MSH6 c.3260_3261del ;(p.P1087Lfs*5)

Variant ID: 2-48030639-ACC-A

NM_000179.2(MSH6):c.3260_3261del;(p.P1087Lfs*5)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer.

Cancer
Ricker, Charité N CN; Hanna, Diana L DL; Peng, Cheng C; Nguyen, Nathalie T NT; Stern, Mariana C MC; Schmit, Stephanie L SL; Idos, Greg E GE; Patel, Ravi R; Tsai, Steven S; Ramirez, Veronica V; Lin, Sonia S; Shamasunadara, Vinay V; Barzi, Afsaneh A; Lenz, Heinz-Josef HJ; Figueiredo, Jane C JC
Publication Date: 2017-10-01

Variant appearance in text: MSH6: 3255_3256del
PubMed Link: 28640387
Variant Present in the following documents:
  • Main text
  • CNCR-123-3732.pdf
View BVdb publication page