MUC16 c.23683C>A ;(p.P7895T)

Variant ID: 19-9063763-G-T

NM_024690.2(MUC16):c.23683C>A;(p.P7895T)

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: MUC16: 23683C>A; P7895T
PubMed Link: 34047476
Variant Present in the following documents:
  • CTM2-11-e399-s003.xls, sheet 1
View BVdb publication page



Genetic alterations associated with progression from pancreatic intraepithelial neoplasia to invasive pancreatic tumor.

Gastroenterology
Murphy, Stephen J SJ; Hart, Steven N SN; Lima, Joema Felipe JF; Kipp, Benjamin R BR; Klebig, Mitchell M; Winters, Jennifer L JL; Szabo, Csilla C; Zhang, Lizhi L; Eckloff, Bruce W BW; Petersen, Gloria M GM; Scherer, Steven E SE; Gibbs, Richard A RA; McWilliams, Robert R RR; Vasmatzis, George G; Couch, Fergus J FJ
Publication Date: 2013-11

Variant appearance in text: MUC16: P7895T
PubMed Link: 23912084
Variant Present in the following documents:
  • Main text
View BVdb publication page