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KMT2C c.965A>T ;(p.H322L)
Variant ID: 7-151970837-T-A
NM_170606.2(
KMT2C
):c.965A>T;(p.H322L)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Exome sequencing reveals aberrant signalling pathways as hallmark of treatment-naive anal squamous cell carcinoma.
Oncotarget
Cacheux, Wulfran W; Dangles-Marie, Virginie V; Rouleau, Etienne E; Lazartigues, Julien J; Girard, Elodie E; Briaux, Adrien A; Mariani, Pascale P; Richon, Sophie S; Vacher, Sophie S; Buecher, Bruno B; Richard-Molard, Marion M; Jeannot, Emmanuelle E; Servant, Nicolas N; Farkhondeh, Fereshteh F; Mariani, Odette O; Rio-Frio, Thomas T; Roman-Roman, Sergio S; Mitry, Emmanuel E; Bieche, Ivan I; Lièvre, Astrid A
Publication Date: 2018-01-02
Variant appearance in text: MLL3: 965A>T
PubMed Link:
29416628
Variant Present in the following documents:
Main text
oncotarget-09-464.pdf
View BVdb publication page