TSC2 c.3712G>A ;(p.A1238T)

Variant ID: 16-2131697-G-A

NM_000548.3(TSC2):c.3712G>A;(p.A1238T)

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:

Clear cell and papillary renal cell carcinomas in hereditary papillary renal cell carcinoma (HPRCC) syndrome: a case report.

Diagnostic Pathology
Ferlicot, Sophie S; Just, Pierre-Alexandre PA; Compérat, Eva E; Rouleau, Etienne E; Tissier, Frédérique F; Vaessen, Christophe C; Richard, Stéphane S
Publication Date: 2021-11-20

Variant appearance in text: TSC2: 3712G>A
PubMed Link: 34801057
Variant Present in the following documents:
  • 13000_2021_Article_1170.pdf
View BVdb publication page