{{Rsnum
|rsid=386134170
|Chromosome=19
|Orientation=plus
|geno1=(GC;GC)
|geno2=(GC;TT)
|geno3=(TT;TT)
|Gene=PRKCG
|position=53889937
|Gene_s=PRKCG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TTT
|CHROM=19
|CLNACC=RCV000034997.1
|CLNALLE=1
|CLNDBN=Spinocerebellar ataxia 14
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
|CLNHGVS=NC_000019.9:g.54393191_54393192delGCinsTT
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1399
|Disease=Spinocerebellar ataxia 14
|FwdALT=TT
|FwdREF=GC
|REF=TGC
|RSPOS=54393190
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=MNV
|VP=0x050168000000000002110800
|WGT=0
|dbSNPBuildID=137
|rsid=386134170
|GENEINFO=PRKCG:5582
|GENE_ID=5582
|GENE_NAME=PRKCG
}}{{PMID Auto
|PMID=16291902
|Title=Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene.
|OA=1
}}