| 155999015 | CV2396349 | single nucleotide variant | NM_002885.4(RAP1GAP):c.-74T>C | not specified [RCV004242074] | uncertain significance | 1 | 21626359 | 21626359 | Human | | name |
| 405658923 | CV3315544 | single nucleotide variant | NM_002885.4(RAP1GAP):c.-62G>A | not specified [RCV004438353] | uncertain significance | 1 | 21626347 | 21626347 | Human | | name |
| 597753875 | CV3592765 | single nucleotide variant | NM_002885.4(RAP1GAP):c.-38C>T | not specified [RCV004847229] | uncertain significance | 1 | 21626323 | 21626323 | Human | | name |
| 405658954 | CV3315551 | single nucleotide variant | NM_002885.4(RAP1GAP):c.-138T>C | not specified [RCV004438360] | uncertain significance | 1 | 21649786 | 21649786 | Human | | name |
| 329397483 | CV2456221 | single nucleotide variant | NM_002885.4(RAP1GAP):c.-148-2005T>C | not specified [RCV004273405] | uncertain significance | 1 | 21651801 | 21651801 | Human | | name |
| 405658944 | CV3315549 | single nucleotide variant | NM_002885.4(RAP1GAP):c.-148-1997C>A | not specified [RCV004438358] | uncertain significance | 1 | 21651793 | 21651793 | Human | | name |
| 156278867 | CV2325131 | single nucleotide variant | NM_002885.4(RAP1GAP):c.31G>C (p.Asp11His) | not specified [RCV004177561] | uncertain significance | 1 | 21619060 | 21619060 | Human | | name |
| 405658935 | CV3315547 | single nucleotide variant | NM_002885.4(RAP1GAP):c.40C>A (p.Arg14Ser) | not specified [RCV004438356] | uncertain significance | 1 | 21619051 | 21619051 | Human | | name |
| 597705093 | CV3592762 | single nucleotide variant | NM_002885.4(RAP1GAP):c.85C>T (p.Pro29Ser) | not specified [RCV004860364] | uncertain significance | 1 | 21617954 | 21617954 | Human | | name |
| 156197797 | CV2259295 | single nucleotide variant | NM_002885.4(RAP1GAP):c.269A>G (p.Tyr90Cys) | not specified [RCV004122310] | uncertain significance | 1 | 21617328 | 21617328 | Human | | name |
| 401935443 | CV2812434 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1803C>T (p.Pro601=) | not provided [RCV003412872] | likely benign | 1 | 21598476 | 21598476 | Human | | name |
| 405658940 | CV3315548 | single nucleotide variant | NM_002885.4(RAP1GAP):c.103G>A (p.Glu35Lys) | not specified [RCV004438357] | uncertain significance | 1 | 21617936 | 21617936 | Human | | name |
| 405658948 | CV3315550 | single nucleotide variant | NM_002885.4(RAP1GAP):c.279C>G (p.His93Gln) | not specified [RCV004438359] | uncertain significance | 1 | 21617318 | 21617318 | Human | | name |
| 597705114 | CV3592764 | single nucleotide variant | NM_002885.4(RAP1GAP):c.272G>A (p.Arg91Gln) | not specified [RCV004860366] | uncertain significance | 1 | 21617325 | 21617325 | Human | | name |
| 597753879 | CV3592766 | single nucleotide variant | NM_002885.4(RAP1GAP):c.226A>C (p.Thr76Pro) | not specified [RCV004847230] | uncertain significance | 1 | 21617371 | 21617371 | Human | | name |
| 156194678 | CV2223363 | single nucleotide variant | NM_002885.4(RAP1GAP):c.596A>G (p.Tyr199Cys) | not specified [RCV004105962] | uncertain significance | 1 | 21612042 | 21612042 | Human | | name |
| 156291018 | CV2226266 | single nucleotide variant | NM_002885.4(RAP1GAP):c.514G>A (p.Val172Met) | not specified [RCV004099510] | uncertain significance | 1 | 21613190 | 21613190 | Human | | name |
| 156316495 | CV2250917 | single nucleotide variant | NM_002885.4(RAP1GAP):c.316G>T (p.Asp106Tyr) | not specified [RCV004123499] | uncertain significance | 1 | 21614065 | 21614065 | Human | | name |
| 156012047 | CV2291211 | single nucleotide variant | NM_002885.4(RAP1GAP):c.652C>A (p.Pro218Thr) | not specified [RCV004153505] | uncertain significance | 1 | 21611777 | 21611777 | Human | | name |
| 155969075 | CV2391535 | single nucleotide variant | NM_002885.4(RAP1GAP):c.355G>A (p.Asp119Asn) | not specified [RCV004239920] | uncertain significance | 1 | 21614026 | 21614026 | Human | | name |
| 401756219 | CV2687037 | single nucleotide variant | NM_002885.4(RAP1GAP):c.322G>T (p.Ala108Ser) | not specified [RCV004304359] | uncertain significance | 1 | 21614059 | 21614059 | Human | | name |
| 405658958 | CV3315552 | single nucleotide variant | NM_002885.4(RAP1GAP):c.569G>C (p.Ser190Thr) | not specified [RCV004438361] | uncertain significance | 1 | 21612069 | 21612069 | Human | | name |
| 407500473 | CV3472319 | single nucleotide variant | NM_002885.4(RAP1GAP):c.641A>T (p.Asn214Ile) | not specified [RCV004669567] | uncertain significance | 1 | 21611788 | 21611788 | Human | | name |
| 407466435 | CV3472321 | single nucleotide variant | NM_002885.4(RAP1GAP):c.383G>A (p.Arg128Gln) | not specified [RCV004660471] | uncertain significance | 1 | 21613998 | 21613998 | Human | | name |
| 597753867 | CV3582815 | single nucleotide variant | NM_002885.4(RAP1GAP):c.924G>C (p.Met308Ile) | not specified [RCV004847227] | uncertain significance | 1 | 21610195 | 21610195 | Human | | name |
| 597753871 | CV3592759 | single nucleotide variant | NM_002885.4(RAP1GAP):c.979C>T (p.Pro327Ser) | not specified [RCV004847228] | uncertain significance | 1 | 21610140 | 21610140 | Human | | name |
| 597705104 | CV3592763 | single nucleotide variant | NM_002885.4(RAP1GAP):c.406C>T (p.Arg136Trp) | not specified [RCV004860365] | uncertain significance | 1 | 21613696 | 21613696 | Human | | name |
| 597753891 | CV3592769 | single nucleotide variant | NM_002885.4(RAP1GAP):c.400A>G (p.Lys134Glu) | not specified [RCV004847233] | uncertain significance | 1 | 21613702 | 21613702 | Human | | name |
| 598175808 | CV3905379 | single nucleotide variant | NM_002885.4(RAP1GAP):c.778C>T (p.Arg260Cys) | not specified [RCV005264055] | uncertain significance | 1 | 21611517 | 21611517 | Human | | name |
| 598175819 | CV3905380 | single nucleotide variant | NM_002885.4(RAP1GAP):c.991C>T (p.Leu331Phe) | not specified [RCV005264056] | uncertain significance | 1 | 21610128 | 21610128 | Human | | name |
| 598175827 | CV3905381 | single nucleotide variant | NM_002885.4(RAP1GAP):c.455A>C (p.Asn152Thr) | not specified [RCV005264057] | uncertain significance | 1 | 21613647 | 21613647 | Human | | name |
| 598175842 | CV3905383 | single nucleotide variant | NM_002885.4(RAP1GAP):c.929C>T (p.Ala310Val) | not specified [RCV005264059] | uncertain significance | 1 | 21610190 | 21610190 | Human | | name |
| 598175863 | CV3905385 | single nucleotide variant | NM_002885.4(RAP1GAP):c.320C>A (p.Ala107Asp) | not specified [RCV005264061] | uncertain significance | 1 | 21614061 | 21614061 | Human | | name |
| 156192608 | CV2202404 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1052A>C (p.Asp351Ala) | not specified [RCV004080717] | uncertain significance | 1 | 21609594 | 21609594 | Human | | name |
| 156040318 | CV2219459 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1187C>T (p.Thr396Met) | not specified [RCV004095232] | uncertain significance | 1 | 21608322 | 21608322 | Human | | name |
| 156335898 | CV2228456 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1601C>T (p.Ser534Leu) | not specified [RCV004098425] | uncertain significance | 1 | 21601735 | 21601735 | Human | | name |
| 155901313 | CV2274493 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1805A>G (p.His602Arg) | not specified [RCV004137119] | uncertain significance | 1 | 21598474 | 21598474 | Human | | name |
| 155923387 | CV2280287 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1112A>G (p.Asn371Ser) | not specified [RCV004140488] | uncertain significance | 1 | 21608896 | 21608896 | Human | | name |
| 156136672 | CV2284841 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1516A>G (p.Ile506Val) | not specified [RCV004143014] | uncertain significance | 1 | 21602826 | 21602826 | Human | | name |
| 156064633 | CV2316179 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1784T>C (p.Val595Ala) | not specified [RCV004174222] | uncertain significance | 1 | 21598495 | 21598495 | Human | | name |
| 156059341 | CV2343697 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1928C>T (p.Ala643Val) | not specified [RCV004190721] | uncertain significance | 1 | 21598016 | 21598016 | Human | | name |
| 156341367 | CV2344782 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1801C>A (p.Pro601Thr) | not specified [RCV004190931] | uncertain significance | 1 | 21598478 | 21598478 | Human | | name |
| 329399586 | CV2443304 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1682C>T (p.Ala561Val) | not specified [RCV004260105] | likely benign | 1 | 21599588 | 21599588 | Human | | name |
| 401718182 | CV2700205 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1765G>C (p.Asp589His) | not specified [RCV004309061] | uncertain significance | 1 | 21599505 | 21599505 | Human | | name |
| 401777631 | CV2718279 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1754T>G (p.Val585Gly) | not specified [RCV004318124] | uncertain significance | 1 | 21599516 | 21599516 | Human | | name |
| 405693955 | CV3315542 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1001T>C (p.Val334Ala) | not specified [RCV004445872] | uncertain significance | 1 | 21609645 | 21609645 | Human | | name |
| 405693961 | CV3315543 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1099A>G (p.Thr367Ala) | not specified [RCV004445873] | uncertain significance | 1 | 21608909 | 21608909 | Human | | name |
| 405658926 | CV3315545 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1732G>A (p.Val578Met) | not specified [RCV004438354] | uncertain significance | 1 | 21599538 | 21599538 | Human | | name |
| 405658932 | CV3315546 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1909G>A (p.Gly637Ser) | not specified [RCV004438355] | uncertain significance | 1 | 21598035 | 21598035 | Human | | name |
| 407500468 | CV3472318 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1675G>C (p.Ala559Pro) | not specified [RCV004669566] | uncertain significance | 1 | 21599595 | 21599595 | Human | | name |
| 597705058 | CV3582814 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1783G>A (p.Val595Met) | not specified [RCV004860361] | uncertain significance | 1 | 21598496 | 21598496 | Human | | name |
| 597705070 | CV3592760 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1759G>A (p.Gly587Arg) | not specified [RCV004860362] | uncertain significance | 1 | 21599511 | 21599511 | Human | | name |
| 597753883 | CV3592767 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1115C>G (p.Ala372Gly) | not specified [RCV004847231] | uncertain significance | 1 | 21608893 | 21608893 | Human | | name |
| 597753887 | CV3592768 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1894C>A (p.Pro632Thr) | not specified [RCV004847232] | uncertain significance | 1 | 21598050 | 21598050 | Human | | name |
| 598175791 | CV3905377 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1699C>T (p.Arg567Cys) | not specified [RCV005264053] | uncertain significance | 1 | 21599571 | 21599571 | Human | | name |
| 598175800 | CV3905378 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1576G>A (p.Gly526Arg) | not specified [RCV005264054] | uncertain significance | 1 | 21601760 | 21601760 | Human | | name |
| 598175834 | CV3905382 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1960T>C (p.Ser654Pro) | not specified [RCV005264058] | uncertain significance | 1 | 21597984 | 21597984 | Human | | name |
| 598175854 | CV3905384 | single nucleotide variant | NM_002885.4(RAP1GAP):c.1480G>A (p.Gly494Ser) | not specified [RCV005264060] | uncertain significance | 1 | 21602862 | 21602862 | Human | | name |
| 15156872 | CV760572 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1494+9G>C | not provided [RCV000924751] | benign | 17 | 3008154 | 3008154 | Human | | name |
| 8585307 | CV119890 | single nucleotide variant | NM_015085.4(RAP1GAP2):c.813+551A>T | Lung cancer [RCV000100410] | uncertain significance | 17 | 2985617 | 2985617 | Human | | name |
| 8585309 | CV119892 | single nucleotide variant | NM_015085.4(RAP1GAP2):c.*30+122A>G | Lung cancer [RCV000100412] | uncertain significance | 17 | 3032571 | 3032571 | Human | | name |
| 407466450 | CV3472325 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.35G>A (p.Gly12Asp) | not specified [RCV004660474] | uncertain significance | 17 | 2796562 | 2796562 | Human | | name |
| 597705141 | CV3592773 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.915T>C (p.Gly305=) | not specified [RCV004860369] | likely benign | 17 | 2995337 | 2995337 | Human | | name |
| 597753911 | CV3592780 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.29T>C (p.Phe10Ser) | not specified [RCV004847238] | uncertain significance | 17 | 2796556 | 2796556 | Human | | name |
| 598175901 | CV3905389 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.95C>T (p.Ala32Val) | not specified [RCV005264065] | uncertain significance | 17 | 2905298 | 2905298 | Human | | name |
| 156171609 | CV2247458 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.250G>A (p.Asp84Asn) | not specified [RCV004108785] | uncertain significance | 17 | 2963433 | 2963433 | Human | | name |
| 329370591 | CV2435598 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.110C>T (p.Ala37Val) | not specified [RCV004254849] | likely benign | 17 | 2905313 | 2905313 | Human | | name |
| 405658967 | CV3315555 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.128C>T (p.Pro43Leu) | not specified [RCV004438364] | uncertain significance | 17 | 2905331 | 2905331 | Human | | name |
| 405658987 | CV3315563 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.262T>C (p.Tyr88His) | not specified [RCV004438372] | uncertain significance | 17 | 2963445 | 2963445 | Human | | name |
| 407466442 | CV3472322 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.109G>T (p.Ala37Ser) | not specified [RCV004660472] | uncertain significance | 17 | 2905312 | 2905312 | Human | | name |
| 598175910 | CV3905390 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.251A>T (p.Asp84Val) | not specified [RCV005264066] | uncertain significance | 17 | 2963434 | 2963434 | Human | | name |
| 15135767 | CV715350 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1407C>T (p.His469=) | not provided [RCV000965341] | benign | 17 | 3008058 | 3008058 | Human | | name |
| 156107473 | CV2214204 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.728A>G (p.Lys243Arg) | not specified [RCV004086199] | uncertain significance | 17 | 2981247 | 2981247 | Human | | name |
| 156035200 | CV2246707 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.332G>A (p.Gly111Asp) | not specified [RCV004110429] | uncertain significance | 17 | 2963908 | 2963908 | Human | | name |
| 155965588 | CV2283984 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.373T>C (p.Ser125Pro) | not specified [RCV004144603] | uncertain significance | 17 | 2963949 | 2963949 | Human | | name |
| 155961454 | CV2285533 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.710A>G (p.Asn237Ser) | not specified [RCV004141415] | uncertain significance | 17 | 2981229 | 2981229 | Human | | name |
| 156050957 | CV2378548 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.547G>A (p.Val183Ile) | not specified [RCV004228596] | likely benign | 17 | 2965594 | 2965594 | Human | | name |
| 156188722 | CV2395494 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.362G>A (p.Gly121Asp) | not specified [RCV004241360] | uncertain significance | 17 | 2963938 | 2963938 | Human | | name |
| 401754285 | CV2726915 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.343G>A (p.Glu115Lys) | not specified [RCV004323201] | uncertain significance | 17 | 2963919 | 2963919 | Human | | name |
| 405658994 | CV3315565 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.613G>A (p.Val205Ile) | not specified [RCV004438374] | uncertain significance | 17 | 2980303 | 2980303 | Human | | name |
| 405658997 | CV3315566 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.940C>G (p.His314Asp) | not specified [RCV004438375] | uncertain significance | 17 | 2995362 | 2995362 | Human | | name |
| 407500481 | CV3472323 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.943G>A (p.Gly315Arg) | not specified [RCV004669568] | uncertain significance | 17 | 2995365 | 2995365 | Human | | name |
| 407500486 | CV3472327 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.299C>G (p.Pro100Arg) | not specified [RCV004669569] | uncertain significance | 17 | 2963875 | 2963875 | Human | | name |
| 598175872 | CV3905386 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.648G>C (p.Lys216Asn) | not specified [RCV005264062] | uncertain significance | 17 | 2980338 | 2980338 | Human | | name |
| 598175920 | CV3905391 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.670G>A (p.Ala224Thr) | not specified [RCV005264067] | uncertain significance | 17 | 2980360 | 2980360 | Human | | name |
| 15161880 | CV704069 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.623G>A (p.Arg208Gln) | not provided [RCV000947752] | benign | 17 | 2980313 | 2980313 | Human | | name |
| 156316788 | CV2193105 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1003G>A (p.Val335Ile) | not specified [RCV004071110] | uncertain significance | 17 | 2995425 | 2995425 | Human | | name |
| 156385771 | CV2228028 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1140C>A (p.Phe380Leu) | not specified [RCV004096269] | uncertain significance | 17 | 2998316 | 2998316 | Human | | name |
| 156219084 | CV2254012 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1324G>T (p.Ala442Ser) | not specified [RCV004129468] | uncertain significance | 17 | 3006006 | 3006006 | Human | | name |
| 155991839 | CV2255735 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1261G>A (p.Val421Ile) | not specified [RCV004120124] | uncertain significance | 17 | 3005429 | 3005429 | Human | | name |
| 156214487 | CV2257478 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1124T>C (p.Met375Thr) | not specified [RCV004125548] | uncertain significance | 17 | 2998300 | 2998300 | Human | | name |
| 155977785 | CV2266447 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2114A>G (p.Lys705Arg) | not specified [RCV004131029] | uncertain significance | 17 | 3030928 | 3030928 | Human | | name |
| 156090257 | CV2302552 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1407C>G (p.His469Gln) | not specified [RCV004160727] | uncertain significance | 17 | 3008058 | 3008058 | Human | | name |
| 156347471 | CV2315302 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1217G>A (p.Arg406Gln) | not specified [RCV004167287] | uncertain significance | 17 | 3005385 | 3005385 | Human | | name |
| 156278989 | CV2316723 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2074G>A (p.Ala692Thr) | not specified [RCV004171947] | uncertain significance | 17 | 3027037 | 3027037 | Human | | name |
| 156360918 | CV2329705 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2153T>G (p.Phe718Cys) | not specified [RCV004180810] | uncertain significance | 17 | 3030967 | 3030967 | Human | | name |
| 155983999 | CV2348178 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2149C>T (p.Arg717Cys) | not specified [RCV004190821] | uncertain significance | 17 | 3030963 | 3030963 | Human | | name |
| 156136541 | CV2357204 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1894C>T (p.Arg632Cys) | not specified [RCV004206987] | uncertain significance | 17 | 3026378 | 3026378 | Human | | name |
| 156389707 | CV2380764 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1652C>T (p.Thr551Met) | not specified [RCV004218330] | uncertain significance | 17 | 3020496 | 3020496 | Human | | name |
| 329359504 | CV2451050 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1397A>G (p.Asp466Gly) | not specified [RCV004269709] | uncertain significance | 17 | 3008048 | 3008048 | Human | | name |
| 329392823 | CV2468975 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1504C>T (p.Arg502Cys) | not specified [RCV004274241] | uncertain significance | 17 | 3018070 | 3018070 | Human | | name |
| 329388417 | CV2471915 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2129C>A (p.Pro710Gln) | not specified [RCV004280938] | uncertain significance | 17 | 3030943 | 3030943 | Human | | name |
| 401879923 | CV2769815 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1447G>T (p.Asp483Tyr) | not specified [RCV004353679] | uncertain significance | 17 | 3008098 | 3008098 | Human | | name |
| 401898247 | CV2790994 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2135C>T (p.Ser712Leu) | not specified [RCV004354614] | uncertain significance | 17 | 3030949 | 3030949 | Human | | name |
| 405658962 | CV3315553 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1159G>A (p.Val387Met) | not specified [RCV004438362] | uncertain significance | 17 | 2998335 | 2998335 | Human | | name |
| 405658965 | CV3315554 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1277C>T (p.Pro426Leu) | not specified [RCV004438363] | uncertain significance | 17 | 3005959 | 3005959 | Human | | name |
| 405658970 | CV3315556 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1348G>A (p.Ala450Thr) | not specified [RCV004438365] | uncertain significance | 17 | 3006030 | 3006030 | Human | | name |
| 405658972 | CV3315557 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1408G>A (p.Ala470Thr) | not specified [RCV004438366] | uncertain significance | 17 | 3008059 | 3008059 | Human | | name |
| 405658975 | CV3315558 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1706G>A (p.Arg569His) | not specified [RCV004438367] | uncertain significance | 17 | 3020550 | 3020550 | Human | | name |
| 405658978 | CV3315559 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1895G>A (p.Arg632His) | not specified [RCV004438368] | uncertain significance | 17 | 3026379 | 3026379 | Human | | name |
| 405658981 | CV3315560 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1930G>A (p.Val644Ile) | not specified [RCV004438369] | uncertain significance | 17 | 3026414 | 3026414 | Human | | name |
| 405658982 | CV3315561 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1991C>T (p.Pro664Leu) | not specified [RCV004438370] | uncertain significance | 17 | 3026954 | 3026954 | Human | | name |
| 405658985 | CV3315562 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2143A>C (p.Lys715Gln) | not specified [RCV004438371] | uncertain significance | 17 | 3030957 | 3030957 | Human | | name |
| 407466446 | CV3472324 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1873A>C (p.Met625Leu) | not specified [RCV004660473] | uncertain significance | 17 | 3026357 | 3026357 | Human | | name |
| 407466454 | CV3472326 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1576A>G (p.Ser526Gly) | not specified [RCV004660475] | uncertain significance | 17 | 3018142 | 3018142 | Human | | name |
| 597705123 | CV3592770 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1337C>T (p.Ser446Leu) | not specified [RCV004860367] | uncertain significance | 17 | 3006019 | 3006019 | Human | | name |
| 597705132 | CV3592771 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1553C>T (p.Ser518Leu) | not specified [RCV004860368] | uncertain significance | 17 | 3018119 | 3018119 | Human | | name |
| 597705150 | CV3592774 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1100A>G (p.Glu367Gly) | not specified [RCV004860370] | uncertain significance | 17 | 2998276 | 2998276 | Human | | name |
| 597705160 | CV3592775 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1997C>T (p.Thr666Met) | not specified [RCV004860371] | uncertain significance | 17 | 3026960 | 3026960 | Human | | name |
| 597753899 | CV3592776 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1783G>C (p.Asp595His) | not specified [RCV004847235] | uncertain significance | 17 | 3026039 | 3026039 | Human | | name |
| 597753903 | CV3592777 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1089C>G (p.Ile363Met) | not specified [RCV004847236] | uncertain significance | 17 | 2998265 | 2998265 | Human | | name |
| 597753907 | CV3592778 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1960A>G (p.Met654Val) | not specified [RCV004847237] | uncertain significance | 17 | 3026444 | 3026444 | Human | | name |
| 597705170 | CV3592779 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.2185G>C (p.Gly729Arg) | not specified [RCV004860372] | uncertain significance | 17 | 3032411 | 3032411 | Human | | name |
| 598175891 | CV3905388 | single nucleotide variant | NM_015085.5(RAP1GAP2):c.1529C>T (p.Thr510Ile) | not specified [RCV005264064] | uncertain significance | 17 | 3018095 | 3018095 | Human | | name |
