TP53 c.1101-221G>A

Variant ID: 17-7573229-C-T

NM_000546.5(TP53):c.1101-221G>A

This variant was identified in 6 publications

View GRCh38 version.




Publications:


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: rs6503048
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: rs6503048
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: rs6503048
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.

Scientific Reports
Castellanos, Elisabeth E; Gel, Bernat B; Rosas, Inma I; Tornero, Eva E; Santín, Sheila S; Pluvinet, Raquel R; Velasco, Juan J; Sumoy, Lauro L; Del Valle, Jesús J; Perucho, Manuel M; Blanco, Ignacio I; Navarro, Matilde M; Brunet, Joan J; Pineda, Marta M; Feliubadaló, Lidia L; Capellá, Gabi G; Lázaro, Conxi C; Serra, Eduard E
Publication Date: 2017-01-04

Variant appearance in text: TP53: 1101-221G>A; rs6503048
PubMed Link: 28051113
Variant Present in the following documents:
  • srep39348-s1.pdf
View BVdb publication page



Re-evaluation of the carcinogenic significance of hepatitis B virus integration in hepatocarcinogenesis.

Plos One
Jiang, Suzhen S; Yang, Ziwei Z; Li, Weijie W; Li, Xiaojun X; Wang, Yongfeng Y; Zhang, Jiangbo J; Xu, Chunhui C; Chen, Pei-Jer PJ; Hou, Jinlin J; McCrae, Malcolm A MA; Chen, Xiangmei X; Zhuang, Hui H; Lu, Fengmin F
Publication Date: 2012

Variant appearance in text: rs6503048
PubMed Link: 22962577
Variant Present in the following documents:
  • Main text
  • pone.0040363.pdf
View BVdb publication page



SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping.

Bmc Bioinformatics
Chang, Hsueh-Wei HW; Cheng, Yu-Huei YH; Chuang, Li-Yeh LY; Yang, Cheng-Hong CH
Publication Date: 2010-04-08

Variant appearance in text: rs6503048
PubMed Link: 20377871
Variant Present in the following documents:
  • Main text
  • 1471-2105-11-173.pdf
View BVdb publication page



Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.

American Journal Of Medical Genetics. Part A
Pangilinan, Faith F; Geiler, Kerry K; Dolle, Jessica J; Troendle, James J; Swanson, Deborah A DA; Molloy, Anne M AM; Sutton, Marie M; Conley, Mary M; Kirke, Peadar N PN; Scott, John M JM; Mills, James L JL; Brody, Lawrence C LC
Publication Date: 2008-10-15

Variant appearance in text: rs6503048
PubMed Link: 18798306
Variant Present in the following documents:
  • Main text
View BVdb publication page