{{Rsnum
|rsid=104886397
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=COL4A5
|position=108680883
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=104886397
|Reversed=0
|FwdREF=A
|FwdALT=G,T
|REF=A
|ALT=G,T
|RSPOS=107924113
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050068000000000002110100
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.107924113A>G; NC_000023.10:g.107924113A>T
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000021577.1; RCV000021576.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|Disease=Alport syndrome
}}{{PMID Auto
|PMID=18332068
|Title=Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.
}}

{{PMID Auto
|PMID=8651296
|Title=X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
|OA=1
}}
{{omim
|id=301050
|rsnum=104886397
}}