| 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 | ClinVar |
| 17 | g.7674960_7675141del | CA913203500 | TP53 | c.472_572del c.76_176del c.193_293del c.451_551del n.728_828del c.355_455del c.-6_95del c.439_539del | |
| 17 | g.7674965_7675432del | CA1139665126 | TP53 | c.376-196_566del c.-21-196_170del c.97-196_287del c.376-217_545del c.-217_170del n.632-196_822del c.259-196_449del c.-298_89del c.341-194_533del | ClinVar |
| 17 | g.7675060_7675112del | CA645588877 | TP53 | c.503_555del (p.His168ArgfsTer23) c.107_159del (p.His36ArgfsTer23) c.224_276del (p.His75ArgfsTer23) c.482_534del (p.His161ArgfsTer23) n.759_811del n.11_63del c.386_438del (p.His129ArgfsTer23) c.26_78del (p.His9ArgfsTer23) c.470_522del (p.His157ArgfsTer23) | COSMIC |
| 17 | g.7675059_7675109del | CA2697552081 | TP53 | c.503_553del (p.His168_Ser185delinsArg) c.107_157del (p.His36_Ser53delinsArg) c.224_274del (p.His75_Ser92delinsArg) c.482_532del (p.His161_Ser178delinsArg) n.759_809del n.11_61del c.386_436del (p.His129_Ser146delinsArg) c.26_76del (p.His9_Ser26delinsArg) c.470_520del (p.His157_Ser174delinsArg) | ClinVar |
| 17 | g.7675080_7675110del | CA645588940 | TP53 | c.502_532del (p.His168ThrfsTer?) c.106_136del (p.His36ThrfsTer?) c.223_253del (p.His75ThrfsTer?) c.481_511del (p.His161ThrfsTer?) n.758_788del n.10_40del c.385_415del (p.His129ThrfsTer?) c.25_55del (p.His9ThrfsTer?) c.469_499del (p.His157ThrfsTer?) | COSMIC |
| 17 | g.7675086_7675145del | CA645588950 | TP53 | c.469_528del (p.Val157_Cys176del) c.73_132del (p.Val25_Cys44del) c.190_249del (p.Val64_Cys83del) c.448_507del (p.Val150_Cys169del) n.725_784del c.352_411del (p.Val118_Cys137del) c.-9_51del c.436_495del (p.Val146_Cys165del) | COSMIC |
| 17 | g.7675089_7675167del | CA645588955 | TP53 | c.445_523del (p.Ser149AlafsTer?) c.49_127del (p.Ser17AlafsTer?) c.166_244del (p.Ser56AlafsTer?) c.424_502del (p.Ser142AlafsTer?) n.701_779del c.328_406del (p.Ser110AlafsTer?) c.-33_46del c.412_490del (p.Ser138AlafsTer?) | COSMIC |
| 17 | g.7675095_7675106del | CA2499224973 | TP53 | c.509_520del (p.Thr170_Val173del) c.113_124del (p.Thr38_Val41del) c.230_241del (p.Thr77_Val80del) c.488_499del (p.Thr163_Val166del) n.765_776del n.17_28del c.392_403del (p.Thr131_Val134del) c.32_43del (p.Thr11_Val14del) c.476_487del (p.Thr159_Val162del) | ClinVar dbSNP |
| 17 | g.7675093_7675161del | CA645588958 | TP53 | c.451_519del (p.Pro151_Val173del) c.55_123del (p.Pro19_Val41del) c.172_240del (p.Pro58_Val80del) c.430_498del (p.Pro144_Val166del) n.707_775del c.334_402del (p.Pro112_Val134del) c.-27_42del c.418_486del (p.Pro140_Val162del) | COSMIC |
| 17 | g.7675099_7675105del | CA645588963 | TP53 | c.508_514del (p.Thr170LeufsTer2) c.112_118del (p.Thr38LeufsTer2) c.229_235del (p.Thr77LeufsTer2) c.487_493del (p.Thr163LeufsTer2) n.764_770del n.16_22del c.391_397del (p.Thr131LeufsTer2) c.31_37del (p.Thr11LeufsTer2) c.475_481del (p.Thr159LeufsTer2) | COSMIC |
| 17 | g.7675102_7675105del | CA658656581 | TP53 | c.509_512del (p.Thr170ArgfsTer3) c.113_116del (p.Thr38ArgfsTer3) c.230_233del (p.Thr77ArgfsTer3) c.488_491del (p.Thr163ArgfsTer3) n.765_768del n.17_20del c.392_395del (p.Thr131ArgfsTer3) c.32_35del (p.Thr11ArgfsTer3) c.476_479del (p.Thr159ArgfsTer3) | ClinVar dbSNP |
| 17 | g.7675102_7675111del | CA645588965 | TP53 | c.502_511del (p.His168ArgfsTer3) c.106_115del (p.His36ArgfsTer3) c.223_232del (p.His75ArgfsTer3) c.481_490del (p.His161ArgfsTer3) n.758_767del n.10_19del c.385_394del (p.His129ArgfsTer3) c.25_34del (p.His9ArgfsTer3) c.469_478del (p.His157ArgfsTer3) | COSMIC |
| 17 | g.7675104_7675110del | CA645588967 | TP53 | c.503_509del (p.His168ArgfsTer4) c.107_113del (p.His36ArgfsTer4) c.224_230del (p.His75ArgfsTer4) c.482_488del (p.His161ArgfsTer4) n.759_765del n.11_17del c.386_392del (p.His129ArgfsTer4) c.26_32del (p.His9ArgfsTer4) c.470_476del (p.His157ArgfsTer4) | COSMIC |
| 17 | g.7675104T>A | CA397841663 | TP53 | c.508A>T (p.Thr170Ser) c.112A>T (p.Thr38Ser) c.229A>T (p.Thr77Ser) c.487A>T (p.Thr163Ser) n.764A>T n.16A>T c.391A>T (p.Thr131Ser) c.31A>T (p.Thr11Ser) c.475A>T (p.Thr159Ser) | COSMIC |
| 17 | g.7675104T>C | CA000244 | TP53 | c.508A>G (p.Thr170Ala) c.112A>G (p.Thr38Ala) c.229A>G (p.Thr77Ala) c.487A>G (p.Thr163Ala) n.764A>G n.16A>G c.391A>G (p.Thr131Ala) c.31A>G (p.Thr11Ala) c.475A>G (p.Thr159Ala) | ClinVar dbSNP COSMIC |
| 17 | g.7675104T>G | CA397841647 | TP53 | c.508A>C (p.Thr170Pro) c.112A>C (p.Thr38Pro) c.229A>C (p.Thr77Pro) c.487A>C (p.Thr163Pro) n.764A>C n.16A>C c.391A>C (p.Thr131Pro) c.31A>C (p.Thr11Pro) c.475A>C (p.Thr159Pro) | COSMIC |
| 17 | g.7675104T= | CA2245956163 | TP53 | c.508A= (p.Thr170=) c.112A= (p.Thr38=) c.229A= (p.Thr77=) c.487A= (p.Thr163=) n.764A= n.16A= c.391A= (p.Thr131=) c.31A= (p.Thr11=) c.475A= (p.Thr159=) | |
| 17 | g.7675105del | CA645588969 | TP53 | c.507del (p.Met169IlefsTer5) c.111del (p.Met37IlefsTer5) c.228del (p.Met76IlefsTer5) c.486del (p.Met162IlefsTer5) n.763del n.15del c.390del (p.Met130IlefsTer5) c.30del (p.Met10IlefsTer5) c.474del (p.Met158IlefsTer5) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675105C>A | CA397841695 | TP53 | c.507G>T (p.Met169Ile) c.111G>T (p.Met37Ile) c.228G>T (p.Met76Ile) c.486G>T (p.Met162Ile) n.763G>T n.15G>T c.390G>T (p.Met130Ile) c.30G>T (p.Met10Ile) c.474G>T (p.Met158Ile) | ClinVar dbSNP COSMIC |
| 17 | g.7675105C= | CA2245956171 | TP53 | c.507G= (p.Met169=) c.111G= (p.Met37=) c.228G= (p.Met76=) c.486G= (p.Met162=) n.763G= n.15G= c.390G= (p.Met130=) c.30G= (p.Met10=) c.474G= (p.Met158=) | |
| 17 | g.7675105C>G | CA397841683 | TP53 | c.507G>C (p.Met169Ile) c.111G>C (p.Met37Ile) c.228G>C (p.Met76Ile) c.486G>C (p.Met162Ile) n.763G>C n.15G>C c.390G>C (p.Met130Ile) c.30G>C (p.Met10Ile) c.474G>C (p.Met158Ile) | dbSNP |
| 17 | g.7675105C>T | CA397841691 | TP53 | c.507G>A (p.Met169Ile) c.111G>A (p.Met37Ile) c.228G>A (p.Met76Ile) c.486G>A (p.Met162Ile) n.763G>A n.15G>A c.390G>A (p.Met130Ile) c.30G>A (p.Met10Ile) c.474G>A (p.Met158Ile) | dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675105_7675109delinsAATGA | CA645588970 | TP53 | c.503_507delinsTCATT (p.His168_Met169delinsLeuIle) c.107_111delinsTCATT (p.His36_Met37delinsLeuIle) c.224_228delinsTCATT (p.His75_Met76delinsLeuIle) c.482_486delinsTCATT (p.His161_Met162delinsLeuIle) n.759_763delinsTCATT n.11_15delinsTCATT c.386_390delinsTCATT (p.His129_Met130delinsLeuIle) c.26_30delinsTCATT (p.His9_Met10delinsLeuIle) c.470_474delinsTCATT (p.His157_Met158delinsLeuIle) | COSMIC |
| 17 | g.7675106_7675120del | CA645588971 | TP53 | c.493_507del (p.Gln165_Met169del) c.97_111del (p.Gln33_Met37del) c.214_228del (p.Gln72_Met76del) c.472_486del (p.Gln158_Met162del) n.749_763del c.376_390del (p.Gln126_Met130del) c.16_30del (p.Gln6_Met10del) c.460_474del (p.Gln154_Met158del) | COSMIC |
| 17 | g.7675106A= | CA2245956180 | TP53 | c.506T= (p.Met169=) c.110T= (p.Met37=) c.227T= (p.Met76=) c.485T= (p.Met162=) n.762T= n.14T= c.389T= (p.Met130=) c.29T= (p.Met10=) c.473T= (p.Met158=) | |
| 17 | g.7675106A>C | CA397841700 | TP53 | c.506T>G (p.Met169Arg) c.110T>G (p.Met37Arg) c.227T>G (p.Met76Arg) c.485T>G (p.Met162Arg) n.762T>G n.14T>G c.389T>G (p.Met130Arg) c.29T>G (p.Met10Arg) c.473T>G (p.Met158Arg) | ClinVar dbSNP |
| 17 | g.7675106A>G | CA397841703 | TP53 | c.506T>C (p.Met169Thr) c.110T>C (p.Met37Thr) c.227T>C (p.Met76Thr) c.485T>C (p.Met162Thr) n.762T>C n.14T>C c.389T>C (p.Met130Thr) c.29T>C (p.Met10Thr) c.473T>C (p.Met158Thr) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675106A>T | CA397841708 | TP53 | c.506T>A (p.Met169Lys) c.110T>A (p.Met37Lys) c.227T>A (p.Met76Lys) c.485T>A (p.Met162Lys) n.762T>A n.14T>A c.389T>A (p.Met130Lys) c.29T>A (p.Met10Lys) c.473T>A (p.Met158Lys) | dbSNP |
| 17 | g.7675106_7675107del | CA2695223090 | TP53 | c.505_506del (p.Met169AspfsTer11) c.109_110del (p.Met37AspfsTer11) c.226_227del (p.Met76AspfsTer11) c.484_485del (p.Met162AspfsTer11) n.761_762del n.13_14del c.388_389del (p.Met130AspfsTer11) c.28_29del (p.Met10AspfsTer11) c.472_473del (p.Met158AspfsTer11) | |
| 17 | g.7675107_7675125del | CA645588972 | TP53 | c.488_506del (p.Tyr163Ter) c.92_110del (p.Tyr31Ter) c.209_227del (p.Tyr70Ter) c.467_485del (p.Tyr156Ter) n.744_762del c.371_389del (p.Tyr124Ter) c.11_29del (p.Tyr4Ter) c.455_473del (p.Tyr152Ter) | COSMIC |
| 17 | g.7675106_7675138del | CA645588973 | TP53 | c.474_506del (p.Ala159_Met169del) c.78_110del (p.Ala27_Met37del) c.195_227del (p.Ala66_Met76del) c.453_485del (p.Ala152_Met162del) n.730_762del c.357_389del (p.Ala120_Met130del) c.-4_29del c.441_473del (p.Ala148_Met158del) | COSMIC |
| 17 | g.7675107T>A | CA397841723 | TP53 | c.505A>T (p.Met169Leu) c.109A>T (p.Met37Leu) c.226A>T (p.Met76Leu) c.484A>T (p.Met162Leu) n.761A>T n.13A>T c.388A>T (p.Met130Leu) c.28A>T (p.Met10Leu) c.472A>T (p.Met158Leu) | ClinVar dbSNP |
| 17 | g.7675107T>C | CA397841719 | TP53 | c.505A>G (p.Met169Val) c.109A>G (p.Met37Val) c.226A>G (p.Met76Val) c.484A>G (p.Met162Val) n.761A>G n.13A>G c.388A>G (p.Met130Val) c.28A>G (p.Met10Val) c.472A>G (p.Met158Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 17 | g.7675107T>G | CA397841715 | TP53 | c.505A>C (p.Met169Leu) c.109A>C (p.Met37Leu) c.226A>C (p.Met76Leu) c.484A>C (p.Met162Leu) n.761A>C n.13A>C c.388A>C (p.Met130Leu) c.28A>C (p.Met10Leu) c.472A>C (p.Met158Leu) | |
| 17 | g.7675107T= | CA2245956188 | TP53 | c.505A= (p.Met169=) c.109A= (p.Met37=) c.226A= (p.Met76=) c.484A= (p.Met162=) n.761A= n.13A= c.388A= (p.Met130=) c.28A= (p.Met10=) c.472A= (p.Met158=) | |
| 17 | g.7675111_7675115del | CA645588974 | TP53 | c.501_505del (p.Gln167HisfsTer12) c.105_109del (p.Gln35HisfsTer12) c.222_226del (p.Gln74HisfsTer12) c.480_484del (p.Gln160HisfsTer12) n.757_761del n.9_13del c.384_388del (p.Gln128HisfsTer12) c.24_28del (p.Gln8HisfsTer12) c.468_472del (p.Gln156HisfsTer12) | gnomAD v4 COSMIC |
| 17 | g.7675108del | CA497925609 | TP53 | c.504del (p.His168GlnfsTer2) c.108del (p.His36GlnfsTer2) c.225del (p.His75GlnfsTer2) c.483del (p.His161GlnfsTer2) n.760del n.12del c.387del (p.His129GlnfsTer2) c.27del (p.His9GlnfsTer2) c.471del (p.His157GlnfsTer2) | COSMIC |
| 17 | g.7675108G>A | CA002473 | TP53 | c.504C>T (p.His168=) c.108C>T (p.His36=) c.225C>T (p.His75=) c.483C>T (p.His161=) n.760C>T n.12C>T c.387C>T (p.His129=) c.27C>T (p.His9=) c.471C>T (p.His157=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 17 | g.7675108G>C | CA397841738 | TP53 | c.504C>G (p.His168Gln) c.108C>G (p.His36Gln) c.225C>G (p.His75Gln) c.483C>G (p.His161Gln) n.760C>G n.12C>G c.387C>G (p.His129Gln) c.27C>G (p.His9Gln) c.471C>G (p.His157Gln) | ClinVar dbSNP |
| 17 | g.7675108G= | CA2245956196 | TP53 | c.504C= (p.His168=) c.108C= (p.His36=) c.225C= (p.His75=) c.483C= (p.His161=) n.760C= n.12C= c.387C= (p.His129=) c.27C= (p.His9=) c.471C= (p.His157=) | |
| 17 | g.7675108G>T | CA397841741 | TP53 | c.504C>A (p.His168Gln) c.108C>A (p.His36Gln) c.225C>A (p.His75Gln) c.483C>A (p.His161Gln) n.760C>A n.12C>A c.387C>A (p.His129Gln) c.27C>A (p.His9Gln) c.471C>A (p.His157Gln) | COSMIC |
| 17 | g.7675108_7675117delinsGTGCTGTGAC | CA2245956197 | TP53 | c.495_504delinsGTCACAGCAC (p.Gln165=) c.99_108delinsGTCACAGCAC (p.Gln33=) c.216_225delinsGTCACAGCAC (p.Gln72=) c.474_483delinsGTCACAGCAC (p.Gln158=) n.751_760delinsGTCACAGCAC n.3_12delinsGTCACAGCAC c.378_387delinsGTCACAGCAC (p.Gln126=) c.18_27delinsGTCACAGCAC (p.Gln6=) c.462_471delinsGTCACAGCAC (p.Gln154=) | |
| 17 | g.7675109del | CA497925610 | TP53 | c.503del (p.His168ProfsTer2) c.107del (p.His36ProfsTer2) c.224del (p.His75ProfsTer2) c.482del (p.His161ProfsTer2) n.759del n.11del c.386del (p.His129ProfsTer2) c.26del (p.His9ProfsTer2) c.470del (p.His157ProfsTer2) | COSMIC |
| 17 | g.7675109T>A | CA397841747 | TP53 | c.503A>T (p.His168Leu) c.107A>T (p.His36Leu) c.224A>T (p.His75Leu) c.482A>T (p.His161Leu) n.759A>T n.11A>T c.386A>T (p.His129Leu) c.26A>T (p.His9Leu) c.470A>T (p.His157Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675109T>C | CA287488569 | TP53 | c.503A>G (p.His168Arg) c.107A>G (p.His36Arg) c.224A>G (p.His75Arg) c.482A>G (p.His161Arg) n.759A>G n.11A>G c.386A>G (p.His129Arg) c.26A>G (p.His9Arg) c.470A>G (p.His157Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675109T>G | CA397841765 | TP53 | c.503A>C (p.His168Pro) c.107A>C (p.His36Pro) c.224A>C (p.His75Pro) c.482A>C (p.His161Pro) n.759A>C n.11A>C c.386A>C (p.His129Pro) c.26A>C (p.His9Pro) c.470A>C (p.His157Pro) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675109T= | CA2245956211 | TP53 | c.503A= (p.His168=) c.107A= (p.His36=) c.224A= (p.His75=) c.482A= (p.His161=) n.759A= n.11A= c.386A= (p.His129=) c.26A= (p.His9=) c.470A= (p.His157=) |