Viewing single variant in MT-RNR2

Uncertain Significance (VUS)Not in ClinVar or MITOMAP — mtDNA classification needs case-level review

MT-RNR2:m.3096T>C

Tutor Research

Nomenclaturem.3096T>CchrMT:3096|Not in ClinVar

Typemitochondrial rRNA variant

InheritanceMitochondrial

gnomAD mtDNA

64 hom · 1 het

of 56,427 genomes

Tutor Research

MITOMAPReported

Live entry

Disease: Possible association with sepsisReported as: heteroplasmicGenBank: 18 sequences

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

Where it sits in the mitochondrial genome

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

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ACCGGAGTAATCCAGGTCGGTTTCTATCTACNTTCAAATTC

MT-RNR2

m.3076–3116 of the revised Cambridge Reference Sequence (NC_012920.1); the boxed base is m.3096 T→C.

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-RNR2 →

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.3096T>C

Resolving variant against ClinVar, gnomAD and Ensembl…

MT-RNR2:m.3096T>C

Where it sits in the mitochondrial genome

Population Allele Frequencies

Mechanism of Pathogenicity

External Resources

MT-RNR2:m.3096T>C

Where it sits in the mitochondrial genome

Population Allele Frequencies

Mechanism of Pathogenicity

External Resources