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

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052577	NM_006133.3(DAGLA):c.12C>T (p.Ile4=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GLikely benign
Select item 3060353	NM_006133.3(DAGLA):c.63G>A (p.Pro21=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GBenign
Select item 3033512	NM_006133.3(DAGLA):c.246C>T (p.Arg82=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GLikely benign
Select item 3030816	NM_006133.3(DAGLA):c.380A>G (p.Asn127Ser)	DAGLA (N127S)	Single nucleotide variant (missense variant)	DAGLA-related condition	GUncertain significance
Select item 3052633	NM_006133.3(DAGLA):c.410-4G>A	DAGLA	Single nucleotide variant (intron variant)	DAGLA-related condition	GLikely benign
Select item 2632571	NM_006133.3(DAGLA):c.856A>T (p.Met286Leu)	DAGLA (M286L)	Single nucleotide variant (missense variant)	DAGLA-related condition	GUncertain significance
Select item 785355	NM_006133.3(DAGLA):c.1005C>T (p.Phe335=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition +1 more	GBenign
Select item 3060723	NM_006133.3(DAGLA):c.1524G>A (p.Ala508=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GBenign
Select item 3045540	NM_006133.3(DAGLA):c.1657-4G>A	DAGLA	Single nucleotide variant (intron variant)	DAGLA-related condition	GLikely benign
Select item 3045733	NM_006133.3(DAGLA):c.1785C>G (p.Ala595=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GLikely benign
Select item 3056430	NM_006133.3(DAGLA):c.1983+10C>T	DAGLA	Single nucleotide variant (intron variant)	DAGLA-related condition	GBenign
Select item 776618	NM_006133.3(DAGLA):c.2204G>T (p.Gly735Val)	DAGLA (G735V)	Single nucleotide variant (missense variant)	DAGLA-related condition +1 more	GBenign
Select item 3052350	NM_006133.3(DAGLA):c.2244G>A (p.Ala748=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GLikely benign
Select item 3057017	NM_006133.3(DAGLA):c.2246C>T (p.Ala749Val)	DAGLA (A749V)	Single nucleotide variant (missense variant)	DAGLA-related condition	GLikely benign
Select item 3037919	NM_006133.3(DAGLA):c.2249C>T (p.Ala750Val)	DAGLA (A750V)	Single nucleotide variant (missense variant)	DAGLA-related condition	GLikely benign
Select item 1274834	NM_006133.3(DAGLA):c.2301G>A (p.Ala767=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition +1 more	GBenign
Select item 3041620	NM_006133.3(DAGLA):c.2439G>A (p.Leu813=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GBenign
Select item 3040997	NM_006133.3(DAGLA):c.2484C>T (p.Pro828=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GLikely benign
Select item 3040716	NM_006133.3(DAGLA):c.2661C>T (p.Gly887=)	DAGLA	Single nucleotide variant (synonymous variant)	DAGLA-related condition	GLikely benign
Select item 3059923	NM_006133.3(DAGLA):c.2666C>T (p.Pro889Leu)	DAGLA (P889L)	Single nucleotide variant (missense variant)	DAGLA-related condition	GBenign

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Items: 20