List of variants in gene TP53 reported as uncertain significance by Mendelics

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.467G>A (p.Arg156His)	rs371524413	0.00003
NM_000546.6(TP53):c.1069A>G (p.Lys357Glu)	rs1567541856
NM_000546.6(TP53):c.234_263del (p.Ala79_Ala88del)	rs754312472
NM_000546.6(TP53):c.31G>C (p.Glu11Gln)	rs201382018
NM_000546.6(TP53):c.320A>G (p.Tyr107Cys)	rs587782447
NM_000546.6(TP53):c.417G>T (p.Lys139Asn)	rs1567554121
NM_000546.6(TP53):c.623A>G (p.Asp208Gly)	rs1464727668
NM_000546.6(TP53):c.66A>G (p.Leu22=)	rs748527030
NM_000546.6(TP53):c.776A>G (p.Asp259Gly)	rs745425759
NM_000546.6(TP53):c.917G>A (p.Arg306Gln)	rs1048095040
NM_000546.6(TP53):c.993+303T>A	rs1567545268
NM_000546.6(TP53):c.993+5T>G	rs1310956961

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