List of variants in gene TP53 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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.1082G>A (p.Gly361Glu)	rs587781663	0.00001
NM_000546.6(TP53):c.376-2dup	rs751253294	0.00001
NM_000546.6(TP53):c.711G>A (p.Met237Ile)	rs587782664	0.00001
NM_000546.6(TP53):c.974G>T (p.Gly325Val)	rs121912659	0.00001
NM_000546.6(TP53):c.318C>G (p.Ser106Arg)	rs1555526581
NM_000546.6(TP53):c.364G>A (p.Val122Met)	rs587781495
NM_000546.6(TP53):c.518T>A (p.Val173Glu)	rs1057519747
NM_000546.6(TP53):c.632C>T (p.Thr211Ile)	rs2073331490
NM_000546.6(TP53):c.646G>A (p.Val216Met)	rs730882025
NM_000546.6(TP53):c.695T>C (p.Ile232Thr)	rs587781589
NM_000546.6(TP53):c.772G>A (p.Glu258Lys)	rs121912652
NM_000546.6(TP53):c.836G>A (p.Gly279Glu)	rs1064793881

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