"PreventionGenetics, part of Exact Sciences"[submitter] AND "DCAF17"[g - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 696807	NM_025000.4(DCAF17):c.192A>G (p.Gly64=)	DCAF17	Single nucleotide variant (synonymous variant +1 more)	DCAF17-related condition +2 more	GConflicting classifications of pathogenicity
Select item 3039368	NM_025000.4(DCAF17):c.322-20_322-19del	DCAF17	Microsatellite (intron variant)	DCAF17-related condition	GLikely benign
Select item 1617873	NM_025000.4(DCAF17):c.322-20A>C	DCAF17	Single nucleotide variant (intron variant)	Woodhouse-Sakati syndrome +1 more	GLikely benign
Select item 1628167	NM_025000.4(DCAF17):c.322-19TC[2]	DCAF17	Microsatellite (intron variant)	Woodhouse-Sakati syndrome +1 more	GLikely benign
Select item 1152174	NM_025000.4(DCAF17):c.322-15_322-14insTT	DCAF17	Insertion (intron variant)	Woodhouse-Sakati syndrome +2 more	GBenign/Likely benign
Select item 191309	NM_025000.4(DCAF17):c.322-14del	DCAF17	Deletion (intron variant)	DCAF17-related condition +2 more	GConflicting classifications of pathogenicity
Select item 332265	NM_025000.4(DCAF17):c.533G>A (p.Arg178Gln)	DCAF17 (R178Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 332266	NM_025000.4(DCAF17):c.579C>A (p.Phe193Leu)	DCAF17 (F193L)	Single nucleotide variant (missense variant +1 more)	DCAF17-related condition +1 more	GLikely benign
Select item 2912860	NM_025000.4(DCAF17):c.723C>T (p.Ile241=)	DCAF17	Single nucleotide variant (synonymous variant +1 more)	Woodhouse-Sakati syndrome +1 more	GLikely benign
Select item 444538	NM_025000.4(DCAF17):c.724G>A (p.Ala242Thr)	DCAF17 (A242T)	Single nucleotide variant (missense variant +1 more)	Woodhouse-Sakati syndrome +2 more	GConflicting classifications of pathogenicity
Select item 332267	NM_025000.4(DCAF17):c.792T>C (p.Thr264=)	DCAF17	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 695583	NM_025000.4(DCAF17):c.981+10del	DCAF17	Deletion (intron variant)	DCAF17-related condition +1 more	GLikely benign