"GeneDx"[submitter] AND "TMEM260"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3373089	NM_017799.4(TMEM260):c.-2C>T	LOC130055718, TMEM260	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 2513718	NM_017799.4(TMEM260):c.284A>G (p.Asn95Ser)	TMEM260 (N95S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1175853	NM_017799.4(TMEM260):c.400C>T (p.Arg134Cys)	TMEM260 (R134C)	Single nucleotide variant (missense variant)	Structural heart defects and renal anomalies syndrome +2 more	GUncertain significance
Select item 3363837	NM_017799.4(TMEM260):c.572A>G (p.His191Arg)	TMEM260 (H191R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363836	NM_017799.4(TMEM260):c.911C>A (p.Ala304Glu)	TMEM260 (A304E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2430741	NM_017799.4(TMEM260):c.998C>T (p.Ser333Leu)	TMEM260 (S333L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2430409	NM_017799.4(TMEM260):c.1889A>G (p.Tyr630Cys)	TMEM260 (Y630C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar