"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "OR13C5" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 778947	NM_001004482.1(OR13C5):c.686G>C (p.Ser229Thr)	OR13C5 (S229T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768315	NM_001004482.1(OR13C5):c.256C>G (p.Leu86Val)	OR13C5 (L86V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768316	NM_001004482.1(OR13C5):c.246A>G (p.Leu82=)	OR13C5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 403269	NM_001004482.1(OR13C5):c.244C>T (p.Leu82=)	OR13C5	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 403270	NM_001004482.1(OR13C5):c.243G>C (p.Thr81=)	OR13C5	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 768317	NM_001004482.1(OR13C5):c.235C>T (p.Pro79Ser)	OR13C5 (P79S)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar