FLNB c.488A>C ;(p.Q163P)

Variant ID: 3-58062968-A-C

NM_001457.3(FLNB):c.488A>C;(p.Q163P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of biomarkers complementary to homologous recombination deficiency for improving the clinical outcome of ovarian serous cystadenocarcinoma.

Clinical And Translational Medicine
Shi, Zhiwen Z; Zhao, Qingguo Q; Lv, Bin B; Qu, Xinyu X; Han, Xiao X; Wang, Hongyan H; Qiu, Junjun J; Hua, Keqin K
Publication Date: 2021-05

Variant appearance in text: FLNB: 488A>C
PubMed Link: 34047476
Variant Present in the following documents:
  • CTM2-11-e399-s003.xls, sheet 1
View BVdb publication page



Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.

Molecules (Basel, Switzerland)
S, Udhaya Kumar UK; Sankar, Srivarshini S; Younes, Salma S; D, Thirumal Kumar TK; Ahmad, Muneera Naseer MN; Okashah, Sarah Samer SS; Kamaraj, Balu B; Al-Subaie, Abeer Mohammed AM; C, George Priya Doss GPD; Zayed, Hatem H
Publication Date: 2020-11-26

Variant appearance in text: FLNB: 488A>C; Q163P
PubMed Link: 33255942
Variant Present in the following documents:
  • Main text
  • molecules-25-05543.pdf
View BVdb publication page