List of variants reported as likely pathogenic for X-linked Alport syndrome by Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.1129G>A (p.Gly377Arg)	rs1603286154
NM_033380.3(COL4A5):c.1387G>C (p.Gly463Arg)	rs1556410516
NM_033380.3(COL4A5):c.1708G>A (p.Gly570Arg)	rs1603290169
NM_033380.3(COL4A5):c.1771G>A (p.Gly591Arg)	rs1569494061
NM_033380.3(COL4A5):c.2183G>A (p.Gly728Glu)	rs1603292422
NM_033380.3(COL4A5):c.2537G>A (p.Gly846Glu)	rs1569497690
NM_033380.3(COL4A5):c.2579G>A (p.Gly860Asp)	rs1556419831
NM_033380.3(COL4A5):c.2587G>A (p.Gly863Ser)	rs1603297305
NM_033380.3(COL4A5):c.2615G>C (p.Gly872Ala)	rs1556419869
NM_033380.3(COL4A5):c.2642G>T (p.Gly881Val)	rs1556419895
NM_033380.3(COL4A5):c.2686G>A (p.Gly896Ser)	rs1556420349
NM_033380.3(COL4A5):c.2695G>A (p.Gly899Ser)	rs1556420358
NM_033380.3(COL4A5):c.2927G>A (p.Gly976Glu)	rs1603298378
NM_033380.3(COL4A5):c.2963G>A (p.Gly988Glu)	rs1569498623
NM_033380.3(COL4A5):c.3052G>T (p.Gly1018Cys)	rs1603298869
NM_033380.3(COL4A5):c.3152G>A (p.Gly1051Glu)	rs1603298993
NM_033380.3(COL4A5):c.3197G>A (p.Gly1066Asp)	rs104886221
NM_033380.3(COL4A5):c.3293G>A (p.Gly1098Asp)	rs1603306716
NM_033380.3(COL4A5):c.3509G>A (p.Gly1170Asp)	rs1060499710
NM_033380.3(COL4A5):c.3554G>T (p.Gly1185Val)	rs2068097992
NM_033380.3(COL4A5):c.3942G>A (p.Gln1314=)	rs281874724
NM_033380.3(COL4A5):c.4475G>T (p.Gly1492Val)	rs104886282
NM_033380.3(COL4A5):c.4529-345A>G	rs1569508899
NM_033380.3(COL4A5):c.4709G>T (p.Cys1570Phe)	rs104886287
NM_033380.3(COL4A5):c.4811C>T (p.Ser1604Phe)	rs1569509257
NM_033380.3(COL4A5):c.547G>A (p.Gly183Ser)	rs1556404985
NM_033380.3(COL4A5):c.584G>T (p.Gly195Val)	rs104886061
NM_033380.3(COL4A5):c.619G>A (p.Gly207Ser)	rs1569490379
NM_033380.3(COL4A5):c.638G>T (p.Gly213Val)	rs104886066
NM_033380.3(COL4A5):c.707G>A (p.Gly236Asp)	rs1556406001
NM_033380.3(COL4A5):c.799G>A (p.Gly267Arg)	rs1603283567
NM_033380.3(COL4A5):c.929G>T (p.Gly310Val)	rs1556407064

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