List of variants in gene TP53 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.704A>G (p.Asn235Ser)	rs144340710	0.00025
NM_000546.6(TP53):c.869G>A (p.Arg290His)	rs55819519	0.00014
NM_000546.6(TP53):c.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_000546.6(TP53):c.341T>C (p.Leu114Ser)	rs781724995	0.00001
NM_000546.6(TP53):c.760A>G (p.Ile254Val)	rs746601313	0.00001
NM_000546.6(TP53):c.79C>T (p.Pro27Ser)	rs922736614	0.00001
NM_000546.6(TP53):c.848G>A (p.Arg283His)	rs371409680	0.00001
NM_000546.6(TP53):c.1073A>T (p.Glu358Val)	rs773553186
NM_000546.6(TP53):c.416A>C (p.Lys139Thr)	rs2151033390
NM_000546.6(TP53):c.703_705dup (p.Asn235dup)	rs2151021881
NM_000546.6(TP53):c.845G>A (p.Arg282Gln)	rs730882008
NM_000546.6(TP53):c.845G>T (p.Arg282Leu)	rs730882008
NM_000546.6(TP53):c.867_868delinsAA (p.Arg290Ser)	rs2151014889

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