List of variants in gene PRODH reported as likely benign 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_016335.6(PRODH):c.1278C>T (p.Asp426=)	rs16983466	0.20443
NM_016335.6(PRODH):c.517+19C>T	rs370155847	0.00088
NM_016335.6(PRODH):c.822C>T (p.Asp274=)	rs146178333	0.00059
NM_016335.6(PRODH):c.1170C>T (p.Ile390=)	rs552700874	0.00039
NM_016335.6(PRODH):c.1104+16C>T	rs182795102	0.00037
NM_016335.6(PRODH):c.1465G>A (p.Ala489Thr)	rs370003523	0.00036
NM_016335.6(PRODH):c.1401C>T (p.Tyr467=)	rs200018716	0.00028
NM_016335.6(PRODH):c.606C>T (p.Tyr202=)	rs149344100	0.00023
NM_016335.6(PRODH):c.780A>G (p.Gln260=)	rs202042437	0.00022
NM_016335.6(PRODH):c.1143C>T (p.Ala381=)	rs560442727	0.00017
NM_016335.6(PRODH):c.873C>T (p.Ile291=)	rs146652616	0.00014
NM_016335.6(PRODH):c.174G>T (p.Ala58=)	rs931875471	0.00009
NM_016335.6(PRODH):c.518-11C>T	rs112526442	0.00004
NM_016335.6(PRODH):c.270G>A (p.Glu90=)	rs562699700
NM_016335.6(PRODH):c.54C>T (p.Val18=)	rs1032634465
NM_016335.6(PRODH):c.87G>A (p.Gln29=)	rs1417739533
NM_016335.6(PRODH):c.90C>T (p.Pro30=)	rs2146224247
NM_016335.6(PRODH):c.930-15C>T	rs201272622

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