ClinVar Miner

List of variants in gene GARS1 reported as benign for not provided

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_002047.4(GARS1):c.570-151C>A rs2709809 0.81338
NM_002047.4(GARS1):c.1031+77G>A rs1986756 0.78867
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.1613+159G>A rs10249885 0.48563
NM_002047.2(GARS1):c.-534T>C rs2270025 0.48489
NM_002047.4(GARS1):c.2095-6C>T rs2240401 0.48477
NM_002047.4(GARS1):c.1359+299A>G rs6970807 0.48094
NC_000007.14:g.30634164A>G rs2214837 0.48022
NM_002047.4(GARS1):c.1360-71A>C rs10951271 0.36177
NM_002047.4(GARS1):c.428-320G>T rs2709806 0.19520
NM_002047.4(GARS1):c.569+173T>C rs10280491 0.12486
NM_002047.4(GARS1):c.1195-80G>A rs78284531 0.11572
NM_002047.4(GARS1):c.223-120G>A rs77213416 0.09798
NM_002047.4(GARS1):c.1699+285G>A rs77121610 0.09754
NM_002047.4(GARS1):c.1032-23A>T rs2527878 0.09645
NM_002047.4(GARS1):c.1468-285T>C rs2527880 0.09612
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.324+259T>G rs722423 0.08267
NM_002047.4(GARS1):c.2145A>G (p.Thr715=) rs4593 0.08113
NM_002047.4(GARS1):c.427+176C>G rs2074779 0.06711
NM_002047.4(GARS1):c.1031+229C>T rs10229836 0.05002
NM_002047.4(GARS1):c.1613+96C>T rs17159291 0.04921
NM_002047.4(GARS1):c.1467+330A>C rs17159289 0.04918
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.223-304G>A rs113551895 0.04104
NM_002047.4(GARS1):c.1032-149A>T rs17159280 0.03786
NM_002047.2(GARS1):c.-217A>G rs2970504 0.02929
NM_002047.4(GARS1):c.428-139G>A rs2952804 0.02919
NM_002047.4(GARS1):c.1614-271A>G rs118095447 0.02712
NM_002047.4(GARS1):c.1700-45T>C rs118002895 0.02313
NM_002047.4(GARS1):c.881+290T>C rs140249264 0.01756
NM_002047.4(GARS1):c.2094+277G>A rs183763845 0.01755
NM_002047.4(GARS1):c.2094+276_2094+277insC rs151154671 0.01754
NM_002047.4(GARS1):c.1194+212C>G rs79036537 0.01732
NM_002047.2(GARS1):c.-317G>A rs116125961 0.01714
NM_002047.4(GARS1):c.2094+129G>A rs79295938 0.01693
NM_002047.4(GARS1):c.1360-335T>C rs113343841 0.01602
NM_002047.4(GARS1):c.747T>C (p.Tyr249=) rs7808770 0.01578
NM_002047.4(GARS1):c.1761G>A (p.Thr587=) rs3886641 0.01523
NM_002047.4(GARS1):c.11C>T (p.Pro4Leu) rs62636572 0.01280
NM_002047.4(GARS1):c.1163G>A (p.Arg388Gln) rs17159287 0.00833
NM_002047.2(GARS1):c.-177T>C rs78980639 0.00437
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.2212G>A (p.Glu738Lys) rs181251337 0.00006
NM_002047.4(GARS1):c.144C>T (p.Ala48=) rs754360926 0.00003
NM_002047.2(GARS1):c.-418T>A rs115725201
NM_002047.4(GARS1):c.*49_*51del
NM_002047.4(GARS1):c.*50_*51del rs70983380
NM_002047.4(GARS1):c.*51del rs70983380
NM_002047.4(GARS1):c.1360-339_1360-336del rs199878197
NM_002047.4(GARS1):c.1613+199del rs74274581
NM_002047.4(GARS1):c.1614-4G>A rs376324026
NM_002047.4(GARS1):c.428-171del rs144012888
NM_002047.4(GARS1):c.570-68_570-64del rs141443294

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