"Revvity Omics, Revvity"[submitter] AND "RBM10"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2435380	NM_005676.5(RBM10):c.856G>A (p.Ala286Thr)	RBM10, LOC126863252 (A209T +2 more)	Single nucleotide variant (missense variant)	TARP syndrome	GUncertain significance
Select item 2435381	NM_005676.5(RBM10):c.995G>A (p.Arg332His)	RBM10 (R255H +2 more)	Single nucleotide variant (missense variant)	TARP syndrome	GUncertain significance
Select item 1323521	NM_005676.5(RBM10):c.1722C>G (p.Tyr574Ter)	RBM10 (Y496* +4 more)	Single nucleotide variant (nonsense)	TARP syndrome	GPathogenic

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