Varaico: Literature-Extracted Genetic Variants

Gene:SLC38A6
Variant:p.M281T
Back to variants list

SLC38A6

NM_153811.3:p.M281T

Associated Papers

Loss-of-function variations in solute carrier family 38 member 6 are associated with essential tremor.

Yuan Z et al.

Signal Transduction and Targeted Therapy, 2025

A Rare Variant of ANK3 Is Associated With Intracranial Aneurysm.

Liu J et al.

Frontiers in Neurology, 2021

Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq.

Gao J et al.

International Journal of Molecular Sciences, 2020

32344918 (PubMed )
Supplement: ijms-21-03040-s001.zip › Supplementary_Data › Supplementary_Data_2.xlsx › S_Data_2

Novel compound heterozygous mutations of ALDH1A3 contribute to anophthalmia in a non-consanguineous Chinese family.

Liu Y et al.

Genetics and Molecular Biology, 0

28590501 (PubMed )
Supplement: 1415-4757-gmb-1678-4685-GMB-2016-0120-Suppl03.pdf
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."