{{Rsnum
|rsid=144003672
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PUSL1
|position=1309724
|Gene_s=PUSL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{PMID|21499247|OA=1
}} Exome sequencing identifies GRIN2A as frequently mutated in melanoma.{{ClinVar
|rsid=144003672
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=1309724
|CHROM=1
|RS=144003672
|dbSNPBuildID=134
|SSR=0
|SAO=3
|VP=0x050268020b05000002100120
|GENEINFO=ACAP3:116983; PUSL1:126789
|GENE_NAME=ACAP3; PUSL1
|GENE_ID=116983; 126789
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.1309724C>A
|CLNORIGIN=2
|CLNSIG=255
|Tags=PM;PMC;S3D;NSM;REF;SYN;R5;ASP;OTHERKG;LSD
|CLNACC=RCV000059856.2
|CLNDBN=Malignant melanoma
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0025202:2092003
|Disease=Malignant melanoma
|CLNSRC=ClinVar
|CLNSRCID=NM_030649.2:c.-1909G>T; NM_153339.1:c.517C>A
}}