ClinVar Miner

List of variants in gene TP53 reported as likely benign by Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.6G>A (p.Glu2=)	rs143458271	0.00009
NM_000546.6(TP53):c.97-52G>A	rs540683791

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