| 243060213 | CV2413759 | single nucleotide variant | NM_021133.4(RNASEL):c.1481-1G>T | Prostate cancer, hereditary, 1 [RCV003135778] | uncertain significance | 1 | 182584167 | 182584167 | Human | 1 | name |
| 404992674 | CV3184341 | deletion | NM_021133.4(RNASEL):c.2039+1del | Prostate cancer, hereditary, 1 [RCV003881675] | uncertain significance | 1 | 182576255 | 182576255 | Human | 1 | name |
| 8599242 | CV28044 | single nucleotide variant | NM_021133.4(RNASEL):c.3G>A (p.Met1Ile) | Prostate cancer, hereditary, 1 [RCV000013879] | pathogenic | 1 | 182586804 | 182586804 | Human | 1 | name |
| 405274937 | CV3204484 | single nucleotide variant | NM_021133.4(RNASEL):c.270G>A (p.Lys90=) | RNASEL-related disorder [RCV003951917] | likely benign | 1 | 182586537 | 182586537 | Human | | name , trait , alternate_id |
| 407475966 | CV3483446 | single nucleotide variant | NM_021133.4(RNASEL):c.22A>C (p.Asn8His) | not specified [RCV004663359] | uncertain significance | 1 | 182586785 | 182586785 | Human | | name |
| 405268487 | CV3198917 | single nucleotide variant | NM_021133.4(RNASEL):c.666G>A (p.Thr222=) | RNASEL-related disorder [RCV003912035] | benign | 1 | 182586141 | 182586141 | Human | | name , trait , alternate_id |
| 405754050 | CV3316341 | single nucleotide variant | NM_021133.4(RNASEL):c.52G>A (p.Gly18Ser) | not specified [RCV004454226] | likely benign | 1 | 182586755 | 182586755 | Human | | name |
| 15195059 | CV696305 | single nucleotide variant | NM_021133.4(RNASEL):c.339T>C (p.Ser113=) | not provided [RCV000955816] | benign | 1 | 182586468 | 182586468 | Human | | name |
| 15194924 | CV718424 | single nucleotide variant | NM_021133.4(RNASEL):c.354C>T (p.Val118=) | not provided [RCV000889355] | benign|conflicting interpretations of pathogenicity | 1 | 182586453 | 182586453 | Human | | name |
| 152981795 | CV1677088 | single nucleotide variant | NM_021133.4(RNASEL):c.221T>C (p.Ile74Thr) | not specified [RCV002248157] | uncertain significance | 1 | 182586586 | 182586586 | Human | | name |
| 153348289 | CV1695310 | single nucleotide variant | NM_021133.4(RNASEL):c.1222C>T (p.Leu408=) | Prostate cancer, hereditary, 1 [RCV002279842] | uncertain significance | 1 | 182585585 | 182585585 | Human | 1 | name |
| 153348290 | CV1695311 | single nucleotide variant | NM_021133.4(RNASEL):c.1239G>A (p.Glu413=) | Prostate cancer, hereditary, 1 [RCV002279843] | uncertain significance | 1 | 182585568 | 182585568 | Human | 1 | name |
| 153348291 | CV1695312 | single nucleotide variant | NM_021133.4(RNASEL):c.1257A>T (p.Thr419=) | Prostate cancer, hereditary, 1 [RCV002279844] | uncertain significance | 1 | 182585550 | 182585550 | Human | 1 | name |
| 153348292 | CV1695313 | single nucleotide variant | NM_021133.4(RNASEL):c.1260C>T (p.Phe420=) | Prostate cancer, hereditary, 1 [RCV002279845] | uncertain significance | 1 | 182585547 | 182585547 | Human | 1 | name |
| 153348293 | CV1695314 | single nucleotide variant | NM_021133.4(RNASEL):c.1263T>C (p.Tyr421=) | Prostate cancer, hereditary, 1 [RCV002279846] | uncertain significance | 1 | 182585544 | 182585544 | Human | 1 | name |
| 153348294 | CV1695315 | single nucleotide variant | NM_021133.4(RNASEL):c.1305C>T (p.Thr435=) | Prostate cancer, hereditary, 1 [RCV002279847] | uncertain significance | 1 | 182585502 | 182585502 | Human | 1 | name |
| 153348295 | CV1695316 | single nucleotide variant | NM_021133.4(RNASEL):c.1416T>C (p.Val472=) | Prostate cancer, hereditary, 1 [RCV002279848] | uncertain significance | 1 | 182585391 | 182585391 | Human | 1 | name |
| 155937298 | CV2379995 | single nucleotide variant | NM_021133.4(RNASEL):c.254C>T (p.Pro85Leu) | not specified [RCV004222136] | uncertain significance | 1 | 182586553 | 182586553 | Human | | name |
| 329355792 | CV2445663 | single nucleotide variant | NM_021133.4(RNASEL):c.145G>A (p.Ala49Thr) | not specified [RCV004259742] | uncertain significance | 1 | 182586662 | 182586662 | Human | | name |
| 405292445 | CV3196325 | single nucleotide variant | NM_021133.4(RNASEL):c.195C>A (p.Asn65Lys) | RNASEL-related disorder [RCV003964514] | likely benign | 1 | 182586612 | 182586612 | Human | | name , trait , alternate_id |
| 405278764 | CV3220388 | single nucleotide variant | NM_021133.4(RNASEL):c.2172G>A (p.Lys724=) | RNASEL-related disorder [RCV003976601] | benign | 1 | 182575446 | 182575446 | Human | | name , trait , alternate_id |
| 405754009 | CV3316335 | single nucleotide variant | NM_021133.4(RNASEL):c.1809C>T (p.Ser603=) | not specified [RCV004454220] | likely benign | 1 | 182581321 | 182581321 | Human | | name |
| 407508554 | CV3483444 | single nucleotide variant | NM_021133.4(RNASEL):c.233T>C (p.Leu78Pro) | not specified [RCV004672080] | uncertain significance | 1 | 182586574 | 182586574 | Human | | name |
| 597754389 | CV3593894 | single nucleotide variant | NM_021133.4(RNASEL):c.117C>A (p.Asp39Glu) | not specified [RCV004847350] | likely benign | 1 | 182586690 | 182586690 | Human | | name |
| 15191679 | CV696304 | single nucleotide variant | NM_021133.4(RNASEL):c.1179G>A (p.Thr393=) | RNASEL-related disorder [RCV003926013]|not provided [RCV000954846] | benign|likely benign|conflicting interpretations of pathogenicity | 1 | 182585628 | 182585628 | Human | 1 | name , trait , alternate_id |
| 15191685 | CV696306 | single nucleotide variant | NM_021133.4(RNASEL):c.175G>A (p.Gly59Ser) | not provided [RCV000954848] | likely benign | 1 | 182586632 | 182586632 | Human | | name |
| 15108265 | CV718423 | single nucleotide variant | NM_021133.4(RNASEL):c.1242C>T (p.Asn414=) | not provided [RCV000893635] | benign | 1 | 182585565 | 182585565 | Human | | name |
| 21072186 | CV794508 | single nucleotide variant | NM_021133.4(RNASEL):c.289A>C (p.Ile97Leu) | not provided [RCV000994205] | benign|likely benign | 1 | 182586518 | 182586518 | Human | | name |
| 126912276 | CV1036977 | single nucleotide variant | NM_021133.4(RNASEL):c.418G>T (p.Ala140Ser) | not provided [RCV001356347] | uncertain significance | 1 | 182586389 | 182586389 | Human | | name |
| 153348244 | CV1695265 | deletion | NM_021133.4(RNASEL):c.1219del (p.Cys407fs) | Prostate cancer, hereditary, 1 [RCV002279797] | uncertain significance | 1 | 182585588 | 182585588 | Human | 1 | name |
| 153348245 | CV1695266 | deletion | NM_021133.4(RNASEL):c.1222del (p.Leu408fs) | Prostate cancer, hereditary, 1 [RCV002279798] | uncertain significance | 1 | 182585585 | 182585585 | Human | 1 | name |
| 153348246 | CV1695267 | deletion | NM_021133.4(RNASEL):c.1234del (p.Arg412fs) | Prostate cancer, hereditary, 1 [RCV002279799] | uncertain significance | 1 | 182585573 | 182585573 | Human | 1 | name |
| 153348247 | CV1695268 | deletion | NM_021133.4(RNASEL):c.1248del (p.Leu417fs) | Prostate cancer, hereditary, 1 [RCV002279800] | uncertain significance | 1 | 182585559 | 182585559 | Human | 1 | name |
| 153348248 | CV1695269 | duplication | NM_021133.4(RNASEL):c.1250dup (p.Leu417fs) | Prostate cancer, hereditary, 1 [RCV002279801] | uncertain significance | 1 | 182585556 | 182585557 | Human | 1 | name |
| 153348249 | CV1695270 | deletion | NM_021133.4(RNASEL):c.1250del (p.Leu417fs) | Prostate cancer, hereditary, 1 [RCV002279802] | uncertain significance | 1 | 182585557 | 182585557 | Human | 1 | name |
| 153348251 | CV1695272 | duplication | NM_021133.4(RNASEL):c.1253dup (p.Thr419fs) | Prostate cancer, hereditary, 1 [RCV002279804] | uncertain significance | 1 | 182585553 | 182585554 | Human | 1 | name |
| 153348252 | CV1695273 | deletion | NM_021133.4(RNASEL):c.1256del (p.Thr419fs) | Prostate cancer, hereditary, 1 [RCV002279805] | uncertain significance | 1 | 182585551 | 182585551 | Human | 1 | name |
| 153348254 | CV1695275 | deletion | NM_021133.4(RNASEL):c.1257del (p.Phe420fs) | Prostate cancer, hereditary, 1 [RCV002279807] | uncertain significance | 1 | 182585550 | 182585550 | Human | 1 | name |
| 153348255 | CV1695276 | duplication | NM_021133.4(RNASEL):c.1259dup (p.Tyr421fs) | Prostate cancer, hereditary, 1 [RCV002279808] | uncertain significance | 1 | 182585547 | 182585548 | Human | 1 | name |
| 153348256 | CV1695277 | duplication | NM_021133.4(RNASEL):c.1266dup (p.Ser423fs) | Prostate cancer, hereditary, 1 [RCV002279809] | uncertain significance | 1 | 182585540 | 182585541 | Human | 1 | name |
| 153348257 | CV1695278 | deletion | NM_021133.4(RNASEL):c.1268del (p.Ser423fs) | Prostate cancer, hereditary, 1 [RCV002279810] | uncertain significance | 1 | 182585539 | 182585539 | Human | 1 | name |
| 153348258 | CV1695279 | duplication | NM_021133.4(RNASEL):c.1273dup (p.Ser425fs) | Prostate cancer, hereditary, 1 [RCV002279811] | uncertain significance | 1 | 182585533 | 182585534 | Human | 1 | name |
| 153348259 | CV1695280 | deletion | NM_021133.4(RNASEL):c.1279del (p.Arg427fs) | Prostate cancer, hereditary, 1 [RCV002279812] | uncertain significance | 1 | 182585528 | 182585528 | Human | 1 | name |
| 153348260 | CV1695281 | duplication | NM_021133.4(RNASEL):c.1285dup (p.His429fs) | Prostate cancer, hereditary, 1 [RCV002279813] | uncertain significance | 1 | 182585521 | 182585522 | Human | 1 | name |
| 153348261 | CV1695282 | deletion | NM_021133.4(RNASEL):c.1286del (p.His429fs) | Prostate cancer, hereditary, 1 [RCV002279814] | uncertain significance | 1 | 182585521 | 182585521 | Human | 1 | name |
| 153348263 | CV1695284 | duplication | NM_021133.4(RNASEL):c.1293dup (p.Val432fs) | Prostate cancer, hereditary, 1 [RCV002279816] | uncertain significance | 1 | 182585513 | 182585514 | Human | 1 | name |
| 153348265 | CV1695286 | deletion | NM_021133.4(RNASEL):c.1300del (p.Val434fs) | Prostate cancer, hereditary, 1 [RCV002279818] | uncertain significance | 1 | 182585507 | 182585507 | Human | 1 | name |
| 153348267 | CV1695288 | deletion | NM_021133.4(RNASEL):c.1311del (p.Cys437fs) | Prostate cancer, hereditary, 1 [RCV002279820] | uncertain significance | 1 | 182585496 | 182585496 | Human | 1 | name |
| 153348268 | CV1695289 | deletion | NM_021133.4(RNASEL):c.1322del (p.Leu441fs) | Prostate cancer, hereditary, 1 [RCV002279821] | uncertain significance | 1 | 182585485 | 182585485 | Human | 1 | name |
| 153348269 | CV1695290 | duplication | NM_021133.4(RNASEL):c.1343dup (p.His448fs) | Prostate cancer, hereditary, 1 [RCV002279822] | uncertain significance | 1 | 182585463 | 182585464 | Human | 1 | name |
| 153348270 | CV1695291 | deletion | NM_021133.4(RNASEL):c.1351del (p.Glu451fs) | Prostate cancer, hereditary, 1 [RCV002279823] | uncertain significance | 1 | 182585456 | 182585456 | Human | 1 | name |
| 153348271 | CV1695292 | deletion | NM_021133.4(RNASEL):c.1358del (p.Val453fs) | Prostate cancer, hereditary, 1 [RCV002279824] | uncertain significance | 1 | 182585449 | 182585449 | Human | 1 | name |
| 153348272 | CV1695293 | deletion | NM_021133.4(RNASEL):c.1360del (p.Glu454fs) | Prostate cancer, hereditary, 1 [RCV002279825] | uncertain significance | 1 | 182585447 | 182585447 | Human | 1 | name |
| 153348273 | CV1695294 | duplication | NM_021133.4(RNASEL):c.1364dup (p.Asn455fs) | Prostate cancer, hereditary, 1 [RCV002279826] | uncertain significance | 1 | 182585442 | 182585443 | Human | 1 | name |
| 153348274 | CV1695295 | deletion | NM_021133.4(RNASEL):c.1369del (p.Glu457fs) | Prostate cancer, hereditary, 1 [RCV002279827] | uncertain significance | 1 | 182585438 | 182585438 | Human | 1 | name |
| 153348276 | CV1695297 | deletion | NM_021133.4(RNASEL):c.1380del (p.Phe460fs) | Prostate cancer, hereditary, 1 [RCV002279829] | uncertain significance | 1 | 182585427 | 182585427 | Human | 1 | name |
| 153348277 | CV1695298 | deletion | NM_021133.4(RNASEL):c.1385del (p.Arg462fs) | Prostate cancer, hereditary, 1 [RCV002279830] | uncertain significance | 1 | 182585422 | 182585422 | Human | 1 | name |
| 153348278 | CV1695299 | deletion | NM_021133.4(RNASEL):c.1395del (p.Ser466fs) | Prostate cancer, hereditary, 1 [RCV002279831] | uncertain significance | 1 | 182585412 | 182585412 | Human | 1 | name |
| 153348280 | CV1695301 | duplication | NM_021133.4(RNASEL):c.1400dup (p.Ile468fs) | Prostate cancer, hereditary, 1 [RCV002279833] | uncertain significance | 1 | 182585406 | 182585407 | Human | 1 | name |
| 153348281 | CV1695302 | deletion | NM_021133.4(RNASEL):c.1403del (p.Ile468fs) | Prostate cancer, hereditary, 1 [RCV002279834] | uncertain significance | 1 | 182585404 | 182585404 | Human | 1 | name |
| 153348282 | CV1695303 | deletion | NM_021133.4(RNASEL):c.1407del (p.Phe469fs) | Prostate cancer, hereditary, 1 [RCV002279835] | uncertain significance | 1 | 182585400 | 182585400 | Human | 1 | name |
| 153348283 | CV1695304 | deletion | NM_021133.4(RNASEL):c.1411del (p.Ala471fs) | Prostate cancer, hereditary, 1 [RCV002279836] | uncertain significance | 1 | 182585396 | 182585396 | Human | 1 | name |
| 153348284 | CV1695305 | deletion | NM_021133.4(RNASEL):c.1413del (p.Val472fs) | Prostate cancer, hereditary, 1 [RCV002279837] | uncertain significance | 1 | 182585394 | 182585394 | Human | 1 | name |
| 153348287 | CV1695308 | deletion | NM_021133.4(RNASEL):c.1430del (p.Leu477fs) | Prostate cancer, hereditary, 1 [RCV002279840] | uncertain significance | 1 | 182585377 | 182585377 | Human | 1 | name |
| 155801014 | CV1861157 | duplication | NM_021133.4(RNASEL):c.1033dup (p.Ala345fs) | Prostate cancer, hereditary, 1 [RCV002468872] | uncertain significance | 1 | 182585773 | 182585774 | Human | 1 | name |
| 156250213 | CV2215639 | single nucleotide variant | NM_021133.4(RNASEL):c.562C>T (p.Leu188Phe) | not specified [RCV004089389] | uncertain significance | 1 | 182586245 | 182586245 | Human | | name |
| 155993713 | CV2377275 | single nucleotide variant | NM_021133.4(RNASEL):c.605G>A (p.Gly202Asp) | not specified [RCV004225465] | uncertain significance | 1 | 182586202 | 182586202 | Human | | name |
| 243060212 | CV2413758 | single nucleotide variant | NM_021133.4(RNASEL):c.526G>A (p.Ala176Thr) | Prostate cancer, hereditary, 1 [RCV003135777] | uncertain significance | 1 | 182586281 | 182586281 | Human | 1 | name |
| 243054580 | CV2418972 | single nucleotide variant | NM_021133.4(RNASEL):c.918G>A (p.Met306Ile) | Ovarian cancer [RCV003154655] | benign | 1 | 182585889 | 182585889 | Human | 2 | name |
| 329374956 | CV2430981 | single nucleotide variant | NM_021133.4(RNASEL):c.976A>G (p.Lys326Glu) | not specified [RCV004248569] | uncertain significance | 1 | 182585831 | 182585831 | Human | | name |
| 329388449 | CV2471937 | single nucleotide variant | NM_021133.4(RNASEL):c.635G>A (p.Ser212Asn) | not specified [RCV004280955] | likely benign | 1 | 182586172 | 182586172 | Human | | name |
| 8599241 | CV28043 | single nucleotide variant | NM_021133.4(RNASEL):c.793G>T (p.Glu265Ter) | Prostate cancer [RCV000991158]|Prostate cancer, hereditary, 1 [RCV000013878]|RNASEL-related disorder [RCV003914838]|not provided [RCV000954847] | pathogenic|likely pathogenic|benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance | 1 | 182586014 | 182586014 | Human | 3 | name , trait , alternate_id |
| 405278503 | CV3216607 | single nucleotide variant | NM_021133.4(RNASEL):c.880A>G (p.Lys294Glu) | RNASEL-related disorder [RCV003954511] | likely benign | 1 | 182585927 | 182585927 | Human | | name , trait , alternate_id |
| 405754045 | CV3316340 | single nucleotide variant | NM_021133.4(RNASEL):c.443G>C (p.Gly148Ala) | not specified [RCV004454225] | uncertain significance | 1 | 182586364 | 182586364 | Human | | name |
| 405754066 | CV3316343 | single nucleotide variant | NM_021133.4(RNASEL):c.704G>T (p.Arg235Met) | not specified [RCV004454228] | uncertain significance | 1 | 182586103 | 182586103 | Human | | name |
| 405754072 | CV3316344 | single nucleotide variant | NM_021133.4(RNASEL):c.938A>T (p.Asp313Val) | not specified [RCV004454229] | uncertain significance | 1 | 182585869 | 182585869 | Human | | name |
| 405754079 | CV3316345 | single nucleotide variant | NM_021133.4(RNASEL):c.965C>G (p.Ser322Cys) | not specified [RCV004454230] | uncertain significance | 1 | 182585842 | 182585842 | Human | | name |
| 407508557 | CV3483445 | single nucleotide variant | NM_021133.4(RNASEL):c.818G>T (p.Gly273Val) | not specified [RCV004672081] | uncertain significance | 1 | 182585989 | 182585989 | Human | | name |
| 597754386 | CV3593891 | single nucleotide variant | NM_021133.4(RNASEL):c.488G>C (p.Arg163Pro) | not specified [RCV004847349] | uncertain significance | 1 | 182586319 | 182586319 | Human | | name |
| 597754393 | CV3593896 | single nucleotide variant | NM_021133.4(RNASEL):c.566A>C (p.Asp189Ala) | not specified [RCV004847351] | uncertain significance | 1 | 182586241 | 182586241 | Human | | name |
| 597754398 | CV3593897 | single nucleotide variant | NM_021133.4(RNASEL):c.333C>G (p.Phe111Leu) | not specified [RCV004847352] | uncertain significance | 1 | 182586474 | 182586474 | Human | | name |
| 598230407 | CV3899349 | single nucleotide variant | NM_021133.4(RNASEL):c.713G>A (p.Arg238Lys) | not specified [RCV005274341] | likely benign | 1 | 182586094 | 182586094 | Human | | name |
| 153348232 | CV1695253 | single nucleotide variant | NM_021133.4(RNASEL):c.1208G>C (p.Arg403Pro) | Prostate cancer, hereditary, 1 [RCV002279785] | uncertain significance | 1 | 182585599 | 182585599 | Human | 1 | name |
| 153348233 | CV1695254 | single nucleotide variant | NM_021133.4(RNASEL):c.1368G>T (p.Glu456Asp) | Prostate cancer, hereditary, 1 [RCV002279786] | uncertain significance | 1 | 182585439 | 182585439 | Human | 1 | name |
| 153348234 | CV1695255 | single nucleotide variant | NM_021133.4(RNASEL):c.1388A>G (p.Asn463Ser) | Prostate cancer, hereditary, 1 [RCV002279787] | uncertain significance | 1 | 182585419 | 182585419 | Human | 1 | name |
| 153348235 | CV1695256 | single nucleotide variant | NM_021133.4(RNASEL):c.1393C>A (p.Leu465Met) | Prostate cancer, hereditary, 1 [RCV002279788] | uncertain significance | 1 | 182585414 | 182585414 | Human | 1 | name |
| 153348236 | CV1695257 | single nucleotide variant | NM_021133.4(RNASEL):c.1405T>A (p.Phe469Ile) | Prostate cancer, hereditary, 1 [RCV002279789] | uncertain significance | 1 | 182585402 | 182585402 | Human | 1 | name |
| 153348237 | CV1695258 | single nucleotide variant | NM_021133.4(RNASEL):c.1407T>A (p.Phe469Leu) | Prostate cancer, hereditary, 1 [RCV002279790] | uncertain significance | 1 | 182585400 | 182585400 | Human | 1 | name |
| 153348238 | CV1695259 | single nucleotide variant | NM_021133.4(RNASEL):c.1409A>C (p.Lys470Thr) | Prostate cancer, hereditary, 1 [RCV002279791] | uncertain significance | 1 | 182585398 | 182585398 | Human | 1 | name |
| 153348239 | CV1695260 | single nucleotide variant | NM_021133.4(RNASEL):c.1412C>T (p.Ala471Val) | Prostate cancer, hereditary, 1 [RCV002279792] | uncertain significance | 1 | 182585395 | 182585395 | Human | 1 | name |
| 153348240 | CV1695261 | single nucleotide variant | NM_021133.4(RNASEL):c.1418A>C (p.Gln473Pro) | Prostate cancer, hereditary, 1 [RCV002279793] | uncertain significance | 1 | 182585389 | 182585389 | Human | 1 | name |
| 153348241 | CV1695262 | single nucleotide variant | NM_021133.4(RNASEL):c.1422A>T (p.Glu474Asp) | Prostate cancer, hereditary, 1 [RCV002279794] | uncertain significance | 1 | 182585385 | 182585385 | Human | 1 | name |
| 153348242 | CV1695263 | single nucleotide variant | NM_021133.4(RNASEL):c.1230C>A (p.Ser410Arg) | Prostate cancer, hereditary, 1 [RCV002279795] | uncertain significance | 1 | 182585577 | 182585577 | Human | 1 | name |
| 153348243 | CV1695264 | single nucleotide variant | NM_021133.4(RNASEL):c.1429T>A (p.Leu477Met) | Prostate cancer, hereditary, 1 [RCV002279796] | uncertain significance | 1 | 182585378 | 182585378 | Human | 1 | name |
| 153348253 | CV1695274 | single nucleotide variant | NM_021133.4(RNASEL):c.1237G>A (p.Glu413Lys) | Prostate cancer, hereditary, 1 [RCV002279806] | uncertain significance | 1 | 182585570 | 182585570 | Human | 1 | name |
| 153348264 | CV1695285 | single nucleotide variant | NM_021133.4(RNASEL):c.1243A>G (p.Ser415Gly) | Prostate cancer, hereditary, 1 [RCV002279817] | uncertain significance | 1 | 182585564 | 182585564 | Human | 1 | name |
| 153348266 | CV1695287 | duplication | NM_021133.4(RNASEL):c.1311dup (p.Glu438Ter) | Prostate cancer, hereditary, 1 [RCV002279819] | uncertain significance | 1 | 182585495 | 182585496 | Human | 1 | name |
| 153348275 | CV1695296 | single nucleotide variant | NM_021133.4(RNASEL):c.1256C>A (p.Thr419Lys) | Prostate cancer, hereditary, 1 [RCV002279828] | uncertain significance | 1 | 182585551 | 182585551 | Human | 1 | name |
| 153348286 | CV1695307 | single nucleotide variant | NM_021133.4(RNASEL):c.1264G>T (p.Gly422Trp) | Prostate cancer, hereditary, 1 [RCV002279839] | uncertain significance | 1 | 182585543 | 182585543 | Human | 1 | name |
| 153348288 | CV1695309 | single nucleotide variant | NM_021133.4(RNASEL):c.1289T>A (p.Leu430Ter) | Prostate cancer, hereditary, 1 [RCV002279841] | uncertain significance | 1 | 182585518 | 182585518 | Human | 1 | name |
| 153348296 | CV1695317 | single nucleotide variant | NM_021133.4(RNASEL):c.1270G>C (p.Glu424Gln) | Prostate cancer, hereditary, 1 [RCV002279849] | uncertain significance | 1 | 182585537 | 182585537 | Human | 1 | name |
| 153348297 | CV1695318 | single nucleotide variant | NM_021133.4(RNASEL):c.1289T>C (p.Leu430Ser) | Prostate cancer, hereditary, 1 [RCV002279850] | uncertain significance | 1 | 182585518 | 182585518 | Human | 1 | name |
| 153348298 | CV1695319 | single nucleotide variant | NM_021133.4(RNASEL):c.1303A>C (p.Thr435Pro) | Prostate cancer, hereditary, 1 [RCV002279851] | uncertain significance | 1 | 182585504 | 182585504 | Human | 1 | name |
| 156331042 | CV2210751 | single nucleotide variant | NM_021133.4(RNASEL):c.1823G>A (p.Arg608Gln) | not specified [RCV004085847] | uncertain significance | 1 | 182581307 | 182581307 | Human | | name |
| 156287686 | CV2288423 | single nucleotide variant | NM_021133.4(RNASEL):c.1376A>T (p.Glu459Val) | not specified [RCV004151971] | uncertain significance | 1 | 182585431 | 182585431 | Human | | name |
| 156358287 | CV2318461 | single nucleotide variant | NM_021133.4(RNASEL):c.1477A>G (p.Ile493Val) | not specified [RCV004173108] | uncertain significance | 1 | 182585330 | 182585330 | Human | | name |
| 243054514 | CV2419015 | single nucleotide variant | NM_021133.4(RNASEL):c.1251G>C (p.Leu417Phe) | Ovarian cancer [RCV003154698] | benign | 1 | 182585556 | 182585556 | Human | 2 | name |
| 243054637 | CV2419019 | single nucleotide variant | NM_021133.4(RNASEL):c.2152C>A (p.Gln718Lys) | Ovarian cancer [RCV003154702] | benign | 1 | 182575466 | 182575466 | Human | 2 | name |
| 243054757 | CV2419065 | single nucleotide variant | NM_021133.4(RNASEL):c.1115C>A (p.Ala372Asp) | Ovarian cancer [RCV003154749] | likely pathogenic | 1 | 182585692 | 182585692 | Human | 2 | name |
| 243055342 | CV2419102 | single nucleotide variant | NM_021133.4(RNASEL):c.1469A>G (p.Asn490Ser) | Ovarian cancer [RCV003154786] | likely pathogenic | 1 | 182585338 | 182585338 | Human | 2 | name |
| 329385676 | CV2432123 | single nucleotide variant | NM_021133.4(RNASEL):c.2194G>A (p.Gly732Arg) | not specified [RCV004249270] | uncertain significance | 1 | 182575424 | 182575424 | Human | | name |
| 401731395 | CV2693776 | single nucleotide variant | NM_021133.4(RNASEL):c.1810G>A (p.Asp604Asn) | not specified [RCV004298098] | uncertain significance | 1 | 182581320 | 182581320 | Human | | name |
| 401749239 | CV2694595 | single nucleotide variant | NM_021133.4(RNASEL):c.2188G>A (p.Ala730Thr) | not specified [RCV004298715] | uncertain significance | 1 | 182575430 | 182575430 | Human | | name |
| 401780163 | CV2725906 | single nucleotide variant | NM_021133.4(RNASEL):c.1164A>C (p.Glu388Asp) | not specified [RCV004324281] | uncertain significance | 1 | 182585643 | 182585643 | Human | | name |
| 401723260 | CV2738125 | single nucleotide variant | NM_021133.4(RNASEL):c.1591G>A (p.Val531Met) | Prostate cancer, hereditary, 1 [RCV003315481] | uncertain significance | 1 | 182582234 | 182582234 | Human | 1 | name |
| 401866044 | CV2786240 | single nucleotide variant | NM_021133.4(RNASEL):c.1696C>T (p.Leu566Phe) | not specified [RCV004361564] | uncertain significance | 1 | 182582129 | 182582129 | Human | | name |
| 8599243 | CV28045 | single nucleotide variant | NM_021133.4(RNASEL):c.1385G>A (p.Arg462Gln) | Hereditary cancer [RCV003492293]|Prostate cancer susceptibility [RCV004794338]|Prostate cancer, hereditary, 1 [RCV002279713] | risk factor|likely benign|uncertain significance | 1 | 182585422 | 182585422 | Human | 3 | name |
| 405273379 | CV3207391 | single nucleotide variant | NM_021133.4(RNASEL):c.1234C>G (p.Arg412Gly) | RNASEL-related disorder [RCV003914666] | likely benign | 1 | 182585573 | 182585573 | Human | | name , trait , alternate_id |
| 405754002 | CV3316334 | single nucleotide variant | NM_021133.4(RNASEL):c.1220G>A (p.Cys407Tyr) | not specified [RCV004454219] | uncertain significance | 1 | 182585587 | 182585587 | Human | | name |
| 405754014 | CV3316336 | single nucleotide variant | NM_021133.4(RNASEL):c.1883G>A (p.Ser628Asn) | not specified [RCV004454221] | uncertain significance | 1 | 182581247 | 182581247 | Human | | name |
| 405754029 | CV3316338 | single nucleotide variant | NM_021133.4(RNASEL):c.1951A>G (p.Arg651Gly) | not specified [RCV004454223] | uncertain significance | 1 | 182576344 | 182576344 | Human | | name |
| 405754039 | CV3316339 | single nucleotide variant | NM_021133.4(RNASEL):c.2000G>A (p.Arg667Gln) | not specified [RCV004454224] | uncertain significance | 1 | 182576295 | 182576295 | Human | | name |
| 597685992 | CV3593892 | single nucleotide variant | NM_021133.4(RNASEL):c.1727G>A (p.Cys576Tyr) | not specified [RCV004858335] | uncertain significance | 1 | 182582098 | 182582098 | Human | | name |
| 597686000 | CV3593893 | single nucleotide variant | NM_021133.4(RNASEL):c.2017A>G (p.Ile673Val) | not specified [RCV004858336] | uncertain significance | 1 | 182576278 | 182576278 | Human | | name |
| 597686021 | CV3593898 | single nucleotide variant | NM_021133.4(RNASEL):c.1833A>C (p.Glu611Asp) | not specified [RCV004858338] | uncertain significance | 1 | 182581297 | 182581297 | Human | | name |
| 597754402 | CV3593899 | single nucleotide variant | NM_021133.4(RNASEL):c.1382C>T (p.Ala461Val) | not specified [RCV004847353] | uncertain significance | 1 | 182585425 | 182585425 | Human | | name |
| 598230414 | CV3899350 | single nucleotide variant | NM_021133.4(RNASEL):c.1198C>T (p.Arg400Cys) | not specified [RCV005274342] | uncertain significance | 1 | 182585609 | 182585609 | Human | | name |
| 598230420 | CV3899351 | single nucleotide variant | NM_021133.4(RNASEL):c.1607G>A (p.Ser536Asn) | not specified [RCV005274343] | uncertain significance | 1 | 182582218 | 182582218 | Human | | name |
| 598230427 | CV3899352 | single nucleotide variant | NM_021133.4(RNASEL):c.1010A>T (p.Lys337Met) | not specified [RCV005274344] | uncertain significance | 1 | 182585797 | 182585797 | Human | | name |
| 598230434 | CV3899353 | single nucleotide variant | NM_021133.4(RNASEL):c.1374T>A (p.Asp458Glu) | not specified [RCV005274345] | uncertain significance | 1 | 182585433 | 182585433 | Human | | name |
| 598176757 | CV4008182 | single nucleotide variant | NM_021133.4(RNASEL):c.1855C>T (p.Gln619Ter) | Prostate cancer, hereditary, 1 [RCV005393698] | uncertain significance | 1 | 182581275 | 182581275 | Human | 1 | name |
| 598176764 | CV4008183 | single nucleotide variant | NM_021133.4(RNASEL):c.2077C>G (p.Gln693Glu) | Prostate cancer, hereditary, 1 [RCV005393699] | uncertain significance | 1 | 182575541 | 182575541 | Human | 1 | name |
| 21072179 | CV794507 | single nucleotide variant | NM_021133.4(RNASEL):c.1567G>A (p.Asp523Asn) | not provided [RCV000994204] | uncertain significance | 1 | 182582258 | 182582258 | Human | | name |
| 42722903 | CV985169 | single nucleotide variant | NM_021133.4(RNASEL):c.1767G>A (p.Trp589Ter) | Prostate cancer, hereditary, 1 [RCV001292911] | pathogenic | 1 | 182582058 | 182582058 | Human | | name |
| 153348285 | CV1695306 | deletion | NM_021133.4(RNASEL):c.1414_1415del (p.Val472fs) | Prostate cancer, hereditary, 1 [RCV002279838] | uncertain significance | 1 | 182585392 | 182585393 | Human | 1 | name |
| 153348250 | CV1695271 | insertion | NM_021133.4(RNASEL):c.1252_1253insA (p.Val418fs) | Prostate cancer, hereditary, 1 [RCV002279803] | uncertain significance | 1 | 182585554 | 182585555 | Human | 1 | name |
| 153348262 | CV1695283 | insertion | NM_021133.4(RNASEL):c.1287_1288insA (p.Leu430fs) | Prostate cancer, hereditary, 1 [RCV002279815] | uncertain significance | 1 | 182585519 | 182585520 | Human | 1 | name |
| 153348279 | CV1695300 | insertion | NM_021133.4(RNASEL):c.1399_1400insA (p.Ser467fs) | Prostate cancer, hereditary, 1 [RCV002279832] | uncertain significance | 1 | 182585407 | 182585408 | Human | 1 | name |
| 405690413 | CV3227391 | deletion | NM_021133.4(RNASEL):c.1127_1129del (p.Glu376del) | Prostate cancer, hereditary, 1 [RCV003991735] | uncertain significance | 1 | 182585678 | 182585680 | Human | 1 | name |
