"Ambry Genetics"[submitter] AND "SIGLEC5"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457608	NM_003830.4(SIGLEC5):c.1498G>A (p.Gly500Arg)	SIGLEC5 (G500R +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2323178	NM_003830.4(SIGLEC5):c.1481C>G (p.Pro494Arg)	SIGLEC5 (P467A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288131	NM_003830.4(SIGLEC5):c.1475A>G (p.Lys492Arg)	SIGLEC5 (K492R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621086	NM_003830.4(SIGLEC5):c.1463C>T (p.Ser488Leu)	SIGLEC5 (S393L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328593	NM_003830.4(SIGLEC5):c.1421A>T (p.Glu474Val)	SIGLEC5 (E379V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162199	NM_003830.4(SIGLEC5):c.1297G>A (p.Gly433Arg)	SIGLEC5 (G338R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2265193	NM_003830.4(SIGLEC5):c.1234G>A (p.Ala412Thr)	SIGLEC5 (A412T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479401	NM_003830.4(SIGLEC5):c.1147G>A (p.Val383Ile)	SIGLEC5 (V383I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315181	NM_003830.4(SIGLEC5):c.1076C>G (p.Pro359Arg)	SIGLEC5 (P359R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408192	NM_003830.4(SIGLEC5):c.1057T>C (p.Cys353Arg)	SIGLEC5 (C353R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460032	NM_003830.4(SIGLEC5):c.1007A>T (p.Gln336Leu)	SIGLEC5 (Q336L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389563	NM_003830.4(SIGLEC5):c.956C>T (p.Pro319Leu)	SIGLEC5 (P319L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552394	NM_003830.4(SIGLEC5):c.950A>G (p.Gln317Arg)	SIGLEC5 (Q317R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530801	NM_003830.4(SIGLEC5):c.943C>G (p.Arg315Gly)	SIGLEC5 (R315G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162202	NM_003830.4(SIGLEC5):c.904C>T (p.Arg302Cys)	SIGLEC5 (R302C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490902	NM_003830.4(SIGLEC5):c.887C>T (p.Thr296Ile)	SIGLEC5 (T296I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302504	NM_003830.4(SIGLEC5):c.878T>C (p.Ile293Thr)	SIGLEC5 (I293T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246552	NM_003830.4(SIGLEC5):c.815C>T (p.Pro272Leu)	SIGLEC5 (P272L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162201	NM_003830.4(SIGLEC5):c.797G>A (p.Arg266Gln)	SIGLEC5 (R266Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3318504	NM_003830.4(SIGLEC5):c.779T>C (p.Leu260Pro)	SIGLEC5 (L260P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461883	NM_003830.4(SIGLEC5):c.773C>T (p.Pro258Leu)	SIGLEC5 (P258L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2605977	NM_003830.4(SIGLEC5):c.770T>A (p.Leu257His)	SIGLEC5 (L257H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218282	NM_003830.4(SIGLEC5):c.733G>T (p.Gly245Cys)	SIGLEC5 (G245C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398032	NM_003830.4(SIGLEC5):c.719C>T (p.Thr240Ile)	SIGLEC5 (T240I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492263	NM_003830.4(SIGLEC5):c.644T>A (p.Met215Lys)	SIGLEC5 (M215K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519370	NM_003830.4(SIGLEC5):c.578C>T (p.Thr193Ile)	SIGLEC5 (T193I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162200	NM_003830.4(SIGLEC5):c.568C>A (p.Pro190Thr)	SIGLEC5 (P190T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231402	NM_003830.4(SIGLEC5):c.523C>T (p.Pro175Ser)	SIGLEC5 (P175S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248480	NM_003830.4(SIGLEC5):c.362A>G (p.Glu121Gly)	SIGLEC5 (E121G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265237	NM_003830.4(SIGLEC5):c.355C>T (p.Arg119Cys)	SIGLEC5 (R119C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592124	NM_003830.4(SIGLEC5):c.316G>A (p.Gly106Arg)	SIGLEC5 (G106R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2282195	NM_003830.4(SIGLEC5):c.268T>G (p.Phe90Val)	SIGLEC5 (F90V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455323	NM_003830.4(SIGLEC5):c.146C>G (p.Ser49Cys)	SIGLEC5 (S49C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241654	NM_003830.4(SIGLEC5):c.86T>C (p.Val29Ala)	SIGLEC5 (V29A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349125	NM_003830.4(SIGLEC5):c.26T>C (p.Leu9Pro)	SIGLEC5 (L9P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 35