TSC2 c.2182T>G ;(p.C728G)

Variant ID: 16-2122326-T-G

NM_000548.3(TSC2):c.2182T>G;(p.C728G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.

Molecular Neurobiology
Zhang, Yi Y; Wang, Tao T; Wang, Yan Y; Xia, Kun K; Li, Jinchen J; Sun, Zhongsheng Z
Publication Date: 2021-08

Variant appearance in text: TSC2: 2182T>G; C728G
PubMed Link: 33860439
Variant Present in the following documents:
  • 12035_2021_2377_MOESM14_ESM.xlsx, sheet 1
View BVdb publication page