List of variants in gene PRODH reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_016335.6(PRODH):c.578G>A (p.Gly193Asp)	rs199907923	0.00029
NM_016335.6(PRODH):c.1729C>T (p.Arg577Trp)	rs184218784	0.00020
NM_016335.6(PRODH):c.319A>G (p.Lys107Glu)	rs140129512	0.00014
NM_016335.6(PRODH):c.392G>A (p.Arg131Gln)	rs145456430	0.00007
NM_016335.6(PRODH):c.1093G>A (p.Val365Ile)	rs768237039	0.00006
NM_016335.6(PRODH):c.1295G>A (p.Arg432His)	rs143011525	0.00006
NM_016335.6(PRODH):c.1181C>T (p.Thr394Met)	rs777930066	0.00005
NM_016335.6(PRODH):c.391C>T (p.Arg131Trp)	rs753625227	0.00003
NM_016335.6(PRODH):c.1763G>A (p.Arg588Lys)	rs1239323884	0.00002
NM_016335.6(PRODH):c.1615+1G>C	rs745902339	0.00001
NM_016335.6(PRODH):c.1163C>T (p.Pro388Leu)	rs147233639
NM_016335.6(PRODH):c.130_156del (p.Thr44_Ala52del)	rs949036081
NM_016335.6(PRODH):c.1402G>A (p.Glu468Lys)	rs372618210
NM_016335.6(PRODH):c.1576C>T (p.Gln526Ter)	rs372187772
NM_016335.6(PRODH):c.1772G>A (p.Arg591Gln)	rs779412444
NM_016335.6(PRODH):c.268G>A (p.Glu90Lys)	rs1023813331
NM_016335.6(PRODH):c.803C>T (p.Ala268Val)	rs375358521

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