MUTYH c.461G>T ;(p.R154L)

Variant ID: 1-45798466-C-A

NM_001048174.1(MUTYH):c.461G>T;(p.R154L)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel.

Cureus
Jinda, Worapoj W; Moungthard, Hathaiwan H; Limwongse, Chanin C; Pithukpakorn, Manop M; Saelee, Pensri P; Pokkasup, Nareerat N; Khunpukdee, Saipan S; Sukthaworn, Suchitraporn S; Jumpasri, Jaruphan J
Publication Date: 2023-05

Variant appearance in text: rs143353451
PubMed Link: 37323311
Variant Present in the following documents:
  • Main text
  • cureus-0015-00000039067.pdf
View BVdb publication page



Evolutionary Origin of MUTYH Germline Pathogenic Variations in Modern Humans.

Biomolecules
Xiao, Fengxia F; Li, Jiaheng J; Lagniton, Philip Naderev Panuringan PNP; Kou, Si Hoi SH; Lei, Huijun H; Tam, Benjamin B; Wang, San Ming SM
Publication Date: 2023-02-24

Variant appearance in text: rs143353451
PubMed Link: 36979362
Variant Present in the following documents:
  • biomolecules-13-00429.pdf
View BVdb publication page



Response prediction in patients with gastric and esophagogastric adenocarcinoma under neoadjuvant chemotherapy using targeted gene expression analysis and next-generation sequencing in pre-therapeutic biopsies.

Journal Of Cancer Research And Clinical Oncology
Kleo, Karsten K; Jovanovic, Vladimir M VM; Arndold, Alexander A; Lehmann, Annika A; Lammert, Hedwig H; Berg, Erika E; Harloff, Hannah H; Treese, Christoph C; Hummel, Michael M; Daum, Severin S
Publication Date: 2022-03-05

Variant appearance in text: rs143353451
PubMed Link: 35246724
Variant Present in the following documents:
  • 432_2022_3944_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



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: rs143353451
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
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 7
  • 41598_2021_93715_MOESM3_ESM.xlsx, sheet 6
  • 41598_2021_93715_MOESM3_ESM.xlsx, sheet 2
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Spectrum of germline cancer susceptibility gene mutations in Turkish colorectal cancer patients: a single center study

Turkish Journal Of Medical Sciences
Erdem, Haktan Bağiş HB; Bahsi, Taha T
Publication Date: 2020-06-23

Variant appearance in text: rs143353451
PubMed Link: 32283892
Variant Present in the following documents:
  • Main text
  • turkjmedsci-50-1015.pdf
View BVdb publication page



Mutation Profiling of Premalignant Colorectal Neoplasia.

Gastroenterology Research And Practice
Karczmarski, Jakub J; Goryca, Krzysztof K; Pachlewski, Jacek J; Dabrowska, Michalina M; Pysniak, Kazimiera K; Paziewska, Agnieszka A; Kulecka, Maria M; Lenarcik, Malgorzata M; Mroz, Andrzej A; Mikula, Michal M; Ostrowski, Jerzy J
Publication Date: 2019

Variant appearance in text: MUTYH: R154L; rs143353451
PubMed Link: 31781186
Variant Present in the following documents:
  • 2542640.f1.xlsx, sheet 1
View BVdb publication page



Optimizing clinical exome design and parallel gene-testing for recessive genetic conditions in preconception carrier screening: Translational research genomic data from 14,125 exomes.

Plos Genetics
Capalbo, Antonio A; Valero, Roberto Alonso RA; Jimenez-Almazan, Jorge J; Pardo, Pere Mir PM; Fabiani, Marco M; Jiménez, David D; Simon, Carlos C; Rodriguez, Julio Martin JM
Publication Date: 2019-10

Variant appearance in text: rs143353451
PubMed Link: 31589614
Variant Present in the following documents:
  • pgen.1008409.s001.xlsx, sheet 1
View BVdb publication page