List of variants in gene TP53 reported as uncertain significance for Breast and/or ovarian cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.869G>A (p.Arg290His)	rs55819519	0.00014
NM_000546.6(TP53):c.920-17C>A	rs911934766	0.00006
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala)	rs17881470	0.00004
NM_000546.6(TP53):c.665C>T (p.Pro222Leu)	rs146340390	0.00002
NM_000546.6(TP53):c.328C>T (p.Arg110Cys)	rs587781371	0.00001
NM_000546.6(TP53):c.672+6G>T	rs766856111	0.00001
NM_000546.6(TP53):c.74+9A>C	rs1057517593	0.00001
NM_000546.6(TP53):c.292C>T (p.Pro98Ser)	rs1597374015
NM_000546.6(TP53):c.382C>A (p.Pro128Thr)	rs1555526327
NM_000546.6(TP53):c.408A>T (p.Gln136His)	rs758781593
NM_000546.6(TP53):c.470T>G (p.Val157Gly)	rs1131691023
NM_000546.6(TP53):c.672+6_672+8delinsTTG	rs2073318029
NM_000546.6(TP53):c.672+8T>G	rs763373602
NM_000546.6(TP53):c.808T>C (p.Phe270Leu)	rs1057519988

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