List of variants in gene TARS2 reported 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
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_025150.5(TARS2):c.773C>T (p.Ser258Leu)	rs145039072	0.00040
NM_025150.5(TARS2):c.1534G>A (p.Glu512Lys)	rs776799586	0.00006
NM_025150.5(TARS2):c.968T>G (p.Phe323Cys)	rs760208518	0.00002
NM_025150.5(TARS2):c.1036C>T (p.Arg346Cys)	rs749476185	0.00001
NM_025150.5(TARS2):c.1255C>T (p.Arg419Trp)	rs778133443	0.00001
NM_025150.5(TARS2):c.1318G>A (p.Glu440Lys)	rs781477512	0.00001
NM_025150.5(TARS2):c.326G>A (p.Arg109Gln)	rs760526545	0.00001
NM_025150.5(TARS2):c.387+6T>C	rs1064797119	0.00001
NM_025150.5(TARS2):c.980G>A (p.Arg327Gln)	rs367984492	0.00001
NM_025150.5(TARS2):c.1026G>C (p.Glu342Asp)	rs371727967
NM_025150.5(TARS2):c.1630C>T (p.Leu544Phe)	rs2526361706
NM_025150.5(TARS2):c.2051G>A (p.Arg684Gln)	rs1322913410
NM_025150.5(TARS2):c.2140G>A (p.Ala714Thr)	rs1064797120
NM_025150.5(TARS2):c.388-1G>C	rs2102476204
NM_025150.5(TARS2):c.464C>T (p.Pro155Leu)	rs2526263331
NM_025150.5(TARS2):c.470C>T (p.Thr157Ile)	rs758088548
NM_025150.5(TARS2):c.774+5G>T	rs2526278171

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