MSH6 c.944C>T ;(p.S315F)

Variant ID: 2-48026066-C-T

NM_000179.2(MSH6):c.944C>T;(p.S315F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Predicting the functional impact of protein mutations: application to cancer genomics.

Nucleic Acids Research
Reva, Boris B; Antipin, Yevgeniy Y; Sander, Chris C
Publication Date: 2011-09-01

Variant appearance in text: MSH6: S315F
PubMed Link: 21727090
Variant Present in the following documents:
  • supp_gkr407_Supplement2_Table_SM1_COSMIC_mutations.xls, sheet 1
View BVdb publication page



Cooperative nuclear localization sequences lend a novel role to the N-terminal region of MSH6.

Plos One
Gassman, Natalie R NR; Clodfelter, Jill E JE; McCauley, Anita K AK; Bonin, Keith K; Salsbury, Freddie R FR; Scarpinato, Karin D KD
Publication Date: 2011-03-17

Variant appearance in text: MSH6: S315F
PubMed Link: 21437237
Variant Present in the following documents:
  • Main text
  • pone.0017907.pdf
View BVdb publication page