List of variants reported as likely benign for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1; Lateral meningocele syndrome; Myofibromatosis, infantile, 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000435.3(NOTCH3):c.1487C>T (p.Pro496Leu)	rs11670799	0.01273
NM_000435.3(NOTCH3):c.1782C>T (p.Gly594=)	rs35793356	0.01231
NM_000435.3(NOTCH3):c.5854G>A (p.Val1952Met)	rs115582213	0.00841
NM_000435.3(NOTCH3):c.1490C>T (p.Ser497Leu)	rs114207045	0.00755
NM_000435.3(NOTCH3):c.2202C>T (p.Ala734=)	rs140040122	0.00306
NM_000435.3(NOTCH3):c.2411-4C>G	rs190177286	0.00295
NM_000435.3(NOTCH3):c.4552C>A (p.Leu1518Met)	rs141320511	0.00217
NM_000435.3(NOTCH3):c.2300G>A (p.Arg767His)	rs75291244	0.00213
NM_000435.3(NOTCH3):c.509A>G (p.His170Arg)	rs147373451	0.00184
NM_000435.3(NOTCH3):c.660C>T (p.Tyr220=)	rs114457076	0.00091
NM_000435.3(NOTCH3):c.3328-8C>A	rs200360207	0.00017
NM_000435.3(NOTCH3):c.3692G>A (p.Arg1231His)	rs778176344	0.00017
NM_000435.3(NOTCH3):c.135C>T (p.Asp45=)	rs370177269	0.00012
NM_000435.3(NOTCH3):c.4560G>T (p.Pro1520=)	rs370010007	0.00010
NM_000435.3(NOTCH3):c.4413C>T (p.Tyr1471=)	rs920286007	0.00005
NM_000435.3(NOTCH3):c.825G>A (p.Val275=)	rs138837495	0.00004
NM_000435.3(NOTCH3):c.4782G>C (p.Ser1594=)	rs748774860	0.00001
NM_000435.3(NOTCH3):c.4974C>T (p.Leu1658=)	rs749616364	0.00001
NM_000435.3(NOTCH3):c.2410+15dup	rs747731340

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