"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PIWIL4- - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 726439	NM_002033.4(FUT4):c.1548C>G (p.Asp516Glu)	FUT4, PIWIL4-AS1 (D516E)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 785377	NM_152431.3(PIWIL4):c.705T>A (p.Ile235=)	PIWIL4, PIWIL4-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 774699	NM_152431.3(PIWIL4):c.766A>C (p.Lys256Gln)	PIWIL4, PIWIL4-AS1 (K256Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 785378	NM_152431.3(PIWIL4):c.801C>T (p.Val267=)	PIWIL4, PIWIL4-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 728680	NM_152431.3(PIWIL4):c.806G>A (p.Arg269Gln)	PIWIL4, PIWIL4-AS1 (R269Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 775296	NM_152431.3(PIWIL4):c.1063A>G (p.Met355Val)	PIWIL4, PIWIL4-AS1 (M355V)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 730869	NM_152431.3(PIWIL4):c.1269-4A>G	PIWIL4, PIWIL4-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 790651	NM_152431.3(PIWIL4):c.1514G>T (p.Cys505Phe)	PIWIL4, PIWIL4-AS1 (C505F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 779311	NM_152431.3(PIWIL4):c.1762A>G (p.Met588Val)	PIWIL4, PIWIL4-AS1 (M588V)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar