Related gene-specific medical variations for Gene (Select 64216) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3176479	NM_022366.3(TFB2M):c.53C>T (p.Ala18Val)	LOC129932930, TFB2M (A18V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176474	NM_022366.3(TFB2M):c.187A>G (p.Lys63Glu)	LOC129932930, TFB2M (K63E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2690230	NM_022366.3(TFB2M):c.1161G>A (p.Trp387Ter)	TFB2M (W387*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2640236	NM_022366.3(TFB2M):c.143C>T (p.Ser48Phe)	LOC129932930, TFB2M (S48F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2606337	NM_022366.3(TFB2M):c.25C>T (p.Pro9Ser)	LOC129932930, TFB2M (P9S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331274	NM_022366.3(TFB2M):c.67T>G (p.Phe23Val)	LOC129932930, TFB2M (F23V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235899	NM_022366.3(TFB2M):c.58G>A (p.Ala20Thr)	LOC129932930, TFB2M (A20T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar