List of variants in gene TP53 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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.994-17C>T	rs368691910	0.00087
NM_000546.6(TP53):c.1014C>T (p.Phe338=)	rs150293825	0.00018
NM_000546.6(TP53):c.869G>A (p.Arg290His)	rs55819519	0.00014
NM_000546.6(TP53):c.673-37C>T	rs374907737	0.00010
NM_000546.6(TP53):c.6G>A (p.Glu2=)	rs143458271	0.00009
NM_000546.6(TP53):c.618G>A (p.Leu206=)	rs142813240	0.00006
NM_000546.6(TP53):c.920-17C>A	rs911934766	0.00006
NM_000546.6(TP53):c.993+312C>T	rs756952434	0.00004
NM_000546.6(TP53):c.249G>A (p.Ala83=)	rs55754907	0.00002
NM_000546.6(TP53):c.90C>T (p.Asn30=)	rs370992294	0.00001
NM_000546.6(TP53):c.994-5T>C	rs375273756	0.00001
NM_000546.6(TP53):c.558T>C (p.Asp186=)	rs375275361

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