List of variants in gene TP53 reported as uncertain significance by Revvity Omics, Revvity

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.466C>T (p.Arg156Cys)	rs563378859	0.00002
NM_000546.6(TP53):c.604C>T (p.Arg202Cys)	rs587780072	0.00001
NM_000546.6(TP53):c.1039G>A (p.Ala347Thr)	rs1597349147

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