{{Rsnum
|rsid=193922136
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CD40LG
|position=136659390
|Gene_s=CD40LG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922136
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=135741549
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.135741549C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Immunodeficiency with hyper IgM type 1
|Disease=Immunodeficiency with hyper IgM type 1
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029466.1
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1402:C0398689:308230
|GENEINFO=CD40LG:959
|GENE_ID=959
|GENE_NAME=CD40LG
}}{{PMID Auto
|PMID=17351
|Title=Assembly of multisubunit respiratory proteins.
}}

{{PMID Auto
|PMID=11037300
|Title=Primary immunodeficiency mutation databases.
}}

{{PMID Auto
|PMID=16509032
|Title=Classification of mutations in the human CD40 ligand, gp39, that are associated with X-linked hyper IgM syndrome.
|OA=1
}}

{{PMID Auto
|PMID=17307885
|Title=The structural basis of hyper IgM deficiency - CD40L mutations.
}}

{{PMID Auto
|PMID=18051214
|Title=Analysis of genetic defects in patients with the common variable immunodeficiency phenotype in a single Taiwanese tertiary care hospital.
}}

{{PMID Auto
|PMID=19575287
|Title=Clinical and laboratory findings in hyper-IgM syndrome with novel CD40L and AICDA mutations.
}}