List of variants in gene TARS2 reported as uncertain significance by Houlden Lab, UCL Institute of Neurology

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_025150.5(TARS2):c.773C>T (p.Ser258Leu)	rs145039072	0.00042
NM_025150.5(TARS2):c.1534G>A (p.Glu512Lys)
NM_025150.5(TARS2):c.1630C>T (p.Leu544Phe)
NM_025150.5(TARS2):c.470C>T (p.Thr157Ile)

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