"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "NT5C1B- - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 731342	NM_033253.4(NT5C1B):c.330G>A (p.Pro110=)	NT5C1B, NT5C1B-RDH14	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 770125	NM_033253.4(NT5C1B):c.312T>C (p.His104=)	NT5C1B, NT5C1B-RDH14	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 726715	NM_033253.4(NT5C1B):c.157C>T (p.Arg53Ter)	NT5C1B, NT5C1B-RDH14 (R130* +3 more)	Single nucleotide variant (nonsense)	not provided	GBenign
Select item 712926	NM_033253.4(NT5C1B):c.140T>C (p.Leu47Pro)	NT5C1B, NT5C1B-RDH14 (L90P +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 725561	NM_033253.4(NT5C1B):c.120+359G>A	NT5C1B, NT5C1B-RDH14	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 710542	NM_033253.4(NT5C1B):c.120+348C>G	NT5C1B, NT5C1B-RDH14 (P47A)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

ClinVar