TP53 c.-28-4460A>G

Variant ID: 17-7584400-T-C

NM_000546.5(TP53):c.-28-4460A>G

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Male and female breast cancer: the two faces of the same genetic susceptibility coin.

Breast Cancer Research And Treatment
Silva, Susana Nunes SN; Gomes, Bruno Costa BC; André, Saudade S; Félix, Ana A; Rodrigues, António Sebastião AS; Rueff, José J
Publication Date: 2021-07

Variant appearance in text: rs11652704
PubMed Link: 33942220
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: rs11652704
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: rs11652704
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Variants in FAT1 and COL9A1 genes in male population with or without substance use to assess the risk factors for oral malignancy.

Plos One
Chung, Chia-Min CM; Hung, Chung-Chieh CC; Lee, Chien-Hung CH; Lee, Chi-Pin CP; Lee, Ka-Wo KW; Chen, Mu-Kuan MK; Yeh, Kun-Tu KT; Ko, Ying-Chin YC
Publication Date: 2019

Variant appearance in text: rs11652704
PubMed Link: 30657779
Variant Present in the following documents:
  • Main text
  • pone.0210901.pdf
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: rs11652704
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.

Journal Of Neuro-Oncology
Dahlin, Anna M AM; Hollegaard, Mads V MV; Wibom, Carl C; Andersson, Ulrika U; Hougaard, David M DM; Deltour, Isabelle I; Hjalmars, Ulf U; Melin, Beatrice B
Publication Date: 2015-10

Variant appearance in text: rs11652704
PubMed Link: 26290144
Variant Present in the following documents:
  • 11060_2015_1891_MOESM1_ESM.pdf
View BVdb publication page