{{Rsnum
|rsid=121918515
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRKCG
|position=53889732
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKCG
}}{{omim
|id=176980
|rsnum=121918515
|variant=0005
}}{{ClinVar
|rsid=121918515
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=54392986
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=PRKCG:5582
|GENE_NAME=PRKCG
|GENE_ID=5582
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.54392986A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1399; 176980.0005
|CLNSIG=5
|CLNCUI=C1854369
|CLNDBN=Spinocerebellar ataxia 14
|Disease=Spinocerebellar ataxia 14
|CLNACC=RCV000014153.24
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
}}{{PMID Auto
|PMID=14676051
|Title=Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
}}