ClinVar Miner

List of variants in gene IARS1 reported as benign for not provided

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_002161.6(IARS1):c.3544A>G (p.Lys1182Glu) rs556155 0.13769
NM_002161.6(IARS1):c.540C>T (p.Pro180=) rs2230402 0.00766
NM_002161.6(IARS1):c.2051C>T (p.Thr684Met) rs2070053 0.00733
NM_002161.6(IARS1):c.950A>G (p.Glu317Gly) rs114279476 0.00690
NM_002161.6(IARS1):c.951A>C (p.Glu317Asp) rs115825549 0.00690
NM_002161.6(IARS1):c.1126A>G (p.Ser376Gly) rs73653050 0.00637
NM_002161.6(IARS1):c.3136G>A (p.Val1046Ile) rs34737051 0.00491
NM_002161.6(IARS1):c.2742G>C (p.Thr914=) rs75415996 0.00204
NM_002161.6(IARS1):c.2016+8C>T rs201446961 0.00183
NM_002161.6(IARS1):c.3727G>A (p.Val1243Met) rs144102700 0.00124
NM_002161.6(IARS1):c.429C>T (p.Asp143=) rs146666049 0.00099
NM_002161.6(IARS1):c.1317G>A (p.Leu439=) rs143120382 0.00091
NM_002161.6(IARS1):c.1290T>C (p.Asn430=) rs139382751 0.00085
NM_002161.6(IARS1):c.2823C>T (p.His941=) rs137864896 0.00036
NM_002161.6(IARS1):c.1170C>T (p.Ala390=) rs79939916 0.00025
NM_002161.6(IARS1):c.2389G>A (p.Asp797Asn) rs199830006 0.00011
NM_002161.6(IARS1):c.2792-3T>C rs748953202 0.00003
NM_002161.6(IARS1):c.1358G>A (p.Arg453His) rs570962385 0.00001
NM_002161.6(IARS1):c.2035C>A (p.Leu679Ile) rs569119560 0.00001
NM_002161.6(IARS1):c.10C>A (p.Gln4Lys)
NM_002161.6(IARS1):c.119+15T>C
NM_002161.6(IARS1):c.1305-7A>G
NM_002161.6(IARS1):c.1569G>C (p.Val523=)
NM_002161.6(IARS1):c.1701-4dup
NM_002161.6(IARS1):c.1788-6dup
NM_002161.6(IARS1):c.1871+19C>T
NM_002161.6(IARS1):c.2138-14T>G
NM_002161.6(IARS1):c.2664T>C (p.Tyr888=)
NM_002161.6(IARS1):c.2791+19_2791+20del
NM_002161.6(IARS1):c.2961T>G (p.Ala987=)
NM_002161.6(IARS1):c.3001-17dup
NM_002161.6(IARS1):c.3177+15C>G
NM_002161.6(IARS1):c.3612A>G (p.Gly1204=)
NM_002161.6(IARS1):c.396+19A>G
NM_002161.6(IARS1):c.407G>A (p.Ser136Asn)
NM_002161.6(IARS1):c.576C>T (p.Phe192=)
NM_002161.6(IARS1):c.833+12A>G
NM_002161.6(IARS1):c.894+15C>T
NM_002161.6(IARS1):c.950_951delinsGC (p.Glu317Gly)

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