RB1 c.1508del ;(p.S503Ffs*16)

Variant ID: 13-48955392-TC-T

NM_000321.2(RB1):c.1508del;(p.S503Ffs*16)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The RB1 Mutation Spectrum and Genetic Management Consultation in Pediatric Patients with Retinoblastoma in Beijing, China.

Risk Management And Healthcare Policy
Xie, Ying Y; Xu, Xiao-Lin XL; Wei, Wen-Bin WB
Publication Date: 2021

Variant appearance in text: RB1: 1508delC; S503Ffs*16
PubMed Link: 34456592
Variant Present in the following documents:
  • Main text
  • rmhp-14-3453.pdf
View BVdb publication page