Related gene-specific medical variations for Gene (Select 10342) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2437053	NM_006070.6(TFG):c.922C>T (p.Pro308Ser)	TFG (P304S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2437052	NM_006070.6(TFG):c.547T>C (p.Ser183Pro)	TFG (S183P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2437051	NM_006070.6(TFG):c.290T>C (p.Leu97Pro)	TFG (L97P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 811936	NM_006070.6(TFG):c.1198C>T (p.Arg400Ter)	TFG (R396* +1 more)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 618425	NM_006070.6(TFG):c.566A>G (p.Asp189Gly)	TFG (D189G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 425303	NM_006070.6(TFG):c.337C>T (p.Arg113Ter)	TFG (R113*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic

ClinVar