List of variants in gene TP53 reported as likely benign 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.672+31A>G	rs34949160	0.00479
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	0.00051
NM_000546.6(TP53):c.96+41A>G	rs139100308	0.00039
NM_000546.6(TP53):c.75-41C>T	rs569425726	0.00005
NM_000546.6(TP53):c.555C>T (p.Ser185=)	rs367560109	0.00002
NM_000546.6(TP53):c.353C>T (p.Thr118Ile)	rs1064794141	0.00001
NM_000546.6(TP53):c.566C>T (p.Ala189Val)	rs121912665	0.00001
NM_000546.6(TP53):c.861G>C (p.Glu287Asp)	rs748891343	0.00001
NM_000546.6(TP53):c.1040C>G (p.Ala347Gly)
NM_000546.6(TP53):c.419C>A (p.Thr140Asn)	rs786202561
NM_000546.6(TP53):c.886C>T (p.His296Tyr)	rs672601296
NM_000546.6(TP53):c.96+41_96+48del	rs780090842
NM_000546.6(TP53):c.993+163AC[3]	rs775788764
NM_000546.6(TP53):c.993+223T>G	rs3021068

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