ClinVar Miner

List of variants in gene GARS1 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_002047.4(GARS1):c.124C>G (p.Pro42Ala) rs1049402 0.70073
NM_002047.4(GARS1):c.659-43C>A rs1558064 0.49314
NM_002047.4(GARS1):c.2095-6C>T rs2240401 0.48477
NM_002047.4(GARS1):c.1032-23A>T rs2527878 0.09645
NM_002047.4(GARS1):c.222+5C>T rs2072236 0.09556
NM_002047.4(GARS1):c.93G>C (p.Leu31=) rs2529438 0.09548
NM_002047.4(GARS1):c.2145A>G (p.Thr715=) rs4593 0.08113
NM_002047.4(GARS1):c.1613+9T>C rs75855065 0.04917
NM_002047.4(GARS1):c.1833T>C (p.Val611=) rs14270 0.04182
NM_002047.4(GARS1):c.1062T>C (p.Phe354=) rs11553502 0.04180
NM_002047.4(GARS1):c.1700-45T>C rs118002895 0.02313
NM_002047.4(GARS1):c.747T>C (p.Tyr249=) rs7808770 0.01578
NM_002047.4(GARS1):c.11C>T (p.Pro4Leu) rs62636572 0.01280
NM_002047.4(GARS1):c.2190G>A (p.Glu730=) rs190132116 0.00437
NM_002047.4(GARS1):c.803C>T (p.Thr268Ile) rs2230310 0.00357
NM_002047.4(GARS1):c.1031+14T>G rs189589556 0.00213
NM_002047.4(GARS1):c.1962C>T (p.Ile654=) rs201927627 0.00120
NM_002047.4(GARS1):c.699C>T (p.Val233=) rs187937286 0.00063
NM_002047.4(GARS1):c.1100A>G (p.Asn367Ser) rs192443850 0.00024
NM_002047.4(GARS1):c.408A>G (p.Gln136=) rs200279483 0.00021
NM_002047.4(GARS1):c.1904-28T>G rs375716806 0.00018
NM_002047.4(GARS1):c.816A>G (p.Leu272=) rs777128525 0.00005
NM_002047.4(GARS1):c.1737C>T (p.Phe579=) rs752464405 0.00004
NM_002047.4(GARS1):c.1581T>C (p.Ile527=) rs960876782 0.00002
NM_002047.4(GARS1):c.1234C>T (p.Arg412Cys) rs770924455 0.00001
NM_002047.4(GARS1):c.1031+1G>A rs1554338272
NM_002047.4(GARS1):c.1359+2dup
NM_002047.4(GARS1):c.1614-4G>A rs376324026
NM_002047.4(GARS1):c.2217A>G (p.Glu739=)
NM_002047.4(GARS1):c.428-6_432del
NM_002047.4(GARS1):c.47TGC[4] (p.Leu20del) rs150213018
NM_002047.4(GARS1):c.969T>G (p.Ala323=)

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