"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 810938	NM_000546.6(TP53):c.1100+30A>T	TP53	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +4 more	GBenign/Likely benign
Select item 93325	NM_000546.6(TP53):c.993+12T>C	TP53	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +6 more	GBenign/Likely benign
Select item 43591	NM_000546.6(TP53):c.639A>G (p.Arg213=)	TP53	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign
Select item 12351	NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	TP53 (P72R +1 more)	Single nucleotide variant (missense variant)	Li-Fraumeni syndrome 1 +16 more	GBenign
Select item 132708	NM_000546.6(TP53):c.108G>A (p.Pro36=)	TP53	Single nucleotide variant (synonymous variant +1 more)	not specified +5 more	GBenign
Select item 256604	NM_000546.6(TP53):c.97-29C>A	TP53	Single nucleotide variant (intron variant)	not provided +4 more	GBenign

ClinVar