| 8632328 | CV87536 | single nucleotide variant | CCDC136:c.1204-5730C>T | Malignant melanoma [RCV000067627] | not provided | 7 | 128812028 | 128812028 | Human | | name |
| 8590389 | CV125080 | single nucleotide variant | NM_001201372.1(CCDC136):c.167-102A>G | Lung cancer [RCV000105599] | uncertain significance | 7 | 128794246 | 128794246 | Human | | name |
| 156195349 | CV2251837 | single nucleotide variant | NM_022742.5(CCDC136):c.58G>C (p.Glu20Gln) | not specified [RCV004119825] | uncertain significance | 7 | 128794389 | 128794389 | Human | | name |
| 15101110 | CV722298 | single nucleotide variant | NM_022742.5(CCDC136):c.663G>C (p.Gly221=) | not provided [RCV000892225] | benign | 7 | 128801502 | 128801502 | Human | | name |
| 156053762 | CV2329116 | single nucleotide variant | NM_022742.5(CCDC136):c.115A>G (p.Ser39Gly) | not specified [RCV004173880] | uncertain significance | 7 | 128794446 | 128794446 | Human | | name |
| 401904488 | CV2823157 | single nucleotide variant | NM_001201372.2(CCDC136):c.30A>C (p.Gly10=) | not provided [RCV003423764] | likely benign | 7 | 128791523 | 128791523 | Human | | name |
| 401922753 | CV2823158 | single nucleotide variant | NM_022742.5(CCDC136):c.2853G>A (p.Glu951=) | not provided [RCV003434127] | likely benign | 7 | 128814727 | 128814727 | Human | | name |
| 405264933 | CV3185402 | single nucleotide variant | NM_022742.5(CCDC136):c.1158C>T (p.Asn386=) | not provided [RCV003885966] | likely benign | 7 | 128806305 | 128806305 | Human | | name |
| 405755287 | CV3302875 | single nucleotide variant | NM_022742.5(CCDC136):c.191A>G (p.Gln64Arg) | not specified [RCV004432735] | uncertain significance | 7 | 128794522 | 128794522 | Human | | name |
| 407483370 | CV3418234 | single nucleotide variant | NM_022742.5(CCDC136):c.227G>A (p.Arg76Gln) | not specified [RCV004602839] | uncertain significance | 7 | 128794558 | 128794558 | Human | | name |
| 598177231 | CV3946709 | single nucleotide variant | NM_022742.5(CCDC136):c.185G>A (p.Arg62Gln) | not specified [RCV005310172] | uncertain significance | 7 | 128794516 | 128794516 | Human | | name |
| 15115227 | CV710758 | single nucleotide variant | NM_022742.5(CCDC136):c.1848G>C (p.Leu616=) | not provided [RCV000961813] | benign | 7 | 128810186 | 128810186 | Human | | name |
| 15180710 | CV710759 | single nucleotide variant | NM_022742.5(CCDC136):c.2061C>T (p.Ala687=) | not provided [RCV000974217] | benign | 7 | 128811832 | 128811832 | Human | | name |
| 156176615 | CV2205336 | single nucleotide variant | NM_022742.5(CCDC136):c.752C>T (p.Thr251Met) | not specified [RCV004079951] | uncertain significance | 7 | 128804731 | 128804731 | Human | | name |
| 156378165 | CV2207648 | single nucleotide variant | NM_022742.5(CCDC136):c.530G>A (p.Arg177Gln) | not specified [RCV004090421] | uncertain significance | 7 | 128801369 | 128801369 | Human | | name |
| 156231112 | CV2235120 | single nucleotide variant | NM_022742.5(CCDC136):c.745A>G (p.Ser249Gly) | not specified [RCV004106863] | uncertain significance | 7 | 128804724 | 128804724 | Human | | name |
| 156079192 | CV2248545 | single nucleotide variant | NM_022742.5(CCDC136):c.460C>T (p.Arg154Trp) | not specified [RCV004119669] | uncertain significance | 7 | 128801299 | 128801299 | Human | | name |
| 156084615 | CV2343289 | single nucleotide variant | NM_022742.5(CCDC136):c.520G>T (p.Asp174Tyr) | not specified [RCV004194910] | uncertain significance | 7 | 128801359 | 128801359 | Human | | name |
| 156385973 | CV2364619 | single nucleotide variant | NM_022742.5(CCDC136):c.474G>T (p.Glu158Asp) | not specified [RCV004219511] | uncertain significance | 7 | 128801313 | 128801313 | Human | | name |
| 156226384 | CV2390819 | single nucleotide variant | NM_022742.5(CCDC136):c.589G>A (p.Ala197Thr) | not specified [RCV004241100] | likely benign | 7 | 128801428 | 128801428 | Human | | name |
| 329399057 | CV2439319 | single nucleotide variant | NM_022742.5(CCDC136):c.874C>T (p.Pro292Ser) | not specified [RCV004249628] | uncertain significance | 7 | 128805450 | 128805450 | Human | | name |
| 401741920 | CV2677467 | single nucleotide variant | NM_022742.5(CCDC136):c.634G>A (p.Gly212Ser) | not specified [RCV004289536] | likely benign | 7 | 128801473 | 128801473 | Human | | name |
| 401744386 | CV2680951 | single nucleotide variant | NM_022742.5(CCDC136):c.860T>C (p.Met287Thr) | not specified [RCV004296023] | uncertain significance | 7 | 128805436 | 128805436 | Human | | name |
| 401773051 | CV2698076 | single nucleotide variant | NM_022742.5(CCDC136):c.404A>C (p.Glu135Ala) | not specified [RCV004302876] | uncertain significance | 7 | 128801243 | 128801243 | Human | | name |
| 401772177 | CV2719559 | single nucleotide variant | NM_022742.5(CCDC136):c.991C>T (p.Arg331Cys) | not specified [RCV004327237] | uncertain significance | 7 | 128805803 | 128805803 | Human | | name |
| 401782436 | CV2719814 | single nucleotide variant | NM_022742.5(CCDC136):c.559C>T (p.Arg187Cys) | not specified [RCV004329235] | uncertain significance | 7 | 128801398 | 128801398 | Human | | name |
| 401922754 | CV2823159 | single nucleotide variant | NM_022742.5(CCDC136):c.3027C>T (p.Ser1009=) | not provided [RCV003434128] | likely benign | 7 | 128814901 | 128814901 | Human | | name |
| 405755371 | CV3302888 | single nucleotide variant | NM_022742.5(CCDC136):c.418G>A (p.Glu140Lys) | not specified [RCV004432748] | uncertain significance | 7 | 128801257 | 128801257 | Human | | name |
| 405755378 | CV3302889 | single nucleotide variant | NM_022742.5(CCDC136):c.554T>G (p.Met185Arg) | not specified [RCV004432749] | uncertain significance | 7 | 128801393 | 128801393 | Human | | name |
| 405755383 | CV3302890 | single nucleotide variant | NM_022742.5(CCDC136):c.688C>T (p.Arg230Trp) | not specified [RCV004432750] | uncertain significance | 7 | 128804667 | 128804667 | Human | | name |
| 405755389 | CV3302891 | single nucleotide variant | NM_022742.5(CCDC136):c.955G>A (p.Glu319Lys) | not specified [RCV004432751] | uncertain significance | 7 | 128805767 | 128805767 | Human | | name |
| 407483364 | CV3418233 | single nucleotide variant | NM_022742.5(CCDC136):c.598C>T (p.Arg200Cys) | not specified [RCV004602838] | uncertain significance | 7 | 128801437 | 128801437 | Human | | name |
| 407483431 | CV3418244 | single nucleotide variant | NM_022742.5(CCDC136):c.364C>T (p.Arg122Trp) | not specified [RCV004602848] | uncertain significance | 7 | 128801203 | 128801203 | Human | | name |
| 597786740 | CV3638066 | single nucleotide variant | NM_022742.5(CCDC136):c.736A>G (p.Ser246Gly) | not specified [RCV004901000] | uncertain significance | 7 | 128804715 | 128804715 | Human | | name |
| 597760765 | CV3638068 | single nucleotide variant | NM_022742.5(CCDC136):c.911G>A (p.Arg304Gln) | not specified [RCV004894840] | uncertain significance | 7 | 128805487 | 128805487 | Human | | name |
| 598177257 | CV3946714 | single nucleotide variant | NM_022742.5(CCDC136):c.757C>A (p.Gln253Lys) | not specified [RCV005310176] | uncertain significance | 7 | 128804736 | 128804736 | Human | | name |
| 15115233 | CV710760 | single nucleotide variant | NM_022742.5(CCDC136):c.3261A>G (p.Glu1087=) | not provided [RCV000961814] | benign | 7 | 128815829 | 128815829 | Human | | name |
| 15101105 | CV722297 | single nucleotide variant | NM_022742.5(CCDC136):c.652G>C (p.Asp218His) | not provided [RCV000892224] | benign | 7 | 128801491 | 128801491 | Human | | name |
| 156185047 | CV2195533 | single nucleotide variant | NM_022742.5(CCDC136):c.1762C>T (p.Leu588Phe) | not specified [RCV004082749] | uncertain significance | 7 | 128809606 | 128809606 | Human | | name |
| 156229407 | CV2199482 | single nucleotide variant | NM_022742.5(CCDC136):c.1595G>A (p.Cys532Tyr) | not specified [RCV004071038] | uncertain significance | 7 | 128807535 | 128807535 | Human | | name |
| 156384029 | CV2220267 | single nucleotide variant | NM_022742.5(CCDC136):c.2679A>C (p.Glu893Asp) | not specified [RCV004095695] | uncertain significance | 7 | 128812845 | 128812845 | Human | | name |
| 156383312 | CV2223866 | single nucleotide variant | NM_022742.5(CCDC136):c.1402A>G (p.Lys468Glu) | not specified [RCV004093884] | uncertain significance | 7 | 128806841 | 128806841 | Human | | name |
| 156112069 | CV2228380 | single nucleotide variant | NM_022742.5(CCDC136):c.1803T>A (p.Ser601Arg) | not specified [RCV004098360] | uncertain significance | 7 | 128810141 | 128810141 | Human | | name |
| 156033258 | CV2236202 | single nucleotide variant | NM_022742.5(CCDC136):c.1291A>C (p.Asn431His) | not specified [RCV004107910] | uncertain significance | 7 | 128806730 | 128806730 | Human | | name |
| 156046894 | CV2268714 | single nucleotide variant | NM_022742.5(CCDC136):c.2321A>T (p.Lys774Met) | not specified [RCV004124114] | uncertain significance | 7 | 128812092 | 128812092 | Human | | name |
| 155901138 | CV2275329 | single nucleotide variant | NM_022742.5(CCDC136):c.2324G>C (p.Ser775Thr) | not specified [RCV004137098] | uncertain significance | 7 | 128812095 | 128812095 | Human | | name |
| 156296834 | CV2297613 | single nucleotide variant | NM_022742.5(CCDC136):c.1729G>A (p.Glu577Lys) | not specified [RCV004155310] | uncertain significance | 7 | 128809573 | 128809573 | Human | | name |
| 156176029 | CV2317349 | single nucleotide variant | NM_022742.5(CCDC136):c.1953G>C (p.Glu651Asp) | not specified [RCV004178831] | uncertain significance | 7 | 128810291 | 128810291 | Human | | name |
| 156189807 | CV2328859 | single nucleotide variant | NM_022742.5(CCDC136):c.2138G>A (p.Arg713Gln) | not specified [RCV004179862] | uncertain significance | 7 | 128811909 | 128811909 | Human | | name |
| 156126519 | CV2350296 | single nucleotide variant | NM_022742.5(CCDC136):c.2233G>A (p.Gly745Arg) | not specified [RCV004202250] | likely benign | 7 | 128812004 | 128812004 | Human | | name |
| 156016257 | CV2360423 | single nucleotide variant | NM_022742.5(CCDC136):c.2939G>C (p.Gly980Ala) | not specified [RCV004208748] | uncertain significance | 7 | 128814813 | 128814813 | Human | | name |
| 156226738 | CV2388041 | single nucleotide variant | NM_022742.5(CCDC136):c.2434A>G (p.Ile812Val) | not specified [RCV004241172] | likely benign | 7 | 128812205 | 128812205 | Human | | name |
| 155996560 | CV2393199 | single nucleotide variant | NM_022742.5(CCDC136):c.1287C>G (p.His429Gln) | not specified [RCV004603403] | uncertain significance | 7 | 128806726 | 128806726 | Human | | name |
| 156250081 | CV2394170 | single nucleotide variant | NM_022742.5(CCDC136):c.2752G>A (p.Asp918Asn) | not specified [RCV004236364] | uncertain significance | 7 | 128812918 | 128812918 | Human | | name |
| 329358488 | CV2425271 | single nucleotide variant | NM_022742.5(CCDC136):c.2045T>G (p.Met682Arg) | not specified [RCV004250942] | uncertain significance | 7 | 128811816 | 128811816 | Human | | name |
| 329360698 | CV2439615 | single nucleotide variant | NM_022742.5(CCDC136):c.1415A>G (p.Glu472Gly) | not specified [RCV004255633] | uncertain significance | 7 | 128806854 | 128806854 | Human | | name |
| 329370428 | CV2461714 | single nucleotide variant | NM_022742.5(CCDC136):c.2657C>T (p.Ala886Val) | not specified [RCV004269866] | uncertain significance | 7 | 128812823 | 128812823 | Human | | name |
| 329375771 | CV2468814 | single nucleotide variant | NM_022742.5(CCDC136):c.2312G>A (p.Ser771Asn) | not specified [RCV004280128] | uncertain significance | 7 | 128812083 | 128812083 | Human | | name |
| 329392983 | CV2469138 | single nucleotide variant | NM_022742.5(CCDC136):c.1700T>C (p.Leu567Pro) | not specified [RCV004274365] | uncertain significance | 7 | 128809544 | 128809544 | Human | | name |
| 329352811 | CV2470558 | single nucleotide variant | NM_022742.5(CCDC136):c.1490G>A (p.Arg497Gln) | not specified [RCV004273562] | uncertain significance | 7 | 128807430 | 128807430 | Human | | name |
| 329392644 | CV2471449 | single nucleotide variant | NM_022742.5(CCDC136):c.1046A>G (p.Gln349Arg) | not specified [RCV004280447] | uncertain significance | 7 | 128805858 | 128805858 | Human | | name |
| 401880157 | CV2769951 | single nucleotide variant | NM_022742.5(CCDC136):c.2914C>G (p.Pro972Ala) | not specified [RCV004353787] | uncertain significance | 7 | 128814788 | 128814788 | Human | | name |
| 401886519 | CV2771308 | single nucleotide variant | NM_022742.5(CCDC136):c.1400T>A (p.Phe467Tyr) | not specified [RCV004346280] | uncertain significance | 7 | 128806839 | 128806839 | Human | | name |
| 401886522 | CV2771309 | single nucleotide variant | NM_022742.5(CCDC136):c.1407G>C (p.Glu469Asp) | not specified [RCV004346281] | uncertain significance | 7 | 128806846 | 128806846 | Human | | name |
| 401865626 | CV2791511 | single nucleotide variant | NM_022742.5(CCDC136):c.1018C>T (p.Arg340Trp) | not specified [RCV004358893] | uncertain significance | 7 | 128805830 | 128805830 | Human | | name |
| 405755243 | CV3302870 | single nucleotide variant | NM_022742.5(CCDC136):c.1220C>G (p.Ser407Cys) | not specified [RCV004432730] | uncertain significance | 7 | 128806367 | 128806367 | Human | | name |
| 405755259 | CV3302872 | single nucleotide variant | NM_022742.5(CCDC136):c.1595G>T (p.Cys532Phe) | not specified [RCV004432732] | uncertain significance | 7 | 128807535 | 128807535 | Human | | name |
| 405755266 | CV3302873 | single nucleotide variant | NM_022742.5(CCDC136):c.1730A>C (p.Glu577Ala) | not specified [RCV004432733] | uncertain significance | 7 | 128809574 | 128809574 | Human | | name |
| 405755293 | CV3302876 | single nucleotide variant | NM_022742.5(CCDC136):c.2141A>T (p.Lys714Met) | not specified [RCV004432736] | uncertain significance | 7 | 128811912 | 128811912 | Human | | name |
| 405755299 | CV3302877 | single nucleotide variant | NM_022742.5(CCDC136):c.2170C>A (p.Leu724Met) | not specified [RCV004432737] | uncertain significance | 7 | 128811941 | 128811941 | Human | | name |
| 405755304 | CV3302878 | single nucleotide variant | NM_022742.5(CCDC136):c.2284T>C (p.Tyr762His) | not specified [RCV004432738] | uncertain significance | 7 | 128812055 | 128812055 | Human | | name |
| 405755312 | CV3302879 | single nucleotide variant | NM_022742.5(CCDC136):c.2585C>T (p.Ala862Val) | not specified [RCV004432739] | uncertain significance | 7 | 128812751 | 128812751 | Human | | name |
| 405755322 | CV3302880 | single nucleotide variant | NM_022742.5(CCDC136):c.2596A>G (p.Met866Val) | not specified [RCV004432740] | uncertain significance | 7 | 128812762 | 128812762 | Human | | name |
| 405755328 | CV3302881 | single nucleotide variant | NM_022742.5(CCDC136):c.2765T>C (p.Ile922Thr) | not specified [RCV004432741] | uncertain significance | 7 | 128814639 | 128814639 | Human | | name |
| 407483406 | CV3418239 | single nucleotide variant | NM_022742.5(CCDC136):c.1985A>G (p.Asp662Gly) | not specified [RCV004602844] | uncertain significance | 7 | 128810323 | 128810323 | Human | | name |
| 407483418 | CV3418241 | single nucleotide variant | NM_022742.5(CCDC136):c.1984G>A (p.Asp662Asn) | not specified [RCV004602846] | uncertain significance | 7 | 128810322 | 128810322 | Human | | name |
| 407483423 | CV3418242 | single nucleotide variant | NM_022742.5(CCDC136):c.1261C>T (p.Arg421Trp) | not specified [RCV004602847] | uncertain significance | 7 | 128806700 | 128806700 | Human | | name |
| 407454343 | CV3418243 | single nucleotide variant | NM_022742.5(CCDC136):c.2741C>T (p.Ala914Val) | not specified [RCV004609818] | uncertain significance | 7 | 128812907 | 128812907 | Human | | name |
| 597786744 | CV3638065 | single nucleotide variant | NM_022742.5(CCDC136):c.1430C>T (p.Thr477Met) | not specified [RCV004900999] | likely benign | 7 | 128807370 | 128807370 | Human | | name |
| 597786735 | CV3638069 | single nucleotide variant | NM_022742.5(CCDC136):c.1814T>G (p.Leu605Arg) | not specified [RCV004901001] | uncertain significance | 7 | 128810152 | 128810152 | Human | | name |
| 597786731 | CV3638070 | single nucleotide variant | NM_022742.5(CCDC136):c.1940G>A (p.Arg647Gln) | not specified [RCV004901002] | uncertain significance | 7 | 128810278 | 128810278 | Human | | name |
| 597786468 | CV3638072 | single nucleotide variant | NM_022742.5(CCDC136):c.1454A>G (p.Lys485Arg) | not specified [RCV004901004] | uncertain significance | 7 | 128807394 | 128807394 | Human | | name |
| 597761169 | CV3638073 | single nucleotide variant | NM_022742.5(CCDC136):c.1823T>C (p.Leu608Ser) | not specified [RCV004894841] | uncertain significance | 7 | 128810161 | 128810161 | Human | | name |
| 597786459 | CV3638074 | single nucleotide variant | NM_022742.5(CCDC136):c.2045T>C (p.Met682Thr) | not specified [RCV004901005] | uncertain significance | 7 | 128811816 | 128811816 | Human | | name |
| 597786464 | CV3638075 | single nucleotide variant | NM_022742.5(CCDC136):c.1501A>G (p.Met501Val) | not specified [RCV004901006] | uncertain significance | 7 | 128807441 | 128807441 | Human | | name |
| 597760774 | CV3638076 | single nucleotide variant | NM_022742.5(CCDC136):c.2995G>T (p.Val999Leu) | not specified [RCV004894842] | uncertain significance | 7 | 128814869 | 128814869 | Human | | name |
| 597760783 | CV3638078 | single nucleotide variant | NM_022742.5(CCDC136):c.1827A>C (p.Glu609Asp) | not specified [RCV004894844] | uncertain significance | 7 | 128810165 | 128810165 | Human | | name |
| 598177237 | CV3946710 | single nucleotide variant | NM_022742.5(CCDC136):c.2668G>T (p.Asp890Tyr) | not specified [RCV005310173] | uncertain significance | 7 | 128812834 | 128812834 | Human | | name |
| 598177243 | CV3946711 | single nucleotide variant | NM_022742.5(CCDC136):c.2699G>A (p.Arg900Lys) | not specified [RCV005310174] | likely benign | 7 | 128812865 | 128812865 | Human | | name |
| 598177251 | CV3946712 | single nucleotide variant | NM_022742.5(CCDC136):c.1480G>A (p.Glu494Lys) | not specified [RCV005310175] | uncertain significance | 7 | 128807420 | 128807420 | Human | | name |
| 598177264 | CV3946715 | single nucleotide variant | NM_022742.5(CCDC136):c.1641G>C (p.Gln547His) | not specified [RCV005310177] | uncertain significance | 7 | 128809485 | 128809485 | Human | | name |
| 598177268 | CV3946716 | single nucleotide variant | NM_022742.5(CCDC136):c.2712G>C (p.Glu904Asp) | not specified [RCV005310178] | uncertain significance | 7 | 128812878 | 128812878 | Human | | name |
| 598177274 | CV3946717 | single nucleotide variant | NM_022742.5(CCDC136):c.2845G>C (p.Val949Leu) | not specified [RCV005310179] | uncertain significance | 7 | 128814719 | 128814719 | Human | | name |
| 598177281 | CV3946718 | single nucleotide variant | NM_022742.5(CCDC136):c.1772C>A (p.Pro591Gln) | not specified [RCV005310180] | uncertain significance | 7 | 128809616 | 128809616 | Human | | name |
| 598177288 | CV3946719 | single nucleotide variant | NM_022742.5(CCDC136):c.2390G>A (p.Ser797Asn) | not specified [RCV005310181] | uncertain significance | 7 | 128812161 | 128812161 | Human | | name |
| 598227179 | CV3946720 | single nucleotide variant | NM_022742.5(CCDC136):c.1376A>G (p.His459Arg) | not specified [RCV005318882] | likely benign | 7 | 128806815 | 128806815 | Human | | name |
| 15100952 | CV699819 | single nucleotide variant | NM_022742.5(CCDC136):c.1294G>A (p.Val432Ile) | not provided [RCV000958992] | benign | 7 | 128806733 | 128806733 | Human | | name |
| 15101118 | CV722299 | single nucleotide variant | NM_022742.5(CCDC136):c.2938G>A (p.Gly980Arg) | not provided [RCV000892226] | benign | 7 | 128814812 | 128814812 | Human | | name |
| 156376290 | CV2210528 | single nucleotide variant | NM_022742.5(CCDC136):c.3025A>C (p.Ser1009Arg) | not specified [RCV004089656] | uncertain significance | 7 | 128814899 | 128814899 | Human | | name |
| 156078036 | CV2248458 | single nucleotide variant | NM_022742.5(CCDC136):c.3147A>T (p.Gln1049His) | not specified [RCV004119592] | uncertain significance | 7 | 128815715 | 128815715 | Human | | name |
| 156387629 | CV2372805 | single nucleotide variant | NM_022742.5(CCDC136):c.3011C>T (p.Ser1004Leu) | not specified [RCV004221989] | likely benign | 7 | 128814885 | 128814885 | Human | | name |
| 156160304 | CV2398178 | single nucleotide variant | NM_022742.5(CCDC136):c.3325G>A (p.Glu1109Lys) | not specified [RCV004241752] | uncertain significance | 7 | 128815893 | 128815893 | Human | | name |
| 329375894 | CV2441189 | single nucleotide variant | NM_022742.5(CCDC136):c.3329A>G (p.Glu1110Gly) | not specified [RCV004263585] | uncertain significance | 7 | 128815897 | 128815897 | Human | | name |
| 405755333 | CV3302882 | single nucleotide variant | NM_022742.5(CCDC136):c.3059T>C (p.Val1020Ala) | not specified [RCV004432742] | uncertain significance | 7 | 128815627 | 128815627 | Human | | name |
| 405755339 | CV3302883 | single nucleotide variant | NM_022742.5(CCDC136):c.3157G>A (p.Glu1053Lys) | not specified [RCV004432743] | uncertain significance | 7 | 128815725 | 128815725 | Human | | name |
| 405755347 | CV3302884 | single nucleotide variant | NM_022742.5(CCDC136):c.3304G>A (p.Asp1102Asn) | not specified [RCV004432744] | uncertain significance | 7 | 128815872 | 128815872 | Human | | name |
| 405755351 | CV3302885 | single nucleotide variant | NM_022742.5(CCDC136):c.3352G>C (p.Glu1118Gln) | not specified [RCV004432745] | uncertain significance | 7 | 128815920 | 128815920 | Human | | name |
| 405755357 | CV3302886 | single nucleotide variant | NM_022742.5(CCDC136):c.3433C>T (p.Leu1145Phe) | not specified [RCV004432746] | uncertain significance | 7 | 128817827 | 128817827 | Human | | name |
| 407483374 | CV3418235 | single nucleotide variant | NM_022742.5(CCDC136):c.3176G>C (p.Gly1059Ala) | not specified [RCV004602840] | uncertain significance | 7 | 128815744 | 128815744 | Human | | name |
| 407483398 | CV3418238 | single nucleotide variant | NM_022742.5(CCDC136):c.3187G>C (p.Val1063Leu) | not specified [RCV004602843] | uncertain significance | 7 | 128815755 | 128815755 | Human | | name |
| 407483413 | CV3418240 | single nucleotide variant | NM_022742.5(CCDC136):c.3137A>G (p.Glu1046Gly) | not specified [RCV004602845] | uncertain significance | 7 | 128815705 | 128815705 | Human | | name |
| 597786601 | CV3638071 | single nucleotide variant | NM_022742.5(CCDC136):c.3358A>C (p.Lys1120Gln) | not specified [RCV004901003] | uncertain significance | 7 | 128815926 | 128815926 | Human | | name |
| 15199134 | CV750399 | single nucleotide variant | NM_022742.5(CCDC136):c.3290A>G (p.Glu1097Gly) | not provided [RCV000912457] | likely benign | 7 | 128815858 | 128815858 | Human | | name |
| 8632327 | CV87535 | single nucleotide variant | NM_001201372.1(CCDC136):c.527C>T (p.Ser176Phe) | Malignant melanoma [RCV000067626] | not provided | 7 | 128801216 | 128801216 | Human | | name |
