List of variants in gene TP53 reported as pathogenic for benign neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.743G>A (p.Arg248Gln)	rs11540652	0.00002
NM_000546.6(TP53):c.1010G>A (p.Arg337His)	rs121912664	0.00001
NM_000546.6(TP53):c.524G>A (p.Arg175His)	rs28934578	0.00001
NM_000546.6(TP53):c.659A>G (p.Tyr220Cys)	rs121912666	0.00001
NM_000546.6(TP53):c.733G>A (p.Gly245Ser)	rs28934575	0.00001
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter)	rs730882029
NM_000546.6(TP53):c.389T>C (p.Leu130Pro)	rs1131691013
NM_000546.6(TP53):c.475_481dup (p.Ala161fs)	rs863223301
NM_000546.6(TP53):c.559+1G>A	rs1131691042
NM_000546.6(TP53):c.72dup (p.Leu25fs)	rs2151047224
NM_000546.6(TP53):c.742C>T (p.Arg248Trp)	rs121912651
NM_000546.6(TP53):c.817C>G (p.Arg273Gly)	rs121913343
NM_000546.6(TP53):c.818G>A (p.Arg273His)	rs28934576
NM_000546.6(TP53):c.818G>T (p.Arg273Leu)	rs28934576
NM_000546.6(TP53):c.845G>C (p.Arg282Pro)	rs730882008
NM_000546.6(TP53):c.854A>T (p.Glu285Val)	rs121912667
NM_000546.6(TP53):c.96+1G>T	rs1131691003

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