Related gene-specific medical variations for Gene (Select 4986) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3204420	NM_000912.5(OPRK1):c.998T>C (p.Leu333Pro)	LOC105375836, OPRK1 (L244P +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2558462	NM_000912.5(OPRK1):c.911A>G (p.His304Arg)	LOC105375836, OPRK1 (H215R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349969	NM_000912.5(OPRK1):c.1015C>T (p.Arg339Trp)	LOC105375836, OPRK1 (R250W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300518	NM_000912.5(OPRK1):c.959A>G (p.Tyr320Cys)	LOC105375836, OPRK1 (Y320C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239631	NM_000912.5(OPRK1):c.723C>G (p.Ile241Met)	LOC105375836, OPRK1 (I152M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790059	NM_000912.5(OPRK1):c.948C>T (p.Ile316=)	LOC105375836, OPRK1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 790058	NM_000912.5(OPRK1):c.1120G>A (p.Asp374Asn)	LOC105375836, OPRK1 (D374N +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 720427	NM_000912.5(OPRK1):c.765C>T (p.Ser255=)	LOC105375836, OPRK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 716915	NM_000912.5(OPRK1):c.852C>T (p.Val284=)	LOC105375836, OPRK1	Single nucleotide variant (synonymous variant)	not provided	GBenign