List of variants in gene DLAT reported as uncertain significance by GeneDx

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001931.5(DLAT):c.946C>T (p.Pro316Ser)	rs149088081	0.00021
NM_001931.5(DLAT):c.109C>G (p.Arg37Gly)	rs183829292	0.00019
NM_001931.5(DLAT):c.572C>T (p.Ala191Val)	rs200500508	0.00016
NM_001931.5(DLAT):c.1406A>G (p.Glu469Gly)	rs376141049	0.00014
NM_001931.5(DLAT):c.1382G>A (p.Arg461Gln)	rs782807951	0.00003
NM_001931.5(DLAT):c.757G>T (p.Ala253Ser)	rs746422062	0.00003
NM_001931.5(DLAT):c.1152C>G (p.Ile384Met)	rs147992445	0.00001
NM_001931.5(DLAT):c.280G>C (p.Val94Leu)	rs781796716	0.00001
NM_001931.5(DLAT):c.410T>G (p.Phe137Cys)	rs138505899	0.00001
NM_001931.5(DLAT):c.478G>A (p.Gly160Arg)	rs782189104	0.00001
NM_001931.5(DLAT):c.998C>G (p.Pro333Arg)	rs782453793	0.00001
NM_001931.5(DLAT):c.1130-6T>G	rs1863147548
NM_001931.5(DLAT):c.1144G>A (p.Gly382Ser)	rs782264757
NM_001931.5(DLAT):c.1225G>C (p.Gly409Arg)
NM_001931.5(DLAT):c.367G>T (p.Asp123Tyr)	rs1555179247
NM_001931.5(DLAT):c.428G>T (p.Cys143Phe)	rs2498425313
NM_001931.5(DLAT):c.458G>A (p.Gly153Asp)	rs2137698269
NM_001931.5(DLAT):c.524C>G (p.Ala175Gly)	rs201046000
NM_001931.5(DLAT):c.79G>A (p.Glu27Lys)
NM_001931.5(DLAT):c.83T>C (p.Val28Ala)	rs1316678815
NM_001931.5(DLAT):c.878T>C (p.Ile293Thr)
NM_001931.5(DLAT):c.953_954inv (p.Val318Ala)
NM_001931.5(DLAT):c.977T>C (p.Val326Ala)	rs1555180793
NM_001931.5(DLAT):c.982G>A (p.Ala328Thr)	rs1862931114

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