List of variants in gene NOTCH1 reported as uncertain significance by Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.3835C>T (p.Arg1279Cys)	rs182330532	0.00058
NM_017617.5(NOTCH1):c.3001G>A (p.Gly1001Ser)	rs763621169	0.00006
NM_017617.5(NOTCH1):c.2908A>G (p.Thr970Ala)	rs201053795	0.00005
NM_017617.5(NOTCH1):c.4031C>T (p.Thr1344Met)	rs201215245
NM_017617.5(NOTCH1):c.5387C>A (p.Pro1796His)	rs557319054

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