ClinVar Miner

List of variants in gene FANCL reported as likely benign for Fanconi anemia complementation group A

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_018062.3(FANCL):c.155+7T>C rs200849840
NM_018062.3(FANCL):c.156-8A>C rs878855045
NM_018062.3(FANCL):c.203G>C (p.Arg68Pro) rs143819820
NM_018062.3(FANCL):c.217-11T>C rs79588315
NM_018062.3(FANCL):c.273+7A>C rs745366278
NM_018062.3(FANCL):c.387G>A (p.Ala129=) rs141400460
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.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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