NOS3 c.466G>C ;(p.E156Q)

Variant ID: 7-150693897-G-C

NM_000603.4(NOS3):c.466G>C;(p.E156Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Effect of parental origin of damaging variants in pro-angiogenic genes on fetal growth in patients with congenital heart defects: Data and analyses.

Data In Brief
Russell, Mark W MW; Moldenhauer, Julie S JS; Rychik, Jack J; Burnham, Nancy B NB; Zullo, Erin E; Parry, Samuel I SI; Simmons, Rebecca A RA; Elovitz, Michal A MA; Nicolson, Susan C SC; Linn, Rebecca L RL; Johnson, Mark P MP; Yu, Sunkyung S; Sampson, Matthew G MG; Hakonarson, Hakon H; Gaynor, J William JW
Publication Date: 2019-08

Variant appearance in text: rs141456642
PubMed Link: 31453292
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility.

Plos Genetics
de Voer, Richarda M RM; Hahn, Marc-Manuel MM; Weren, Robbert D A RD; Mensenkamp, Arjen R AR; Gilissen, Christian C; van Zelst-Stams, Wendy A WA; Spruijt, Liesbeth L; Kets, C Marleen CM; Zhang, Junxiao J; Venselaar, Hanka H; Vreede, Lilian L; Schubert, Nil N; Tychon, Marloes M; Derks, Ronny R; Schackert, Hans K HK; Geurts van Kessel, Ad A; Hoogerbrugge, Nicoline N; Ligtenberg, Marjolijn J L MJ; Kuiper, Roland P RP
Publication Date: 2016-02

Variant appearance in text: rs141456642
PubMed Link: 26901136
Variant Present in the following documents:
  • pgen.1005880.s003.xlsx, sheet 1
View BVdb publication page