TSPAN17[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3183811	NM_130465.5(TSPAN17):c.190G>A (p.Val64Met)	TSPAN17 (V64M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183812	NM_130465.5(TSPAN17):c.259C>T (p.Arg87Trp)	TSPAN17 (R87W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398281	NM_130465.5(TSPAN17):c.259C>G (p.Arg87Gly)	TSPAN17 (R87G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597628	NM_130465.5(TSPAN17):c.616G>A (p.Val206Ile)	TSPAN17 (V206I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593287	NM_130465.5(TSPAN17):c.707T>C (p.Ile236Thr)	TSPAN17 (I236T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183813	NM_130465.5(TSPAN17):c.719G>C (p.Gly240Ala)	TSPAN17 (G174A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328174	NM_130465.5(TSPAN17):c.737C>T (p.Ala246Val)	TSPAN17 (A180V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183814	NM_130465.5(TSPAN17):c.751T>G (p.Phe251Val)	TSPAN17 (F277V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar