List of variants in gene combination LOC130067862, TYMP reported as uncertain significance for mitochondrial DNA depletion syndrome

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.931G>A (p.Gly311Ser)	rs121913040	0.00004
NM_001953.5(TYMP):c.929-1G>A	rs1180285291	0.00001
NM_001953.5(TYMP):c.930G>A (p.Gly310=)	rs773100466	0.00001
NM_001953.5(TYMP):c.952G>C (p.Gly318Arg)	rs1412132331

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