"Ambry Genetics"[submitter] AND "DLG2"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2300239	NM_001142699.3(DLG2):c.2873T>C (p.Val958Ala)	DLG2 (V331A +23 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082773	NM_001142699.3(DLG2):c.2852T>C (p.Ile951Thr)	DLG2 (I293T +23 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082772	NM_001142699.3(DLG2):c.2618G>A (p.Arg873Lys)	DLG2 (R215K +21 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272236	NM_001142699.3(DLG2):c.2615A>G (p.Glu872Gly)	DLG2 (E768G +21 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545032	NM_001142699.3(DLG2):c.2389C>G (p.Arg797Gly)	DLG2 (R589G +21 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400409	NM_001142699.3(DLG2):c.2354C>T (p.Thr785Ile)	DLG2 (T158I +21 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619233	NM_001142699.3(DLG2):c.2276A>G (p.Glu759Gly)	DLG2 (E641G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272235	NM_001142699.3(DLG2):c.2254A>G (p.Asn752Asp)	DLG2 (N634D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334012	NM_001142699.3(DLG2):c.1924C>T (p.Arg642Cys)	DLG2 (R434C +13 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082771	NM_001142699.3(DLG2):c.1784C>A (p.Ala595Asp)	DLG2 (A448D +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550836	NM_001142699.3(DLG2):c.1781G>C (p.Gly594Ala)	DLG2 (G386A +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082770	NM_001142699.3(DLG2):c.1748C>T (p.Ala583Val)	DLG2 (A436V +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082769	NM_001142699.3(DLG2):c.1693G>A (p.Glu565Lys)	DLG2 (E479K +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293999	NM_001142699.3(DLG2):c.1637G>A (p.Gly546Glu)	DLG2 (G338E +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082768	NM_001142699.3(DLG2):c.1556C>T (p.Ser519Phe)	DLG2 (S414F +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082767	NM_001142699.3(DLG2):c.1546C>T (p.Arg516Trp)	DLG2 (R369W +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570513	NM_001142699.3(DLG2):c.1534A>G (p.Met512Val)	DLG2 (M322V +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3082766	NM_001142699.3(DLG2):c.1444G>C (p.Ala482Pro)	DLG2 (A344P +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3272234	NM_001142699.3(DLG2):c.1435C>T (p.Leu479Phe)	DLG2 (L479F +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2288026	NM_001142699.3(DLG2):c.1430G>A (p.Ser477Asn)	DLG2 (S488N +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2368107	NM_001142699.3(DLG2):c.1411C>T (p.Pro471Ser)	DLG2 (P333S +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3082764	NM_001142699.3(DLG2):c.1345C>T (p.Pro449Ser)	DLG2 (P302S +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2469701	NM_001142699.3(DLG2):c.1316T>A (p.Met439Lys)	DLG2 (M292K +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2664635	NM_001142699.3(DLG2):c.1300C>G (p.Pro434Ala)	DLG2 (P278A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335070	NM_001142699.3(DLG2):c.1178A>G (p.Tyr393Cys)	DLG2 (Y307C +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594391	NM_001142699.3(DLG2):c.1001A>G (p.Asp334Gly)	DLG2 (D178G +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234663	NM_001142699.3(DLG2):c.986T>C (p.Val329Ala)	DLG2 (V182A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296406	NM_001142699.3(DLG2):c.800C>T (p.Ser267Phe)	DLG2, LOC126861281 (S279F +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281452	NM_001142699.3(DLG2):c.394C>T (p.His132Tyr)	DLG2 (H144Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240571	NM_001142699.3(DLG2):c.382G>C (p.Ala128Pro)	DLG2 (A128P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30