"Ambry Genetics"[submitter] AND "RAB29"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312125	NM_003929.3(RAB29):c.545T>C (p.Met182Thr)	RAB29 (M158T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312123	NM_003929.3(RAB29):c.539A>T (p.Asp180Val)	RAB29 (D156V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526383	NM_003929.3(RAB29):c.527A>T (p.Asn176Ile)	RAB29 (N104I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150668	NM_003929.3(RAB29):c.454A>C (p.Thr152Pro)	RAB29 (T80P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150667	NM_003929.3(RAB29):c.439G>A (p.Gly147Ser)	RAB29 (G147S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150666	NM_003929.3(RAB29):c.422G>A (p.Arg141Gln)	RAB29 (R141Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358355	NM_003929.3(RAB29):c.421C>G (p.Arg141Gly)	RAB29 (R69G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400277	NM_003929.3(RAB29):c.406C>G (p.Arg136Gly)	RAB29 (R136G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150665	NM_003929.3(RAB29):c.395G>T (p.Trp132Leu)	RAB29 (W132L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520550	NM_003929.3(RAB29):c.224G>A (p.Arg75Gln)	RAB29 (R3Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537115	NM_003929.3(RAB29):c.193G>T (p.Ala65Ser)	RAB29 (A65S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3150664	NM_003929.3(RAB29):c.173G>A (p.Arg58Gln)	RAB29 (R58Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3312124	NM_003929.3(RAB29):c.107A>T (p.Tyr36Phe)	RAB29 (Y36F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance