List of variants reported as uncertain significance for Apert syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.2426T>C (p.Leu809Pro)	rs368003279	0.00011
NM_000141.5(FGFR2):c.289G>A (p.Ala97Thr)	rs372430349	0.00011
NM_000141.5(FGFR2):c.989G>A (p.Arg330Gln)	rs199757302	0.00011
NM_000141.5(FGFR2):c.182G>A (p.Arg61His)	rs199575491	0.00007
NM_000141.5(FGFR2):c.16C>T (p.Arg6Cys)	rs141724446	0.00005
NM_000141.5(FGFR2):c.362T>C (p.Met121Thr)	rs748322657	0.00003
NM_000141.5(FGFR2):c.772C>T (p.Leu258Phe)	rs747171741	0.00003
NM_000141.5(FGFR2):c.1085C>T (p.Ala362Val)	rs757846343	0.00002
NM_000141.5(FGFR2):c.1238C>T (p.Pro413Leu)	rs372348666	0.00002
NM_000141.5(FGFR2):c.1328C>T (p.Pro443Leu)	rs757125418	0.00002
NM_000141.5(FGFR2):c.1348C>T (p.Arg450Cys)	rs536181987	0.00002
NM_000141.5(FGFR2):c.1561+6C>T	rs781352732	0.00002
NM_000141.5(FGFR2):c.*1369C>T	rs886046759	0.00001
NM_000141.5(FGFR2):c.1240G>A (p.Ala414Thr)	rs769880096	0.00001
NM_000141.5(FGFR2):c.138A>C (p.Gln46His)	rs748117555	0.00001
NM_000141.5(FGFR2):c.1985A>G (p.Asn662Ser)	rs962103382	0.00001
NM_000141.5(FGFR2):c.2077A>G (p.Met693Val)	rs774682374	0.00001
NM_000141.5(FGFR2):c.788C>T (p.Pro263Leu)	rs779326224	0.00001
NM_000141.5(FGFR2):c.910G>A (p.Asp304Asn)	rs370877537	0.00001
NM_000141.5(FGFR2):c.-17G>C	rs766629665
NM_000141.5(FGFR2):c.1562-9_1562-7delinsAA	rs2133978031
NM_000141.5(FGFR2):c.1735C>T (p.Arg579Trp)	rs1564875549
NM_000141.5(FGFR2):c.2444_2445del (p.Ile815fs)	rs771208561
NM_000141.5(FGFR2):c.287G>A (p.Gly96Asp)	rs1277734487
NM_000141.5(FGFR2):c.781G>A (p.Gly261Arg)	rs2134317947
NM_000141.5(FGFR2):c.877C>T (p.His293Tyr)	rs748526473

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