{{Rsnum
|rsid=111033319
|Chromosome=MT
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ACTR6
|position=7471
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=AC
|CHROM=MT
|CLNACC=RCV000035051.1
|CLNALLE=1
|CLNDBN=Hereditary hearing loss and deafness
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002
|CLNHGVS=NC_012920.1:m.7471_7472insC
|CLNORIGIN=1
|CLNSIG=5
|Disease=Hereditary hearing loss and deafness
|FwdALT=C
|REF=A
|RSPOS=7465
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD
|VC=DIV
|VP=0x050068000000000002100200
|WGT=0
|dbSNPBuildID=132
|rsid=111033319
}}{{PMID Auto
|PMID=7581383
|Title=Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.
}}

{{PMID Auto
|PMID=9708714
|Title=Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472.
}}

{{PMID Auto
|PMID=9832034
|Title=A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy.
|OA=1
}}

{{PMID Auto
|PMID=10094190
|Title=Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
}}

{{PMID Auto
|PMID=11378827
|Title=Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction.
}}