List of variants in gene TP53 reported as likely pathogenic by Molecular Diagnostics Laboratory, Catalan Institute of Oncology

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.374C>T (p.Thr125Met)	rs786201057	0.00001
NM_000546.6(TP53):c.535C>T (p.His179Tyr)	rs587780070	0.00001
NM_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NM_000546.6(TP53):c.725G>A (p.Cys242Tyr)	rs121912655	0.00001
NM_000546.6(TP53):c.783-1G>A	rs1555525367	0.00001
NM_000546.6(TP53):c.332T>C (p.Leu111Pro)	rs1057519997
NM_000546.6(TP53):c.374C>G (p.Thr125Arg)	rs786201057
NM_000546.6(TP53):c.452C>G (p.Pro151Arg)	rs1057520000
NM_000546.6(TP53):c.586del (p.Arg196fs)
NM_000546.6(TP53):c.638G>A (p.Arg213Gln)	rs587778720
NM_000546.6(TP53):c.646G>T (p.Val216Leu)	rs730882025
NM_000546.6(TP53):c.724T>G (p.Cys242Gly)	rs1057519982
NM_000546.6(TP53):c.857A>G (p.Glu286Gly)	rs1057519985

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