List of variants in gene NOTCH3 reported as uncertain significance for benign soft tissue neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000435.3(NOTCH3):c.*306C>T	rs181930934	0.00036
NM_000435.3(NOTCH3):c.2183G>A (p.Arg728His)	rs144935367	0.00024
NM_000435.3(NOTCH3):c.3227G>A (p.Arg1076His)	rs771803651	0.00008
NM_000435.3(NOTCH3):c.359C>T (p.Pro120Leu)	rs778715118	0.00006
NM_000435.3(NOTCH3):c.6619C>T (p.Arg2207Trp)	rs753170185	0.00006
NM_000435.3(NOTCH3):c.2960C>G (p.Thr987Ser)	rs752995216	0.00005
NM_000435.3(NOTCH3):c.451C>G (p.Gln151Glu)	rs371491165	0.00005
NM_000435.3(NOTCH3):c.6521G>A (p.Arg2174Gln)	rs1337328035	0.00005
NM_000435.3(NOTCH3):c.4914A>G (p.Glu1638=)	rs149222385	0.00003
NM_000435.3(NOTCH3):c.2051C>T (p.Pro684Leu)	rs770737365	0.00002
NM_000435.3(NOTCH3):c.119C>T (p.Ala40Val)	rs766139231	0.00001
NM_000435.3(NOTCH3):c.1783G>A (p.Gly595Ser)	rs770146452	0.00001
NM_000435.3(NOTCH3):c.214G>A (p.Val72Met)	rs2046938247	0.00001
NM_000435.3(NOTCH3):c.21CCG[4] (p.Arg13del)	rs894374843
NM_000435.3(NOTCH3):c.3970T>A (p.Cys1324Ser)
NM_000435.3(NOTCH3):c.5114+11T>G	rs2046721049
NM_000435.3(NOTCH3):c.6681C>G (p.His2227Gln)	rs1366113655

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.