List of variants in gene TP53 reported as uncertain significance for Malignant tumor of breast

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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.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_000546.6(TP53):c.329G>A (p.Arg110His)	rs11540654	0.00003
NM_000546.6(TP53):c.1093C>T (p.His365Tyr)	rs267605075	0.00001
NM_000546.6(TP53):c.245C>T (p.Pro82Leu)	rs534447939	0.00001
NM_000546.6(TP53):c.328C>T (p.Arg110Cys)	rs587781371	0.00001
NM_000546.6(TP53):c.605G>A (p.Arg202His)	rs587778719	0.00001
NM_000546.6(TP53):c.800G>A (p.Arg267Gln)	rs587780075	0.00001
NM_000546.6(TP53):c.176G>A (p.Gly59Asp)	rs1597374828
NM_000546.6(TP53):c.427G>A (p.Val143Met)	rs587782620
NM_000546.6(TP53):c.673-9A>G	rs754628512
NM_000546.6(TP53):c.830G>A (p.Cys277Tyr)	rs763098116
NM_000546.6(TP53):c.892G>A (p.Glu298Lys)	rs201744589

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