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MLH1 c.69A>T ;(p.E23D)
Variant ID: 3-37035107-A-T
NM_000249.3(
MLH1
):c.69A>T;(p.E23D)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.
Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12
Variant appearance in text: HNPCC2: E23D
PubMed Link:
34253785
Variant Present in the following documents:
41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
41598_2021_93715_MOESM3_ESM.xlsx, sheet 4
View BVdb publication page
Identification of MLH2/hPMS1 dominant mutations that prevent DNA mismatch repair function.
Communications Biology
Reyes, Gloria X GX; Zhao, Boyu B; Schmidt, Tobias T TT; Gries, Kerstin K; Kloor, Matthias M; Hombauer, Hans H
Publication Date: 2020-12-10
Variant appearance in text: MLH1: E23D
PubMed Link:
33303966
Variant Present in the following documents:
Main text
42003_2020_Article_1481.pdf
View BVdb publication page
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome.
Elife
Abildgaard, Amanda B AB; Stein, Amelie A; Nielsen, Sofie V SV; Schultz-Knudsen, Katrine K; Papaleo, Elena E; Shrikhande, Amruta A; Hoffmann, Eva R ER; Bernstein, Inge I; Gerdes, Anne-Marie AM; Takahashi, Masanobu M; Ishioka, Chikashi C; Lindorff-Larsen, Kresten K; Hartmann-Petersen, Rasmus R
Publication Date: 2019-11-07
Variant appearance in text: MLH1: E23D
PubMed Link:
31697235
Variant Present in the following documents:
Main text
elife-49138.pdf
View BVdb publication page