List of variants in gene TP53 reported as likely benign by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.993+12T>C	rs1800899	0.01614
NM_000546.6(TP53):c.74+14T>C	rs184743157	0.00018
NM_000546.6(TP53):c.97-9C>T	rs202217267	0.00011
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala)	rs17881470	0.00004
NM_000546.6(TP53):c.459C>T (p.Pro153=)	rs72661116	0.00003
NM_000546.6(TP53):c.903A>G (p.Pro301=)	rs72661120	0.00003
NM_000546.6(TP53):c.18A>C (p.Ser6=)	rs573130482	0.00002
NM_000546.6(TP53):c.891C>T (p.His297=)	rs750578863	0.00001
NM_000546.6(TP53):c.168A>G (p.Glu56=)	rs574255227
NM_000546.6(TP53):c.558T>C (p.Asp186=)	rs375275361
NM_000546.6(TP53):c.63C>T (p.Asp21=)	rs1800369
NM_000546.6(TP53):c.782+14T>G	rs1437756379

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