"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "HUS1B"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 768058	NM_148959.4(HUS1B):c.529A>G (p.Ser177Gly)	EXOC2, HUS1B (S177G)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 792029	NM_148959.4(HUS1B):c.406G>T (p.Val136Leu)	EXOC2, HUS1B (V136L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 732647	NM_148959.4(HUS1B):c.264C>T (p.Ser88=)	EXOC2, HUS1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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