TSC2 c.3472C>T ;(p.P1158S)

Variant ID: 16-2130240-C-T

NM_000548.3(TSC2):c.3472C>T;(p.P1158S)

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:

Validity of an NGS-based multiple gene panel in identifying actionable mutations for patients with NSCLC in a Chinese hospital.

Oncology Letters
Cao, Wei W; Yan, Chenghai C; Wang, Hailong H; Tang, Tom T; Wang, Haifeng H; Liu, Dujuan D
Publication Date: 2019-06

Variant appearance in text: TSC2: P1158S
PubMed Link: 31186761
Variant Present in the following documents:
  • Main text
  • ol-17-06-5425.pdf
View BVdb publication page