ClinVar Miner

List of variants in gene DARS1 reported as likely benign for not provided

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001349.4(DARS1):c.504+34G>A rs111716305 0.00938
NM_001349.4(DARS1):c.67-149T>G rs115691888 0.00910
NC_000002.12:g.135985829T>C rs79018926 0.00825
NM_001349.4(DARS1):c.676+125del rs200100343 0.00822
NM_001349.4(DARS1):c.590G>A (p.Arg197His) rs141522501 0.00244
NM_001349.4(DARS1):c.1088G>A (p.Gly363Glu) rs2228660 0.00113
NM_001349.4(DARS1):c.1150-5T>G rs199776135 0.00075
NM_001349.4(DARS1):c.1391C>T (p.Pro464Leu) rs148806569 0.00058
NM_001349.4(DARS1):c.124+15G>T rs181377990 0.00028
NM_001349.4(DARS1):c.1149+7C>A rs373337130 0.00020
NM_001349.4(DARS1):c.1158A>G (p.Thr386=) rs373077996 0.00018
NM_001349.4(DARS1):c.753G>A (p.Gln251=) rs145963861 0.00009
NM_001349.4(DARS1):c.1230+17T>C rs369649828 0.00006
NM_001349.4(DARS1):c.125-18C>T rs777497235 0.00006
NM_001349.4(DARS1):c.366A>G (p.Lys122=) rs200029648 0.00004
NM_001349.4(DARS1):c.1104G>C (p.Leu368=) rs769215712 0.00001
NM_001349.4(DARS1):c.1125G>A (p.Leu375=) rs769425671 0.00001
NM_001349.4(DARS1):c.466C>T (p.Leu156=) rs571189613 0.00001
NM_001349.4(DARS1):c.570A>G (p.Ser190=) rs765566198 0.00001
NM_001349.4(DARS1):c.858T>C (p.Phe286=) rs369617769 0.00001
NC_000002.12:g.135985740G>T rs16832394
NM_001349.4(DARS1):c.1080C>T (p.Val360=)
NM_001349.4(DARS1):c.1083A>G (p.Glu361=) rs760769694
NM_001349.4(DARS1):c.1102C>T (p.Leu368=)
NM_001349.4(DARS1):c.1107-13G>A
NM_001349.4(DARS1):c.1119A>G (p.Glu373=)
NM_001349.4(DARS1):c.1149+15A>G
NM_001349.4(DARS1):c.1149+7C>G
NM_001349.4(DARS1):c.1191T>C (p.Ala397=)
NM_001349.4(DARS1):c.1230+13G>A
NM_001349.4(DARS1):c.1230+8A>G
NM_001349.4(DARS1):c.125-10G>A
NM_001349.4(DARS1):c.125-18C>G
NM_001349.4(DARS1):c.125-6T>C
NM_001349.4(DARS1):c.1342+12A>G
NM_001349.4(DARS1):c.1342+19T>C
NM_001349.4(DARS1):c.1342+9_1342+13del
NM_001349.4(DARS1):c.1343-7T>A
NM_001349.4(DARS1):c.1343-7T>C rs199507494
NM_001349.4(DARS1):c.1374C>G (p.Ser458=)
NM_001349.4(DARS1):c.1380C>T (p.Arg460=)
NM_001349.4(DARS1):c.1414+19T>G
NM_001349.4(DARS1):c.1415-11del
NM_001349.4(DARS1):c.159A>C (p.Ile53=)
NM_001349.4(DARS1):c.217+9G>C
NM_001349.4(DARS1):c.218-22_218-19del rs2104834109
NM_001349.4(DARS1):c.258T>C (p.Asn86=)
NM_001349.4(DARS1):c.276G>A (p.Ala92=)
NM_001349.4(DARS1):c.276G>C (p.Ala92=) rs746768443
NM_001349.4(DARS1):c.320+12A>G
NM_001349.4(DARS1):c.320+8A>G
NM_001349.4(DARS1):c.357T>C (p.Val119=)
NM_001349.4(DARS1):c.423+15A>C
NM_001349.4(DARS1):c.423+17T>C
NM_001349.4(DARS1):c.424-14T>C rs2104811058
NM_001349.4(DARS1):c.456G>T (p.Leu152=) rs1575391182
NM_001349.4(DARS1):c.484C>T (p.Pro162Ser) rs149170955
NM_001349.4(DARS1):c.504+17T>C
NM_001349.4(DARS1):c.505-15_505-14insC
NM_001349.4(DARS1):c.505-18_505-14del
NM_001349.4(DARS1):c.505-18_505-6del rs781360476
NM_001349.4(DARS1):c.505-4T>C
NM_001349.4(DARS1):c.505-4_505-3del rs34744196
NM_001349.4(DARS1):c.507A>G (p.Glu169=)
NM_001349.4(DARS1):c.564+16T>G
NM_001349.4(DARS1):c.565-13T>C
NM_001349.4(DARS1):c.565-6T>C
NM_001349.4(DARS1):c.603C>T (p.Gly201=)
NM_001349.4(DARS1):c.67-17A>G
NM_001349.4(DARS1):c.762G>A (p.Lys254=)
NM_001349.4(DARS1):c.84A>G (p.Arg28=)
NM_001349.4(DARS1):c.87T>C (p.Tyr29=)
NM_001349.4(DARS1):c.900C>T (p.His300=)
NM_001349.4(DARS1):c.959+17G>A rs1426607525
NM_001349.4(DARS1):c.960-15T>C
NM_001349.4(DARS1):c.987T>C (p.Asn329=)

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