ClinVar Miner

List of variants in gene CENPF reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_016343.4(CENPF):c.3811A>G (p.Lys1271Glu) rs62000407 0.00238
NM_016343.4(CENPF):c.1055A>G (p.Gln352Arg) rs6697155 0.00207
NM_016343.4(CENPF):c.3617A>G (p.Tyr1206Cys) rs144237457 0.00181
NM_016343.4(CENPF):c.9158G>A (p.Arg3053Gln) rs143976001 0.00065
NM_016343.4(CENPF):c.4355A>G (p.Asn1452Ser) rs140952090 0.00041
NM_016343.4(CENPF):c.635C>A (p.Ala212Asp) rs141892982 0.00039
NM_016343.4(CENPF):c.6026T>C (p.Val2009Ala) rs202092147 0.00030
NM_016343.4(CENPF):c.3974G>A (p.Arg1325Lys) rs150048811 0.00024
NM_016343.4(CENPF):c.7721C>T (p.Ser2574Phe) rs201477597 0.00022
NM_016343.4(CENPF):c.9116C>G (p.Thr3039Arg) rs141439443 0.00021
NM_016343.4(CENPF):c.9007C>A (p.Arg3003=) rs767547548 0.00004
NM_016343.4(CENPF):c.4892C>T (p.Thr1631Met) rs769388025 0.00003
NM_016343.4(CENPF):c.8485+3G>C rs527897605 0.00003
NM_016343.4(CENPF):c.1816A>G (p.Lys606Glu) rs1553288629 0.00001
NM_016343.4(CENPF):c.533G>A (p.Arg178Gln) rs760951737 0.00001
NM_016343.4(CENPF):c.8509G>A (p.Asp2837Asn) rs138734779 0.00001
NM_016343.4(CENPF):c.8526G>C (p.Glu2842Asp) rs1039446040 0.00001
NM_016343.4(CENPF):c.2206G>A (p.Glu736Lys) rs1553288720
NM_016343.4(CENPF):c.7060C>G (p.His2354Asp) rs2102567951
NM_016343.4(CENPF):c.945T>G (p.Phe315Leu) rs1657523717

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