TTC28 c.4566C>A ;(p.P1522=)

Variant ID: 22-28395081-G-T

NM_001145418.1(TTC28):c.4566C>A;(p.P1522=)

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:

Cancer of Unknown Primary (CUP): genetic evidence for a novel nosological entity? A case report.

Embo Molecular Medicine
Benvenuti, Silvia S; Milan, Melissa M; Geuna, Elena E; Pisacane, Alberto A; Senetta, Rebecca R; Gambardella, Gennaro G; Stella, Giulia M GM; Montemurro, Filippo F; Sapino, Anna A; Boccaccio, Carla C; Comoglio, Paolo M PM
Publication Date: 2020-07-07

Variant appearance in text: TTC28: P1522P
PubMed Link: 32511869
Variant Present in the following documents:
  • EMMM-12-e11756-s005.xlsx, sheet 1
View BVdb publication page