MSH6 c.3978_3979insT ;(p.N1327*)

Variant ID: 2-48033767-G-GT

NM_000179.2(MSH6):c.3978_3979insT;(p.N1327*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing.

Bmc Medical Genomics
Cheng, Donavan T DT; Prasad, Meera M; Chekaluk, Yvonne Y; Benayed, Ryma R; Sadowska, Justyna J; Zehir, Ahmet A; Syed, Aijazuddin A; Wang, Yan Elsa YE; Somar, Joshua J; Li, Yirong Y; Yelskaya, Zarina Z; Wong, Donna D; Robson, Mark E ME; Offit, Kenneth K; Berger, Michael F MF; Nafa, Khedoudja K; Ladanyi, Marc M; Zhang, Liying L
Publication Date: 2017-05-19

Variant appearance in text: N/A
PubMed Link: 28526081
Variant Present in the following documents:
View BVdb publication page