Varaico: Literature-Extracted Genetic Variants

Gene:SULT1A2
Variant:p.E217*
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SULT1A2

NM_001054.4:p.E217*

Associated Papers

Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China.

Wei SJ et al.

Bmc Genomics, 2023

36721086 (PubMed )
Supplement: 12864_2022_9097_MOESM2_ESM.xls › Sheet1

Energy metabolism and whole-exome sequencing-based analysis of Sasang constitution: a pilot study.

Kim HK et al.

Integrative Medicine Research, 2017

A complex intragenic rearrangement of ERCC8 in Chinese siblings with Cockayne syndrome.

Xie H et al.

Scientific Reports, 2017

28333167 (PubMed )
Supplement: srep44271-s1.pdf

Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease?

Oh SH et al.

Gut and Liver, 2015

Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss.

Zhao Y et al.

Plos One, 2013

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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."