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Article

m6AVar: a database of functional variants involved in m6A modification.

Nucleic acids research - 4 Jan 2018

Zheng Yueyuan, Nie Peng, Peng Di, He Zhihao, Liu Mengni, Xie Yubin, Miao Yanyan, Zuo Zhixiang, Ren Jian

Abstract excerpt

Identifying disease-causing variants among a large number of single nucleotide variants (SNVs) is still a major challenge. Recently, N6-methyladenosine (m6A) has become a research hotspot because of its critical roles in many fundamental biological processes and a variety of diseases. Therefore, it is important to evaluate the effect of variants on m6A modification, in order to gain a better understanding of...

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Identifiers

PMID: 29036329
DOI: 10.1093/nar/gkx895
PMCID: PMC5753261

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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