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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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