List of variants in gene QARS1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_005051.3(QARS1):c.1570C>T (p.Arg524Trp)	rs774980346	0.00002
NM_005051.3(QARS1):c.1132C>T (p.Arg378Cys)	rs185476065	0.00001
NM_005051.3(QARS1):c.1164+1G>C	rs1262558494	0.00001
NM_005051.3(QARS1):c.1385C>T (p.Ala462Val)	rs373289986	0.00001
NM_005051.3(QARS1):c.1451del (p.Tyr484fs)	rs1064795119	0.00001
NM_005051.3(QARS1):c.1543C>T (p.Arg515Trp)	rs587777334	0.00001
NM_005051.3(QARS1):c.487A>G (p.Lys163Glu)	rs1398173228	0.00001
NM_005051.3(QARS1):c.1058G>T (p.Gly353Val)	rs752600100
NM_005051.3(QARS1):c.1314C>G (p.Tyr438Ter)	rs1294643628
NM_005051.3(QARS1):c.1430A>G (p.Tyr477Cys)	rs1172486173
NM_005051.3(QARS1):c.169T>C (p.Tyr57His)	rs587777333
NM_005051.3(QARS1):c.1700G>A (p.Arg567Gln)	rs1468382416
NM_005051.3(QARS1):c.322G>T (p.Glu108Ter)
NM_005051.3(QARS1):c.533G>T (p.Gly178Val)	rs2107109028
NM_005051.3(QARS1):c.793C>T (p.Arg265Cys)	rs1559968699

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