{{Rsnum
|rsid=387906733
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SMARCE1P4
|position=12201
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000022899.1
|CLNALLE=1
|CLNDBN=Deafness, nonsyndromic sensorineural, mitochondrial
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1422:NBK1434:C3151897:500008:90641
|CLNHGVS=NC_012920.1:m.12201T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590040.0004
|Disease=Deafness
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=12201
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906733
}}