{{Rsnum
|rsid=145449783
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NOL9
|position=6529168
|Gene_s=NOL9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=145449783
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=6529168
|CHROM=1
|dbSNPBuildID=134
|SSR=0
|SAO=3
|VP=0x050068000a05000002100120
|GENEINFO=NOL9:79707
|GENE_NAME=NOL9
|GENE_ID=79707
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.6529168G>A
|CLNORIGIN=2
|CLNSIG=255
|Tags=PM;PMC;NSM;REF;ASP;OTHERKG;LSD
|CLNACC=RCV000060234.2
|CLNDBN=Malignant melanoma
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0025202:2092003
|Disease=Malignant melanoma
|CLNSRC=ClinVar
|CLNSRCID=NM_024654.4:c.1651C>T
}}{{PMID Auto
|PMID=21499247
|Title=Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
|OA=1
}}