| 405280938 | CV3190665 | single nucleotide variant | NM_003728.4(UNC5C):c.124+6G>A | UNC5C-related disorder [RCV003907101] | likely benign | 4 | 95548728 | 95548728 | Human | | name , trait , alternate_id |
| 408380287 | CV3512778 | single nucleotide variant | NM_003728.4(UNC5C):c.490+8A>G | UNC5C-related disorder [RCV004754057] | likely benign | 4 | 95301598 | 95301598 | Human | | name , trait , alternate_id |
| 8580158 | CV114584 | single nucleotide variant | NM_003728.3(UNC5C):c.125-49125C>A | Lung cancer [RCV000095107] | uncertain significance | 4 | 95384756 | 95384756 | Human | | name |
| 8580159 | CV114585 | single nucleotide variant | NM_003728.3(UNC5C):c.125-61844A>G | Lung cancer [RCV000095108] | uncertain significance | 4 | 95397475 | 95397475 | Human | | name |
| 156279961 | CV2206335 | single nucleotide variant | NM_003728.4(UNC5C):c.26C>A (p.Ala9Glu) | not specified [RCV004078672] | uncertain significance | 4 | 95548832 | 95548832 | Human | | name |
| 329386839 | CV2439436 | single nucleotide variant | NM_003728.4(UNC5C):c.10G>T (p.Gly4Cys) | not specified [RCV004249726] | uncertain significance | 4 | 95548848 | 95548848 | Human | | name |
| 405275949 | CV3193160 | single nucleotide variant | NM_003728.4(UNC5C):c.291T>C (p.Ser97=) | UNC5C-related disorder [RCV003974326] | benign | 4 | 95335465 | 95335465 | Human | | name , trait , alternate_id |
| 401928353 | CV2820042 | single nucleotide variant | NM_003728.4(UNC5C):c.933G>A (p.Thr311=) | UNC5C-related disorder [RCV003919192]|not provided [RCV003439421] | likely benign | 4 | 95244987 | 95244987 | Human | | name , trait , alternate_id |
| 405274748 | CV3199803 | single nucleotide variant | NM_003728.4(UNC5C):c.801G>A (p.Thr267=) | UNC5C-related disorder [RCV003973856] | benign | 4 | 95245119 | 95245119 | Human | | name , trait , alternate_id |
| 405809928 | CV3345043 | single nucleotide variant | NM_003728.4(UNC5C):c.38G>A (p.Gly13Glu) | not specified [RCV004482003] | uncertain significance | 4 | 95548820 | 95548820 | Human | | name |
| 597721155 | CV3632886 | single nucleotide variant | NM_003728.4(UNC5C):c.66G>T (p.Met22Ile) | not specified [RCV004887893] | uncertain significance | 4 | 95548792 | 95548792 | Human | | name |
| 598191234 | CV3925640 | single nucleotide variant | NM_003728.4(UNC5C):c.70G>C (p.Val24Leu) | not specified [RCV005288324] | uncertain significance | 4 | 95548788 | 95548788 | Human | | name |
| 150456846 | CV1248708 | single nucleotide variant | NM_003728.4(UNC5C):c.1614G>A (p.Ser538=) | UNC5C-related disorder [RCV003975856]|not provided [RCV001668884] | benign | 4 | 95219000 | 95219000 | Human | | name , trait , alternate_id |
| 401928348 | CV2820040 | single nucleotide variant | NM_003728.4(UNC5C):c.2514G>A (p.Gly838=) | UNC5C-related disorder [RCV003938999]|not provided [RCV003439419] | likely benign | 4 | 95170270 | 95170270 | Human | | name , trait , alternate_id |
| 401928350 | CV2820041 | single nucleotide variant | NM_003728.4(UNC5C):c.1524G>A (p.Ser508=) | UNC5C-related disorder [RCV003966407]|not provided [RCV003439420] | likely benign | 4 | 95219090 | 95219090 | Human | | name , trait , alternate_id |
| 405286154 | CV3192009 | single nucleotide variant | NM_003728.4(UNC5C):c.2709T>C (p.Asp903=) | UNC5C-related disorder [RCV003923939] | benign | 4 | 95169321 | 95169321 | Human | | name , trait , alternate_id |
| 405276520 | CV3193381 | single nucleotide variant | NM_003728.4(UNC5C):c.1812A>C (p.Pro604=) | UNC5C-related disorder [RCV003974548] | benign | 4 | 95206718 | 95206718 | Human | | name , trait , alternate_id |
| 405275544 | CV3196335 | single nucleotide variant | NM_003728.4(UNC5C):c.2221C>T (p.Leu741=) | UNC5C-related disorder [RCV003974185] | likely benign | 4 | 95185112 | 95185112 | Human | | name , trait , alternate_id |
| 405275819 | CV3196440 | single nucleotide variant | NM_003728.4(UNC5C):c.1494G>A (p.Thr498=) | UNC5C-related disorder [RCV003974272] | likely benign | 4 | 95219120 | 95219120 | Human | | name , trait , alternate_id |
| 405290733 | CV3197125 | single nucleotide variant | NM_003728.4(UNC5C):c.2037G>A (p.Ala679=) | UNC5C-related disorder [RCV003984687] | benign | 4 | 95202830 | 95202830 | Human | | name , trait , alternate_id |
| 405275804 | CV3199438 | single nucleotide variant | NM_003728.4(UNC5C):c.2442C>T (p.Thr814=) | UNC5C-related disorder [RCV003916845] | likely benign | 4 | 95182906 | 95182906 | Human | | name , trait , alternate_id |
| 405291095 | CV3203960 | single nucleotide variant | NM_003728.4(UNC5C):c.2448A>G (p.Ser816=) | UNC5C-related disorder [RCV003927364] | likely benign | 4 | 95182900 | 95182900 | Human | | name , trait , alternate_id |
| 405281874 | CV3216148 | single nucleotide variant | NM_003728.4(UNC5C):c.2772C>T (p.Ser924=) | UNC5C-related disorder [RCV003956682] | likely benign | 4 | 95169258 | 95169258 | Human | | name , trait , alternate_id |
| 597790628 | CV3632887 | single nucleotide variant | NM_003728.4(UNC5C):c.103G>A (p.Gly35Ser) | not specified [RCV004876398] | uncertain significance | 4 | 95548755 | 95548755 | Human | | name |
| 598191248 | CV3925643 | single nucleotide variant | NM_003728.4(UNC5C):c.132C>A (p.Asp44Glu) | not specified [RCV005288326] | uncertain significance | 4 | 95335624 | 95335624 | Human | | name |
| 616939535 | CV4014030 | single nucleotide variant | NM_003728.4(UNC5C):c.1374C>T (p.Asp458=) | not provided [RCV005413522] | likely benign | 4 | 95219240 | 95219240 | Human | | name |
| 15150927 | CV709534 | single nucleotide variant | NM_003728.4(UNC5C):c.2670C>T (p.Gly890=) | not provided [RCV000968036] | benign | 4 | 95169360 | 95169360 | Human | | name |
| 8631333 | CV86494 | single nucleotide variant | NM_003728.3(UNC5C):c.2176C>T (p.Leu726=) | Malignant melanoma [RCV000066585] | not provided | 4 | 95185157 | 95185157 | Human | | name |
| 156123062 | CV2227195 | single nucleotide variant | NM_003728.4(UNC5C):c.857C>A (p.Thr286Asn) | not specified [RCV004091804] | uncertain significance | 4 | 95245063 | 95245063 | Human | | name |
| 156335997 | CV2228475 | single nucleotide variant | NM_003728.4(UNC5C):c.686C>T (p.Ala229Val) | not specified [RCV004098441] | uncertain significance | 4 | 95250576 | 95250576 | Human | | name |
| 156052949 | CV2246363 | single nucleotide variant | NM_003728.4(UNC5C):c.631G>C (p.Val211Leu) | not specified [RCV004107802] | uncertain significance | 4 | 95250631 | 95250631 | Human | | name |
| 156141832 | CV2288592 | single nucleotide variant | NM_003728.4(UNC5C):c.340A>T (p.Thr114Ser) | not specified [RCV004152111] | uncertain significance | 4 | 95335416 | 95335416 | Human | | name |
| 156263321 | CV2329363 | single nucleotide variant | NM_003728.4(UNC5C):c.800C>T (p.Thr267Met) | not specified [RCV004187381] | uncertain significance | 4 | 95245120 | 95245120 | Human | | name |
| 401773795 | CV2691410 | single nucleotide variant | NM_003728.4(UNC5C):c.541G>A (p.Glu181Lys) | not specified [RCV004305272] | uncertain significance | 4 | 95278312 | 95278312 | Human | | name |
| 405284753 | CV3201851 | single nucleotide variant | NM_003728.4(UNC5C):c.319G>C (p.Val107Leu) | UNC5C-related disorder [RCV003909374] | benign | 4 | 95335437 | 95335437 | Human | | name , trait , alternate_id |
| 405809929 | CV3345044 | single nucleotide variant | NM_003728.4(UNC5C):c.848G>A (p.Arg283His) | not specified [RCV004482004] | uncertain significance | 4 | 95245072 | 95245072 | Human | | name |
| 407462501 | CV3489341 | single nucleotide variant | NM_003728.4(UNC5C):c.354T>G (p.Ile118Met) | not specified [RCV004687983] | uncertain significance | 4 | 95301742 | 95301742 | Human | | name |
| 407462505 | CV3489342 | single nucleotide variant | NM_003728.4(UNC5C):c.751A>G (p.Thr251Ala) | not specified [RCV004687984] | uncertain significance | 4 | 95250511 | 95250511 | Human | | name |
| 407454715 | CV3489343 | single nucleotide variant | NM_003728.4(UNC5C):c.884G>C (p.Gly295Ala) | not specified [RCV004685194] | uncertain significance | 4 | 95245036 | 95245036 | Human | | name |
| 597721142 | CV3632883 | single nucleotide variant | NM_003728.4(UNC5C):c.382C>T (p.Arg128Cys) | not specified [RCV004887892] | uncertain significance | 4 | 95301714 | 95301714 | Human | | name |
| 597721169 | CV3632889 | single nucleotide variant | NM_003728.4(UNC5C):c.449C>T (p.Ala150Val) | not specified [RCV004887894] | uncertain significance | 4 | 95301647 | 95301647 | Human | | name |
| 598274637 | CV3925639 | single nucleotide variant | NM_003728.4(UNC5C):c.388C>A (p.Gln130Lys) | not specified [RCV005304035] | uncertain significance | 4 | 95301708 | 95301708 | Human | | name |
| 598191242 | CV3925641 | single nucleotide variant | NM_003728.4(UNC5C):c.463A>G (p.Ser155Gly) | not specified [RCV005288325] | uncertain significance | 4 | 95301633 | 95301633 | Human | | name |
| 155916475 | CV2197446 | single nucleotide variant | NM_003728.4(UNC5C):c.2443G>A (p.Val815Met) | not specified [RCV004081181] | uncertain significance | 4 | 95182905 | 95182905 | Human | | name |
| 155915066 | CV2242904 | single nucleotide variant | NM_003728.4(UNC5C):c.2688G>C (p.Trp896Cys) | not specified [RCV004107493] | uncertain significance | 4 | 95169342 | 95169342 | Human | | name |
| 156077642 | CV2248125 | single nucleotide variant | NM_003728.4(UNC5C):c.2587G>A (p.Gly863Ser) | not specified [RCV004117529] | uncertain significance | 4 | 95170197 | 95170197 | Human | | name |
| 155922877 | CV2251795 | single nucleotide variant | NM_003728.4(UNC5C):c.2265C>G (p.Ser755Arg) | not specified [RCV004119786] | uncertain significance | 4 | 95185068 | 95185068 | Human | | name |
| 155990028 | CV2259761 | single nucleotide variant | NM_003728.4(UNC5C):c.1738C>A (p.Pro580Thr) | not specified [RCV004116771] | uncertain significance | 4 | 95206792 | 95206792 | Human | | name |
| 156158215 | CV2262463 | single nucleotide variant | NM_003728.4(UNC5C):c.2389C>T (p.Leu797Phe) | not specified [RCV004128901] | uncertain significance | 4 | 95182959 | 95182959 | Human | | name |
| 155977497 | CV2266417 | single nucleotide variant | NM_003728.4(UNC5C):c.2434A>C (p.Asn812His) | not specified [RCV004131008] | uncertain significance | 4 | 95182914 | 95182914 | Human | | name |
| 156122065 | CV2276063 | single nucleotide variant | NM_003728.4(UNC5C):c.2312G>A (p.Ser771Asn) | not specified [RCV004141737] | uncertain significance | 4 | 95183036 | 95183036 | Human | | name |
| 156065512 | CV2287371 | single nucleotide variant | NM_003728.4(UNC5C):c.2789A>G (p.Gln930Arg) | not specified [RCV004146984] | uncertain significance | 4 | 95169241 | 95169241 | Human | | name |
| 156094537 | CV2300306 | single nucleotide variant | NM_003728.4(UNC5C):c.1025C>T (p.Ala342Val) | not specified [RCV004153258] | uncertain significance | 4 | 95242512 | 95242512 | Human | | name |
| 156019041 | CV2301731 | single nucleotide variant | NM_003728.4(UNC5C):c.2163G>A (p.Met721Ile) | not specified [RCV004156548] | uncertain significance | 4 | 95185170 | 95185170 | Human | | name |
| 155911479 | CV2303827 | single nucleotide variant | NM_003728.4(UNC5C):c.2534C>T (p.Pro845Leu) | not specified [RCV004163664] | uncertain significance | 4 | 95170250 | 95170250 | Human | | name |
| 156241454 | CV2310205 | single nucleotide variant | NM_003728.4(UNC5C):c.1315C>A (p.Pro439Thr) | not specified [RCV004163310] | uncertain significance | 4 | 95219299 | 95219299 | Human | | name |
| 156115648 | CV2349318 | single nucleotide variant | NM_003728.4(UNC5C):c.1154T>C (p.Ile385Thr) | not specified [RCV004199262] | uncertain significance | 4 | 95220131 | 95220131 | Human | | name |
| 156126708 | CV2351022 | single nucleotide variant | NM_003728.4(UNC5C):c.2388A>T (p.Lys796Asn) | not specified [RCV004211846] | uncertain significance | 4 | 95182960 | 95182960 | Human | | name |
| 156011696 | CV2358764 | single nucleotide variant | NM_003728.4(UNC5C):c.1400A>G (p.Asn467Ser) | not specified [RCV004210072] | uncertain significance | 4 | 95219214 | 95219214 | Human | | name |
| 156249630 | CV2358932 | single nucleotide variant | NM_003728.4(UNC5C):c.2401C>G (p.Gln801Glu) | not specified [RCV004212267] | uncertain significance | 4 | 95182947 | 95182947 | Human | | name |
| 155910590 | CV2366508 | single nucleotide variant | NM_003728.4(UNC5C):c.2791T>C (p.Tyr931His) | not specified [RCV004208484] | uncertain significance | 4 | 95169239 | 95169239 | Human | | name |
| 156265603 | CV2372268 | single nucleotide variant | NM_003728.4(UNC5C):c.1666G>A (p.Ala556Thr) | not specified [RCV004217045] | uncertain significance | 4 | 95216191 | 95216191 | Human | | name |
| 156219338 | CV2393579 | single nucleotide variant | NM_003728.4(UNC5C):c.2707G>A (p.Asp903Asn) | not specified [RCV004231395] | uncertain significance | 4 | 95169323 | 95169323 | Human | | name |
| 156225289 | CV2399613 | single nucleotide variant | NM_003728.4(UNC5C):c.2416G>A (p.Gly806Arg) | not specified [RCV004244132] | uncertain significance | 4 | 95182932 | 95182932 | Human | | name |
| 329382745 | CV2424541 | single nucleotide variant | NM_003728.4(UNC5C):c.2225G>A (p.Arg742His) | not specified [RCV004254042] | uncertain significance | 4 | 95185108 | 95185108 | Human | | name |
| 329374788 | CV2431046 | single nucleotide variant | NM_003728.4(UNC5C):c.2582C>T (p.Thr861Met) | not specified [RCV004250416] | uncertain significance | 4 | 95170202 | 95170202 | Human | | name |
| 329396759 | CV2459014 | single nucleotide variant | NM_003728.4(UNC5C):c.2156G>C (p.Arg719Thr) | not specified [RCV004272493] | uncertain significance | 4 | 95185177 | 95185177 | Human | | name |
| 401751723 | CV2672555 | single nucleotide variant | NM_003728.4(UNC5C):c.2452G>C (p.Glu818Gln) | not specified [RCV004287589] | uncertain significance | 4 | 95170332 | 95170332 | Human | | name |
| 401734174 | CV2694461 | single nucleotide variant | NM_003728.4(UNC5C):c.1375G>C (p.Val459Leu) | not specified [RCV004304625] | uncertain significance | 4 | 95219239 | 95219239 | Human | | name |
| 401750793 | CV2715764 | single nucleotide variant | NM_003728.4(UNC5C):c.1318C>G (p.Pro440Ala) | not specified [RCV004328901] | uncertain significance | 4 | 95219296 | 95219296 | Human | | name |
| 401728590 | CV2729678 | single nucleotide variant | NM_003728.4(UNC5C):c.2467G>A (p.Asp823Asn) | not specified [RCV004331938] | uncertain significance | 4 | 95170317 | 95170317 | Human | | name |
| 401920057 | CV2796394 | single nucleotide variant | NM_003728.4(UNC5C):c.2537T>C (p.Leu846Pro) | UNC5C-related disorder [RCV003402449] | uncertain significance | 4 | 95170247 | 95170247 | Human | | name , trait , alternate_id |
| 401928346 | CV2820039 | single nucleotide variant | NM_003728.4(UNC5C):c.2521G>A (p.Ala841Thr) | UNC5C-related disorder [RCV003980923]|not provided [RCV003439418] | benign | 4 | 95170263 | 95170263 | Human | | name , trait , alternate_id |
| 401944157 | CV2840515 | single nucleotide variant | NM_003728.4(UNC5C):c.1807C>T (p.Arg603Cys) | not provided [RCV003457123] | likely benign | 4 | 95206723 | 95206723 | Human | | name |
| 404996683 | CV2851465 | single nucleotide variant | NM_003728.4(UNC5C):c.2676C>G (p.Ile892Met) | not provided [RCV003491841] | uncertain significance | 4 | 95169354 | 95169354 | Human | | name |
| 404996690 | CV2851466 | single nucleotide variant | NM_003728.4(UNC5C):c.2578C>A (p.Gln860Lys) | not provided [RCV003491842] | uncertain significance | 4 | 95170206 | 95170206 | Human | | name |
| 405277034 | CV3192571 | single nucleotide variant | NM_003728.4(UNC5C):c.1882G>A (p.Ala628Thr) | UNC5C-related disorder [RCV003917311] | benign | 4 | 95206648 | 95206648 | Human | | name , trait , alternate_id |
| 405292170 | CV3199792 | single nucleotide variant | NM_003728.4(UNC5C):c.2065C>G (p.Pro689Ala) | UNC5C-related disorder [RCV003964414] | benign | 4 | 95202802 | 95202802 | Human | | name , trait , alternate_id |
| 405255973 | CV3208510 | single nucleotide variant | NM_003728.4(UNC5C):c.2036C>T (p.Ala679Val) | UNC5C-related disorder [RCV003939597] | likely benign | 4 | 95202831 | 95202831 | Human | | name , trait , alternate_id |
| 405293911 | CV3210506 | single nucleotide variant | NM_003728.4(UNC5C):c.1883C>A (p.Ala628Glu) | UNC5C-related disorder [RCV003932325] | benign | 4 | 95206647 | 95206647 | Human | | name , trait , alternate_id |
| 405288027 | CV3218088 | single nucleotide variant | NM_003728.4(UNC5C):c.2162T>C (p.Met721Thr) | UNC5C-related disorder [RCV003982213] | benign | 4 | 95185171 | 95185171 | Human | | name , trait , alternate_id |
| 405809914 | CV3345035 | single nucleotide variant | NM_003728.4(UNC5C):c.1237A>G (p.Ile413Val) | not specified [RCV004481995] | uncertain significance | 4 | 95220048 | 95220048 | Human | | name |
| 405809916 | CV3345036 | single nucleotide variant | NM_003728.4(UNC5C):c.1450A>C (p.Thr484Pro) | not specified [RCV004481996] | uncertain significance | 4 | 95219164 | 95219164 | Human | | name |
| 405809917 | CV3345037 | single nucleotide variant | NM_003728.4(UNC5C):c.1599T>G (p.Phe533Leu) | not specified [RCV004481997] | uncertain significance | 4 | 95219015 | 95219015 | Human | | name |
| 405809919 | CV3345038 | single nucleotide variant | NM_003728.4(UNC5C):c.1837G>A (p.Ala613Thr) | not specified [RCV004481998] | uncertain significance | 4 | 95206693 | 95206693 | Human | | name |
| 405809921 | CV3345039 | single nucleotide variant | NM_003728.4(UNC5C):c.1918G>A (p.Gly640Arg) | not specified [RCV004481999] | uncertain significance | 4 | 95202949 | 95202949 | Human | | name |
| 405809923 | CV3345040 | single nucleotide variant | NM_003728.4(UNC5C):c.2210G>C (p.Ser737Thr) | not specified [RCV004482000] | uncertain significance | 4 | 95185123 | 95185123 | Human | | name |
| 405809924 | CV3345041 | single nucleotide variant | NM_003728.4(UNC5C):c.2239G>A (p.Asp747Asn) | not specified [RCV004482001] | uncertain significance | 4 | 95185094 | 95185094 | Human | | name |
| 405809926 | CV3345042 | single nucleotide variant | NM_003728.4(UNC5C):c.2462G>A (p.Gly821Asp) | not specified [RCV004482002] | uncertain significance | 4 | 95170322 | 95170322 | Human | | name |
| 407462498 | CV3489337 | single nucleotide variant | NM_003728.4(UNC5C):c.1328C>T (p.Thr443Met) | not specified [RCV004687982] | uncertain significance | 4 | 95219286 | 95219286 | Human | | name |
| 407454708 | CV3489338 | single nucleotide variant | NM_003728.4(UNC5C):c.1559A>G (p.Gln520Arg) | not specified [RCV004685191] | uncertain significance | 4 | 95219055 | 95219055 | Human | | name |
| 407454710 | CV3489339 | single nucleotide variant | NM_003728.4(UNC5C):c.1462G>A (p.Val488Ile) | not specified [RCV004685192] | uncertain significance | 4 | 95219152 | 95219152 | Human | | name |
| 407454713 | CV3489340 | single nucleotide variant | NM_003728.4(UNC5C):c.2542A>C (p.Ile848Leu) | not specified [RCV004685193] | uncertain significance | 4 | 95170242 | 95170242 | Human | | name |
| 407454716 | CV3489344 | single nucleotide variant | NM_003728.4(UNC5C):c.2695C>G (p.Gln899Glu) | not specified [RCV004685195] | uncertain significance | 4 | 95169335 | 95169335 | Human | | name |
| 407454720 | CV3489346 | single nucleotide variant | NM_003728.4(UNC5C):c.2207G>A (p.Gly736Asp) | not specified [RCV004685197] | uncertain significance | 4 | 95185126 | 95185126 | Human | | name |
| 407462509 | CV3489347 | single nucleotide variant | NM_003728.4(UNC5C):c.1310C>T (p.Ala437Val) | not specified [RCV004687985] | uncertain significance | 4 | 95219304 | 95219304 | Human | | name |
| 597790624 | CV3632885 | single nucleotide variant | NM_003728.4(UNC5C):c.1590T>G (p.Cys530Trp) | not specified [RCV004876397] | uncertain significance | 4 | 95219024 | 95219024 | Human | | name |
| 597790632 | CV3632888 | single nucleotide variant | NM_003728.4(UNC5C):c.2780C>G (p.Ala927Gly) | not specified [RCV004876399] | uncertain significance | 4 | 95169250 | 95169250 | Human | | name |
| 597790636 | CV3632890 | single nucleotide variant | NM_003728.4(UNC5C):c.1364C>T (p.Ala455Val) | not specified [RCV004876400] | uncertain significance | 4 | 95219250 | 95219250 | Human | | name |
| 597790640 | CV3632891 | single nucleotide variant | NM_003728.4(UNC5C):c.2671G>A (p.Val891Ile) | not specified [RCV004876401] | uncertain significance | 4 | 95169359 | 95169359 | Human | | name |
| 597790642 | CV3632892 | single nucleotide variant | NM_003728.4(UNC5C):c.2288A>C (p.Glu763Ala) | not specified [RCV004876402] | uncertain significance | 4 | 95183060 | 95183060 | Human | | name |
| 597790646 | CV3632893 | single nucleotide variant | NM_003728.4(UNC5C):c.1465A>C (p.Thr489Pro) | not specified [RCV004876403] | uncertain significance | 4 | 95219149 | 95219149 | Human | | name |
| 598274635 | CV3925638 | single nucleotide variant | NM_003728.4(UNC5C):c.2405T>G (p.Val802Gly) | not specified [RCV005304034] | uncertain significance | 4 | 95182943 | 95182943 | Human | | name |
| 598274639 | CV3925642 | single nucleotide variant | NM_003728.4(UNC5C):c.2545C>T (p.Arg849Trp) | not specified [RCV005304036] | uncertain significance | 4 | 95170239 | 95170239 | Human | | name |
| 156369924 | CV2263442 | single nucleotide variant | NM_173561.3(UNC5CL):c.70G>T (p.Val24Phe) | not specified [RCV004133688] | uncertain significance | 6 | 41035005 | 41035005 | Human | | name |
| 401866082 | CV2762517 | single nucleotide variant | NM_173561.3(UNC5CL):c.40C>G (p.Leu14Val) | not specified [RCV004338052] | uncertain significance | 6 | 41035035 | 41035035 | Human | | name |
| 405809936 | CV3345048 | single nucleotide variant | NM_173561.3(UNC5CL):c.38T>C (p.Phe13Ser) | not specified [RCV004482008] | uncertain significance | 6 | 41035037 | 41035037 | Human | | name |
| 156277859 | CV2209966 | single nucleotide variant | NM_173561.3(UNC5CL):c.143G>T (p.Gly48Val) | not specified [RCV004076408] | uncertain significance | 6 | 41034932 | 41034932 | Human | | name |
| 156173638 | CV2326864 | single nucleotide variant | NM_173561.3(UNC5CL):c.229G>C (p.Val77Leu) | not specified [RCV004176690] | uncertain significance | 6 | 41034846 | 41034846 | Human | | name |
| 329372181 | CV2443010 | single nucleotide variant | NM_173561.3(UNC5CL):c.124G>T (p.Ala42Ser) | not specified [RCV004253601] | uncertain significance | 6 | 41034951 | 41034951 | Human | | name |
| 401867521 | CV2780487 | single nucleotide variant | NM_173561.3(UNC5CL):c.274A>G (p.Met92Val) | not specified [RCV004358182] | likely benign | 6 | 41034801 | 41034801 | Human | | name |
| 407454724 | CV3489350 | single nucleotide variant | NM_173561.3(UNC5CL):c.157G>A (p.Val53Met) | not specified [RCV004685199] | uncertain significance | 6 | 41034918 | 41034918 | Human | | name |
| 598191258 | CV3925644 | single nucleotide variant | NM_173561.3(UNC5CL):c.212C>A (p.Ala71Asp) | not specified [RCV005288327] | uncertain significance | 6 | 41034863 | 41034863 | Human | | name |
| 156316146 | CV2193013 | single nucleotide variant | NM_173561.3(UNC5CL):c.730C>T (p.Arg244Cys) | not specified [RCV004069564] | uncertain significance | 6 | 41033103 | 41033103 | Human | | name |
| 156028583 | CV2238242 | single nucleotide variant | NM_173561.3(UNC5CL):c.784C>G (p.His262Asp) | not specified [RCV004113331] | uncertain significance | 6 | 41033049 | 41033049 | Human | | name |
| 156201614 | CV2313157 | single nucleotide variant | NM_173561.3(UNC5CL):c.653G>A (p.Arg218Gln) | not specified [RCV004161417] | uncertain significance | 6 | 41033914 | 41033914 | Human | | name |
| 156075605 | CV2331748 | single nucleotide variant | NM_173561.3(UNC5CL):c.869G>A (p.Arg290His) | not specified [RCV004184373] | uncertain significance | 6 | 41032964 | 41032964 | Human | | name |
| 155978685 | CV2335139 | single nucleotide variant | NM_173561.3(UNC5CL):c.493G>T (p.Ala165Ser) | not specified [RCV004184670] | uncertain significance | 6 | 41034074 | 41034074 | Human | | name |
| 156383563 | CV2361601 | single nucleotide variant | NM_173561.3(UNC5CL):c.575G>A (p.Arg192His) | not specified [RCV004221227] | uncertain significance | 6 | 41033992 | 41033992 | Human | | name |
| 155910682 | CV2366586 | single nucleotide variant | NM_173561.3(UNC5CL):c.797G>A (p.Arg266His) | not specified [RCV004210604] | uncertain significance | 6 | 41033036 | 41033036 | Human | | name |
| 329372723 | CV2433995 | single nucleotide variant | NM_173561.3(UNC5CL):c.578C>A (p.Thr193Asn) | not specified [RCV004249901] | uncertain significance | 6 | 41033989 | 41033989 | Human | | name |
| 329357777 | CV2453783 | single nucleotide variant | NM_173561.3(UNC5CL):c.515C>G (p.Ser172Cys) | not specified [RCV004269404] | uncertain significance | 6 | 41034052 | 41034052 | Human | | name |
| 405809938 | CV3345049 | single nucleotide variant | NM_173561.3(UNC5CL):c.662G>C (p.Cys221Ser) | not specified [RCV004482009] | uncertain significance | 6 | 41033905 | 41033905 | Human | | name |
| 405810046 | CV3345050 | single nucleotide variant | NM_173561.3(UNC5CL):c.818C>T (p.Thr273Met) | not specified [RCV004482010] | uncertain significance | 6 | 41033015 | 41033015 | Human | | name |
| 405809942 | CV3345051 | single nucleotide variant | NM_173561.3(UNC5CL):c.826G>A (p.Ala276Thr) | not specified [RCV004482011] | uncertain significance | 6 | 41033007 | 41033007 | Human | | name |
| 407454722 | CV3489348 | single nucleotide variant | NM_173561.3(UNC5CL):c.391G>A (p.Val131Met) | not specified [RCV004685198] | uncertain significance | 6 | 41034176 | 41034176 | Human | | name |
| 597790650 | CV3632896 | single nucleotide variant | NM_173561.3(UNC5CL):c.572C>A (p.Ala191Asp) | not specified [RCV004876404] | uncertain significance | 6 | 41033995 | 41033995 | Human | | name |
| 597790654 | CV3632897 | single nucleotide variant | NM_173561.3(UNC5CL):c.764C>T (p.Pro255Leu) | not specified [RCV004876405] | uncertain significance | 6 | 41033069 | 41033069 | Human | | name |
| 597721194 | CV3632898 | single nucleotide variant | NM_173561.3(UNC5CL):c.844A>G (p.Thr282Ala) | not specified [RCV004887896] | uncertain significance | 6 | 41032989 | 41032989 | Human | | name |
| 597721206 | CV3632899 | single nucleotide variant | NM_173561.3(UNC5CL):c.332G>A (p.Arg111His) | not specified [RCV004887897] | uncertain significance | 6 | 41034743 | 41034743 | Human | | name |
| 597790658 | CV3632901 | single nucleotide variant | NM_173561.3(UNC5CL):c.650C>T (p.Ser217Phe) | not specified [RCV004876406] | uncertain significance | 6 | 41033917 | 41033917 | Human | | name |
| 597790662 | CV3632902 | single nucleotide variant | NM_173561.3(UNC5CL):c.304G>A (p.Val102Met) | not specified [RCV004876407] | uncertain significance | 6 | 41034771 | 41034771 | Human | | name |
| 597790666 | CV3632903 | single nucleotide variant | NM_173561.3(UNC5CL):c.665G>A (p.Arg222His) | not specified [RCV004876408] | uncertain significance | 6 | 41033902 | 41033902 | Human | | name |
| 597790668 | CV3632904 | single nucleotide variant | NM_173561.3(UNC5CL):c.922T>C (p.Cys308Arg) | not specified [RCV004876409] | uncertain significance | 6 | 41032911 | 41032911 | Human | | name |
| 598274641 | CV3925645 | single nucleotide variant | NM_173561.3(UNC5CL):c.799A>G (p.Ile267Val) | not specified [RCV005304037] | likely benign | 6 | 41033034 | 41033034 | Human | | name |
| 598274645 | CV3925647 | single nucleotide variant | NM_173561.3(UNC5CL):c.413G>A (p.Arg138Gln) | not specified [RCV005304039] | uncertain significance | 6 | 41034154 | 41034154 | Human | | name |
| 598274649 | CV3925649 | single nucleotide variant | NM_173561.3(UNC5CL):c.695C>T (p.Thr232Ile) | not specified [RCV005304041] | uncertain significance | 6 | 41033138 | 41033138 | Human | | name |
| 156379291 | CV2207934 | single nucleotide variant | NM_173561.3(UNC5CL):c.1485C>G (p.His495Gln) | not specified [RCV004084353] | likely benign | 6 | 41028445 | 41028445 | Human | | name |
| 155957551 | CV2282084 | single nucleotide variant | NM_173561.3(UNC5CL):c.1025G>T (p.Arg342Leu) | not specified [RCV004138830] | uncertain significance | 6 | 41032062 | 41032062 | Human | | name |
| 156278460 | CV2316688 | single nucleotide variant | NM_173561.3(UNC5CL):c.1249C>T (p.Arg417Trp) | not specified [RCV004171918] | uncertain significance | 6 | 41030473 | 41030473 | Human | | name |
| 156062568 | CV2321008 | single nucleotide variant | NM_173561.3(UNC5CL):c.1205C>A (p.Pro402Gln) | not specified [RCV004172801] | uncertain significance | 6 | 41030670 | 41030670 | Human | | name |
| 156337584 | CV2343072 | single nucleotide variant | NM_173561.3(UNC5CL):c.1304C>T (p.Ser435Phe) | not specified [RCV004192669] | uncertain significance | 6 | 41030418 | 41030418 | Human | | name |
| 156195033 | CV2347408 | single nucleotide variant | NM_173561.3(UNC5CL):c.1039C>T (p.Arg347Trp) | not specified [RCV004207246] | uncertain significance | 6 | 41032048 | 41032048 | Human | | name |
| 155917518 | CV2362326 | single nucleotide variant | NM_173561.3(UNC5CL):c.1448G>A (p.Cys483Tyr) | not specified [RCV004212960] | uncertain significance | 6 | 41028482 | 41028482 | Human | | name |
| 156043870 | CV2381582 | single nucleotide variant | NM_173561.3(UNC5CL):c.1024C>T (p.Arg342Cys) | not specified [RCV004232060] | uncertain significance | 6 | 41032063 | 41032063 | Human | | name |
| 156390946 | CV2384966 | single nucleotide variant | NM_173561.3(UNC5CL):c.1184C>T (p.Ala395Val) | not specified [RCV004226194] | uncertain significance | 6 | 41030691 | 41030691 | Human | | name |
| 401865309 | CV2791602 | single nucleotide variant | NM_173561.3(UNC5CL):c.1502C>A (p.Pro501His) | not specified [RCV004358968] | uncertain significance | 6 | 41028428 | 41028428 | Human | | name |
| 405809931 | CV3345045 | single nucleotide variant | NM_173561.3(UNC5CL):c.1238T>C (p.Phe413Ser) | not specified [RCV004482005] | uncertain significance | 6 | 41030484 | 41030484 | Human | | name |
| 405809933 | CV3345046 | single nucleotide variant | NM_173561.3(UNC5CL):c.1333C>T (p.Arg445Trp) | not specified [RCV004482006] | uncertain significance | 6 | 41030389 | 41030389 | Human | | name |
| 405809934 | CV3345047 | single nucleotide variant | NM_173561.3(UNC5CL):c.1442T>C (p.Leu481Pro) | not specified [RCV004482007] | uncertain significance | 6 | 41028488 | 41028488 | Human | | name |
| 407462513 | CV3489349 | single nucleotide variant | NM_173561.3(UNC5CL):c.1250G>A (p.Arg417Gln) | not specified [RCV004687986] | likely benign | 6 | 41030472 | 41030472 | Human | | name |
| 407454726 | CV3489351 | single nucleotide variant | NM_173561.3(UNC5CL):c.1031T>C (p.Phe344Ser) | not specified [RCV004685200] | uncertain significance | 6 | 41032056 | 41032056 | Human | | name |
| 597721183 | CV3632895 | single nucleotide variant | NM_173561.3(UNC5CL):c.1391A>G (p.Gln464Arg) | not specified [RCV004887895] | uncertain significance | 6 | 41028539 | 41028539 | Human | | name |
| 597721218 | CV3632900 | single nucleotide variant | NM_173561.3(UNC5CL):c.1070G>A (p.Cys357Tyr) | not specified [RCV004887898] | uncertain significance | 6 | 41031730 | 41031730 | Human | | name |
| 597790672 | CV3632905 | single nucleotide variant | NM_173561.3(UNC5CL):c.1094T>C (p.Ile365Thr) | not specified [RCV004876410] | uncertain significance | 6 | 41031706 | 41031706 | Human | | name |
| 598274643 | CV3925646 | single nucleotide variant | NM_173561.3(UNC5CL):c.1534C>G (p.Leu512Val) | not specified [RCV005304038] | uncertain significance | 6 | 41028396 | 41028396 | Human | | name |
| 598274647 | CV3925648 | single nucleotide variant | NM_173561.3(UNC5CL):c.1025G>A (p.Arg342His) | not specified [RCV005304040] | uncertain significance | 6 | 41032062 | 41032062 | Human | | name |
