TSC2 c.1204_1206delinsAGC ;(p.G402S)

Variant ID: 16-2111956-GGG-AGC

NM_000548.3(TSC2):c.1204_1206delinsAGC;(p.G402S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.

Hereditary Cancer In Clinical Practice
Wallander, Karin K; Thonberg, Håkan H; Nilsson, Daniel D; Tham, Emma E
Publication Date: 2021-10-28

Variant appearance in text: TSC2: Gly402Ser
PubMed Link: 34711244
Variant Present in the following documents:
  • Main text
View BVdb publication page



Autism throughout genetics: Perusal of the implication of ion channels.

Brain And Behavior
Daghsni, Marwa M; Rima, Mohamad M; Fajloun, Ziad Z; Ronjat, Michel M; Brusés, Juan L JL; M'rad, Ridha R; De Waard, Michel M
Publication Date: 2018-08

Variant appearance in text: TSC2: G402S
PubMed Link: 29934975
Variant Present in the following documents:
  • Main text
View BVdb publication page