List of variants reported as likely benign for Tuberous sclerosis 2 by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.1362-32C>G	rs45517166	0.00391
NM_000548.5(TSC2):c.3420C>T (p.Gly1140=)	rs373968155	0.00020
NM_000548.5(TSC2):c.5289C>T (p.Pro1763=)	rs144965811	0.00015
NM_000548.5(TSC2):c.1946+20C>T	rs372149311	0.00011
NM_000548.5(TSC2):c.3468A>G (p.Pro1156=)	rs147242130	0.00010
NM_000548.5(TSC2):c.3815-16C>T	rs546810161	0.00008
NM_000548.5(TSC2):c.363C>T (p.Ala121=)	rs45517106	0.00006
NM_000548.5(TSC2):c.1361+20C>G	rs538626543	0.00005
NM_000548.5(TSC2):c.3225C>T (p.Thr1075=)	rs374145104	0.00004
NM_000548.5(TSC2):c.1600-10C>T	rs768188836	0.00003
NM_000548.5(TSC2):c.672C>T (p.Ala224=)	rs138897064	0.00003
NM_000548.5(TSC2):c.2484G>A (p.Val828=)	rs780395534	0.00002
NM_000548.5(TSC2):c.2607C>T (p.Phe869=)	rs750336814	0.00002
NM_000548.5(TSC2):c.411C>T (p.His137=)	rs776129896	0.00002
NM_000548.5(TSC2):c.1854G>C (p.Leu618=)	rs1060504088	0.00001
NM_000548.5(TSC2):c.2128C>T (p.Leu710=)	rs1225700612	0.00001
NM_000548.5(TSC2):c.2748G>A (p.Leu916=)	rs757674443	0.00001
NM_000548.5(TSC2):c.3699C>T (p.Asn1233=)	rs773240506	0.00001
NM_000548.5(TSC2):c.3814+15G>A	rs201225719	0.00001
NM_000548.5(TSC2):c.481+9C>T	rs201026150	0.00001
NM_000548.5(TSC2):c.5043C>T (p.Asn1681=)	rs45476793	0.00001
NM_000548.5(TSC2):c.5061C>T (p.Cys1687=)	rs779923426	0.00001
NM_000548.5(TSC2):c.704G>A (p.Ser235Asn)	rs397514957	0.00001
NM_000548.5(TSC2):c.711G>A (p.Pro237=)	rs189380607	0.00001
NM_000548.5(TSC2):c.2763C>T (p.Leu921=)	rs771817176
NM_000548.5(TSC2):c.3102C>G (p.Val1034=)	rs562998574
NM_000548.5(TSC2):c.3126G>A (p.Pro1042=)	rs36078782

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