Viewing single variant in MT-RNR1

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

MT-RNR1:m.965C>CC

Tutor Research

Nomenclaturem.965C>CCchrMT:962|Not in ClinVar

Typemitochondrial rRNA variant

InheritanceMitochondrial

gnomAD mtDNA

Absent

~56k genomes

Tutor Research

MITOMAPNot in MITOMAP’s disease table (as of 2026-10-07); it may have been added since.

Check MITOMAP

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)

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-RNR1 →

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.965C>CC

Resolving variant against ClinVar, gnomAD and Ensembl…

MT-RNR1:m.965C>CC

Where it sits in the mitochondrial genome

Population Allele Frequencies

Mechanism of Pathogenicity

External Resources

MT-RNR1:m.965C>CC

Where it sits in the mitochondrial genome

Population Allele Frequencies

Mechanism of Pathogenicity

External Resources