RB1 c.155C>T ;(p.T52I)

Variant ID: 13-48881433-C-T

NM_000321.2(RB1):c.155C>T;(p.T52I)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Somatic mutations in benign breast disease tissue and risk of subsequent invasive breast cancer.

British Journal Of Cancer
Rohan, Thomas E TE; Miller, Christopher A CA; Li, Tiandao T; Wang, Yihong Y; Loudig, Olivier O; Ginsberg, Mindy M; Glass, Andrew A; Mardis, Elaine E
Publication Date: 2018-06

Variant appearance in text: RB1: T52I
PubMed Link: 29872146
Variant Present in the following documents:
  • 41416_2018_89_MOESM2_ESM.xls, sheet 1
View BVdb publication page