List of variants in gene TP53 reported as pathogenic by Institute of Human Genetics, University of Leipzig Medical Center

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.455C>T (p.Pro152Leu)	rs587782705	0.00001
NM_000546.6(TP53):c.711G>A (p.Met237Ile)	rs587782664	0.00001
NM_000546.6(TP53):c.159G>A (p.Trp53Ter)	rs1064794618
NM_000546.6(TP53):c.394A>G (p.Lys132Glu)	rs747342068
NM_000546.6(TP53):c.636del (p.Arg213fs)	rs864309495
NM_000546.6(TP53):c.637C>T (p.Arg213Ter)	rs397516436
NM_000546.6(TP53):c.638G>A (p.Arg213Gln)	rs587778720

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