C3280492[trait identifier] AND "Genetics and Molecular Pathology, SA P - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1698777	NM_004656.4(BAP1):c.1480_1481del (p.Asp494fs)	BAP1 (D494fs)	Deletion (frameshift variant)	BAP1-related tumor predisposition syndrome	GPathogenic
Select item 1698872	NM_004656.4(BAP1):c.932-151G>A	BAP1	Single nucleotide variant (intron variant)	Uveal melanoma +1 more	GConflicting classifications of pathogenicity
Select item 1803172	NM_004656.4(BAP1):c.206del (p.Thr69fs)	BAP1 (T69fs)	Deletion (frameshift variant)	BAP1-related tumor predisposition syndrome	GPathogenic

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