List of variants in gene TP53 reported as benign for Acute myeloid leukemia

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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: 7

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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.805A>T (p.Ser269Cys)	rs1597362155
NM_000546.6(TP53):c.952C>T (p.Pro318Ser)	rs2151011743
NM_000546.6(TP53):c.954A>T (p.Pro318=)	rs761322293
NM_000546.6(TP53):c.969G>C (p.Leu323=)	rs672601297
NM_000546.6(TP53):c.970G>A (p.Asp324Asn)	rs1064794810
NM_000546.6(TP53):c.978A>G (p.Glu326=)	rs1000256867

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