ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia, complementation group I by Baylor Genetics

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Total variants: 15
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HGVS dbSNP
NM_001113378.2(FANCI):c.1084A>G (p.Thr362Ala)
NM_001113378.2(FANCI):c.1264G>A (p.Gly422Arg) rs146040966
NM_001113378.2(FANCI):c.1573A>G (p.Met525Val) rs144908351
NM_001113378.2(FANCI):c.233C>T (p.Ser78Leu) rs754443451
NM_001113378.2(FANCI):c.25G>A (p.Ala9Thr)
NM_001113378.2(FANCI):c.3055C>T (p.Arg1019Trp) rs149167939
NM_001113378.2(FANCI):c.349A>G (p.Arg117Gly) rs548947826
NM_001113378.2(FANCI):c.3656A>G (p.Lys1219Arg) rs757964620
NM_001113378.2(FANCI):c.3721G>A (p.Ala1241Thr) rs140357734
NM_001113378.2(FANCI):c.3985T>A (p.Ter1329Lys) rs1411317487
NM_001113378.2(FANCI):c.467G>A (p.Cys156Tyr) rs112387610
NM_001113378.2(FANCI):c.546-5C>T rs2052826764
NM_001113378.2(FANCI):c.775G>A (p.Val259Met) rs2053062704
NM_001113378.2(FANCI):c.824T>C (p.Ile275Thr) rs142906652
NM_001113378.2(FANCI):c.850G>A (p.Glu284Lys) rs368711186

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