Related gene-specific medical variations for Gene (Select 10077) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329656	NM_139022.3(TSPAN32):c.88A>T (p.Thr30Ser)	C11orf21, TSPAN32 (T30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183828	NM_139022.3(TSPAN32):c.116C>T (p.Ala39Val)	C11orf21, TSPAN32 (A39V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606204	NM_139022.3(TSPAN32):c.112G>T (p.Gly38Trp)	C11orf21, TSPAN32 (G38W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603290	NM_139022.3(TSPAN32):c.133C>T (p.Arg45Cys)	C11orf21, TSPAN32 (R45C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530909	NM_139022.3(TSPAN32):c.25G>T (p.Val9Phe)	C11orf21, TSPAN32 (V9F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516981	NM_139022.3(TSPAN32):c.137G>T (p.Arg46Leu)	C11orf21, TSPAN32 (R46L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261042	NM_139022.3(TSPAN32):c.166G>C (p.Ala56Pro)	C11orf21, TSPAN32 (A56P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar