ClinVar Miner

List of variants reported as likely benign for Alport syndrome by Illumina Laboratory Services, Illumina

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_000091.5(COL4A3):c.1352A>G (p.His451Arg) rs11677877 0.08050
NM_000091.5(COL4A3):c.2715C>T (p.Pro905=) rs75519005 0.01995
NM_000092.5(COL4A4):c.*581G>A rs79659665 0.01689
NM_000092.5(COL4A4):c.3486A>G (p.Pro1162=) rs2229815 0.01659
NM_000092.5(COL4A4):c.2008G>A (p.Val670Ile) rs34236495 0.01622
NM_000092.5(COL4A4):c.2439A>T (p.Gly813=) rs34835657 0.01612
NM_000092.5(COL4A4):c.1323T>C (p.Pro441=) rs35830639 0.01576
NM_000092.5(COL4A4):c.2791G>A (p.Ala931Thr) rs75875272 0.01243
NM_000092.5(COL4A4):c.2717-5A>T rs1800519 0.01182
NM_000091.5(COL4A3):c.*1360T>A rs116377856 0.00953
NM_000092.5(COL4A4):c.*3690A>G rs149243282 0.00945
NM_000092.5(COL4A4):c.*841G>A rs11556632 0.00854
NM_000092.5(COL4A4):c.*4164C>T rs147109071 0.00850
NM_000092.5(COL4A4):c.198A>G (p.Pro66=) rs147947155 0.00681
NM_000092.5(COL4A4):c.*472A>T rs77268230 0.00670
NM_000092.5(COL4A4):c.*2311C>T rs77079951 0.00666
NM_000092.5(COL4A4):c.*2239T>C rs79443960 0.00664
NM_000092.5(COL4A4):c.3871C>G (p.Pro1291Ala) rs34728338 0.00619
NM_000091.5(COL4A3):c.*2145A>C rs115394347 0.00614
NM_000091.5(COL4A3):c.*2182C>T rs114535536 0.00613
NM_000092.5(COL4A4):c.-101-4A>G rs147186690 0.00562
NM_000092.5(COL4A4):c.*718G>C rs183147767 0.00543
NM_000092.5(COL4A4):c.2907A>C (p.Ser969=) rs116354015 0.00506
NM_000091.5(COL4A3):c.*811A>C rs116568659 0.00504
NM_000092.5(COL4A4):c.1833T>C (p.Gly611=) rs145806603 0.00479
NM_000092.5(COL4A4):c.*3636C>T rs147995299 0.00469
NM_000092.5(COL4A4):c.4082-8C>T rs139571413 0.00420
NM_000092.5(COL4A4):c.50A>G (p.Lys17Arg) rs114969026 0.00341
NM_000091.5(COL4A3):c.3566-10T>C rs114719458 0.00331
NM_000092.5(COL4A4):c.5016A>G (p.Glu1672=) rs34761049 0.00264
NM_000092.5(COL4A4):c.4731G>A (p.Ala1577=) rs200639109 0.00257
NM_000092.5(COL4A4):c.2717-15C>A rs143886681 0.00199
NM_000091.5(COL4A3):c.222G>T (p.Pro74=) rs187950806 0.00096
NM_000092.5(COL4A4):c.195T>C (p.Gly65=) rs201278620 0.00082
NM_000092.5(COL4A4):c.2877C>T (p.Pro959=) rs79470996 0.00035
NM_000091.5(COL4A3):c.*2228T>C rs367785196 0.00034
NM_000091.5(COL4A3):c.1353C>T (p.His451=) rs189364374 0.00025
NM_000092.5(COL4A4):c.4195A>T (p.Met1399Leu) rs149117087 0.00019
NM_000092.5(COL4A4):c.4857T>C (p.Pro1619=) rs184776061 0.00017
NM_000092.5(COL4A4):c.1202C>T (p.Ala401Val) rs199581317 0.00003
NM_000091.5(COL4A3):c.*2834ATA[1] rs137947510
NM_000092.5(COL4A4):c.*4491_*4494dup rs151077907
NM_000092.5(COL4A4):c.2165-13del rs140965334
NM_000092.5(COL4A4):c.2367A>T (p.Gly789=) rs56247709

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