ClinVar Miner

List of variants in gene NOTCH3 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP
GRCh37/hg19 19p13.12(chr19:15270636-15325310)x3
GRCh37/hg19 19p13.12(chr19:15276755-15290236)x3
GRCh37/hg19 19p13.12(chr19:15278099-15290236)x3
NM_000435.3(NOTCH3):c.*338A>C rs7247906
NM_000435.3(NOTCH3):c.*4G>A rs182111655
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.*890C>T rs1044123
NM_000435.3(NOTCH3):c.1036+10C>T rs776962888
NM_000435.3(NOTCH3):c.1140T>C (p.Pro380=) rs61749020
NM_000435.3(NOTCH3):c.1192+15A>G rs10423702
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.1493-8C>T rs201202842
NM_000435.3(NOTCH3):c.1607-5C>A rs372869012
NM_000435.3(NOTCH3):c.1620G>T (p.Thr540=) rs75617410
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.1840+8C>T rs372100017
NM_000435.3(NOTCH3):c.2039G>A (p.Arg680His) rs10406745
NM_000435.3(NOTCH3):c.2175T>C (p.Ser725=) rs141993521
NM_000435.3(NOTCH3):c.2202C>T (p.Ala734=) rs140040122
NM_000435.3(NOTCH3):c.2300G>A (p.Arg767His) rs75291244
NM_000435.3(NOTCH3):c.2538C>T (p.Cys846=) rs1043996
NM_000435.3(NOTCH3):c.2682C>T (p.Asn894=) rs138245070
NM_000435.3(NOTCH3):c.2742A>G (p.Pro914=) rs1043997
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.3399C>A (p.His1133Gln) rs112197217
NM_000435.3(NOTCH3):c.3547G>A (p.Val1183Met) rs10408676
NM_000435.3(NOTCH3):c.3575C>T (p.Thr1192Ile) rs150811543
NM_000435.3(NOTCH3):c.4044C>T (p.Gly1348=) rs78926093
NM_000435.3(NOTCH3):c.432C>T (p.Cys144=) rs748339634
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.5114+10C>G rs369547319
NM_000435.3(NOTCH3):c.5362+3T>C rs1548555
NM_000435.3(NOTCH3):c.5363-17C>T rs2074619
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.5816-8T>C rs4809030
NM_000435.3(NOTCH3):c.5854G>A (p.Val1952Met) rs115582213
NM_000435.3(NOTCH3):c.5895G>A (p.Lys1965=) rs140567100
NM_000435.3(NOTCH3):c.6031G>A (p.Val2011Ile) rs142007575
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.6504G>C (p.Val2168=) rs546608637
NM_000435.3(NOTCH3):c.6573G>A (p.Pro2191=) rs576653145
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.6809C>T (p.Thr2270Met) rs148716935
NM_000435.3(NOTCH3):c.6813T>C (p.Pro2271=) rs61731974

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