"Ambry Genetics"[submitter] AND "SLAMF6"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2589636	NM_001184714.2(SLAMF6):c.994G>A (p.Val332Met)	SLAMF6 (V282M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162727	NM_001184714.2(SLAMF6):c.977C>T (p.Thr326Ile)	SLAMF6 (T326I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162726	NM_001184714.2(SLAMF6):c.962C>T (p.Thr321Ile)	SLAMF6 (T210I +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2241575	NM_001184714.2(SLAMF6):c.888A>T (p.Glu296Asp)	SLAMF6 (E246D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303615	NM_001184714.2(SLAMF6):c.728T>C (p.Leu243Pro)	LOC126805892, SLAMF6 (L243P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459334	NM_001184714.2(SLAMF6):c.715G>A (p.Gly239Ser)	LOC126805892, SLAMF6 (G128S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162724	NM_001184714.2(SLAMF6):c.685T>C (p.Phe229Leu)	LOC126805892, SLAMF6 (F229L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280399	NM_001184714.2(SLAMF6):c.682C>A (p.Leu228Met)	LOC126805892, SLAMF6 (L179M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469751	NM_001184714.2(SLAMF6):c.643G>A (p.Glu215Lys)	LOC126805892, SLAMF6 (E104K +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3162723	NM_001184714.2(SLAMF6):c.590C>T (p.Ala197Val)	LOC126805892, SLAMF6 (A148V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492264	NM_001184714.2(SLAMF6):c.539C>A (p.Thr180Asn)	LOC126805892, SLAMF6 (T69N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318769	NM_001184714.2(SLAMF6):c.277T>G (p.Ser93Ala)	SLAMF6 (S44A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3318767	NM_001184714.2(SLAMF6):c.215G>A (p.Ser72Asn)	SLAMF6 (S23N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3318768	NM_001184714.2(SLAMF6):c.137C>A (p.Ala46Glu)	SLAMF6 (A46E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162725	NM_001184714.2(SLAMF6):c.94G>A (p.Gly32Arg)	SLAMF6 (G32R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance