"Ambry Genetics"[submitter] AND "GAGE12I"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2399003	NM_001098405.3(GAGE12F):c.125A>T (p.Glu42Val)	GAGE12B, GAGE12I (E42V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591744	NM_001477.1:c.178G>C	GAGE12I	Single nucleotide variant	not specified	GUncertain significance
Select item 2273432	NM_001477.1:c.148C>A	GAGE12I	Single nucleotide variant	not specified	GLikely benign
Select item 3097941	NM_001477.1:c.98G>T	GAGE12I	Single nucleotide variant	not specified	GUncertain significance
Select item 3097940	NM_001477.1:c.140C>G	GAGE12I	Single nucleotide variant	not specified	GUncertain significance
Select item 3097939	NM_001477.1:c.133G>C	GAGE12I	Single nucleotide variant	not specified	GUncertain significance
Select item 3097938	NM_001477.1:c.129A>C	GAGE12I	Single nucleotide variant	not specified	GUncertain significance

ClinVar