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

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2361956	NM_021920.4(SCT):c.280G>A (p.Gly94Arg)	SCT (G94R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2326754	NM_021920.4(SCT):c.277G>A (p.Asp93Asn)	SCT (D93N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321166	NM_021920.4(SCT):c.227T>G (p.Leu76Arg)	SCT (L76R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412089	NM_021920.4(SCT):c.175G>A (p.Glu59Lys)	SCT (E59K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219532	NM_021920.4(SCT):c.130G>A (p.Ala44Thr)	SCT (A44T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363551	NM_021920.4(SCT):c.128G>A (p.Gly43Asp)	SCT (G43D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158736	NM_021920.4(SCT):c.122G>C (p.Arg41Pro)	SCT (R41P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391399	NM_021920.4(SCT):c.115C>T (p.Arg39Cys)	SCT (R39C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596698	NM_021920.4(SCT):c.13C>T (p.Pro5Ser)	SCT (P5S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361274	NM_021920.4(SCT):c.10C>T (p.Arg4Trp)	SCT (R4W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance