| 401732022 | CV2712262 | single nucleotide variant | NM_001308173.3(CCNJL):c.11A>C (p.Glu4Ala) | not specified [RCV004313760] | uncertain significance | 5 | 160311913 | 160311913 | Human | | name |
| 405263549 | CV3185172 | single nucleotide variant | NM_001308173.3(CCNJL):c.189C>G (p.Ala63=) | not provided [RCV003885736] | benign | 5 | 160280616 | 160280616 | Human | | name |
| 156399224 | CV2204991 | single nucleotide variant | NM_001308173.3(CCNJL):c.133A>T (p.Ile45Phe) | not specified [RCV004077610] | uncertain significance | 5 | 160280672 | 160280672 | Human | | name |
| 155919777 | CV2254926 | single nucleotide variant | NM_001308173.3(CCNJL):c.226G>A (p.Val76Ile) | Inborn genetic diseases [RCV002772831] | likely benign | 5 | 160280579 | 160280579 | Human | 1 | name |
| 156180909 | CV2374800 | single nucleotide variant | NM_001308173.3(CCNJL):c.178C>T (p.Arg60Trp) | not specified [RCV004225401] | uncertain significance | 5 | 160280627 | 160280627 | Human | | name |
| 405742047 | CV3303160 | single nucleotide variant | NM_001308173.3(CCNJL):c.253G>A (p.Val85Met) | not specified [RCV004430781] | uncertain significance | 5 | 160280552 | 160280552 | Human | | name |
| 405742041 | CV3303161 | single nucleotide variant | NM_001308173.3(CCNJL):c.296G>A (p.Arg99Gln) | not specified [RCV004430782] | uncertain significance | 5 | 160259756 | 160259756 | Human | | name |
| 156399047 | CV2194953 | single nucleotide variant | NM_001308173.3(CCNJL):c.523C>T (p.Arg175Cys) | not specified [RCV004075476] | uncertain significance | 5 | 160259529 | 160259529 | Human | | name |
| 156092867 | CV2256705 | single nucleotide variant | NM_001308173.3(CCNJL):c.872C>T (p.Pro291Leu) | not specified [RCV004118878] | uncertain significance | 5 | 160253670 | 160253670 | Human | | name |
| 156265819 | CV2312266 | single nucleotide variant | NM_001308173.3(CCNJL):c.875C>T (p.Ala292Val) | not specified [RCV004166979] | uncertain significance | 5 | 160253667 | 160253667 | Human | | name |
| 156360847 | CV2329681 | single nucleotide variant | NM_001308173.3(CCNJL):c.793T>G (p.Leu265Val) | not specified [RCV004180792] | uncertain significance | 5 | 160253749 | 160253749 | Human | | name |
| 155989077 | CV2355220 | single nucleotide variant | NM_001308173.3(CCNJL):c.820A>C (p.Thr274Pro) | not specified [RCV004198595] | uncertain significance | 5 | 160253722 | 160253722 | Human | | name |
| 155999369 | CV2373408 | single nucleotide variant | NM_001308173.3(CCNJL):c.611C>G (p.Ser204Cys) | not specified [RCV004220109] | uncertain significance | 5 | 160255681 | 160255681 | Human | | name |
| 156252793 | CV2390082 | single nucleotide variant | NM_001308173.3(CCNJL):c.715C>G (p.Leu239Val) | not specified [RCV004238684] | uncertain significance | 5 | 160255577 | 160255577 | Human | | name |
| 156248547 | CV2393977 | single nucleotide variant | NM_001308173.3(CCNJL):c.928C>T (p.Arg310Trp) | not specified [RCV004236203] | uncertain significance | 5 | 160253614 | 160253614 | Human | | name |
| 329398403 | CV2464530 | single nucleotide variant | NM_001308173.3(CCNJL):c.967T>C (p.Ser323Pro) | not specified [RCV004278228] | uncertain significance | 5 | 160253575 | 160253575 | Human | | name |
| 401727228 | CV2684523 | single nucleotide variant | NM_001308173.3(CCNJL):c.890A>G (p.Gln297Arg) | not specified [RCV004291592] | uncertain significance | 5 | 160253652 | 160253652 | Human | | name |
| 401899047 | CV2785978 | single nucleotide variant | NM_001308173.3(CCNJL):c.857C>A (p.Pro286Gln) | not specified [RCV004359817] | uncertain significance | 5 | 160253685 | 160253685 | Human | | name |
| 401918112 | CV2825503 | single nucleotide variant | NM_001308173.3(CCNJL):c.307G>A (p.Val103Ile) | not provided [RCV003429959] | benign | 5 | 160259745 | 160259745 | Human | | name |
| 405741532 | CV3292688 | single nucleotide variant | NM_001308173.3(CCNJL):c.865G>A (p.Gly289Ser) | not specified [RCV004430777] | likely benign | 5 | 160253677 | 160253677 | Human | | name |
| 405742066 | CV3292689 | single nucleotide variant | NM_001308173.3(CCNJL):c.871C>G (p.Pro291Ala) | not specified [RCV004430778] | uncertain significance | 5 | 160253671 | 160253671 | Human | | name |
| 405742061 | CV3303158 | single nucleotide variant | NM_001308173.3(CCNJL):c.904G>A (p.Val302Met) | not specified [RCV004430779] | uncertain significance | 5 | 160253638 | 160253638 | Human | | name |
| 405742034 | CV3303162 | single nucleotide variant | NM_001308173.3(CCNJL):c.377A>T (p.Glu126Val) | not specified [RCV004430783] | uncertain significance | 5 | 160259675 | 160259675 | Human | | name |
| 405742028 | CV3303163 | single nucleotide variant | NM_001308173.3(CCNJL):c.437C>T (p.Thr146Met) | not specified [RCV004430784] | uncertain significance | 5 | 160259615 | 160259615 | Human | | name |
| 405742022 | CV3303164 | single nucleotide variant | NM_001308173.3(CCNJL):c.442G>A (p.Ala148Thr) | not specified [RCV004430785] | uncertain significance | 5 | 160259610 | 160259610 | Human | | name |
| 405742017 | CV3303165 | single nucleotide variant | NM_001308173.3(CCNJL):c.486G>C (p.Lys162Asn) | not specified [RCV004430786] | uncertain significance | 5 | 160259566 | 160259566 | Human | | name |
| 405742010 | CV3303166 | single nucleotide variant | NM_001308173.3(CCNJL):c.697A>C (p.Ser233Arg) | not specified [RCV004430787] | uncertain significance | 5 | 160255595 | 160255595 | Human | | name |
| 405742001 | CV3303167 | single nucleotide variant | NM_001308173.3(CCNJL):c.799A>G (p.Met267Val) | not specified [RCV004430788] | uncertain significance | 5 | 160253743 | 160253743 | Human | | name |
| 407491997 | CV3428652 | single nucleotide variant | NM_001308173.3(CCNJL):c.301G>C (p.Asp101His) | not specified [RCV004604848] | uncertain significance | 5 | 160259751 | 160259751 | Human | | name |
| 407492000 | CV3428653 | single nucleotide variant | NM_001308173.3(CCNJL):c.689G>A (p.Arg230Lys) | not specified [RCV004604849] | uncertain significance | 5 | 160255603 | 160255603 | Human | | name |
| 407492003 | CV3428654 | single nucleotide variant | NM_001308173.3(CCNJL):c.875C>G (p.Ala292Gly) | not specified [RCV004604850] | uncertain significance | 5 | 160253667 | 160253667 | Human | | name |
| 597766125 | CV3638227 | single nucleotide variant | NM_001308173.3(CCNJL):c.931G>A (p.Asp311Asn) | not specified [RCV004896075] | uncertain significance | 5 | 160253611 | 160253611 | Human | | name |
| 597766126 | CV3638228 | single nucleotide variant | NM_001308173.3(CCNJL):c.965T>C (p.Leu322Pro) | not specified [RCV004896076] | uncertain significance | 5 | 160253577 | 160253577 | Human | | name |
| 597762182 | CV3638229 | single nucleotide variant | NM_001308173.3(CCNJL):c.757G>A (p.Val253Ile) | not specified [RCV004895098] | uncertain significance | 5 | 160253785 | 160253785 | Human | | name |
| 598205285 | CV3939812 | single nucleotide variant | NM_001308173.3(CCNJL):c.722C>G (p.Thr241Arg) | not specified [RCV005314929] | uncertain significance | 5 | 160255570 | 160255570 | Human | | name |
| 598205294 | CV3939813 | single nucleotide variant | NM_001308173.3(CCNJL):c.808G>T (p.Gly270Cys) | not specified [RCV005314930] | uncertain significance | 5 | 160253734 | 160253734 | Human | | name |
| 598205308 | CV3939815 | single nucleotide variant | NM_001308173.3(CCNJL):c.929G>A (p.Arg310Gln) | not specified [RCV005314932] | uncertain significance | 5 | 160253613 | 160253613 | Human | | name |
| 598205315 | CV3939816 | single nucleotide variant | NM_001308173.3(CCNJL):c.571G>T (p.Val191Phe) | not specified [RCV005314933] | uncertain significance | 5 | 160259481 | 160259481 | Human | | name |
| 598205325 | CV3939817 | single nucleotide variant | NM_001308173.3(CCNJL):c.524G>T (p.Arg175Leu) | not specified [RCV005314934] | uncertain significance | 5 | 160259528 | 160259528 | Human | | name |
| 598228382 | CV3939818 | single nucleotide variant | NM_001308173.3(CCNJL):c.968C>T (p.Ser323Leu) | not specified [RCV005319075] | uncertain significance | 5 | 160253574 | 160253574 | Human | | name |
| 598205334 | CV3939819 | single nucleotide variant | NM_001308173.3(CCNJL):c.619G>T (p.Ala207Ser) | not specified [RCV005314935] | uncertain significance | 5 | 160255673 | 160255673 | Human | | name |
| 598205342 | CV3939820 | single nucleotide variant | NM_001308173.3(CCNJL):c.851C>T (p.Ala284Val) | not specified [RCV005314936] | uncertain significance | 5 | 160253691 | 160253691 | Human | | name |
| 155931476 | CV2221040 | single nucleotide variant | NM_001308173.3(CCNJL):c.1148G>C (p.Gly383Ala) | not specified [RCV004092718] | uncertain significance | 5 | 160253394 | 160253394 | Human | | name |
| 155979097 | CV2247188 | single nucleotide variant | NM_001308173.3(CCNJL):c.1051C>T (p.Leu351Phe) | not specified [RCV004114709] | uncertain significance | 5 | 160253491 | 160253491 | Human | | name |
| 155991745 | CV2355519 | single nucleotide variant | NM_001308173.3(CCNJL):c.1148G>T (p.Gly383Val) | not specified [RCV004205369] | uncertain significance | 5 | 160253394 | 160253394 | Human | | name |
| 401751942 | CV2723064 | single nucleotide variant | NM_001308173.3(CCNJL):c.1100C>A (p.Thr367Asn) | not specified [RCV004327544] | uncertain significance | 5 | 160253442 | 160253442 | Human | | name |
| 405742054 | CV3303159 | single nucleotide variant | NM_001308173.3(CCNJL):c.1138T>C (p.Phe380Leu) | not specified [RCV004430780] | uncertain significance | 5 | 160253404 | 160253404 | Human | | name |
| 407492007 | CV3428655 | single nucleotide variant | NM_001308173.3(CCNJL):c.1160G>A (p.Arg387Lys) | not specified [RCV004604851] | uncertain significance | 5 | 160253382 | 160253382 | Human | | name |
| 598205300 | CV3939814 | single nucleotide variant | NM_001308173.3(CCNJL):c.1067C>T (p.Ala356Val) | not specified [RCV005314931] | uncertain significance | 5 | 160253475 | 160253475 | Human | | name |
