"Ambry Genetics"[submitter] AND "SLAMF8"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2388737	NM_020125.3(SLAMF8):c.23G>A (p.Ser8Asn)	SLAMF8 (S8N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2400047	NM_020125.3(SLAMF8):c.56C>T (p.Thr19Ile)	SLAMF8 (T19I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2230741	NM_020125.3(SLAMF8):c.91G>A (p.Gly31Ser)	SLAMF8 (G31S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2511411	NM_020125.3(SLAMF8):c.92G>A (p.Gly31Asp)	SLAMF8 (G31D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2524864	NM_020125.3(SLAMF8):c.119C>G (p.Pro40Arg)	SLAMF8 (P40R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2488546	NM_020125.3(SLAMF8):c.128T>C (p.Phe43Ser)	SLAMF8 (F43S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2530311	NM_020125.3(SLAMF8):c.235C>G (p.Arg79Gly)	SLAMF8 (R79G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2397357	NM_020125.3(SLAMF8):c.271G>A (p.Gly91Arg)	SLAMF8 (G91R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2489602	NM_020125.3(SLAMF8):c.298A>C (p.Asn100His)	SLAMF8 (N100H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2604154	NM_020125.3(SLAMF8):c.406G>A (p.Val136Ile)	SLAMF8 (V136I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2387573	NM_020125.3(SLAMF8):c.413G>A (p.Arg138Lys)	SLAMF8 (R138K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2479498	NM_020125.3(SLAMF8):c.496C>T (p.Arg166Trp)	SLAMF8 (R166W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236506	NM_020125.3(SLAMF8):c.497G>T (p.Arg166Leu)	SLAMF8 (R57L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263161	NM_020125.3(SLAMF8):c.513C>G (p.Asp171Glu)	SLAMF8 (D62E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2294133	NM_020125.3(SLAMF8):c.650G>T (p.Trp217Leu)	SLAMF8 (W217L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461866	NM_020125.3(SLAMF8):c.667G>A (p.Glu223Lys)	SLAMF8 (E114K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618305	NM_020125.3(SLAMF8):c.707T>C (p.Leu236Pro)	SLAMF8 (L236P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556649	NM_020125.3(SLAMF8):c.710T>A (p.Val237Glu)	SLAMF8 (V128E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602943	NM_020125.3(SLAMF8):c.725C>T (p.Ser242Leu)	SLAMF8 (S133L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance