Varaico: Literature-Extracted Genetic Variants

Gene:TACR3
Variant:p.W331*
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TACR3

NM_001059.3:p.W331*

Associated Papers

How exome sequencing improves the diagnostics and management of men with non-syndromic infertility.

Stallmeyer B et al.

Andrology, 2025

39120565 (PubMed )
Supplement: ANDR-13-1011-s001.xlsx › Table_S1

Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.

Ozturk S

Cell Cycle (georgetown, Tex.), 2023

Transitioning the Molecular Tumor Board from Proof of Concept to Clinical Routine: A German Single-Center Analysis.

Hoefflin R et al.

Cancers, 2021

33800365 (PubMed )
Supplement: cancers-13-01151-s001.zip › Supplementary_Data_2.xlsx › Unknown_Mutations

A single-nucleotide polymorphism induced alternative splicing in Tacr3 involves in hypoxic-ischemic brain damage.

Xue LL et al.

Brain Research Bulletin, 2020

A novel stopgain mutation c.G992A (p.W331X) in TACR3 gene was identified in nonobstructive azoospermia by targeted next-generation sequencing.

Geng D et al.

Journal of Clinical Laboratory Analysis, 2019

Identification of the Germline Mutation Profile in Esophageal Squamous Cell Carcinoma by Whole Exome Sequencing.

Deng J et al.

Frontiers in Genetics, 2019

30833958 (PubMed )
Supplement: Table_1.XLSX › susceptibility_genes
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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."