{{Rsnum
|rsid=386134158
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PRKCG
|position=53882616
|Gene_s=PRKCG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=19
|CLNACC=RCV000034959.1
|CLNALLE=1
|CLNDBN=Spinocerebellar ataxia 14
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
|CLNHGVS=NC_000019.9:g.54385870G>C
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1399
|Disease=Spinocerebellar ataxia 14
|FwdALT=C
|FwdREF=G
|REF=G
|RSPOS=54385870
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386134158
|GENEINFO=PRKCG:5582
|GENE_ID=5582
|GENE_NAME=PRKCG
}}{{PMID Auto
|PMID=15824357
|Title=The clinical and genetic spectrum of spinocerebellar ataxia 14.
}}