TSC2 c.2710_2711delinsGC ;(p.F904A)

Variant ID: 16-2126139-TT-GC

NM_000548.3(TSC2):c.2710_2711delinsGC;(p.F904A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder.

Molecular Autism
Bahl, Samira S; Chiang, Colby C; Beauchamp, Roberta L RL; Neale, Benjamin M BM; Daly, Mark J MJ; Gusella, James F JF; Talkowski, Michael E ME; Ramesh, Vijaya V
Publication Date: 2013-03-20

Variant appearance in text: TSC2: F904A
PubMed Link: 23514105
Variant Present in the following documents:
  • Main text
  • 2040-2392-4-5.pdf
View BVdb publication page