Related gene-specific medical variations for Gene (Select 84951) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180878	NM_032865.6(TNS4):c.1687G>T (p.Asp563Tyr)	LOC126862556, TNS4 (D563Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180877	NM_032865.6(TNS4):c.1682G>A (p.Gly561Asp)	LOC126862556, TNS4 (G561D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 747380	NM_032865.6(TNS4):c.1739C>T (p.Ala580Val)	LOC126862556, TNS4 (A580V)	Single nucleotide variant (missense variant)	not provided	GBenign

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