List of variants in gene TP53 reported as benign for carcinoma

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	rs1042522	0.62654
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
NM_000546.6(TP53):c.704A>G (p.Asn235Ser)	rs144340710	0.00025
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala)	rs17881470	0.00004
NM_000546.6(TP53):c.28G>A (p.Val10Ile)	rs535274413	0.00004
NM_000546.6(TP53):c.665C>T (p.Pro222Leu)	rs146340390	0.00002
NM_000546.6(TP53):c.245C>T (p.Pro82Leu)	rs534447939	0.00001
NM_000546.6(TP53):c.997C>T (p.Arg333Cys)	rs769934890

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