Related gene-specific medical variations for Gene (Select 11339) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302240	NM_007280.2(OIP5):c.58T>A (p.Phe20Ile)	LOC130056891, OIP5 (F20I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302239	NM_007280.2(OIP5):c.583A>G (p.Lys195Glu)	OIP5, OIP5-AS1 (K154E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204166	NM_007280.2(OIP5):c.613C>G (p.Leu205Val)	OIP5, OIP5-AS1 (L164V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204165	NM_007280.2(OIP5):c.155C>T (p.Pro52Leu)	LOC130056891, OIP5 (P52L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204164	NM_007280.2(OIP5):c.137G>A (p.Gly46Glu)	LOC130056891, OIP5 (G46E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539272	NM_007280.2(OIP5):c.115T>C (p.Trp39Arg)	LOC130056891, OIP5 (W39R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535571	NM_007280.2(OIP5):c.658G>T (p.Val220Leu)	OIP5, OIP5-AS1 (V179L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517064	NM_007280.2(OIP5):c.596T>C (p.Leu199Pro)	OIP5, OIP5-AS1 (L158P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361752	NM_007280.2(OIP5):c.32G>A (p.Arg11His)	LOC130056891, OIP5 (R11H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355888	NM_007280.2(OIP5):c.35G>A (p.Cys12Tyr)	LOC130056891, OIP5 (C12Y)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2354871	NM_007280.2(OIP5):c.70A>C (p.Thr24Pro)	LOC130056891, OIP5 (T24P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337956	NM_007280.2(OIP5):c.38C>T (p.Ala13Val)	LOC130056891, OIP5 (A13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211688	NM_007280.2(OIP5):c.628T>G (p.Leu210Val)	OIP5, OIP5-AS1 (L210V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance