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