List of variants in gene TP53 reported as likely benign for 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.993+12T>C	rs1800899	0.01614
NM_000546.6(TP53):c.97-6C>T	rs35117667	0.00847
NM_000546.6(TP53):c.783-33T>C	rs113302588	0.00051
NM_000546.5(TP53):c.319T>C (p.Tyr107His)	rs368771578	0.00028
NM_000546.6(TP53):c.1014C>T (p.Phe338=)	rs150293825	0.00018
NM_000546.6(TP53):c.74+14T>C	rs184743157	0.00018
NM_000546.6(TP53):c.648G>C (p.Val216=)	rs199693249	0.00017
NM_000546.6(TP53):c.672+18G>C	rs199578278	0.00014
NM_000546.6(TP53):c.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala)	rs17881470	0.00004
NM_000546.6(TP53):c.1149C>T (p.Leu383=)	rs373710656	0.00004
NM_000546.6(TP53):c.459C>T (p.Pro153=)	rs72661116	0.00003
NM_000546.6(TP53):c.903A>G (p.Pro301=)	rs72661120	0.00003
NM_000546.6(TP53):c.-12C>T	rs375229869	0.00002
NM_000546.6(TP53):c.18A>C (p.Ser6=)	rs573130482	0.00002
NM_000546.6(TP53):c.555C>T (p.Ser185=)	rs367560109	0.00002
NM_000546.6(TP53):c.354A>T (p.Thr118=)	rs751978853	0.00001
NM_000546.6(TP53):c.783-34C>T	rs376988747	0.00001
NM_000546.6(TP53):c.885T>C (p.Pro295=)	rs200073907	0.00001
NM_000546.6(TP53):c.891C>T (p.His297=)	rs750578863	0.00001
NM_000546.6(TP53):c.285T>G (p.Ser95=)	rs876658696
NM_000546.6(TP53):c.376-158del	rs5819162
NM_000546.6(TP53):c.376-160_376-158del	rs5819162
NM_000546.6(TP53):c.376-161_376-158del	rs5819162
NM_000546.6(TP53):c.576G>C (p.Gln192His)	rs2073344721
NM_000546.6(TP53):c.63C>T (p.Asp21=)	rs1800369
NM_000546.6(TP53):c.782+14T>G	rs1437756379
NM_000546.6(TP53):c.993+257del	rs1373684374

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