PC c.70_71delinsCA ;(p.A24H)

Variant ID: 11-66639560-GC-TG

NM_001040716.1(PC):c.70_71delinsCA;(p.A24H)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Genetic fusions favor tumorigenesis through degron loss in oncogenes.

Nature Communications
Liu, Jing J; Tokheim, Collin C; Lee, Jonathan D JD; Gan, Wenjian W; North, Brian J BJ; Liu, X Shirley XS; Pandolfi, Pier Paolo PP; Wei, Wenyi W
Publication Date: 2021-11-18

Variant appearance in text: PC: A24H
PubMed Link: 34795215
Variant Present in the following documents:
  • 41467_2021_26871_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: PC: A24H
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM3_ESM.xlsx, sheet 2
  • 41598_2021_93715_MOESM3_ESM.xlsx, sheet 4
View BVdb publication page



FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome.

Thorax
Min, Haiyan H; Ma, Dehua D; Zou, Wei W; Wu, Yongzheng Y; Ding, Yibing Y; Zhu, Chengchu C; Lin, Anqi A; Song, Shiyu S; Liang, Qiao Q; Chen, Baofu B; Zhang, Bin B; Wan, Yueming Y; Ye, Minhua M; Pan, Yanqing Y; Wen, Yanting Y; Yi, Long L; Gao, Qian Q
Publication Date: 2020-06

Variant appearance in text: PC: A24h
PubMed Link: 32184379
Variant Present in the following documents:
  • thoraxjnl-2019-213225.pdf
View BVdb publication page



Parsimonious Gene Correlation Network Analysis (PGCNA): a tool to define modular gene co-expression for refined molecular stratification in cancer.

Npj Systems Biology And Applications
Care, Matthew A MA; Westhead, David R DR; Tooze, Reuben M RM
Publication Date: 2019

Variant appearance in text: PC: A24H
PubMed Link: 30993001
Variant Present in the following documents:
  • 41540_2019_90_MOESM2_ESM.pdf
View BVdb publication page



The prognostic effects of somatic mutations in ER-positive breast cancer.

Nature Communications
Griffith, Obi L OL; Spies, Nicholas C NC; Anurag, Meenakshi M; Griffith, Malachi M; Luo, Jingqin J; Tu, Dongsheng D; Yeo, Belinda B; Kunisaki, Jason J; Miller, Christopher A CA; Krysiak, Kilannin K; Hundal, Jasreet J; Ainscough, Benjamin J BJ; Skidmore, Zachary L ZL; Campbell, Katie K; Kumar, Runjun R; Fronick, Catrina C; Cook, Lisa L; Snider, Jacqueline E JE; Davies, Sherri S; Kavuri, Shyam M SM; Chang, Eric C EC; Magrini, Vincent V; Larson, David E DE; Fulton, Robert S RS; Liu, Shuzhen S; Leung, Samuel S; Voduc, David D; Bose, Ron R; Dowsett, Mitch M; Wilson, Richard K RK; Nielsen, Torsten O TO; Mardis, Elaine R ER; Ellis, Matthew J MJ
Publication Date: 2018-09-04

Variant appearance in text: PC: A24H
PubMed Link: 30181556
Variant Present in the following documents:
  • 41467_2018_5914_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



The landscape and therapeutic relevance of cancer-associated transcript fusions.

Oncogene
Yoshihara, K K; Wang, Q Q; Torres-Garcia, W W; Zheng, S S; Vegesna, R R; Kim, H H; Verhaak, R G W RG
Publication Date: 2015-09-10

Variant appearance in text: PC: A24H
PubMed Link: 25500544
Variant Present in the following documents:
  • NIHMS632238-supplement-2.xlsx, sheet 2
View BVdb publication page



Microsatellite genotyping reveals a signature in breast cancer exomes.

Breast Cancer Research And Treatment
McIver, L J LJ; Fonville, N C NC; Karunasena, E E; Garner, H R HR
Publication Date: 2014-06

Variant appearance in text: PC: A24H
PubMed Link: 24838940
Variant Present in the following documents:
View BVdb publication page