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MLH1 c.2182_2184delinsG ;(p.I728Afs*4)
Variant ID: 3-37092055-ATT-G
NM_000249.3(
MLH1
):c.2182_2184delinsG;(p.I728Afs*4)
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:
Impact of Different Selection Approaches for Identifying Lynch Syndrome-Related Colorectal Cancer Patients: Unity Is Strength.
Frontiers In Oncology
Fanale, Daniele D; Corsini, Lidia Rita LR; Brando, Chiara C; Dimino, Alessandra A; Filorizzo, Clarissa C; Magrin, Luigi L; Sciacchitano, Roberta R; Fiorino, Alessia A; Bazan Russo, Tancredi Didier TD; Calò, Valentina V; Iovanna, Juan Lucio JL; Francini, Edoardo E; Russo, Antonio A; Bazan, Viviana V
Publication Date: 2022
Variant appearance in text: MLH1: 2182_2184delinsG
PubMed Link:
35223509
Variant Present in the following documents:
fonc-12-827822.pdf
View BVdb publication page