"GeneDx"[submitter] AND "DGKE"[gene] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1238240	NM_003647.3(DGKE):c.-19+217G>T	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249672	NM_003647.3(DGKE):c.-18-210G>A	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 783790	NM_003647.3(DGKE):c.59G>A (p.Gly20Glu)	DGKE (G20E)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1235190	NM_003647.3(DGKE):c.183G>A (p.Gly61=)	DGKE	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1286426	NM_003647.3(DGKE):c.464+117A>G	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1292022	NM_003647.3(DGKE):c.465-205dup	DGKE	Duplication (intron variant)	not provided	GBenign
Select item 1243279	NM_003647.3(DGKE):c.465-209_465-205dup	DGKE	Duplication (intron variant)	not provided	GBenign
Select item 1238428	NM_003647.3(DGKE):c.465-210_465-205dup	DGKE	Duplication (intron variant)	not provided	GBenign
Select item 1242093	NM_003647.3(DGKE):c.465-58G>A	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 259116	NM_003647.3(DGKE):c.579A>C (p.Thr193=)	DGKE	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1700509	NM_003647.3(DGKE):c.624+4A>T	DGKE	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1260841	NM_003647.3(DGKE):c.624+175C>T	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241400	NM_003647.3(DGKE):c.625-247G>C	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1312987	NM_003647.3(DGKE):c.713G>A (p.Gly238Glu)	DGKE (G238E)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 1219839	NM_003647.3(DGKE):c.744+158G>A	DGKE	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1294524	NM_003647.3(DGKE):c.744+284_744+285del	DGKE	Microsatellite (intron variant)	not provided	GBenign
Select item 1255480	NM_003647.3(DGKE):c.745-21G>T	DGKE	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1220836	NM_003647.3(DGKE):c.798T>A (p.Leu266=)	DGKE	Single nucleotide variant (synonymous variant)	Immunoglobulin-mediated membranoproliferative glomerulonephritis +2 more	GBenign/Likely benign
Select item 1280501	NM_003647.3(DGKE):c.888+55AT[9]	DGKE	Microsatellite (intron variant)	not provided	GBenign
Select item 1259985	NM_003647.3(DGKE):c.888+55AT[10]	DGKE	Microsatellite (intron variant)	not provided	GBenign
Select item 1196931	NM_003647.3(DGKE):c.888+101G>T	DGKE	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3369582	NM_003647.3(DGKE):c.1018A>G (p.Met340Val)	DGKE (M340V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1250449	NM_003647.3(DGKE):c.1046+124C>T	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236781	NM_003647.3(DGKE):c.1047-31C>T	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234095	NM_003647.3(DGKE):c.1098+232G>A	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1205214	NM_003647.3(DGKE):c.1099-245G>A	DGKE	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1182535	NM_003647.3(DGKE):c.1212+223A>G	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289377	NM_003647.3(DGKE):c.1212+330G>A	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1196630	NM_003647.3(DGKE):c.1213-264T>C	DGKE	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1220894	NM_003647.3(DGKE):c.1284+105T>C	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1191095	NM_003647.3(DGKE):c.1285-153C>A	DGKE	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1196231	NM_003647.3(DGKE):c.1285-72A>G	DGKE	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1272625	NM_003647.3(DGKE):c.1524+103T>C	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179804	NM_003647.3(DGKE):c.1524+125T>A	DGKE	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276221	NM_003647.3(DGKE):c.*229A>G	DGKE	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1271043	NM_003647.3(DGKE):c.*239A>G	DGKE	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1261465	NM_003647.3(DGKE):c.*279G>A	DGKE	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

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Items: 37