List of variants reported as likely pathogenic for Autosomal dominant Alport syndrome by Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.4981C>T (p.Arg1661Cys)	rs201697532	0.00039
NM_000091.5(COL4A3):c.3829G>A (p.Gly1277Ser)	rs190598500	0.00032
NM_000091.5(COL4A3):c.1450G>A (p.Gly484Arg)	rs777401300	0.00003
NM_000091.5(COL4A3):c.898G>A (p.Gly300Arg)	rs772708743	0.00002
NM_000091.5(COL4A3):c.1814G>T (p.Gly605Val)	rs2469700028
NM_000091.5(COL4A3):c.2711G>A (p.Gly904Glu)	rs1174417447
NM_000091.5(COL4A3):c.3312AAGTCCTGG[1] (p.1105SPG[1])	rs756539994
NM_000091.5(COL4A3):c.3546_3548dup (p.Gly1183dup)	rs1175052474
NM_000091.5(COL4A3):c.370G>C (p.Gly124Arg)	rs2469502863

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