"PreventionGenetics, part of Exact Sciences"[submitter] AND "GOT1"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039802	NM_002079.3(GOT1):c.570C>T (p.His190=)	GOT1	Single nucleotide variant (synonymous variant)	GOT1-related disorder	GLikely benign
Select item 3047043	NM_002079.3(GOT1):c.479G>A (p.Arg160His)	GOT1 (R160H)	Single nucleotide variant (missense variant)	GOT1-related disorder	GLikely benign
Select item 3060094	NM_002079.3(GOT1):c.363G>A (p.Ala121=)	GOT1	Single nucleotide variant (synonymous variant)	GOT1-related disorder	GBenign

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