List of variants reported as likely benign for mesothelial neoplasm

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1161A>G (p.Ala387=)	rs141834493	0.00051
NM_024426.6(WT1):c.1264+19C>T	rs2234592	0.00010
NM_024426.6(WT1):c.849C>T (p.Thr283=)	rs145425799	0.00010
NM_024426.6(WT1):c.887+14G>A	rs757237600	0.00008
NM_024426.6(WT1):c.1016+15C>T	rs752756426	0.00004
NM_024426.6(WT1):c.1038C>T (p.Ser346=)	rs750018485	0.00003
NM_024426.6(WT1):c.115C>A (p.Arg39=)	rs763147828	0.00001
NM_024426.6(WT1):c.27G>A (p.Pro9=)	rs556835183	0.00001
NM_024426.6(WT1):c.945C>T (p.Asn315=)	rs775085343	0.00001
NM_024426.6(WT1):c.1448-10G>A	rs185744719
NM_024426.6(WT1):c.543C>T (p.Arg181=)	rs369870529
NM_024426.6(WT1):c.662-10G>T	rs1554945255
NM_024426.6(WT1):c.708G>A (p.Thr236=)	rs768828897
NM_024426.6(WT1):c.764T>A (p.Met255Lys)	rs377573993
NM_024426.6(WT1):c.780G>A (p.Ser260=)	rs1403311573

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