ClinVar Miner

List of variants in gene NOTCH1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP
NC_000009.12:g.136508789dup
NC_000009.12:g.136515849_136515856del
NM_017617.5(NOTCH1):c.*6G>A rs73668310
NM_017617.5(NOTCH1):c.-152T>C
NM_017617.5(NOTCH1):c.1100-140G>A
NM_017617.5(NOTCH1):c.1100-16G>C rs146815871
NM_017617.5(NOTCH1):c.1100-85T>C
NM_017617.5(NOTCH1):c.141-230T>C
NM_017617.5(NOTCH1):c.1441+131A>G
NM_017617.5(NOTCH1):c.1441+7C>T rs9411208
NM_017617.5(NOTCH1):c.1442-43C>T
NM_017617.5(NOTCH1):c.1555+102C>T
NM_017617.5(NOTCH1):c.1555+10A>G rs11145767
NM_017617.5(NOTCH1):c.1555+245C>T
NM_017617.5(NOTCH1):c.1555+272C>T
NM_017617.5(NOTCH1):c.1556-133A>G
NM_017617.5(NOTCH1):c.1556-43T>C
NM_017617.5(NOTCH1):c.1635C>T (p.Asp545=) rs11574889
NM_017617.5(NOTCH1):c.1665G>A (p.Thr555=) rs148331061
NM_017617.5(NOTCH1):c.1669+13G>A rs147260092
NM_017617.5(NOTCH1):c.1669+9T>C rs3125006
NM_017617.5(NOTCH1):c.1670-9A>G rs3124603
NM_017617.5(NOTCH1):c.2205C>T (p.Asn735=) rs2229970
NM_017617.5(NOTCH1):c.2207+206T>C
NM_017617.5(NOTCH1):c.2207+70G>A
NM_017617.5(NOTCH1):c.2265T>C (p.Asn755=) rs2229971
NM_017617.5(NOTCH1):c.2467+21G>A
NM_017617.5(NOTCH1):c.2467+34C>G
NM_017617.5(NOTCH1):c.2468-19G>A rs116515776
NM_017617.5(NOTCH1):c.2542G>A (p.Glu848Lys) rs35136134
NM_017617.5(NOTCH1):c.2587+103T>C
NM_017617.5(NOTCH1):c.2587+20G>A rs148381982
NM_017617.5(NOTCH1):c.2588-104T>C
NM_017617.5(NOTCH1):c.2588-4G>A rs3125001
NM_017617.5(NOTCH1):c.2646A>T (p.Ala882=) rs61751550
NM_017617.5(NOTCH1):c.2664C>T (p.His888=) rs61751548
NM_017617.5(NOTCH1):c.2691C>T (p.Ala897=) rs11574895
NM_017617.5(NOTCH1):c.2740+12C>T rs36119806
NM_017617.5(NOTCH1):c.2769A>G (p.Thr923=) rs201985795
NM_017617.5(NOTCH1):c.2813G>A (p.Arg938Gln) rs35962301
NM_017617.5(NOTCH1):c.2969+13C>T rs7864720
NM_017617.5(NOTCH1):c.2970-31A>G
NM_017617.5(NOTCH1):c.312T>C (p.Asn104=) rs4489420
NM_017617.5(NOTCH1):c.3171+220A>G
NM_017617.5(NOTCH1):c.3171+54A>G
NM_017617.5(NOTCH1):c.3172-122T>C
NM_017617.5(NOTCH1):c.3172-71A>G
NM_017617.5(NOTCH1):c.3249C>T (p.Cys1083=) rs139994842
NM_017617.5(NOTCH1):c.3315G>T (p.Ala1105=) rs3812602
NM_017617.5(NOTCH1):c.3325+21A>G
NM_017617.5(NOTCH1):c.3333C>T (p.Asp1111=) rs61751545
NM_017617.5(NOTCH1):c.3511-10G>A rs139838537
NM_017617.5(NOTCH1):c.3644-152G>C
NM_017617.5(NOTCH1):c.3644-79C>T
NM_017617.5(NOTCH1):c.3767C>T (p.Pro1256Leu) rs80340744
NM_017617.5(NOTCH1):c.3780G>C (p.Val1260=) rs201354526
NM_017617.5(NOTCH1):c.3836G>A (p.Arg1279His) rs61751543
NM_017617.5(NOTCH1):c.4014+75G>A
NM_017617.5(NOTCH1):c.4015-73G>A
NM_017617.5(NOTCH1):c.4129C>T (p.Pro1377Ser) rs61751542
NM_017617.5(NOTCH1):c.4536C>T (p.Ala1512=) rs61751540
NM_017617.5(NOTCH1):c.4626C>T (p.Asp1542=) rs142375989
NM_017617.5(NOTCH1):c.4823G>A (p.Arg1608His) rs76371972
NM_017617.5(NOTCH1):c.4827C>T (p.Asp1609=) rs113634293
NM_017617.5(NOTCH1):c.5011G>A (p.Val1671Ile) rs2229968
NM_017617.5(NOTCH1):c.5019-13A>G rs148002954
NM_017617.5(NOTCH1):c.5019-13_5019-10del rs374419074
NM_017617.5(NOTCH1):c.5073G>A (p.Gln1691=) rs61751538
NM_017617.5(NOTCH1):c.5094C>T (p.Asp1698=) rs10521
NM_017617.5(NOTCH1):c.5124G>T (p.Ser1708=) rs35980907
NM_017617.5(NOTCH1):c.5167+189C>A
NM_017617.5(NOTCH1):c.5167+208C>T rs11574905
NM_017617.5(NOTCH1):c.5168-10G>A rs199903655
NM_017617.5(NOTCH1):c.5175C>T (p.Thr1725=) rs61751536
NM_017617.5(NOTCH1):c.5226C>T (p.Ala1742=) rs116316039
NM_017617.5(NOTCH1):c.5384+13C>T rs112582298
NM_017617.5(NOTCH1):c.5385-70C>T
NM_017617.5(NOTCH1):c.5445C>T (p.Asp1815=) rs61751535
NM_017617.5(NOTCH1):c.5473-43T>C
NM_017617.5(NOTCH1):c.5639-12C>T rs11574908
NM_017617.5(NOTCH1):c.5639-174G>A
NM_017617.5(NOTCH1):c.5679C>T (p.Gly1893=) rs2229973
NM_017617.5(NOTCH1):c.5934+45G>A
NM_017617.5(NOTCH1):c.5935-148G>A
NM_017617.5(NOTCH1):c.5935-209G>A
NM_017617.5(NOTCH1):c.5988G>A (p.Thr1996=) rs186453356
NM_017617.5(NOTCH1):c.6180+176T>C
NM_017617.5(NOTCH1):c.6180+189C>T
NM_017617.5(NOTCH1):c.6180+284G>A
NM_017617.5(NOTCH1):c.62-8C>T rs202023246
NM_017617.5(NOTCH1):c.6397C>T (p.Pro2133Ser) rs61733294
NM_017617.5(NOTCH1):c.6454G>C (p.Gly2152Arg) rs116317506
NM_017617.5(NOTCH1):c.64C>T (p.Pro22Ser) rs114832250
NM_017617.5(NOTCH1):c.6555C>T (p.Asp2185=) rs2229974
NM_017617.5(NOTCH1):c.663C>T (p.Pro221=) rs11574872
NM_017617.5(NOTCH1):c.6648G>A (p.Pro2216=) rs3812596
NM_017617.5(NOTCH1):c.6777T>C (p.Gly2259=) rs61751490
NM_017617.5(NOTCH1):c.6853G>A (p.Val2285Ile) rs61751489
NM_017617.5(NOTCH1):c.6870C>T (p.Ser2290=) rs61751488
NM_017617.5(NOTCH1):c.6991G>A (p.Ala2331Thr) rs111309246
NM_017617.5(NOTCH1):c.711C>T (p.Gly237=) rs61751557
NM_017617.5(NOTCH1):c.7209G>A (p.Gln2403=) rs61751486
NM_017617.5(NOTCH1):c.7233A>G (p.Pro2411=) rs11574911
NM_017617.5(NOTCH1):c.7338G>A (p.Leu2446=) rs35320927
NM_017617.5(NOTCH1):c.7515T>G (p.Pro2505=) rs34152221
NM_017617.5(NOTCH1):c.852G>A (p.Pro284=) rs2229975
NM_017617.5(NOTCH1):c.866-257G>A
NM_017617.5(NOTCH1):c.866-263G>A
NM_017617.5(NOTCH1):c.873C>T (p.Tyr291=) rs143654474

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