List of variants in gene TP53 reported as likely pathogenic 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.701A>G (p.Tyr234Cys)	rs587780073
NM_000546.6(TP53):c.715A>G (p.Asn239Asp)	rs876660807
NM_000546.6(TP53):c.799C>T (p.Arg267Trp)	rs55832599

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