List of variants in gene TP53 reported as benign by Sema4, Sema4

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_000546.5(TP53):c.319T>C (p.Tyr107His)	rs368771578	0.00027
NM_000546.6(TP53):c.704A>G (p.Asn235Ser)	rs144340710	0.00025
NM_000546.6(TP53):c.216C>T (p.Pro72=)	rs56275308	0.00022
NM_000546.6(TP53):c.1014C>T (p.Phe338=)	rs150293825	0.00018
NM_000546.6(TP53):c.560-8G>C	rs373797299	0.00018
NM_000546.6(TP53):c.935C>G (p.Thr312Ser)	rs145151284	0.00018
NM_000546.6(TP53):c.97-9C>T	rs202217267	0.00011
NM_000546.6(TP53):c.474C>T (p.Arg158=)	rs139200646	0.00009
NM_000546.6(TP53):c.903A>G (p.Pro301=)	rs72661120	0.00007
NM_000546.6(TP53):c.63C>T (p.Asp21=)	rs1800369
NM_000546.6(TP53):c.672+48G>A	rs17884607

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