"Ambry Genetics"[submitter] AND "SIGLEC10-AS1"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2520767	NM_033130.5(SIGLEC10):c.920G>A (p.Gly307Glu)	SIGLEC10, SIGLEC10-AS1 (G249E +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 3162142	NM_033130.5(SIGLEC10):c.914C>T (p.Pro305Leu)	SIGLEC10, SIGLEC10-AS1 (P247L +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3162141	NM_033130.5(SIGLEC10):c.797C>T (p.Ala266Val)	SIGLEC10, SIGLEC10-AS1 (A208V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2590381	NM_033130.5(SIGLEC10):c.688G>T (p.Val230Phe)	SIGLEC10, SIGLEC10-AS1 (D90E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334546	NM_033130.5(SIGLEC10):c.668G>C (p.Gly223Ala)	SIGLEC10, SIGLEC10-AS1 (G175A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162139	NM_033130.5(SIGLEC10):c.575C>A (p.Pro192Gln)	SIGLEC10, SIGLEC10-AS1 (P144Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162138	NM_033130.5(SIGLEC10):c.547G>A (p.Ala183Thr)	SIGLEC10, SIGLEC10-AS1 (A183T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2267444	NM_033130.5(SIGLEC10):c.491G>T (p.Cys164Phe)	SIGLEC10, SIGLEC10-AS1 (C164F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306823	NM_033130.5(SIGLEC10):c.466C>T (p.Pro156Ser)	SIGLEC10, SIGLEC10-AS1 (P156S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554685	NM_033130.5(SIGLEC10):c.449T>C (p.Ile150Thr)	SIGLEC10, SIGLEC10-AS1 (I150T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267967	NM_033130.5(SIGLEC10):c.268T>C (p.Phe90Leu)	SIGLEC10, SIGLEC10-AS1 (F90L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2568775	NM_033130.5(SIGLEC10):c.259C>T (p.Arg87Trp)	SIGLEC10, SIGLEC10-AS1 (R87W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2554013	NM_033130.5(SIGLEC10):c.244G>C (p.Val82Leu)	SIGLEC10, SIGLEC10-AS1 (V82L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2489339	NM_033130.5(SIGLEC10):c.191T>C (p.Val64Ala)	SIGLEC10, SIGLEC10-AS1 (V64A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2205962	NM_033130.5(SIGLEC10):c.152C>T (p.Thr51Ile)	SIGLEC10, SIGLEC10-AS1 (T51I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2477725	NM_033130.5(SIGLEC10):c.127T>C (p.Phe43Leu)	SIGLEC10, SIGLEC10-AS1 (F43L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2409198	NM_033130.5(SIGLEC10):c.71G>A (p.Arg24Gln)	SIGLEC10, SIGLEC10-AS1 (R24Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3162140	NM_033130.5(SIGLEC10):c.65G>T (p.Trp22Leu)	SIGLEC10, SIGLEC10-AS1 (W22L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2319906	NM_033130.5(SIGLEC10):c.53A>G (p.Asp18Gly)	SIGLEC10, SIGLEC10-AS1 (D18G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2210947	NM_033130.5(SIGLEC10):c.26C>T (p.Ser9Leu)	SIGLEC10, SIGLEC10-AS1 (S9L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign

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Items: 20