ClinVar Miner

List of variants in gene COL4A1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP
NM_001845.5(COL4A1):c.*1404T>C rs56406633
NM_001845.6(COL4A1):c.*1014C>T rs139916479
NM_001845.6(COL4A1):c.*1099G>A rs193065628
NM_001845.6(COL4A1):c.*176A>G rs11545877
NM_001845.6(COL4A1):c.*265A>G rs555157539
NM_001845.6(COL4A1):c.*609T>C rs189966143
NM_001845.6(COL4A1):c.*766G>A rs371130027
NM_001845.6(COL4A1):c.*975A>C rs28362515
NM_001845.6(COL4A1):c.-103G>A rs538721412
NM_001845.6(COL4A1):c.1000-13C>G rs115358624
NM_001845.6(COL4A1):c.1000-5T>G rs75711155
NM_001845.6(COL4A1):c.1065A>G (p.Arg355=) rs1594575843
NM_001845.6(COL4A1):c.1092A>T (p.Pro364=) rs141208458
NM_001845.6(COL4A1):c.1110C>T (p.Pro370=) rs368143409
NM_001845.6(COL4A1):c.1360A>G (p.Ile454Val) rs373712845
NM_001845.6(COL4A1):c.1381+8A>G rs1054421900
NM_001845.6(COL4A1):c.1425T>C (p.Tyr475=) rs1594566831
NM_001845.6(COL4A1):c.1426C>T (p.Arg476Trp) rs369960952
NM_001845.6(COL4A1):c.145-5T>C rs749251030
NM_001845.6(COL4A1):c.1466-6C>T rs183563055
NM_001845.6(COL4A1):c.1588C>T (p.Pro530Ser) rs145172612
NM_001845.6(COL4A1):c.161C>T (p.Pro54Leu) rs34004222
NM_001845.6(COL4A1):c.1673C>T (p.Ala558Val) rs200252122
NM_001845.6(COL4A1):c.1725G>A (p.Ser575=) rs370332353
NM_001845.6(COL4A1):c.1735G>A (p.Val579Ile) rs141527136
NM_001845.6(COL4A1):c.1758C>A (p.Gly586=) rs1594560899
NM_001845.6(COL4A1):c.1838C>G (p.Pro613Arg) rs146091004
NM_001845.6(COL4A1):c.1858G>C (p.Ala620Pro) rs372803920
NM_001845.6(COL4A1):c.2028C>A (p.Gly676=) rs778947922
NM_001845.6(COL4A1):c.2085C>T (p.Pro695=) rs377505775
NM_001845.6(COL4A1):c.2103C>T (p.Asp701=) rs561116319
NM_001845.6(COL4A1):c.2160C>T (p.Gly720=) rs781133776
NM_001845.6(COL4A1):c.2285T>C (p.Val762Ala)
NM_001845.6(COL4A1):c.2313G>A (p.Ala771=) rs781701888
NM_001845.6(COL4A1):c.234+9G>T rs374115295
NM_001845.6(COL4A1):c.2392G>C (p.Val798Leu) rs146950993
NM_001845.6(COL4A1):c.2517G>A (p.Pro839=) rs773443475
NM_001845.6(COL4A1):c.2542C>G (p.Gln848Glu) rs144207910
NM_001845.6(COL4A1):c.2571G>A (p.Ser857=)
NM_001845.6(COL4A1):c.2624C>G (p.Pro875Arg) rs201964644
NM_001845.6(COL4A1):c.2627-4dup rs1555303159
NM_001845.6(COL4A1):c.2647G>A (p.Val883Ile) rs41275090
NM_001845.6(COL4A1):c.2704C>T (p.Pro902Ser) rs779350720
NM_001845.6(COL4A1):c.2716+9G>C rs756352312
NM_001845.6(COL4A1):c.2811C>T (p.Ser937=) rs765239658
NM_001845.6(COL4A1):c.2869+6T>C rs557198622
NM_001845.6(COL4A1):c.2955G>C (p.Gln985His) rs145018661
NM_001845.6(COL4A1):c.2968+12A>G rs752476229
NM_001845.6(COL4A1):c.2968+4C>T rs1555303033
NM_001845.6(COL4A1):c.2985A>G (p.Pro995=)
NM_001845.6(COL4A1):c.3054G>A (p.Leu1018=)
NM_001845.6(COL4A1):c.3164C>T (p.Pro1055Leu) rs375787099
NM_001845.6(COL4A1):c.3198+10G>A rs202002553
NM_001845.6(COL4A1):c.3285C>T (p.Ser1095=) rs267603751
NM_001845.6(COL4A1):c.3288A>G (p.Pro1096=) rs2305082
NM_001845.6(COL4A1):c.329T>C (p.Ile110Thr) rs138269346
NM_001845.6(COL4A1):c.3326-13dup rs139122216
NM_001845.6(COL4A1):c.3506-7C>G rs377592935
NM_001845.6(COL4A1):c.3634A>T (p.Met1212Leu) rs199557190
NM_001845.6(COL4A1):c.367C>T (p.Pro123Ser) rs138503916
NM_001845.6(COL4A1):c.3714C>T (p.Arg1238=) rs377765047
NM_001845.6(COL4A1):c.3743-15C>T
NM_001845.6(COL4A1):c.3774T>C (p.Leu1258=) rs139578640
NM_001845.6(COL4A1):c.3776C>G (p.Pro1259Arg) rs146329532
NM_001845.6(COL4A1):c.3822A>G (p.Pro1274=) rs746243053
NM_001845.6(COL4A1):c.3877-8G>A rs370539477
NM_001845.6(COL4A1):c.3915T>G (p.Gly1305=) rs1396040382
NM_001845.6(COL4A1):c.393G>A (p.Glu131=) rs34458255
NM_001845.6(COL4A1):c.3949+10C>T rs188122235
NM_001845.6(COL4A1):c.3972C>T (p.Leu1324=) rs535848796
NM_001845.6(COL4A1):c.4005C>T (p.Gly1335=) rs140722653
NM_001845.6(COL4A1):c.4010C>T (p.Pro1337Leu) rs189728415
NM_001845.6(COL4A1):c.4056C>T (p.Tyr1352=) rs140210015
NM_001845.6(COL4A1):c.405C>T (p.Leu135=) rs138888319
NM_001845.6(COL4A1):c.4134C>A (p.Gly1378=) rs1250683195
NM_001845.6(COL4A1):c.4150+3G>A rs545498227
NM_001845.6(COL4A1):c.4229T>C (p.Met1410Thr) rs200734000
NM_001845.6(COL4A1):c.4250-12C>T rs202055679
NM_001845.6(COL4A1):c.4271C>T (p.Pro1424Leu) rs760889798
NM_001845.6(COL4A1):c.4332C>T (p.His1444=) rs756069308
NM_001845.6(COL4A1):c.442-10T>C rs1400870120
NM_001845.6(COL4A1):c.4441C>T (p.Arg1481Trp) rs199586038
NM_001845.6(COL4A1):c.4442G>A (p.Arg1481Gln) rs376607450
NM_001845.6(COL4A1):c.4608C>T (p.Ile1536=) rs377100994
NM_001845.6(COL4A1):c.4640+3G>T rs770167198
NM_001845.6(COL4A1):c.4640+8G>A rs117566874
NM_001845.6(COL4A1):c.4658C>T (p.Ala1553Val) rs201150281
NM_001845.6(COL4A1):c.477A>T (p.Pro159=) rs141067230
NM_001845.6(COL4A1):c.4797G>A (p.Ala1599=) rs146638269
NM_001845.6(COL4A1):c.4797G>T (p.Ala1599=) rs146638269
NM_001845.6(COL4A1):c.4803C>T (p.Pro1601=) rs190097900
NM_001845.6(COL4A1):c.4851C>T (p.His1617=) rs748558670
NM_001845.6(COL4A1):c.4912A>C (p.Arg1638=) rs1594527347
NM_001845.6(COL4A1):c.4929-9G>A rs756038842
NM_001845.6(COL4A1):c.4941G>A (p.Pro1647=) rs115834242
NM_001845.6(COL4A1):c.501C>T (p.Pro167=) rs16975612
NM_001845.6(COL4A1):c.504G>A (p.Gly168=) rs539633643
NM_001845.6(COL4A1):c.606C>T (p.Thr202=)
NM_001845.6(COL4A1):c.651+4_651+5insCAC rs760194800
NM_001845.6(COL4A1):c.690C>T (p.Asp230=) rs149688210
NM_001845.6(COL4A1):c.708C>G (p.Val236=) rs139523466
NM_001845.6(COL4A1):c.762C>T (p.Phe254=) rs145029443
NM_001845.6(COL4A1):c.781-12G>A rs202198648
NM_001845.6(COL4A1):c.7C>A (p.Pro3Thr) rs751749989
NM_001845.6(COL4A1):c.807+3C>T rs192723236
NM_001845.6(COL4A1):c.831A>G (p.Lys277=) rs140978802
NM_001845.6(COL4A1):c.904-9C>T rs201481886
NM_001845.6(COL4A1):c.966G>A (p.Lys322=) rs372969177
NM_001845.6(COL4A1):c.994G>C (p.Gly332Arg) rs150182714

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