ClinVar Miner

List of variants in gene FANCL reported as likely benign for aplastic anemia

Included ClinVar conditions (107):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_001114636.1(FANCL):c.108C>G (p.Phe36Leu) rs149726602
NM_001114636.1(FANCL):c.203G>C (p.Arg68Pro) rs143819820
NM_001114636.1(FANCL):c.273+7A>C rs745366278
NM_001114636.1(FANCL):c.387G>A (p.Ala129=) rs141400460
NM_001114636.1(FANCL):c.51C>G (p.Pro17=) rs772700022
NM_001114636.1(FANCL):c.534A>G (p.Thr178=) rs151181785
NM_001114636.1(FANCL):c.685A>G (p.Thr229Ala) rs149731356
NM_001114636.1(FANCL):c.81A>C (p.Gly27=) rs1553459821
NM_001114636.1(FANCL):c.96+10C>T rs184741617
NM_018062.4(FANCL):c.420A>G (p.Ala140=)
NM_018062.4(FANCL):c.546C>T (p.Ser182=)
NM_018062.4(FANCL):c.621C>T (p.Ile207=)

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