List of variants in gene TP53 reported as likely benign by German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne

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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.353C>T (p.Thr118Ile)	rs1064794141	0.00001
NM_000546.6(TP53):c.861G>C (p.Glu287Asp)	rs748891343	0.00001
NM_000546.6(TP53):c.1040C>G (p.Ala347Gly)	rs397516434
NM_000546.6(TP53):c.419C>A (p.Thr140Asn)	rs786202561
NM_000546.6(TP53):c.886C>T (p.His296Tyr)	rs672601296

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