"Ambry Genetics"[submitter] AND "LOC130061165"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2335429	NM_018346.3(RSAD1):c.16G>T (p.Ala6Ser)	LOC130061165, RSAD1 (A6S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266833	NM_018346.3(RSAD1):c.17C>A (p.Ala6Asp)	LOC130061165, RSAD1 (A6D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354232	NM_018346.3(RSAD1):c.38C>T (p.Ala13Val)	LOC130061165, RSAD1 (A13V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315503	NM_018346.3(RSAD1):c.68G>A (p.Arg23His)	LOC130061165, RSAD1 (R23H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315498	NM_018346.3(RSAD1):c.79G>A (p.Ala27Thr)	RSAD1, LOC130061165 (A27T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315497	NM_018346.3(RSAD1):c.98C>T (p.Pro33Leu)	LOC130061165, RSAD1 (P33L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619547	NM_018346.3(RSAD1):c.116G>A (p.Arg39His)	LOC130061165, RSAD1 (R39H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156572	NM_018346.3(RSAD1):c.125T>C (p.Leu42Pro)	LOC130061165, RSAD1 (L42P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar