List of variants in gene TP53 reported as benign by Ambry Genetics

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	rs1042522	0.62654
NM_000546.6(TP53):c.993+12T>C	rs1800899	0.01614
NM_000546.6(TP53):c.639A>G (p.Arg213=)	rs1800372	0.01275
NM_000546.6(TP53):c.108G>A (p.Pro36=)	rs1800370	0.00974
NM_000546.6(TP53):c.1100+30A>T	rs17880847	0.00929
NM_000546.6(TP53):c.97-6C>T	rs35117667	0.00847
NM_000546.6(TP53):c.782+17C>T	rs17880172	0.00184
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
NM_000546.6(TP53):c.869G>A (p.Arg290His)	rs55819519	0.00014
NM_000546.6(TP53):c.386C>A (p.Ala129Asp)
NM_000546.6(TP53):c.666G>T (p.Pro222=)	rs72661118
NM_000546.6(TP53):c.673-19G>A	rs564974117
NM_000546.6(TP53):c.673-36G>C	rs17880604
NM_000546.6(TP53):c.673-44C>T
NM_000546.6(TP53):c.932A>G (p.Asn311Ser)	rs56184981

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