"Ambry Genetics"[submitter] AND "LOC126806546"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2305411	NM_152527.5(SLC16A14):c.1067C>T (p.Thr356Met)	LOC126806546, SLC16A14 (T356M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239319	NM_152527.5(SLC16A14):c.1061C>T (p.Pro354Leu)	LOC126806546, SLC16A14 (P354L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220755	NM_152527.5(SLC16A14):c.1028T>C (p.Leu343Ser)	LOC126806546, SLC16A14 (L343S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318933	NM_152527.5(SLC16A14):c.982A>G (p.Ser328Gly)	LOC126806546, SLC16A14 (S328G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519278	NM_152527.5(SLC16A14):c.890T>C (p.Phe297Ser)	LOC126806546, SLC16A14 (F297S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377672	NM_152527.5(SLC16A14):c.831G>A (p.Met277Ile)	LOC126806546, SLC16A14 (M277I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163087	NM_152527.5(SLC16A14):c.737C>T (p.Thr246Ile)	LOC126806546, SLC16A14 (T246I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487232	NM_152527.5(SLC16A14):c.631C>T (p.Pro211Ser)	LOC126806546, SLC16A14 (P211S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163086	NM_152527.5(SLC16A14):c.484G>A (p.Gly162Ser)	LOC126806546, SLC16A14 (G162S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance