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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.214657088T>A | CA344856827 | CENPF | c.8464T>A (p.Leu2822Ile) n.740T>A c.8641T>A (p.Leu2881Ile) n.412T>A c.7576T>A (p.Leu2526Ile) | |
| 1 | g.214657088T>C | CA423429484 | CENPF | c.8464T>C (p.Leu2822=) n.740T>C c.8641T>C (p.Leu2881=) n.412T>C c.7576T>C (p.Leu2526=) | |
| 1 | g.214657088T>G | CA344856828 | CENPF | c.8464T>G (p.Leu2822Val) n.740T>G c.8641T>G (p.Leu2881Val) n.412T>G c.7576T>G (p.Leu2526Val) | |
| 1 | g.214657089T>A | CA344856831 | CENPF | c.8465T>A (p.Leu2822Ter) n.741T>A c.8642T>A (p.Leu2881Ter) n.413T>A c.7577T>A (p.Leu2526Ter) | |
| 1 | g.214657089T>C | CA344856830 | CENPF | c.8465T>C (p.Leu2822Ser) n.741T>C c.8642T>C (p.Leu2881Ser) n.413T>C c.7577T>C (p.Leu2526Ser) | dbSNP |
| 1 | g.214657089T>G | CA344856829 | CENPF | c.8465T>G (p.Leu2822Ter) n.741T>G c.8642T>G (p.Leu2881Ter) n.413T>G c.7577T>G (p.Leu2526Ter) | |
| 1 | g.214657089T= | CA2486377607 | CENPF | c.8465T= (p.Leu2822=) n.741T= c.8642T= (p.Leu2881=) n.413T= c.7577T= (p.Leu2526=) | |
| 1 | g.214657090A>C | CA344856832 | CENPF | c.8466A>C (p.Leu2822Phe) n.742A>C c.8643A>C (p.Leu2881Phe) n.414A>C c.7578A>C (p.Leu2526Phe) | |
| 1 | g.214657090A>G | CA423429489 | CENPF | c.8466A>G (p.Leu2822=) n.742A>G c.8643A>G (p.Leu2881=) n.414A>G c.7578A>G (p.Leu2526=) | gnomAD v4 |
| 1 | g.214657090A>T | CA344856833 | CENPF | c.8466A>T (p.Leu2822Phe) n.742A>T c.8643A>T (p.Leu2881Phe) n.414A>T c.7578A>T (p.Leu2526Phe) | |
| 1 | g.214657091G>A | CA344856834 | CENPF | c.8467G>A (p.Glu2823Lys) n.743G>A c.8644G>A (p.Glu2882Lys) n.415G>A c.7579G>A (p.Glu2527Lys) | |
| 1 | g.214657091G>C | CA344856835 | CENPF | c.8467G>C (p.Glu2823Gln) n.743G>C c.8644G>C (p.Glu2882Gln) n.415G>C c.7579G>C (p.Glu2527Gln) | |
| 1 | g.214657091G>T | CA344856836 | CENPF | c.8467G>T (p.Glu2823Ter) n.743G>T c.8644G>T (p.Glu2882Ter) n.415G>T c.7579G>T (p.Glu2527Ter) | |
| 1 | g.214657092A= | CA2486377608 | CENPF | c.8468A= (p.Glu2823=) n.744A= c.8645A= (p.Glu2882=) n.416A= c.7580A= (p.Glu2527=) | |
| 1 | g.214657092A>C | CA344856837 | CENPF | c.8468A>C (p.Glu2823Ala) n.744A>C c.8645A>C (p.Glu2882Ala) n.416A>C c.7580A>C (p.Glu2527Ala) | gnomAD v4 |
| 1 | g.214657092A>G | CA1391466 | CENPF | c.8468A>G (p.Glu2823Gly) n.744A>G c.8645A>G (p.Glu2882Gly) n.416A>G c.7580A>G (p.Glu2527Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657092A>T | CA344856838 | CENPF | c.8468A>T (p.Glu2823Val) n.744A>T c.8645A>T (p.Glu2882Val) n.416A>T c.7580A>T (p.Glu2527Val) | |
| 1 | g.214657093G>A | CA423429496 | CENPF | c.8469G>A (p.Glu2823=) n.745G>A c.8646G>A (p.Glu2882=) n.417G>A c.7581G>A (p.Glu2527=) | |
| 1 | g.214657093G>C | CA344856839 | CENPF | c.8469G>C (p.Glu2823Asp) n.745G>C c.8646G>C (p.Glu2882Asp) n.417G>C c.7581G>C (p.Glu2527Asp) | |
| 1 | g.214657093G>T | CA344856840 | CENPF | c.8469G>T (p.Glu2823Asp) n.745G>T c.8646G>T (p.Glu2882Asp) n.417G>T c.7581G>T (p.Glu2527Asp) | |
| 1 | g.214657094A= | CA1142064894 | CENPF | c.8470A= (p.Thr2824=) n.746A= c.8647A= (p.Thr2883=) n.418A= c.7582A= (p.Thr2528=) | |
| 1 | g.214657094A>C | CA344856841 | CENPF | c.8470A>C (p.Thr2824Pro) n.746A>C c.8647A>C (p.Thr2883Pro) n.418A>C c.7582A>C (p.Thr2528Pro) | |
| 1 | g.214657094A>G | CA37381015 | CENPF | c.8470A>G (p.Thr2824Ala) n.746A>G c.8647A>G (p.Thr2883Ala) n.418A>G c.7582A>G (p.Thr2528Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.214657094A>T | CA344856842 | CENPF | c.8470A>T (p.Thr2824Ser) n.746A>T c.8647A>T (p.Thr2883Ser) n.418A>T c.7582A>T (p.Thr2528Ser) | |
| 1 | g.214657095C>A | CA344856844 | CENPF | c.8471C>A (p.Thr2824Lys) n.747C>A c.8648C>A (p.Thr2883Lys) n.419C>A c.7583C>A (p.Thr2528Lys) | |
| 1 | g.214657095C>G | CA344856845 | CENPF | c.8471C>G (p.Thr2824Arg) n.747C>G c.8648C>G (p.Thr2883Arg) n.419C>G c.7583C>G (p.Thr2528Arg) | |
| 1 | g.214657095C>T | CA344856843 | CENPF | c.8471C>T (p.Thr2824Ile) n.747C>T c.8648C>T (p.Thr2883Ile) n.419C>T c.7583C>T (p.Thr2528Ile) | |
| 1 | g.214657096A>C | CA423429501 | CENPF | c.8472A>C (p.Thr2824=) n.748A>C c.8649A>C (p.Thr2883=) n.420A>C c.7584A>C (p.Thr2528=) | |
| 1 | g.214657096A>G | CA423429502 | CENPF | c.8472A>G (p.Thr2824=) n.748A>G c.8649A>G (p.Thr2883=) n.420A>G c.7584A>G (p.Thr2528=) | |
| 1 | g.214657096A>T | CA423429503 | CENPF | c.8472A>T (p.Thr2824=) n.748A>T c.8649A>T (p.Thr2883=) n.420A>T c.7584A>T (p.Thr2528=) | |
| 1 | g.214657097C>A | CA344856848 | CENPF | c.8473C>A (p.Gln2825Lys) n.749C>A c.8650C>A (p.Gln2884Lys) n.421C>A c.7585C>A (p.Gln2529Lys) | |
| 1 | g.214657097C>G | CA344856846 | CENPF | c.8473C>G (p.Gln2825Glu) n.749C>G c.8650C>G (p.Gln2884Glu) n.421C>G c.7585C>G (p.Gln2529Glu) | |
| 1 | g.214657097C>T | CA344856847 | CENPF | c.8473C>T (p.Gln2825Ter) n.749C>T c.8650C>T (p.Gln2884Ter) n.421C>T c.7585C>T (p.Gln2529Ter) | |
| 1 | g.214657098A= | CA2486377614 | CENPF | c.8474A= (p.Gln2825=) n.750A= c.8651A= (p.Gln2884=) n.422A= c.7586A= (p.Gln2529=) | |
| 1 | g.214657098A>C | CA344856849 | CENPF | c.8474A>C (p.Gln2825Pro) n.750A>C c.8651A>C (p.Gln2884Pro) n.422A>C c.7586A>C (p.Gln2529Pro) | |
| 1 | g.214657098A>G | CA344856850 | CENPF | c.8474A>G (p.Gln2825Arg) n.750A>G c.8651A>G (p.Gln2884Arg) n.422A>G c.7586A>G (p.Gln2529Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.214657098A>T | CA344856851 | CENPF | c.8474A>T (p.Gln2825Leu) n.750A>T c.8651A>T (p.Gln2884Leu) n.422A>T c.7586A>T (p.Gln2529Leu) | |
| 1 | g.214657099A= | CA2486377616 | CENPF | c.8475A= (p.Gln2825=) n.751A= c.8652A= (p.Gln2884=) n.423A= c.7587A= (p.Gln2529=) | |
| 1 | g.214657099A>C | CA344856852 | CENPF | c.8475A>C (p.Gln2825His) n.751A>C c.8652A>C (p.Gln2884His) n.423A>C c.7587A>C (p.Gln2529His) | |
| 1 | g.214657099A>G | CA423429508 | CENPF | c.8475A>G (p.Gln2825=) n.751A>G c.8652A>G (p.Gln2884=) n.423A>G c.7587A>G (p.Gln2529=) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.214657099A>T | CA344856853 | CENPF | c.8475A>T (p.Gln2825His) n.751A>T c.8652A>T (p.Gln2884His) n.423A>T c.7587A>T (p.Gln2529His) | COSMIC |
| 1 | g.214657100G>A | CA344856854 | CENPF | c.8476G>A (p.Val2826Met) n.752G>A c.8653G>A (p.Val2885Met) n.424G>A c.7588G>A (p.Val2530Met) | |
| 1 | g.214657100G>C | CA344856856 | CENPF | c.8476G>C (p.Val2826Leu) n.752G>C c.8653G>C (p.Val2885Leu) n.424G>C c.7588G>C (p.Val2530Leu) | |
| 1 | g.214657100G>T | CA344856855 | CENPF | c.8476G>T (p.Val2826Leu) n.752G>T c.8653G>T (p.Val2885Leu) n.424G>T c.7588G>T (p.Val2530Leu) | |
| 1 | g.214657101T>A | CA344856857 | CENPF | c.8477T>A (p.Val2826Glu) n.753T>A c.8654T>A (p.Val2885Glu) n.425T>A c.7589T>A (p.Val2530Glu) | |
| 1 | g.214657101T>C | CA344856858 | CENPF | c.8477T>C (p.Val2826Ala) n.753T>C c.8654T>C (p.Val2885Ala) n.425T>C c.7589T>C (p.Val2530Ala) | |
| 1 | g.214657101T>G | CA344856859 | CENPF | c.8477T>G (p.Val2826Gly) n.753T>G c.8654T>G (p.Val2885Gly) n.425T>G c.7589T>G (p.Val2530Gly) | |
| 1 | g.214657102G>A | CA1391467 | CENPF | c.8478G>A (p.Val2826=) n.754G>A c.8655G>A (p.Val2885=) n.426G>A c.7590G>A (p.Val2530=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657102G>C | CA423429513 | CENPF | c.8478G>C (p.Val2826=) n.754G>C c.8655G>C (p.Val2885=) n.426G>C c.7590G>C (p.Val2530=) | |
| 1 | g.214657102G= | CA2486377619 | CENPF | c.8478G= (p.Val2826=) n.754G= c.8655G= (p.Val2885=) n.426G= c.7590G= (p.Val2530=) | |
| 1 | g.214657102G>T | CA423429514 | CENPF | c.8478G>T (p.Val2826=) n.754G>T c.8655G>T (p.Val2885=) n.426G>T c.7590G>T (p.Val2530=) | |
| 1 | g.214657103G>A | CA344856860 | CENPF | c.8479G>A (p.Ala2827Thr) n.755G>A c.8656G>A (p.Ala2886Thr) n.427G>A c.7591G>A (p.Ala2531Thr) | gnomAD v4 |
| 1 | g.214657103G>C | CA344856862 | CENPF | c.8479G>C (p.Ala2827Pro) n.755G>C c.8656G>C (p.Ala2886Pro) n.427G>C c.7591G>C (p.Ala2531Pro) | |
| 1 | g.214657103G= | CA2486377622 | CENPF | c.8479G= (p.Ala2827=) n.755G= c.8656G= (p.Ala2886=) n.427G= c.7591G= (p.Ala2531=) | |
| 1 | g.214657103G>T | CA344856861 | CENPF | c.8479G>T (p.Ala2827Ser) n.755G>T c.8656G>T (p.Ala2886Ser) n.427G>T c.7591G>T (p.Ala2531Ser) | dbSNP |
| 1 | g.214657104C>A | CA344856863 | CENPF | c.8480C>A (p.Ala2827Asp) n.756C>A c.8657C>A (p.Ala2886Asp) n.428C>A c.7592C>A (p.Ala2531Asp) | |
| 1 | g.214657104C>G | CA344856864 | CENPF | c.8480C>G (p.Ala2827Gly) n.756C>G c.8657C>G (p.Ala2886Gly) n.428C>G c.7592C>G (p.Ala2531Gly) | |
| 1 | g.214657104C>T | CA344856865 | CENPF | c.8480C>T (p.Ala2827Val) n.756C>T c.8657C>T (p.Ala2886Val) n.428C>T c.7592C>T (p.Ala2531Val) | COSMIC |
| 1 | g.214657105C>A | CA423429519 | CENPF | c.8481C>A (p.Ala2827=) n.757C>A c.8658C>A (p.Ala2886=) n.429C>A c.7593C>A (p.Ala2531=) | |
| 1 | g.214657105C>G | CA423429524 | CENPF | c.8481C>G (p.Ala2827=) n.757C>G c.8658C>G (p.Ala2886=) n.429C>G c.7593C>G (p.Ala2531=) | |
| 1 | g.214657105C>T | CA423429520 | CENPF | c.8481C>T (p.Ala2827=) n.757C>T c.8658C>T (p.Ala2886=) n.429C>T c.7593C>T (p.Ala2531=) | |
| 1 | g.214657106C>A | CA1391468 | CENPF | c.8482C>A (p.His2828Asn) n.758C>A c.8659C>A (p.His2887Asn) n.430C>A c.7594C>A (p.His2532Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657106C= | CA1148869134 | CENPF | c.8482C= (p.His2828=) n.758C= c.8659C= (p.His2887=) n.430C= c.7594C= (p.His2532=) | |
| 1 | g.214657106C>G | CA344856866 | CENPF | c.8482C>G (p.His2828Asp) n.758C>G c.8659C>G (p.His2887Asp) n.430C>G c.7594C>G (p.His2532Asp) | |
| 1 | g.214657106C>T | CA344856867 | CENPF | c.8482C>T (p.His2828Tyr) n.758C>T c.8659C>T (p.His2887Tyr) n.430C>T c.7594C>T (p.His2532Tyr) | gnomAD v4 |
| 1 | g.214657107A>C | CA344856868 | CENPF | c.8483A>C (p.His2828Pro) n.759A>C c.8660A>C (p.His2887Pro) n.431A>C c.7595A>C (p.His2532Pro) | |
| 1 | g.214657107A>G | CA344856869 | CENPF | c.8483A>G (p.His2828Arg) n.759A>G c.8660A>G (p.His2887Arg) n.431A>G c.7595A>G (p.His2532Arg) | gnomAD v4 |
| 1 | g.214657107A>T | CA344856870 | CENPF | c.8483A>T (p.His2828Leu) n.759A>T c.8660A>T (p.His2887Leu) n.431A>T c.7595A>T (p.His2532Leu) | |
| 1 | g.214657108T>A | CA344856871 | CENPF | c.8484T>A (p.His2828Gln) n.760T>A c.8661T>A (p.His2887Gln) n.432T>A c.7596T>A (p.His2532Gln) | |
| 1 | g.214657108T>C | CA423429529 | CENPF | c.8484T>C (p.His2828=) n.760T>C c.8661T>C (p.His2887=) n.432T>C c.7596T>C (p.His2532=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657108T>G | CA344856872 | CENPF | c.8484T>G (p.His2828Gln) n.760T>G c.8661T>G (p.His2887Gln) n.432T>G c.7596T>G (p.His2532Gln) | |
| 1 | g.214657108T= | CA2486377629 | CENPF | c.8484T= (p.His2828=) n.760T= c.8661T= (p.His2887=) n.432T= c.7596T= (p.His2532=) | |
| 1 | g.214657109_214657114dup | CA2747692469 | CENPF | c.8485_8490dup (p.Cys2830_Ser2831insLeuCys) n.761_766dup c.8662_8667dup (p.Cys2889_Ser2890insLeuCys) n.433_438dup c.7597_7602dup (p.Cys2534_Ser2535insLeuCys) | |
| 1 | g.214657109C>A | CA344856874 | CENPF | c.8485C>A (p.Leu2829Met) n.761C>A c.8662C>A (p.Leu2888Met) n.433C>A c.7597C>A (p.Leu2533Met) | |
| 1 | g.214657109C>G | CA344856873 | CENPF | c.8485C>G (p.Leu2829Val) n.761C>G c.8662C>G (p.Leu2888Val) n.433C>G c.7597C>G (p.Leu2533Val) | |
| 1 | g.214657109C>T | CA423429531 | CENPF | c.8485C>T (p.Leu2829=) n.761C>T c.8662C>T (p.Leu2888=) n.433C>T c.7597C>T (p.Leu2533=) | |
| 1 | g.214657110T>A | CA344856875 | CENPF | c.8486T>A (p.Leu2829Gln) n.762T>A c.8663T>A (p.Leu2888Gln) n.434T>A c.7598T>A (p.Leu2533Gln) | |
| 1 | g.214657110T>C | CA344856877 | CENPF | c.8486T>C (p.Leu2829Pro) n.762T>C c.8663T>C (p.Leu2888Pro) n.434T>C c.7598T>C (p.Leu2533Pro) | |
| 1 | g.214657110T>G | CA344856876 | CENPF | c.8486T>G (p.Leu2829Arg) n.762T>G c.8663T>G (p.Leu2888Arg) n.434T>G c.7598T>G (p.Leu2533Arg) | dbSNP |
| 1 | g.214657110T= | CA2486377631 | CENPF | c.8486T= (p.Leu2829=) n.762T= c.8663T= (p.Leu2888=) n.434T= c.7598T= (p.Leu2533=) | |
| 1 | g.214657111G>A | CA423429536 | CENPF | c.8487G>A (p.Leu2829=) n.763G>A c.8664G>A (p.Leu2888=) n.435G>A c.7599G>A (p.Leu2533=) | dbSNP |
| 1 | g.214657111G>C | CA423429538 | CENPF | c.8487G>C (p.Leu2829=) n.763G>C c.8664G>C (p.Leu2888=) n.435G>C c.7599G>C (p.Leu2533=) | |
| 1 | g.214657111G= | CA2486377632 | CENPF | c.8487G= (p.Leu2829=) n.763G= c.8664G= (p.Leu2888=) n.435G= c.7599G= (p.Leu2533=) | |
| 1 | g.214657111G>T | CA423429539 | CENPF | c.8487G>T (p.Leu2829=) n.763G>T c.8664G>T (p.Leu2888=) n.435G>T c.7599G>T (p.Leu2533=) | |
| 1 | g.214657112T>A | CA344856878 | CENPF | c.8488T>A (p.Cys2830Ser) n.764T>A c.8665T>A (p.Cys2889Ser) n.436T>A c.7600T>A (p.Cys2534Ser) | |
| 1 | g.214657112T>C | CA344856879 | CENPF | c.8488T>C (p.Cys2830Arg) n.764T>C c.8665T>C (p.Cys2889Arg) n.436T>C c.7600T>C (p.Cys2534Arg) | dbSNP COSMIC |
| 1 | g.214657112T>G | CA344856880 | CENPF | c.8488T>G (p.Cys2830Gly) n.764T>G c.8665T>G (p.Cys2889Gly) n.436T>G c.7600T>G (p.Cys2534Gly) | |
| 1 | g.214657112T= | CA2486377633 | CENPF | c.8488T= (p.Cys2830=) n.764T= c.8665T= (p.Cys2889=) n.436T= c.7600T= (p.Cys2534=) | |
| 1 | g.214657113G>A | CA344856881 | CENPF | c.8489G>A (p.Cys2830Tyr) n.765G>A c.8666G>A (p.Cys2889Tyr) n.437G>A c.7601G>A (p.Cys2534Tyr) | gnomAD v4 |
| 1 | g.214657113G>C | CA344856882 | CENPF | c.8489G>C (p.Cys2830Ser) n.765G>C c.8666G>C (p.Cys2889Ser) n.437G>C c.7601G>C (p.Cys2534Ser) | |
| 1 | g.214657113G>T | CA344856883 | CENPF | c.8489G>T (p.Cys2830Phe) n.765G>T c.8666G>T (p.Cys2889Phe) n.437G>T c.7601G>T (p.Cys2534Phe) | |
| 1 | g.214657114T>A | CA344856884 | CENPF | c.8490T>A (p.Cys2830Ter) n.766T>A c.8667T>A (p.Cys2889Ter) n.438T>A c.7602T>A (p.Cys2534Ter) | |
| 1 | g.214657114T>C | CA423429544 | CENPF | c.8490T>C (p.Cys2830=) n.766T>C c.8667T>C (p.Cys2889=) n.438T>C c.7602T>C (p.Cys2534=) | |
| 1 | g.214657114T>G | CA344856885 | CENPF | c.8490T>G (p.Cys2830Trp) n.766T>G c.8667T>G (p.Cys2889Trp) n.438T>G c.7602T>G (p.Cys2534Trp) | |
| 1 | g.214657115T>A | CA344856886 | CENPF | c.8491T>A (p.Ser2831Thr) n.767T>A c.8668T>A (p.Ser2890Thr) n.439T>A c.7603T>A (p.Ser2535Thr) | |
| 1 | g.214657115T>C | CA344856887 | CENPF | c.8491T>C (p.Ser2831Pro) n.767T>C c.8668T>C (p.Ser2890Pro) n.439T>C c.7603T>C (p.Ser2535Pro) | |
| 1 | g.214657115T>G | CA344856888 | CENPF | c.8491T>G (p.Ser2831Ala) n.767T>G c.8668T>G (p.Ser2890Ala) n.439T>G c.7603T>G (p.Ser2535Ala) | |
| 1 | g.214657116C>A | CA344856891 | CENPF | c.8492C>A (p.Ser2831Ter) n.768C>A c.8669C>A (p.Ser2890Ter) n.440C>A c.7604C>A (p.Ser2535Ter) | |
| 1 | g.214657116C= | CA2486377634 | CENPF | c.8492C= (p.Ser2831=) n.768C= c.8669C= (p.Ser2890=) n.440C= c.7604C= (p.Ser2535=) | |
| 1 | g.214657116C>G | CA344856890 | CENPF | c.8492C>G (p.Ser2831Ter) n.768C>G c.8669C>G (p.Ser2890Ter) n.440C>G c.7604C>G (p.Ser2535Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657116C>T | CA344856889 | CENPF | c.8492C>T (p.Ser2831Leu) n.768C>T c.8669C>T (p.Ser2890Leu) n.440C>T c.7604C>T (p.Ser2535Leu) | gnomAD v4 |
| 1 | g.214657117A= | CA2486377635 | CENPF | c.8493A= (p.Ser2831=) n.769A= c.8670A= (p.Ser2890=) n.441A= c.7605A= (p.Ser2535=) | |
| 1 | g.214657117A>C | CA423429548 | CENPF | c.8493A>C (p.Ser2831=) n.769A>C c.8670A>C (p.Ser2890=) n.441A>C c.7605A>C (p.Ser2535=) | |
| 1 | g.214657117A>G | CA1391469 | CENPF | c.8493A>G (p.Ser2831=) n.769A>G c.8670A>G (p.Ser2890=) n.441A>G c.7605A>G (p.Ser2535=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657117A>T | CA423429549 | CENPF | c.8493A>T (p.Ser2831=) n.769A>T c.8670A>T (p.Ser2890=) n.441A>T c.7605A>T (p.Ser2535=) | |
| 1 | g.214657118C>A | CA344856892 | CENPF | c.8494C>A (p.Gln2832Lys) n.770C>A c.8671C>A (p.Gln2891Lys) n.442C>A c.7606C>A (p.Gln2536Lys) | |
| 1 | g.214657118C>G | CA344856893 | CENPF | c.8494C>G (p.Gln2832Glu) n.770C>G c.8671C>G (p.Gln2891Glu) n.442C>G c.7606C>G (p.Gln2536Glu) | |
| 1 | g.214657118C>T | CA344856894 | CENPF | c.8494C>T (p.Gln2832Ter) n.770C>T c.8671C>T (p.Gln2891Ter) n.442C>T c.7606C>T (p.Gln2536Ter) | |
| 1 | g.214657119A= | CA2486377636 | CENPF | c.8495A= (p.Gln2832=) n.771A= c.8672A= (p.Gln2891=) n.443A= c.7607A= (p.Gln2536=) | |
| 1 | g.214657119A>C | CA344856895 | CENPF | c.8495A>C (p.Gln2832Pro) n.771A>C c.8672A>C (p.Gln2891Pro) n.443A>C c.7607A>C (p.Gln2536Pro) | |
| 1 | g.214657119A>G | CA344856896 | CENPF | c.8495A>G (p.Gln2832Arg) n.771A>G c.8672A>G (p.Gln2891Arg) n.443A>G c.7607A>G (p.Gln2536Arg) | |
| 1 | g.214657119A>T | CA1391470 | CENPF | c.8495A>T (p.Gln2832Leu) n.771A>T c.8672A>T (p.Gln2891Leu) n.443A>T c.7607A>T (p.Gln2536Leu) | dbSNP ExAC gnomAD v2 |
| 1 | g.214657119_214657136del | CA2650488221 | CENPF | c.8495_8512del (p.Gln2832_Ser2838delinsPro) n.771_788del c.8672_8689del (p.Gln2891_Ser2897delinsPro) n.443_460del c.7607_7624del (p.Gln2536_Ser2542delinsPro) | gnomAD v4 |
| 1 | g.214657120G>A | CA1391472 | CENPF | c.8496G>A (p.Gln2832=) n.772G>A c.8673G>A (p.Gln2891=) n.444G>A c.7608G>A (p.Gln2536=) | dbSNP ExAC gnomAD v2 COSMIC |
| 1 | g.214657120G>C | CA1391471 | CENPF | c.8496G>C (p.Gln2832His) n.772G>C c.8673G>C (p.Gln2891His) n.444G>C c.7608G>C (p.Gln2536His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657120G= | CA2486377637 | CENPF | c.8496G= (p.Gln2832=) n.772G= c.8673G= (p.Gln2891=) n.444G= c.7608G= (p.Gln2536=) | |
| 1 | g.214657120G>T | CA344856897 | CENPF | c.8496G>T (p.Gln2832His) n.772G>T c.8673G>T (p.Gln2891His) n.444G>T c.7608G>T (p.Gln2536His) | |
| 1 | g.214657121C>A | CA344856898 | CENPF | c.8497C>A (p.Gln2833Lys) n.773C>A c.8674C>A (p.Gln2892Lys) n.445C>A c.7609C>A (p.Gln2537Lys) | dbSNP gnomAD v2 |
| 1 | g.214657121C= | CA1141301873 | CENPF | c.8497C= (p.Gln2833=) n.773C= c.8674C= (p.Gln2892=) n.445C= c.7609C= (p.Gln2537=) | |
| 1 | g.214657121C>G | CA344856899 | CENPF | c.8497C>G (p.Gln2833Glu) n.773C>G c.8674C>G (p.Gln2892Glu) n.445C>G c.7609C>G (p.Gln2537Glu) | |
| 1 | g.214657121C>T | CA37381076 | CENPF | c.8497C>T (p.Gln2833Ter) n.773C>T c.8674C>T (p.Gln2892Ter) n.445C>T c.7609C>T (p.Gln2537Ter) | dbSNP |
| 1 | g.214657122A>C | CA344856902 | CENPF | c.8498A>C (p.Gln2833Pro) n.774A>C c.8675A>C (p.Gln2892Pro) n.446A>C c.7610A>C (p.Gln2537Pro) | |
| 1 | g.214657122A>G | CA344856901 | CENPF | c.8498A>G (p.Gln2833Arg) n.774A>G c.8675A>G (p.Gln2892Arg) n.446A>G c.7610A>G (p.Gln2537Arg) | |
| 1 | g.214657122A>T | CA344856900 | CENPF | c.8498A>T (p.Gln2833Leu) n.774A>T c.8675A>T (p.Gln2892Leu) n.446A>T c.7610A>T (p.Gln2537Leu) | |
| 1 | g.214657123A= | CA2486377638 | CENPF | c.8499A= (p.Gln2833=) n.775A= c.8676A= (p.Gln2892=) n.447A= c.7611A= (p.Gln2537=) | |
| 1 | g.214657123A>C | CA344856903 | CENPF | c.8499A>C (p.Gln2833His) n.775A>C c.8676A>C (p.Gln2892His) n.447A>C c.7611A>C (p.Gln2537His) | |
| 1 | g.214657123A>G | CA1391473 | CENPF | c.8499A>G (p.Gln2833=) n.775A>G c.8676A>G (p.Gln2892=) n.447A>G c.7611A>G (p.Gln2537=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657123A>T | CA344856904 | CENPF | c.8499A>T (p.Gln2833His) n.775A>T c.8676A>T (p.Gln2892His) n.447A>T c.7611A>T (p.Gln2537His) | |
| 1 | g.214657124T>A | CA344856905 | CENPF | c.8500T>A (p.Ser2834Thr) n.776T>A c.8677T>A (p.Ser2893Thr) n.448T>A c.7612T>A (p.Ser2538Thr) | |
| 1 | g.214657124T>C | CA344856906 | CENPF | c.8500T>C (p.Ser2834Pro) n.776T>C c.8677T>C (p.Ser2893Pro) n.448T>C c.7612T>C (p.Ser2538Pro) | |
| 1 | g.214657124T>G | CA344856907 | CENPF | c.8500T>G (p.Ser2834Ala) n.776T>G c.8677T>G (p.Ser2893Ala) n.448T>G c.7612T>G (p.Ser2538Ala) | |
| 1 | g.214657125C>A | CA344856908 | CENPF | c.8501C>A (p.Ser2834Tyr) n.777C>A c.8678C>A (p.Ser2893Tyr) n.449C>A c.7613C>A (p.Ser2538Tyr) | |
| 1 | g.214657125C>G | CA344856909 | CENPF | c.8501C>G (p.Ser2834Cys) n.777C>G c.8678C>G (p.Ser2893Cys) n.449C>G c.7613C>G (p.Ser2538Cys) | |
| 1 | g.214657125C>T | CA344856910 | CENPF | c.8501C>T (p.Ser2834Phe) n.777C>T c.8678C>T (p.Ser2893Phe) n.449C>T c.7613C>T (p.Ser2538Phe) | |
| 1 | g.214657126T>A | CA423429561 | CENPF | c.8502T>A (p.Ser2834=) n.778T>A c.8679T>A (p.Ser2893=) n.450T>A c.7614T>A (p.Ser2538=) | |
| 1 | g.214657126T>C | CA423429562 | CENPF | c.8502T>C (p.Ser2834=) n.778T>C c.8679T>C (p.Ser2893=) n.450T>C c.7614T>C (p.Ser2538=) | gnomAD v4 |
| 1 | g.214657126T>G | CA423429563 | CENPF | c.8502T>G (p.Ser2834=) n.778T>G c.8679T>G (p.Ser2893=) n.450T>G c.7614T>G (p.Ser2538=) | |
| 1 | g.214657127A= | CA2486377639 | CENPF | c.8503A= (p.Lys2835=) n.779A= c.8680A= (p.Lys2894=) n.451A= c.7615A= (p.Lys2539=) | |
| 1 | g.214657127A>C | CA344856913 | CENPF | c.8503A>C (p.Lys2835Gln) n.779A>C c.8680A>C (p.Lys2894Gln) n.451A>C c.7615A>C (p.Lys2539Gln) | |
| 1 | g.214657127A>G | CA344856911 | CENPF | c.8503A>G (p.Lys2835Glu) n.779A>G c.8680A>G (p.Lys2894Glu) n.451A>G c.7615A>G (p.Lys2539Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657127A>T | CA344856912 | CENPF | c.8503A>T (p.Lys2835Ter) n.779A>T c.8680A>T (p.Lys2894Ter) n.451A>T c.7615A>T (p.Lys2539Ter) | |
| 1 | g.214657128A>C | CA344856914 | CENPF | c.8504A>C (p.Lys2835Thr) n.780A>C c.8681A>C (p.Lys2894Thr) n.452A>C c.7616A>C (p.Lys2539Thr) | |
| 1 | g.214657128A>G | CA344856915 | CENPF | c.8504A>G (p.Lys2835Arg) n.780A>G c.8681A>G (p.Lys2894Arg) n.452A>G c.7616A>G (p.Lys2539Arg) | gnomAD v4 |
| 1 | g.214657128A>T | CA344856916 | CENPF | c.8504A>T (p.Lys2835Ile) n.780A>T c.8681A>T (p.Lys2894Ile) n.452A>T c.7616A>T (p.Lys2539Ile) | |
| 1 | g.214657129A>C | CA344856917 | CENPF | c.8505A>C (p.Lys2835Asn) n.781A>C c.8682A>C (p.Lys2894Asn) n.453A>C c.7617A>C (p.Lys2539Asn) | |
| 1 | g.214657129A>G | CA423429571 | CENPF | c.8505A>G (p.Lys2835=) n.781A>G c.8682A>G (p.Lys2894=) n.453A>G c.7617A>G (p.Lys2539=) | |
| 1 | g.214657129A>T | CA344856918 | CENPF | c.8505A>T (p.Lys2835Asn) n.781A>T c.8682A>T (p.Lys2894Asn) n.453A>T c.7617A>T (p.Lys2539Asn) | |
| 1 | g.214657130C>A | CA344856921 | CENPF | c.8506C>A (p.Gln2836Lys) n.782C>A c.8683C>A (p.Gln2895Lys) n.454C>A c.7618C>A (p.Gln2540Lys) | gnomAD v4 |
| 1 | g.214657130C>G | CA344856919 | CENPF | c.8506C>G (p.Gln2836Glu) n.782C>G c.8683C>G (p.Gln2895Glu) n.454C>G c.7618C>G (p.Gln2540Glu) | |
| 1 | g.214657130C>T | CA344856920 | CENPF | c.8506C>T (p.Gln2836Ter) n.782C>T c.8683C>T (p.Gln2895Ter) n.454C>T c.7618C>T (p.Gln2540Ter) | |
| 1 | g.214657131A>C | CA344856922 | CENPF | c.8507A>C (p.Gln2836Pro) n.783A>C c.8684A>C (p.Gln2895Pro) n.455A>C c.7619A>C (p.Gln2540Pro) | |
| 1 | g.214657131A>G | CA344856923 | CENPF | c.8507A>G (p.Gln2836Arg) n.783A>G c.8684A>G (p.Gln2895Arg) n.455A>G c.7619A>G (p.Gln2540Arg) | gnomAD v4 |
| 1 | g.214657131A>T | CA344856924 | CENPF | c.8507A>T (p.Gln2836Leu) n.783A>T c.8684A>T (p.Gln2895Leu) n.455A>T c.7619A>T (p.Gln2540Leu) | |
| 1 | g.214657132A>C | CA344856925 | CENPF | c.8508A>C (p.Gln2836His) n.784A>C c.8685A>C (p.Gln2895His) n.456A>C c.7620A>C (p.Gln2540His) | |
| 1 | g.214657132A>G | CA423429580 | CENPF | c.8508A>G (p.Gln2836=) n.784A>G c.8685A>G (p.Gln2895=) n.456A>G c.7620A>G (p.Gln2540=) | gnomAD v4 |
| 1 | g.214657132A>T | CA344856926 | CENPF | c.8508A>T (p.Gln2836His) n.784A>T c.8685A>T (p.Gln2895His) n.456A>T c.7620A>T (p.Gln2540His) | |
| 1 | g.214657133G>A | CA344856927 | CENPF | c.8509G>A (p.Asp2837Asn) n.785G>A c.8686G>A (p.Asp2896Asn) n.457G>A c.7621G>A (p.Asp2541Asn) | |
| 1 | g.214657133G>C | CA344856928 | CENPF | c.8509G>C (p.Asp2837His) n.785G>C c.8686G>C (p.Asp2896His) n.457G>C c.7621G>C (p.Asp2541His) | |
| 1 | g.214657133G>T | CA344856929 | CENPF | c.8509G>T (p.Asp2837Tyr) n.785G>T c.8686G>T (p.Asp2896Tyr) n.457G>T c.7621G>T (p.Asp2541Tyr) | |
| 1 | g.214657134A= | CA1144240322 | CENPF | c.8510A= (p.Asp2837=) n.786A= c.8687A= (p.Asp2896=) n.458A= c.7622A= (p.Asp2541=) | |
| 1 | g.214657134A>C | CA344856930 | CENPF | c.8510A>C (p.Asp2837Ala) n.786A>C c.8687A>C (p.Asp2896Ala) n.458A>C c.7622A>C (p.Asp2541Ala) | |
| 1 | g.214657134A>G | CA1391474 | CENPF | c.8510A>G (p.Asp2837Gly) n.786A>G c.8687A>G (p.Asp2896Gly) n.458A>G c.7622A>G (p.Asp2541Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657134A>T | CA344856931 | CENPF | c.8510A>T (p.Asp2837Val) n.786A>T c.8687A>T (p.Asp2896Val) n.458A>T c.7622A>T (p.Asp2541Val) | gnomAD v4 |
| 1 | g.214657135T>A | CA344856932 | CENPF | c.8511T>A (p.Asp2837Glu) n.787T>A c.8688T>A (p.Asp2896Glu) n.459T>A c.7623T>A (p.Asp2541Glu) | |
| 1 | g.214657135T>C | CA423429590 | CENPF | c.8511T>C (p.Asp2837=) n.787T>C c.8688T>C (p.Asp2896=) n.459T>C c.7623T>C (p.Asp2541=) | |
| 1 | g.214657135T>G | CA344856933 | CENPF | c.8511T>G (p.Asp2837Glu) n.787T>G c.8688T>G (p.Asp2896Glu) n.459T>G c.7623T>G (p.Asp2541Glu) | |
| 1 | g.214657136T>A | CA344856934 | CENPF | c.8512T>A (p.Ser2838Thr) n.788T>A c.8689T>A (p.Ser2897Thr) n.460T>A c.7624T>A (p.Ser2542Thr) | |
| 1 | g.214657136T>C | CA344856936 | CENPF | c.8512T>C (p.Ser2838Pro) n.788T>C c.8689T>C (p.Ser2897Pro) n.460T>C c.7624T>C (p.Ser2542Pro) | |
| 1 | g.214657136T>G | CA344856935 | CENPF | c.8512T>G (p.Ser2838Ala) n.788T>G c.8689T>G (p.Ser2897Ala) n.460T>G c.7624T>G (p.Ser2542Ala) | dbSNP |
| 1 | g.214657136T= | CA2486377640 | CENPF | c.8512T= (p.Ser2838=) n.788T= c.8689T= (p.Ser2897=) n.460T= c.7624T= (p.Ser2542=) | |
| 1 | g.214657137C>A | CA1391475 | CENPF | c.8513C>A (p.Ser2838Tyr) n.789C>A c.8690C>A (p.Ser2897Tyr) n.461C>A c.7625C>A (p.Ser2542Tyr) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 1 | g.214657137C= | CA2486377641 | CENPF | c.8513C= (p.Ser2838=) n.789C= c.8690C= (p.Ser2897=) n.461C= c.7625C= (p.Ser2542=) | |
| 1 | g.214657137C>G | CA344856937 | CENPF | c.8513C>G (p.Ser2838Cys) n.789C>G c.8690C>G (p.Ser2897Cys) n.461C>G c.7625C>G (p.Ser2542Cys) | |
| 1 | g.214657137C>T | CA344856938 | CENPF | c.8513C>T (p.Ser2838Phe) n.789C>T c.8690C>T (p.Ser2897Phe) n.461C>T c.7625C>T (p.Ser2542Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657138C>A | CA423429594 | CENPF | c.8514C>A (p.Ser2838=) n.790C>A c.8691C>A (p.Ser2897=) n.462C>A c.7626C>A (p.Ser2542=) | |
| 1 | g.214657138C>G | CA423429595 | CENPF | c.8514C>G (p.Ser2838=) n.790C>G c.8691C>G (p.Ser2897=) n.462C>G c.7626C>G (p.Ser2542=) | |
| 1 | g.214657138C>T | CA423429596 | CENPF | c.8514C>T (p.Ser2838=) n.790C>T c.8691C>T (p.Ser2897=) n.462C>T c.7626C>T (p.Ser2542=) | |
| 1 | g.214657139C>A | CA423429598 | CENPF | c.8515C>A (p.Arg2839=) n.791C>A c.8692C>A (p.Arg2898=) n.463C>A c.7627C>A (p.Arg2543=) | |
| 1 | g.214657139C= | CA2486377642 | CENPF | c.8515C= (p.Arg2839=) n.791C= c.8692C= (p.Arg2898=) n.463C= c.7627C= (p.Arg2543=) | |
| 1 | g.214657139C>G | CA344856939 | CENPF | c.8515C>G (p.Arg2839Gly) n.791C>G c.8692C>G (p.Arg2898Gly) n.463C>G c.7627C>G (p.Arg2543Gly) | |
| 1 | g.214657139C>T | CA199685 | CENPF | c.8515C>T (p.Arg2839Ter) n.791C>T c.8692C>T (p.Arg2898Ter) n.463C>T c.7627C>T (p.Arg2543Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
| 1 | g.214657140G>A | CA1391476 | CENPF | c.8516G>A (p.Arg2839Gln) n.792G>A c.8693G>A (p.Arg2898Gln) n.464G>A c.7628G>A (p.Arg2543Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657140G>C | CA344856940 | CENPF | c.8516G>C (p.Arg2839Pro) n.792G>C c.8693G>C (p.Arg2898Pro) n.464G>C c.7628G>C (p.Arg2543Pro) | |
| 1 | g.214657140G= | CA2486377643 | CENPF | c.8516G= (p.Arg2839=) n.792G= c.8693G= (p.Arg2898=) n.464G= c.7628G= (p.Arg2543=) | |
| 1 | g.214657140G>T | CA344856941 | CENPF | c.8516G>T (p.Arg2839Leu) n.792G>T c.8693G>T (p.Arg2898Leu) n.464G>T c.7628G>T (p.Arg2543Leu) | |
| 1 | g.214657141A>C | CA423429600 | CENPF | c.8517A>C (p.Arg2839=) n.793A>C c.8694A>C (p.Arg2898=) n.465A>C c.7629A>C (p.Arg2543=) | |
| 1 | g.214657141A>G | CA423429601 | CENPF | c.8517A>G (p.Arg2839=) n.793A>G c.8694A>G (p.Arg2898=) n.465A>G c.7629A>G (p.Arg2543=) | |
| 1 | g.214657141A>T | CA423429602 | CENPF | c.8517A>T (p.Arg2839=) n.793A>T c.8694A>T (p.Arg2898=) n.465A>T c.7629A>T (p.Arg2543=) | |
| 1 | g.214657142G>A | CA344856942 | CENPF | c.8518G>A (p.Gly2840Arg) n.794G>A c.8695G>A (p.Gly2899Arg) n.466G>A c.7630G>A (p.Gly2544Arg) | |
| 1 | g.214657142G>C | CA344856943 | CENPF | c.8518G>C (p.Gly2840Arg) n.794G>C c.8695G>C (p.Gly2899Arg) n.466G>C c.7630G>C (p.Gly2544Arg) | gnomAD v4 |
| 1 | g.214657142G>T | CA344856944 | CENPF | c.8518G>T (p.Gly2840Trp) n.794G>T c.8695G>T (p.Gly2899Trp) n.466G>T c.7630G>T (p.Gly2544Trp) | |
| 1 | g.214657143G>A | CA344856947 | CENPF | c.8519G>A (p.Gly2840Glu) n.795G>A c.8696G>A (p.Gly2899Glu) n.467G>A c.7631G>A (p.Gly2544Glu) | |
| 1 | g.214657143G>C | CA344856946 | CENPF | c.8519G>C (p.Gly2840Ala) n.795G>C c.8696G>C (p.Gly2899Ala) n.467G>C c.7631G>C (p.Gly2544Ala) | |
| 1 | g.214657143G>T | CA344856945 | CENPF | c.8519G>T (p.Gly2840Val) n.795G>T c.8696G>T (p.Gly2899Val) n.467G>T c.7631G>T (p.Gly2544Val) | |
| 1 | g.214657144G>A | CA1391477 | CENPF | c.8520G>A (p.Gly2840=) n.796G>A c.8697G>A (p.Gly2899=) n.468G>A c.7632G>A (p.Gly2544=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657144G>C | CA423429608 | CENPF | c.8520G>C (p.Gly2840=) n.796G>C c.8697G>C (p.Gly2899=) n.468G>C c.7632G>C (p.Gly2544=) | |
| 1 | g.214657144G= | CA1143624337 | CENPF | c.8520G= (p.Gly2840=) n.796G= c.8697G= (p.Gly2899=) n.468G= c.7632G= (p.Gly2544=) | |
| 1 | g.214657144G>T | CA423429609 | CENPF | c.8520G>T (p.Gly2840=) n.796G>T c.8697G>T (p.Gly2899=) n.468G>T c.7632G>T (p.Gly2544=) | |
| 1 | g.214657145T>A | CA344856948 | CENPF | c.8521T>A (p.Ser2841Thr) n.797T>A c.8698T>A (p.Ser2900Thr) n.469T>A c.7633T>A (p.Ser2545Thr) | |
| 1 | g.214657145T>C | CA344856949 | CENPF | c.8521T>C (p.Ser2841Pro) n.797T>C c.8698T>C (p.Ser2900Pro) n.469T>C c.7633T>C (p.Ser2545Pro) | |
| 1 | g.214657145T>G | CA344856950 | CENPF | c.8521T>G (p.Ser2841Ala) n.797T>G c.8698T>G (p.Ser2900Ala) n.469T>G c.7633T>G (p.Ser2545Ala) | |
| 1 | g.214657146C>A | CA344856951 | CENPF | c.8522C>A (p.Ser2841Tyr) n.798C>A c.8699C>A (p.Ser2900Tyr) n.470C>A c.7634C>A (p.Ser2545Tyr) | |
| 1 | g.214657146C>G | CA344856952 | CENPF | c.8522C>G (p.Ser2841Cys) n.798C>G c.8699C>G (p.Ser2900Cys) n.470C>G c.7634C>G (p.Ser2545Cys) | |
| 1 | g.214657146C>T | CA344856953 | CENPF | c.8522C>T (p.Ser2841Phe) n.798C>T c.8699C>T (p.Ser2900Phe) n.470C>T c.7634C>T (p.Ser2545Phe) | |
| 1 | g.214657147T>A | CA423429610 | CENPF | c.8523T>A (p.Ser2841=) n.799T>A c.8700T>A (p.Ser2900=) n.471T>A c.7635T>A (p.Ser2545=) | |
| 1 | g.214657147T>C | CA423429611 | CENPF | c.8523T>C (p.Ser2841=) n.799T>C c.8700T>C (p.Ser2900=) n.471T>C c.7635T>C (p.Ser2545=) | |
| 1 | g.214657147T>G | CA423429612 | CENPF | c.8523T>G (p.Ser2841=) n.799T>G c.8700T>G (p.Ser2900=) n.471T>G c.7635T>G (p.Ser2545=) | |
| 1 | g.214657148C>A | CA344856954 | CENPF | c.8524C>A (p.Pro2842Thr) n.800C>A c.8701C>A (p.Pro2901Thr) n.472C>A c.7636C>A (p.Pro2546Thr) | |
| 1 | g.214657148C>G | CA344856955 | CENPF | c.8524C>G (p.Pro2842Ala) n.800C>G c.8701C>G (p.Pro2901Ala) n.472C>G c.7636C>G (p.Pro2546Ala) | |
| 1 | g.214657148C>T | CA344856956 | CENPF | c.8524C>T (p.Pro2842Ser) n.800C>T c.8701C>T (p.Pro2901Ser) n.472C>T c.7636C>T (p.Pro2546Ser) | |
| 1 | g.214657149del | CA2574132260 | CENPF | c.8525del (p.Pro2842LeufsTer3) n.801del c.8702del (p.Pro2901LeufsTer3) n.473del c.7637del (p.Pro2546LeufsTer3) | |
| 1 | g.214657149C>A | CA344856957 | CENPF | c.8525C>A (p.Pro2842His) n.801C>A c.8702C>A (p.Pro2901His) n.473C>A c.7637C>A (p.Pro2546His) | |
| 1 | g.214657149C>G | CA344856958 | CENPF | c.8525C>G (p.Pro2842Arg) n.801C>G c.8702C>G (p.Pro2901Arg) n.473C>G c.7637C>G (p.Pro2546Arg) | |
| 1 | g.214657149C>T | CA344856959 | CENPF | c.8525C>T (p.Pro2842Leu) n.801C>T c.8702C>T (p.Pro2901Leu) n.473C>T c.7637C>T (p.Pro2546Leu) | gnomAD v4 |
| 1 | g.214657150T>A | CA423429614 | CENPF | c.8526T>A (p.Pro2842=) n.802T>A c.8703T>A (p.Pro2901=) n.474T>A c.7638T>A (p.Pro2546=) | |
| 1 | g.214657150T>C | CA423429618 | CENPF | c.8526T>C (p.Pro2842=) n.802T>C c.8703T>C (p.Pro2901=) n.474T>C c.7638T>C (p.Pro2546=) | |
| 1 | g.214657150T>G | CA423429617 | CENPF | c.8526T>G (p.Pro2842=) n.802T>G c.8703T>G (p.Pro2901=) n.474T>G c.7638T>G (p.Pro2546=) | |
| 1 | g.214657151T>A | CA344856960 | CENPF | c.8527T>A (p.Leu2843Met) n.803T>A c.8704T>A (p.Leu2902Met) n.475T>A c.7639T>A (p.Leu2547Met) | |
| 1 | g.214657151T>C | CA423429620 | CENPF | c.8527T>C (p.Leu2843=) n.803T>C c.8704T>C (p.Leu2902=) n.475T>C c.7639T>C (p.Leu2547=) | |
| 1 | g.214657151T>G | CA344856961 | CENPF | c.8527T>G (p.Leu2843Val) n.803T>G c.8704T>G (p.Leu2902Val) n.475T>G c.7639T>G (p.Leu2547Val) | |
| 1 | g.214657152T>A | CA344856962 | CENPF | c.8528T>A (p.Leu2843Ter) n.804T>A c.8705T>A (p.Leu2902Ter) n.476T>A c.7640T>A (p.Leu2547Ter) | |
| 1 | g.214657152T>C | CA344856964 | CENPF | c.8528T>C (p.Leu2843Ser) n.804T>C c.8705T>C (p.Leu2902Ser) n.476T>C c.7640T>C (p.Leu2547Ser) | |
| 1 | g.214657152T>G | CA344856963 | CENPF | c.8528T>G (p.Leu2843Trp) n.804T>G c.8705T>G (p.Leu2902Trp) n.476T>G c.7640T>G (p.Leu2547Trp) | |
| 1 | g.214657153G>A | CA423429627 | CENPF | c.8529G>A (p.Leu2843=) n.805G>A c.8706G>A (p.Leu2902=) n.477G>A c.7641G>A (p.Leu2547=) | |
| 1 | g.214657153G>C | CA344856965 | CENPF | c.8529G>C (p.Leu2843Phe) n.805G>C c.8706G>C (p.Leu2902Phe) n.477G>C c.7641G>C (p.Leu2547Phe) | |
| 1 | g.214657153G>T | CA344856966 | CENPF | c.8529G>T (p.Leu2843Phe) n.805G>T c.8706G>T (p.Leu2902Phe) n.477G>T c.7641G>T (p.Leu2547Phe) | |
| 1 | g.214657154C>A | CA344856967 | CENPF | c.8530C>A (p.Leu2844Ile) n.806C>A c.8707C>A (p.Leu2903Ile) n.478C>A c.7642C>A (p.Leu2548Ile) | |
| 1 | g.214657154C>G | CA344856968 | CENPF | c.8530C>G (p.Leu2844Val) n.806C>G c.8707C>G (p.Leu2903Val) n.478C>G c.7642C>G (p.Leu2548Val) | |
| 1 | g.214657154C>T | CA423429634 | CENPF | c.8530C>T (p.Leu2844=) n.806C>T c.8707C>T (p.Leu2903=) n.478C>T c.7642C>T (p.Leu2548=) | |
| 1 | g.214657155T>A | CA344856969 | CENPF | c.8531T>A (p.Leu2844Gln) n.807T>A c.8708T>A (p.Leu2903Gln) n.479T>A c.7643T>A (p.Leu2548Gln) | |
| 1 | g.214657155T>C | CA344856970 | CENPF | c.8531T>C (p.Leu2844Pro) n.807T>C c.8708T>C (p.Leu2903Pro) n.479T>C c.7643T>C (p.Leu2548Pro) | |
| 1 | g.214657155T>G | CA344856971 | CENPF | c.8531T>G (p.Leu2844Arg) n.807T>G c.8708T>G (p.Leu2903Arg) n.479T>G c.7643T>G (p.Leu2548Arg) | COSMIC |
| 1 | g.214657156A= | CA2486377644 | CENPF | c.8532A= (p.Leu2844=) n.808A= c.8709A= (p.Leu2903=) n.480A= c.7644A= (p.Leu2548=) | |
| 1 | g.214657156A>C | CA423429640 | CENPF | c.8532A>C (p.Leu2844=) n.808A>C c.8709A>C (p.Leu2903=) n.480A>C c.7644A>C (p.Leu2548=) | |
| 1 | g.214657156A>G | CA1391478 | CENPF | c.8532A>G (p.Leu2844=) n.808A>G c.8709A>G (p.Leu2903=) n.480A>G c.7644A>G (p.Leu2548=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657156A>T | CA423429641 | CENPF | c.8532A>T (p.Leu2844=) n.808A>T c.8709A>T (p.Leu2903=) n.480A>T c.7644A>T (p.Leu2548=) | gnomAD v4 |
| 1 | g.214657157G>A | CA37381142 | CENPF | c.8533G>A (p.Gly2845Ser) n.809G>A c.8710G>A (p.Gly2904Ser) n.481G>A c.7645G>A (p.Gly2549Ser) | dbSNP |
| 1 | g.214657157G>C | CA37381150 | CENPF | c.8533G>C (p.Gly2845Arg) n.809G>C c.8710G>C (p.Gly2904Arg) n.481G>C c.7645G>C (p.Gly2549Arg) | dbSNP gnomAD v4 |
| 1 | g.214657157G= | CA2486377645 | CENPF | c.8533G= (p.Gly2845=) n.809G= c.8710G= (p.Gly2904=) n.481G= c.7645G= (p.Gly2549=) | |
| 1 | g.214657157G>T | CA344856972 | CENPF | c.8533G>T (p.Gly2845Cys) n.809G>T c.8710G>T (p.Gly2904Cys) n.481G>T c.7645G>T (p.Gly2549Cys) | |
| 1 | g.214657158G>A | CA344856974 | CENPF | c.8534G>A (p.Gly2845Asp) n.810G>A c.8711G>A (p.Gly2904Asp) n.482G>A c.7646G>A (p.Gly2549Asp) | dbSNP |
| 1 | g.214657158G>C | CA344856973 | CENPF | c.8534G>C (p.Gly2845Ala) n.810G>C c.8711G>C (p.Gly2904Ala) n.482G>C c.7646G>C (p.Gly2549Ala) | |
| 1 | g.214657158G= | CA1145746558 | CENPF | c.8534G= (p.Gly2845=) n.810G= c.8711G= (p.Gly2904=) n.482G= c.7646G= (p.Gly2549=) | |
| 1 | g.214657158G>T | CA1391479 | CENPF | c.8534G>T (p.Gly2845Val) n.810G>T c.8711G>T (p.Gly2904Val) n.482G>T c.7646G>T (p.Gly2549Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657159T>A | CA423429651 | CENPF | c.8535T>A (p.Gly2845=) n.811T>A c.8712T>A (p.Gly2904=) n.483T>A c.7647T>A (p.Gly2549=) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.214657159T>C | CA423429652 | CENPF | c.8535T>C (p.Gly2845=) n.811T>C c.8712T>C (p.Gly2904=) n.483T>C c.7647T>C (p.Gly2549=) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.214657159T>G | CA423429654 | CENPF | c.8535T>G (p.Gly2845=) n.811T>G c.8712T>G (p.Gly2904=) n.483T>G c.7647T>G (p.Gly2549=) | |
| 1 | g.214657159T= | CA2486377646 | CENPF | c.8535T= (p.Gly2845=) n.811T= c.8712T= (p.Gly2904=) n.483T= c.7647T= (p.Gly2549=) | |
| 1 | g.214657160C>A | CA344856975 | CENPF | c.8536C>A (p.Pro2846Thr) n.812C>A c.8713C>A (p.Pro2905Thr) n.484C>A c.7648C>A (p.Pro2550Thr) | |
| 1 | g.214657160C>G | CA344856976 | CENPF | c.8536C>G (p.Pro2846Ala) n.812C>G c.8713C>G (p.Pro2905Ala) n.484C>G c.7648C>G (p.Pro2550Ala) | |
| 1 | g.214657160C>T | CA344856977 | CENPF | c.8536C>T (p.Pro2846Ser) n.812C>T c.8713C>T (p.Pro2905Ser) n.484C>T c.7648C>T (p.Pro2550Ser) | |
| 1 | g.214657161C>A | CA344856978 | CENPF | c.8537C>A (p.Pro2846Gln) n.813C>A c.8714C>A (p.Pro2905Gln) n.485C>A c.7649C>A (p.Pro2550Gln) | |
| 1 | g.214657161C>G | CA344856979 | CENPF | c.8537C>G (p.Pro2846Arg) n.813C>G c.8714C>G (p.Pro2905Arg) n.485C>G c.7649C>G (p.Pro2550Arg) | |
| 1 | g.214657161C>T | CA344856980 | CENPF | c.8537C>T (p.Pro2846Leu) n.813C>T c.8714C>T (p.Pro2905Leu) n.485C>T c.7649C>T (p.Pro2550Leu) | gnomAD v4 |
| 1 | g.214657162A= | CA2486377647 | CENPF | c.8538A= (p.Pro2846=) n.814A= c.8715A= (p.Pro2905=) n.486A= c.7650A= (p.Pro2550=) | |
| 1 | g.214657162A>C | CA423429662 | CENPF | c.8538A>C (p.Pro2846=) n.814A>C c.8715A>C (p.Pro2905=) n.486A>C c.7650A>C (p.Pro2550=) | |
| 1 | g.214657162A>G | CA423429664 | CENPF | c.8538A>G (p.Pro2846=) n.814A>G c.8715A>G (p.Pro2905=) n.486A>G c.7650A>G (p.Pro2550=) | dbSNP gnomAD v4 |
| 1 | g.214657162A>T | CA423429665 | CENPF | c.8538A>T (p.Pro2846=) n.814A>T c.8715A>T (p.Pro2905=) n.486A>T c.7650A>T (p.Pro2550=) | |
| 1 | g.214657163G>A | CA344856981 | CENPF | c.8539G>A (p.Val2847Ile) n.815G>A c.8716G>A (p.Val2906Ile) n.487G>A c.7651G>A (p.Val2551Ile) | gnomAD v4 |
| 1 | g.214657163G>C | CA344856982 | CENPF | c.8539G>C (p.Val2847Leu) n.815G>C c.8716G>C (p.Val2906Leu) n.487G>C c.7651G>C (p.Val2551Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.214657163G= | CA2486377648 | CENPF | c.8539G= (p.Val2847=) n.815G= c.8716G= (p.Val2906=) n.487G= c.7651G= (p.Val2551=) | |
| 1 | g.214657163G>T | CA37381165 | CENPF | c.8539G>T (p.Val2847Phe) n.815G>T c.8716G>T (p.Val2906Phe) n.487G>T c.7651G>T (p.Val2551Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657164T>A | CA344856983 | CENPF | c.8540T>A (p.Val2847Asp) n.816T>A c.8717T>A (p.Val2906Asp) n.488T>A c.7652T>A (p.Val2551Asp) | |
| 1 | g.214657164T>C | CA344856984 | CENPF | c.8540T>C (p.Val2847Ala) n.816T>C c.8717T>C (p.Val2906Ala) n.488T>C c.7652T>C (p.Val2551Ala) | |
| 1 | g.214657164T>G | CA344856985 | CENPF | c.8540T>G (p.Val2847Gly) n.816T>G c.8717T>G (p.Val2906Gly) n.488T>G c.7652T>G (p.Val2551Gly) | |
| 1 | g.214657165T>A | CA423429671 | CENPF | c.8541T>A (p.Val2847=) n.817T>A c.8718T>A (p.Val2906=) n.489T>A c.7653T>A (p.Val2551=) | |
| 1 | g.214657165T>C | CA423429672 | CENPF | c.8541T>C (p.Val2847=) n.817T>C c.8718T>C (p.Val2906=) n.489T>C c.7653T>C (p.Val2551=) | |
| 1 | g.214657165T>G | CA423429674 | CENPF | c.8541T>G (p.Val2847=) n.817T>G c.8718T>G (p.Val2906=) n.489T>G c.7653T>G (p.Val2551=) | |
| 1 | g.214657166G>A | CA344856988 | CENPF | c.8542G>A (p.Val2848Ile) n.818G>A c.8719G>A (p.Val2907Ile) n.490G>A c.7654G>A (p.Val2552Ile) | |
| 1 | g.214657166G>C | CA344856987 | CENPF | c.8542G>C (p.Val2848Leu) n.818G>C c.8719G>C (p.Val2907Leu) n.490G>C c.7654G>C (p.Val2552Leu) | |
| 1 | g.214657166G>T | CA344856986 | CENPF | c.8542G>T (p.Val2848Phe) n.818G>T c.8719G>T (p.Val2907Phe) n.490G>T c.7654G>T (p.Val2552Phe) | gnomAD v4 |
| 1 | g.214657167T>A | CA344856989 | CENPF | c.8543T>A (p.Val2848Asp) n.819T>A c.8720T>A (p.Val2907Asp) n.491T>A c.7655T>A (p.Val2552Asp) | |
| 1 | g.214657167T>C | CA344856990 | CENPF | c.8543T>C (p.Val2848Ala) n.819T>C c.8720T>C (p.Val2907Ala) n.491T>C c.7655T>C (p.Val2552Ala) | |
| 1 | g.214657167T>G | CA344856991 | CENPF | c.8543T>G (p.Val2848Gly) n.819T>G c.8720T>G (p.Val2907Gly) n.491T>G c.7655T>G (p.Val2552Gly) | |
| 1 | g.214657168T>A | CA423429678 | CENPF | c.8544T>A (p.Val2848=) n.820T>A c.8721T>A (p.Val2907=) n.492T>A c.7656T>A (p.Val2552=) | |
| 1 | g.214657168T>C | CA423429679 | CENPF | c.8544T>C (p.Val2848=) n.820T>C c.8721T>C (p.Val2907=) n.492T>C c.7656T>C (p.Val2552=) | |
| 1 | g.214657168T>G | CA423429680 | CENPF | c.8544T>G (p.Val2848=) n.820T>G c.8721T>G (p.Val2907=) n.492T>G c.7656T>G (p.Val2552=) | |
| 1 | g.214657169C>A | CA344856992 | CENPF | c.8545C>A (p.Pro2849Thr) n.821C>A c.8722C>A (p.Pro2908Thr) n.493C>A c.7657C>A (p.Pro2553Thr) | |
| 1 | g.214657169C= | CA2486377649 | CENPF | c.8545C= (p.Pro2849=) n.821C= c.8722C= (p.Pro2908=) n.493C= c.7657C= (p.Pro2553=) | |
| 1 | g.214657169C>G | CA344856993 | CENPF | c.8545C>G (p.Pro2849Ala) n.821C>G c.8722C>G (p.Pro2908Ala) n.493C>G c.7657C>G (p.Pro2553Ala) | dbSNP |
| 1 | g.214657169C>T | CA344856994 | CENPF | c.8545C>T (p.Pro2849Ser) n.821C>T c.8722C>T (p.Pro2908Ser) n.493C>T c.7657C>T (p.Pro2553Ser) | COSMIC |
| 1 | g.214657170C>A | CA344856995 | CENPF | c.8546C>A (p.Pro2849Gln) n.822C>A c.8723C>A (p.Pro2908Gln) n.494C>A c.7658C>A (p.Pro2553Gln) | |
| 1 | g.214657170C>G | CA344856996 | CENPF | c.8546C>G (p.Pro2849Arg) n.822C>G c.8723C>G (p.Pro2908Arg) n.494C>G c.7658C>G (p.Pro2553Arg) | |
| 1 | g.214657170C>T | CA344856997 | CENPF | c.8546C>T (p.Pro2849Leu) n.822C>T c.8723C>T (p.Pro2908Leu) n.494C>T c.7658C>T (p.Pro2553Leu) | |
| 1 | g.214657171A= | CA1147510854 | CENPF | c.8547A= (p.Pro2849=) n.823A= c.8724A= (p.Pro2908=) n.495A= c.7659A= (p.Pro2553=) | |
| 1 | g.214657171A>C | CA423429696 | CENPF | c.8547A>C (p.Pro2849=) n.823A>C c.8724A>C (p.Pro2908=) n.495A>C c.7659A>C (p.Pro2553=) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.214657171A>G | CA37381169 | CENPF | c.8547A>G (p.Pro2849=) n.823A>G c.8724A>G (p.Pro2908=) n.495A>G c.7659A>G (p.Pro2553=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657171A>T | CA423429694 | CENPF | c.8547A>T (p.Pro2849=) n.823A>T c.8724A>T (p.Pro2908=) n.495A>T c.7659A>T (p.Pro2553=) | |
| 1 | g.214657172G>A | CA344856998 | CENPF | c.8548G>A (p.Gly2850Arg) n.824G>A c.8725G>A (p.Gly2909Arg) n.496G>A c.7660G>A (p.Gly2554Arg) | gnomAD v4 |
| 1 | g.214657172G>C | CA344856999 | CENPF | c.8548G>C (p.Gly2850Arg) n.824G>C c.8725G>C (p.Gly2909Arg) n.496G>C c.7660G>C (p.Gly2554Arg) | |
| 1 | g.214657172G>T | CA344857000 | CENPF | c.8548G>T (p.Gly2850Ter) n.824G>T c.8725G>T (p.Gly2909Ter) n.496G>T c.7660G>T (p.Gly2554Ter) | |
| 1 | g.214657173G>A | CA344857003 | CENPF | c.8549G>A (p.Gly2850Glu) n.825G>A c.8726G>A (p.Gly2909Glu) n.497G>A c.7661G>A (p.Gly2554Glu) | |
| 1 | g.214657173G>C | CA344857001 | CENPF | c.8549G>C (p.Gly2850Ala) n.825G>C c.8726G>C (p.Gly2909Ala) n.497G>C c.7661G>C (p.Gly2554Ala) | |
| 1 | g.214657173G>T | CA344857002 | CENPF | c.8549G>T (p.Gly2850Val) n.825G>T c.8726G>T (p.Gly2909Val) n.497G>T c.7661G>T (p.Gly2554Val) | |
| 1 | g.214657174A>C | CA423429701 | CENPF | c.8550A>C (p.Gly2850=) n.826A>C c.8727A>C (p.Gly2909=) n.498A>C c.7662A>C (p.Gly2554=) | |
| 1 | g.214657174A>G | CA423429703 | CENPF | c.8550A>G (p.Gly2850=) n.826A>G c.8727A>G (p.Gly2909=) n.498A>G c.7662A>G (p.Gly2554=) | |
| 1 | g.214657174A>T | CA423429704 | CENPF | c.8550A>T (p.Gly2850=) n.826A>T c.8727A>T (p.Gly2909=) n.498A>T c.7662A>T (p.Gly2554=) | |
| 1 | g.214657174_214657175delinsAC | CA2486377650 | CENPF | c.8550_8551delinsAC (p.Gly2850=) n.826_827delinsAC c.8727_8728delinsAC (p.Gly2909=) n.498_499delinsAC c.7662_7663delinsAC (p.Gly2554=) | |
| 1 | g.214657175C>A | CA344857004 | CENPF | c.8551C>A (p.Pro2851Thr) n.827C>A c.8728C>A (p.Pro2910Thr) n.499C>A c.7663C>A (p.Pro2555Thr) | |
| 1 | g.214657175C>G | CA344857005 | CENPF | c.8551C>G (p.Pro2851Ala) n.827C>G c.8728C>G (p.Pro2910Ala) n.499C>G c.7663C>G (p.Pro2555Ala) | |
| 1 | g.214657175C>T | CA344857006 | CENPF | c.8551C>T (p.Pro2851Ser) n.827C>T c.8728C>T (p.Pro2910Ser) n.499C>T c.7663C>T (p.Pro2555Ser) | |
| 1 | g.214657176del | CA1391480 | CENPF | c.8552del (p.Pro2851HisfsTer?) n.828del c.8729del (p.Pro2910HisfsTer?) n.500del c.7664del (p.Pro2555HisfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657176C>A | CA344857007 | CENPF | c.8552C>A (p.Pro2851Gln) n.828C>A c.8729C>A (p.Pro2910Gln) n.500C>A c.7664C>A (p.Pro2555Gln) | |
| 1 | g.214657176C= | CA2486377651 | CENPF | c.8552C= (p.Pro2851=) n.828C= c.8729C= (p.Pro2910=) n.500C= c.7664C= (p.Pro2555=) | |
| 1 | g.214657176C>G | CA344857008 | CENPF | c.8552C>G (p.Pro2851Arg) n.828C>G c.8729C>G (p.Pro2910Arg) n.500C>G c.7664C>G (p.Pro2555Arg) | |
| 1 | g.214657176C>T | CA1391481 | CENPF | c.8552C>T (p.Pro2851Leu) n.828C>T c.8729C>T (p.Pro2910Leu) n.500C>T c.7664C>T (p.Pro2555Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657177A>C | CA423429714 | CENPF | c.8553A>C (p.Pro2851=) n.829A>C c.8730A>C (p.Pro2910=) n.501A>C c.7665A>C (p.Pro2555=) | |
| 1 | g.214657177A>G | CA423429717 | CENPF | c.8553A>G (p.Pro2851=) n.829A>G c.8730A>G (p.Pro2910=) n.501A>G c.7665A>G (p.Pro2555=) | gnomAD v4 |
| 1 | g.214657177A>T | CA423429718 | CENPF | c.8553A>T (p.Pro2851=) n.829A>T c.8730A>T (p.Pro2910=) n.501A>T c.7665A>T (p.Pro2555=) | |
| 1 | g.214657178T>A | CA344857009 | CENPF | c.8554T>A (p.Ser2852Thr) n.830T>A c.8731T>A (p.Ser2911Thr) n.502T>A c.7666T>A (p.Ser2556Thr) | |
| 1 | g.214657178T>C | CA344857010 | CENPF | c.8554T>C (p.Ser2852Pro) n.830T>C c.8731T>C (p.Ser2911Pro) n.502T>C c.7666T>C (p.Ser2556Pro) | |
| 1 | g.214657178T>G | CA344857011 | CENPF | c.8554T>G (p.Ser2852Ala) n.830T>G c.8731T>G (p.Ser2911Ala) n.502T>G c.7666T>G (p.Ser2556Ala) | gnomAD v4 |
| 1 | g.214657179C>A | CA344857012 | CENPF | c.8555C>A (p.Ser2852Tyr) n.831C>A c.8732C>A (p.Ser2911Tyr) n.503C>A c.7667C>A (p.Ser2556Tyr) | |
| 1 | g.214657179C= | CA2486377652 | CENPF | c.8555C= (p.Ser2852=) n.831C= c.8732C= (p.Ser2911=) n.503C= c.7667C= (p.Ser2556=) | |
| 1 | g.214657179C>G | CA344857013 | CENPF | c.8555C>G (p.Ser2852Cys) n.831C>G c.8732C>G (p.Ser2911Cys) n.503C>G c.7667C>G (p.Ser2556Cys) | |
| 1 | g.214657179C>T | CA1391482 | CENPF | c.8555C>T (p.Ser2852Phe) n.831C>T c.8732C>T (p.Ser2911Phe) n.503C>T c.7667C>T (p.Ser2556Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657180T>A | CA423429723 | CENPF | c.8556T>A (p.Ser2852=) n.832T>A c.8733T>A (p.Ser2911=) n.504T>A c.7668T>A (p.Ser2556=) | |
| 1 | g.214657180T>C | CA423429726 | CENPF | c.8556T>C (p.Ser2852=) n.832T>C c.8733T>C (p.Ser2911=) n.504T>C c.7668T>C (p.Ser2556=) | |
| 1 | g.214657180T>G | CA423429728 | CENPF | c.8556T>G (p.Ser2852=) n.832T>G c.8733T>G (p.Ser2911=) n.504T>G c.7668T>G (p.Ser2556=) | |
| 1 | g.214657181C>A | CA344857014 | CENPF | c.8557C>A (p.Pro2853Thr) n.833C>A c.8734C>A (p.Pro2912Thr) n.505C>A c.7669C>A (p.Pro2557Thr) | |
| 1 | g.214657181C= | CA2486377653 | CENPF | c.8557C= (p.Pro2853=) n.833C= c.8734C= (p.Pro2912=) n.505C= c.7669C= (p.Pro2557=) | |
| 1 | g.214657181C>G | CA344857015 | CENPF | c.8557C>G (p.Pro2853Ala) n.833C>G c.8734C>G (p.Pro2912Ala) n.505C>G c.7669C>G (p.Pro2557Ala) | gnomAD v4 |
| 1 | g.214657181C>T | CA1391483 | CENPF | c.8557C>T (p.Pro2853Ser) n.833C>T c.8734C>T (p.Pro2912Ser) n.505C>T c.7669C>T (p.Pro2557Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657182C>A | CA344857016 | CENPF | c.8558C>A (p.Pro2853Gln) n.834C>A c.8735C>A (p.Pro2912Gln) n.506C>A c.7670C>A (p.Pro2557Gln) | |
| 1 | g.214657182C>G | CA344857018 | CENPF | c.8558C>G (p.Pro2853Arg) n.834C>G c.8735C>G (p.Pro2912Arg) n.506C>G c.7670C>G (p.Pro2557Arg) | |
| 1 | g.214657182C>T | CA344857017 | CENPF | c.8558C>T (p.Pro2853Leu) n.834C>T c.8735C>T (p.Pro2912Leu) n.506C>T c.7670C>T (p.Pro2557Leu) | |
| 1 | g.214657183A= | CA1141770945 | CENPF | c.8559A= (p.Pro2853=) n.835A= c.8736A= (p.Pro2912=) n.507A= c.7671A= (p.Pro2557=) | |
| 1 | g.214657183A>C | CA1391484 | CENPF | c.8559A>C (p.Pro2853=) n.835A>C c.8736A>C (p.Pro2912=) n.507A>C c.7671A>C (p.Pro2557=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.214657183A>G | CA423429734 | CENPF | c.8559A>G (p.Pro2853=) n.835A>G c.8736A>G (p.Pro2912=) n.507A>G c.7671A>G (p.Pro2557=) | |
| 1 | g.214657183A>T | CA423429735 | CENPF | c.8559A>T (p.Pro2853=) n.835A>T c.8736A>T (p.Pro2912=) n.507A>T c.7671A>T (p.Pro2557=) | |
| 1 | g.214657184A= | CA2486377654 | CENPF | c.8560A= (p.Ile2854=) n.836A= c.8737A= (p.Ile2913=) n.508A= c.7672A= (p.Ile2558=) | |
| 1 | g.214657184A>C | CA344857020 | CENPF | c.8560A>C (p.Ile2854Leu) n.836A>C c.8737A>C (p.Ile2913Leu) n.508A>C c.7672A>C (p.Ile2558Leu) | gnomAD v4 |
| 1 | g.214657184A>G | CA1391485 | CENPF | c.8560A>G (p.Ile2854Val) n.836A>G c.8737A>G (p.Ile2913Val) n.508A>G c.7672A>G (p.Ile2558Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657184A>T | CA344857019 | CENPF | c.8560A>T (p.Ile2854Phe) n.836A>T c.8737A>T (p.Ile2913Phe) n.508A>T c.7672A>T (p.Ile2558Phe) | |
| 1 | g.214657185T>A | CA344857021 | CENPF | c.8561T>A (p.Ile2854Asn) n.837T>A c.8738T>A (p.Ile2913Asn) n.509T>A c.7673T>A (p.Ile2558Asn) | |
| 1 | g.214657185T>C | CA344857022 | CENPF | c.8561T>C (p.Ile2854Thr) n.837T>C c.8738T>C (p.Ile2913Thr) n.509T>C c.7673T>C (p.Ile2558Thr) | |
| 1 | g.214657185T>G | CA344857023 | CENPF | c.8561T>G (p.Ile2854Ser) n.837T>G c.8738T>G (p.Ile2913Ser) n.509T>G c.7673T>G (p.Ile2558Ser) | |
| 1 | g.214657186C>A | CA423429743 | CENPF | c.8562C>A (p.Ile2854=) n.838C>A c.8739C>A (p.Ile2913=) n.510C>A c.7674C>A (p.Ile2558=) | dbSNP gnomAD v4 |
| 1 | g.214657186C= | CA2486377655 | CENPF | c.8562C= (p.Ile2854=) n.838C= c.8739C= (p.Ile2913=) n.510C= c.7674C= (p.Ile2558=) | |
| 1 | g.214657186C>G | CA344857024 | CENPF | c.8562C>G (p.Ile2854Met) n.838C>G c.8739C>G (p.Ile2913Met) n.510C>G c.7674C>G (p.Ile2558Met) | gnomAD v4 |
| 1 | g.214657186C>T | CA423429746 | CENPF | c.8562C>T (p.Ile2854=) n.838C>T c.8739C>T (p.Ile2913=) n.510C>T c.7674C>T (p.Ile2558=) | |
| 1 | g.214657187C>A | CA344857025 | CENPF | c.8563C>A (p.Pro2855Thr) n.839C>A c.8740C>A (p.Pro2914Thr) n.511C>A c.7675C>A (p.Pro2559Thr) | |
| 1 | g.214657187C= | CA2486377656 | CENPF | c.8563C= (p.Pro2855=) n.839C= c.8740C= (p.Pro2914=) n.511C= c.7675C= (p.Pro2559=) | |
| 1 | g.214657187C>G | CA344857026 | CENPF | c.8563C>G (p.Pro2855Ala) n.839C>G c.8740C>G (p.Pro2914Ala) n.511C>G c.7675C>G (p.Pro2559Ala) | |
| 1 | g.214657187C>T | CA344857027 | CENPF | c.8563C>T (p.Pro2855Ser) n.839C>T c.8740C>T (p.Pro2914Ser) n.511C>T c.7675C>T (p.Pro2559Ser) | dbSNP gnomAD v4 |
| 1 | g.214657188C>A | CA344857028 | CENPF | c.8564C>A (p.Pro2855His) n.840C>A c.8741C>A (p.Pro2914His) n.512C>A c.7676C>A (p.Pro2559His) | |
| 1 | g.214657188C= | CA2486377657 | CENPF | c.8564C= (p.Pro2855=) n.840C= c.8741C= (p.Pro2914=) n.512C= c.7676C= (p.Pro2559=) | |
| 1 | g.214657188C>G | CA344857029 | CENPF | c.8564C>G (p.Pro2855Arg) n.840C>G c.8741C>G (p.Pro2914Arg) n.512C>G c.7676C>G (p.Pro2559Arg) | |
| 1 | g.214657188C>T | CA344857030 | CENPF | c.8564C>T (p.Pro2855Leu) n.840C>T c.8741C>T (p.Pro2914Leu) n.512C>T c.7676C>T (p.Pro2559Leu) | dbSNP gnomAD v2 gnomAD v4 COSMIC |