CR2 c.2654G>A ;(p.R885H)

Variant ID: 1-207648499-G-A

NM_001006658.2(CR2):c.2654G>A;(p.R885H)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


A Phase II Trial of Guadecitabine plus Atezolizumab in Metastatic Urothelial Carcinoma Progressing after Initial Immune Checkpoint Inhibitor Therapy.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Jang, H Josh HJ; Hostetter, Galen G; MacFarlane, Alexander W AW; Madaj, Zachary Z; Ross, Eric A EA; Hinoue, Toshinori T; Kulchycki, Justin R JR; Burgos, Ryan S RS; Tafseer, Mahvish M; Alpaugh, R Katherine RK; Schwebel, Candice L CL; Kokate, Rutika R; Geynisman, Daniel M DM; Zibelman, Matthew R MR; Ghatalia, Pooja P; Nichols, Peter W PW; Chung, Woonbok W; Madzo, Jozef J; Hahn, Noah M NM; Quinn, David I DI; Issa, Jean-Pierre J JJ; Topper, Michael J MJ; Baylin, Stephen B SB; Shen, Hui H; Campbell, Kerry S KS; Jones, Peter A PA; Plimack, Elizabeth R ER
Publication Date: 2023-03-16

Variant appearance in text: CR2: R885H
PubMed Link: 36928921
Variant Present in the following documents:
  • ccr-22-3642_supplementary_tables_1_suppts1.xlsx, sheet 3
View BVdb publication page



Identification of a novel mutation in complement receptor 2 in Chinese familial systemic lupus erythematosus.

Archives Of Rheumatology
Tang, Yuewu Y; Luo, Yi Y
Publication Date: 2022-12

Variant appearance in text: CR2: 2654G>A; Arg885His
PubMed Link: 36879571
Variant Present in the following documents:
  • ArchRheumatol-2022-37-566.pdf
View BVdb publication page



Expanding horizons in complement drug discovery: challenges and emerging strategies.

Seminars In Immunopathology
Harris, Claire L CL
Publication Date: 2018-01

Variant appearance in text: CR2: R885H
PubMed Link: 28986638
Variant Present in the following documents:
  • Main text
View BVdb publication page



Complement, a target for therapy in inflammatory and degenerative diseases.

Nature Reviews. Drug Discovery
Morgan, B Paul BP; Harris, Claire L CL
Publication Date: 2015-12

Variant appearance in text: CR2: R885H
PubMed Link: 26493766
Variant Present in the following documents:
  • Main text
  • 41573_2015_Article_BFnrd4657.pdf
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: rs140808707
PubMed Link: 25032700
Variant Present in the following documents:
  • pone.0101670.s004.xlsx, sheet 1
View BVdb publication page



Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.

Nature Genetics
Seddon, Johanna M JM; Yu, Yi Y; Miller, Elizabeth C EC; Reynolds, Robyn R; Tan, Perciliz L PL; Gowrisankar, Sivakumar S; Goldstein, Jacqueline I JI; Triebwasser, Michael M; Anderson, Holly E HE; Zerbib, Jennyfer J; Kavanagh, David D; Souied, Eric E; Katsanis, Nicholas N; Daly, Mark J MJ; Atkinson, John P JP; Raychaudhuri, Soumya S
Publication Date: 2013-11

Variant appearance in text: rs140808707
PubMed Link: 24036952
Variant Present in the following documents:
  • NIHMS512112-supplement-2.xlsx, sheet 2
View BVdb publication page