All screenings for gene APC

45 entries on 1 page. Showing entries 1 - 45.
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Type of test     

Variants found     

Owner     
0000000137 00000126 DNA SEQ-NG;z-score-CNV Héritas - 03-may-2017 Specific pathology 10 Alejandra Mampel-Hospital Universitario de Mendoza
0000000172 00000153 DNA SEQ-NG Genia - 09-feb-2017 Specific pathology 10 Maria Laura Gonzalez-Hospital Italiano
0000000173 00000153 DNA MLPA Genia - 09-feb-2017 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000000179 00000159 DNA SEQ-NG CEMIC - 04-jul-2016 Specific pathology 9 Maria Laura Gonzalez-Hospital Italiano
0000000180 00000159 DNA MLPA CEMIC - 01-nov-2017 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000000214 00000188 DNA SEQ-NG CEMIC - 15-mar-2017 Specific pathology 13 Alejandra Mampel-COIR
0000000235 00000208 DNA SEQ-NG CEMIC - 22-mar-2017 Specific pathology 10 Pablo Kalfayan-CEMIC
0000000248 00000153 DNA MLPA Genia - 30-jun-2017 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000000250 00000218 DNA SEQ-NG CEMIC - 09-may-2017 Specific pathology 11 Maria Laura Gonzalez-Hospital Italiano
0000000333 00000284 DNA SEQ-NG Genia - 06-sep-2017 Specific pathology 10 Maria Laura Gonzalez-Hospital Italiano
0000000585 00000517 DNA SEQ-NG;z-score-CNV Héritas - 20-mar-2018 Specific pathology - Erika Stegmayer-Hospital Zenon Santillan
0000000812 00000694 DNA SEQ Centogene - 30-jul-2018 Known familial mutation - Maria Laura Gonzalez-Hospital Italiano
0000000848 00000728 DNA SEQ Hospital Privado Centro Médico de Córdoba - 07-jan-2019 Known familial mutation - Lina Nuñez-Private Practice
0000001068 00000897 DNA z-score-CNV Héritas - 03-mar-2018 Multigenetic panel - Laura Vargas Roig-IMBECU
0000001079 00000901 DNA z-score-CNV Héritas - 16-may-2018 Multigenetic panel - Laura Vargas Roig-IMBECU
0000001220 00001018 DNA SEQ-NG Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 05-dec-2018 Specific pathology 10 Maria Laura Gonzalez-Hospital Italiano
0000001221 00001018 DNA MLPA Dasa Genómica - Genia;INVITAE - 05-dec-2018 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000001223 00001019 DNA SEQ-NG Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 16-apr-2019 Specific pathology 8 Maria Laura Gonzalez-Hospital Italiano
0000001224 00001019 DNA MLPA Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 16-apr-2019 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000001331 00001115 DNA MLPA Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 22-mar-2019 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000001332 00001115 DNA SEQ-NG Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 22-mar-2019 Specific pathology 8 Maria Laura Gonzalez-Hospital Italiano
0000001335 00001017 DNA MLPA Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 03-apr-2019 Specific pathology - Maria Laura Gonzalez-Hospital Italiano
0000001336 00001017 DNA SEQ-NG Dasa Genómica - Genia;Hospital Italiano de Buenos Aires - 03-apr-2019 Specific pathology 7 Maria Laura Gonzalez-Hospital Italiano
0000001350 00001126 DNA SEQ CEMIC - 31-jul-2019 Known familial mutation - Lina Nuñez-Private Practice
0000001452 00001216 DNA CNV;SEQ-NG Hospital Privado Centro Médico de Córdoba Panel Tiroides 05-dec-2019 Multigenetic panel - Claudia Martin-Hospital de Córdoba
0000001615 00001366 DNA SEQ Hospital Privado Centro Médico de Córdoba - 18-mar-2020 Known familial mutation - Claudia Martin-Hospital de Córdoba
0000001625 00001376 DNA SEQ Hospital Privado Centro Médico de Córdoba - 18-mar-2020 Known familial mutation 1 Claudia Martin-Hospital de Córdoba
0000001756 00001488 DNA SEQ-NG CEMIC - 24-aug-2020 Specific pathology 7 Maria Laura Gonzalez-Hospital Italiano
0000002006 00001727 DNA SEQ-NG Myriad Genetics NGS de APC y MUTYH 07-feb-2019 Specific pathology 1 Marcela Lopez - Instituto Donna
0000002014 00001735 DNA SEQ CIBIC Sanger APC 05-feb-2019 Known familial mutation 1 Marcela Lopez-CEMAFE
0000002015 00001736 DNA SEQ CIBIC Sanger APC 05-feb-2019 Known familial mutation 1 Marcela Lopez-CEMAFE
0000002016 00001737 DNA SEQ-NG CIBIC/Héritas Panel Polipomatosis adenomatosa familiar (5 genes) APC, BMPRA1, MUTYH, PTEN, SMAD4 01-oct-2018 Multigenetic panel 1 Marcela Lopez-CEMAFE
0000002017 00001738 DNA SEQ CIBIC Sanger APC 24-oct-2020 Known familial mutation 1 Marcela Lopez-CEMAFE
0000002020 00001741 DNA SEQ-NG CIBIC/Héritas Panel cáncer de colon hereditario Héritas (14 genes) APC,ATM,BMPR1A,CHEK2, EPCAM,MLH1,MSH2,MSH6,MUTYH,PMS2,PTEN,SMAD4,STK11,TP53 26-jun-2019 Multigenetic panel 1 Marcela Lopez-CEMAFE
0000002252 00001965 DNA SEQ-NG Genia Secuenciacion por NGS de genes asociados a Adenopoliposis Colónica Familiar (PAF) APC, MUTYH 17-feb-2022 Specific pathology 1 Pablo Kalfayan-Hospital Italiano
0000002258 00001971 DNA SEQ-NG PRICAI-Primer Centro Argentino de Inmunogenética-Fundación Favaloro Panel NGS para Poliposis Adenomatosa Familiar (mutaciones puntuales) (10 genes) APC, AXIN2, BMPR1A, GREM1, MSH, MUTYH, PTEN, POLD1, POLE, SMAD4 01-apr-2022 Multigenetic panel 1 Maria Laura Gonzalez-Hospital Italiano
0000002529 00002236 DNA SEQ-NG Domeq&Lafage complete gene sequencing: MLH1, MSH2, MSH6, PMS2, APC, MUTYH, GREM1, POLE, POLD1, PTEN, NTHL1, STK11 08-10-20 Multigenetic panel - Lina Nuñez-Hospital Alemán
0000002702 00002416 DNA SEQ-NG;CNV Laboratorio Tucumán Hereditary cancer panel (7 genes) APC, MUTYH, POLD1, POLE, PTEN, SMAD4, STK11. 28-apr-2022 Multigenetic panel 1 Erika Stegmayer-CIOC
0000002923 00002600 DNA SEQ Laboratorio NANNI NM_000038.6(APC): c.3080A>G (rs869312784) 25-apr-2023 Known familial mutation 1 Maria Laura Gonzalez-Hospital Italiano
0000002936 00002634 DNA SEQ Hospital Alemán NM_000038.6(APC): c.3920T>A; p.(Ile1307Lys) 06-oct-2023 Known familial mutation - Pablo Kalfayan-Hospital Italiano
0000003252 00002937 DNA SEQ Centro de Educación Médica e Investigaciones Clínicas (CEMIC) - 29-may-2012 Specific pathology 1 Guillermo Alberto-Instituto Fleming
0000010148 00005937 DNA SEQ-NG;CNV CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS ABRAXAST, ACD, AIR, AKT1, APC, ATM, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, CTRC, DDB2, DICER1, DIS3L2, EPCAM, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FH, FLCN, GALNT12, GATA2, GPC3, GREM1, HOXB13, KIF1B, KIT, LZTR1, MAX, MEN1, MET, MITF, MLH1, MRE11A, MSH2, MSH3, MSHE6, MUTYH, NBN, NF1, NF2, NSD1, NTHL1, PALB2, PDGFRA, PHOX2B, PIKSCA, PMS2, POLD1, POLE, POT1, PRKART1A, PTCH1, PTEN, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RB1, RET, RHBDF2, RINT1, RUNX1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SLX4, SMAD4, SMARCA4, SMARCB1, SMARCET1, SPINK1, SPRED1, STK11, SUFU, TERF2IF, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WT1, XPA, XPC, XRCC2 01-apr-2026 Multigenetic panel 5 Guillermo Alberto-Instituto Fleming
0000010163 00005952 DNA SEQ-NG;CNV CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS APC, ATM, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDKN2A, CHEK2, DICER1, EPCAM, FANCC, FANCM, GALNT12, GREM1, HOXB13, MLH1, MRE11A, MSH2, MSH3, MSHE6, MUTYH, NBN, NF1, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD50, RAD51C, RAD51D, RINT1, SMAD4, SMARCA4, STK11, TP53, XRCC2 20-apr-2026 Multigenetic panel 3 Guillermo Alberto-Instituto Fleming
0000010166 00005955 DNA SEQ-NG;CNV CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS APC, ATM, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDKN2A, CHEK2, DICER1, EPCAM, FANCC, FANCM, GALNT12, GREM1, HOXB13, MLH1, MRE11A, MSH2, MSH3, MSHE6, MUTYH, NBN, NF1, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD50, RAD51C, RAD51D, RINT1, SMAD4, SMARCA4, STK11, TP53, XRCC2 27-apr-2026 Multigenetic panel 2 Guillermo Alberto-Instituto Fleming
0000010201 00005990 DNA SEQ-NG;CNV CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS ACD, AIP, AKT1, APC, ATM, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, DICER1, EPCAM, FANCA, FANCC, FANCL, FANCM, FH, FLCN, GALNT12, GREM1, HOXB13, KIT, LZTR1, MAX, MENT, MET, MITF, MLH1, MRE11A, MSH2, MSH3, MSHE6, MUTYH, NBN, NF1, NF2, NTHL1, PALB2, PIK3CA, PMS2, POLD1, POLE, POT1, PTEN, RAD50, RAD51B, RAD51C, RAD51D, RB1, RET, RINT1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, SMARCB1, SPRED1, STK11, TERF2IR, TERT, TMEM127, TP53, TSC1, TSC2, VHL, XRCC2 13-apr-2026 Multigenetic panel 2 Andres Rodriguez-Instituto Fleming
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