{{Rsnum
|rsid=121918514
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRKCG
|position=53889705
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKCG
}}{{omim
|id=176980
|rsnum=121918514
|variant=0004
}}{{ClinVar
|rsid=121918514
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=54392959
|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.54392959G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1399; 176980.0004
|CLNSIG=5
|CLNCUI=C1854369
|CLNDBN=Spinocerebellar ataxia 14
|Disease=Spinocerebellar ataxia 14
|CLNACC=RCV000014152.25
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
}}{{PMID Auto
|PMID=14694043
|Title=Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
}}

{{PMID Auto
|PMID=15841389
|Title=Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.
}}

{{PMID Auto
|PMID=17343273
|Title=PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotype.
}}