C0025500[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 6250	NM_003921.5(BCL10):c.499dup (p.Ser167fs)	BCL10 (S156fs +1 more)	Duplication (frameshift variant)	Mesothelioma +2 more	GPathogenic
Select item 6263	NM_003921.5(BCL10):c.136del (p.Ile46fs)	BCL10 (I46fs)	Deletion (frameshift variant)	Mesothelioma	GPathogenic
Select item 3499	NM_024426.6(WT1):c.1036A>G (p.Ser346Gly)	WT1 (S129G +7 more)	Single nucleotide variant (missense variant +2 more)	Mesothelioma	GPathogenic

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