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

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033599	NM_001347.4(DGKQ):c.2637C>A (p.Val879=)	DGKQ	Single nucleotide variant (synonymous variant)	DGKQ-related disorder	GLikely benign
Select item 3050037	NM_001347.4(DGKQ):c.2575-7G>A	DGKQ	Single nucleotide variant (intron variant)	DGKQ-related disorder	GLikely benign
Select item 3038607	NM_001347.4(DGKQ):c.2574+8G>C	DGKQ	Single nucleotide variant (intron variant)	DGKQ-related disorder	GLikely benign
Select item 3052604	NM_001347.4(DGKQ):c.2566G>A (p.Val856Met)	DGKQ (V856M)	Single nucleotide variant (missense variant)	DGKQ-related disorder	GBenign
Select item 3043989	NM_001347.4(DGKQ):c.1886+10G>T	DGKQ	Single nucleotide variant (intron variant)	DGKQ-related disorder	GLikely benign
Select item 3046447	NM_001347.4(DGKQ):c.1884C>T (p.Pro628=)	DGKQ	Single nucleotide variant (synonymous variant)	DGKQ-related disorder	GLikely benign
Select item 3050114	NM_001347.4(DGKQ):c.1734+10C>T	DGKQ	Single nucleotide variant (intron variant)	DGKQ-related disorder	GLikely benign
Select item 3041208	NM_001347.4(DGKQ):c.1619-4G>A	DGKQ	Single nucleotide variant (intron variant)	DGKQ-related disorder	GLikely benign
Select item 3053600	NM_001347.4(DGKQ):c.1015C>A (p.Pro339Thr)	DGKQ (P339T)	Single nucleotide variant (missense variant)	DGKQ-related disorder	GLikely benign
Select item 3044052	NM_001347.4(DGKQ):c.719G>A (p.Arg240His)	DGKQ (R240H)	Single nucleotide variant (missense variant)	DGKQ-related disorder	GLikely benign
Select item 3056660	NM_001347.4(DGKQ):c.633C>T (p.Ala211=)	DGKQ	Single nucleotide variant (synonymous variant)	DGKQ-related disorder	GBenign
Select item 3045545	NM_001347.4(DGKQ):c.609G>C (p.Thr203=)	DGKQ	Single nucleotide variant (synonymous variant)	DGKQ-related disorder	GLikely benign
Select item 3042093	NM_001347.4(DGKQ):c.592G>C (p.Glu198Gln)	DGKQ (E198Q)	Single nucleotide variant (missense variant)	DGKQ-related disorder	GLikely benign
Select item 3046878	NM_001347.4(DGKQ):c.538-10C>T	DGKQ	Single nucleotide variant (intron variant)	DGKQ-related disorder	GLikely benign
Select item 3041681	NM_001347.4(DGKQ):c.447C>T (p.Cys149=)	DGKQ	Single nucleotide variant (synonymous variant)	DGKQ-related disorder	GLikely benign