"Ambry Genetics"[submitter] AND "LOC126861894"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2263417	NM_001386863.1(ACIN1):c.1949G>A (p.Arg650His)	ACIN1, LOC126861894 (R708H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261725	NM_001386863.1(ACIN1):c.1924T>C (p.Ser642Pro)	ACIN1, LOC126861894 (S700P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533441	NM_001386863.1(ACIN1):c.1879G>C (p.Val627Leu)	ACIN1, LOC126861894 (V627L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376603	NM_001386863.1(ACIN1):c.1874C>T (p.Pro625Leu)	ACIN1, LOC126861894 (P643L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358361	NM_001386863.1(ACIN1):c.1817G>C (p.Ser606Thr)	ACIN1, LOC126861894 (S606T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329845	NM_001386863.1(ACIN1):c.1763G>A (p.Arg588His)	ACIN1, LOC126861894 (R588H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar