"Ambry Genetics"[submitter] AND "DLEU7-AS1"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2242415	NM_001306135.2(DLEU7):c.419G>A (p.Gly140Glu)	DLEU7, DLEU7-AS1 (G140E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466657	NM_001306135.2(DLEU7):c.386C>T (p.Ser129Leu)	DLEU7, DLEU7-AS1 (S129L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559538	NM_001306135.2(DLEU7):c.367C>G (p.Arg123Gly)	DLEU7, DLEU7-AS1 (R123G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082750	NM_001306135.2(DLEU7):c.309C>A (p.Phe103Leu)	DLEU7, DLEU7-AS1 (F103L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082749	NM_001306135.2(DLEU7):c.238G>A (p.Ala80Thr)	DLEU7, DLEU7-AS1 (A80T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399560	NM_001306135.2(DLEU7):c.228T>G (p.Ser76Arg)	DLEU7, DLEU7-AS1 (S76R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225160	NM_001306135.2(DLEU7):c.214G>A (p.Val72Met)	DLEU7, DLEU7-AS1 (V72M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082748	NM_001306135.2(DLEU7):c.196G>C (p.Glu66Gln)	DLEU7-AS1, DLEU7 (E66Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082747	NM_001306135.2(DLEU7):c.187C>A (p.Pro63Thr)	DLEU7, DLEU7-AS1 (P63T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082746	NM_001306135.2(DLEU7):c.182C>A (p.Pro61Gln)	DLEU7, DLEU7-AS1 (P61Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215176	NM_001306135.2(DLEU7):c.173G>A (p.Arg58Gln)	DLEU7, DLEU7-AS1 (R58Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382310	NM_001306135.2(DLEU7):c.151G>A (p.Ala51Thr)	DLEU7, DLEU7-AS1 (A51T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082745	NM_001306135.2(DLEU7):c.145G>A (p.Ala49Thr)	DLEU7, DLEU7-AS1 (A49T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262057	NM_001306135.2(DLEU7):c.136G>A (p.Val46Met)	DLEU7, DLEU7-AS1 (V46M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216072	NM_001306135.2(DLEU7):c.127C>A (p.Pro43Thr)	DLEU7, DLEU7-AS1 (P43T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410980	NM_001306135.2(DLEU7):c.113G>A (p.Gly38Glu)	DLEU7, DLEU7-AS1 (G38E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511502	NM_001306135.2(DLEU7):c.89G>T (p.Trp30Leu)	DLEU7, DLEU7-AS1 (W30L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361595	NM_001306135.2(DLEU7):c.25G>T (p.Ala9Ser)	DLEU7, DLEU7-AS1 (A9S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205977	NM_001306135.2(DLEU7):c.5C>T (p.Ala2Val)	DLEU7, DLEU7-AS1 (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance