ClinVar Miner

List of variants in gene TP53 reported as benign by GeneDx

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Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_000546.5(TP53):c.1014C>T (p.Phe338=) rs150293825
NM_000546.5(TP53):c.139C>T (p.Pro47Ser) rs1800371
NM_000546.5(TP53):c.18A>C (p.Ser6=) rs573130482
NM_000546.5(TP53):c.216C>T (p.Pro72=) rs56275308
NM_000546.5(TP53):c.354A>T (p.Thr118=) rs751978853
NM_000546.5(TP53):c.376-17C>T rs376713749
NM_000546.5(TP53):c.459C>T (p.Pro153=) rs72661116
NM_000546.5(TP53):c.510G>A (p.Thr170=) rs757544615
NM_000546.5(TP53):c.582T>C (p.Leu194=) rs370216745
NM_000546.5(TP53):c.63C>T (p.Asp21=) rs1800369
NM_000546.5(TP53):c.672+18G>C rs199578278
NM_000546.5(TP53):c.672+220G>T
NM_000546.5(TP53):c.782+10C>T rs200277687
NM_000546.5(TP53):c.782+12C>T rs17881780
NM_000546.5(TP53):c.782+17C>T rs17880172
NM_000546.5(TP53):c.885T>C (p.Pro295=) rs200073907
NM_000546.5(TP53):c.96+15_96+30del rs730882010
NM_000546.5(TP53):c.96+15_96+31del rs730882011
NM_000546.5(TP53):c.96+18del rs730882012
NM_000546.5(TP53):c.96+41_97-54del rs59758982
NM_000546.5(TP53):c.97-9C>T rs202217267
NM_000546.5(TP53):c.993+13G>C rs369599972
NM_000546.5(TP53):c.993+326_993+341del rs730882013
NM_000546.5(TP53):c.994-17C>T rs368691910

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