| 8575176 | CV109521 | single nucleotide variant | NM_170692.2(RASAL2):c.203-12809T>C | Lung cancer [RCV000090046] | uncertain significance | 1 | 178270755 | 178270755 | Human | | name |
| 401906286 | CV2806198 | single nucleotide variant | NM_170692.4(RASAL2):c.90C>T (p.Pro30=) | not provided [RCV003421232] | likely benign | 1 | 178094582 | 178094582 | Human | | name |
| 597706218 | CV3593036 | single nucleotide variant | NM_170692.4(RASAL2):c.8T>G (p.Leu3Arg) | not specified [RCV004860481] | uncertain significance | 1 | 178094500 | 178094500 | Human | | name |
| 401768266 | CV2675209 | single nucleotide variant | NM_170692.4(RASAL2):c.13C>T (p.Pro5Ser) | not specified [RCV004289980] | uncertain significance | 1 | 178094505 | 178094505 | Human | | name |
| 401879749 | CV2788499 | single nucleotide variant | NM_170692.4(RASAL2):c.97G>T (p.Asp33Tyr) | not specified [RCV004359481] | uncertain significance | 1 | 178094589 | 178094589 | Human | | name |
| 598184186 | CV3902115 | single nucleotide variant | NM_170692.4(RASAL2):c.76G>T (p.Asp26Tyr) | not specified [RCV005265722] | uncertain significance | 1 | 178094568 | 178094568 | Human | | name |
| 15104049 | CV718406 | single nucleotide variant | NM_170692.4(RASAL2):c.834C>T (p.Thr278=) | not provided [RCV000892807] | benign | 1 | 178441554 | 178441554 | Human | | name |
| 15116838 | CV731891 | single nucleotide variant | NM_170692.4(RASAL2):c.83C>A (p.Pro28Gln) | not provided [RCV000895271] | likely benign | 1 | 178094575 | 178094575 | Human | | name |
| 156081557 | CV2292821 | single nucleotide variant | NM_170692.4(RASAL2):c.212G>A (p.Gly71Glu) | not specified [RCV004148340] | uncertain significance | 1 | 178283573 | 178283573 | Human | | name |
| 156090459 | CV2299965 | single nucleotide variant | NM_170692.4(RASAL2):c.226C>T (p.Arg76Cys) | not specified [RCV004151183] | uncertain significance | 1 | 178283587 | 178283587 | Human | | name |
| 405659667 | CV3312282 | single nucleotide variant | NM_170692.4(RASAL2):c.165G>T (p.Glu55Asp) | not specified [RCV004438602] | uncertain significance | 1 | 178094657 | 178094657 | Human | | name |
| 405659672 | CV3312284 | single nucleotide variant | NM_170692.4(RASAL2):c.185G>C (p.Ser62Thr) | not specified [RCV004438604] | uncertain significance | 1 | 178094677 | 178094677 | Human | | name |
| 407466821 | CV3472466 | single nucleotide variant | NM_170692.4(RASAL2):c.227G>T (p.Arg76Leu) | not specified [RCV004660565] | uncertain significance | 1 | 178283588 | 178283588 | Human | | name |
| 597706207 | CV3593035 | single nucleotide variant | NM_170692.4(RASAL2):c.253A>C (p.Thr85Pro) | not specified [RCV004860480] | uncertain significance | 1 | 178283614 | 178283614 | Human | | name |
| 15157047 | CV718407 | single nucleotide variant | NM_170692.4(RASAL2):c.1299G>A (p.Arg433=) | not provided [RCV000880748] | likely benign | 1 | 178443046 | 178443046 | Human | | name |
| 15131056 | CV731892 | single nucleotide variant | NM_170692.4(RASAL2):c.1107T>C (p.Leu369=) | not provided [RCV000897707] | likely benign | 1 | 178442854 | 178442854 | Human | | name |
| 15131063 | CV731893 | single nucleotide variant | NM_170692.4(RASAL2):c.2541C>T (p.Ser847=) | not provided [RCV000897708] | likely benign | 1 | 178457833 | 178457833 | Human | | name |
| 156252721 | CV2212475 | single nucleotide variant | NM_170692.4(RASAL2):c.904C>T (p.Arg302Cys) | not specified [RCV004091368] | uncertain significance | 1 | 178441624 | 178441624 | Human | | name |
| 155977160 | CV2246230 | single nucleotide variant | NM_170692.4(RASAL2):c.730C>G (p.Pro244Ala) | not specified [RCV004107689] | uncertain significance | 1 | 178439477 | 178439477 | Human | | name |
| 156280184 | CV2325428 | single nucleotide variant | NM_170692.4(RASAL2):c.922A>T (p.Asn308Tyr) | not specified [RCV004177787] | uncertain significance | 1 | 178441642 | 178441642 | Human | | name |
| 156043921 | CV2342355 | single nucleotide variant | NM_170692.4(RASAL2):c.599A>G (p.Lys200Arg) | not specified [RCV004191921] | uncertain significance | 1 | 178420545 | 178420545 | Human | | name |
| 155936738 | CV2376025 | single nucleotide variant | NM_170692.4(RASAL2):c.941G>A (p.Arg314Gln) | not specified [RCV004220270] | uncertain significance | 1 | 178442688 | 178442688 | Human | | name |
| 156031906 | CV2376431 | single nucleotide variant | NM_170692.4(RASAL2):c.442G>A (p.Gly148Ser) | not specified [RCV004220614] | uncertain significance | 1 | 178300103 | 178300103 | Human | | name |
| 156196924 | CV2400684 | single nucleotide variant | NM_170692.4(RASAL2):c.488G>A (p.Arg163Gln) | not specified [RCV004242360] | uncertain significance | 1 | 178390130 | 178390130 | Human | | name |
| 156007431 | CV2401311 | single nucleotide variant | NM_170692.4(RASAL2):c.350A>T (p.Gln117Leu) | not specified [RCV004245851] | uncertain significance | 1 | 178300011 | 178300011 | Human | | name |
| 401779033 | CV2702052 | single nucleotide variant | NM_170692.4(RASAL2):c.445G>A (p.Ala149Thr) | not specified [RCV004320631] | likely benign | 1 | 178300106 | 178300106 | Human | | name |
| 401754565 | CV2722740 | single nucleotide variant | NM_170692.4(RASAL2):c.706C>T (p.Arg236Cys) | not specified [RCV004325172] | uncertain significance | 1 | 178439453 | 178439453 | Human | | name |
| 405659697 | CV3312293 | single nucleotide variant | NM_170692.4(RASAL2):c.380G>A (p.Arg127Gln) | not specified [RCV004438613] | uncertain significance | 1 | 178300041 | 178300041 | Human | | name |
| 405659701 | CV3312294 | single nucleotide variant | NM_170692.4(RASAL2):c.427G>A (p.Glu143Lys) | not specified [RCV004438614] | uncertain significance | 1 | 178300088 | 178300088 | Human | | name |
| 405659704 | CV3312295 | single nucleotide variant | NM_170692.4(RASAL2):c.473G>A (p.Arg158Lys) | not specified [RCV004438615] | uncertain significance | 1 | 178390115 | 178390115 | Human | | name |
| 405659708 | CV3312296 | single nucleotide variant | NM_170692.4(RASAL2):c.565G>C (p.Gly189Arg) | not specified [RCV004438616] | uncertain significance | 1 | 178420511 | 178420511 | Human | | name |
| 405659711 | CV3312297 | single nucleotide variant | NM_170692.4(RASAL2):c.643C>T (p.Arg215Trp) | not specified [RCV004438617] | uncertain significance | 1 | 178420589 | 178420589 | Human | | name |
| 407466811 | CV3472461 | single nucleotide variant | NM_170692.4(RASAL2):c.531G>T (p.Met177Ile) | not specified [RCV004660562] | uncertain significance | 1 | 178390173 | 178390173 | Human | | name |
| 407466815 | CV3472463 | single nucleotide variant | NM_170692.4(RASAL2):c.659G>A (p.Arg220His) | not specified [RCV004660563] | uncertain significance | 1 | 178420605 | 178420605 | Human | | name |
| 407466827 | CV3472470 | single nucleotide variant | NM_170692.4(RASAL2):c.626A>G (p.Asp209Gly) | not specified [RCV004660567] | uncertain significance | 1 | 178420572 | 178420572 | Human | | name |
| 597706158 | CV3593020 | single nucleotide variant | NM_170692.4(RASAL2):c.679C>T (p.Arg227Cys) | not specified [RCV004860475] | uncertain significance | 1 | 178439426 | 178439426 | Human | | name |
| 597783840 | CV3593023 | single nucleotide variant | NM_170692.4(RASAL2):c.459G>C (p.Glu153Asp) | not specified [RCV004854337] | uncertain significance | 1 | 178390101 | 178390101 | Human | | name |
| 597783849 | CV3593025 | single nucleotide variant | NM_170692.4(RASAL2):c.719C>G (p.Ser240Cys) | not specified [RCV004854339] | uncertain significance | 1 | 178439466 | 178439466 | Human | | name |
| 597706180 | CV3593030 | single nucleotide variant | NM_170692.4(RASAL2):c.843T>G (p.Ser281Arg) | not specified [RCV004860477] | uncertain significance | 1 | 178441563 | 178441563 | Human | | name |
| 598184173 | CV3902112 | single nucleotide variant | NM_170692.4(RASAL2):c.331A>T (p.Ile111Leu) | not specified [RCV005265720] | uncertain significance | 1 | 178299992 | 178299992 | Human | | name |
| 598184194 | CV3902116 | single nucleotide variant | NM_170692.4(RASAL2):c.638G>C (p.Ser213Thr) | not specified [RCV005265723] | uncertain significance | 1 | 178420584 | 178420584 | Human | | name |
| 15165384 | CV696290 | single nucleotide variant | NM_170692.4(RASAL2):c.3132G>C (p.Val1044=) | not provided [RCV000948574] | benign | 1 | 178458424 | 178458424 | Human | | name |
| 8629122 | CV84267 | single nucleotide variant | NM_004841.3(RASAL2):c.919T>G (p.Phe307Val) | Malignant melanoma [RCV000064349] | not provided | 1 | 178443110 | 178443110 | Human | | name |
| 156067851 | CV2193635 | single nucleotide variant | NM_170692.4(RASAL2):c.2689C>T (p.Pro897Ser) | not specified [RCV004074239] | uncertain significance | 1 | 178457981 | 178457981 | Human | | name |
| 156251060 | CV2215724 | single nucleotide variant | NM_170692.4(RASAL2):c.2342G>A (p.Gly781Glu) | not specified [RCV004091246] | uncertain significance | 1 | 178456851 | 178456851 | Human | | name |
| 156331857 | CV2218224 | single nucleotide variant | NM_170692.4(RASAL2):c.2654C>T (p.Ala885Val) | not specified [RCV004088426] | uncertain significance | 1 | 178457946 | 178457946 | Human | | name |
| 156381195 | CV2218623 | single nucleotide variant | NM_170692.4(RASAL2):c.2542G>A (p.Val848Ile) | not specified [RCV004090881] | likely benign | 1 | 178457834 | 178457834 | Human | | name |
| 156040430 | CV2219470 | single nucleotide variant | NM_170692.4(RASAL2):c.2699C>T (p.Ala900Val) | not specified [RCV004095238] | uncertain significance | 1 | 178457991 | 178457991 | Human | | name |
| 156235650 | CV2245450 | single nucleotide variant | NM_170692.4(RASAL2):c.2133T>G (p.Phe711Leu) | not specified [RCV004109230] | uncertain significance | 1 | 178454570 | 178454570 | Human | | name |
| 156335022 | CV2263616 | single nucleotide variant | NM_170692.4(RASAL2):c.1355T>A (p.Phe452Tyr) | not specified [RCV004135620] | uncertain significance | 1 | 178443102 | 178443102 | Human | | name |
| 156252391 | CV2286967 | single nucleotide variant | NM_170692.4(RASAL2):c.2278C>T (p.Pro760Ser) | not specified [RCV004144568] | uncertain significance | 1 | 178456787 | 178456787 | Human | | name |
| 156201455 | CV2313147 | single nucleotide variant | NM_170692.4(RASAL2):c.2187G>C (p.Trp729Cys) | not specified [RCV004161410] | uncertain significance | 1 | 178454624 | 178454624 | Human | | name |
| 156166817 | CV2315262 | single nucleotide variant | NM_170692.4(RASAL2):c.1714C>G (p.Gln572Glu) | not specified [RCV004167251] | uncertain significance | 1 | 178451657 | 178451657 | Human | | name |
| 156051265 | CV2323333 | single nucleotide variant | NM_170692.4(RASAL2):c.1262C>T (p.Thr421Ile) | not specified [RCV004171741] | uncertain significance | 1 | 178443009 | 178443009 | Human | | name |
| 155975219 | CV2342645 | single nucleotide variant | NM_170692.4(RASAL2):c.1924C>G (p.Leu642Val) | not specified [RCV004196730] | uncertain significance | 1 | 178452567 | 178452567 | Human | | name |
| 156346270 | CV2353491 | single nucleotide variant | NM_170692.4(RASAL2):c.2969C>T (p.Thr990Met) | not specified [RCV004199477] | uncertain significance | 1 | 178458261 | 178458261 | Human | | name |
| 156012260 | CV2358875 | single nucleotide variant | NM_170692.4(RASAL2):c.2729C>T (p.Ala910Val) | not specified [RCV004212218] | uncertain significance | 1 | 178458021 | 178458021 | Human | | name |
| 156263910 | CV2364194 | single nucleotide variant | NM_170692.4(RASAL2):c.2855G>C (p.Ser952Thr) | not specified [RCV004223433] | uncertain significance | 1 | 178458147 | 178458147 | Human | | name |
| 156344152 | CV2384696 | single nucleotide variant | NM_170692.4(RASAL2):c.1223G>A (p.Arg408His) | not specified [RCV004232469] | uncertain significance | 1 | 178442970 | 178442970 | Human | | name |
| 329385307 | CV2451216 | single nucleotide variant | NM_170692.4(RASAL2):c.2140T>C (p.Tyr714His) | not specified [RCV004270130] | uncertain significance | 1 | 178454577 | 178454577 | Human | | name |
| 329367864 | CV2457145 | single nucleotide variant | NM_170692.4(RASAL2):c.2243G>A (p.Arg748His) | not specified [RCV004264919] | uncertain significance | 1 | 178456752 | 178456752 | Human | | name |
| 329360419 | CV2458730 | single nucleotide variant | NM_170692.4(RASAL2):c.2949G>C (p.Glu983Asp) | not specified [RCV004268382] | uncertain significance | 1 | 178458241 | 178458241 | Human | | name |
| 401759245 | CV2690838 | single nucleotide variant | NM_170692.4(RASAL2):c.2942A>G (p.Gln981Arg) | not specified [RCV004298545] | uncertain significance | 1 | 178458234 | 178458234 | Human | | name |
| 401774491 | CV2691755 | single nucleotide variant | NM_170692.4(RASAL2):c.2218G>A (p.Val740Met) | not specified [RCV004299210] | uncertain significance | 1 | 178456727 | 178456727 | Human | | name |
| 401783554 | CV2723700 | single nucleotide variant | NM_170692.4(RASAL2):c.1900A>G (p.Ile634Val) | not specified [RCV004325868] | uncertain significance | 1 | 178452543 | 178452543 | Human | | name |
| 401761595 | CV2726829 | single nucleotide variant | NM_170692.4(RASAL2):c.1763A>G (p.Asn588Ser) | not specified [RCV004323134] | uncertain significance | 1 | 178451706 | 178451706 | Human | | name |
| 401769663 | CV2731515 | single nucleotide variant | NM_170692.4(RASAL2):c.2230G>A (p.Gly744Arg) | not specified [RCV004330865] | uncertain significance | 1 | 178456739 | 178456739 | Human | | name |
| 401870046 | CV2765588 | single nucleotide variant | NM_170692.4(RASAL2):c.2945G>A (p.Ser982Asn) | not specified [RCV004335603] | uncertain significance | 1 | 178458237 | 178458237 | Human | | name |
| 401865996 | CV2775371 | single nucleotide variant | NM_170692.4(RASAL2):c.2372T>C (p.Phe791Ser) | not specified [RCV004348775] | uncertain significance | 1 | 178456881 | 178456881 | Human | | name |
| 401900067 | CV2780316 | single nucleotide variant | NM_170692.4(RASAL2):c.2524C>A (p.Leu842Ile) | not specified [RCV004357725] | uncertain significance | 1 | 178457816 | 178457816 | Human | | name |
| 405659657 | CV3312279 | single nucleotide variant | NM_170692.4(RASAL2):c.1184T>C (p.Val395Ala) | not specified [RCV004438599] | uncertain significance | 1 | 178442931 | 178442931 | Human | | name |
| 405659661 | CV3312280 | single nucleotide variant | NM_170692.4(RASAL2):c.1271A>G (p.Lys424Arg) | not specified [RCV004438600] | uncertain significance | 1 | 178443018 | 178443018 | Human | | name |
| 405659664 | CV3312281 | single nucleotide variant | NM_170692.4(RASAL2):c.1310G>A (p.Arg437His) | not specified [RCV004438601] | uncertain significance | 1 | 178443057 | 178443057 | Human | | name |
| 405659669 | CV3312283 | single nucleotide variant | NM_170692.4(RASAL2):c.1706T>C (p.Ile569Thr) | not specified [RCV004438603] | uncertain significance | 1 | 178451649 | 178451649 | Human | | name |
| 405659675 | CV3312285 | single nucleotide variant | NM_170692.4(RASAL2):c.2060A>G (p.His687Arg) | not specified [RCV004438605] | uncertain significance | 1 | 178454497 | 178454497 | Human | | name |
| 405659678 | CV3312286 | single nucleotide variant | NM_170692.4(RASAL2):c.2080C>T (p.Arg694Cys) | not specified [RCV004438606] | uncertain significance | 1 | 178454517 | 178454517 | Human | | name |
| 405659680 | CV3312287 | single nucleotide variant | NM_170692.4(RASAL2):c.2282C>T (p.Thr761Met) | not specified [RCV004438607] | uncertain significance | 1 | 178456791 | 178456791 | Human | | name |
| 405659683 | CV3312288 | single nucleotide variant | NM_170692.4(RASAL2):c.2537G>A (p.Arg846Gln) | not specified [RCV004438608] | uncertain significance | 1 | 178457829 | 178457829 | Human | | name |
| 407466818 | CV3472464 | single nucleotide variant | NM_170692.4(RASAL2):c.2096T>C (p.Ile699Thr) | not specified [RCV004660564] | uncertain significance | 1 | 178454533 | 178454533 | Human | | name |
| 407500729 | CV3472469 | single nucleotide variant | NM_170692.4(RASAL2):c.2143A>G (p.Ile715Val) | not specified [RCV004669620] | uncertain significance | 1 | 178454580 | 178454580 | Human | | name |
| 407466831 | CV3472471 | single nucleotide variant | NM_170692.4(RASAL2):c.1912A>G (p.Ser638Gly) | not specified [RCV004660568] | uncertain significance | 1 | 178452555 | 178452555 | Human | | name |
| 407500734 | CV3472472 | single nucleotide variant | NM_170692.4(RASAL2):c.1697G>T (p.Ser566Ile) | not specified [RCV004669621] | uncertain significance | 1 | 178451640 | 178451640 | Human | | name |
| 407500740 | CV3472475 | single nucleotide variant | NM_170692.4(RASAL2):c.1771T>C (p.Cys591Arg) | not specified [RCV004669622] | uncertain significance | 1 | 178451714 | 178451714 | Human | | name |
| 407500746 | CV3472476 | single nucleotide variant | NM_170692.4(RASAL2):c.1601G>C (p.Gly534Ala) | not specified [RCV004669623] | uncertain significance | 1 | 178445636 | 178445636 | Human | | name |
| 407459620 | CV3496844 | single nucleotide variant | NM_170692.4(RASAL2):c.2236C>A (p.Leu746Ile) | Autism [RCV004698659] | uncertain significance | 1 | 178456745 | 178456745 | Human | 2 | name |
| 597706169 | CV3593021 | single nucleotide variant | NM_170692.4(RASAL2):c.2263A>G (p.Lys755Glu) | not specified [RCV004860476] | uncertain significance | 1 | 178456772 | 178456772 | Human | | name |
| 597783856 | CV3593027 | single nucleotide variant | NM_170692.4(RASAL2):c.2626G>A (p.Gly876Arg) | not specified [RCV004854341] | uncertain significance | 1 | 178457918 | 178457918 | Human | | name |
| 597783860 | CV3593028 | single nucleotide variant | NM_170692.4(RASAL2):c.1577T>C (p.Ile526Thr) | not specified [RCV004854342] | uncertain significance | 1 | 178445612 | 178445612 | Human | | name |
| 597783868 | CV3593032 | single nucleotide variant | NM_170692.4(RASAL2):c.2081G>A (p.Arg694His) | not specified [RCV004854344] | uncertain significance | 1 | 178454518 | 178454518 | Human | | name |
| 598184150 | CV3902109 | single nucleotide variant | NM_170692.4(RASAL2):c.1561A>G (p.Ile521Val) | not specified [RCV005265717] | uncertain significance | 1 | 178445596 | 178445596 | Human | | name |
| 598184166 | CV3902111 | single nucleotide variant | NM_170692.4(RASAL2):c.2614A>G (p.Ile872Val) | not specified [RCV005265719] | uncertain significance | 1 | 178457906 | 178457906 | Human | | name |
| 598184179 | CV3902114 | single nucleotide variant | NM_170692.4(RASAL2):c.1226A>C (p.Gln409Pro) | not specified [RCV005265721] | uncertain significance | 1 | 178442973 | 178442973 | Human | | name |
| 598184201 | CV3902117 | single nucleotide variant | NM_170692.4(RASAL2):c.2578C>A (p.Gln860Lys) | not specified [RCV005265724] | uncertain significance | 1 | 178457870 | 178457870 | Human | | name |
| 9686942 | CV171308 | single nucleotide variant | NM_170692.4(RASAL2):c.3820G>T (p.Glu1274Ter) | Prostate cancer [RCV000149161] | uncertain significance | 1 | 178473216 | 178473216 | Human | 2 | name |
| 156235861 | CV2193430 | single nucleotide variant | NM_170692.4(RASAL2):c.3157G>C (p.Val1053Leu) | not specified [RCV004072924] | uncertain significance | 1 | 178458449 | 178458449 | Human | | name |
| 156258777 | CV2204686 | single nucleotide variant | NM_170692.4(RASAL2):c.3074C>T (p.Ala1025Val) | not specified [RCV004081789] | uncertain significance | 1 | 178458366 | 178458366 | Human | | name |
| 156399171 | CV2204959 | single nucleotide variant | NM_170692.4(RASAL2):c.3007C>A (p.Gln1003Lys) | not specified [RCV004077582] | uncertain significance | 1 | 178458299 | 178458299 | Human | | name |
| 156240242 | CV2236023 | single nucleotide variant | NM_170692.4(RASAL2):c.3458G>A (p.Arg1153His) | not specified [RCV004113889] | uncertain significance | 1 | 178465990 | 178465990 | Human | | name |
| 156202486 | CV2256250 | single nucleotide variant | NM_170692.4(RASAL2):c.3790C>G (p.Pro1264Ala) | not specified [RCV004116504] | uncertain significance | 1 | 178473186 | 178473186 | Human | | name |
| 156261284 | CV2314709 | single nucleotide variant | NM_170692.4(RASAL2):c.3106C>G (p.Arg1036Gly) | not specified [RCV004170854] | uncertain significance | 1 | 178458398 | 178458398 | Human | | name |
| 156058066 | CV2316859 | single nucleotide variant | NM_170692.4(RASAL2):c.3773G>C (p.Gly1258Ala) | not specified [RCV004174387] | uncertain significance | 1 | 178473169 | 178473169 | Human | | name |
| 156289023 | CV2327465 | single nucleotide variant | NM_170692.4(RASAL2):c.3076C>T (p.Pro1026Ser) | not specified [RCV004174879] | uncertain significance | 1 | 178458368 | 178458368 | Human | | name |
| 155980256 | CV2336892 | single nucleotide variant | NM_170692.4(RASAL2):c.3610G>A (p.Glu1204Lys) | not specified [RCV004190509] | uncertain significance | 1 | 178467353 | 178467353 | Human | | name |
| 156115978 | CV2349342 | single nucleotide variant | NM_170692.4(RASAL2):c.3088C>T (p.Pro1030Ser) | not specified [RCV004199281] | uncertain significance | 1 | 178458380 | 178458380 | Human | | name |
| 156059557 | CV2391769 | single nucleotide variant | NM_170692.4(RASAL2):c.3082T>G (p.Ser1028Ala) | not specified [RCV004235652] | uncertain significance | 1 | 178458374 | 178458374 | Human | | name |
| 156260835 | CV2395579 | single nucleotide variant | NM_170692.4(RASAL2):c.3793A>G (p.Thr1265Ala) | not specified [RCV004241430] | uncertain significance | 1 | 178473189 | 178473189 | Human | | name |
| 329381791 | CV2441531 | single nucleotide variant | NM_170692.4(RASAL2):c.3571A>C (p.Met1191Leu) | not specified [RCV004257317] | uncertain significance | 1 | 178466103 | 178466103 | Human | | name |
| 401732101 | CV2690298 | single nucleotide variant | NM_170692.4(RASAL2):c.3542G>A (p.Arg1181Gln) | not specified [RCV004302294] | uncertain significance | 1 | 178466074 | 178466074 | Human | | name |
| 401759444 | CV2701865 | single nucleotide variant | NM_170692.4(RASAL2):c.3440G>A (p.Arg1147Gln) | not specified [RCV004307829] | uncertain significance | 1 | 178465972 | 178465972 | Human | | name |
| 401863345 | CV2776769 | single nucleotide variant | NM_170692.4(RASAL2):c.3091C>G (p.His1031Asp) | not specified [RCV004357918] | uncertain significance | 1 | 178458383 | 178458383 | Human | | name |
| 405659690 | CV3312290 | single nucleotide variant | NM_170692.4(RASAL2):c.3437G>A (p.Arg1146Gln) | not specified [RCV004438610] | uncertain significance | 1 | 178465969 | 178465969 | Human | | name |
| 405659692 | CV3312291 | single nucleotide variant | NM_170692.4(RASAL2):c.3766C>T (p.Arg1256Cys) | not specified [RCV004438611] | uncertain significance | 1 | 178473162 | 178473162 | Human | | name |
| 405659694 | CV3312292 | single nucleotide variant | NM_170692.4(RASAL2):c.3805A>G (p.Ile1269Val) | not specified [RCV004438612] | uncertain significance | 1 | 178473201 | 178473201 | Human | | name |
| 407500714 | CV3472462 | single nucleotide variant | NM_170692.4(RASAL2):c.3340G>A (p.Val1114Met) | not specified [RCV004669617] | uncertain significance | 1 | 178464365 | 178464365 | Human | | name |
| 407500718 | CV3472465 | single nucleotide variant | NM_170692.4(RASAL2):c.3178C>T (p.Arg1060Trp) | not specified [RCV004669618] | uncertain significance | 1 | 178458470 | 178458470 | Human | | name |
| 407466835 | CV3472473 | single nucleotide variant | NM_170692.4(RASAL2):c.3359A>C (p.Asn1120Thr) | not specified [RCV004660569] | uncertain significance | 1 | 178464384 | 178464384 | Human | | name |
| 407466839 | CV3472474 | single nucleotide variant | NM_170692.4(RASAL2):c.3123G>A (p.Met1041Ile) | not specified [RCV004660570] | uncertain significance | 1 | 178458415 | 178458415 | Human | | name |
| 597783836 | CV3593022 | single nucleotide variant | NM_170692.4(RASAL2):c.3816T>A (p.Asn1272Lys) | not specified [RCV004854336] | uncertain significance | 1 | 178473212 | 178473212 | Human | | name |
| 597783852 | CV3593026 | single nucleotide variant | NM_170692.4(RASAL2):c.3436C>T (p.Arg1146Trp) | not specified [RCV004854340] | uncertain significance | 1 | 178465968 | 178465968 | Human | | name |
| 597783864 | CV3593029 | single nucleotide variant | NM_170692.4(RASAL2):c.3077C>T (p.Pro1026Leu) | not specified [RCV004854343] | uncertain significance | 1 | 178458369 | 178458369 | Human | | name |
| 597706190 | CV3593031 | single nucleotide variant | NM_170692.4(RASAL2):c.3536G>A (p.Arg1179Gln) | not specified [RCV004860478] | uncertain significance | 1 | 178466068 | 178466068 | Human | | name |
| 597706199 | CV3593033 | single nucleotide variant | NM_170692.4(RASAL2):c.3173G>A (p.Arg1058Gln) | not specified [RCV004860479] | uncertain significance | 1 | 178458465 | 178458465 | Human | | name |
| 597706228 | CV3593037 | single nucleotide variant | NM_170692.4(RASAL2):c.3067G>T (p.Ala1023Ser) | not specified [RCV004860482] | uncertain significance | 1 | 178458359 | 178458359 | Human | | name |
| 598184159 | CV3902110 | single nucleotide variant | NM_170692.4(RASAL2):c.3748C>T (p.Arg1250Trp) | not specified [RCV005265718] | uncertain significance | 1 | 178473144 | 178473144 | Human | | name |
| 598203554 | CV3902113 | single nucleotide variant | NM_170692.4(RASAL2):c.3449A>T (p.Glu1150Val) | not specified [RCV005269394] | uncertain significance | 1 | 178465981 | 178465981 | Human | | name |
