{{Rsnum
|rsid=121918511
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRKCG
|position=53889653
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKCG
}}{{omim
|id=176980
|rsnum=121918511
|variant=0001
}}{{ClinVar
|rsid=121918511
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=54392907
|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.54392907C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1399; 176980.0001
|CLNSIG=5
|CLNCUI=C1854369
|CLNDBN=Spinocerebellar ataxia 14
|Disease=Spinocerebellar ataxia 14
|CLNACC=RCV000014149.24
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
}}{{PMID Auto
|PMID=12644968
|Title=Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
|OA=1
}}

{{PMID Auto
|PMID=17659643
|Title=Codon 101 of PRKCG, a preferential mutation site in SCA14.
}}