ClinVar Miner

List of variants in gene DLAT reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001931.5(DLAT):c.572C>T (p.Ala191Val)	rs200500508	0.00016
NM_001931.5(DLAT):c.1202C>T (p.Pro401Leu)	rs781794850	0.00001

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