"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DOCK2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718903	NM_004946.3(DOCK2):c.264A>G (p.Ala88=)	DOCK2	Single nucleotide variant (synonymous variant +1 more)	DOCK2 deficiency	GBenign
Select item 578432	NM_004946.3(DOCK2):c.286T>C (p.Trp96Arg)	DOCK2 (W96R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 573836	NM_004946.3(DOCK2):c.5165G>A (p.Arg1722Gln)	DOCK2 (R1722Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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