MMP9 c.559C>G ;(p.L187V)

Variant ID: 20-44639599-C-G

NM_004994.2(MMP9):c.559C>G;(p.L187V)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic variation in human drug-related genes.

Genome Medicine
Schärfe, Charlotta Pauline Irmgard CPI; Tremmel, Roman R; Schwab, Matthias M; Kohlbacher, Oliver O; Marks, Debora Susan DS
Publication Date: 2017-12-22

Variant appearance in text: rs55789927
PubMed Link: 29273096
Variant Present in the following documents:
  • 13073_2017_502_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



NCI-60 whole exome sequencing and pharmacological CellMiner analyses.

Plos One
Reinhold, William C WC; Varma, Sudhir S; Sousa, Fabricio F; Sunshine, Margot M; Abaan, Ogan D OD; Davis, Sean R SR; Reinhold, Spencer W SW; Kohn, Kurt W KW; Morris, Joel J; Meltzer, Paul S PS; Doroshow, James H JH; Pommier, Yves Y
Publication Date: 2014

Variant appearance in text: rs55789927
PubMed Link: 25032700
Variant Present in the following documents:
  • pone.0101670.s004.xlsx, sheet 1
View BVdb publication page



Matrix metalloproteinase-9 genotype as a potential genetic marker for abdominal aortic aneurysm.

Circulation. Cardiovascular Genetics
Duellman, Tyler T; Warren, Christopher L CL; Peissig, Peggy P; Wynn, Martha M; Yang, Jay J
Publication Date: 2012-10-01

Variant appearance in text: rs55789927
PubMed Link: 22942228
Variant Present in the following documents:
  • Main text
View BVdb publication page