Related gene-specific medical variations for Gene (Select 696) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2615672	NM_001732.3(BTN1A1):c.169A>T (p.Ser57Cys)	BTN1A1, LOC129996064 (S57C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362436	NM_001732.3(BTN1A1):c.205A>G (p.Lys69Glu)	BTN1A1, LOC129996064 (K69E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223604	NM_001732.3(BTN1A1):c.182T>C (p.Leu61Ser)	BTN1A1, LOC129996064 (L61S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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