"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "UBE2F-S - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 785025	NM_016510.7(SCLY):c.258A>G (p.Ile86Met)	SCLY, UBE2F-SCLY (I86M)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 785026	NM_016510.7(SCLY):c.612+7C>T	SCLY, UBE2F-SCLY	Single nucleotide variant	not provided	GBenign
Select item 775836	NM_016510.7(SCLY):c.827T>C (p.Phe276Ser)	SCLY, UBE2F-SCLY (F276S)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 785027	NM_016510.7(SCLY):c.976G>A (p.Val326Ile)	SCLY, UBE2F-SCLY (V326I)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 716841	NM_016510.7(SCLY):c.1161G>C (p.Ala387=)	SCLY, UBE2F-SCLY	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 782740	NM_016510.7(SCLY):c.1233G>A (p.Arg411=)	LOC112840914, SCLY +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 788481	NM_016510.7(SCLY):c.1275C>T (p.Ala425=)	LOC112840914, SCLY +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

ClinVar