MSH2 c.602dup ;(p.L201Ffs*31)

Variant ID: 2-47637464-G-GT

NM_000251.2(MSH2):c.602dup;(p.L201Ffs*31)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Counseling for Hereditary Gastric and Pancreatic Cancer in High-Risk Gastrointestinal Cancer Clinics: An Effective Strategy.

Cancers
Llach, Joan J; Moreno, Lorena L; Sánchez, Ariadna A; Herrera-Pariente, Cristina C; Ocaña, Teresa T; Cuatrecasas, Miriam M; Rivero-Sánchez, Liseth L; Moreira, Rebeca R; Díaz, Mireia M; Jung, Gerhard G; Pellisé, Maria M; Castells, Antoni A; Balaguer, Francesc F; Carballal, Sabela S; Moreira, Leticia L
Publication Date: 2020-08-23

Variant appearance in text: MSH2: 602dupT
PubMed Link: 32842532
Variant Present in the following documents:
  • Main text
  • cancers-12-02386.pdf
View BVdb publication page



A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.

Scientific Reports
Castellanos, Elisabeth E; Gel, Bernat B; Rosas, Inma I; Tornero, Eva E; Santín, Sheila S; Pluvinet, Raquel R; Velasco, Juan J; Sumoy, Lauro L; Del Valle, Jesús J; Perucho, Manuel M; Blanco, Ignacio I; Navarro, Matilde M; Brunet, Joan J; Pineda, Marta M; Feliubadaló, Lidia L; Capellá, Gabi G; Lázaro, Conxi C; Serra, Eduard E
Publication Date: 2017-01-04

Variant appearance in text: MSH2: 602_603insT
PubMed Link: 28051113
Variant Present in the following documents:
  • srep39348-s1.pdf
View BVdb publication page