.Ala70=) c.-21-923T>G (n.-21-923T>G) c.96+223T>G (n.96+223T>G) n.466T>G c.93T>G (p.Ala31=) | COSMIC |
17 | g.7676159A>G | CA000068 | TP53 | c.210T>C (p.Ala70=) c.-21-923T>C (n.-21-923T>C) c.96+223T>C (n.96+223T>C) n.466T>C c.93T>C (p.Ala31=) | ClinVar dbSNP gnomAD v4 |
17 | g.7676159A>T | CA16616004 | TP53 | c.210T>A (p.Ala70=) c.-21-923T>A (n.-21-923T>A) c.96+223T>A (n.96+223T>A) n.466T>A c.93T>A (p.Ala31=) | ClinVar dbSNP gnomAD v4 |
17 | g.7676162_7676164del | CA658820767 | TP53 | c.208_210del (p.Ala70del) c.-21-925_-21-923del (n.-21-925_-21-923del) c.96+221_96+223del (n.96+221_96+223del) n.464_466del c.91_93del (p.Ala31del) | |
17 | g.7676160G>A | CA397845860 | TP53 | c.209C>T (p.Ala70Val) c.-21-924C>T (n.-21-924C>T) c.96+222C>T (n.96+222C>T) n.465C>T c.92C>T (p.Ala31Val) | ClinVar dbSNP |
17 | g.7676160G>C | CA397845851 | TP53 | c.209C>G (p.Ala70Gly) c.-21-924C>G (n.-21-924C>G) c.96+222C>G (n.96+222C>G) n.465C>G c.92C>G (p.Ala31Gly) | dbSNP |
17 | g.7676160G= | CA2245934862 | TP53 | c.209C= (p.Ala70=) c.-21-924C= (n.-21-924C=) c.96+222C= (n.96+222C=) n.465C= c.92C= (p.Ala31=) | |
17 | g.7676160G>T | CA397845855 | TP53 | c.209C>A (p.Ala70Asp) c.-21-924C>A (n.-21-924C>A) c.96+222C>A (n.96+222C>A) n.465C>A c.92C>A (p.Ala31Asp) | dbSNP |
17 | g.7676161C>A | CA397845864 | TP53 | c.208G>T (p.Ala70Ser) c.-21-925G>T (n.-21-925G>T) c.96+221G>T (n.96+221G>T) n.464G>T c.91G>T (p.Ala31Ser) | dbSNP |
17 | g.7676161C>G | CA397845865 | TP53 | c.208G>C (p.Ala70Pro) c.-21-925G>C (n.-21-925G>C) c.96+221G>C (n.96+221G>C) n.464G>C c.91G>C (p.Ala31Pro) | dbSNP |
17 | g.7676161C>T | CA397845866 | TP53 | c.208G>A (p.Ala70Thr) c.-21-925G>A (n.-21-925G>A) c.96+221G>A (n.96+221G>A) n.464G>A c.91G>A (p.Ala31Thr) | dbSNP COSMIC |
17 | g.7676162del | CA2635874979 | TP53 | c.207del (p.Ala70LeufsTer?) c.-21-926del (n.-21-926del) c.96+220del (n.96+220del) n.463del c.90del (p.Ala31LeufsTer?) | gnomAD v4 |
17 | g.7676162A= | CA2245934871 | TP53 | c.207T= (p.Ala69=) c.-21-926T= (n.-21-926T=) c.96+220T= (n.96+220T=) n.463T= c.90T= (p.Ala30=) | |
17 | g.7676162A>C | CA497925995 | TP53 | c.207T>G (p.Ala69=) c.-21-926T>G (n.-21-926T>G) c.96+220T>G (n.96+220T>G) n.463T>G c.90T>G (p.Ala30=) | |
17 | g.7676162A>G | CA003098 | TP53 | c.207T>C (p.Ala69=) c.-21-926T>C (n.-21-926T>C) c.96+220T>C (n.96+220T>C) n.463T>C c.90T>C (p.Ala30=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676162A>T | CA497925996 | TP53 | c.207T>A (p.Ala69=) c.-21-926T>A (n.-21-926T>A) c.96+220T>A (n.96+220T>A) n.463T>A c.90T>A (p.Ala30=) | dbSNP |
17 | g.7676163G>A | CA287489112 | TP53 | c.206C>T (p.Ala69Val) c.-21-927C>T (n.-21-927C>T) c.96+219C>T (n.96+219C>T) n.462C>T c.89C>T (p.Ala30Val) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7676163G>C | CA10580956 | TP53 | c.206C>G (p.Ala69Gly) c.-21-927C>G (n.-21-927C>G) c.96+219C>G (n.96+219C>G) n.462C>G c.89C>G (p.Ala30Gly) | ClinVar dbSNP COSMIC |
17 | g.7676163G= | CA2245934893 | TP53 | c.206C= (p.Ala69=) c.-21-927C= (n.-21-927C=) c.96+219C= (n.96+219C=) n.462C= c.89C= (p.Ala30=) | |
17 | g.7676163G>T | CA397845889 | TP53 | c.206C>A (p.Ala69Asp) c.-21-927C>A (n.-21-927C>A) c.96+219C>A (n.96+219C>A) n.462C>A c.89C>A (p.Ala30Asp) | dbSNP |
17 | g.7676163_7676164del | CA645589374 | TP53 | c.205_206del (p.Ala69CysfsTer?) c.-21-928_-21-927del (n.-21-928_-21-927del) c.96+218_96+219del (n.96+218_96+219del) n.461_462del c.88_89del (p.Ala30CysfsTer?) | COSMIC |
17 | g.7676164C>A | CA397845894 | TP53 | c.205G>T (p.Ala69Ser) c.-21-928G>T (n.-21-928G>T) c.96+218G>T (n.96+218G>T) n.461G>T c.88G>T (p.Ala30Ser) | dbSNP |
17 | g.7676164C= | CA2245934909 | TP53 | c.205G= (p.Ala69=) c.-21-928G= (n.-21-928G=) c.96+218G= (n.96+218G=) n.461G= c.88G= (p.Ala30=) | |
17 | g.7676164C>G | CA397845901 | TP53 | c.205G>C (p.Ala69Pro) c.-21-928G>C (n.-21-928G>C) c.96+218G>C (n.96+218G>C) n.461G>C c.88G>C (p.Ala30Pro) | ClinVar dbSNP gnomAD v4 |
17 | g.7676164C>T | CA397845904 | TP53 | c.205G>A (p.Ala69Thr) c.-21-928G>A (n.-21-928G>A) c.96+218G>A (n.96+218G>A) n.461G>A c.88G>A (p.Ala30Thr) | ClinVar dbSNP gnomAD v4 |
17 | g.7676165del | CA497925997 | TP53 | c.205del (p.Ala69LeufsTer?) c.-21-928del (n.-21-928del) c.96+218del (n.96+218del) n.461del c.88del (p.Ala30LeufsTer?) | ClinVar dbSNP COSMIC |
17 | g.7676165C>A | CA397845922 | TP53 | c.204G>T (p.Glu68Asp) c.-21-929G>T (n.-21-929G>T) c.96+217G>T (n.96+217G>T) n.460G>T c.87G>T (p.Glu29Asp) | dbSNP |
17 | g.7676165C= | CA2245934918 | TP53 | c.204G= (p.Glu68=) c.-21-929G= (n.-21-929G=) c.96+217G= (n.96+217G=) n.460G= c.87G= (p.Glu29=) | |
17 | g.7676165C>G | CA397845918 | TP53 | c.204G>C (p.Glu68Asp) c.-21-929G>C (n.-21-929G>C) c.96+217G>C (n.96+217G>C) n.460G>C c.87G>C (p.Glu29Asp) | dbSNP |
17 | g.7676165C>T | CA000067 | TP53 | c.204G>A (p.Glu68=) c.-21-929G>A (n.-21-929G>A) c.96+217G>A (n.96+217G>A) n.460G>A c.87G>A (p.Glu29=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7676166T>A | CA397845932 | TP53 | c.203A>T (p.Glu68Val) c.-21-930A>T (n.-21-930A>T) c.96+216A>T (n.96+216A>T) n.459A>T c.86A>T (p.Glu29Val) | dbSNP |
17 | g.7676166T>C | CA397845936 | TP53 | c.203A>G (p.Glu68Gly) c.-21-930A>G (n.-21-930A>G) c.96+216A>G (n.96+216A>G) n.459A>G c.86A>G (p.Glu29Gly) | dbSNP COSMIC |
17 | g.7676166T>G | CA397845940 | TP53 | c.203A>C (p.Glu68Ala) c.-21-930A>C (n.-21-930A>C) c.96+216A>C (n.96+216A>C) n.459A>C c.86A>C (p.Glu29Ala) | |
17 | g.7676171_7676178del | CA645589375 | TP53 | c.196_203del (p.Met66GlyfsTer?) c.-21-937_-21-930del (n.-21-937_-21-930del) c.96+209_96+216del (n.96+209_96+216del) n.452_459del c.79_86del (p.Met27GlyfsTer?) | COSMIC |
17 | g.7676167del | CA497925998 | TP53 | c.202del (p.Glu68ArgfsTer?) c.-21-931del (n.-21-931del) c.96+215del (n.96+215del) n.458del c.85del (p.Glu29ArgfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676167C>A | CA353535 | TP53 | c.202G>T (p.Glu68Ter) c.-21-931G>T (n.-21-931G>T) c.96+215G>T (n.96+215G>T) n.458G>T c.85G>T (p.Glu29Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676167C= | CA2245934936 | TP53 | c.202G= (p.Glu68=) c.-21-931G= (n.-21-931G=) c.96+215G= (n.96+215G=) n.458G= c.85G= (p.Glu29=) | |
17 | g.7676167C>G | CA397845956 | TP53 | c.202G>C (p.Glu68Gln) c.-21-931G>C (n.-21-931G>C) c.96+215G>C (n.96+215G>C) n.458G>C c.85G>C (p.Glu29Gln) | ClinVar dbSNP COSMIC |
17 | g.7676167C>T | CA397845957 | TP53 | c.202G>A (p.Glu68Lys) c.-21-931G>A (n.-21-931G>A) c.96+215G>A (n.96+215G>A) n.458G>A c.85G>A (p.Glu29Lys) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676168T>A | CA497926000 | TP53 | c.201A>T (p.Pro67=) c.-21-932A>T (n.-21-932A>T) c.96+214A>T (n.96+214A>T) n.457A>T c.84A>T (p.Pro28=) | |
17 | g.7676168T>C | CA000066 | TP53 | c.201A>G (p.Pro67=) c.-21-932A>G (n.-21-932A>G) c.96+214A>G (n.96+214A>G) n.457A>G c.84A>G (p.Pro28=) | ClinVar dbSNP COSMIC |
17 | g.7676168T>G | CA497925999 | TP53 | c.201A>C (p.Pro67=) c.-21-932A>C (n.-21-932A>C) c.96+214A>C (n.96+214A>C) n.457A>C c.84A>C (p.Pro28=) | |
17 | g.7676168T= | CA2245934952 | TP53 | c.201A= (p.Pro67=) c.-21-932A= (n.-21-932A=) c.96+214A= (n.96+214A=) n.457A= c.84A= (p.Pro28=) | |
17 | g.7676168_7676169del | CA645589376 | TP53 | c.200_201del (p.Pro67ArgfsTer?) c.-21-933_-21-932del (n.-21-933_-21-932del) c.96+213_96+214del (n.96+213_96+214del) n.456_457del c.83_84del (p.Pro28ArgfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676169G>A | CA397845965 | TP53 | c.200C>T (p.Pro67Leu) c.-21-933C>T (n.-21-933C>T) c.96+213C>T (n.96+213C>T) n.456C>T c.83C>T (p.Pro28Leu) | dbSNP COSMIC |
17 | g.7676169G>C | CA397845968 | TP53 | c.200C>G (p.Pro67Arg) c.-21-933C>G (n.-21-933C>G) c.96+213C>G (n.96+213C>G) n.456C>G c.83C>G (p.Pro28Arg) | dbSNP COSMIC |
17 | g.7676169G= | CA2245934966 | TP53 | c.200C= (p.Pro67=) c.-21-933C= (n.-21-933C=) c.96+213C= (n.96+213C=) n.456C= c.83C= (p.Pro28=) | |
17 | g.7676169G>T | CA397845972 | TP53 | c.200C>A (p.Pro67Gln) c.-21-933C>A (n.-21-933C>A) c.96+213C>A (n.96+213C>A) n.456C>A c.83C>A (p.Pro28Gln) | ClinVar dbSNP |
17 | g.7676170dup | CA645589377 | TP53 | c.200dup (p.Glu68ArgfsTer?) c.-21-933dup (n.-21-933dup) c.96+213dup (n.96+213dup) n.456dup c.83dup (p.Glu29ArgfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676170del | CA497926001 | TP53 | c.200del (p.Pro67GlnfsTer?) c.-21-933del (n.-21-933del) c.96+213del (n.96+213del) n.456del c.83del (p.Pro28GlnfsTer?) | ClinVar COSMIC |
17 | g.7676170G>A | CA397845977 | TP53 | c.199C>T (p.Pro67Ser) c.-21-934C>T (n.-21-934C>T) c.96+212C>T (n.96+212C>T) n.455C>T c.82C>T (p.Pro28Ser) | ClinVar dbSNP COSMIC |
17 | g.7676170G>C | CA397845985 | TP53 | c.199C>G (p.Pro67Ala) c.-21-934C>G (n.-21-934C>G) c.96+212C>G (n.96+212C>G) n.455C>G c.82C>G (p.Pro28Ala) | ClinVar dbSNP |
17 | g.7676170G= | CA2245934977 | TP53 | c.199C= (p.Pro67=) c.-21-934C= (n.-21-934C=) c.96+212C= (n.96+212C=) n.455C= c.82C= (p.Pro28=) | |
17 | g.7676170G>T | CA397845998 | TP53 | c.199C>A (p.Pro67Thr) c.-21-934C>A (n.-21-934C>A) c.96+212C>A (n.96+212C>A) n.455C>A c.82C>A (p.Pro28Thr) | dbSNP |
17 | g.7676170_7676171delinsGC | CA2245934976 | TP53 | c.198_199delinsGC (p.Met66=) c.-21-935_-21-934delinsGC (n.-21-935_-21-934delinsGC) c.96+211_96+212delinsGC (n.96+211_96+212delinsGC) n.454_455delinsGC c.81_82delinsGC (p.Met27=) | |
17 | g.7676171del | CA287489129 | TP53 | c.198del (p.Met66IlefsTer?) c.-21-935del (n.-21-935del) c.96+211del (n.96+211del) n.454del c.81del (p.Met27IlefsTer?) | dbSNP |
17 | g.7676171C>A | CA397846013 | TP53 | c.198G>T (p.Met66Ile) c.-21-935G>T (n.-21-935G>T) c.96+211G>T (n.96+211G>T) n.454G>T c.81G>T (p.Met27Ile) | dbSNP |
17 | g.7676171C= | CA2245934987 | TP53 | c.198G= (p.Met66=) c.-21-935G= (n.-21-935G=) c.96+211G= (n.96+211G=) n.454G= c.81G= (p.Met27=) | |
17 | g.7676171C>G | CA397846016 | TP53 | c.198G>C (p.Met66Ile) c.-21-935G>C (n.-21-935G>C) c.96+211G>C (n.96+211G>C) n.454G>C c.81G>C (p.Met27Ile) | dbSNP |
17 | g.7676171C>T | CA397846006 | TP53 | c.198G>A (p.Met66Ile) c.-21-935G>A (n.-21-935G>A) c.96+211G>A (n.96+211G>A) n.454G>A c.81G>A (p.Met27Ile) | ClinVar dbSNP COSMIC |
17 | g.7676172A= | CA2245935006 | TP53 | c.197T= (p.Met66=) c.-21-936T= (n.-21-936T=) c.96+210T= (n.96+210T=) n.453T= c.80T= (p.Met27=) | |
17 | g.7676172A>C | CA397846032 | TP53 | c.197T>G (p.Met66Arg) c.-21-936T>G (n.-21-936T>G) c.96+210T>G (n.96+210T>G) n.453T>G c.80T>G (p.Met27Arg) | ClinVar dbSNP COSMIC |
17 | g.7676172A>G | CA397846021 | TP53 | c.197T>C (p.Met66Thr) c.-21-936T>C (n.-21-936T>C) c.96+210T>C (n.96+210T>C) n.453T>C c.80T>C (p.Met27Thr) | ClinVar dbSNP |
17 | g.7676172A>T | CA397846037 | TP53 | c.197T>A (p.Met66Lys) c.-21-936T>A (n.-21-936T>A) c.96+210T>A (n.96+210T>A) n.453T>A c.80T>A (p.Met27Lys) | dbSNP |
17 | g.7676172_7676173insATTCTGGG | CA645589378 | TP53 | c.196_197insCCCAGAAT (p.Met66ThrfsTer?) c.-21-937_-21-936insCCCAGAAT (n.-21-937_-21-936insCCCAGAAT) c.96+209_96+210insCCCAGAAT (n.96+209_96+210insCCCAGAAT) n.452_453insCCCAGAAT c.79_80insCCCAGAAT (p.Met27ThrfsTer?) | COSMIC COSMIC COSMIC |
17 | g.7676173T>A | CA397846045 | TP53 | c.196A>T (p.Met66Leu) c.-21-937A>T (n.-21-937A>T) c.96+209A>T (n.96+209A>T) n.452A>T c.79A>T (p.Met27Leu) | dbSNP |
17 | g.7676173T>C | CA397846060 | TP53 | c.196A>G (p.Met66Val) c.-21-937A>G (n.-21-937A>G) c.96+209A>G (n.96+209A>G) n.452A>G c.79A>G (p.Met27Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7676173T>G | CA397846047 | TP53 | c.196A>C (p.Met66Leu) c.-21-937A>C (n.-21-937A>C) c.96+209A>C (n.96+209A>C) n.452A>C c.79A>C (p.Met27Leu) | dbSNP |
17 | g.7676173T= | CA2245935022 | TP53 | c.196A= (p.Met66=) c.-21-937A= (n.-21-937A=) c.96+209A= (n.96+209A=) n.452A= c.79A= (p.Met27=) | |
17 | g.7676174dup | CA645589379 | TP53 | c.196dup (p.Met66AsnfsTer?) c.-21-937dup (n.-21-937dup) c.96+209dup (n.96+209dup) n.452dup c.79dup (p.Met27AsnfsTer?) | ClinVar dbSNP COSMIC |
17 | g.7676173_7676174insA | CA497926002 | TP53 | c.195_196insT (p.Met66TyrfsTer?) c.-21-938_-21-937insT (n.-21-938_-21-937insT) c.96+208_96+209insT (n.96+208_96+209insT) n.451_452insT c.78_79insT (p.Met27TyrfsTer?) | |
17 | g.7676174T>A | CA397846063 | TP53 | c.195A>T (p.Arg65Ser) c.-21-938A>T (n.-21-938A>T) c.96+208A>T (n.96+208A>T) n.451A>T c.78A>T (p.Arg26Ser) | dbSNP |
17 | g.7676174T>C | CA497926003 | TP53 | c.195A>G (p.Arg65=) c.-21-938A>G (n.-21-938A>G) c.96+208A>G (n.96+208A>G) n.451A>G c.78A>G (p.Arg26=) | ClinVar dbSNP |
17 | g.7676174T>G | CA397846065 | TP53 | c.195A>C (p.Arg65Ser) c.-21-938A>C (n.-21-938A>C) c.96+208A>C (n.96+208A>C) n.451A>C c.78A>C (p.Arg26Ser) | dbSNP |
17 | g.7676174T= | CA2245935027 | TP53 | c.195A= (p.Arg65=) c.-21-938A= (n.-21-938A=) c.96+208A= (n.96+208A=) n.451A= c.78A= (p.Arg26=) | |
17 | g.7676175C>A | CA397846071 | TP53 | c.194G>T (p.Arg65Ile) c.-21-939G>T (n.-21-939G>T) c.96+207G>T (n.96+207G>T) n.450G>T c.77G>T (p.Arg26Ile) | dbSNP |
17 | g.7676175C= | CA2245935032 | TP53 | c.194G= (p.Arg65=) c.-21-939G= (n.-21-939G=) c.96+207G= (n.96+207G=) n.450G= c.77G= (p.Arg26=) | |
17 | g.7676175C>G | CA16615958 | TP53 | c.194G>C (p.Arg65Thr) c.-21-939G>C (n.-21-939G>C) c.96+207G>C (n.96+207G>C) n.450G>C c.77G>C (p.Arg26Thr) | ClinVar dbSNP |
17 | g.7676175C>T | CA397846082 | TP53 | c.194G>A (p.Arg65Lys) c.-21-939G>A (n.-21-939G>A) c.96+207G>A (n.96+207G>A) n.450G>A c.77G>A (p.Arg26Lys) | dbSNP |
17 | g.7676175_7676176insG | CA645589380 | TP53 | c.193_194insC (p.Arg65ThrfsTer?) c.-21-940_-21-939insC (n.-21-940_-21-939insC) c.96+206_96+207insC (n.96+206_96+207insC) n.449_450insC c.76_77insC (p.Arg26ThrfsTer?) | COSMIC COSMIC COSMIC |
17 | g.7676176T>A | CA397846088 | TP53 | c.193A>T (p.Arg65Ter) c.-21-940A>T (n.-21-940A>T) c.96+206A>T (n.96+206A>T) n.449A>T c.76A>T (p.Arg26Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676176T>C | CA397846091 | TP53 | c.193A>G (p.Arg65Gly) c.-21-940A>G (n.-21-940A>G) c.96+206A>G (n.96+206A>G) n.449A>G c.76A>G (p.Arg26Gly) | ClinVar dbSNP |
17 | g.7676176T>G | CA497926004 | TP53 | c.193A>C (p.Arg65=) c.-21-940A>C (n.-21-940A>C) c.96+206A>C (n.96+206A>C) n.449A>C c.76A>C (p.Arg26=) | ClinVar dbSNP |
17 | g.7676176T= | CA2245935060 | TP53 | c.193A= (p.Arg65=) c.-21-940A= (n.-21-940A=) c.96+206A= (n.96+206A=) n.449A= c.76A= (p.Arg26=) | |
17 | g.7676176dup | CA645589381 | TP53 | c.193dup (p.Arg65LysfsTer?) c.-21-940dup (n.-21-940dup) c.96+206dup (n.96+206dup) n.449dup c.76dup (p.Arg26LysfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676176_7676177insC | CA497926008 | TP53 | c.192_193insG (p.Arg65GlufsTer?) c.-21-941_-21-940insG (n.-21-941_-21-940insG) c.96+205_96+206insG (n.96+205_96+206insG) n.448_449insG c.75_76insG (p.Arg26GlufsTer?) | |
17 | g.7676177G>A | CA497926007 | TP53 | c.192C>T (p.Pro64=) c.-21-941C>T (n.-21-941C>T) c.96+205C>T (n.96+205C>T) n.448C>T c.75C>T (p.Pro25=) | ClinVar dbSNP gnomAD v4 |
17 | g.7676177G>C | CA497926006 | TP53 | c.192C>G (p.Pro64=) c.-21-941C>G (n.-21-941C>G) c.96+205C>G (n.96+205C>G) n.448C>G c.75C>G (p.Pro25=) | ClinVar dbSNP |
17 | g.7676177G= | CA2245935083 | TP53 | c.192C= (p.Pro64=) c.-21-941C= (n.-21-941C=) c.96+205C= (n.96+205C=) n.448C= c.75C= (p.Pro25=) | |
17 | g.7676177G>T | CA497926005 | TP53 | c.192C>A (p.Pro64=) c.-21-941C>A (n.-21-941C>A) c.96+205C>A (n.96+205C>A) n.448C>A c.75C>A (p.Pro25=) | dbSNP |
17 | g.7676179dup | CA645589383 | TP53 | c.192dup (p.Arg65GlnfsTer?) c.-21-941dup (n.-21-941dup) c.96+205dup (n.96+205dup) n.448dup c.75dup (p.Arg26GlnfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676179del | CA645589382 | TP53 | c.192del (p.Arg65GlufsTer?) c.-21-941del (n.-21-941del) c.96+205del (n.96+205del) n.448del c.75del (p.Arg26GlufsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676178_7676179del | CA2695223138 | TP53 | c.191_192del (p.Pro64GlnfsTer?) c.-21-942_-21-941del (n.-21-942_-21-941del) c.96+204_96+205del (n.96+204_96+205del) n.447_448del c.74_75del (p.Pro25GlnfsTer?) | |
17 | g.7676181_7676233del | CA1139768370 | TP53 | c.140_192del (p.Pro47GlnfsTer?) c.-21-993_-21-941del (n.-21-993_-21-941del) c.96+153_96+205del (n.96+153_96+205del) n.396_448del c.23_75del (p.Pro8GlnfsTer?) | |
17 | g.7676177_7676178insC | CA497926009 | TP53 | c.191_192insG (p.Arg65GlnfsTer?) c.-21-942_-21-941insG (n.-21-942_-21-941insG) c.96+204_96+205insG (n.96+204_96+205insG) n.447_448insG c.74_75insG (p.Arg26GlnfsTer?) | |
17 | g.7676178G>A | CA397846114 | TP53 | c.191C>T (p.Pro64Leu) c.-21-942C>T (n.-21-942C>T) c.96+204C>T (n.96+204C>T) n.447C>T c.74C>T (p.Pro25Leu) | dbSNP |
17 | g.7676178G>C | CA397846118 | TP53 | c.191C>G (p.Pro64Arg) c.-21-942C>G (n.-21-942C>G) c.96+204C>G (n.96+204C>G) n.447C>G c.74C>G (p.Pro25Arg) | dbSNP |
17 | g.7676178G>T | CA397846119 | TP53 | c.191C>A (p.Pro64His) c.-21-942C>A (n.-21-942C>A) c.96+204C>A (n.96+204C>A) n.447C>A c.74C>A (p.Pro25His) | dbSNP |
17 | g.7676179G>A | CA397846122 | TP53 | c.190C>T (p.Pro64Ser) c.-21-943C>T (n.-21-943C>T) c.96+203C>T (n.96+203C>T) n.446C>T c.73C>T (p.Pro25Ser) | ClinVar |
17 | g.7676179G>C | CA397846123 | TP53 | c.190C>G (p.Pro64Ala) c.-21-943C>G (n.-21-943C>G) c.96+203C>G (n.96+203C>G) n.446C>G c.73C>G (p.Pro25Ala) | |
17 | g.7676179G>T | CA397846125 | TP53 | c.190C>A (p.Pro64Thr) c.-21-943C>A (n.-21-943C>A) c.96+203C>A (n.96+203C>A) n.446C>A c.73C>A (p.Pro25Thr) | gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676180A>C | CA497926010 | TP53 | c.189T>G (p.Ala63=) c.-21-944T>G (n.-21-944T>G) c.96+202T>G (n.96+202T>G) n.445T>G c.72T>G (p.Ala24=) | |
17 | g.7676180A>G | CA497926011 | TP53 | c.189T>C (p.Ala63=) c.-21-944T>C (n.-21-944T>C) c.96+202T>C (n.96+202T>C) n.445T>C c.72T>C (p.Ala24=) | ClinVar dbSNP |
17 | g.7676180A>T | CA497926012 | TP53 | c.189T>A (p.Ala63=) c.-21-944T>A (n.-21-944T>A) c.96+202T>A (n.96+202T>A) n.445T>A c.72T>A (p.Ala24=) | dbSNP |
17 | g.7676180delinsTCT | CA2695223139 | TP53 | c.189delinsAGA (p.Pro64AspfsTer?) c.-21-944delinsAGA (n.-21-944delinsAGA) c.96+202delinsAGA (n.96+202delinsAGA) n.445delinsAGA c.72delinsAGA (p.Pro25AspfsTer?) | |
17 | g.7676181_7676220del | CA645589384 | TP53 | c.150_189del (p.Glu51ProfsTer?) c.-21-983_-21-944del (n.-21-983_-21-944del) c.96+163_96+202del (n.96+163_96+202del) n.406_445del c.33_72del (p.Glu12ProfsTer?) | COSMIC |
17 | g.7676181G>A | CA000063 | TP53 | c.188C>T (p.Ala63Val) c.-21-945C>T (n.-21-945C>T) c.96+201C>T (n.96+201C>T) n.444C>T c.71C>T (p.Ala24Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7676181G>C | CA10580957 | TP53 | c.188C>G (p.Ala63Gly) c.-21-945C>G (n.-21-945C>G) c.96+201C>G (n.96+201C>G) n.444C>G c.71C>G (p.Ala24Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7676181G= | CA2245935091 | TP53 | c.188C= (p.Ala63=) c.-21-945C= (n.-21-945C=) c.96+201C= (n.96+201C=) n.444C= c.71C= (p.Ala24=) | |
17 | g.7676181G>T | CA397846132 | TP53 | c.188C>A (p.Ala63Asp) c.-21-945C>A (n.-21-945C>A) c.96+201C>A (n.96+201C>A) n.444C>A c.71C>A (p.Ala24Asp) | dbSNP |
17 | g.7676182C>A | CA397846140 | TP53 | c.187G>T (p.Ala63Ser) c.-21-946G>T (n.-21-946G>T) c.96+200G>T (n.96+200G>T) n.443G>T c.70G>T (p.Ala24Ser) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676182C= | CA2245935102 | TP53 | c.187G= (p.Ala63=) c.-21-946G= (n.-21-946G=) c.96+200G= (n.96+200G=) n.443G= c.70G= (p.Ala24=) | |
17 | g.7676182C>G | CA397846142 | TP53 | c.187G>C (p.Ala63Pro) c.-21-946G>C (n.-21-946G>C) c.96+200G>C (n.96+200G>C) n.443G>C c.70G>C (p.Ala24Pro) | dbSNP |
17 | g.7676182C>T | CA10580958 | TP53 | c.187G>A (p.Ala63Thr) c.-21-946G>A (n.-21-946G>A) c.96+200G>A (n.96+200G>A) n.443G>A c.70G>A (p.Ala24Thr) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676183T>A | CA397846150 | TP53 | c.186A>T (p.Glu62Asp) c.-21-947A>T (n.-21-947A>T) c.96+199A>T (n.96+199A>T) n.442A>T c.69A>T (p.Glu23Asp) | dbSNP |
17 | g.7676183T>C | CA497926014 | TP53 | c.186A>G (p.Glu62=) c.-21-947A>G (n.-21-947A>G) c.96+199A>G (n.96+199A>G) n.442A>G c.69A>G (p.Glu23=) | dbSNP COSMIC |
17 | g.7676183T>G | CA397846152 | TP53 | c.186A>C (p.Glu62Asp) c.-21-947A>C (n.-21-947A>C) c.96+199A>C (n.96+199A>C) n.442A>C c.69A>C (p.Glu23Asp) | COSMIC |
17 | g.7676184del | CA497926013 | TP53 | c.186del (p.Ala63LeufsTer?) c.-21-947del (n.-21-947del) c.96+199del (n.96+199del) n.442del c.69del (p.Ala24LeufsTer?) | COSMIC |
17 | g.7676184T>A | CA397846156 | TP53 | c.185A>T (p.Glu62Val) c.-21-948A>T (n.-21-948A>T) c.96+198A>T (n.96+198A>T) n.441A>T c.68A>T (p.Glu23Val) | dbSNP |
17 | g.7676184T>C | CA397846161 | TP53 | c.185A>G (p.Glu62Gly) c.-21-948A>G (n.-21-948A>G) c.96+198A>G (n.96+198A>G) n.441A>G c.68A>G (p.Glu23Gly) | dbSNP |
17 | g.7676184T>G | CA397846174 | TP53 | c.185A>C (p.Glu62Ala) c.-21-948A>C (n.-21-948A>C) c.96+198A>C (n.96+198A>C) n.441A>C c.68A>C (p.Glu23Ala) | ClinVar dbSNP |
17 | g.7676185_7676201dup | CA645589385 | TP53 | c.169_185dup (p.Ala63ThrfsTer?) c.-21-964_-21-948dup (n.-21-964_-21-948dup) c.96+182_96+198dup (n.96+182_96+198dup) n.425_441dup c.52_68dup (p.Ala24ThrfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676185_7676201del | CA645589386 | TP53 | c.169_185del (p.Asp57SerfsTer?) c.-21-964_-21-948del (n.-21-964_-21-948del) c.96+182_96+198del (n.96+182_96+198del) n.425_441del c.52_68del (p.Asp18SerfsTer?) | COSMIC |
17 | g.7676185C>A | CA397846175 | TP53 | c.184G>T (p.Glu62Ter) c.-21-949G>T (n.-21-949G>T) c.96+197G>T (n.96+197G>T) n.440G>T c.67G>T (p.Glu23Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7676185C= | CA2245935118 | TP53 | c.184G= (p.Glu62=) c.-21-949G= (n.-21-949G=) c.96+197G= (n.96+197G=) n.440G= c.67G= (p.Glu23=) | |
17 | g.7676185C>G | CA397846176 | TP53 | c.184G>C (p.Glu62Gln) c.-21-949G>C (n.-21-949G>C) c.96+197G>C (n.96+197G>C) n.440G>C c.67G>C (p.Glu23Gln) | dbSNP |
17 | g.7676185C>T | CA397846178 | TP53 | c.184G>A (p.Glu62Lys) c.-21-949G>A (n.-21-949G>A) c.96+197G>A (n.96+197G>A) n.440G>A c.67G>A (p.Glu23Lys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676186del | CA2733133702 | TP53 | c.183del (p.Asp61GlufsTer?) c.-21-950del (n.-21-950del) c.96+196del (n.96+196del) n.439del c.66del (p.Asp22GlufsTer?) | dbSNP |
17 | g.7676186A= | CA2245935143 | TP53 | c.183T= (p.Asp61=) c.-21-950T= (n.-21-950T=) c.96+196T= (n.96+196T=) n.439T= c.66T= (p.Asp22=) | |
17 | g.7676186A>C | CA397846181 | TP53 | c.183T>G (p.Asp61Glu) c.-21-950T>G (n.-21-950T>G) c.96+196T>G (n.96+196T>G) n.439T>G c.66T>G (p.Asp22Glu) | dbSNP |
17 | g.7676186A>G | CA497926015 | TP53 | c.183T>C (p.Asp61=) c.-21-950T>C (n.-21-950T>C) c.96+196T>C (n.96+196T>C) n.439T>C c.66T>C (p.Asp22=) | ClinVar dbSNP |
17 | g.7676186A>T | CA397846186 | TP53 | c.183T>A (p.Asp61Glu) c.-21-950T>A (n.-21-950T>A) c.96+196T>A (n.96+196T>A) n.439T>A c.66T>A (p.Asp22Glu) | ClinVar dbSNP gnomAD v4 |
17 | g.7676195_7676196insTATCTGGACCT | CA645589387 | TP53 | c.183_184insAAGGTCCAGAT (p.Glu62LysfsTer?) c.-21-950_-21-949insAAGGTCCAGAT (n.-21-950_-21-949insAAGGTCCAGAT) c.96+196_96+197insAAGGTCCAGAT (n.96+196_96+197insAAGGTCCAGAT) n.439_440insAAGGTCCAGAT c.66_67insAAGGTCCAGAT (p.Glu23LysfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676187del | CA645589389 | TP53 | c.182del (p.Asp61ValfsTer?) c.-21-951del (n.-21-951del) c.96+195del (n.96+195del) n.438del c.65del (p.Asp22ValfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676187T>A | CA397846191 | TP53 | c.182A>T (p.Asp61Val) c.-21-951A>T (n.-21-951A>T) c.96+195A>T (n.96+195A>T) n.438A>T c.65A>T (p.Asp22Val) | ClinVar dbSNP |
17 | g.7676187T>C | CA397846192 | TP53 | c.182A>G (p.Asp61Gly) c.-21-951A>G (n.-21-951A>G) c.96+195A>G (n.96+195A>G) n.438A>G c.65A>G (p.Asp22Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.7676187T>G | CA397846193 | TP53 | c.182A>C (p.Asp61Ala) c.-21-951A>C (n.-21-951A>C) c.96+195A>C (n.96+195A>C) n.438A>C c.65A>C (p.Asp22Ala) | |
17 | g.7676187T= | CA2245935150 | TP53 | c.182A= (p.Asp61=) c.-21-951A= (n.-21-951A=) c.96+195A= (n.96+195A=) n.438A= c.65A= (p.Asp22=) | |
17 | g.7676188_7676189del | CA645589388 | TP53 | c.181_182del (p.Asp61Ter) c.-21-952_-21-951del (n.-21-952_-21-951del) c.96+194_96+195del (n.96+194_96+195del) n.437_438del c.64_65del (p.Asp22Ter) | COSMIC COSMIC COSMIC |
17 | g.7676188C>A | CA397846194 | TP53 | c.181G>T (p.Asp61Tyr) c.-21-952G>T (n.-21-952G>T) c.96+194G>T (n.96+194G>T) n.437G>T c.64G>T (p.Asp22Tyr) | ClinVar dbSNP |
17 | g.7676188C>G | CA397846204 | TP53 | c.181G>C (p.Asp61His) c.-21-952G>C (n.-21-952G>C) c.96+194G>C (n.96+194G>C) n.437G>C c.64G>C (p.Asp22His) | dbSNP |
17 | g.7676188C>T | CA397846209 | TP53 | c.181G>A (p.Asp61Asn) c.-21-952G>A (n.-21-952G>A) c.96+194G>A (n.96+194G>A) n.437G>A c.64G>A (p.Asp22Asn) | dbSNP COSMIC |
17 | g.7676189_7676211dup | CA2635875042 | TP53 | c.159_181dup (p.Asp61GlyfsTer?) c.-21-974_-21-952dup (n.-21-974_-21-952dup) c.96+172_96+194dup (n.96+172_96+194dup) n.415_437dup c.42_64dup (p.Asp22GlyfsTer?) | gnomAD v4 |
17 | g.7676189T>A | CA497926016 | TP53 | c.180A>T (p.Pro60=) c.-21-953A>T (n.-21-953A>T) c.96+193A>T (n.96+193A>T) n.436A>T c.63A>T (p.Pro21=) | COSMIC |
17 | g.7676189T>C | CA497926017 | TP53 | c.180A>G (p.Pro60=) c.-21-953A>G (n.-21-953A>G) c.96+193A>G (n.96+193A>G) n.436A>G c.63A>G (p.Pro21=) | ClinVar |
17 | g.7676189T>G | CA000062 | TP53 | c.180A>C (p.Pro60=) c.-21-953A>C (n.-21-953A>C) c.96+193A>C (n.96+193A>C) n.436A>C c.63A>C (p.Pro21=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676189T= | CA2245935158 | TP53 | c.180A= (p.Pro60=) c.-21-953A= (n.-21-953A=) c.96+193A= (n.96+193A=) n.436A= c.63A= (p.Pro21=) | |
17 | g.7676190G>A | CA397846216 | TP53 | c.179C>T (p.Pro60Leu) c.-21-954C>T (n.-21-954C>T) c.96+192C>T (n.96+192C>T) n.435C>T c.62C>T (p.Pro21Leu) | ClinVar dbSNP COSMIC |
17 | g.7676190G>C | CA397846222 | TP53 | c.179C>G (p.Pro60Arg) c.-21-954C>G (n.-21-954C>G) c.96+192C>G (n.96+192C>G) n.435C>G c.62C>G (p.Pro21Arg) | dbSNP COSMIC |
17 | g.7676190G= | CA2245935169 | TP53 | c.179C= (p.Pro60=) c.-21-954C= (n.-21-954C=) c.96+192C= (n.96+192C=) n.435C= c.62C= (p.Pro21=) | |
17 | g.7676190G>T | CA397846223 | TP53 | c.179C>A (p.Pro60Gln) c.-21-954C>A (n.-21-954C>A) c.96+192C>A (n.96+192C>A) n.435C>A c.62C>A (p.Pro21Gln) | COSMIC |
17 | g.7676191del | CA497926018 | TP53 | c.179del (p.Pro60GlnfsTer?) c.-21-954del (n.-21-954del) c.96+192del (n.96+192del) n.435del c.62del (p.Pro21GlnfsTer?) | COSMIC COSMIC COSMIC |
17 | g.7676191G>A | CA397846224 | TP53 | c.178C>T (p.Pro60Ser) c.-21-955C>T (n.-21-955C>T) c.96+191C>T (n.96+191C>T) n.434C>T c.61C>T (p.Pro21Ser) | dbSNP COSMIC |
17 | g.7676191G>C | CA397846226 | TP53 | c.178C>G (p.Pro60Ala) c.-21-955C>G (n.-21-955C>G) c.96+191C>G (n.96+191C>G) n.434C>G c.61C>G (p.Pro21Ala) | dbSNP COSMIC |
17 | g.7676191G>T | CA397846228 | TP53 | c.178C>A (p.Pro60Thr) c.-21-955C>A (n.-21-955C>A) c.96+191C>A (n.96+191C>A) n.434C>A c.61C>A (p.Pro21Thr) | dbSNP COSMIC |
17 | g.7676192A>C | CA497926021 | TP53 | c.177T>G (p.Gly59=) c.-21-956T>G (n.-21-956T>G) c.96+190T>G (n.96+190T>G) n.433T>G c.60T>G (p.Gly20=) | dbSNP |
17 | g.7676192A>G | CA497926020 | TP53 | c.177T>C (p.Gly59=) c.-21-956T>C (n.-21-956T>C) c.96+190T>C (n.96+190T>C) n.433T>C c.60T>C (p.Gly20=) | dbSNP |
17 | g.7676192A>T | CA497926019 | TP53 | c.177T>A (p.Gly59=) c.-21-956T>A (n.-21-956T>A) c.96+190T>A (n.96+190T>A) n.433T>A c.60T>A (p.Gly20=) | ClinVar dbSNP |
17 | g.7676192_7676193delinsAC | CA2245935173 | TP53 | c.176_177delinsGT (p.Gly59=) c.-21-957_-21-956delinsGT (n.-21-957_-21-956delinsGT) c.96+189_96+190delinsGT (n.96+189_96+190delinsGT) n.432_433delinsGT c.59_60delinsGT (p.Gly20=) | |
17 | g.7676193C>A | CA397846241 | TP53 | c.176G>T (p.Gly59Val) c.-21-957G>T (n.-21-957G>T) c.96+189G>T (n.96+189G>T) n.432G>T c.59G>T (p.Gly20Val) | dbSNP |
17 | g.7676193C= | CA2245935181 | TP53 | c.176G= (p.Gly59=) c.-21-957G= (n.-21-957G=) c.96+189G= (n.96+189G=) n.432G= c.59G= (p.Gly20=) | |
17 | g.7676193C>G | CA397846232 | TP53 | c.176G>C (p.Gly59Ala) c.-21-957G>C (n.-21-957G>C) c.96+189G>C (n.96+189G>C) n.432G>C c.59G>C (p.Gly20Ala) | ClinVar dbSNP |
17 | g.7676193C>T | CA397846235 | TP53 | c.176G>A (p.Gly59Asp) c.-21-957G>A (n.-21-957G>A) c.96+189G>A (n.96+189G>A) n.432G>A c.59G>A (p.Gly20Asp) | ClinVar dbSNP COSMIC |
17 | g.7676193_7676194delinsTT | CA645589391 | TP53 | c.175_176delinsAA (p.Gly59Asn) c.-21-958_-21-957delinsAA (n.-21-958_-21-957delinsAA) c.96+188_96+189delinsAA (n.96+188_96+189delinsAA) n.431_432delinsAA c.58_59delinsAA (p.Gly20Asn) | COSMIC |
17 | g.7676194del | CA913191063 | TP53 | c.176del (p.Gly59ValfsTer?) c.-21-957del (n.-21-957del) c.96+189del (n.96+189del) n.432del c.59del (p.Gly20ValfsTer?) | ClinVar dbSNP |
17 | g.7676194_7676218del | CA645589390 | TP53 | c.152_176del (p.Glu51ValfsTer?) c.-21-981_-21-957del (n.-21-981_-21-957del) c.96+165_96+189del (n.96+165_96+189del) n.408_432del c.35_59del (p.Glu12ValfsTer?) | COSMIC |
17 | g.7676194C>A | CA397846253 | TP53 | c.175G>T (p.Gly59Cys) c.-21-958G>T (n.-21-958G>T) c.96+188G>T (n.96+188G>T) n.431G>T c.58G>T (p.Gly20Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7676194C= | CA2245935189 | TP53 | c.175G= (p.Gly59=) c.-21-958G= (n.-21-958G=) c.96+188G= (n.96+188G=) n.431G= c.58G= (p.Gly20=) | |
17 | g.7676194C>G | CA397846263 | TP53 | c.175G>C (p.Gly59Arg) c.-21-958G>C (n.-21-958G>C) c.96+188G>C (n.96+188G>C) n.431G>C c.58G>C (p.Gly20Arg) | ClinVar dbSNP |
17 | g.7676194C>T | CA397846266 | TP53 | c.175G>A (p.Gly59Ser) c.-21-958G>A (n.-21-958G>A) c.96+188G>A (n.96+188G>A) n.431G>A c.58G>A (p.Gly20Ser) | ClinVar |
17 | g.7676195del | CA645589392 | TP53 | c.174del (p.Gly59ValfsTer?) c.-21-959del (n.-21-959del) c.96+187del (n.96+187del) n.430del c.57del (p.Gly20ValfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676195T>A | CA497926022 | TP53 | c.174A>T (p.Pro58=) c.-21-959A>T (n.-21-959A>T) c.96+187A>T (n.96+187A>T) n.430A>T c.57A>T (p.Pro19=) | |
17 | g.7676195T>C | CA16616006 | TP53 | c.174A>G (p.Pro58=) c.-21-959A>G (n.-21-959A>G) c.96+187A>G (n.96+187A>G) n.430A>G c.57A>G (p.Pro19=) | ClinVar dbSNP |
17 | g.7676195T>G | CA497926023 | TP53 | c.174A>C (p.Pro58=) c.-21-959A>C (n.-21-959A>C) c.96+187A>C (n.96+187A>C) n.430A>C c.57A>C (p.Pro19=) | |
17 | g.7676195T= | CA2245935204 | TP53 | c.174A= (p.Pro58=) c.-21-959A= (n.-21-959A=) c.96+187A= (n.96+187A=) n.430A= c.57A= (p.Pro19=) | |
17 | g.7676196G>A | CA397846274 | TP53 | c.173C>T (p.Pro58Leu) c.-21-960C>T (n.-21-960C>T) c.96+186C>T (n.96+186C>T) n.429C>T c.56C>T (p.Pro19Leu) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676196G>C | CA000061 | TP53 | c.173C>G (p.Pro58Arg) c.-21-960C>G (n.-21-960C>G) c.96+186C>G (n.96+186C>G) n.429C>G c.56C>G (p.Pro19Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7676196G= | CA2245935224 | TP53 | c.173C= (p.Pro58=) c.-21-960C= (n.-21-960C=) c.96+186C= (n.96+186C=) n.429C= c.56C= (p.Pro19=) | |
17 | g.7676196G>T | CA397846279 | TP53 | c.173C>A (p.Pro58Gln) c.-21-960C>A (n.-21-960C>A) c.96+186C>A (n.96+186C>A) n.429C>A c.56C>A (p.Pro19Gln) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7676198del | CA497926024 | TP53 | c.173del (p.Pro58GlnfsTer?) c.-21-960del (n.-21-960del) c.96+186del (n.96+186del) n.429del c.56del (p.Pro19GlnfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676197G>A | CA397846284 | TP53 | c.172C>T (p.Pro58Ser) c.-21-961C>T (n.-21-961C>T) c.96+185C>T (n.96+185C>T) n.428C>T c.55C>T (p.Pro19Ser) | dbSNP |
17 | g.7676197G>C | CA397846288 | TP53 | c.172C>G (p.Pro58Ala) c.-21-961C>G (n.-21-961C>G) c.96+185C>G (n.96+185C>G) n.428C>G c.55C>G (p.Pro19Ala) | ClinVar dbSNP |
17 | g.7676197G= | CA2245935252 | TP53 | c.172C= (p.Pro58=) c.-21-961C= (n.-21-961C=) c.96+185C= (n.96+185C=) n.428C= c.55C= (p.Pro19=) | |
17 | g.7676197G>T | CA397846289 | TP53 | c.172C>A (p.Pro58Thr) c.-21-961C>A (n.-21-961C>A) c.96+185C>A (n.96+185C>A) n.428C>A c.55C>A (p.Pro19Thr) | ClinVar dbSNP |
17 | g.7676197_7676200dup | CA645589393 | TP53 | c.169_172dup (p.Pro58ArgfsTer6) c.-21-964_-21-961dup (n.-21-964_-21-961dup) c.96+182_96+185dup (n.96+182_96+185dup) n.425_428dup c.52_55dup (p.Pro19ArgfsTer6) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676198G>A | CA497926025 | TP53 | c.171C>T (p.Asp57=) c.-21-962C>T (n.-21-962C>T) c.96+184C>T (n.96+184C>T) n.427C>T c.54C>T (p.Asp18=) | ClinVar dbSNP |
17 | g.7676198G>C | CA397846290 | TP53 | c.171C>G (p.Asp57Glu) c.-21-962C>G (n.-21-962C>G) c.96+184C>G (n.96+184C>G) n.427C>G c.54C>G (p.Asp18Glu) | dbSNP |
17 | g.7676198G= | CA2245935268 | TP53 | c.171C= (p.Asp57=) c.-21-962C= (n.-21-962C=) c.96+184C= (n.96+184C=) n.427C= c.54C= (p.Asp18=) | |
17 | g.7676198G>T | CA000060 | TP53 | c.171C>A (p.Asp57Glu) c.-21-962C>A (n.-21-962C>A) c.96+184C>A (n.96+184C>A) n.427C>A c.54C>A (p.Asp18Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7676199T>A | CA397846310 | TP53 | c.170A>T (p.Asp57Val) c.-21-963A>T (n.-21-963A>T) c.96+183A>T (n.96+183A>T) n.426A>T c.53A>T (p.Asp18Val) | ClinVar |
17 | g.7676199T>C | CA397846305 | TP53 | c.170A>G (p.Asp57Gly) c.-21-963A>G (n.-21-963A>G) c.96+183A>G (n.96+183A>G) n.426A>G c.53A>G (p.Asp18Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7676199T>G | CA397846304 | TP53 | c.170A>C (p.Asp57Ala) c.-21-963A>C (n.-21-963A>C) c.96+183A>C (n.96+183A>C) n.426A>C c.53A>C (p.Asp18Ala) | ClinVar dbSNP |
17 | g.7676199T= | CA2245935273 | TP53 | c.170A= (p.Asp57=) c.-21-963A= (n.-21-963A=) c.96+183A= (n.96+183A=) n.426A= c.53A= (p.Asp18=) | |
17 | g.7676200_7676213del | CA891842285 | TP53 | c.157_170del (p.Trp53ProfsTer5) c.-21-976_-21-963del (n.-21-976_-21-963del) c.96+170_96+183del (n.96+170_96+183del) n.413_426del c.40_53del (p.Trp14ProfsTer5) | |
17 | g.7676200C>A | CA397846323 | TP53 | c.169G>T (p.Asp57Tyr) c.-21-964G>T (n.-21-964G>T) c.96+182G>T (n.96+182G>T) n.425G>T c.52G>T (p.Asp18Tyr) | dbSNP |
17 | g.7676200C>G | CA397846331 | TP53 | c.169G>C (p.Asp57His) c.-21-964G>C (n.-21-964G>C) c.96+182G>C (n.96+182G>C) n.425G>C c.52G>C (p.Asp18His) | dbSNP |
17 | g.7676200C>T | CA397846329 | TP53 | c.169G>A (p.Asp57Asn) c.-21-964G>A (n.-21-964G>A) c.96+182G>A (n.96+182G>A) n.425G>A c.52G>A (p.Asp18Asn) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676201T>A | CA397846348 | TP53 | c.168A>T (p.Glu56Asp) c.-21-965A>T (n.-21-965A>T) c.96+181A>T (n.96+181A>T) n.424A>T c.51A>T (p.Glu17Asp) | dbSNP |
17 | g.7676201T>C | CA003148 | TP53 | c.168A>G (p.Glu56=) c.-21-965A>G (n.-21-965A>G) c.96+181A>G (n.96+181A>G) n.424A>G c.51A>G (p.Glu17=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7676201T>G | CA397846370 | TP53 | c.168A>C (p.Glu56Asp) c.-21-965A>C (n.-21-965A>C) c.96+181A>C (n.96+181A>C) n.424A>C c.51A>C (p.Glu17Asp) | |
17 | g.7676201T= | CA2245935282 | TP53 | c.168A= (p.Glu56=) c.-21-965A= (n.-21-965A=) c.96+181A= (n.96+181A=) n.424A= c.51A= (p.Glu17=) | |
17 | g.7676202del | CA2580095112 | TP53 | c.168del (p.Asp57ThrfsTer?) c.-21-965del (n.-21-965del) c.96+181del (n.96+181del) n.424del c.51del (p.Asp18ThrfsTer?) | ClinVar |
17 | g.7676202T>A | CA397846381 | TP53 | c.167A>T (p.Glu56Val) c.-21-966A>T (n.-21-966A>T) c.96+180A>T (n.96+180A>T) n.423A>T c.50A>T (p.Glu17Val) | dbSNP COSMIC |
17 | g.7676202T>C | CA397846383 | TP53 | c.167A>G (p.Glu56Gly) c.-21-966A>G (n.-21-966A>G) c.96+180A>G (n.96+180A>G) n.423A>G c.50A>G (p.Glu17Gly) | dbSNP |
17 | g.7676202T>G | CA397846387 | TP53 | c.167A>C (p.Glu56Ala) c.-21-966A>C (n.-21-966A>C) c.96+180A>C (n.96+180A>C) n.423A>C c.50A>C (p.Glu17Ala) | |
17 | g.7676204_7676205insTCTGGACCTGGGTCTCA | CA645589394 | TP53 | c.167_168insGACCCAGGTCCAGATGA (p.Asp57ThrfsTer?) c.-21-966_-21-965insGACCCAGGTCCAGATGA (n.-21-966_-21-965insGACCCAGGTCCAGATGA) c.96+180_96+181insGACCCAGGTCCAGATGA (n.96+180_96+181insGACCCAGGTCCAGATGA) n.423_424insGACCCAGGTCCAGATGA c.50_51insGACCCAGGTCCAGATGA (p.Asp18ThrfsTer?) | COSMIC COSMIC |
17 | g.7676202_7676203insA | CA891842286 | TP53 | c.166_167insT (p.Glu56ValfsTer7) c.-21-967_-21-966insT (n.-21-967_-21-966insT) c.96+179_96+180insT (n.96+179_96+180insT) n.422_423insT c.49_50insT (p.Glu17ValfsTer7) | |
17 | g.7676202_7676203insGTAGACCTGGACCCAGA | CA645589395 | TP53 | c.166_167insTCTGGGTCCAGGTCTAC (p.Glu56ValfsTer?) c.-21-967_-21-966insTCTGGGTCCAGGTCTAC (n.-21-967_-21-966insTCTGGGTCCAGGTCTAC) c.96+179_96+180insTCTGGGTCCAGGTCTAC (n.96+179_96+180insTCTGGGTCCAGGTCTAC) n.422_423insTCTGGGTCCAGGTCTAC c.49_50insTCTGGGTCCAGGTCTAC (p.Glu17ValfsTer?) | COSMIC COSMIC COSMIC |
17 | g.7676203del | CA497926026 | TP53 | c.166del (p.Glu56LysfsTer?) c.-21-967del (n.-21-967del) c.96+179del (n.96+179del) n.422del c.49del (p.Glu17LysfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676203C>A | CA397846394 | TP53 | c.166G>T (p.Glu56Ter) c.-21-967G>T (n.-21-967G>T) c.96+179G>T (n.96+179G>T) n.422G>T c.49G>T (p.Glu17Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676203C>G | CA397846398 | TP53 | c.166G>C (p.Glu56Gln) c.-21-967G>C (n.-21-967G>C) c.96+179G>C (n.96+179G>C) n.422G>C c.49G>C (p.Glu17Gln) | |
17 | g.7676203C>T | CA397846399 | TP53 | c.166G>A (p.Glu56Lys) c.-21-967G>A (n.-21-967G>A) c.96+179G>A (n.96+179G>A) n.422G>A c.49G>A (p.Glu17Lys) | ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676203_7676204del | CA645589397 | TP53 | c.165_166del (p.Glu56ArgfsTer6) c.-21-968_-21-967del (n.-21-968_-21-967del) c.96+178_96+179del (n.96+178_96+179del) n.421_422del c.48_49del (p.Glu17ArgfsTer6) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676203_7676215del | CA645589396 | TP53 | c.154_166del (p.Gln52LysfsTer?) c.-21-979_-21-967del (n.-21-979_-21-967del) c.96+167_96+179del (n.96+167_96+179del) n.410_422del c.37_49del (p.Gln13LysfsTer?) | COSMIC |
17 | g.7676204A>C | CA497926027 | TP53 | c.165T>G (p.Thr55=) c.-21-968T>G (n.-21-968T>G) c.96+178T>G (n.96+178T>G) n.421T>G c.48T>G (p.Thr16=) | ClinVar dbSNP |
17 | g.7676204A>G | CA497926028 | TP53 | c.165T>C (p.Thr55=) c.-21-968T>C (n.-21-968T>C) c.96+178T>C (n.96+178T>C) n.421T>C c.48T>C (p.Thr16=) | dbSNP |
17 | g.7676204A>T | CA497926029 | TP53 | c.165T>A (p.Thr55=) c.-21-968T>A (n.-21-968T>A) c.96+178T>A (n.96+178T>A) n.421T>A c.48T>A (p.Thr16=) | dbSNP |
17 | g.7676205del | CA645589399 | TP53 | c.164del (p.Thr55MetfsTer?) c.-21-969del (n.-21-969del) c.96+177del (n.96+177del) n.420del c.47del (p.Thr16MetfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676205G>A | CA397846403 | TP53 | c.164C>T (p.Thr55Ile) c.-21-969C>T (n.-21-969C>T) c.96+177C>T (n.96+177C>T) n.420C>T c.47C>T (p.Thr16Ile) | dbSNP |
17 | g.7676205G>C | CA397846406 | TP53 | c.164C>G (p.Thr55Ser) c.-21-969C>G (n.-21-969C>G) c.96+177C>G (n.96+177C>G) n.420C>G c.47C>G (p.Thr16Ser) | ClinVar dbSNP |
17 | g.7676205G>T | CA397846407 | TP53 | c.164C>A (p.Thr55Asn) c.-21-969C>A (n.-21-969C>A) c.96+177C>A (n.96+177C>A) n.420C>A c.47C>A (p.Thr16Asn) | |
17 | g.7676205dup | CA645589398 | TP53 | c.164dup (p.Glu56Ter) c.-21-969dup (n.-21-969dup) c.96+177dup (n.96+177dup) n.420dup c.47dup (p.Glu17Ter) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676207_7676216del | CA2580095113 | TP53 | c.155_164del (p.Gln52LeufsTer?) c.-21-978_-21-969del (n.-21-978_-21-969del) c.96+168_96+177del (n.96+168_96+177del) n.411_420del c.38_47del (p.Gln13LeufsTer?) | ClinVar |
17 | g.7676206T>A | CA397846418 | TP53 | c.163A>T (p.Thr55Ser) c.-21-970A>T (n.-21-970A>T) c.96+176A>T (n.96+176A>T) n.419A>T c.46A>T (p.Thr16Ser) | dbSNP |
17 | g.7676206T>C | CA397846410 | TP53 | c.163A>G (p.Thr55Ala) c.-21-970A>G (n.-21-970A>G) c.96+176A>G (n.96+176A>G) n.419A>G c.46A>G (p.Thr16Ala) | dbSNP |
17 | g.7676206T>G | CA397846416 | TP53 | c.163A>C (p.Thr55Pro) c.-21-970A>C (n.-21-970A>C) c.96+176A>C (n.96+176A>C) n.419A>C c.46A>C (p.Thr16Pro) | ClinVar dbSNP |
17 | g.7676206_7676211delinsAT | CA2573154645 | TP53 | c.158_163delinsAT (p.Trp53TyrfsTer?) c.-21-975_-21-970delinsAT (n.-21-975_-21-970delinsAT) c.96+171_96+176delinsAT (n.96+171_96+176delinsAT) n.414_419delinsAT c.41_46delinsAT (p.Trp14TyrfsTer?) | ClinVar dbSNP |
17 | g.7676207del | CA2573154646 | TP53 | c.162del (p.Phe54LeufsTer?) c.-21-971del (n.-21-971del) c.96+175del (n.96+175del) n.418del c.45del (p.Phe15LeufsTer?) | ClinVar dbSNP |
17 | g.7676207G>A | CA497926030 | TP53 | c.162C>T (p.Phe54=) c.-21-971C>T (n.-21-971C>T) c.96+175C>T (n.96+175C>T) n.418C>T c.45C>T (p.Phe15=) | dbSNP COSMIC |
17 | g.7676207G>C | CA397846420 | TP53 | c.162C>G (p.Phe54Leu) c.-21-971C>G (n.-21-971C>G) c.96+175C>G (n.96+175C>G) n.418C>G c.45C>G (p.Phe15Leu) | dbSNP |
17 | g.7676207G>T | CA397846422 | TP53 | c.162C>A (p.Phe54Leu) c.-21-971C>A (n.-21-971C>A) c.96+175C>A (n.96+175C>A) n.418C>A c.45C>A (p.Phe15Leu) | COSMIC |
17 | g.7676208_7676230del | CA645589400 | TP53 | c.140_162del (p.Pro47HisfsTer2) c.-21-993_-21-971del (n.-21-993_-21-971del) c.96+153_96+175del (n.96+153_96+175del) n.396_418del c.23_45del (p.Pro8HisfsTer2) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676208A>C | CA397846423 | TP53 | c.161T>G (p.Phe54Cys) c.-21-972T>G (n.-21-972T>G) c.96+174T>G (n.96+174T>G) n.417T>G c.44T>G (p.Phe15Cys) | dbSNP |
17 | g.7676208A>G | CA397846424 | TP53 | c.161T>C (p.Phe54Ser) c.-21-972T>C (n.-21-972T>C) c.96+174T>C (n.96+174T>C) n.417T>C c.44T>C (p.Phe15Ser) | dbSNP |
17 | g.7676208A>T | CA397846434 | TP53 | c.161T>A (p.Phe54Tyr) c.-21-972T>A (n.-21-972T>A) c.96+174T>A (n.96+174T>A) n.417T>A c.44T>A (p.Phe15Tyr) | dbSNP |
17 | g.7676209del | CA497926031 | TP53 | c.161del (p.Phe54SerfsTer?) c.-21-972del (n.-21-972del) c.96+174del (n.96+174del) n.417del c.44del (p.Phe15SerfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676209A= | CA2245935293 | TP53 | c.160T= (p.Phe54=) c.-21-973T= (n.-21-973T=) c.96+173T= (n.96+173T=) n.416T= c.43T= (p.Phe15=) | |
17 | g.7676209A>C | CA397846435 | TP53 | c.160T>G (p.Phe54Val) c.-21-973T>G (n.-21-973T>G) c.96+173T>G (n.96+173T>G) n.416T>G c.43T>G (p.Phe15Val) | |
17 | g.7676209A>G | CA397846436 | TP53 | c.160T>C (p.Phe54Leu) c.-21-973T>C (n.-21-973T>C) c.96+173T>C (n.96+173T>C) n.416T>C c.43T>C (p.Phe15Leu) | ClinVar dbSNP COSMIC |
17 | g.7676209A>T | CA397846438 | TP53 | c.160T>A (p.Phe54Ile) c.-21-973T>A (n.-21-973T>A) c.96+173T>A (n.96+173T>A) n.416T>A c.43T>A (p.Phe15Ile) | |
17 | g.7676210C>A | CA397846443 | TP53 | c.159G>T (p.Trp53Cys) c.-21-974G>T (n.-21-974G>T) c.96+172G>T (n.96+172G>T) n.415G>T c.42G>T (p.Trp14Cys) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676210C= | CA2245935301 | TP53 | c.159G= (p.Trp53=) c.-21-974G= (n.-21-974G=) c.96+172G= (n.96+172G=) n.415G= c.42G= (p.Trp14=) | |
17 | g.7676210C>G | CA397846446 | TP53 | c.159G>C (p.Trp53Cys) c.-21-974G>C (n.-21-974G>C) c.96+172G>C (n.96+172G>C) n.415G>C c.42G>C (p.Trp14Cys) | dbSNP COSMIC |
17 | g.7676210C>T | CA16620640 | TP53 | c.159G>A (p.Trp53Ter) c.-21-974G>A (n.-21-974G>A) c.96+172G>A (n.96+172G>A) n.415G>A c.42G>A (p.Trp14Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676211dup | CA2825002625 | TP53 | c.159dup (p.Phe54ValfsTer3) c.-21-974dup (n.-21-974dup) c.96+172dup (n.96+172dup) n.415dup c.42dup (p.Phe15ValfsTer3) | ClinVar |
17 | g.7676211C>A | CA397846483 | TP53 | c.158G>T (p.Trp53Leu) c.-21-975G>T (n.-21-975G>T) c.96+171G>T (n.96+171G>T) n.414G>T c.41G>T (p.Trp14Leu) | ClinVar dbSNP |
17 | g.7676211C= | CA2245935318 | TP53 | c.158G= (p.Trp53=) c.-21-975G= (n.-21-975G=) c.96+171G= (n.96+171G=) n.414G= c.41G= (p.Trp14=) | |
17 | g.7676211C>G | CA397846478 | TP53 | c.158G>C (p.Trp53Ser) c.-21-975G>C (n.-21-975G>C) c.96+171G>C (n.96+171G>C) n.414G>C c.41G>C (p.Trp14Ser) | dbSNP |
17 | g.7676211C>T | CA10580959 | TP53 | c.158G>A (p.Trp53Ter) c.-21-975G>A (n.-21-975G>A) c.96+171G>A (n.96+171G>A) n.414G>A c.41G>A (p.Trp14Ter) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676211_7676213dup | CA2580095114 | TP53 | c.156_158dup (p.Trp53Ter) c.-21-977_-21-975dup (n.-21-977_-21-975dup) c.96+169_96+171dup (n.96+169_96+171dup) n.412_414dup c.39_41dup (p.Trp14Ter) | ClinVar |
17 | g.7676211_7676214dup | CA624865029 | TP53 | c.155_158dup (p.Trp53Ter) c.-21-978_-21-975dup (n.-21-978_-21-975dup) c.96+168_96+171dup (n.96+168_96+171dup) n.411_414dup c.38_41dup (p.Trp14Ter) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
17 | g.7676213_7676219del | CA891842288 | TP53 | c.152_158del (p.Glu51GlyfsTer?) c.-21-981_-21-975del (n.-21-981_-21-975del) c.96+165_96+171del (n.96+165_96+171del) n.408_414del c.35_41del (p.Glu12GlyfsTer?) | |
17 | g.7676212del | CA645589401 | TP53 | c.157del (p.Trp53GlyfsTer?) c.-21-976del (n.-21-976del) c.96+170del (n.96+170del) n.413del c.40del (p.Trp14GlyfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676212A= | CA2245935332 | TP53 | c.157T= (p.Trp53=) c.-21-976T= (n.-21-976T=) c.96+170T= (n.96+170T=) n.413T= c.40T= (p.Trp14=) | |
17 | g.7676212A>C | CA397846495 | TP53 | c.157T>G (p.Trp53Gly) c.-21-976T>G (n.-21-976T>G) c.96+170T>G (n.96+170T>G) n.413T>G c.40T>G (p.Trp14Gly) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676212A>G | CA397846498 | TP53 | c.157T>C (p.Trp53Arg) c.-21-976T>C (n.-21-976T>C) c.96+170T>C (n.96+170T>C) n.413T>C c.40T>C (p.Trp14Arg) | ClinVar dbSNP gnomAD v4 |
17 | g.7676212A>T | CA397846503 | TP53 | c.157T>A (p.Trp53Arg) c.-21-976T>A (n.-21-976T>A) c.96+170T>A (n.96+170T>A) n.413T>A c.40T>A (p.Trp14Arg) | ClinVar dbSNP |
17 | g.7676212_7676214delinsATT | CA2245935333 | TP53 | c.155_157delinsAAT (p.Gln52=) c.-21-978_-21-976delinsAAT (n.-21-978_-21-976delinsAAT) c.96+168_96+170delinsAAT (n.96+168_96+170delinsAAT) n.411_413delinsAAT c.38_40delinsAAT (p.Gln13=) | |
17 | g.7676212_7676214dup | CA168994 | TP53 | c.155_157dup (p.Trp53Ter) c.-21-978_-21-976dup (n.-21-978_-21-976dup) c.96+168_96+170dup (n.96+168_96+170dup) n.411_413dup c.38_40dup (p.Trp14Ter) | ClinVar dbSNP |
17 | g.7676214_7676221del | CA645589402 | TP53 | c.150_157del (p.Ile50MetfsTer4) c.-21-983_-21-976del (n.-21-983_-21-976del) c.96+163_96+170del (n.96+163_96+170del) n.406_413del c.33_40del (p.Ile11MetfsTer4) | COSMIC |
17 | g.7676213T>A | CA397846509 | TP53 | c.156A>T (p.Gln52His) c.-21-977A>T (n.-21-977A>T) c.96+169A>T (n.96+169A>T) n.412A>T c.39A>T (p.Gln13His) | dbSNP COSMIC |
17 | g.7676213T>C | CA16608669 | TP53 | c.156A>G (p.Gln52=) c.-21-977A>G (n.-21-977A>G) c.96+169A>G (n.96+169A>G) n.412A>G c.39A>G (p.Gln13=) | ClinVar dbSNP gnomAD v4 |
17 | g.7676213T>G | CA397846515 | TP53 | c.156A>C (p.Gln52His) c.-21-977A>C (n.-21-977A>C) c.96+169A>C (n.96+169A>C) n.412A>C c.39A>C (p.Gln13His) | dbSNP |
17 | g.7676213T= | CA2245935357 | TP53 | c.156A= (p.Gln52=) c.-21-977A= (n.-21-977A=) c.96+169A= (n.96+169A=) n.412A= c.39A= (p.Gln13=) | |
17 | g.7676213_7676214del | CA658798707 | TP53 | c.155_156del (p.Gln52LeufsTer4) c.-21-978_-21-977del (n.-21-978_-21-977del) c.96+168_96+169del (n.96+168_96+169del) n.411_412del c.38_39del (p.Gln13LeufsTer4) | ClinVar dbSNP |
17 | g.7676214dup | CA645589403 | TP53 | c.156dup (p.Trp53MetfsTer4) c.-21-977dup (n.-21-977dup) c.96+169dup (n.96+169dup) n.412dup c.39dup (p.Trp14MetfsTer4) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676214del | CA2695223140 | TP53 | c.156del (p.Gln52HisfsTer?) c.-21-977del (n.-21-977del) c.96+169del (n.96+169del) n.412del c.39del (p.Gln13HisfsTer?) | |
17 | g.7676214_7676217del | CA891842289 | TP53 | c.153_156del (p.Glu51AspfsTer?) c.-21-980_-21-977del (n.-21-980_-21-977del) c.96+166_96+169del (n.96+166_96+169del) n.409_412del c.36_39del (p.Glu12AspfsTer?) | |
17 | g.7676214T>A | CA397846516 | TP53 | c.155A>T (p.Gln52Leu) c.-21-978A>T (n.-21-978A>T) c.96+168A>T (n.96+168A>T) n.411A>T c.38A>T (p.Gln13Leu) | dbSNP |
17 | g.7676214T>C | CA003159 | TP53 | c.155A>G (p.Gln52Arg) c.-21-978A>G (n.-21-978A>G) c.96+168A>G (n.96+168A>G) n.411A>G c.38A>G (p.Gln13Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676214T>G | CA397846519 | TP53 | c.155A>C (p.Gln52Pro) c.-21-978A>C (n.-21-978A>C) c.96+168A>C (n.96+168A>C) n.411A>C c.38A>C (p.Gln13Pro) | |
17 | g.7676214T= | CA2245935364 | TP53 | c.155A= (p.Gln52=) c.-21-978A= (n.-21-978A=) c.96+168A= (n.96+168A=) n.411A= c.38A= (p.Gln13=) | |
17 | g.7676215G>A | CA397846527 | TP53 | c.154C>T (p.Gln52Ter) c.-21-979C>T (n.-21-979C>T) c.96+167C>T (n.96+167C>T) n.410C>T c.37C>T (p.Gln13Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676215G>C | CA397846538 | TP53 | c.154C>G (p.Gln52Glu) c.-21-979C>G (n.-21-979C>G) c.96+167C>G (n.96+167C>G) n.410C>G c.37C>G (p.Gln13Glu) | |
17 | g.7676215G= | CA2245935368 | TP53 | c.154C= (p.Gln52=) c.-21-979C= (n.-21-979C=) c.96+167C= (n.96+167C=) n.410C= c.37C= (p.Gln13=) | |
17 | g.7676215G>T | CA397846541 | TP53 | c.154C>A (p.Gln52Lys) c.-21-979C>A (n.-21-979C>A) c.96+167C>A (n.96+167C>A) n.410C>A c.37C>A (p.Gln13Lys) | |
17 | g.7676216T>A | CA397846552 | TP53 | c.153A>T (p.Glu51Asp) c.-21-980A>T (n.-21-980A>T) c.96+166A>T (n.96+166A>T) n.409A>T c.36A>T (p.Glu12Asp) | dbSNP |
17 | g.7676216T>C | CA497926032 | TP53 | c.153A>G (p.Glu51=) c.-21-980A>G (n.-21-980A>G) c.96+166A>G (n.96+166A>G) n.409A>G c.36A>G (p.Glu12=) | dbSNP gnomAD v4 COSMIC |
17 | g.7676216T>G | CA397846548 | TP53 | c.153A>C (p.Glu51Asp) c.-21-980A>C (n.-21-980A>C) c.96+166A>C (n.96+166A>C) n.409A>C c.36A>C (p.Glu12Asp) | dbSNP |
17 | g.7676216T= | CA2245935384 | TP53 | c.153A= (p.Glu51=) c.-21-980A= (n.-21-980A=) c.96+166A= (n.96+166A=) n.409A= c.36A= (p.Glu12=) | |
17 | g.7676217dup | CA913191064 | TP53 | c.153dup (p.Gln52ThrfsTer5) c.-21-980dup (n.-21-980dup) c.96+166dup (n.96+166dup) n.409dup c.36dup (p.Gln13ThrfsTer5) | ClinVar dbSNP |
17 | g.7676217del | CA645589404 | TP53 | c.153del (p.Glu51AspfsTer?) c.-21-980del (n.-21-980del) c.96+166del (n.96+166del) n.409del c.36del (p.Glu12AspfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676217_7676239dup | CA916081953 | TP53 | c.131_153dup (p.Gln52CysfsTer?) c.-21-1002_-21-980dup (n.-21-1002_-21-980dup) c.96+144_96+166dup (n.96+144_96+166dup) n.387_409dup c.14_36dup (p.Gln13CysfsTer?) | ClinVar dbSNP |
17 | g.7676217T>A | CA397846557 | TP53 | c.152A>T (p.Glu51Val) c.-21-981A>T (n.-21-981A>T) c.96+165A>T (n.96+165A>T) n.408A>T c.35A>T (p.Glu12Val) | dbSNP |
17 | g.7676217T>C | CA397846560 | TP53 | c.152A>G (p.Glu51Gly) c.-21-981A>G (n.-21-981A>G) c.96+165A>G (n.96+165A>G) n.408A>G c.35A>G (p.Glu12Gly) | ClinVar dbSNP |
17 | g.7676217T>G | CA397846563 | TP53 | c.152A>C (p.Glu51Ala) c.-21-981A>C (n.-21-981A>C) c.96+165A>C (n.96+165A>C) n.408A>C c.35A>C (p.Glu12Ala) | |
17 | g.7676217T= | CA2245935394 | TP53 | c.152A= (p.Glu51=) c.-21-981A= (n.-21-981A=) c.96+165A= (n.96+165A=) n.408A= c.35A= (p.Glu12=) | |
17 | g.7676218_7676221del | CA645589405 | TP53 | c.149_152del (p.Ile50AsnfsTer?) c.-21-984_-21-981del (n.-21-984_-21-981del) c.96+162_96+165del (n.96+162_96+165del) n.405_408del c.32_35del (p.Ile11AsnfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676217_7676227dup | CA913203396 | TP53 | c.142_152dup (p.Gln52ThrfsTer?) c.-21-991_-21-981dup (n.-21-991_-21-981dup) c.96+155_96+165dup (n.96+155_96+165dup) n.398_408dup c.25_35dup (p.Gln13ThrfsTer?) | ClinVar dbSNP |
17 | g.7676218del | CA497926033 | TP53 | c.151del (p.Glu51AsnfsTer?) c.-21-982del (n.-21-982del) c.96+164del (n.96+164del) n.407del c.34del (p.Glu12AsnfsTer?) | COSMIC |
17 | g.7676218C>A | CA397846566 | TP53 | c.151G>T (p.Glu51Ter) c.-21-982G>T (n.-21-982G>T) c.96+164G>T (n.96+164G>T) n.407G>T c.34G>T (p.Glu12Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676218C= | CA2245935421 | TP53 | c.151G= (p.Glu51=) c.-21-982G= (n.-21-982G=) c.96+164G= (n.96+164G=) n.407G= c.34G= (p.Glu12=) | |
17 | g.7676218C>G | CA397846570 | TP53 | c.151G>C (p.Glu51Gln) c.-21-982G>C (n.-21-982G>C) c.96+164G>C (n.96+164G>C) n.407G>C c.34G>C (p.Glu12Gln) | |
17 | g.7676218C>T | CA397846575 | TP53 | c.151G>A (p.Glu51Lys) c.-21-982G>A (n.-21-982G>A) c.96+164G>A (n.96+164G>A) n.407G>A c.34G>A (p.Glu12Lys) | ClinVar dbSNP gnomAD v4 |
17 | g.7676218dup | CA645589406 | TP53 | c.151dup (p.Glu51GlyfsTer6) c.-21-982dup (n.-21-982dup) c.96+164dup (n.96+164dup) n.407dup c.34dup (p.Glu12GlyfsTer6) | COSMIC COSMIC COSMIC |
17 | g.7676218_7676219insG | CA497926034 | TP53 | c.150_151insC (p.Glu51ArgfsTer6) c.-21-983_-21-982insC (n.-21-983_-21-982insC) c.96+163_96+164insC (n.96+163_96+164insC) n.406_407insC c.33_34insC (p.Glu12ArgfsTer6) | |
17 | g.7676219A>C | CA397846576 | TP53 | c.150T>G (p.Ile50Met) c.-21-983T>G (n.-21-983T>G) c.96+163T>G (n.96+163T>G) n.406T>G c.33T>G (p.Ile11Met) | |
17 | g.7676219A>G | CA497926035 | TP53 | c.150T>C (p.Ile50=) c.-21-983T>C (n.-21-983T>C) c.96+163T>C (n.96+163T>C) n.406T>C c.33T>C (p.Ile11=) | dbSNP gnomAD v4 |
17 | g.7676219A>T | CA497926036 | TP53 | c.150T>A (p.Ile50=) c.-21-983T>A (n.-21-983T>A) c.96+163T>A (n.96+163T>A) n.406T>A c.33T>A (p.Ile11=) | dbSNP |
17 | g.7676220del | CA497926037 | TP53 | c.150del (p.Ile50MetfsTer?) c.-21-983del (n.-21-983del) c.96+163del (n.96+163del) n.406del c.33del (p.Ile11MetfsTer?) | COSMIC COSMIC COSMIC |
17 | g.7676220A= | CA2245935439 | TP53 | c.149T= (p.Ile50=) c.-21-984T= (n.-21-984T=) c.96+162T= (n.96+162T=) n.405T= c.32T= (p.Ile11=) | |
17 | g.7676220A>C | CA397846579 | TP53 | c.149T>G (p.Ile50Ser) c.-21-984T>G (n.-21-984T>G) c.96+162T>G (n.96+162T>G) n.405T>G c.32T>G (p.Ile11Ser) | |
17 | g.7676220A>G | CA337284 | TP53 | c.149T>C (p.Ile50Thr) c.-21-984T>C (n.-21-984T>C) c.96+162T>C (n.96+162T>C) n.405T>C c.32T>C (p.Ile11Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7676220A>T | CA000059 | TP53 | c.149T>A (p.Ile50Asn) c.-21-984T>A (n.-21-984T>A) c.96+162T>A (n.96+162T>A) n.405T>A c.32T>A (p.Ile11Asn) | ClinVar dbSNP |
17 | g.7676222_7676223del | CA645589407 | TP53 | c.148_149del (p.Ile50Ter) c.-21-985_-21-984del (n.-21-985_-21-984del) c.96+161_96+162del (n.96+161_96+162del) n.404_405del c.31_32del (p.Ile11Ter) | COSMIC |
17 | g.7676221T>A | CA397846591 | TP53 | c.148A>T (p.Ile50Phe) c.-21-985A>T (n.-21-985A>T) c.96+161A>T (n.96+161A>T) n.404A>T c.31A>T (p.Ile11Phe) | dbSNP |
17 | g.7676221T>C | CA397846598 | TP53 | c.148A>G (p.Ile50Val) c.-21-985A>G (n.-21-985A>G) c.96+161A>G (n.96+161A>G) n.404A>G c.31A>G (p.Ile11Val) | dbSNP |
17 | g.7676221T>G | CA397846601 | TP53 | c.148A>C (p.Ile50Leu) c.-21-985A>C (n.-21-985A>C) c.96+161A>C (n.96+161A>C) n.404A>C c.31A>C (p.Ile11Leu) | ClinVar |
17 | g.7676221dup | CA919785522 | TP53 | c.148dup (p.Ile50AsnfsTer2) c.-21-985dup (n.-21-985dup) c.96+161dup (n.96+161dup) n.404dup c.31dup (p.Ile11AsnfsTer2) | ClinVar dbSNP |
17 | g.7676222A= | CA2245935457 | TP53 | c.147T= (p.Asp49=) c.-21-986T= (n.-21-986T=) c.96+160T= (n.96+160T=) n.403T= c.30T= (p.Asp10=) | |
17 | g.7676222A>C | CA397846612 | TP53 | c.147T>G (p.Asp49Glu) c.-21-986T>G (n.-21-986T>G) c.96+160T>G (n.96+160T>G) n.403T>G c.30T>G (p.Asp10Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7676222A>G | CA000058 | TP53 | c.147T>C (p.Asp49=) c.-21-986T>C (n.-21-986T>C) c.96+160T>C (n.96+160T>C) n.403T>C c.30T>C (p.Asp10=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676222A>T | CA397846609 | TP53 | c.147T>A (p.Asp49Glu) c.-21-986T>A (n.-21-986T>A) c.96+160T>A (n.96+160T>A) n.403T>A c.30T>A (p.Asp10Glu) | ClinVar dbSNP |
17 | g.7676222_7676233del | CA645589408 | TP53 | c.136_147del (p.Ser46_Asp49del) c.-21-997_-21-986del (n.-21-997_-21-986del) c.96+149_96+160del (n.96+149_96+160del) n.392_403del c.19_30del (p.Ser7_Asp10del) | COSMIC |
17 | g.7676223T>A | CA397846617 | TP53 | c.146A>T (p.Asp49Val) c.-21-987A>T (n.-21-987A>T) c.96+159A>T (n.96+159A>T) n.402A>T c.29A>T (p.Asp10Val) | dbSNP |
17 | g.7676223T>C | CA003170 | TP53 | c.146A>G (p.Asp49Gly) c.-21-987A>G (n.-21-987A>G) c.96+159A>G (n.96+159A>G) n.402A>G c.29A>G (p.Asp10Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7676223T>G | CA397846664 | TP53 | c.146A>C (p.Asp49Ala) c.-21-987A>C (n.-21-987A>C) c.96+159A>C (n.96+159A>C) n.402A>C c.29A>C (p.Asp10Ala) | |
17 | g.7676223T= | CA2245935467 | TP53 | c.146A= (p.Asp49=) c.-21-987A= (n.-21-987A=) c.96+159A= (n.96+159A=) n.402A= c.29A= (p.Asp10=) | |
17 | g.7676223dup | CA645589409 | TP53 | c.146dup (p.Asp49GlufsTer3) c.-21-987dup (n.-21-987dup) c.96+159dup (n.96+159dup) n.402dup c.29dup (p.Asp10GlufsTer3) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676223_7676224del | CA645589410 | TP53 | c.145_146del (p.Asp49TyrfsTer2) c.-21-988_-21-987del (n.-21-988_-21-987del) c.96+158_96+159del (n.96+158_96+159del) n.401_402del c.28_29del (p.Asp10TyrfsTer2) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676224C>A | CA397846678 | TP53 | c.145G>T (p.Asp49Tyr) c.-21-988G>T (n.-21-988G>T) c.96+158G>T (n.96+158G>T) n.401G>T c.28G>T (p.Asp10Tyr) | dbSNP COSMIC |
17 | g.7676224C= | CA2245935484 | TP53 | c.145G= (p.Asp49=) c.-21-988G= (n.-21-988G=) c.96+158G= (n.96+158G=) n.401G= c.28G= (p.Asp10=) | |
17 | g.7676224C>G | CA000057 | TP53 | c.145G>C (p.Asp49His) c.-21-988G>C (n.-21-988G>C) c.96+158G>C (n.96+158G>C) n.401G>C c.28G>C (p.Asp10His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7676224C>T | CA000056 | TP53 | c.145G>A (p.Asp49Asn) c.-21-988G>A (n.-21-988G>A) c.96+158G>A (n.96+158G>A) n.401G>A c.28G>A (p.Asp10Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
17 | g.7676225del | CA645589411 | TP53 | c.144del (p.Asp48GlufsTer?) c.-21-989del (n.-21-989del) c.96+157del (n.96+157del) n.400del c.27del (p.Asp9GlufsTer?) | COSMIC |
17 | g.7676225G>A | CA10580960 | TP53 | c.144C>T (p.Asp48=) c.-21-989C>T (n.-21-989C>T) c.96+157C>T (n.96+157C>T) n.400C>T c.27C>T (p.Asp9=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676225G>C | CA397846713 | TP53 | c.144C>G (p.Asp48Glu) c.-21-989C>G (n.-21-989C>G) c.96+157C>G (n.96+157C>G) n.400C>G c.27C>G (p.Asp9Glu) | dbSNP |
17 | g.7676225G= | CA2245935500 | TP53 | c.144C= (p.Asp48=) c.-21-989C= (n.-21-989C=) c.96+157C= (n.96+157C=) n.400C= c.27C= (p.Asp9=) | |
17 | g.7676225G>T | CA000055 | TP53 | c.144C>A (p.Asp48Glu) c.-21-989C>A (n.-21-989C>A) c.96+157C>A (n.96+157C>A) n.400C>A c.27C>A (p.Asp9Glu) | ClinVar dbSNP gnomAD v4 |
17 | g.7676226T>A | CA397846724 | TP53 | c.143A>T (p.Asp48Val) c.-21-990A>T (n.-21-990A>T) c.96+156A>T (n.96+156A>T) n.399A>T c.26A>T (p.Asp9Val) | |
17 | g.7676226T>C | CA397846727 | TP53 | c.143A>G (p.Asp48Gly) c.-21-990A>G (n.-21-990A>G) c.96+156A>G (n.96+156A>G) n.399A>G c.26A>G (p.Asp9Gly) | ClinVar |
17 | g.7676226T>G | CA397846730 | TP53 | c.143A>C (p.Asp48Ala) c.-21-990A>C (n.-21-990A>C) c.96+156A>C (n.96+156A>C) n.399A>C c.26A>C (p.Asp9Ala) | |
17 | g.7676227C>A | CA397846736 | TP53 | c.142G>T (p.Asp48Tyr) c.-21-991G>T (n.-21-991G>T) c.96+155G>T (n.96+155G>T) n.398G>T c.25G>T (p.Asp9Tyr) | dbSNP |
17 | g.7676227C>G | CA397846739 | TP53 | c.142G>C (p.Asp48His) c.-21-991G>C (n.-21-991G>C) c.96+155G>C (n.96+155G>C) n.398G>C c.25G>C (p.Asp9His) | dbSNP |
17 | g.7676227C>T | CA397846743 | TP53 | c.142G>A (p.Asp48Asn) c.-21-991G>A (n.-21-991G>A) c.96+155G>A (n.96+155G>A) n.398G>A c.25G>A (p.Asp9Asn) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676228del | CA645589412 | TP53 | c.142del (p.Asp48ThrfsTer?) c.-21-991del (n.-21-991del) c.96+155del (n.96+155del) n.398del c.25del (p.Asp9ThrfsTer?) | gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676228_7676264del | CA645589413 | TP53 | c.106_142del (p.Pro36ThrfsTer?) c.-21-1027_-21-991del (n.-21-1027_-21-991del) c.96+119_96+155del (n.96+119_96+155del) n.362_398del c.-12_25del | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676228C>A | CA497926038 | TP53 | c.141G>T (p.Pro47=) c.-21-992G>T (n.-21-992G>T) c.96+154G>T (n.96+154G>T) n.397G>T c.24G>T (p.Pro8=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7676228C= | CA2245935518 | TP53 | c.141G= (p.Pro47=) c.-21-992G= (n.-21-992G=) c.96+154G= (n.96+154G=) n.397G= c.24G= (p.Pro8=) | |
17 | g.7676228C>G | CA497926039 | TP53 | c.141G>C (p.Pro47=) c.-21-992G>C (n.-21-992G>C) c.96+154G>C (n.96+154G>C) n.397G>C c.24G>C (p.Pro8=) | |
17 | g.7676228C>T | CA000054 | TP53 | c.141G>A (p.Pro47=) c.-21-992G>A (n.-21-992G>A) c.96+154G>A (n.96+154G>A) n.397G>A c.24G>A (p.Pro8=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7676228_7676229delinsCG | CA2245935520 | TP53 | c.140_141delinsCG (p.Pro47=) c.-21-993_-21-992delinsCG (n.-21-993_-21-992delinsCG) c.96+153_96+154delinsCG (n.96+153_96+154delinsCG) n.396_397delinsCG c.23_24delinsCG (p.Pro8=) | |
17 | g.7676228_7676231delinsCGGG | CA2245935522 | TP53 | c.138_141delinsCCCG (p.Ser46=) c.-21-995_-21-992delinsCCCG (n.-21-995_-21-992delinsCCCG) c.96+151_96+154delinsCCCG (n.96+151_96+154delinsCCCG) n.394_397delinsCCCG c.21_24delinsCCCG (p.Ser7=) | |
17 | g.7676229G>A | CA397846754 | TP53 | c.140C>T (p.Pro47Leu) c.-21-993C>T (n.-21-993C>T) c.96+153C>T (n.96+153C>T) n.396C>T c.23C>T (p.Pro8Leu) | dbSNP COSMIC |
17 | g.7676229G>C | CA397846755 | TP53 | c.140C>G (p.Pro47Arg) c.-21-993C>G (n.-21-993C>G) c.96+153C>G (n.96+153C>G) n.396C>G c.23C>G (p.Pro8Arg) | ClinVar dbSNP |
17 | g.7676229G= | CA2245935547 | TP53 | c.140C= (p.Pro47=) c.-21-993C= (n.-21-993C=) c.96+153C= (n.96+153C=) n.396C= c.23C= (p.Pro8=) | |
17 | g.7676229G>T | CA397846756 | TP53 | c.140C>A (p.Pro47Gln) c.-21-993C>A (n.-21-993C>A) c.96+153C>A (n.96+153C>A) n.396C>A c.23C>A (p.Pro8Gln) | |
17 | g.7676229_7676231delinsC | CA919785524 | TP53 | c.138_140delinsG (p.Pro47GlyfsTer4) c.-21-995_-21-993delinsG (n.-21-995_-21-993delinsG) c.96+151_96+153delinsG (n.96+151_96+153delinsG) n.394_396delinsG c.21_23delinsG (p.Pro8GlyfsTer4) | dbSNP |
17 | g.7676232dup | CA2580095117 | TP53 | c.140dup (p.Asp48GlyfsTer4) c.-21-993dup (n.-21-993dup) c.96+153dup (n.96+153dup) n.396dup c.23dup (p.Asp9GlyfsTer4) | ClinVar dbSNP |
17 | g.7676232del | CA497926040 | TP53 | c.140del (p.Pro47ArgfsTer?) c.-21-993del (n.-21-993del) c.96+153del (n.96+153del) n.396del c.23del (p.Pro8ArgfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676231_7676232del | CA645589414 | TP53 | c.139_140del (p.Pro47GlyfsTer4) c.-21-994_-21-993del (n.-21-994_-21-993del) c.96+152_96+153del (n.96+152_96+153del) n.395_396del c.22_23del (p.Pro8GlyfsTer4) | COSMIC |
17 | g.7676230G>A | CA000053 | TP53 | c.139C>T (p.Pro47Ser) c.-21-994C>T (n.-21-994C>T) c.96+152C>T (n.96+152C>T) n.395C>T c.22C>T (p.Pro8Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676230G>C | CA397846769 | TP53 | c.139C>G (p.Pro47Ala) c.-21-994C>G (n.-21-994C>G) c.96+152C>G (n.96+152C>G) n.395C>G c.22C>G (p.Pro8Ala) | ClinVar dbSNP |
17 | g.7676230G= | CA2245935554 | TP53 | c.139C= (p.Pro47=) c.-21-994C= (n.-21-994C=) c.96+152C= (n.96+152C=) n.395C= c.22C= (p.Pro8=) | |
17 | g.7676230G>T | CA16615959 | TP53 | c.139C>A (p.Pro47Thr) c.-21-994C>A (n.-21-994C>A) c.96+152C>A (n.96+152C>A) n.395C>A c.22C>A (p.Pro8Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676231G>A | CA497926043 | TP53 | c.138C>T (p.Ser46=) c.-21-995C>T (n.-21-995C>T) c.96+151C>T (n.96+151C>T) n.394C>T c.21C>T (p.Ser7=) | ClinVar dbSNP |
17 | g.7676231G>C | CA497926042 | TP53 | c.138C>G (p.Ser46=) c.-21-995C>G (n.-21-995C>G) c.96+151C>G (n.96+151C>G) n.394C>G c.21C>G (p.Ser7=) | dbSNP |
17 | g.7676231G>T | CA497926041 | TP53 | c.138C>A (p.Ser46=) c.-21-995C>A (n.-21-995C>A) c.96+151C>A (n.96+151C>A) n.394C>A c.21C>A (p.Ser7=) | dbSNP |
17 | g.7676231_7676232delinsGG | CA2245935564 | TP53 | c.137_138delinsCC (p.Ser46=) c.-21-996_-21-995delinsCC (n.-21-996_-21-995delinsCC) c.96+150_96+151delinsCC (n.96+150_96+151delinsCC) n.393_394delinsCC c.20_21delinsCC (p.Ser7=) | |
17 | g.7676232G>A | CA397846782 | TP53 | c.137C>T (p.Ser46Phe) c.-21-996C>T (n.-21-996C>T) c.96+150C>T (n.96+150C>T) n.393C>T c.20C>T (p.Ser7Phe) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676232G>C | CA397846788 | TP53 | c.137C>G (p.Ser46Cys) c.-21-996C>G (n.-21-996C>G) c.96+150C>G (n.96+150C>G) n.393C>G c.20C>G (p.Ser7Cys) | dbSNP |
17 | g.7676232G= | CA2245935586 | TP53 | c.137C= (p.Ser46=) c.-21-996C= (n.-21-996C=) c.96+150C= (n.96+150C=) n.393C= c.20C= (p.Ser7=) | |
17 | g.7676232G>T | CA397846789 | TP53 | c.137C>A (p.Ser46Tyr) c.-21-996C>A (n.-21-996C>A) c.96+150C>A (n.96+150C>A) n.393C>A c.20C>A (p.Ser7Tyr) | ClinVar dbSNP |
17 | g.7676232delinsAC | CA169169 | TP53 | c.137delinsGT (p.Ser46CysfsTer6) c.-21-996delinsGT (n.-21-996delinsGT) c.96+150delinsGT (n.96+150delinsGT) n.393delinsGT c.20delinsGT (p.Ser7CysfsTer6) | ClinVar dbSNP |
17 | g.7676233del | CA645589415 | TP53 | c.136del (p.Ser46ProfsTer?) c.-21-997del (n.-21-997del) c.96+149del (n.96+149del) n.392del c.19del (p.Ser7ProfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676233A= | CA2245935605 | TP53 | c.136T= (p.Ser46=) c.-21-997T= (n.-21-997T=) c.96+149T= (n.96+149T=) n.392T= c.19T= (p.Ser7=) | |
17 | g.7676233A>C | CA397846790 | TP53 | c.136T>G (p.Ser46Ala) c.-21-997T>G (n.-21-997T>G) c.96+149T>G (n.96+149T>G) n.392T>G c.19T>G (p.Ser7Ala) | dbSNP |
17 | g.7676233A>G | CA10580961 | TP53 | c.136T>C (p.Ser46Pro) c.-21-997T>C (n.-21-997T>C) c.96+149T>C (n.96+149T>C) n.392T>C c.19T>C (p.Ser7Pro) | ClinVar dbSNP COSMIC |
17 | g.7676233A>T | CA397846799 | TP53 | c.136T>A (p.Ser46Thr) c.-21-997T>A (n.-21-997T>A) c.96+149T>A (n.96+149T>A) n.392T>A c.19T>A (p.Ser7Thr) | dbSNP |
17 | g.7676234del | CA891842290 | TP53 | c.135del (p.Ser46ProfsTer?) c.-21-998del (n.-21-998del) c.96+148del (n.96+148del) n.391del c.18del (p.Ser7ProfsTer?) | |
17 | g.7676234C>A | CA497926044 | TP53 | c.135G>T (p.Leu45=) c.-21-998G>T (n.-21-998G>T) c.96+148G>T (n.96+148G>T) n.391G>T c.18G>T (p.Leu6=) | |
17 | g.7676234C= | CA2245935612 | TP53 | c.135G= (p.Leu45=) c.-21-998G= (n.-21-998G=) c.96+148G= (n.96+148G=) n.391G= c.18G= (p.Leu6=) | |
17 | g.7676234C>G | CA497926045 | TP53 | c.135G>C (p.Leu45=) c.-21-998G>C (n.-21-998G>C) c.96+148G>C (n.96+148G>C) n.391G>C c.18G>C (p.Leu6=) | dbSNP |
17 | g.7676234C>T | CA16615734 | TP53 | c.135G>A (p.Leu45=) c.-21-998G>A (n.-21-998G>A) c.96+148G>A (n.96+148G>A) n.391G>A c.18G>A (p.Leu6=) | ClinVar dbSNP |
17 | g.7676235A= | CA2245935635 | TP53 | c.134T= (p.Leu45=) c.-21-999T= (n.-21-999T=) c.96+147T= (n.96+147T=) n.390T= c.17T= (p.Leu6=) | |
17 | g.7676235A>C | CA397846812 | TP53 | c.134T>G (p.Leu45Arg) c.-21-999T>G (n.-21-999T>G) c.96+147T>G (n.96+147T>G) n.390T>G c.17T>G (p.Leu6Arg) | |
17 | g.7676235A>G | CA10584594 | TP53 | c.134T>C (p.Leu45Pro) c.-21-999T>C (n.-21-999T>C) c.96+147T>C (n.96+147T>C) n.390T>C c.17T>C (p.Leu6Pro) | ClinVar dbSNP COSMIC |
17 | g.7676235A>T | CA397846819 | TP53 | c.134T>A (p.Leu45Gln) c.-21-999T>A (n.-21-999T>A) c.96+147T>A (n.96+147T>A) n.390T>A c.17T>A (p.Leu6Gln) | dbSNP |
17 | g.7676235dup | CA645589417 | TP53 | c.134dup (p.Ser46ValfsTer6) c.-21-999dup (n.-21-999dup) c.96+147dup (n.96+147dup) n.390dup c.17dup (p.Ser7ValfsTer6) | COSMIC |
17 | g.7676235_7676236del | CA645589416 | TP53 | c.133_134del (p.Leu45ValfsTer6) c.-21-1000_-21-999del (n.-21-1000_-21-999del) c.96+146_96+147del (n.96+146_96+147del) n.389_390del c.16_17del (p.Leu6ValfsTer6) | COSMIC |
17 | g.7676236G>A | CA497926046 | TP53 | c.133C>T (p.Leu45=) c.-21-1000C>T (n.-21-1000C>T) c.96+146C>T (n.96+146C>T) n.389C>T c.16C>T (p.Leu6=) | dbSNP gnomAD v4 |
17 | g.7676236G>C | CA397846833 | TP53 | c.133C>G (p.Leu45Val) c.-21-1000C>G (n.-21-1000C>G) c.96+146C>G (n.96+146C>G) n.389C>G c.16C>G (p.Leu6Val) | ClinVar dbSNP gnomAD v4 |
17 | g.7676236G= | CA2245935647 | TP53 | c.133C= (p.Leu45=) c.-21-1000C= (n.-21-1000C=) c.96+146C= (n.96+146C=) n.389C= c.16C= (p.Leu6=) | |
17 | g.7676236G>T | CA397846837 | TP53 | c.133C>A (p.Leu45Met) c.-21-1000C>A (n.-21-1000C>A) c.96+146C>A (n.96+146C>A) n.389C>A c.16C>A (p.Leu6Met) | |
17 | g.7676237del | CA2579908747 | TP53 | c.132del (p.Met44IlefsTer?) c.-21-1001del (n.-21-1001del) c.96+145del (n.96+145del) n.388del c.15del (p.Met5IlefsTer?) | |
17 | g.7676237C>A | CA397846847 | TP53 | c.132G>T (p.Met44Ile) c.-21-1001G>T (n.-21-1001G>T) c.96+145G>T (n.96+145G>T) n.388G>T c.15G>T (p.Met5Ile) | dbSNP COSMIC |
17 | g.7676237C= | CA2245935656 | TP53 | c.132G= (p.Met44=) c.-21-1001G= (n.-21-1001G=) c.96+145G= (n.96+145G=) n.388G= c.15G= (p.Met5=) | |
17 | g.7676237C>G | CA397846851 | TP53 | c.132G>C (p.Met44Ile) c.-21-1001G>C (n.-21-1001G>C) c.96+145G>C (n.96+145G>C) n.388G>C c.15G>C (p.Met5Ile) | dbSNP |
17 | g.7676237C>T | CA16615713 | TP53 | c.132G>A (p.Met44Ile) c.-21-1001G>A (n.-21-1001G>A) c.96+145G>A (n.96+145G>A) n.388G>A c.15G>A (p.Met5Ile) | ClinVar dbSNP gnomAD v4 |
17 | g.7676237_7676245del | CA2499224980 | TP53 | c.124_132del (p.Asp42_Met44del) c.-21-1009_-21-1001del (n.-21-1009_-21-1001del) c.96+137_96+145del (n.96+137_96+145del) n.380_388del c.7_15del (p.Asp3_Met5del) | ClinVar dbSNP |
17 | g.7676238del | CA497926047 | TP53 | c.131del (p.Met44SerfsTer?) c.-21-1002del (n.-21-1002del) c.96+144del (n.96+144del) n.387del c.14del (p.Met5SerfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676238A= | CA2245935677 | TP53 | c.131T= (p.Met44=) c.-21-1002T= (n.-21-1002T=) c.96+144T= (n.96+144T=) n.387T= c.14T= (p.Met5=) | |
17 | g.7676238A>C | CA397846861 | TP53 | c.131T>G (p.Met44Arg) c.-21-1002T>G (n.-21-1002T>G) c.96+144T>G (n.96+144T>G) n.387T>G c.14T>G (p.Met5Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676238A>G | CA397846863 | TP53 | c.131T>C (p.Met44Thr) c.-21-1002T>C (n.-21-1002T>C) c.96+144T>C (n.96+144T>C) n.387T>C c.14T>C (p.Met5Thr) | ClinVar dbSNP COSMIC |
17 | g.7676238A>T | CA397846867 | TP53 | c.131T>A (p.Met44Lys) c.-21-1002T>A (n.-21-1002T>A) c.96+144T>A (n.96+144T>A) n.387T>A c.14T>A (p.Met5Lys) | ClinVar dbSNP |
17 | g.7676242_7676246del | CA645589419 | TP53 | c.127_131del (p.Leu43AlafsTer7) c.-21-1006_-21-1002del (n.-21-1006_-21-1002del) c.96+140_96+144del (n.96+140_96+144del) n.383_387del c.10_14del (p.Leu4AlafsTer7) | COSMIC |
17 | g.7676239_7676260del | CA645589418 | TP53 | c.110_131del (p.Ser37CysfsTer?) c.-21-1023_-21-1002del (n.-21-1023_-21-1002del) c.96+123_96+144del (n.96+123_96+144del) n.366_387del c.-8_14del | COSMIC |
17 | g.7676239del | CA497926048 | TP53 | c.130del (p.Met44CysfsTer?) c.-21-1003del (n.-21-1003del) c.96+143del (n.96+143del) n.386del c.13del (p.Met5CysfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676239T>A | CA397846872 | TP53 | c.130A>T (p.Met44Leu) c.-21-1003A>T (n.-21-1003A>T) c.96+143A>T (n.96+143A>T) n.386A>T c.13A>T (p.Met5Leu) | dbSNP |
17 | g.7676239T>C | CA397846879 | TP53 | c.130A>G (p.Met44Val) c.-21-1003A>G (n.-21-1003A>G) c.96+143A>G (n.96+143A>G) n.386A>G c.13A>G (p.Met5Val) | dbSNP COSMIC |
17 | g.7676239T>G | CA397846886 | TP53 | c.130A>C (p.Met44Leu) c.-21-1003A>C (n.-21-1003A>C) c.96+143A>C (n.96+143A>C) n.386A>C c.13A>C (p.Met5Leu) | ClinVar dbSNP gnomAD v4 |
17 | g.7676239_7676278delinsTCAAATCATCCATTGCTTGGGACGGCAAGGGGGACTGTAG | CA2245935693 | TP53 | c.97-6_130delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA c.-21-1042_-21-1003delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA (n.-21-1042_-21-1003delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA) c.96+104_96+143delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA (n.96+104_96+143delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA) n.353-6_386delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA c.-21-6_13delinsCTACAGTCCCCCTTGCCGTCCCAAGCAATGGATGATTTGA | |
17 | g.7676240del | CA645589420 | TP53 | c.129del (p.Met44CysfsTer?) c.-21-1004del (n.-21-1004del) c.96+142del (n.96+142del) n.385del c.12del (p.Met5CysfsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676240C>A | CA397846888 | TP53 | c.129G>T (p.Leu43Phe) c.-21-1004G>T (n.-21-1004G>T) c.96+142G>T (n.96+142G>T) n.385G>T c.12G>T (p.Leu4Phe) | ClinVar dbSNP |
17 | g.7676240C= | CA2245935709 | TP53 | c.129G= (p.Leu43=) c.-21-1004G= (n.-21-1004G=) c.96+142G= (n.96+142G=) n.385G= c.12G= (p.Leu4=) | |
17 | g.7676240C>G | CA003217 | TP53 | c.129G>C (p.Leu43Phe) c.-21-1004G>C (n.-21-1004G>C) c.96+142G>C (n.96+142G>C) n.385G>C c.12G>C (p.Leu4Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7676240C>T | CA497926049 | TP53 | c.129G>A (p.Leu43=) c.-21-1004G>A (n.-21-1004G>A) c.96+142G>A (n.96+142G>A) n.385G>A c.12G>A (p.Leu4=) | ClinVar dbSNP |
17 | g.7676240_7676241delinsCA | CA2245935718 | TP53 | c.128_129delinsTG (p.Leu43=) c.-21-1005_-21-1004delinsTG (n.-21-1005_-21-1004delinsTG) c.96+141_96+142delinsTG (n.96+141_96+142delinsTG) n.384_385delinsTG c.11_12delinsTG (p.Leu4=) | |
17 | g.7676240_7676278del | CA2245935701 | TP53 | c.97-6_129del c.-21-1042_-21-1004del (n.-21-1042_-21-1004del) c.96+104_96+142del (n.96+104_96+142del) n.353-6_385del c.-21-6_12del | ClinVar dbSNP |
17 | g.7676241A= | CA2245935731 | TP53 | c.128T= (p.Leu43=) c.-21-1005T= (n.-21-1005T=) c.96+141T= (n.96+141T=) n.384T= c.11T= (p.Leu4=) | |
17 | g.7676241A>C | CA397846896 | TP53 | c.128T>G (p.Leu43Trp) c.-21-1005T>G (n.-21-1005T>G) c.96+141T>G (n.96+141T>G) n.384T>G c.11T>G (p.Leu4Trp) | |
17 | g.7676241A>G | CA397846897 | TP53 | c.128T>C (p.Leu43Ser) c.-21-1005T>C (n.-21-1005T>C) c.96+141T>C (n.96+141T>C) n.384T>C c.11T>C (p.Leu4Ser) | |
17 | g.7676241A>T | CA397846898 | TP53 | c.128T>A (p.Leu43Ter) c.-21-1005T>A (n.-21-1005T>A) c.96+141T>A (n.96+141T>A) n.384T>A c.11T>A (p.Leu4Ter) | ClinVar dbSNP |
17 | g.7676243del | CA497926050 | TP53 | c.128del (p.Leu43Ter) c.-21-1005del (n.-21-1005del) c.96+141del (n.96+141del) n.384del c.11del (p.Leu4Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC |
17 | g.7676241_7676242insC | CA645589421 | TP53 | c.127_128insG (p.Leu43CysfsTer9) c.-21-1006_-21-1005insG (n.-21-1006_-21-1005insG) c.96+140_96+141insG (n.96+140_96+141insG) n.383_384insG c.10_11insG (p.Leu4CysfsTer9) | COSMIC COSMIC COSMIC |
17 | g.7676242A= | CA2245935744 | TP53 | c.127T= (p.Leu43=) c.-21-1006T= (n.-21-1006T=) c.96+140T= (n.96+140T=) n.383T= c.10T= (p.Leu4=) | |
17 | g.7676242A>C | CA397846899 | TP53 | c.127T>G (p.Leu43Val) c.-21-1006T>G (n.-21-1006T>G) c.96+140T>G (n.96+140T>G) n.383T>G c.10T>G (p.Leu4Val) | ClinVar |
17 | g.7676242A>G | CA497926051 | TP53 | c.127T>C (p.Leu43=) c.-21-1006T>C (n.-21-1006T>C) c.96+140T>C (n.96+140T>C) n.383T>C c.10T>C (p.Leu4=) | ClinVar |
17 | g.7676242A>T | CA397846903 | TP53 | c.127T>A (p.Leu43Met) c.-21-1006T>A (n.-21-1006T>A) c.96+140T>A (n.96+140T>A) n.383T>A c.10T>A (p.Leu4Met) | ClinVar dbSNP |
17 | g.7676242_7676243insG | CA497926052 | TP53 | c.126_127insC (p.Met44AspfsTer8) c.-21-1007_-21-1006insC (n.-21-1007_-21-1006insC) c.96+139_96+140insC (n.96+139_96+140insC) n.382_383insC c.9_10insC (p.Met5AspfsTer8) | |
17 | g.7676243A= | CA2245935753 | TP53 | c.126T= (p.Asp42=) c.-21-1007T= (n.-21-1007T=) c.96+139T= (n.96+139T=) n.382T= c.9T= (p.Asp3=) | |
17 | g.7676243A>C | CA397846909 | TP53 | c.126T>G (p.Asp42Glu) c.-21-1007T>G (n.-21-1007T>G) c.96+139T>G (n.96+139T>G) n.382T>G c.9T>G (p.Asp3Glu) | |
17 | g.7676243A>G | CA497926053 | TP53 | c.126T>C (p.Asp42=) c.-21-1007T>C (n.-21-1007T>C) c.96+139T>C (n.96+139T>C) n.382T>C c.9T>C (p.Asp3=) | ClinVar dbSNP |
17 | g.7676243A>T | CA397846913 | TP53 | c.126T>A (p.Asp42Glu) c.-21-1007T>A (n.-21-1007T>A) c.96+139T>A (n.96+139T>A) n.382T>A c.9T>A (p.Asp3Glu) | dbSNP |
17 | g.7676244T>A | CA397846919 | TP53 | c.125A>T (p.Asp42Val) c.-21-1008A>T (n.-21-1008A>T) c.96+138A>T (n.96+138A>T) n.381A>T c.8A>T (p.Asp3Val) | dbSNP |
17 | g.7676244T>C | CA000052 | TP53 | c.125A>G (p.Asp42Gly) c.-21-1008A>G (n.-21-1008A>G) c.96+138A>G (n.96+138A>G) n.381A>G c.8A>G (p.Asp3Gly) | ClinVar dbSNP |
17 | g.7676244T>G | CA397846936 | TP53 | c.125A>C (p.Asp42Ala) c.-21-1008A>C (n.-21-1008A>C) c.96+138A>C (n.96+138A>C) n.381A>C c.8A>C (p.Asp3Ala) | dbSNP |
17 | g.7676244T= | CA2245935765 | TP53 | c.125A= (p.Asp42=) c.-21-1008A= (n.-21-1008A=) c.96+138A= (n.96+138A=) n.381A= c.8A= (p.Asp3=) | |
17 | g.7676245C>A | CA397846948 | TP53 | c.124G>T (p.Asp42Tyr) c.-21-1009G>T (n.-21-1009G>T) c.96+137G>T (n.96+137G>T) n.380G>T c.7G>T (p.Asp3Tyr) | dbSNP COSMIC |
17 | g.7676245C= | CA2245935777 | TP53 | c.124G= (p.Asp42=) c.-21-1009G= (n.-21-1009G=) c.96+137G= (n.96+137G=) n.380G= c.7G= (p.Asp3=) | |
17 | g.7676245C>G | CA397846962 | TP53 | c.124G>C (p.Asp42His) c.-21-1009G>C (n.-21-1009G>C) c.96+137G>C (n.96+137G>C) n.380G>C c.7G>C (p.Asp3His) | dbSNP |
17 | g.7676245C>T | CA003226 | TP53 | c.124G>A (p.Asp42Asn) c.-21-1009G>A (n.-21-1009G>A) c.96+137G>A (n.96+137G>A) n.380G>A c.7G>A (p.Asp3Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7676248_7676251dup | CA658656662 | TP53 | c.121_124dup (p.Asp42GlyfsTer2) c.-21-1012_-21-1009dup (n.-21-1012_-21-1009dup) c.96+134_96+137dup (n.96+134_96+137dup) n.377_380dup c.4_7dup (p.Asp3GlyfsTer2) | ClinVar dbSNP |
17 | g.7676246_7676261del | CA2573154651 | TP53 | c.109_124del (p.Ser37IlefsTer2) c.-21-1024_-21-1009del (n.-21-1024_-21-1009del) c.96+122_96+137del (n.96+122_96+137del) n.365_380del c.-9_7del | ClinVar dbSNP |
17 | g.7676246A= | CA2245935784 | TP53 | c.123T= (p.Asp41=) c.-21-1010T= (n.-21-1010T=) c.96+136T= (n.96+136T=) n.379T= c.6T= (p.Asp2=) | |
17 | g.7676246A>C | CA397846981 | TP53 | c.123T>G (p.Asp41Glu) c.-21-1010T>G (n.-21-1010T>G) c.96+136T>G (n.96+136T>G) n.379T>G c.6T>G (p.Asp2Glu) | dbSNP |
17 | g.7676246A>G | CA000051 | TP53 | c.123T>C (p.Asp41=) c.-21-1010T>C (n.-21-1010T>C) c.96+136T>C (n.96+136T>C) n.379T>C c.6T>C (p.Asp2=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7676246A>T | CA397846984 | TP53 | c.123T>A (p.Asp41Glu) c.-21-1010T>A (n.-21-1010T>A) c.96+136T>A (n.96+136T>A) n.379T>A c.6T>A (p.Asp2Glu) | dbSNP |
17 | g.7676247T>A | CA397847016 | TP53 | c.122A>T (p.Asp41Val) c.-21-1011A>T (n.-21-1011A>T) c.96+135A>T (n.96+135A>T) n.378A>T c.5A>T (p.Asp2Val) | |
17 | g.7676247T>C | CA397847012 | TP53 | c.122A>G (p.Asp41Gly) c.-21-1011A>G (n.-21-1011A>G) c.96+135A>G (n.96+135A>G) n.378A>G c.5A>G (p.Asp2Gly) | ClinVar dbSNP |
17 | g.7676247T>G | CA397846990 | TP53 | c.122A>C (p.Asp41Ala) c.-21-1011A>C (n.-21-1011A>C) c.96+135A>C (n.96+135A>C) n.378A>C c.5A>C (p.Asp2Ala) | |
17 | g.7676247T= | CA2245935792 | TP53 | c.122A= (p.Asp41=) c.-21-1011A= (n.-21-1011A=) c.96+135A= (n.96+135A=) n.378A= c.5A= (p.Asp2=) | |
17 | g.7676248C>A | CA397847019 | TP53 | c.121G>T (p.Asp41Tyr) c.-21-1012G>T (n.-21-1012G>T) c.96+134G>T (n.96+134G>T) n.377G>T c.4G>T (p.Asp2Tyr) | dbSNP |
17 | g.7676248C= | CA2245935806 | TP53 | c.121G= (p.Asp41=) c.-21-1012G= (n.-21-1012G=) c.96+134G= (n.96+134G=) n.377G= c.4G= (p.Asp2=) | |
17 | g.7676248C>G | CA397847037 | TP53 | c.121G>C (p.Asp41His) c.-21-1012G>C (n.-21-1012G>C) c.96+134G>C (n.96+134G>C) n.377G>C c.4G>C (p.Asp2His) | dbSNP |
17 | g.7676248C>T | CA397847025 | TP53 | c.121G>A (p.Asp41Asn) c.-21-1012G>A (n.-21-1012G>A) c.96+134G>A (n.96+134G>A) n.377G>A c.4G>A (p.Asp2Asn) | ClinVar dbSNP |
17 | g.7676249del | CA497926054 | TP53 | c.121del (p.Asp41MetfsTer3) c.-21-1012del (n.-21-1012del) c.96+134del (n.96+134del) n.377del c.4del (p.Asp2MetfsTer3) | ClinVar COSMIC |
17 | g.7676249C>A | CA397847042 | TP53 | c.120G>T (p.Met40Ile) c.-21-1013G>T (n.-21-1013G>T) c.96+133G>T (n.96+133G>T) n.376G>T c.3G>T (p.Met1Ile) | dbSNP |
17 | g.7676249C>G | CA397847045 | TP53 | c.120G>C (p.Met40Ile) c.-21-1013G>C (n.-21-1013G>C) c.96+133G>C (n.96+133G>C) n.376G>C c.3G>C (p.Met1Ile) | dbSNP |
17 | g.7676249C>T | CA397847050 | TP53 | c.120G>A (p.Met40Ile) c.-21-1013G>A (n.-21-1013G>A) c.96+133G>A (n.96+133G>A) n.376G>A c.3G>A (p.Met1Ile) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |