List of variants reported as uncertain significance for fumaric aciduria by Fulgent Genetics, Fulgent Genetics

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_000143.4(FH):c.1303G>A (p.Val435Met)	rs147528200	0.00021
NM_000143.4(FH):c.217G>A (p.Val73Met)	rs201878591	0.00010
NM_000143.4(FH):c.556-4A>G	rs370229813	0.00004
NM_000143.4(FH):c.580G>A (p.Ala194Thr)	rs587782215	0.00004
NM_000143.4(FH):c.917T>C (p.Val306Ala)	rs147991516	0.00004
NM_000143.4(FH):c.616G>A (p.Val206Ile)	rs763183520	0.00003
NM_000143.4(FH):c.1049G>A (p.Arg350Gln)	rs749316923	0.00002
NM_000143.4(FH):c.352A>G (p.Asn118Asp)	rs200738857	0.00002
NM_000143.4(FH):c.926C>T (p.Pro309Leu)	rs756528378	0.00002
NM_000143.4(FH):c.1259C>T (p.Ala420Val)	rs766377516	0.00001
NM_000143.4(FH):c.193G>A (p.Asp65Asn)	rs769956664	0.00001
NM_000143.4(FH):c.292A>G (p.Ile98Val)	rs1660147766	0.00001
NM_000143.4(FH):c.776T>C (p.Met259Thr)	rs1407485828	0.00001
NM_000143.4(FH):c.133G>T (p.Ala45Ser)	rs1260007300
NM_000143.4(FH):c.1508C>G (p.Pro503Arg)	rs1659661748
NM_000143.4(FH):c.194A>T (p.Asp65Val)	rs145116688
NM_000143.4(FH):c.251T>C (p.Val84Ala)	rs878853692
NM_000143.4(FH):c.254C>G (p.Thr85Arg)	rs1324632356
NM_000143.4(FH):c.354T>G (p.Asn118Lys)	rs1465574376
NM_000143.4(FH):c.378+11A>G
NM_000143.4(FH):c.37C>G (p.Pro13Ala)	rs587778360
NM_000143.4(FH):c.382G>A (p.Ala128Thr)	rs1553341620
NM_000143.4(FH):c.47G>A (p.Arg16Gln)
NM_000143.4(FH):c.526C>T (p.His176Tyr)
NM_000143.4(FH):c.578C>T (p.Thr193Ile)	rs1573883332
NM_000143.4(FH):c.593C>G (p.Ala198Gly)	rs1414507017
NM_000143.4(FH):c.648T>G (p.Asp216Glu)	rs199536615
NM_000143.4(FH):c.707C>T (p.Thr236Ile)	rs773382103
NM_000143.4(FH):c.800C>G (p.Pro267Arg)
NM_000143.4(FH):c.907T>G (p.Leu303Val)	rs1057523697
NM_000143.4(FH):c.958G>T (p.Ala320Ser)	rs766441385

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