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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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