ClinVar Miner

List of variants in gene COL4A1 reported as likely pathogenic for Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome; Brain small vessel disease 1 with or without ocular anomalies; Hemorrhage, intracerebral, susceptibility to; Retinal arterial tortuosity; Microangiopathy and leukoencephalopathy, pontine, autosomal dominant

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001845.6(COL4A1):c.922G>A (p.Gly308Arg) rs370677625 0.00003
NM_001845.6(COL4A1):c.1702G>T (p.Gly568Cys) rs375477517 0.00001
NM_001845.6(COL4A1):c.2458+2T>C rs1436175370 0.00001
NM_001845.6(COL4A1):c.3187C>T (p.Arg1063Ter) rs1877827904 0.00001
NM_001845.6(COL4A1):c.4204G>A (p.Gly1402Ser) rs1179536054 0.00001
NM_001845.6(COL4A1):c.518G>A (p.Gly173Asp) rs567124920 0.00001
NM_001845.6(COL4A1):c.1022G>C (p.Gly341Ala)
NM_001845.6(COL4A1):c.1067G>C (p.Gly356Ala)
NM_001845.6(COL4A1):c.1438G>A (p.Gly480Arg) rs1461754052
NM_001845.6(COL4A1):c.1456G>A (p.Gly486Arg)
NM_001845.6(COL4A1):c.1466-1G>C
NM_001845.6(COL4A1):c.1484G>A (p.Gly495Glu)
NM_001845.6(COL4A1):c.1504_1505dup (p.Leu502fs)
NM_001845.6(COL4A1):c.1720G>C (p.Gly574Arg)
NM_001845.6(COL4A1):c.1730G>T (p.Gly577Val)
NM_001845.6(COL4A1):c.1996C>T (p.Arg666Ter)
NM_001845.6(COL4A1):c.2100dup (p.Asp701Ter)
NM_001845.6(COL4A1):c.2132G>C (p.Gly711Ala)
NM_001845.6(COL4A1):c.2182C>T (p.Gln728Ter)
NM_001845.6(COL4A1):c.2269_2276del (p.Lys757fs)
NM_001845.6(COL4A1):c.2593C>T (p.Gln865Ter)
NM_001845.6(COL4A1):c.3771del (p.Leu1258fs)
NM_001845.6(COL4A1):c.3778G>A (p.Gly1260Arg)
NM_001845.6(COL4A1):c.3991C>T (p.Gln1331Ter)
NM_001845.6(COL4A1):c.4049del (p.Gly1350fs)
NM_001845.6(COL4A1):c.4098_4104del (p.Pro1367fs)
NM_001845.6(COL4A1):c.4163T>A (p.Leu1388Ter)
NM_001845.6(COL4A1):c.4187G>A (p.Gly1396Asp)
NM_001845.6(COL4A1):c.4250-1G>A rs2139146298
NM_001845.6(COL4A1):c.4286G>T (p.Gly1429Val)
NM_001845.6(COL4A1):c.4546C>T (p.Arg1516Ter) rs1594535661
NM_001845.6(COL4A1):c.4886dup (p.Tyr1629Ter)
NM_001845.6(COL4A1):c.536G>C (p.Gly179Ala)
NM_001845.6(COL4A1):c.807+1G>A
NM_001845.6(COL4A1):c.868G>T (p.Gly290Ter)
NM_001845.6(COL4A1):c.958-1G>C

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