NOTCH1 c.4978_4980delinsTGT ;(p.G1660C)

Variant ID: 9-139399163-CCC-ACA

NM_017617.3(NOTCH1):c.4978_4980delinsTGT;(p.G1660C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive Genomic Profile of Heterogeneous Long Follow-Up Triple-Negative Breast Cancer and Its Clinical Characteristics Shows DNA Repair Deficiency Has Better Prognostic.

Genes
Rojas-Jiménez, Ernesto E; Mejía-Gómez, Javier César JC; Díaz-Velásquez, Clara C; Quezada-Urban, Rosalía R; Martínez Gregorio, Héctor H; Vallejo-Lecuona, Fernando F; de la Cruz-Montoya, Aldo A; Porras Reyes, Fany Iris FI; Pérez-Sánchez, Víctor Manuel VM; Maldonado-Martínez, Héctor Aquiles HA; Robles-Estrada, Maybelline M; Bargalló-Rocha, Enrique E; Cabrera-Galeana, Paula P; Ramos-Ramírez, Maritza M; Chirino, Yolanda Irasema YI; Alonso Herrera, Luis L; Terrazas, Luis Ignacio LI; Oliver, Javier J; Frecha, Cecilia C; Perdomo, Sandra S; Vaca-Paniagua, Felipe F
Publication Date: 2020-11-19

Variant appearance in text: NOTCH1: G1660C
PubMed Link: 33227964
Variant Present in the following documents:
  • genes-11-01367-s001.pdf
View BVdb publication page