Related gene-specific medical variations for Gene (Select 9026) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284312	NM_003959.3(HIP1R):c.2725G>A (p.Glu909Lys)	HIP1R, LOC124849271 (E909K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105904	NM_003959.3(HIP1R):c.2713G>A (p.Val905Ile)	HIP1R, LOC124849271 (V905I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461974	NM_003959.3(HIP1R):c.2656C>A (p.Leu886Met)	HIP1R, LOC124849271 (L886M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333169	NM_003959.3(HIP1R):c.2710A>G (p.Ile904Val)	HIP1R, LOC124849271 (I904V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269567	NM_003959.3(HIP1R):c.2692G>A (p.Gly898Ser)	HIP1R, LOC124849271 (G898S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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