PC c.2380G>T ;(p.V794L)

Variant ID: 11-66618238-C-A

NM_001040716.1(PC):c.2380G>T;(p.V794L)

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:

Detection of genetic mutations in patients with breast cancer from Saudi Arabia using Ion AmpliSeq™ Cancer Hotspot Panel v.2.0.

Biomedical Reports
Messaoudi, Safia A SA; Al Sharhan, Nourah A NA; Alharthi, Bandar B; Babu, Saranya R SR; Alsaleh, Abrar B AB; Alasiri, Alanoud M AM; Assidi, Mourad M; Buhmeida, Abdelbaset A; Almawi, Wassim Y WY
Publication Date: 2022-04

Variant appearance in text: PC: 2380G>T; Val794Leu
PubMed Link: 35251613
Variant Present in the following documents:
  • br-16-04-01509.pdf
View BVdb publication page