BRCA2 c.4134T>C ;(p.T1378=)

Variant ID: 13-32912626-T-C

NM_000059.3(BRCA2):c.4134T>C;(p.T1378=)

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:

BRCA1/2 NGS Somatic Testing in Clinical Practice: A Short Report.

Genes
Pepe, Francesco F; Pisapia, Pasquale P; Russo, Gianluca G; Nacchio, Mariantonia M; Pallante, Pierlorenzo P; Vigliar, Elena E; De Angelis, Carmine C; Insabato, Luigi L; Bellevicine, Claudio C; De Placido, Sabino S; Troncone, Giancarlo G; Malapelle, Umberto U
Publication Date: 2021-11-28

Variant appearance in text: BRCA2: T1378T
PubMed Link: 34946865
Variant Present in the following documents:
  • Main text
  • genes-12-01917.pdf
View BVdb publication page


BRCA1/2 NGS Somatic Testing in Clinical Practice: A Short Report.

Genes
Pepe, Francesco F; Pisapia, Pasquale P; Russo, Gianluca G; Nacchio, Mariantonia M; Pallante, Pierlorenzo P; Vigliar, Elena E; De Angelis, Carmine C; Insabato, Luigi L; Bellevicine, Claudio C; De Placido, Sabino S; Troncone, Giancarlo G; Malapelle, Umberto U
Publication Date: 2021-11-28

Variant appearance in text: BRCA2: T1378T
PubMed Link: 34946865
Variant Present in the following documents:
  • Main text
  • genes-12-01917.pdf
View BVdb publication page