Varaico: Literature-Extracted Genetic Variants

Gene:NTRK3
Variant:p.T332M
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NTRK3

NM_001012338.3:p.T332M

Associated Papers

Case Report: a novel missense variant of FGD5 in a family with tetralogy of Fallot.

Liu MW et al.

Frontiers in Genetics, 2025

Evolutionary history of adenomas to colorectal cancer in FAP families.

Yang C et al.

Frontiers in Genetics, 2024

39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 2016-04836A1.xls › SNVIndel

Germline Variants Associated with Nasopharyngeal Carcinoma Predisposition Identified through Whole-Exome Sequencing.

Lee NY et al.

Cancers, 2022

35954343 (PubMed )
Supplement: cancers-14-03680-s001.zip › NPC_WES_study_Table_S3.xlsx › All

Germline variants of ATG7 in familial cholangiocarcinoma alter autophagy and p62.

Greer SU et al.

Scientific Reports, 2022

35725745 (PubMed )
Supplement: 41598_2022_13569_MOESM1_ESM.xlsx › Table_S9

Mutational Profile and Potential Molecular Therapeutic Targets of Pheochromocytoma.

Ma X et al.

Frontiers in Endocrinology, 2022

35966080 (PubMed )
Supplement: Table_1.xlsx › Table_S4

EGFR-Mutated Squamous Cell Lung Cancer and Its Association With Outcomes.

Jin R et al.

Frontiers in Oncology, 2021

34195081 (PubMed )
Supplement: Table_2.xlsx › EGFR_wild-type_SCC

Patient-derived ovarian cancer organoids capture the genomic profiles of primary tumours applicable for drug sensitivity and resistance testing.

Nanki Y et al.

Scientific Reports, 2020

32724113 (PubMed )
Supplement: 41598_2020_69488_MOESM2_ESM.xlsx › Sheet1

Roles of TrkC Signaling in the Regulation of Tumorigenicity and Metastasis of Cancer.

Jin W

Cancers, 2020

Discovery of actionable genetic alterations with targeted panel sequencing in children with relapsed or refractory solid tumors.

Lee JW et al.

Plos One, 2019

31747416 (PubMed )
Supplement: pone.0224227.s002.xlsx › SNV

Clinical Relevance of Genomic Changes in Recurrent Pediatric Solid Tumors.

Lee B et al.

Translational Oncology, 2018

30216764 (PubMed )
Supplement: mmc3.xlsx › Supplementary_Table_S4

Profiling cancer-related gene mutations in oral squamous cell carcinoma from Japanese patients by targeted amplicon sequencing.

Nakagaki T et al.

Oncotarget, 2017

28938622 (PubMed )
Supplement: oncotarget-08-59113-s006.xlsx › Table_S5
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."