TP53 c.*485G>A

Variant ID: 17-7572442-C-T

NM_000546.5(TP53):c.*485G>A

This variant was identified in 15 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs4968187
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs4968187
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Case Report: Clinicopathological and Genetic Features of IDH-Mutant Brainstem Glioma in Adults: Report of Five Cases.

Pathology Oncology Research : Por
Zhou, Jiangfen J; Lai, Mingyao M; Ni, Yang Y; Li, Shaoqun S; Zhen, Junjie J; Du, Furong F; Zhang, Xing X; Song, Chao C; Cai, Linbo L
Publication Date: 2022

Variant appearance in text: rs4968187
PubMed Link: 35991838
Variant Present in the following documents:
  • Main text
  • pore-28-1610408.pdf
View BVdb publication page



A New Insight for the Identification of Oncogenic Variants in Breast and Prostate Cancers in Diverse Human Populations, With a Focus on Latinos.

Frontiers In Pharmacology
Varela, Nelson M NM; Guevara-Ramírez, Patricia P; Acevedo, Cristian C; Zambrano, Tomás T; Armendáriz-Castillo, Isaac I; Guerrero, Santiago S; Quiñones, Luis A LA; López-Cortés, Andrés A
Publication Date: 2021

Variant appearance in text: rs4968187
PubMed Link: 33912047
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.

Cell Death And Differentiation
Doffe, Flora F; Carbonnier, Vincent V; Tissier, Manon M; Leroy, Bernard B; Martins, Isabelle I; Mattsson, Johanna S M JSM; Micke, Patrick P; Pavlova, Sarka S; Pospisilova, Sarka S; Smardova, Jana J; Joerger, Andreas C AC; Wiman, Klas G KG; Kroemer, Guido G; Soussi, Thierry T
Publication Date: 2021-05

Variant appearance in text: rs4968187
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.

Cell Death And Differentiation
Doffe, Flora F; Carbonnier, Vincent V; Tissier, Manon M; Leroy, Bernard B; Martins, Isabelle I; Mattsson, Johanna S M JSM; Micke, Patrick P; Pavlova, Sarka S; Pospisilova, Sarka S; Smardova, Jana J; Joerger, Andreas C AC; Wiman, Klas G KG; Kroemer, Guido G; Soussi, Thierry T
Publication Date: 2021-05

Variant appearance in text: rs4968187
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs4968187
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Pathway-Based Analysis of Genome-Wide Association Data Identified SNPs in HMMR as Biomarker for Chemotherapy- Induced Neutropenia in Breast Cancer Patients.

Frontiers In Pharmacology
Bidadi, Behzad B; Liu, Duan D; Kalari, Krishna R KR; Rubner, Matthias M; Hein, Alexander A; Beckmann, Matthias W MW; Rack, Brigitte B; Janni, Wolfgang W; Fasching, Peter A PA; Weinshilboum, Richard M RM; Wang, Liewei L
Publication Date: 2018

Variant appearance in text: rs4968187
PubMed Link: 29593529
Variant Present in the following documents:
  • Main text
  • fphar-09-00158.pdf
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The screening of the functional microRNA binding site SNPs in sporadic colorectal cancer genes.

Cancer Biology & Therapy
He, Hongjuan H; Lei, Lei L; Chen, Erfei E; Xu, Xiaona X; Wang, Lili L; Pan, Junqiang J; Yang, Fangfang F; Wang, Min M; Dong, Jing J; Yang, Jin J
Publication Date: 2017-06-03

Variant appearance in text: rs4968187
PubMed Link: 28494187
Variant Present in the following documents:
  • Main text
View BVdb publication page



A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.

Bmc Medical Genomics
Mucaki, Eliseos J EJ; Caminsky, Natasha G NG; Perri, Ami M AM; Lu, Ruipeng R; Laederach, Alain A; Halvorsen, Matthew M; Knoll, Joan H M JH; Rogan, Peter K PK
Publication Date: 2016-04-11

Variant appearance in text: rs4968187
PubMed Link: 27067391
Variant Present in the following documents:
  • Main text
  • 12920_2016_178_MOESM14_ESM.xlsx, sheet 1
  • 12920_2016_Article_178.pdf
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: rs4968187
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach.

American Journal Of Epidemiology
O'Brien, Katie M KM; Cole, Stephen R SR; Poole, Charles C; Bensen, Jeannette T JT; Herring, Amy H AH; Engel, Lawrence S LS; Millikan, Robert C RC
Publication Date: 2014-02-01

Variant appearance in text: rs4968187
PubMed Link: 24218030
Variant Present in the following documents:
  • Main text
View BVdb publication page



Breast cancer subtypes and previously established genetic risk factors: a bayesian approach.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
O'Brien, Katie M KM; Cole, Stephen R SR; Engel, Lawrence S LS; Bensen, Jeannette T JT; Poole, Charles C; Herring, Amy H AH; Millikan, Robert C RC
Publication Date: 2014-01

Variant appearance in text: rs4968187
PubMed Link: 24177593
Variant Present in the following documents:
  • Main text
View BVdb publication page



Single nucleotide variation in the TP53 3' untranslated region in diffuse large B-cell lymphoma treated with rituximab-CHOP: a report from the International DLBCL Rituximab-CHOP Consortium Program.

Blood
Li, Yong Y; Gordon, Michael W MW; Xu-Monette, Zijun Y ZY; Visco, Carlo C; Tzankov, Alexander A; Zou, Dehui D; Qiu, Lugui L; Montes-Moreno, Santiago S; Dybkaer, Karen K; Orazi, Attilio A; Zu, Youli Y; Bhagat, Govind G; Richards, Kristy L KL; Hsi, Eric D ED; Choi, William W L WW; van Krieken, J Han JH; Huang, Qin Q; Ai, Weiyun W; Ponzoni, Maurilio M; Ferreri, Andrés J M AJ; Winter, Jane N JN; Go, Ronald S RS; Piris, Miguel A MA; Møller, Michael B MB; Wu, Lin L; Wang, Michael M; Ramos, Kenneth S KS; Medeiros, L Jeffrey LJ; Young, Ken H KH
Publication Date: 2013-05-30

Variant appearance in text: rs4968187
PubMed Link: 23515929
Variant Present in the following documents:
  • Main text
View BVdb publication page



Quantification of rare allelic variants from pooled genomic DNA.

Nature Methods
Druley, Todd E TE; Vallania, Francesco L M FL; Wegner, Daniel J DJ; Varley, Katherine E KE; Knowles, Olivia L OL; Bonds, Jacqueline A JA; Robison, Sarah W SW; Doniger, Scott W SW; Hamvas, Aaron A; Cole, F Sessions FS; Fay, Justin C JC; Mitra, Robi D RD
Publication Date: 2009-04

Variant appearance in text: rs4968187
PubMed Link: 19252504
Variant Present in the following documents:
  • NIHMS92733-supplement-1.pdf
View BVdb publication page



Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.

American Journal Of Kidney Diseases : The Official Journal Of The National Kidney Foundation
Israni, Ajay K AK; Li, Na N; Cizman, Bojana B BB; Snyder, Jon J; Abrams, John J; Joffe, Marshall M; Rebbeck, Timothy T; Feldman, Harold I HI
Publication Date: 2008-08

Variant appearance in text: rs4968187
PubMed Link: 18640487
Variant Present in the following documents:
  • Main text
View BVdb publication page