| 15103222 | CV763848 | single nucleotide variant | NM_020873.7(LRRN1):c.90T>C (p.Ser30=) | not provided [RCV000937155] | likely benign | 3 | 3844731 | 3844731 | Human | | name |
| 8630793 | CV85948 | single nucleotide variant | NM_020873.5(LRRN1):c.252C>T (p.Ile84=) | Malignant melanoma [RCV000066032] | not provided | 3 | 3844893 | 3844893 | Human | | name |
| 156061528 | CV2280428 | single nucleotide variant | NM_020873.7(LRRN1):c.93G>C (p.Glu31Asp) | not specified [RCV004140603] | uncertain significance | 3 | 3844734 | 3844734 | Human | | name |
| 401922030 | CV2819824 | single nucleotide variant | NM_020873.7(LRRN1):c.984C>T (p.Ile328=) | not provided [RCV003433353] | likely benign | 3 | 3845625 | 3845625 | Human | | name |
| 15098821 | CV698058 | single nucleotide variant | NM_020873.7(LRRN1):c.459C>T (p.Asn153=) | not provided [RCV000958646] | benign | 3 | 3845100 | 3845100 | Human | 1 | name |
| 15098821 | CV698058 | single nucleotide variant | NM_020873.7(LRRN1):c.459C>T (p.Asn153=) | not provided [RCV000958646] | benign | 3 | 3845100 | 3845101 | Human | 1 | name |
| 15195601 | CV720422 | single nucleotide variant | NM_020873.7(LRRN1):c.396C>T (p.Thr132=) | not provided [RCV000889547] | benign | 3 | 3845037 | 3845037 | Human | | name |
| 8630795 | CV85950 | single nucleotide variant | NM_020873.5(LRRN1):c.900C>T (p.Leu300=) | Malignant melanoma [RCV000066034] | not provided | 3 | 3845541 | 3845541 | Human | | name |
| 156080778 | CV2337575 | single nucleotide variant | NM_020873.7(LRRN1):c.176A>G (p.Asn59Ser) | not specified [RCV004181141] | uncertain significance | 3 | 3844817 | 3844817 | Human | | name |
| 401922031 | CV2819825 | single nucleotide variant | NM_020873.7(LRRN1):c.1209C>T (p.Pro403=) | not provided [RCV003433354] | likely benign | 3 | 3845850 | 3845850 | Human | | name |
| 405810502 | CV3288249 | single nucleotide variant | NM_020873.7(LRRN1):c.287A>C (p.Asn96Thr) | not specified [RCV004408019] | uncertain significance | 3 | 3844928 | 3844928 | Human | | name |
| 407482324 | CV3453010 | single nucleotide variant | NM_020873.7(LRRN1):c.157G>A (p.Ala53Thr) | not specified [RCV004640112] | uncertain significance | 3 | 3844798 | 3844798 | Human | | name |
| 598223356 | CV3984974 | single nucleotide variant | NM_020873.7(LRRN1):c.161C>T (p.Thr54Ile) | not specified [RCV005380039] | uncertain significance | 3 | 3844802 | 3844802 | Human | | name |
| 15170596 | CV698059 | single nucleotide variant | NM_020873.7(LRRN1):c.1308C>T (p.Asn436=) | not provided [RCV000949680] | benign | 3 | 3845949 | 3845949 | Human | | name |
| 15103811 | CV698060 | single nucleotide variant | NM_020873.7(LRRN1):c.1647C>T (p.Val549=) | not provided [RCV000959556] | benign | 3 | 3846288 | 3846288 | Human | | name |
| 15157666 | CV708819 | single nucleotide variant | NM_020873.7(LRRN1):c.1221G>A (p.Gly407=) | not provided [RCV000969350] | likely benign | 3 | 3845862 | 3845862 | Human | | name |
| 15154986 | CV708820 | single nucleotide variant | NM_020873.7(LRRN1):c.1827C>T (p.Cys609=) | not provided [RCV000968839] | benign | 3 | 3846468 | 3846468 | Human | | name |
| 15105340 | CV748222 | single nucleotide variant | NM_020873.7(LRRN1):c.1152C>T (p.Ser384=) | not provided [RCV000915526] | likely benign | 3 | 3845793 | 3845793 | Human | | name |
| 8630792 | CV85947 | single nucleotide variant | NM_020873.5(LRRN1):c.124C>T (p.Pro42Ser) | Malignant melanoma [RCV000066031] | not provided | 3 | 3844765 | 3844765 | Human | | name |
| 156143332 | CV2208625 | single nucleotide variant | NM_020873.7(LRRN1):c.451A>C (p.Asn151His) | not specified [RCV004091142] | uncertain significance | 3 | 3845092 | 3845092 | Human | | name |
| 329398929 | CV2443154 | single nucleotide variant | NM_020873.7(LRRN1):c.830A>G (p.Lys277Arg) | not specified [RCV004255349] | uncertain significance | 3 | 3845471 | 3845471 | Human | | name |
| 401731721 | CV2674462 | single nucleotide variant | NM_020873.7(LRRN1):c.917A>G (p.Tyr306Cys) | not specified [RCV004291366] | uncertain significance | 3 | 3845558 | 3845558 | Human | | name |
| 401718597 | CV2704689 | single nucleotide variant | NM_020873.7(LRRN1):c.948G>C (p.Lys316Asn) | not specified [RCV004307296] | uncertain significance | 3 | 3845589 | 3845589 | Human | | name |
| 401882029 | CV2774672 | single nucleotide variant | NM_020873.7(LRRN1):c.490G>T (p.Ala164Ser) | not specified [RCV004350132] | likely benign | 3 | 3845131 | 3845131 | Human | | name |
| 401860780 | CV2776188 | single nucleotide variant | NM_020873.7(LRRN1):c.623A>T (p.Asp208Val) | not specified [RCV004353272] | uncertain significance | 3 | 3845264 | 3845264 | Human | | name |
| 405810504 | CV3288250 | single nucleotide variant | NM_020873.7(LRRN1):c.481C>A (p.His161Asn) | not specified [RCV004408020] | likely benign | 3 | 3845122 | 3845122 | Human | | name |
| 405810506 | CV3288251 | single nucleotide variant | NM_020873.7(LRRN1):c.571C>T (p.Pro191Ser) | not specified [RCV004408021] | uncertain significance | 3 | 3845212 | 3845212 | Human | | name |
| 405810508 | CV3288252 | single nucleotide variant | NM_020873.7(LRRN1):c.589A>C (p.Met197Leu) | not specified [RCV004408022] | uncertain significance | 3 | 3845230 | 3845230 | Human | | name |
| 405810510 | CV3288253 | single nucleotide variant | NM_020873.7(LRRN1):c.858G>A (p.Met286Ile) | not specified [RCV004408023] | uncertain significance | 3 | 3845499 | 3845499 | Human | | name |
| 405810512 | CV3288254 | single nucleotide variant | NM_020873.7(LRRN1):c.988C>G (p.Arg330Gly) | not specified [RCV004408024] | uncertain significance | 3 | 3845629 | 3845629 | Human | | name |
| 407482335 | CV3453012 | single nucleotide variant | NM_020873.7(LRRN1):c.763C>T (p.Pro255Ser) | not specified [RCV004640114] | uncertain significance | 3 | 3845404 | 3845404 | Human | | name |
| 407482340 | CV3453013 | single nucleotide variant | NM_020873.7(LRRN1):c.337G>C (p.Val113Leu) | not specified [RCV004640115] | uncertain significance | 3 | 3844978 | 3844978 | Human | | name |
| 597634284 | CV3702397 | single nucleotide variant | NM_020873.7(LRRN1):c.537G>C (p.Leu179Phe) | not specified [RCV004940395] | uncertain significance | 3 | 3845178 | 3845178 | Human | | name |
| 597634289 | CV3702398 | single nucleotide variant | NM_020873.7(LRRN1):c.491C>G (p.Ala164Gly) | not specified [RCV004940396] | uncertain significance | 3 | 3845132 | 3845132 | Human | | name |
| 597634294 | CV3702399 | single nucleotide variant | NM_020873.7(LRRN1):c.820C>G (p.Pro274Ala) | not specified [RCV004940397] | uncertain significance | 3 | 3845461 | 3845461 | Human | | name |
| 598251622 | CV3984976 | single nucleotide variant | NM_020873.7(LRRN1):c.833T>C (p.Ile278Thr) | not specified [RCV005366728] | uncertain significance | 3 | 3845474 | 3845474 | Human | | name |
| 598251627 | CV3984977 | single nucleotide variant | NM_020873.7(LRRN1):c.624T>A (p.Asp208Glu) | not specified [RCV005366729] | uncertain significance | 3 | 3845265 | 3845265 | Human | | name |
| 598223363 | CV3984978 | single nucleotide variant | NM_020873.7(LRRN1):c.625A>G (p.Met209Val) | not specified [RCV005380040] | uncertain significance | 3 | 3845266 | 3845266 | Human | | name |
| 598251637 | CV3984981 | single nucleotide variant | NM_020873.7(LRRN1):c.782A>G (p.Lys261Arg) | not specified [RCV005366731] | uncertain significance | 3 | 3845423 | 3845423 | Human | | name |
| 598223378 | CV3984984 | single nucleotide variant | NM_020873.7(LRRN1):c.989G>T (p.Arg330Leu) | not specified [RCV005380042] | uncertain significance | 3 | 3845630 | 3845630 | Human | | name |
| 8630794 | CV85949 | single nucleotide variant | NM_020873.5(LRRN1):c.580G>A (p.Glu194Lys) | Malignant melanoma [RCV000066033] | not provided | 3 | 3845221 | 3845221 | Human | | name |
| 156389564 | CV2226395 | single nucleotide variant | NM_020873.7(LRRN1):c.1799A>G (p.Asn600Ser) | not specified [RCV004099615] | uncertain significance | 3 | 3846440 | 3846440 | Human | | name |
| 156020278 | CV2270244 | single nucleotide variant | NM_020873.7(LRRN1):c.1441G>A (p.Glu481Lys) | not specified [RCV004135463] | uncertain significance | 3 | 3846082 | 3846082 | Human | | name |
| 155923965 | CV2280427 | single nucleotide variant | NM_020873.7(LRRN1):c.1971G>C (p.Lys657Asn) | not specified [RCV004140602] | uncertain significance | 3 | 3846612 | 3846612 | Human | | name |
| 156250465 | CV2286720 | single nucleotide variant | NM_020873.7(LRRN1):c.1576G>T (p.Val526Leu) | not specified [RCV004142543] | uncertain significance | 3 | 3846217 | 3846217 | Human | | name |
| 156290121 | CV2342527 | single nucleotide variant | NM_020873.7(LRRN1):c.1090C>T (p.Arg364Cys) | not specified [RCV004196625] | uncertain significance | 3 | 3845731 | 3845731 | Human | | name |
| 156006965 | CV2401258 | single nucleotide variant | NM_020873.7(LRRN1):c.1529G>A (p.Arg510Gln) | not specified [RCV004245807] | uncertain significance | 3 | 3846170 | 3846170 | Human | | name |
| 329387003 | CV2436199 | single nucleotide variant | NM_020873.7(LRRN1):c.1160C>T (p.Thr387Ile) | not specified [RCV004249832] | uncertain significance | 3 | 3845801 | 3845801 | Human | | name |
| 401748100 | CV2687682 | single nucleotide variant | NM_020873.7(LRRN1):c.1385C>T (p.Pro462Leu) | not specified [RCV004302677] | uncertain significance | 3 | 3846026 | 3846026 | Human | | name |
| 401922032 | CV2819826 | single nucleotide variant | NM_020873.7(LRRN1):c.1255A>G (p.Ser419Gly) | not provided [RCV003433355] | likely benign | 3 | 3845896 | 3845896 | Human | | name |
| 405810483 | CV3288240 | single nucleotide variant | NM_020873.7(LRRN1):c.1207C>T (p.Pro403Ser) | not specified [RCV004408010] | uncertain significance | 3 | 3845848 | 3845848 | Human | | name |
| 405810486 | CV3288241 | single nucleotide variant | NM_020873.7(LRRN1):c.1273A>G (p.Met425Val) | not specified [RCV004408011] | uncertain significance | 3 | 3845914 | 3845914 | Human | | name |
| 405810487 | CV3288242 | single nucleotide variant | NM_020873.7(LRRN1):c.1511T>A (p.Val504Asp) | not specified [RCV004408012] | uncertain significance | 3 | 3846152 | 3846152 | Human | | name |
| 405810490 | CV3288243 | single nucleotide variant | NM_020873.7(LRRN1):c.1643A>G (p.Asn548Ser) | not specified [RCV004408013] | uncertain significance | 3 | 3846284 | 3846284 | Human | | name |
| 405810492 | CV3288244 | single nucleotide variant | NM_020873.7(LRRN1):c.1652C>A (p.Thr551Lys) | not specified [RCV004408014] | uncertain significance | 3 | 3846293 | 3846293 | Human | | name |
| 405810494 | CV3288245 | single nucleotide variant | NM_020873.7(LRRN1):c.1652C>T (p.Thr551Met) | not specified [RCV004408015] | uncertain significance | 3 | 3846293 | 3846293 | Human | | name |
| 405810496 | CV3288246 | single nucleotide variant | NM_020873.7(LRRN1):c.1670C>T (p.Ser557Leu) | not specified [RCV004408016] | uncertain significance | 3 | 3846311 | 3846311 | Human | | name |
| 405810498 | CV3288247 | single nucleotide variant | NM_020873.7(LRRN1):c.1681A>G (p.Met561Val) | not specified [RCV004408017] | uncertain significance | 3 | 3846322 | 3846322 | Human | | name |
| 405810500 | CV3288248 | single nucleotide variant | NM_020873.7(LRRN1):c.1852G>T (p.Ala618Ser) | not specified [RCV004408018] | uncertain significance | 3 | 3846493 | 3846493 | Human | | name |
| 407502226 | CV3453005 | single nucleotide variant | NM_020873.7(LRRN1):c.1852G>A (p.Ala618Thr) | not specified [RCV004645095] | uncertain significance | 3 | 3846493 | 3846493 | Human | | name |
| 407502230 | CV3453006 | single nucleotide variant | NM_020873.7(LRRN1):c.1169G>A (p.Arg390His) | not specified [RCV004645096] | uncertain significance | 3 | 3845810 | 3845810 | Human | | name |
| 407482306 | CV3453007 | single nucleotide variant | NM_020873.7(LRRN1):c.1589A>G (p.Tyr530Cys) | not specified [RCV004640109] | uncertain significance | 3 | 3846230 | 3846230 | Human | | name |
| 407482313 | CV3453008 | single nucleotide variant | NM_020873.7(LRRN1):c.1168C>T (p.Arg390Cys) | not specified [RCV004640110] | uncertain significance | 3 | 3845809 | 3845809 | Human | | name |
| 407482318 | CV3453009 | single nucleotide variant | NM_020873.7(LRRN1):c.1224C>G (p.His408Gln) | not specified [RCV004640111] | likely benign | 3 | 3845865 | 3845865 | Human | | name |
| 407482330 | CV3453011 | single nucleotide variant | NM_020873.7(LRRN1):c.1063A>G (p.Lys355Glu) | not specified [RCV004640113] | uncertain significance | 3 | 3845704 | 3845704 | Human | | name |
| 597634298 | CV3702400 | single nucleotide variant | NM_020873.7(LRRN1):c.1630A>C (p.Lys544Gln) | not specified [RCV004940398] | uncertain significance | 3 | 3846271 | 3846271 | Human | | name |
| 598223350 | CV3984973 | single nucleotide variant | NM_020873.7(LRRN1):c.1091G>A (p.Arg364His) | not specified [RCV005380038] | uncertain significance | 3 | 3845732 | 3845732 | Human | | name |
| 598251617 | CV3984975 | single nucleotide variant | NM_020873.7(LRRN1):c.1414C>G (p.Leu472Val) | not specified [RCV005366727] | uncertain significance | 3 | 3846055 | 3846055 | Human | | name |
| 598223369 | CV3984980 | single nucleotide variant | NM_020873.7(LRRN1):c.1343G>A (p.Arg448Gln) | not specified [RCV005380041] | uncertain significance | 3 | 3845984 | 3845984 | Human | | name |
| 598251642 | CV3984982 | single nucleotide variant | NM_020873.7(LRRN1):c.1858G>T (p.Ala620Ser) | not specified [RCV005366732] | uncertain significance | 3 | 3846499 | 3846499 | Human | | name |
| 598251648 | CV3984983 | single nucleotide variant | NM_020873.7(LRRN1):c.1720G>A (p.Val574Ile) | not specified [RCV005366733] | uncertain significance | 3 | 3846361 | 3846361 | Human | | name |
| 15156719 | CV708821 | single nucleotide variant | NM_020873.7(LRRN1):c.2104A>C (p.Thr702Pro) | not provided [RCV000969168] | benign | 3 | 3846745 | 3846745 | Human | | name |
| 15105347 | CV748223 | single nucleotide variant | NM_020873.7(LRRN1):c.2067A>T (p.Glu689Asp) | not provided [RCV000915527] | likely benign | 3 | 3846708 | 3846708 | Human | | name |
