"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC5A10"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043072	NM_006613.4(GRAP):c.603C>T (p.Cys201=)	GRAP, SLC5A10 (A145V)	Single nucleotide variant (missense variant +2 more)	GRAP-related disorder	GLikely benign
Select item 3036303	NM_006613.4(GRAP):c.595C>A (p.Arg199=)	GRAP, SLC5A10	Single nucleotide variant (synonymous variant +1 more)	GRAP-related disorder	GLikely benign
Select item 3051338	NM_006613.4(GRAP):c.546C>T (p.Gly182=)	GRAP, SLC5A10 (A126V)	Single nucleotide variant (missense variant +2 more)	GRAP-related disorder	GLikely benign

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