List of variants in gene TARS2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_025150.5(TARS2):c.1034A>G (p.His345Arg)	rs115390773	0.00560
NM_025150.5(TARS2):c.1251C>T (p.Ala417=)	rs41264465	0.00537
NM_025150.5(TARS2):c.1160C>T (p.Pro387Leu)	rs141179905	0.00202
NM_025150.5(TARS2):c.562C>A (p.Leu188Ile)	rs140418026	0.00153
NM_025150.5(TARS2):c.1812G>C (p.Gly604=)	rs144477069	0.00018
NM_025150.5(TARS2):c.900G>C (p.Arg300=)	rs775382225	0.00004
NM_025150.5(TARS2):c.1821-5A>G

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