ClinVar Miner

List of variants in gene NOTCH3 reported as likely benign for Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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Gene type:
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Total variants: 45
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HGVS dbSNP
NM_000435.3(NOTCH3):c.*23T>A rs73504084
NM_000435.3(NOTCH3):c.*370A>G rs139792065
NM_000435.3(NOTCH3):c.*544C>T rs368577217
NM_000435.3(NOTCH3):c.*563T>C rs77669983
NM_000435.3(NOTCH3):c.*608C>T rs577953923
NM_000435.3(NOTCH3):c.*937T>C rs16980378
NM_000435.3(NOTCH3):c.*96C>T rs117165744
NM_000435.3(NOTCH3):c.1140T>C (p.Pro380=) rs61749020
NM_000435.3(NOTCH3):c.1487C>T (p.Pro496Leu) rs11670799
NM_000435.3(NOTCH3):c.1490C>T (p.Ser497Leu) rs114207045
NM_000435.3(NOTCH3):c.1620G>T (p.Thr540=) rs75617410
NM_000435.3(NOTCH3):c.1690G>A (p.Ala564Thr) rs374767079
NM_000435.3(NOTCH3):c.1725G>A (p.Thr575=) rs79926127
NM_000435.3(NOTCH3):c.1782C>T (p.Gly594=) rs35793356
NM_000435.3(NOTCH3):c.2039G>A (p.Arg680His) rs10406745
NM_000435.3(NOTCH3):c.2202C>T (p.Ala734=) rs140040122
NM_000435.3(NOTCH3):c.2411-4C>G rs190177286
NM_000435.3(NOTCH3):c.2580C>T (p.Asn860=) rs201436750
NM_000435.3(NOTCH3):c.338G>A (p.Arg113Gln) rs143385744
NM_000435.3(NOTCH3):c.3399C>A (p.His1133Gln) rs112197217
NM_000435.3(NOTCH3):c.3523C>T (p.Arg1175Trp) rs200504060
NM_000435.3(NOTCH3):c.3704A>T (p.His1235Leu) rs55882518
NM_000435.3(NOTCH3):c.3719-11C>T rs78907190
NM_000435.3(NOTCH3):c.4044C>T (p.Gly1348=) rs78926093
NM_000435.3(NOTCH3):c.4071C>T (p.Pro1357=) rs542856470
NM_000435.3(NOTCH3):c.4348G>A (p.Ala1450Thr) rs201082692
NM_000435.3(NOTCH3):c.4444G>C (p.Gly1482Arg) rs202085803
NM_000435.3(NOTCH3):c.4552C>A (p.Leu1518Met) rs141320511
NM_000435.3(NOTCH3):c.4679G>C (p.Arg1560Pro) rs78501403
NM_000435.3(NOTCH3):c.509A>G (p.His170Arg) rs147373451
NM_000435.3(NOTCH3):c.5370C>T (p.Phe1790=) rs35887416
NM_000435.3(NOTCH3):c.5376G>A (p.Pro1792=) rs374875084
NM_000435.3(NOTCH3):c.5400G>T (p.Gly1800=) rs34480308
NM_000435.3(NOTCH3):c.5466C>T (p.Ser1822=) rs148053028
NM_000435.3(NOTCH3):c.5501G>A (p.Arg1834Gln) rs202027632
NM_000435.3(NOTCH3):c.5668-11C>T rs199850662
NM_000435.3(NOTCH3):c.5854G>A (p.Val1952Met) rs115582213
NM_000435.3(NOTCH3):c.6031G>A (p.Val2011Ile) rs142007575
NM_000435.3(NOTCH3):c.6166G>A (p.Ala2056Thr) rs556851818
NM_000435.3(NOTCH3):c.6532C>T (p.Pro2178Ser) rs751951476
NM_000435.3(NOTCH3):c.660C>T (p.Tyr220=) rs114457076
NM_000435.3(NOTCH3):c.6611C>T (p.Pro2204Leu) rs371738874
NM_000435.3(NOTCH3):c.6813T>C (p.Pro2271=) rs61731974
NM_000435.3(NOTCH3):c.945C>T (p.Ile315=) rs116239440
NM_000435.3(NOTCH3):c.964G>A (p.Val322Met) rs115029695

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