ClinVar Miner

List of variants in gene LIG1 reported as benign for not provided

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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_000234.3(LIG1):c.2406T>C (p.Asp802=) rs20581 0.64373
NM_000234.3(LIG1):c.510C>A (p.Ala170=) rs20580 0.50510
NM_000234.3(LIG1):c.2442G>C (p.Ala814=) rs13436 0.48854
NM_000234.3(LIG1):c.1821+14A>T rs392891 0.47637
NM_000234.3(LIG1):c.370+20_370+27del rs3730867 0.46965
NM_000234.3(LIG1):c.17+12C>T rs3730849 0.29697
NM_000234.3(LIG1):c.-7C>T rs20579 0.17185
NM_000234.3(LIG1):c.2439+19G>A rs3729512 0.15533
NM_000234.3(LIG1):c.2286C>T (p.Ile762=) rs3731027 0.01682
NM_000234.3(LIG1):c.2232+10G>A rs3731011 0.01591
NM_000234.3(LIG1):c.2439+12C>T rs56271590 0.01562
NM_000234.3(LIG1):c.1226G>A (p.Arg409His) rs4987068 0.01247
NM_000234.3(LIG1):c.777-5C>T rs3730932 0.01239
NM_000234.3(LIG1):c.1841C>T (p.Thr614Ile) rs3731003 0.01236
NM_000234.3(LIG1):c.800A>G (p.Asn267Ser) rs3730933 0.01234
NM_000234.3(LIG1):c.2700A>G (p.Gln900=) rs1803907 0.01196
NM_000234.3(LIG1):c.2652G>A (p.Pro884=) rs35100567 0.00965
NM_000234.3(LIG1):c.1131C>T (p.Gly377=) rs4987069 0.00950
NM_000234.3(LIG1):c.1438A>G (p.Met480Val) rs3730980 0.00896
NM_000234.3(LIG1):c.507G>A (p.Val169=) rs77648519 0.00719
NM_000234.3(LIG1):c.2257G>A (p.Val753Met) rs146309259 0.00627
NM_000234.3(LIG1):c.370+7A>G rs3730866 0.00576
NM_000234.3(LIG1):c.1523+12G>A rs3730981 0.00520
NM_000234.3(LIG1):c.914+15C>A rs3730935 0.00473
NM_000234.3(LIG1):c.954C>T (p.Ser318=) rs41542416 0.00451
NM_000234.3(LIG1):c.71C>T (p.Ala24Val) rs3730855 0.00447
NM_000234.3(LIG1):c.2030G>T (p.Arg677Leu) rs3731008 0.00417
NM_000234.3(LIG1):c.1726-8C>T rs112820248 0.00340
NM_000234.3(LIG1):c.1045G>A (p.Val349Met) rs3730947 0.00271
NM_000234.3(LIG1):c.2205C>T (p.Ile735=) rs56191641 0.00239
NM_000234.3(LIG1):c.2187T>C (p.Val729=) rs116999747 0.00230
NM_000234.3(LIG1):c.1105G>A (p.Val369Ile) rs3730966 0.00195
NM_000234.3(LIG1):c.2584-10G>A rs182766545 0.00160
NM_000234.3(LIG1):c.2233-15C>T rs369067038 0.00140
NM_000234.3(LIG1):c.140C>T (p.Ser47Phe) rs41555118 0.00105
NM_000234.3(LIG1):c.681G>A (p.Thr227=) rs201868704 0.00089
NM_000234.3(LIG1):c.108-5T>C rs200668350 0.00056
NM_000234.3(LIG1):c.2343C>T (p.Ala781=) rs201469086 0.00036
NM_000234.3(LIG1):c.746G>A (p.Gly249Glu) rs3730911 0.00036
NM_000234.3(LIG1):c.1933-18C>T rs200847147 0.00027
NM_000234.3(LIG1):c.108-9A>G rs200174656 0.00011
NM_000234.3(LIG1):c.1818C>T (p.Pro606=) rs750492076 0.00009
NM_000234.3(LIG1):c.467-18C>T rs568854434 0.00008
NM_000234.3(LIG1):c.1866C>T (p.Ala622=) rs375967541 0.00005
NM_000234.3(LIG1):c.1290C>G (p.Leu430=) rs549831617 0.00001
NM_000234.3(LIG1):c.1821+17C>G rs201975345
NM_000234.3(LIG1):c.2232+16dup
NM_000234.3(LIG1):c.466+10dup rs762247170
NM_000234.3(LIG1):c.915-15del rs776431829

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