Viewing single variant in MT-RNR1

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

MT-RNR1:m.961T>CC

Tutor Research

Nomenclaturem.961T>CCchrMT:961|Not in ClinVar

Typemitochondrial rRNA variant

InheritanceMitochondrial

gnomAD mtDNA

Absent

~56k genomes

Tutor Research

MITOMAPLikely benignreported

Live entry

Disease: Maternally inherited or aminoglycoside-induced deafness (DEAF) · AD-associated · Intellectual disabilityReported as: homoplasmic and heteroplasmicGenBank: 0 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)

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.