RAB25[gene] and "single gene"[properties] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3150646	NM_020387.4(RAB25):c.5G>A (p.Gly2Glu)	RAB25 (G2E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3150642	NM_020387.4(RAB25):c.19G>A (p.Glu7Lys)	RAB25 (E7K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513057	NM_020387.4(RAB25):c.26A>G (p.Tyr9Cys)	RAB25 (Y9C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312114	NM_020387.4(RAB25):c.44T>C (p.Val15Ala)	RAB25 (V15A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3234162	NM_020387.4(RAB25):c.59A>G (p.Glu20Gly)	RAB25 (E20G)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2466963	NM_020387.4(RAB25):c.106G>A (p.Glu36Lys)	RAB25 (E36K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322905	NM_020387.4(RAB25):c.152C>T (p.Thr51Ile)	RAB25 (T51I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304061	NM_020387.4(RAB25):c.155G>A (p.Arg52His)	RAB25 (R52H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150643	NM_020387.4(RAB25):c.224G>A (p.Arg75Gln)	RAB25 (R75Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312115	NM_020387.4(RAB25):c.236C>T (p.Ser79Leu)	RAB25 (S79L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319692	NM_020387.4(RAB25):c.236C>G (p.Ser79Trp)	RAB25 (S79W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392471	NM_020387.4(RAB25):c.272T>G (p.Val91Gly)	RAB25 (V91G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223029	NM_020387.4(RAB25):c.350C>T (p.Thr117Met)	RAB25 (T117M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312116	NM_020387.4(RAB25):c.352A>T (p.Ile118Phe)	RAB25 (I118F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279807	NM_020387.4(RAB25):c.398G>A (p.Arg133Gln)	RAB25 (R133Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339332	NM_020387.4(RAB25):c.418G>T (p.Ala140Ser)	RAB25 (A140S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239641	NM_020387.4(RAB25):c.451T>C (p.Phe151Leu)	RAB25 (F151L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3150644	NM_020387.4(RAB25):c.501G>C (p.Glu167Asp)	RAB25 (E167D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590029	NM_020387.4(RAB25):c.524C>A (p.Ala175Glu)	RAB25 (A175E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543898	NM_020387.4(RAB25):c.536A>G (p.Lys179Arg)	RAB25 (K179R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3150645	NM_020387.4(RAB25):c.544C>G (p.Gln182Glu)	RAB25 (Q182E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312117	NM_020387.4(RAB25):c.589G>C (p.Ala197Pro)	RAB25 (A197P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 22