{{Rsnum
|rsid=121918516
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRKCG
|position=53906728
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKCG
}}{{omim
|id=176980
|rsnum=121918516
|variant=0006
}}{{ClinVar
|rsid=121918516
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=54409982
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PRKCG:5582
|GENE_NAME=PRKCG
|GENE_ID=5582
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.54409982T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1399; 176980.0006
|CLNSIG=5
|CLNCUI=C1854369
|CLNDBN=Spinocerebellar ataxia 14
|Disease=Spinocerebellar ataxia 14
|CLNACC=RCV000014154.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
}}