"Ambry Genetics"[submitter] AND "LOC126806176"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2610838	NM_014860.3(SUPT7L):c.1184G>C (p.Ser395Thr)	LOC126806176, SUPT7L (S260T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488434	NM_014860.3(SUPT7L):c.1166G>A (p.Gly389Asp)	LOC126806176, SUPT7L (G387D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477838	NM_014860.3(SUPT7L):c.1114A>G (p.Met372Val)	LOC126806176, SUPT7L (M372V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357810	NM_014860.3(SUPT7L):c.1063T>G (p.Ser355Ala)	LOC126806176, SUPT7L (S353A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510036	NM_014860.3(SUPT7L):c.1052A>G (p.Glu351Gly)	LOC126806176, SUPT7L (E216G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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