{{Rsnum
|rsid=104886389
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=COL4A5
|position=108666513
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNALLE=1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=OMIM
|CLNDSDBID=301050
|CLNHGVS=NC_000023.10:g.107909743G>T
|CLNSIG=4
|Disease=Alport syndrome
|FwdALT=T
|FwdREF=G
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=G
|RSPOS=107909743
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000a01000002110100
|WGT=1
|dbSNPBuildID=132
|rsid=104886389
}}{{PMID Auto
|PMID=10561141
|Title=Detection of mutations in the COL4A5 gene in over 90% of male patients with X-linked Alport's syndrome by RT-PCR and direct sequencing.
}}