List of variants in gene TP53 reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.523C>T (p.Arg175Cys)	rs138729528	0.00002
NM_000546.6(TP53):c.1000G>C (p.Gly334Arg)	rs730882028	0.00001
NM_000546.6(TP53):c.374C>T (p.Thr125Met)	rs786201057	0.00001
NM_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NC_000017.10:g.(7574034_7576852)_(7576927_7577018)dup
NM_000546.6(TP53):c.1028del (p.Glu343fs)	rs2150994907
NM_000546.6(TP53):c.324_331delinsAAA (p.Phe109fs)	rs2073455679
NM_000546.6(TP53):c.375+2T>C	rs1555526469
NM_000546.6(TP53):c.464C>A (p.Thr155Asn)	rs786202752
NM_000546.6(TP53):c.557_559+2delinsGGGG	rs1567552467
NM_000546.6(TP53):c.559+2del	rs1567552459
NM_000546.6(TP53):c.713G>T (p.Cys238Phe)	rs730882005
NM_000546.6(TP53):c.749C>T (p.Pro250Leu)	rs1064794311
NM_000546.6(TP53):c.782+1G>T	rs1555525429
NM_000546.6(TP53):c.799C>T (p.Arg267Trp)	rs55832599
NM_000546.6(TP53):c.891_915dup (p.Ala307_Leu308insAlaProArgGluHisTer)	rs2073171970

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