TP53 c.171_172insATCCGGGTGA ;(p.P58Ifs*8)

Variant ID: 17-7579515-G-GTCACCCGGAT

NM_000546.5(TP53):c.171_172insATCCGGGTGA;(p.P58Ifs*8)

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:

Primary malignant pericardial tumour in Lynch syndrome.

Bmc Cancer
Paolisso, Pasquale P; Saturi, Giulia G; Foà, Alberto A; Saponara, Maristella M; Nannini, Margherita M; Pantaleo, Maria Abbondanza MA; Leone, Ornella O; Turchetti, Daniela D; Calistri, Daniele D; Savini, Carlo C; Pacini, Davide D; Pizzi, Carmine C; Galiè, Nazzareno N
Publication Date: 2020-03-06

Variant appearance in text: TP53: 171_172insATCCGGGTGA
PubMed Link: 32143595
Variant Present in the following documents:
  • Main text
View BVdb publication page