ClinVar Miner

List of variants in gene LIG3 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_013975.4(LIG3):c.2472A>G (p.Gln824=) rs3136022 0.02750
NM_013975.4(LIG3):c.2367C>T (p.Phe789=) rs114522796 0.00569
NM_013975.4(LIG3):c.2961G>A (p.Ala987=) rs76122405 0.00266
NM_013975.4(LIG3):c.2331+19G>A rs3136015 0.00186
NM_013975.4(LIG3):c.471C>A (p.Ile157=) rs61749869 0.00138
NM_013975.4(LIG3):c.67C>T (p.Leu23=) rs144307769 0.00111
NM_013975.4(LIG3):c.1041+11C>T rs116677517 0.00093
NM_013975.4(LIG3):c.2660C>T (p.Ser887Phe) rs35501315 0.00073
NM_013975.4(LIG3):c.670C>T (p.Arg224Trp) rs3744356 0.00062
NM_013975.4(LIG3):c.2701G>A (p.Ala901Thr) rs139474938 0.00039
NM_013975.4(LIG3):c.1383G>A (p.Val461=) rs3135988 0.00021
NM_013975.4(LIG3):c.1332G>A (p.Ser444=) rs111958156 0.00020
NM_013975.4(LIG3):c.722C>T (p.Ser241Leu) rs201814781 0.00019
NM_013975.4(LIG3):c.1835A>T (p.Glu612Val) rs201705066 0.00013
NM_013975.4(LIG3):c.2825G>A (p.Arg942Gln) rs200974999 0.00011
NM_013975.4(LIG3):c.2316C>T (p.Ile772=) rs775019742 0.00010
NM_013975.4(LIG3):c.1028G>A (p.Arg343Gln) rs370882864 0.00006
NM_013975.4(LIG3):c.452G>A (p.Arg151Gln) rs537076655 0.00006
NM_013975.4(LIG3):c.2796+20C>T rs778468086 0.00004
NM_013975.4(LIG3):c.1208+3G>T rs375260860 0.00003
NM_013975.4(LIG3):c.3008G>A (p.Arg1003Gln) rs140462567 0.00003
NM_013975.4(LIG3):c.446G>A (p.Arg149Gln) rs772050625 0.00002
NM_013975.4(LIG3):c.1193A>G (p.Gln398Arg) rs781367751 0.00001
NM_013975.4(LIG3):c.1440T>C (p.Pro480=) rs193922690 0.00001
NM_013975.4(LIG3):c.1555A>G (p.Asn519Asp) rs763624496 0.00001
NM_013975.4(LIG3):c.2211G>A (p.Thr737=) rs368207452 0.00001
NM_013975.4(LIG3):c.1073T>C (p.Phe358Ser)
NM_013975.4(LIG3):c.1166A>G (p.Lys389Arg)
NM_013975.4(LIG3):c.123A>G (p.Thr41=)
NM_013975.4(LIG3):c.1690A>C (p.Ile564Leu) rs1555556264
NM_013975.4(LIG3):c.1824-13C>T
NM_013975.4(LIG3):c.1857C>T (p.Asp619=)
NM_013975.4(LIG3):c.1859A>G (p.Asn620Ser)
NM_013975.4(LIG3):c.1990-17_1990-14del rs147265750
NM_013975.4(LIG3):c.2133C>T (p.Phe711=)
NM_013975.4(LIG3):c.2200G>C (p.Asp734His) rs1567693216
NM_013975.4(LIG3):c.2332-19G>C
NM_013975.4(LIG3):c.2712G>C (p.Val904=) rs372207276
NM_013975.4(LIG3):c.2727C>G (p.Ala909=)
NM_013975.4(LIG3):c.2860C>A (p.Arg954Ser)
NM_013975.4(LIG3):c.2931C>T (p.His977=)
NM_013975.4(LIG3):c.3023C>T (p.Pro1008Leu) rs1319167353
NM_013975.4(LIG3):c.382T>G (p.Ser128Ala) rs1021764612
NM_013975.4(LIG3):c.744T>A (p.Ser248Arg)
NM_013975.4(LIG3):c.74G>A (p.Arg25Gln)

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