"GeneDx"[submitter] AND "ERAL1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1294695	NM_005702.4(ERAL1):c.284-178G>A	ERAL1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231247	NM_005702.4(ERAL1):c.284-127C>G	ERAL1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182082	NM_005702.4(ERAL1):c.411+53G>A	ERAL1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288338	NM_005702.4(ERAL1):c.489+147del	ERAL1	Deletion (intron variant)	not provided	GBenign
Select item 1255389	NM_005702.4(ERAL1):c.945C>T (p.Asp315=)	ERAL1, LOC126862526	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1275659	NM_005702.4(ERAL1):c.1191+177T>C	ERAL1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256947	NM_005702.4(ERAL1):c.*65G>T	ERAL1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1267992	NM_005702.4(ERAL1):c.*218C>T	ERAL1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

ClinVar