"Athena Diagnostics"[submitter] AND "LOC127814297"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 44583	NM_002700.3(POU4F3):c.90C>T (p.Ala30=)	LOC127814297, POU4F3	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 164978	NM_002700.3(POU4F3):c.103T>C (p.Cys35Arg)	LOC127814297, POU4F3 (C35R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 164983	NM_002700.3(POU4F3):c.663C>A (p.Gly221=)	LOC127814297, POU4F3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign

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