"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DOCK5"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658489	NM_024940.8(DOCK5):c.564G>A (p.Glu188=)	DOCK5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658490	NM_024940.8(DOCK5):c.738C>T (p.Tyr246=)	DOCK5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 771876	NM_024940.8(DOCK5):c.1406C>T (p.Thr469Met)	DOCK5 (T469M)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2658491	NM_024940.8(DOCK5):c.1653C>T (p.Phe551=)	DOCK5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658492	NM_024940.8(DOCK5):c.5322A>G (p.Leu1774=)	DOCK5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2499083	GRCh37/hg19 8p21.3-21.2(chr8:21925038-26372195)x1	ADAM28, ADAM7 +46 more	Copy number loss	not provided	GLikely pathogenic
Select item 624504	GRCh37/hg19 8p23.1-12(chr8:12556004-34374150)x3	ADAM28, ADAM7 +123 more	Copy number gain	not provided	GLikely pathogenic
Select item 547132	GRCh37/hg19 8p21.2(chr8:25165444-25587783)x3	CDCA2, DOCK5 +2 more	Copy number gain	not provided	GLikely benign

ClinVar