Related gene-specific medical variations for Gene (Select 222967) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315551	NM_173565.5(RSPH10B):c.2557G>A (p.Asp853Asn)	CCZ1, RSPH10B (D853N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315549	NM_173565.5(RSPH10B):c.2478C>G (p.Asp826Glu)	CCZ1, RSPH10B (D826E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315548	NM_173565.5(RSPH10B):c.2539C>A (p.Leu847Met)	CCZ1, RSPH10B (L847M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156680	NM_173565.5(RSPH10B):c.2465C>T (p.Ala822Val)	CCZ1, RSPH10B (A822V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386036	NM_173565.5(RSPH10B):c.2482G>A (p.Glu828Lys)	CCZ1, RSPH10B (E828K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385362	NM_173565.5(RSPH10B):c.2485G>A (p.Val829Met)	CCZ1, RSPH10B (V829M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363793	NM_173565.5(RSPH10B):c.2510C>T (p.Pro837Leu)	CCZ1, RSPH10B (P837L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348789	NM_173565.5(RSPH10B):c.2580C>G (p.Ser860Arg)	CCZ1, RSPH10B (S860R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241650	NM_173565.5(RSPH10B):c.2495C>T (p.Thr832Ile)	CCZ1, RSPH10B (T832I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance