List of variants in gene TP53 reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys)	rs17882252	0.00006
NM_000546.6(TP53):c.91G>A (p.Val31Ile)	rs201753350	0.00004
NM_000546.6(TP53):c.467G>A (p.Arg156His)	rs371524413	0.00003
NM_000546.6(TP53):c.472C>T (p.Arg158Cys)	rs587780068	0.00001
NM_000546.6(TP53):c.523C>T (p.Arg175Cys)	rs138729528	0.00001
NM_000546.6(TP53):c.116C>T (p.Ala39Val)	rs1353016807
NM_000546.6(TP53):c.145G>C (p.Asp49His)	rs587780728
NM_000546.6(TP53):c.211C>T (p.Pro71Ser)	rs1567556576
NM_000546.6(TP53):c.283TCT[1] (p.Ser96del)	rs878854068
NM_000546.6(TP53):c.31G>C (p.Glu11Gln)	rs201382018
NM_000546.6(TP53):c.322G>A (p.Gly108Ser)	rs587782461
NM_000546.6(TP53):c.529_546del (p.Pro177_Cys182del)	rs2073361326
NM_000546.6(TP53):c.569CTC[1] (p.Pro191del)	rs1555525902
NM_000546.6(TP53):c.605G>A (p.Arg202His)	rs587778719
NM_000546.6(TP53):c.782+89del	rs2073229980
NM_000546.6(TP53):c.845G>A (p.Arg282Gln)	rs730882008
NM_000546.6(TP53):c.85AAC[1] (p.Asn30del)	rs587782270
NM_000546.6(TP53):c.97-52G>A	rs540683791

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