| 8650286 | CV126861 | single nucleotide variant | NM_080872.2(UNC5D):c.751+170T>C | Lung cancer [RCV000107348] | uncertain significance | 8 | 35683897 | 35683897 | Human | | name |
| 8650285 | CV126860 | single nucleotide variant | NM_080872.2(UNC5D):c.467-9598A>T | Lung cancer [RCV000107347] | uncertain significance | 8 | 35585956 | 35585956 | Human | | name |
| 8650281 | CV126856 | single nucleotide variant | NM_080872.2(UNC5D):c.103+29333G>T | Lung cancer [RCV000107343] | uncertain significance | 8 | 35265220 | 35265220 | Human | | name |
| 8650282 | CV126857 | single nucleotide variant | NM_080872.2(UNC5D):c.103+81421C>A | Lung cancer [RCV000107344] | uncertain significance | 8 | 35317308 | 35317308 | Human | | name |
| 8650284 | CV126859 | single nucleotide variant | NM_080872.2(UNC5D):c.104-99064C>A | Lung cancer [RCV000107346] | uncertain significance | 8 | 35450228 | 35450228 | Human | | name |
| 8650283 | CV126858 | single nucleotide variant | NM_080872.2(UNC5D):c.103+129615A>G | Lung cancer [RCV000107345] | uncertain significance | 8 | 35365502 | 35365502 | Human | | name |
| 15100918 | CV700572 | single nucleotide variant | NM_080872.4(UNC5D):c.12G>T (p.Ala4=) | not provided [RCV000958987] | likely benign | 8 | 35235796 | 35235796 | Human | | name |
| 405809962 | CV3345062 | single nucleotide variant | NM_080872.4(UNC5D):c.23C>G (p.Ala8Gly) | not specified [RCV004482022] | likely benign | 8 | 35235807 | 35235807 | Human | | name |
| 156177104 | CV2327155 | single nucleotide variant | NM_080872.4(UNC5D):c.91G>T (p.Ala31Ser) | not specified [RCV004178719] | uncertain significance | 8 | 35235875 | 35235875 | Human | | name |
| 401897652 | CV2776624 | single nucleotide variant | NM_080872.4(UNC5D):c.40G>A (p.Ala14Thr) | not specified [RCV004357496] | uncertain significance | 8 | 35235824 | 35235824 | Human | | name |
| 405809971 | CV3345067 | single nucleotide variant | NM_080872.4(UNC5D):c.43C>T (p.Arg15Cys) | not specified [RCV004482027] | uncertain significance | 8 | 35235827 | 35235827 | Human | | name |
| 15185373 | CV723072 | single nucleotide variant | NM_080872.4(UNC5D):c.336C>T (p.Arg112=) | not provided [RCV000886677] | benign | 8 | 35568111 | 35568111 | Human | | name |
| 8632988 | CV88203 | single nucleotide variant | NM_080872.2(UNC5D):c.597C>T (p.Pro199=) | Malignant melanoma [RCV000068295] | not provided | 8 | 35683573 | 35683573 | Human | | name |
| 156082916 | CV2384904 | single nucleotide variant | NM_080872.4(UNC5D):c.177G>T (p.Glu59Asp) | not specified [RCV004225778] | uncertain significance | 8 | 35549365 | 35549365 | Human | | name |
| 155998465 | CV2396246 | single nucleotide variant | NM_080872.4(UNC5D):c.230C>T (p.Ala77Val) | not specified [RCV004240198] | uncertain significance | 8 | 35549418 | 35549418 | Human | | name |
| 401857535 | CV2756028 | single nucleotide variant | NM_080872.4(UNC5D):c.130G>A (p.Glu44Lys) | not specified [RCV004338154] | uncertain significance | 8 | 35549318 | 35549318 | Human | | name |
| 405809957 | CV3345059 | single nucleotide variant | NM_080872.4(UNC5D):c.211A>G (p.Ile71Val) | not specified [RCV004482019] | uncertain significance | 8 | 35549399 | 35549399 | Human | | name |
| 405809966 | CV3345064 | single nucleotide variant | NM_080872.4(UNC5D):c.265G>A (p.Gly89Ser) | not specified [RCV004482024] | uncertain significance | 8 | 35549453 | 35549453 | Human | | name |
| 597790697 | CV3632913 | single nucleotide variant | NM_080872.4(UNC5D):c.194T>G (p.Ile65Ser) | not specified [RCV004876417] | uncertain significance | 8 | 35549382 | 35549382 | Human | | name |
| 598191265 | CV3925650 | single nucleotide variant | NM_080872.4(UNC5D):c.217C>T (p.Leu73Phe) | not specified [RCV005288328] | uncertain significance | 8 | 35549405 | 35549405 | Human | | name |
| 8626574 | CV81718 | single nucleotide variant | NM_080872.2(UNC5D):c.1344G>A (p.Leu448=) | Malignant melanoma [RCV000061796] | not provided | 8 | 35726192 | 35726192 | Human | | name |
| 8632987 | CV88202 | single nucleotide variant | NM_080872.4(UNC5D):c.286G>A (p.Glu96Lys) | not specified [RCV004322518] | uncertain significance|not provided | 8 | 35549474 | 35549474 | Human | | name |
| 155909845 | CV2360048 | single nucleotide variant | NM_080872.4(UNC5D):c.676T>G (p.Ser226Ala) | not specified [RCV004212881] | uncertain significance | 8 | 35683652 | 35683652 | Human | | name |
| 401735964 | CV2692241 | single nucleotide variant | NM_080872.4(UNC5D):c.511C>T (p.Pro171Ser) | not specified [RCV004303719] | uncertain significance | 8 | 35595598 | 35595598 | Human | | name |
| 401892304 | CV2776059 | single nucleotide variant | NM_080872.4(UNC5D):c.695T>G (p.Met232Arg) | not specified [RCV004353165] | uncertain significance | 8 | 35683671 | 35683671 | Human | | name |
| 405809968 | CV3345065 | single nucleotide variant | NM_080872.4(UNC5D):c.332T>G (p.Val111Gly) | not specified [RCV004482025] | uncertain significance | 8 | 35568107 | 35568107 | Human | | name |
| 405809970 | CV3345066 | single nucleotide variant | NM_080872.4(UNC5D):c.388G>A (p.Glu130Lys) | not specified [RCV004482026] | uncertain significance | 8 | 35568163 | 35568163 | Human | | name |
| 405809973 | CV3345068 | single nucleotide variant | NM_080872.4(UNC5D):c.713C>T (p.Ala238Val) | not specified [RCV004482028] | uncertain significance | 8 | 35683689 | 35683689 | Human | | name |
| 407454730 | CV3489353 | single nucleotide variant | NM_080872.4(UNC5D):c.335G>A (p.Arg112His) | not specified [RCV004685202] | uncertain significance | 8 | 35568110 | 35568110 | Human | | name |
| 597790691 | CV3632910 | single nucleotide variant | NM_080872.4(UNC5D):c.866C>A (p.Ala289Asp) | not specified [RCV004876415] | uncertain significance | 8 | 35684696 | 35684696 | Human | | name |
| 598274655 | CV3925653 | single nucleotide variant | NM_080872.4(UNC5D):c.334C>T (p.Arg112Cys) | not specified [RCV005304044] | uncertain significance | 8 | 35568109 | 35568109 | Human | | name |
| 156338764 | CV2224983 | single nucleotide variant | NM_080872.4(UNC5D):c.2015G>A (p.Ser672Asn) | not specified [RCV004094828] | uncertain significance | 8 | 35750661 | 35750661 | Human | | name |
| 155963879 | CV2261540 | single nucleotide variant | NM_080872.4(UNC5D):c.1913G>C (p.Arg638Thr) | not specified [RCV004125880] | uncertain significance | 8 | 35748673 | 35748673 | Human | | name |
| 155965498 | CV2261802 | single nucleotide variant | NM_080872.4(UNC5D):c.2107T>C (p.Ser703Pro) | not specified [RCV004126081] | uncertain significance | 8 | 35750753 | 35750753 | Human | | name |
| 155962446 | CV2388241 | single nucleotide variant | NM_080872.4(UNC5D):c.2329C>T (p.Arg777Cys) | not specified [RCV004234699] | uncertain significance | 8 | 35766917 | 35766917 | Human | | name |
| 329391329 | CV2452244 | single nucleotide variant | NM_080872.4(UNC5D):c.2231A>G (p.Lys744Arg) | not specified [RCV004278937] | uncertain significance | 8 | 35759387 | 35759387 | Human | | name |
| 329351837 | CV2455366 | single nucleotide variant | NM_080872.4(UNC5D):c.2579G>A (p.Arg860Gln) | not specified [RCV004274866] | uncertain significance | 8 | 35774399 | 35774399 | Human | | name |
| 401735647 | CV2672706 | single nucleotide variant | NM_080872.4(UNC5D):c.1639G>A (p.Val547Ile) | not specified [RCV004287719] | uncertain significance | 8 | 35726487 | 35726487 | Human | | name |
| 401781011 | CV2681860 | single nucleotide variant | NM_080872.4(UNC5D):c.1967C>A (p.Ser656Tyr) | not specified [RCV004296854] | uncertain significance | 8 | 35750613 | 35750613 | Human | | name |
| 401723868 | CV2684895 | single nucleotide variant | NM_080872.4(UNC5D):c.2095A>C (p.Met699Leu) | not specified [RCV004296400] | uncertain significance | 8 | 35750741 | 35750741 | Human | | name |
| 401770331 | CV2711086 | single nucleotide variant | NM_080872.4(UNC5D):c.1118G>A (p.Ser373Asn) | not specified [RCV004310775] | uncertain significance | 8 | 35722210 | 35722210 | Human | | name |
| 401877137 | CV2769349 | single nucleotide variant | NM_080872.4(UNC5D):c.1052C>A (p.Ser351Tyr) | not specified [RCV004357343] | uncertain significance | 8 | 35686677 | 35686677 | Human | | name |
| 401891573 | CV2780547 | single nucleotide variant | NM_080872.4(UNC5D):c.1915A>G (p.Thr639Ala) | not specified [RCV004358232] | uncertain significance | 8 | 35748675 | 35748675 | Human | | name |
| 401892778 | CV2791782 | single nucleotide variant | NM_080872.4(UNC5D):c.2804T>G (p.Ile935Ser) | not specified [RCV004353100] | uncertain significance | 8 | 35790505 | 35790505 | Human | | name |
| 405809944 | CV3345052 | single nucleotide variant | NM_080872.4(UNC5D):c.1135G>A (p.Asp379Asn) | not specified [RCV004482012] | uncertain significance | 8 | 35722227 | 35722227 | Human | | name |
| 405809946 | CV3345053 | single nucleotide variant | NM_080872.4(UNC5D):c.1160G>A (p.Gly387Asp) | not specified [RCV004482013] | uncertain significance | 8 | 35722252 | 35722252 | Human | | name |
| 405809947 | CV3345054 | single nucleotide variant | NM_080872.4(UNC5D):c.1171G>A (p.Val391Met) | not specified [RCV004482014] | uncertain significance | 8 | 35722263 | 35722263 | Human | | name |
| 405809949 | CV3345055 | single nucleotide variant | NM_080872.4(UNC5D):c.1354C>T (p.Arg452Trp) | not specified [RCV004482015] | uncertain significance | 8 | 35726202 | 35726202 | Human | | name |
| 405809951 | CV3345056 | single nucleotide variant | NM_080872.4(UNC5D):c.1366G>A (p.Gly456Arg) | not specified [RCV004482016] | uncertain significance | 8 | 35726214 | 35726214 | Human | | name |
| 405809953 | CV3345057 | single nucleotide variant | NM_080872.4(UNC5D):c.1841C>T (p.Thr614Ile) | not specified [RCV004482017] | uncertain significance | 8 | 35748601 | 35748601 | Human | | name |
| 405809955 | CV3345058 | single nucleotide variant | NM_080872.4(UNC5D):c.2077G>A (p.Val693Met) | not specified [RCV004482018] | uncertain significance | 8 | 35750723 | 35750723 | Human | | name |
| 405809958 | CV3345060 | single nucleotide variant | NM_080872.4(UNC5D):c.2263C>G (p.Leu755Val) | not specified [RCV004482020] | uncertain significance | 8 | 35759419 | 35759419 | Human | | name |
| 405809964 | CV3345063 | single nucleotide variant | NM_080872.4(UNC5D):c.2486G>A (p.Arg829Gln) | not specified [RCV004482023] | uncertain significance | 8 | 35774306 | 35774306 | Human | | name |
| 407454728 | CV3489352 | single nucleotide variant | NM_080872.4(UNC5D):c.1355G>A (p.Arg452Gln) | not specified [RCV004685201] | uncertain significance | 8 | 35726203 | 35726203 | Human | | name |
| 407454732 | CV3489354 | single nucleotide variant | NM_080872.4(UNC5D):c.2566T>C (p.Ser856Pro) | not specified [RCV004685203] | uncertain significance | 8 | 35774386 | 35774386 | Human | | name |
| 597790675 | CV3632906 | single nucleotide variant | NM_080872.4(UNC5D):c.2477A>C (p.Glu826Ala) | not specified [RCV004876411] | uncertain significance | 8 | 35767065 | 35767065 | Human | | name |
| 597790679 | CV3632907 | single nucleotide variant | NM_080872.4(UNC5D):c.2380C>T (p.Arg794Cys) | not specified [RCV004876412] | uncertain significance | 8 | 35766968 | 35766968 | Human | | name |
| 597790684 | CV3632908 | single nucleotide variant | NM_080872.4(UNC5D):c.1767C>G (p.Ser589Arg) | not specified [RCV004876413] | uncertain significance | 8 | 35748527 | 35748527 | Human | | name |
| 597790687 | CV3632909 | single nucleotide variant | NM_080872.4(UNC5D):c.2470A>G (p.Ile824Val) | not specified [RCV004876414] | uncertain significance | 8 | 35767058 | 35767058 | Human | | name |
| 597790693 | CV3632911 | single nucleotide variant | NM_080872.4(UNC5D):c.1121T>C (p.Ile374Thr) | not specified [RCV004876416] | uncertain significance | 8 | 35722213 | 35722213 | Human | | name |
| 597721231 | CV3632912 | single nucleotide variant | NM_080872.4(UNC5D):c.1447G>A (p.Val483Met) | not specified [RCV004887899] | uncertain significance | 8 | 35726295 | 35726295 | Human | | name |
| 598274651 | CV3925651 | single nucleotide variant | NM_080872.4(UNC5D):c.2789C>T (p.Thr930Met) | not specified [RCV005304042] | uncertain significance | 8 | 35790490 | 35790490 | Human | | name |
| 598274653 | CV3925652 | single nucleotide variant | NM_080872.4(UNC5D):c.1214G>A (p.Arg405Gln) | not specified [RCV005304043] | uncertain significance | 8 | 35722306 | 35722306 | Human | | name |
| 598191270 | CV3925654 | single nucleotide variant | NM_080872.4(UNC5D):c.2341A>C (p.Ser781Arg) | not specified [RCV005288329] | uncertain significance | 8 | 35766929 | 35766929 | Human | | name |
| 598274657 | CV3925655 | single nucleotide variant | NM_080872.4(UNC5D):c.1930T>A (p.Trp644Arg) | not specified [RCV005304045] | uncertain significance | 8 | 35748690 | 35748690 | Human | | name |
| 598274659 | CV3925656 | single nucleotide variant | NM_080872.4(UNC5D):c.1283A>C (p.Asn428Thr) | not specified [RCV005304046] | uncertain significance | 8 | 35722375 | 35722375 | Human | | name |
| 8632989 | CV88204 | single nucleotide variant | NM_080872.2(UNC5D):c.1532C>T (p.Pro511Leu) | Malignant melanoma [RCV000068296] | not provided | 8 | 35726380 | 35726380 | Human | | name |
