"Ambry Genetics"[submitter] AND "SSX5"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2549286	NM_175723.2(SSX5):c.562G>C (p.Glu188Gln)	SSX5 (E229Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322907	NM_175723.2(SSX5):c.537G>T (p.Glu179Asp)	SSX5 (E179D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359247	NM_175723.2(SSX5):c.506G>A (p.Arg169His)	SSX5 (R210H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312697	NM_175723.2(SSX5):c.478G>A (p.Gly160Arg)	SSX5 (G160R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551913	NM_175723.2(SSX5):c.442T>C (p.Ser148Pro)	SSX5 (S189P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397341	NM_175723.2(SSX5):c.419G>A (p.Arg140His)	SSX5 (R140H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170578	NM_175723.2(SSX5):c.401A>C (p.Asn134Thr)	SSX5 (N134T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170577	NM_175723.2(SSX5):c.347C>T (p.Pro116Leu)	SSX5 (P157L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207502	NM_175723.2(SSX5):c.316G>A (p.Gly106Arg)	SSX5 (G147R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2207501	NM_175723.2(SSX5):c.315G>T (p.Gln105His)	SSX5 (Q105H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314542	NM_175723.2(SSX5):c.311T>C (p.Leu104Pro)	SSX5 (L104P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322908	NM_175723.2(SSX5):c.287A>G (p.His96Arg)	SSX5 (H137R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2325413	NM_175723.2(SSX5):c.268C>A (p.Arg90Ser)	SSX5 (R90S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461895	NM_175723.2(SSX5):c.259G>A (p.Asp87Asn)	SSX5 (D87N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170574	NM_175723.2(SSX5):c.239A>G (p.Gln80Arg)	SSX5 (Q80R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257719	NM_175723.2(SSX5):c.224G>A (p.Arg75Gln)	SSX5 (R116Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2215947	NM_175723.2(SSX5):c.205C>T (p.Pro69Ser)	SSX5 (P110S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170573	NM_175723.2(SSX5):c.162G>C (p.Lys54Asn)	SSX5 (K54N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3322910	NM_175723.2(SSX5):c.143A>G (p.Tyr48Cys)	SSX5 (Y89C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322909	NM_175723.2(SSX5):c.128C>T (p.Ser43Leu)	SSX5 (S43L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228049	NM_175723.2(SSX5):c.70-196C>A	SSX5 (A50D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392976	NM_175723.2(SSX5):c.69+213C>G	SSX5 (P41R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533255	NM_175723.2(SSX5):c.69+212C>T	SSX5 (P41S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170576	NM_175723.2(SSX5):c.40G>T (p.Gly14Cys)	SSX5 (G14C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 24