"PreventionGenetics, part of Exact Sciences"[submitter] AND "TARS2"[ge - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 380568	NM_025150.5(TARS2):c.81C>T (p.Thr27=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder +2 more	GBenign
Select item 3040414	NM_025150.5(TARS2):c.264-9C>T	TARS2	Single nucleotide variant (intron variant)	TARS2-related disorder	GLikely benign
Select item 389371	NM_025150.5(TARS2):c.366C>T (p.Phe122=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder +2 more	GLikely benign
Select item 2066981	NM_025150.5(TARS2):c.696-5C>T	MIR6878, TARS2	Single nucleotide variant (non-coding transcript variant +1 more)	TARS2-related disorder +1 more	GLikely benign
Select item 381177	NM_025150.5(TARS2):c.1076C>T (p.Thr359Met)	TARS2 (T359M +2 more)	Single nucleotide variant (missense variant +1 more)	TARS2-related disorder +2 more	GBenign
Select item 516719	NM_025150.5(TARS2):c.1160C>T (p.Pro387Leu)	TARS2 (P387L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 3051461	NM_025150.5(TARS2):c.1176C>T (p.Asp392=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder	GLikely benign
Select item 380197	NM_025150.5(TARS2):c.1197A>G (p.Thr399=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder +2 more	GBenign
Select item 3040077	NM_025150.5(TARS2):c.1206C>T (p.Leu402=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder	GLikely benign
Select item 380558	NM_025150.5(TARS2):c.1317C>T (p.Ala439=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder +2 more	GBenign
Select item 513487	NM_025150.5(TARS2):c.1353G>A (p.Leu451=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GLikely benign
Select item 3055229	NM_025150.5(TARS2):c.1470C>T (p.Phe490=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related disorder	GLikely benign
Select item 3046733	NM_025150.5(TARS2):c.1617+5G>A	TARS2	Single nucleotide variant (intron variant)	TARS2-related disorder	GLikely benign