List of variants in gene TP53 reported as likely pathogenic for Papillary renal cell carcinoma, sporadic

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.578A>C (p.His193Pro)	rs786201838	0.00001
NM_000546.6(TP53):c.659A>G (p.Tyr220Cys)	rs121912666	0.00001
NM_000546.6(TP53):c.577C>A (p.His193Asn)	rs876658468
NM_000546.6(TP53):c.577C>G (p.His193Asp)	rs876658468
NM_000546.6(TP53):c.577C>T (p.His193Tyr)	rs876658468
NM_000546.6(TP53):c.578A>G (p.His193Arg)	rs786201838
NM_000546.6(TP53):c.578A>T (p.His193Leu)	rs786201838
NM_000546.6(TP53):c.658T>A (p.Tyr220Asn)	rs530941076
NM_000546.6(TP53):c.658T>C (p.Tyr220His)	rs530941076
NM_000546.6(TP53):c.658T>G (p.Tyr220Asp)	rs530941076
NM_000546.6(TP53):c.659A>C (p.Tyr220Ser)	rs121912666
NM_000546.6(TP53):c.721T>C (p.Ser241Pro)	rs1057520002
NM_000546.6(TP53):c.721T>G (p.Ser241Ala)	rs1057520002
NM_000546.6(TP53):c.722C>A (p.Ser241Tyr)	rs28934573
NM_000546.6(TP53):c.722C>G (p.Ser241Cys)	rs28934573
NM_000546.6(TP53):c.722C>T (p.Ser241Phe)	rs28934573

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