| 401751323 | CV2716354 | single nucleotide variant | NM_014397.6(NEK6):c.-26G>A | not specified [RCV004325350] | uncertain significance | 9 | 124301939 | 124301939 | Human | | name |
| 156090592 | CV2206621 | single nucleotide variant | NM_014397.6(NEK6):c.-29-8925G>T | not specified [RCV004080962] | uncertain significance | 9 | 124293011 | 124293011 | Human | | name |
| 156186738 | CV2236258 | single nucleotide variant | NM_014397.6(NEK6):c.-29-8974T>A | not specified [RCV004107958] | uncertain significance | 9 | 124292962 | 124292962 | Human | | name |
| 401752572 | CV2707054 | single nucleotide variant | NM_014397.6(NEK6):c.-29-8925G>A | not specified [RCV004321640] | uncertain significance | 9 | 124293011 | 124293011 | Human | | name |
| 407489584 | CV3454882 | single nucleotide variant | NM_014397.6(NEK6):c.-29-8971G>A | not specified [RCV004641494] | uncertain significance | 9 | 124292965 | 124292965 | Human | | name |
| 598231849 | CV3990719 | single nucleotide variant | NM_014397.6(NEK6):c.11A>G (p.Gln4Arg) | not specified [RCV005381432] | uncertain significance | 9 | 124301975 | 124301975 | Human | | name |
| 15199972 | CV723328 | single nucleotide variant | NM_014397.6(NEK6):c.270T>C (p.Cys90=) | not provided [RCV000890783] | benign | 9 | 124313961 | 124313961 | Human | | name |
| 156312965 | CV2196442 | single nucleotide variant | NM_014397.6(NEK6):c.29A>G (p.His10Arg) | not specified [RCV004073743] | uncertain significance | 9 | 124301993 | 124301993 | Human | | name |
| 155978610 | CV2247091 | single nucleotide variant | NM_014397.6(NEK6):c.37A>T (p.Ser13Cys) | not specified [RCV004114630] | uncertain significance | 9 | 124302001 | 124302001 | Human | | name |
| 156265962 | CV2247092 | single nucleotide variant | NM_014397.6(NEK6):c.40T>C (p.Ser14Pro) | not specified [RCV004114631] | likely benign | 9 | 124302004 | 124302004 | Human | | name |
| 401768778 | CV2686368 | single nucleotide variant | NM_014397.6(NEK6):c.64G>T (p.Gly22Trp) | not specified [RCV004297442] | uncertain significance | 9 | 124302028 | 124302028 | Human | | name |
| 405808425 | CV3353149 | single nucleotide variant | NM_014397.6(NEK6):c.48C>A (p.Asn16Lys) | not specified [RCV004481175] | uncertain significance | 9 | 124302012 | 124302012 | Human | | name |
| 156388192 | CV2221771 | single nucleotide variant | NM_014397.6(NEK6):c.142G>A (p.Glu48Lys) | not specified [RCV004098528] | uncertain significance | 9 | 124312560 | 124312560 | Human | | name |
| 156210568 | CV2370247 | single nucleotide variant | NM_014397.6(NEK6):c.104C>T (p.Thr35Met) | not specified [RCV004213167] | uncertain significance | 9 | 124312522 | 124312522 | Human | | name |
| 405808439 | CV3353156 | single nucleotide variant | NM_014397.6(NEK6):c.103A>G (p.Thr35Ala) | not specified [RCV004481182] | likely benign | 9 | 124312521 | 124312521 | Human | | name |
| 405808472 | CV3353172 | single nucleotide variant | NM_014397.6(NEK6):c.282C>G (p.Ile94Met) | not specified [RCV004481198] | uncertain significance | 9 | 124313973 | 124313973 | Human | | name |
| 407489579 | CV3454881 | single nucleotide variant | NM_014397.6(NEK6):c.172G>A (p.Glu58Lys) | not specified [RCV004641493] | uncertain significance | 9 | 124312590 | 124312590 | Human | | name |
| 156245679 | CV2310411 | single nucleotide variant | NM_014397.6(NEK6):c.478G>A (p.Val160Met) | not specified [RCV004163452] | uncertain significance | 9 | 124326402 | 124326402 | Human | | name |
| 156069820 | CV2341147 | single nucleotide variant | NM_014397.6(NEK6):c.895G>A (p.Val299Met) | not specified [RCV004181623] | uncertain significance | 9 | 124350900 | 124350900 | Human | | name |
| 155935485 | CV2371809 | single nucleotide variant | NM_014397.6(NEK6):c.496C>T (p.Arg166Cys) | not specified [RCV004219466] | uncertain significance | 9 | 124326420 | 124326420 | Human | | name |
| 156178368 | CV2374591 | single nucleotide variant | NM_014397.6(NEK6):c.826G>A (p.Glu276Lys) | not specified [RCV004225217] | uncertain significance | 9 | 124347817 | 124347817 | Human | | name |
| 156066837 | CV2381039 | single nucleotide variant | NM_014397.6(NEK6):c.434C>T (p.Pro145Leu) | not specified [RCV004225078] | uncertain significance | 9 | 124326358 | 124326358 | Human | | name |
| 329399135 | CV2469958 | single nucleotide variant | NM_014397.6(NEK6):c.920A>G (p.His307Arg) | not specified [RCV004285415] | uncertain significance | 9 | 124350925 | 124350925 | Human | | name |
| 401730287 | CV2680083 | single nucleotide variant | NM_014397.6(NEK6):c.811G>A (p.Gly271Arg) | not specified [RCV004286575] | uncertain significance | 9 | 124347802 | 124347802 | Human | | name |
| 401782983 | CV2716073 | single nucleotide variant | NM_014397.6(NEK6):c.402C>G (p.Ile134Met) | not specified [RCV004323320] | uncertain significance | 9 | 124321566 | 124321566 | Human | | name |
| 401878308 | CV2774166 | single nucleotide variant | NM_014397.6(NEK6):c.694T>G (p.Ser232Ala) | not specified [RCV004345756] | uncertain significance | 9 | 124339642 | 124339642 | Human | | name |
| 405808529 | CV3353201 | single nucleotide variant | NM_014397.6(NEK6):c.756G>A (p.Met252Ile) | not specified [RCV004481227] | uncertain significance | 9 | 124347747 | 124347747 | Human | | name |
| 597638893 | CV3555951 | single nucleotide variant | NM_014397.6(NEK6):c.565G>A (p.Gly189Ser) | not specified [RCV004831822] | uncertain significance | 9 | 124327388 | 124327388 | Human | | name |
| 597638899 | CV3555952 | single nucleotide variant | NM_014397.6(NEK6):c.756G>C (p.Met252Ile) | not specified [RCV004831823] | uncertain significance | 9 | 124347747 | 124347747 | Human | | name |
| 597638904 | CV3555953 | single nucleotide variant | NM_014397.6(NEK6):c.406T>C (p.Tyr136His) | not specified [RCV004831824] | uncertain significance | 9 | 124326330 | 124326330 | Human | | name |
| 597638910 | CV3555954 | single nucleotide variant | NM_014397.6(NEK6):c.851T>C (p.Met284Thr) | not specified [RCV004831825] | uncertain significance | 9 | 124350856 | 124350856 | Human | | name |
| 597638916 | CV3555955 | single nucleotide variant | NM_014397.6(NEK6):c.803C>G (p.Pro268Arg) | not specified [RCV004831826] | uncertain significance | 9 | 124347794 | 124347794 | Human | | name |
| 597638921 | CV3555956 | single nucleotide variant | NM_014397.6(NEK6):c.715G>A (p.Glu239Lys) | not specified [RCV004831827] | uncertain significance | 9 | 124339663 | 124339663 | Human | | name |
| 598231854 | CV3990720 | single nucleotide variant | NM_014397.6(NEK6):c.299T>G (p.Leu100Arg) | not specified [RCV005381433] | uncertain significance | 9 | 124321463 | 124321463 | Human | | name |
| 598231861 | CV3990721 | single nucleotide variant | NM_014397.6(NEK6):c.919C>T (p.His307Tyr) | not specified [RCV005381434] | uncertain significance | 9 | 124350924 | 124350924 | Human | | name |