TP53 c.502_503delinsGT ;(p.H168V)

Variant ID: 17-7578427-TG-AC

NM_000546.5(TP53):c.502_503delinsGT;(p.H168V)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: TP53: H168V
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations.

Genome Biology
Martelotto, Luciano G LG; Ng, Charlotte Ky CK; De Filippo, Maria R MR; Zhang, Yan Y; Piscuoglio, Salvatore S; Lim, Raymond S RS; Shen, Ronglai R; Norton, Larry L; Reis-Filho, Jorge S JS; Weigelt, Britta B
Publication Date: 2014-10-28

Variant appearance in text: TP53: H168V
PubMed Link: 25348012
Variant Present in the following documents:
  • 13059_2014_484_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Major and essential role for the DNA methylation mark in mouse embryogenesis and stable association of DNMT1 with newly replicated regions.

Molecular And Cellular Biology
Takebayashi, Shin-ichiro S; Tamura, Takashi T; Matsuoka, Chisa C; Okano, Masaki M
Publication Date: 2007-12

Variant appearance in text: p53: H168V
PubMed Link: 17893328
Variant Present in the following documents:
  • Main text
View BVdb publication page