List of variants in gene TP53 reported as likely benign by National Health Laboratory Service, Universitas Academic Hospital and University of the Free State

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.672+31A>G	rs34949160	0.00543
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.783-33T>C	rs113302588	0.00047
NM_000546.6(TP53):c.96+41A>G	rs139100308	0.00039
NM_000546.6(TP53):c.993+223T>G	rs3021068	0.00011
NM_000546.6(TP53):c.555C>T (p.Ser185=)	rs367560109	0.00002
NM_000546.6(TP53):c.75-41C>T	rs569425726	0.00001
NM_000546.6(TP53):c.96+41_96+48del	rs780090842
NM_000546.6(TP53):c.993+163AC[3]	rs775788764

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