{{Rsnum
|rsid=386134160
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=PRKCG
|position=53884187
|Gene_s=PRKCG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000034975.2
|CLNALLE=1
|CLNDBN=Spinocerebellar ataxia 14
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
|CLNHGVS=NC_000019.9:g.54387441T>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1399
|Disease=Spinocerebellar ataxia 14
|FwdALT=A
|FwdREF=T
|REF=T
|RSPOS=54387441
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386134160
|GENEINFO=PRKCG:5582
|GENE_ID=5582
|GENE_NAME=PRKCG
}}{{PMID Auto
|PMID=17708558
|Title=Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene.
}}