TMEM14B[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2542195	NM_030969.5(TMEM14B):c.58G>A (p.Ala20Thr)	TMEM14B (A20T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326810	NM_030969.5(TMEM14B):c.59C>T (p.Ala20Val)	TMEM14B (A20V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178855	NM_030969.5(TMEM14B):c.71C>T (p.Ser24Phe)	TMEM14B (S24F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178856	NM_030969.5(TMEM14B):c.82G>A (p.Val28Ile)	TMEM14B (V28I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2343135	NM_030969.5(TMEM14B):c.148G>A (p.Gly50Ser)	TMEM14B (G39S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336510	NM_030969.5(TMEM14B):c.161A>T (p.Tyr54Phe)	TMEM14B (Y43F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344941	NM_030969.5(TMEM14B):c.191G>C (p.Trp64Ser)	TMEM14B (W64S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178854	NM_030969.5(TMEM14B):c.323G>A (p.Arg108His)	TMEM14B (R74H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar