| 597798987 | CV3653963 | single nucleotide variant | NM_015442.3(CNOT10):c.4G>A (p.Ala2Thr) | not specified [RCV004904977] | uncertain significance | 3 | 32685464 | 32685464 | Human | | name |
| 405674083 | CV3304581 | single nucleotide variant | NM_015442.3(CNOT10):c.29G>A (p.Gly10Glu) | not specified [RCV004441966] | uncertain significance | 3 | 32703874 | 32703874 | Human | | name |
| 597798982 | CV3653960 | single nucleotide variant | NM_015442.3(CNOT10):c.71C>G (p.Thr24Ser) | not specified [RCV004904974] | uncertain significance | 3 | 32703916 | 32703916 | Human | | name |
| 597798985 | CV3653962 | single nucleotide variant | NM_015442.3(CNOT10):c.549C>T (p.Asn183=) | not specified [RCV004904976] | likely benign | 3 | 32713345 | 32713345 | Human | | name |
| 598257801 | CV3941293 | single nucleotide variant | NM_015442.3(CNOT10):c.32C>G (p.Ala11Gly) | not specified [RCV005324491] | uncertain significance | 3 | 32703877 | 32703877 | Human | | name |
| 598257807 | CV3941295 | single nucleotide variant | NM_015442.3(CNOT10):c.41A>G (p.His14Arg) | not specified [RCV005324492] | uncertain significance | 3 | 32703886 | 32703886 | Human | | name |
| 156366505 | CV2203343 | single nucleotide variant | NM_015442.3(CNOT10):c.853A>G (p.Met285Val) | not specified [RCV004072575] | uncertain significance | 3 | 32720222 | 32720222 | Human | | name |
| 155978559 | CV2222707 | single nucleotide variant | NM_015442.3(CNOT10):c.749C>T (p.Ala250Val) | not specified [RCV004101563] | uncertain significance | 3 | 32720118 | 32720118 | Human | | name |
| 156390061 | CV2223014 | single nucleotide variant | NM_015442.3(CNOT10):c.703T>C (p.Cys235Arg) | not specified [RCV004103601] | uncertain significance | 3 | 32717196 | 32717196 | Human | | name |
| 156359797 | CV2257949 | single nucleotide variant | NM_015442.3(CNOT10):c.371G>A (p.Arg124Gln) | not specified [RCV004129763] | uncertain significance | 3 | 32708761 | 32708761 | Human | | name |
| 156153066 | CV2265961 | single nucleotide variant | NM_015442.3(CNOT10):c.674C>T (p.Ala225Val) | not specified [RCV004126801] | uncertain significance | 3 | 32717167 | 32717167 | Human | | name |
| 155910380 | CV2303583 | single nucleotide variant | NM_015442.3(CNOT10):c.300A>C (p.Glu100Asp) | not specified [RCV004161669] | uncertain significance | 3 | 32708690 | 32708690 | Human | | name |
| 156248491 | CV2307206 | single nucleotide variant | NM_015442.3(CNOT10):c.607C>T (p.His203Tyr) | not specified [RCV004159673] | uncertain significance | 3 | 32716258 | 32716258 | Human | | name |
| 155922354 | CV2340607 | single nucleotide variant | NM_015442.3(CNOT10):c.587A>G (p.Asn196Ser) | not specified [RCV004197315] | uncertain significance | 3 | 32716238 | 32716238 | Human | | name |
| 156217663 | CV2348170 | single nucleotide variant | NM_015442.3(CNOT10):c.370C>T (p.Arg124Trp) | not specified [RCV004190814] | uncertain significance | 3 | 32708760 | 32708760 | Human | | name |
| 156080105 | CV2351241 | single nucleotide variant | NM_015442.3(CNOT10):c.808G>A (p.Val270Met) | not specified [RCV004214088] | uncertain significance | 3 | 32720177 | 32720177 | Human | | name |
| 329365736 | CV2441088 | single nucleotide variant | NM_015442.3(CNOT10):c.652A>C (p.Ile218Leu) | not specified [RCV004261447] | uncertain significance | 3 | 32716303 | 32716303 | Human | | name |
| 401740002 | CV2709766 | single nucleotide variant | NM_015442.3(CNOT10):c.752C>T (p.Pro251Leu) | not specified [RCV004320750] | uncertain significance | 3 | 32720121 | 32720121 | Human | | name |
| 401736970 | CV2717868 | single nucleotide variant | NM_015442.3(CNOT10):c.451G>A (p.Val151Met) | not specified [RCV004321840] | uncertain significance | 3 | 32713247 | 32713247 | Human | | name |
| 401889965 | CV2762037 | single nucleotide variant | NM_015442.3(CNOT10):c.881T>C (p.Met294Thr) | not specified [RCV004341857] | uncertain significance | 3 | 32725468 | 32725468 | Human | | name |
| 405674087 | CV3304582 | single nucleotide variant | NM_015442.3(CNOT10):c.352G>A (p.Val118Ile) | not specified [RCV004441967] | uncertain significance | 3 | 32708742 | 32708742 | Human | | name |
| 405674091 | CV3304583 | single nucleotide variant | NM_015442.3(CNOT10):c.551A>G (p.Asn184Ser) | not specified [RCV004441968] | uncertain significance | 3 | 32713347 | 32713347 | Human | | name |
| 405674095 | CV3304584 | single nucleotide variant | NM_015442.3(CNOT10):c.649A>C (p.Lys217Gln) | not specified [RCV004441969] | uncertain significance | 3 | 32716300 | 32716300 | Human | | name |
| 405674099 | CV3304585 | single nucleotide variant | NM_015442.3(CNOT10):c.835G>A (p.Ala279Thr) | not specified [RCV004441970] | uncertain significance | 3 | 32720204 | 32720204 | Human | | name |
| 405674102 | CV3304586 | single nucleotide variant | NM_015442.3(CNOT10):c.944A>G (p.Tyr315Cys) | not specified [RCV004441971] | uncertain significance | 3 | 32725531 | 32725531 | Human | | name |
| 407470534 | CV3425694 | single nucleotide variant | NM_015442.3(CNOT10):c.844C>T (p.Pro282Ser) | not specified [RCV004615470] | uncertain significance | 3 | 32720213 | 32720213 | Human | | name |
| 407470542 | CV3425696 | single nucleotide variant | NM_015442.3(CNOT10):c.955G>T (p.Ala319Ser) | not specified [RCV004615472] | uncertain significance | 3 | 32725542 | 32725542 | Human | | name |
| 407470546 | CV3425697 | single nucleotide variant | NM_015442.3(CNOT10):c.729G>A (p.Met243Ile) | not specified [RCV004615473] | uncertain significance | 3 | 32717222 | 32717222 | Human | | name |
| 597798991 | CV3650459 | single nucleotide variant | NM_015442.3(CNOT10):c.331A>T (p.Met111Leu) | not specified [RCV004904979] | uncertain significance | 3 | 32708721 | 32708721 | Human | | name |
| 597798978 | CV3653958 | single nucleotide variant | NM_015442.3(CNOT10):c.329G>A (p.Ser110Asn) | not specified [RCV004904972] | uncertain significance | 3 | 32708719 | 32708719 | Human | | name |
| 598257812 | CV3941296 | single nucleotide variant | NM_015442.3(CNOT10):c.478A>G (p.Ile160Val) | not specified [RCV005324493] | uncertain significance | 3 | 32713274 | 32713274 | Human | | name |
| 598257823 | CV3941298 | single nucleotide variant | NM_015442.3(CNOT10):c.914C>T (p.Ala305Val) | not specified [RCV005324495] | uncertain significance | 3 | 32725501 | 32725501 | Human | | name |
| 155968048 | CV2261951 | single nucleotide variant | NM_015442.3(CNOT10):c.2150A>T (p.Glu717Val) | not specified [RCV004126447] | uncertain significance | 3 | 32773526 | 32773526 | Human | | name |
| 156096120 | CV2297424 | single nucleotide variant | NM_015442.3(CNOT10):c.2116A>C (p.Asn706His) | not specified [RCV004153365] | uncertain significance | 3 | 32773492 | 32773492 | Human | | name |
| 156056178 | CV2320592 | single nucleotide variant | NM_015442.3(CNOT10):c.1517G>T (p.Ser506Ile) | not specified [RCV004172213] | uncertain significance | 3 | 32737412 | 32737412 | Human | | name |
| 155902890 | CV2356546 | single nucleotide variant | NM_015442.3(CNOT10):c.1543A>G (p.Ile515Val) | not specified [RCV004199456] | uncertain significance | 3 | 32737438 | 32737438 | Human | | name |
| 156386876 | CV2364874 | single nucleotide variant | NM_015442.3(CNOT10):c.1543A>C (p.Ile515Leu) | not specified [RCV004219733] | uncertain significance | 3 | 32737438 | 32737438 | Human | | name |
| 329385629 | CV2432134 | single nucleotide variant | NM_015442.3(CNOT10):c.1387A>G (p.Ile463Val) | not specified [RCV004249280] | uncertain significance | 3 | 32734849 | 32734849 | Human | | name |
| 329395177 | CV2458186 | single nucleotide variant | NM_015442.3(CNOT10):c.1313A>G (p.Gln438Arg) | not specified [RCV004265854] | uncertain significance | 3 | 32733520 | 32733520 | Human | | name |
| 401780375 | CV2673996 | single nucleotide variant | NM_015442.3(CNOT10):c.2006C>T (p.Ala669Val) | not specified [RCV004293364] | uncertain significance | 3 | 32769888 | 32769888 | Human | | name |
| 401738465 | CV2711900 | single nucleotide variant | NM_015442.3(CNOT10):c.1063T>G (p.Tyr355Asp) | not specified [RCV004309522] | uncertain significance | 3 | 32727718 | 32727718 | Human | | name |
| 401892839 | CV2791829 | single nucleotide variant | NM_015442.3(CNOT10):c.2140A>T (p.Thr714Ser) | not specified [RCV004359278] | uncertain significance | 3 | 32773516 | 32773516 | Human | | name |
| 405673972 | CV3304577 | single nucleotide variant | NM_015442.3(CNOT10):c.1433A>T (p.Asp478Val) | not specified [RCV004441962] | uncertain significance | 3 | 32734895 | 32734895 | Human | | name |
| 405674071 | CV3304578 | single nucleotide variant | NM_015442.3(CNOT10):c.1585G>A (p.Glu529Lys) | not specified [RCV004441963] | uncertain significance | 3 | 32737480 | 32737480 | Human | | name |
| 405674075 | CV3304579 | single nucleotide variant | NM_015442.3(CNOT10):c.1999C>T (p.His667Tyr) | not specified [RCV004441964] | uncertain significance | 3 | 32764804 | 32764804 | Human | | name |
| 405674078 | CV3304580 | single nucleotide variant | NM_015442.3(CNOT10):c.2192A>G (p.Gln731Arg) | not specified [RCV004441965] | uncertain significance | 3 | 32773568 | 32773568 | Human | | name |
| 407470538 | CV3425695 | single nucleotide variant | NM_015442.3(CNOT10):c.1082G>C (p.Cys361Ser) | not specified [RCV004615471] | uncertain significance | 3 | 32727737 | 32727737 | Human | | name |
| 407470555 | CV3425699 | single nucleotide variant | NM_015442.3(CNOT10):c.1682A>G (p.Gln561Arg) | not specified [RCV004615475] | uncertain significance | 3 | 32759544 | 32759544 | Human | | name |
| 597798989 | CV3650458 | single nucleotide variant | NM_015442.3(CNOT10):c.2189T>C (p.Ile730Thr) | not specified [RCV004904978] | uncertain significance | 3 | 32773565 | 32773565 | Human | | name |
| 597798983 | CV3653961 | single nucleotide variant | NM_015442.3(CNOT10):c.2134G>A (p.Val712Met) | not specified [RCV004904975] | uncertain significance | 3 | 32773510 | 32773510 | Human | | name |
| 598264693 | CV3941294 | single nucleotide variant | NM_015442.3(CNOT10):c.1037T>C (p.Met346Thr) | not specified [RCV005326184] | uncertain significance | 3 | 32727692 | 32727692 | Human | | name |
| 598257818 | CV3941297 | single nucleotide variant | NM_015442.3(CNOT10):c.1963C>G (p.Leu655Val) | not specified [RCV005324494] | uncertain significance | 3 | 32764768 | 32764768 | Human | | name |
| 8625602 | CV80726 | single nucleotide variant | NM_015442.2(CNOT10):c.1180C>T (p.Arg394Trp) | Malignant melanoma [RCV000060803] | not provided | 3 | 32727835 | 32727835 | Human | | name |
