| 405674238 | CV3304616 | single nucleotide variant | NM_001370472.1(CNOT6):c.5C>T (p.Pro2Leu) | not specified [RCV004442001] | uncertain significance | 5 | 180529281 | 180529281 | Human | | name |
| 597799034 | CV3650492 | single nucleotide variant | NM_001370472.1(CNOT6):c.21G>T (p.Glu7Asp) | not specified [RCV004905002] | uncertain significance | 5 | 180529297 | 180529297 | Human | | name |
| 405674235 | CV3304615 | single nucleotide variant | NM_001370472.1(CNOT6):c.34C>T (p.Arg12Trp) | not specified [RCV004442000] | uncertain significance | 5 | 180529310 | 180529310 | Human | | name |
| 405674254 | CV3304620 | single nucleotide variant | NM_001370472.1(CNOT6):c.94G>A (p.Ala32Thr) | not specified [RCV004442005] | uncertain significance | 5 | 180529370 | 180529370 | Human | | name |
| 407470655 | CV3425726 | single nucleotide variant | NM_001370472.1(CNOT6):c.65A>G (p.Glu22Gly) | not specified [RCV004615502] | uncertain significance | 5 | 180529341 | 180529341 | Human | | name |
| 597799026 | CV3650488 | single nucleotide variant | NM_001370472.1(CNOT6):c.83A>G (p.Lys28Arg) | not specified [RCV004904998] | uncertain significance | 5 | 180529359 | 180529359 | Human | | name |
| 156180574 | CV2324474 | single nucleotide variant | NM_001370472.1(CNOT6):c.122G>A (p.Arg41Lys) | not specified [RCV004178958] | uncertain significance | 5 | 180549940 | 180549940 | Human | | name |
| 155968149 | CV2337812 | single nucleotide variant | NM_001370472.1(CNOT6):c.260G>A (p.Arg87His) | not specified [RCV004183826] | uncertain significance | 5 | 180550078 | 180550078 | Human | | name |
| 156003202 | CV2258040 | single nucleotide variant | NM_001370472.1(CNOT6):c.302A>T (p.Glu101Val) | not specified [RCV004129837] | uncertain significance | 5 | 180553388 | 180553388 | Human | | name |
| 156086210 | CV2289915 | single nucleotide variant | NM_001370472.1(CNOT6):c.353A>G (p.Lys118Arg) | not specified [RCV004150569] | uncertain significance | 5 | 180553439 | 180553439 | Human | | name |
| 401762980 | CV2720150 | single nucleotide variant | NM_001370472.1(CNOT6):c.619T>C (p.Tyr207His) | not specified [RCV004323708] | uncertain significance | 5 | 180565879 | 180565879 | Human | | name |
| 401857959 | CV2774124 | single nucleotide variant | NM_001370472.1(CNOT6):c.557C>T (p.Thr186Ile) | not specified [RCV004345717] | uncertain significance | 5 | 180564741 | 180564741 | Human | | name |
| 405674242 | CV3304617 | single nucleotide variant | NM_001370472.1(CNOT6):c.622G>A (p.Gly208Ser) | not specified [RCV004442002] | uncertain significance | 5 | 180565882 | 180565882 | Human | | name |
| 405674246 | CV3304618 | single nucleotide variant | NM_001370472.1(CNOT6):c.830G>A (p.Arg277Lys) | not specified [RCV004442003] | uncertain significance | 5 | 180567200 | 180567200 | Human | | name |
| 405674250 | CV3304619 | single nucleotide variant | NM_001370472.1(CNOT6):c.853A>G (p.Ile285Val) | not specified [RCV004442004] | uncertain significance | 5 | 180567223 | 180567223 | Human | | name |
| 407470651 | CV3425725 | single nucleotide variant | NM_001370472.1(CNOT6):c.814A>G (p.Met272Val) | not specified [RCV004615501] | uncertain significance | 5 | 180567184 | 180567184 | Human | | name |
| 597799030 | CV3650490 | single nucleotide variant | NM_001370472.1(CNOT6):c.703A>G (p.Ile235Val) | not specified [RCV004905000] | uncertain significance | 5 | 180565963 | 180565963 | Human | | name |
| 597799032 | CV3650491 | single nucleotide variant | NM_001370472.1(CNOT6):c.455A>G (p.Tyr152Cys) | not specified [RCV004905001] | uncertain significance | 5 | 180564558 | 180564558 | Human | | name |
| 597799036 | CV3650493 | single nucleotide variant | NM_001370472.1(CNOT6):c.641C>T (p.Ala214Val) | not specified [RCV004905003] | uncertain significance | 5 | 180565901 | 180565901 | Human | | name |
| 156111658 | CV2261783 | single nucleotide variant | NM_001370472.1(CNOT6):c.1378G>A (p.Gly460Arg) | not specified [RCV004126069] | uncertain significance | 5 | 180571349 | 180571349 | Human | | name |
| 156282727 | CV2317411 | single nucleotide variant | NM_001370472.1(CNOT6):c.1420A>G (p.Ser474Gly) | not specified [RCV004172383] | uncertain significance | 5 | 180571391 | 180571391 | Human | | name |
| 329359327 | CV2450959 | single nucleotide variant | NM_001370472.1(CNOT6):c.1042C>T (p.Leu348Phe) | not specified [RCV004267848] | uncertain significance | 5 | 180569124 | 180569124 | Human | | name |
| 401776949 | CV2721540 | single nucleotide variant | NM_001370472.1(CNOT6):c.1174C>T (p.Arg392Cys) | not specified [RCV004316056] | uncertain significance | 5 | 180569256 | 180569256 | Human | | name |
| 405674231 | CV3304614 | single nucleotide variant | NM_001370472.1(CNOT6):c.1199G>A (p.Gly400Glu) | not specified [RCV004441999] | uncertain significance | 5 | 180569281 | 180569281 | Human | | name |
| 407470646 | CV3425724 | single nucleotide variant | NM_001370472.1(CNOT6):c.1355A>G (p.His452Arg) | not specified [RCV004615500] | uncertain significance | 5 | 180571326 | 180571326 | Human | | name |
| 597799024 | CV3650487 | single nucleotide variant | NM_001370472.1(CNOT6):c.1045G>A (p.Gly349Arg) | not specified [RCV004904997] | uncertain significance | 5 | 180569127 | 180569127 | Human | | name |
| 598257901 | CV3941317 | single nucleotide variant | NM_001370472.1(CNOT6):c.1181T>C (p.Leu394Pro) | not specified [RCV005324513] | uncertain significance | 5 | 180569263 | 180569263 | Human | | name |
| 156246941 | CV2196306 | single nucleotide variant | NM_144571.3(CNOT6L):c.89A>C (p.Asn30Thr) | not specified [RCV004073651] | uncertain significance | 4 | 77776309 | 77776309 | Human | | name |
| 156028569 | CV2278541 | single nucleotide variant | NM_144571.3(CNOT6L):c.140G>A (p.Ser47Asn) | not specified [RCV004132975] | uncertain significance | 4 | 77774704 | 77774704 | Human | | name |
| 156335119 | CV2333482 | single nucleotide variant | NM_144571.3(CNOT6L):c.179C>T (p.Ala60Val) | not specified [RCV004190179] | uncertain significance | 4 | 77774665 | 77774665 | Human | | name |
| 156106219 | CV2387064 | single nucleotide variant | NM_144571.3(CNOT6L):c.160T>G (p.Ser54Ala) | not specified [RCV004226808] | uncertain significance | 4 | 77774684 | 77774684 | Human | | name |
| 407470660 | CV3425727 | single nucleotide variant | NM_144571.3(CNOT6L):c.209G>A (p.Arg70His) | not specified [RCV004615503] | uncertain significance | 4 | 77774635 | 77774635 | Human | | name |
| 598257912 | CV3941319 | single nucleotide variant | NM_144571.3(CNOT6L):c.206G>C (p.Ser69Thr) | not specified [RCV005324515] | uncertain significance | 4 | 77774638 | 77774638 | Human | | name |
| 15156192 | CV749062 | single nucleotide variant | NM_144571.3(CNOT6L):c.1420T>C (p.Leu474=) | not provided [RCV000924620] | likely benign | 4 | 77726202 | 77726202 | Human | | name |
| 156315612 | CV2192924 | single nucleotide variant | NM_144571.3(CNOT6L):c.428A>G (p.Asn143Ser) | not specified [RCV004069485] | uncertain significance | 4 | 77756924 | 77756924 | Human | | name |
| 156134133 | CV2216981 | single nucleotide variant | NM_144571.3(CNOT6L):c.554C>T (p.Pro185Leu) | not specified [RCV004085346] | uncertain significance | 4 | 77748321 | 77748321 | Human | | name |
| 155972344 | CV2309397 | single nucleotide variant | NM_144571.3(CNOT6L):c.779A>C (p.Asp260Ala) | not specified [RCV004165545] | uncertain significance | 4 | 77742234 | 77742234 | Human | | name |
| 155986068 | CV2344045 | single nucleotide variant | NM_144571.3(CNOT6L):c.539G>A (p.Arg180Gln) | not specified [RCV004195654] | uncertain significance | 4 | 77748336 | 77748336 | Human | | name |
| 597799042 | CV3650496 | single nucleotide variant | NM_144571.3(CNOT6L):c.770G>T (p.Arg257Leu) | not specified [RCV004905006] | uncertain significance | 4 | 77742243 | 77742243 | Human | | name |
| 597799044 | CV3650497 | single nucleotide variant | NM_144571.3(CNOT6L):c.853A>G (p.Ile285Val) | not specified [RCV004905007] | uncertain significance | 4 | 77742160 | 77742160 | Human | | name |
| 156199087 | CV2312966 | single nucleotide variant | NM_144571.3(CNOT6L):c.1349A>G (p.Asn450Ser) | not specified [RCV004159471] | uncertain significance | 4 | 77726273 | 77726273 | Human | | name |
| 156308481 | CV2332352 | single nucleotide variant | NM_144571.3(CNOT6L):c.1547A>G (p.Asn516Ser) | not specified [RCV004182514] | uncertain significance | 4 | 77720552 | 77720552 | Human | | name |
| 155969486 | CV2335471 | single nucleotide variant | NM_144571.3(CNOT6L):c.1334T>C (p.Met445Thr) | not specified [RCV004191642] | uncertain significance | 4 | 77726288 | 77726288 | Human | | name |
| 329384433 | CV2435064 | single nucleotide variant | NM_144571.3(CNOT6L):c.1526C>G (p.Pro509Arg) | not specified [RCV004252713] | uncertain significance | 4 | 77720573 | 77720573 | Human | | name |
| 329393372 | CV2466898 | single nucleotide variant | NM_144571.3(CNOT6L):c.1657A>G (p.Asn553Asp) | not specified [RCV004282668] | uncertain significance | 4 | 77720442 | 77720442 | Human | | name |
| 401724297 | CV2681373 | single nucleotide variant | NM_144571.3(CNOT6L):c.1201A>C (p.Asn401His) | not specified [RCV004291920] | uncertain significance | 4 | 77728905 | 77728905 | Human | | name |
| 401729384 | CV2733008 | single nucleotide variant | NM_144571.3(CNOT6L):c.1619C>A (p.Pro540His) | not specified [RCV004331181] | uncertain significance | 4 | 77720480 | 77720480 | Human | | name |
| 405674257 | CV3304621 | single nucleotide variant | NM_144571.3(CNOT6L):c.1540G>C (p.Glu514Gln) | not specified [RCV004442006] | uncertain significance | 4 | 77720559 | 77720559 | Human | | name |
| 405674260 | CV3304622 | single nucleotide variant | NM_144571.3(CNOT6L):c.1660C>T (p.Arg554Trp) | not specified [RCV004442007] | uncertain significance | 4 | 77720439 | 77720439 | Human | | name |
| 597799038 | CV3650494 | single nucleotide variant | NM_144571.3(CNOT6L):c.1209C>G (p.Ile403Met) | not specified [RCV004905004] | uncertain significance | 4 | 77728897 | 77728897 | Human | | name |
| 597799040 | CV3650495 | single nucleotide variant | NM_144571.3(CNOT6L):c.1051A>C (p.Lys351Gln) | not specified [RCV004905005] | uncertain significance | 4 | 77729055 | 77729055 | Human | | name |
