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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 343441	NM_001063.4(TF):c.887A>G (p.Asp296Gly)	TF (D296G +2 more)	Single nucleotide variant (missense variant)	Atransferrinemia +1 more	GBenign/Likely benign
Select item 900555	NM_001063.4(TF):c.1027C>T (p.Arg343Trp)	TF (R216W +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 12617	NM_001063.4(TF):c.1765C>T (p.Pro589Ser)	TF (P589S +2 more)	Single nucleotide variant (missense variant)	Atransferrinemia +1 more	GBenign

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