C3280030[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 404088	NM_032638.5(GATA2):c.1348G>A (p.Gly450Arg)	GATA2 (G450R +1 more)	Single nucleotide variant (missense variant)	Acute myeloid leukemia +4 more	GUncertain significance
Select item 404078	NM_032638.5(GATA2):c.1286G>C (p.Ser429Thr)	GATA2 (S429T +1 more)	Single nucleotide variant (missense variant)	Acute myeloid leukemia +6 more	GConflicting classifications of pathogenicity
Select item 472438	NM_032638.5(GATA2):c.1232C>T (p.Ala411Val)	GATA2 (A411V +1 more)	Single nucleotide variant (missense variant)	Deafness-lymphedema-leukemia syndrome +5 more	GUncertain significance
Select item 435283	NM_032638.5(GATA2):c.829A>G (p.Ser277Gly)	GATA2 (S277G)	Single nucleotide variant (missense variant)	Acute myeloid leukemia +6 more	GUncertain significance
Select item 343139	NM_032638.5(GATA2):c.710G>A (p.Gly237Asp)	GATA2 (G237D)	Single nucleotide variant (missense variant)	Deafness-lymphedema-leukemia syndrome +4 more	GBenign/Likely benign
Select item 656906	NM_032638.5(GATA2):c.494A>T (p.His165Leu)	GATA2 (H165L)	Single nucleotide variant (missense variant)	Acute myeloid leukemia +3 more	GUncertain significance
Select item 1051776	NM_032638.5(GATA2):c.479C>G (p.Thr160Ser)	GATA2 (T160S)	Single nucleotide variant (missense variant)	Acute myeloid leukemia +3 more	GUncertain significance
Select item 404080	NM_032638.5(GATA2):c.445G>A (p.Gly149Arg)	GATA2 (G149R)	Single nucleotide variant (missense variant)	Acute myeloid leukemia +6 more	GConflicting classifications of pathogenicity
Select item 241721	NM_032638.5(GATA2):c.182C>T (p.Ala61Val)	GATA2 (A61V)	Single nucleotide variant (missense variant)	Deafness-lymphedema-leukemia syndrome +4 more	GUncertain significance