"Ambry Genetics"[submitter] AND "LOC112577472"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2222465	NM_138346.3(KIAA2013):c.176C>T (p.Ala59Val)	KIAA2013, LOC112577472 (A59V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347212	NM_138346.3(KIAA2013):c.163G>T (p.Gly55Cys)	KIAA2013, LOC112577472 (G55C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288237	NM_138346.3(KIAA2013):c.127G>T (p.Ala43Ser)	KIAA2013, LOC112577472 (A43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525133	NM_138346.3(KIAA2013):c.124C>T (p.Arg42Trp)	KIAA2013, LOC112577472 (R42W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288233	NM_138346.3(KIAA2013):c.113C>T (p.Ser38Phe)	KIAA2013, LOC112577472 (S38F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484420	NM_138346.3(KIAA2013):c.103T>C (p.Phe35Leu)	KIAA2013, LOC112577472 (F35L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar