List of variants in gene TP53 reported as likely pathogenic by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NM_000546.6(TP53):c.202G>T (p.Glu68Ter)	rs869312782
NM_000546.6(TP53):c.469G>T (p.Val157Phe)	rs121912654
NM_000546.6(TP53):c.535C>G (p.His179Asp)	rs587780070
NM_000546.6(TP53):c.646G>T (p.Val216Leu)	rs730882025

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