"Hematological Lab, University of Education"[submitter] AND "TP53"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2446886	NM_000546.6(TP53):c.576del (p.Gln192fs)	TP53 (Q153fs +3 more)	Deletion (frameshift variant)	Acute myeloid leukemia	GPathogenic
Select item 2502898	NM_000546.6(TP53):c.549A>T (p.Ser183=)	TP53	Single nucleotide variant (synonymous variant +1 more)	Acute myeloid leukemia	GPathogenic
Select item 406578	NM_000546.6(TP53):c.537T>A (p.His179Gln)	TP53 (H140Q +3 more)	Single nucleotide variant (missense variant)	Li-Fraumeni syndrome	GPathogenic FDA Recognized database
Select item 2446885	NM_000546.6(TP53):c.513G>T (p.Glu171Asp)	TP53 (E12D +3 more)	Single nucleotide variant (missense variant +1 more)	Acute myeloid leukemia	GPathogenic
Select item 2505496	NM_000546.6(TP53):c.494A>T (p.Gln165Leu)	TP53 (Q126L +3 more)	Single nucleotide variant (missense variant +1 more)	Acute myeloid leukemia	GPathogenic
Select item 1350373	NM_000546.6(TP53):c.449C>T (p.Thr150Ile)	TP53 (T150I +2 more)	Single nucleotide variant (missense variant +1 more)	Li-Fraumeni syndrome	GUncertain significance

ClinVar