{{Rsnum
|rsid=150855676
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CHD5
|position=6112171
|Gene_s=CHD5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=150855676
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=6112171
|CHROM=1
|dbSNPBuildID=134
|SSR=0
|SAO=3
|VP=0x050068000305000002100120
|GENEINFO=CHD5:26038
|GENE_NAME=CHD5
|GENE_ID=26038
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.6112171G>A
|CLNORIGIN=2
|CLNSIG=255
|Tags=PM;PMC;REF;SYN;ASP;OTHERKG;LSD
|RS=150855676
|CLNACC=RCV000060228.2
|CLNDBN=Malignant melanoma
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0025202:2092003
|Disease=Malignant melanoma
|CLNSRC=ClinVar
|CLNSRCID=NM_015557.2:c.5109C>T
}}{{PMID|21499247|OA=1
}} Exome sequencing identifies GRIN2A as frequently mutated in melanoma.