"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "SP1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 735857	NM_138473.3(SP1):c.8-10A>G	SP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 710019	NM_138473.3(SP1):c.243C>G (p.Ser81=)	LOC130007983, SP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 745328	NM_138473.3(SP1):c.957C>G (p.Ser319=)	SP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 715649	NM_138473.3(SP1):c.1587C>A (p.Leu529=)	SP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 748746	NM_138473.3(SP1):c.1851G>A (p.Ser617=)	SP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 716435	NM_138473.3(SP1):c.2304C>T (p.Asn768=)	SP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710359	NM_138473.3(SP1):c.2355C>T (p.Phe785=)	SP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar