CTNNB1 c.36G>T ;(p.M12I)

Variant ID: 3-41266039-G-T

NM_001904.3(CTNNB1):c.36G>T;(p.M12I)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Targeted Next-Generation Sequencing of Plasma Cell-Free DNA in Korean Patients with Hepatocellular Carcinoma.

Annals Of Laboratory Medicine
Chae, Hyojin H; Sung, Pil Soo PS; Choi, Hayoung H; Kwon, Ahlm A; Kang, Dain D; Kim, Yonggoo Y; Kim, Myungshin M; Yoon, Seung Kew SK
Publication Date: 2021-03-01

Variant appearance in text: CTNNB1: 36G>T; M12I
PubMed Link: 33063681
Variant Present in the following documents:
  • Main text
  • ALM-41-198.pdf
View BVdb publication page



Clinical significance of frequent somatic mutations detected by high-throughput targeted sequencing in archived colorectal cancer samples.

Journal Of Translational Medicine
Dallol, Ashraf A; Buhmeida, Abdelbaset A; Al-Ahwal, Mahmoud Shaheen MS; Al-Maghrabi, Jaudah J; Bajouh, Osama O; Al-Khayyat, Shadi S; Alam, Rania R; Abusanad, Atlal A; Turki, Rola R; Elaimi, Aisha A; Alhadrami, Hani A HA; Abuzenadah, Mohammed M; Banni, Huda H; Al-Qahtani, Mohammed H MH; Abuzenadah, Adel M AM
Publication Date: 2016-05-04

Variant appearance in text: CTNNB1: Met12Ile
PubMed Link: 27146902
Variant Present in the following documents:
  • Main text
  • 12967_2016_Article_878.pdf
View BVdb publication page