List of variants in gene TP53 reported as uncertain significance by MGZ Medical Genetics Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.472C>T (p.Arg158Cys)	rs587780068	0.00001
NM_000546.6(TP53):c.100C>A (p.Pro34Thr)	rs786201968
NM_000546.6(TP53):c.234_263del (p.Ala79_Ala88del)	rs754312472
NM_000546.6(TP53):c.266C>T (p.Pro89Leu)	rs730881994
NM_000546.6(TP53):c.782+5G>C	rs2151019771
NM_000546.6(TP53):c.783-6G>A	rs2073210368

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