List of variants in gene TP53 reported as likely pathogenic by BRCAlab, Lund University

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.328C>T (p.Arg110Cys)	rs587781371	0.00001
NM_000546.6(TP53):c.374C>T (p.Thr125Met)	rs786201057	0.00001
NM_000546.6(TP53):c.395A>G (p.Lys132Arg)	rs1057519996	0.00001
NM_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NM_000546.6(TP53):c.1009C>T (p.Arg337Cys)	rs587782529
NM_000546.6(TP53):c.402T>G (p.Phe134Leu)	rs1555526278
NM_000546.6(TP53):c.528C>G (p.Cys176Trp)	rs1057519980

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