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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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