ClinVar Miner

List of variants in gene TOP1MT reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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_052963.3(TOP1MT):c.332G>A (p.Arg111Gln)	rs147714048	0.00064
NM_052963.3(TOP1MT):c.880C>T (p.Arg294Cys)	rs144092447	0.00006

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