List of variants in gene TP53 reported as likely pathogenic by Clinical Genetics Laboratory, Skane University Hospital Lund

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.541C>T (p.Arg181Cys)	rs587782596	0.00001
NM_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NM_000546.6(TP53):c.713G>A (p.Cys238Tyr)	rs730882005	0.00001
NM_000546.6(TP53):c.325T>A (p.Phe109Ile)	rs1057523496

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