PC c.2575T>G ;(p.S859A)

Variant ID: 11-66617834-A-C

NM_001040716.1(PC):c.2575T>G;(p.S859A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: PC: S859A
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



HGF and MET: From Brain Development to Neurological Disorders.

Frontiers In Cell And Developmental Biology
Desole, Claudia C; Gallo, Simona S; Vitacolonna, Annapia A; Montarolo, Francesca F; Bertolotto, Antonio A; Vivien, Denis D; Comoglio, Paolo P; Crepaldi, Tiziana T
Publication Date: 2021

Variant appearance in text: PC: 2575T>G
PubMed Link: 34179015
Variant Present in the following documents:
  • Main text
  • fcell-09-683609.pdf
View BVdb publication page