MSH6 c.1807_1808delinsGC ;(p.K603A)

Variant ID: 2-48026929-AA-GC

NM_000179.2(MSH6):c.1807_1808delinsGC;(p.K603A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1.

Genes & Development
Terui, Riki R; Nagao, Koji K; Kawasoe, Yoshitaka Y; Taki, Kanae K; Higashi, Torahiko L TL; Tanaka, Seiji S; Nakagawa, Takuro T; Obuse, Chikashi C; Masukata, Hisao H; Takahashi, Tatsuro S TS
Publication Date: 2018-06-01

Variant appearance in text: MSH6: K603A
PubMed Link: 29899141
Variant Present in the following documents:
  • Main text
  • 806.pdf
View BVdb publication page