"PreventionGenetics, part of Exact Sciences"[submitter] AND "DAB1"[gen - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058113	NM_001365792.1(DAB1):c.1272G>A (p.Pro424=)	DAB1	Single nucleotide variant (synonymous variant)	DAB1-related disorder	GLikely benign
Select item 3053243	NM_001365792.1(DAB1):c.1074C>T (p.Ala358=)	DAB1	Single nucleotide variant (synonymous variant)	DAB1-related disorder	GLikely benign
Select item 3046012	NM_001365792.1(DAB1):c.1017C>T (p.Ile339=)	DAB1	Single nucleotide variant (synonymous variant)	DAB1-related disorder	GLikely benign
Select item 3041471	NM_001365792.1(DAB1):c.860G>A (p.Ser287Asn)	DAB1 (S285N +1 more)	Single nucleotide variant (missense variant)	DAB1-related disorder	GBenign
Select item 726037	NM_001365792.1(DAB1):c.793G>A (p.Ala265Thr)	DAB1 (A263T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3058144	NM_001365792.1(DAB1):c.669C>T (p.Pro223=)	DAB1	Single nucleotide variant (synonymous variant)	DAB1-related disorder	GLikely benign
Select item 2638844	NM_001365792.1(DAB1):c.439-3C>T	DAB1	Single nucleotide variant (intron variant)	DAB1-related disorder +1 more	GLikely benign
Select item 2635858	NM_001365792.1(DAB1):c.438G>A (p.Ala146=)	DAB1	Single nucleotide variant (synonymous variant)	DAB1-related disorder	GUncertain significance
Select item 3051613	NM_001365792.1(DAB1):c.318T>G (p.His106Gln)	DAB1 (H106Q)	Single nucleotide variant (missense variant)	DAB1-related disorder	GLikely benign
Select item 3044537	NM_001365792.1(DAB1):c.307-10dup	DAB1	Duplication (intron variant)	DAB1-related disorder	GBenign
Select item 3030885	NM_001365792.1(DAB1):c.42C>T (p.Ser14=)	DAB1	Single nucleotide variant (synonymous variant)	DAB1-related disorder	GLikely benign