List of variants in gene TP53 reported as pathogenic by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.375G>A (p.Thr125=)	rs55863639	0.00001
NM_000546.6(TP53):c.524G>A (p.Arg175His)	rs28934578	0.00001
NM_000546.6(TP53):c.659A>G (p.Tyr220Cys)	rs121912666	0.00001
NM_000546.6(TP53):c.733G>A (p.Gly245Ser)	rs28934575	0.00001
NM_000546.6(TP53):c.1015G>T (p.Glu339Ter)	rs17882252
NM_000546.6(TP53):c.375G>C (p.Thr125=)	rs55863639
NM_000546.6(TP53):c.527G>A (p.Cys176Tyr)	rs786202962
NM_000546.6(TP53):c.626_627del (p.Arg209fs)	rs1057517840
NM_000546.6(TP53):c.702C>A (p.Tyr234Ter)
NM_000546.6(TP53):c.779_782+13del
NM_000546.6(TP53):c.891_915dup (p.Ala307_Leu308insAlaProArgGluHisTer)	rs2073171970

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