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MLH1 c.1692del ;(p.I565Ffs*26)
Variant ID: 3-37083783-TC-T
NM_000249.3(
MLH1
):c.1692del;(p.I565Ffs*26)
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:
Real-world outcome of universal screening for Lynch syndrome in Japanese patients with colorectal cancer highlights the importance of targeting patients with young-onset disease.
Molecular And Clinical Oncology
Yamada, Atsushi A; Matsuoka, Yui Y; Minamiguchi, Sachiko S; Yamamoto, Yoshihiro Y; Kondo, Tomohiro T; Sunami, Tomohiko T; Horimatsu, Takahiro T; Kawada, Kenji K; Seno, Hiroshi H; Torishima, Masako M; Murakami, Hiromi H; Yamada, Takahiro T; Kosugi, Shinji S; Sugano, Kokichi K; Muto, Manabu M
Publication Date: 2021-12
Variant appearance in text: MLH1: 1692delC; Ile565PhefsX26
PubMed Link:
34712484
Variant Present in the following documents:
Main text
View BVdb publication page