List of variants in gene TP53 reported as likely pathogenic by Sema4, Sema4

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: 5

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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.298C>T (p.Gln100Ter)	rs1567555994
NM_000546.6(TP53):c.375+1G>C	rs1567555445
NM_000546.6(TP53):c.587G>C (p.Arg196Pro)	rs483352697
NM_000546.6(TP53):c.643A>G (p.Ser215Gly)	rs886039484

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