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

Variant ID: 3-41266039-G-A

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

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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



Bioinformatics Knowledge Map for Analysis of Beta-Catenin Function in Cancer.

Plos One
Çelen, İrem İ; Ross, Karen E KE; Arighi, Cecilia N CN; Wu, Cathy H CH
Publication Date: 2015

Variant appearance in text: CTNNB1: 36G>A; M12I
PubMed Link: 26509276
Variant Present in the following documents:
  • pone.0141773.s003.xlsx, sheet 1
View BVdb publication page