MT-TQ:m.4381A>G

Tutor Research

Nomenclaturem.4381A>GchrMT:4381|ClinVar #689898

Typemitochondrial tRNA variant

InheritanceMitochondrial

gnomAD mtDNA

4 hom · 0 het

of 56,432 genomes

MitoTIP

5.4 · Q4 likely benign

PON-mt-tRNA

0.35 · likely neutral

Tutor Research

ClinVarBenign

VCV000689898

Review: criteria provided, single submitterSubmitters: 1view ↗Last evaluated: 2019/07/12 00:00

MELAS syndrome[OMIM][MedGen][Orphanet][MONDO]

MITOMAPReported

Live entry

Disease: Leber hereditary optic neuropathy (LHON)Reported as: homoplasmicGenBank: 4 sequences

MITOMAP (mitomap.org), CC BY 3.0 · disease table as of 2026-10-07

Where it sits in the mitochondrial genome

Tap or hover a gene, landmark or tick; genes open their page, ticks their variant.

proteinrRNAtRNAouter ring H-strand · inner L-strandMITOMAP confirmedreported (as of 2026-10-07)

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AATCCAAAATTCTCCGTGCCACCTATCACACCCCATCCTAA

MT-TQ (L-strand) · ends m.4400

m.4361–4401 of the revised Cambridge Reference Sequence (NC_012920.1); the boxed base is m.4381 A→G.

37 genes from Ensembl (rCRS numbering, matched to MITOMAP’s Gene Loci); landmarks and disease alleles from MITOMAP (CC BY 3.0). Circular layout after MitoWheel.

Open Research Assistant for MT-TQ →

External Resources

Franklin (Genoox)

AI-powered curation

MITOMAP

mtDNA variant database · expect a security check

VarSome

Variant interpretation · expect a security check

OMIM

Gene & phenotype

gnomAD

mtDNA frequencies (v3.1)

UCSC Browser

Genome browser

m.4381A>G

Resolving variant against ClinVar, gnomAD and Ensembl…

MT-TQ:m.4381A>G

Where it sits in the mitochondrial genome

Population Allele Frequencies

External Resources

MT-TQ:m.4381A>G

Where it sits in the mitochondrial genome

Population Allele Frequencies

External Resources