List of variants reported as likely benign for Apert syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.2232C>T (p.Pro744=)	rs142639988	0.00035
NM_000141.5(FGFR2):c.1986+7C>T	rs199697707	0.00032
NM_000141.5(FGFR2):c.1761C>T (p.Ser587=)	rs147173572	0.00027
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=)	rs149008039	0.00026
NM_000141.5(FGFR2):c.64C>T (p.Arg22Trp)	rs377570596	0.00023
NM_000141.5(FGFR2):c.748+18C>T	rs377269009	0.00012
NM_000141.5(FGFR2):c.454+15G>A	rs200275522	0.00010
NM_000141.5(FGFR2):c.420G>A (p.Ala140=)	rs765024365	0.00006
NM_000141.5(FGFR2):c.1086G>A (p.Ala362=)	rs151250769	0.00003
NM_000141.5(FGFR2):c.1545C>T (p.Ala515=)	rs778789088	0.00003
NM_000141.5(FGFR2):c.1155C>G (p.Val385=)	rs531426519	0.00001
NM_000141.5(FGFR2):c.1335G>T (p.Val445=)	rs1460282965	0.00001
NM_000141.5(FGFR2):c.1356T>A (p.Ser452=)	rs2134060289
NM_000141.5(FGFR2):c.1746C>T (p.Pro582=)	rs369850306
NM_000141.5(FGFR2):c.1987-20A>T	rs772633227
NM_000141.5(FGFR2):c.390C>G (p.Ser130=)	rs1029635273

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