"PreventionGenetics, part of Exact Sciences"[submitter] AND "DOCK4"[ge - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056048	NM_001363540.2(DOCK4):c.5804C>T (p.Ser1935Leu)	DOCK4 (S1926L +1 more)	Single nucleotide variant (missense variant)	DOCK4-related disorder	GBenign
Select item 3032406	NM_001363540.2(DOCK4):c.5738G>A (p.Ser1913Asn)	DOCK4 (S1904N +1 more)	Single nucleotide variant (missense variant)	DOCK4-related disorder	GLikely benign
Select item 2634986	NM_001363540.2(DOCK4):c.5504C>T (p.Pro1835Leu)	DOCK4 (P1826L +1 more)	Single nucleotide variant (missense variant)	DOCK4-related disorder	GUncertain significance
Select item 3057729	NM_001363540.2(DOCK4):c.5418T>A (p.Thr1806=)	DOCK4	Single nucleotide variant (synonymous variant)	DOCK4-related disorder	GLikely benign
Select item 3040477	NM_001363540.2(DOCK4):c.4417-2A>G	DOCK4	Single nucleotide variant (splice acceptor variant)	DOCK4-related disorder	GUncertain significance
Select item 2628428	NM_001363540.2(DOCK4):c.4286G>A (p.Arg1429Gln)	DOCK4, LOC126860152 (R1420Q +1 more)	Single nucleotide variant (missense variant)	DOCK4-related disorder	GUncertain significance
Select item 3033254	NM_001363540.2(DOCK4):c.3778C>T (p.Arg1260Cys)	DOCK4 (R1251C +1 more)	Single nucleotide variant (missense variant)	DOCK4-related disorder	GUncertain significance
Select item 3030775	NM_001363540.2(DOCK4):c.3112G>A (p.Gly1038Ser)	DOCK4, DOCK4-AS1 (G1038S)	Single nucleotide variant (missense variant)	DOCK4-related disorder	GUncertain significance
Select item 717552	NM_001363540.2(DOCK4):c.2878C>A (p.Arg960Ser)	DOCK4 (R960S)	Single nucleotide variant (missense variant)	DOCK4-related disorder +1 more	GLikely benign