"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 240055	NM_004656.4(BAP1):c.2057-4G>T	BAP1	Single nucleotide variant (intron variant)	BAP1-related tumor predisposition syndrome +4 more	GConflicting classifications of pathogenicity
Select item 240050	NM_004656.4(BAP1):c.1729+8T>C	BAP1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 346118	NM_004656.4(BAP1):c.1413T>G (p.Ala471=)	BAP1	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign
Select item 240047	NM_004656.4(BAP1):c.1407C>T (p.Ser469=)	BAP1	Single nucleotide variant (synonymous variant)	not provided +3 more	GLikely benign
Select item 220780	NM_004656.4(BAP1):c.1026C>T (p.Ser342=)	BAP1	Single nucleotide variant (synonymous variant)	BAP1-related tumor predisposition syndrome +5 more	GBenign/Likely benign
Select item 220641	NM_004656.4(BAP1):c.1002A>G (p.Leu334=)	BAP1	Single nucleotide variant (synonymous variant)	BAP1-related tumor predisposition syndrome +4 more	GBenign/Likely benign
Select item 240070	NM_004656.4(BAP1):c.960C>T (p.Cys320=)	BAP1	Single nucleotide variant (synonymous variant)	Melanoma, uveal, susceptibility to, 2 +3 more	GBenign/Likely benign

ClinVar