"Ambry Genetics"[submitter] AND "RAB2B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2599719	NM_032846.4(RAB2B):c.620G>A (p.Arg207His)	RAB2B (R161H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274275	NM_032846.4(RAB2B):c.610C>T (p.Arg204Trp)	RAB2B (R158W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210967	NM_032846.4(RAB2B):c.524T>C (p.Leu175Ser)	RAB2B (L129S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495474	NM_032846.4(RAB2B):c.451A>C (p.Lys151Gln)	RAB2B (K105Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296138	NM_032846.4(RAB2B):c.401G>A (p.Gly134Glu)	RAB2B (G134E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404114	NM_032846.4(RAB2B):c.265A>G (p.Thr89Ala)	RAB2B (T89A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323218	NM_032846.4(RAB2B):c.259G>A (p.Asp87Asn)	RAB2B (D41N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312126	NM_032846.4(RAB2B):c.206G>A (p.Arg69His)	RAB2B (R23H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar