{{Rsnum
|rsid=121434595
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NRAS
|position=114716124
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NRAS
}}{{omim
|id=164790
|rsnum=121434595
|variant=0001
}}{{ClinVar
|rsid=121434595
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=114716124
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=3
|VP=0x050260000a05000002110124
|GENEINFO=NRAS:4893
|GENE_NAME=NRAS
|GENE_ID=4893
|WGT=1
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000001.11:g.114716124C>G
|CLNORIGIN=2
|CLNSRCID=
NM_002524.4:c.37G>C; 164790.0001
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000014913.2; RCV000114743.1
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM;NOV
|CLNDBN=Rectal cancer, somatic; MELANOCYTIC NEVUS SYNDROME, CONGENITAL, SOMATIC
|CLNSRC=ClinVar; OMIM Allelic Variant
|Disease=Rectal cancer; MELANOCYTIC NEVUS SYNDROME
}}