ClinVar Miner

List of variants reported as benign for CADASIL

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_000435.3(NOTCH3):c.*23T>A rs73504084
NM_000435.3(NOTCH3):c.*338A>C rs7247906
NM_000435.3(NOTCH3):c.*370A>G rs139792065
NM_000435.3(NOTCH3):c.*463G>A
NM_000435.3(NOTCH3):c.*4G>A rs182111655
NM_000435.3(NOTCH3):c.*544C>T rs368577217
NM_000435.3(NOTCH3):c.*668G>T rs1044055
NM_000435.3(NOTCH3):c.*808G>A rs1044116
NM_000435.3(NOTCH3):c.*837G>A rs12082
NM_000435.3(NOTCH3):c.*845G>T rs571584841
NM_000435.3(NOTCH3):c.*85G>T
NM_000435.3(NOTCH3):c.*890C>T rs1044123
NM_000435.3(NOTCH3):c.1140T>C (p.Pro380=) rs61749020
NM_000435.3(NOTCH3):c.1192+15A>G rs10423702
NM_000435.3(NOTCH3):c.1194C>T (p.Gly398=)
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.1567G>A (p.Val523Met)
NM_000435.3(NOTCH3):c.1677C>T (p.Cys559=) rs113216024
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.1725G>C (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.2163G>A (p.Glu721=) rs375173938
NM_000435.3(NOTCH3):c.2202C>T (p.Ala734=) rs140040122
NM_000435.3(NOTCH3):c.2411-4C>G rs190177286
NM_000435.3(NOTCH3):c.2538C>T (p.Cys846=) rs1043996
NM_000435.3(NOTCH3):c.2580C>T (p.Asn860=) rs201436750
NM_000435.3(NOTCH3):c.2742A>G (p.Pro914=) rs1043997
NM_000435.3(NOTCH3):c.2792+6C>T rs376329316
NM_000435.3(NOTCH3):c.303C>T (p.Thr101=) rs3815188
NM_000435.3(NOTCH3):c.3058G>C (p.Ala1020Pro) rs35769976
NM_000435.3(NOTCH3):c.3327+11G>A
NM_000435.3(NOTCH3):c.3399C>A (p.His1133Gln) rs112197217
NM_000435.3(NOTCH3):c.3461-15C>T rs564737009
NM_000435.3(NOTCH3):c.3547G>A (p.Val1183Met) rs10408676
NM_000435.3(NOTCH3):c.3704A>T (p.His1235Leu) rs55882518
NM_000435.3(NOTCH3):c.3718+13G>T
NM_000435.3(NOTCH3):c.4348G>A (p.Ala1450Thr) rs201082692
NM_000435.3(NOTCH3):c.4552C>A (p.Leu1518Met) rs141320511
NM_000435.3(NOTCH3):c.4563A>G (p.Pro1521=) rs1044006
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.5362+3T>C rs1548555
NM_000435.3(NOTCH3):c.5370C>T (p.Phe1790=) rs35887416
NM_000435.3(NOTCH3):c.5400G>T (p.Gly1800=) rs34480308
NM_000435.3(NOTCH3):c.5526T>C (p.Ala1842=) rs16980398
NM_000435.3(NOTCH3):c.5668-11C>T rs199850662
NM_000435.3(NOTCH3):c.5678G>A (p.Arg1893Gln) rs372834264
NM_000435.3(NOTCH3):c.5816-8T>C rs4809030
NM_000435.3(NOTCH3):c.5854G>A (p.Val1952Met) rs115582213
NM_000435.3(NOTCH3):c.593C>T (p.Ala198Val)
NM_000435.3(NOTCH3):c.5992C>T (p.Arg1998Cys) rs201105335
NM_000435.3(NOTCH3):c.606A>G (p.Ala202=) rs1043994
NM_000435.3(NOTCH3):c.6102C>T (p.Pro2034=) rs114887570
NM_000435.3(NOTCH3):c.6221C>T (p.Pro2074Leu) rs114447350
NM_000435.3(NOTCH3):c.6237G>A (p.Gly2079=) rs376598183
NM_000435.3(NOTCH3):c.6438G>A (p.Ala2146=) rs1044008
NM_000435.3(NOTCH3):c.6569C>T (p.Ala2190Val) rs528151296
NM_000435.3(NOTCH3):c.6668C>T (p.Ala2223Val) rs1044009
NM_000435.3(NOTCH3):c.6753C>T (p.Ser2251=) rs61731975
NM_000435.3(NOTCH3):c.6813T>C (p.Pro2271=) rs61731974
NM_000435.3(NOTCH3):c.850G>A (p.Ala284Thr) rs149307620

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