CT47A6[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2239342	NM_001080141.2(CT47A6):c.719C>A (p.Ala240Glu)	CT47A6 (A240E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230051	NM_001080141.2(CT47A6):c.718G>A (p.Ala240Thr)	CT47A6 (A240T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078473	NM_001080141.2(CT47A6):c.688G>A (p.Ala230Thr)	CT47A6 (A230T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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