"Ambry Genetics"[submitter] AND "LOC125371467"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2596902	NM_001042462.2(TRAPPC5):c.47C>G (p.Ala16Gly)	LOC125371467, TRAPPC5 (A16G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182007	NM_001042462.2(TRAPPC5):c.53C>T (p.Ala18Val)	LOC125371467, TRAPPC5 (A18V)	Single nucleotide variant (missense variant)	not specified	GLikely benign