Related gene-specific medical variations for Gene (Select 7018) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1699991	NM_001063.4(TF):c.1444C>T (p.Pro482Ser)	TF (P355S +2 more)	Single nucleotide variant (missense variant)	Atransferrinemia	GLikely pathogenic
Select item 1174118	NM_001063.4(TF):c.2063-11_2063-10del	TF	Microsatellite (intron variant)	Atransferrinemia	GUncertain significance
Select item 161508	NM_001063.4(TF):c.1069G>T (p.Glu357Ter)	TF (E357* +2 more)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance

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