"Phenosystems SA"[submitter] AND "HNRNPUL2-BSCL2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128533	NM_001122955.4(BSCL2):c.1137A>G (p.Glu379=)	BSCL2, HNRNPUL2-BSCL2 (K268R)	Single nucleotide variant (non-coding transcript variant +2 more)	Hereditary spastic paraplegia +8 more	GBenign
Select item 1320031	NC_000011.10:g.62707486C>T	GNG3, HNRNPUL2-BSCL2 +1 more	Single nucleotide variant (intron variant)	Breast carcinoma +2 more	GPathogenic