List of variants in gene TP53 reported as likely pathogenic by GeneKor MSA

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.844C>T (p.Arg282Trp)	rs28934574	0.00001
NM_000546.6(TP53):c.1025G>C (p.Arg342Pro)	rs375338359
NM_000546.6(TP53):c.469G>T (p.Val157Phe)	rs121912654
NM_000546.6(TP53):c.818G>A (p.Arg273His)	rs28934576

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