List of variants reported as uncertain significance for Developmental and epileptic encephalopathy, 50 by Baylor Genetics

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004341.5(CAD):c.5392C>A (p.Gln1798Lys)	rs138840581	0.00064
NM_004341.5(CAD):c.461A>G (p.Asn154Ser)	rs147694325	0.00027
NM_004341.5(CAD):c.1118G>A (p.Arg373Gln)	rs779009526	0.00012
NM_004341.5(CAD):c.5488A>G (p.Met1830Val)	rs747817554	0.00006
NM_004341.5(CAD):c.4208G>A (p.Arg1403Gln)	rs368332006	0.00005
NM_004341.5(CAD):c.1352A>G (p.Tyr451Cys)	rs770953907	0.00001
NM_004341.5(CAD):c.208T>C (p.Phe70Leu)	rs1674954573	0.00001
NM_004341.5(CAD):c.4315-3C>T	rs867496821	0.00001
NM_004341.5(CAD):c.4564-9C>G	rs575379595	0.00001
NM_004341.5(CAD):c.4655C>T (p.Ala1552Val)	rs1041556030	0.00001
NM_004341.5(CAD):c.625C>G (p.Leu209Val)	rs374182358	0.00001
NM_004341.5(CAD):c.859C>T (p.Arg287Cys)	rs753478495	0.00001
NM_004341.5(CAD):c.1100G>A (p.Gly367Asp)	rs766915720
NM_004341.5(CAD):c.223-2A>G	rs1675149924
NM_004341.5(CAD):c.2401-5A>G	rs759687469
NM_004341.5(CAD):c.4669C>G (p.Leu1557Val)	rs199990394
NM_004341.5(CAD):c.6329G>T (p.Arg2110Leu)	rs759380014

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