List of variants reported as benign for X-linked Alport syndrome

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.3979G>A (p.Val1327Met)	rs2229813	0.46716
NM_033380.3(COL4A5):c.1033-72C>T	rs2272944	0.23733
NM_033380.3(COL4A5):c.609+21T>C	rs6622333	0.18370
NM_033380.3(COL4A5):c.1587+136A>G	rs4308887	0.18242
NM_033380.3(COL4A5):c.3513A>G (p.Gln1171=)	rs2273051	0.14310
NM_033380.3(COL4A5):c.2349G>A (p.Pro783=)	rs3747408	0.11046
NM_033380.3(COL4A5):c.1331T>G (p.Ile444Ser)	rs2272946	0.11020
NM_033380.3(COL4A5):c.2055T>C (p.Leu685=)	rs7884085	0.10905
NM_033380.3(COL4A5):c.1095G>C (p.Gly365=)	rs2272945	0.10302
NM_033380.3(COL4A5):c.4293C>T (p.Asp1431=)	rs61746140	0.10149
NM_033380.3(COL4A5):c.438+36G>T	rs73526282	0.09880
NM_033380.3(COL4A5):c.2768-11A>G	rs1006269	0.09324
NM_033380.3(COL4A5):c.3519T>G (p.Gly1173=)	rs61735627	0.03239
NM_033380.3(COL4A5):c.276+69T>C	rs149638471	0.01263
NM_033380.3(COL4A5):c.1992G>T (p.Lys664Asn)	rs34077552	0.00745
NM_033380.3(COL4A5):c.1289C>A (p.Ala430Asp)	rs142883891	0.00418
NM_033380.3(COL4A5):c.4223C>G (p.Thr1408Ser)	rs151278542	0.00294
NM_033380.3(COL4A5):c.2858G>T (p.Gly953Val)	rs78972735	0.00119
NM_033380.3(COL4A5):c.2215C>G (p.Pro739Ala)	rs104886164	0.00034
NM_033380.3(COL4A5):c.2692A>G (p.Met898Val)	rs104886192	0.00017
NM_033380.3(COL4A5):c.3029A>G (p.Asn1010Ser)	rs151077921	0.00015
NM_033380.3(COL4A5):c.2107A>G (p.Ile703Val)	rs104886155	0.00002
NM_033380.3(COL4A5):c.779A>G (p.Gln260Arg)	rs372889859	0.00001
NM_033380.3(COL4A5):c.1032+17del	rs761615270
NM_033380.3(COL4A5):c.1032+17dup	rs761615270
NM_033380.3(COL4A5):c.1032+25G>A	rs58190747
NM_033380.3(COL4A5):c.1033-15del	rs104886089
NM_033380.3(COL4A5):c.2999G>T (p.Gly1000Val)	rs281874709
NM_033380.3(COL4A5):c.406A>G (p.Ser136Gly)	rs768580195
NM_033380.3(COL4A5):c.891+37A>G	rs2294543

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