"Fulgent Genetics, Fulgent Genetics"[submitter] AND "IDH2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 158668	NM_002168.4(IDH2):c.993G>A (p.Thr331=)	IDH2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 211177	NM_002168.4(IDH2):c.782G>A (p.Arg261His)	IDH2 (R209H +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 211175	NM_002168.4(IDH2):c.429G>C (p.Leu143=)	IDH2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign

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