All screenings for gene FANCM

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AscendingScreening ID     

Individual ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Variants found     

Owner     
0000002197 00001911 DNA SEQ Fundación para el Progreso de la Medicina Analisis de variantes: ATM (NM:000051):c.790del (p.Tyr264fs), FANCM (NM_020937.4): c.997C>T (p.Gln333Ter) 28-sep-2021 Known familial mutation 1 Norma Rossi - Fundacion Para el Progreso de la Medicina
0000010185 00005974 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 15-apr-2026 Multigenetic panel 3 Luisina Bruno-Instituto Fleming
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