ClinVar Miner

List of variants in gene FANCL studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Total variants: 46
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HGVS dbSNP
FANCL, 3-BP DEL, 1007TAT
FANCL, 4-BP DUP, 1095AATT
NM_018062.3(FANCL):c.-13C>T rs757714548
NM_018062.3(FANCL):c.-39A>C rs41281511
NM_018062.3(FANCL):c.-39A>G rs41281511
NM_018062.3(FANCL):c.-40C>A rs199661008
NM_018062.3(FANCL):c.-44C>T rs780348127
NM_018062.3(FANCL):c.108C>G (p.Phe36Leu) rs149726602
NM_018062.3(FANCL):c.112C>T (p.Leu38Phe) rs55849827
NM_018062.3(FANCL):c.134A>T (p.Asp45Val)
NM_018062.3(FANCL):c.142C>G (p.Leu48Val) rs148516173
NM_018062.3(FANCL):c.147_148delinsTT (p.Lys49_Asn50delinsAsnTyr) rs1558825558
NM_018062.3(FANCL):c.155+7T>C rs200849840
NM_018062.3(FANCL):c.156-8A>C rs878855045
NM_018062.3(FANCL):c.182C>G (p.Thr61Arg) rs1315405264
NM_018062.3(FANCL):c.203G>C (p.Arg68Pro) rs143819820
NM_018062.3(FANCL):c.211C>T (p.Gln71Ter) rs753105795
NM_018062.3(FANCL):c.216+1G>T rs1205006300
NM_018062.3(FANCL):c.217-11T>C rs79588315
NM_018062.3(FANCL):c.238C>G (p.Leu80Val) rs563513081
NM_018062.3(FANCL):c.246C>G (p.Ser82Arg)
NM_018062.3(FANCL):c.268del (p.Leu90fs) rs869320684
NM_018062.3(FANCL):c.273+1G>A
NM_018062.3(FANCL):c.273+7A>C rs745366278
NM_018062.3(FANCL):c.288G>T (p.Lys96Asn) rs770368316
NM_018062.3(FANCL):c.2T>C (p.Met1Thr)
NM_018062.3(FANCL):c.319C>G (p.Pro107Ala) rs754028115
NM_018062.3(FANCL):c.332A>G (p.Tyr111Cys) rs757683704
NM_018062.3(FANCL):c.335C>T (p.Ser112Leu)
NM_018062.3(FANCL):c.343A>G (p.Ile115Val) rs149414332
NM_018062.3(FANCL):c.344T>C (p.Ile115Thr) rs1060501895
NM_018062.3(FANCL):c.355G>A (p.Gly119Arg)
NM_018062.3(FANCL):c.387G>A (p.Ala129=) rs141400460
NM_018062.3(FANCL):c.394T>C (p.Cys132Arg)
NM_018062.3(FANCL):c.402T>C (p.Ser134=) rs145284589
NM_018062.3(FANCL):c.40dup (p.Leu14fs) rs761039364
NM_018062.3(FANCL):c.426_438del (p.Asp142fs) rs878855046
NM_018062.3(FANCL):c.430del (p.Ser144fs) rs869320685
NM_018062.3(FANCL):c.4G>T (p.Ala2Ser) rs144057264
NM_018062.3(FANCL):c.51C>G (p.Pro17=) rs772700022
NM_018062.3(FANCL):c.534A>G (p.Thr178=) rs151181785
NM_018062.3(FANCL):c.548_550TAA[1] (p.Ile184del)
NM_018062.3(FANCL):c.622G>A (p.Asp208Asn) rs199564543
NM_018062.3(FANCL):c.670A>G (p.Thr224Ala) rs149731356
NM_018062.3(FANCL):c.81A>C (p.Gly27=) rs1553459821
NM_018062.3(FANCL):c.96+10C>T rs184741617

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