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

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.523C>T (p.Arg175Cys)	rs138729528	0.00002
NM_000546.6(TP53):c.472C>T (p.Arg158Cys)	rs587780068	0.00001
NM_000546.6(TP53):c.283TCT[1] (p.Ser96del)	rs878854068
NM_000546.6(TP53):c.529_546del (p.Pro177_Cys182del)	rs2073361326
NM_000546.6(TP53):c.569CTC[1] (p.Pro191del)	rs1555525902
NM_000546.6(TP53):c.845G>A (p.Arg282Gln)	rs730882008
NM_000546.6(TP53):c.85AAC[1] (p.Asn30del)	rs587782270

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