"Ambry Genetics"[submitter] AND "RAB26"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3150648	NM_014353.5(RAB26):c.17C>T (p.Thr6Ile)	RAB26 (T6I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2349564	NM_014353.5(RAB26):c.40A>C (p.Thr14Pro)	RAB26 (T14P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2348054	NM_014353.5(RAB26):c.82C>T (p.Pro28Ser)	RAB26 (P28S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3150647	NM_014353.5(RAB26):c.175T>C (p.Phe59Leu)	RAB26 (F59L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2302846	NM_014353.5(RAB26):c.184G>A (p.Val62Ile)	RAB26 (V62I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2216232	NM_014353.5(RAB26):c.190T>C (p.Phe64Leu)	RAB26 (F64L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2550351	NM_014353.5(RAB26):c.193A>C (p.Lys65Gln)	RAB26 (K65Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2607039	NM_014353.5(RAB26):c.203T>C (p.Leu68Pro)	RAB26 (L2P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304682	NM_014353.5(RAB26):c.253G>A (p.Asp85Asn)	RAB26 (D19N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150649	NM_014353.5(RAB26):c.289G>A (p.Val97Ile)	RAB26 (V97I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608219	NM_014353.5(RAB26):c.298G>C (p.Asp100His)	RAB26 (D100H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602273	NM_014353.5(RAB26):c.321C>A (p.Asp107Glu)	RAB26 (D41E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514807	NM_014353.5(RAB26):c.334A>C (p.Lys112Gln)	RAB26 (K112Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508039	NM_014353.5(RAB26):c.356A>G (p.Asp119Gly)	RAB26 (D119G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243857	NM_014353.5(RAB26):c.380G>A (p.Arg127His)	RAB26 (R127H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312119	NM_014353.5(RAB26):c.433G>A (p.Asp145Asn)	RAB26 (D79N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150651	NM_014353.5(RAB26):c.504C>A (p.His168Gln)	RAB26 (H102Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355269	NM_014353.5(RAB26):c.508G>A (p.Val170Met)	RAB26 (V104M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312118	NM_014353.5(RAB26):c.509T>C (p.Val170Ala)	RAB26 (V170A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150652	NM_014353.5(RAB26):c.512C>T (p.Ala171Val)	RAB26 (A105V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3150653	NM_014353.5(RAB26):c.566G>A (p.Arg189Lys)	RAB26 (R123K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369439	NM_014353.5(RAB26):c.622G>A (p.Ala208Thr)	RAB26 (A208T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519369	NM_014353.5(RAB26):c.627G>C (p.Lys209Asn)	RAB26 (K209N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3150654	NM_014353.5(RAB26):c.670G>A (p.Glu224Lys)	RAB26 (E224K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236632	NM_014353.5(RAB26):c.690G>A (p.Met230Ile)	RAB26 (M164I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379133	NM_014353.5(RAB26):c.703G>A (p.Glu235Lys)	RAB26 (E169K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290945	NM_014353.5(RAB26):c.709C>T (p.Arg237Cys)	RAB26 (R237C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595621	NM_014353.5(RAB26):c.715C>T (p.Arg239Trp)	RAB26 (R239W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589088	NM_014353.5(RAB26):c.716G>A (p.Arg239Gln)	RAB26 (R173Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303865	NM_014353.5(RAB26):c.725A>T (p.Asp242Val)	RAB26 (D176V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265966	NM_014353.5(RAB26):c.737G>A (p.Arg246Lys)	RAB26 (R246K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507924	NM_014353.5(RAB26):c.764G>A (p.Arg255His)	RAB26 (R189H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32