List of variants in gene TP53 reported as likely pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.1039G>A (p.Ala347Thr)	rs1597349147
NM_000546.6(TP53):c.485T>G (p.Ile162Ser)	rs587780069
NM_000546.6(TP53):c.560-15_560-5del	rs2543589630

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