MST1R c.179C>G ;(p.T60S)

Variant ID: 3-49940864-G-C

NM_002447.2(MST1R):c.179C>G;(p.T60S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.

Journal Of Molecular Biology
Pal, Lipika R LR; Moult, John J
Publication Date: 2015-07-03

Variant appearance in text: RON: T60S
PubMed Link: 25937569
Variant Present in the following documents:
  • Main text
View BVdb publication page