ClinVar Miner

List of variants reported as uncertain significance for BBS9-related ciliopathy by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 169
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HGVS dbSNP gnomAD frequency
NM_198428.3(BBS9):c.2294A>G (p.Glu765Gly) rs140882212 0.00037
NM_198428.3(BBS9):c.1559C>T (p.Pro520Leu) rs769669385 0.00019
NM_198428.3(BBS9):c.736C>T (p.Leu246Phe) rs140821420 0.00018
NM_198428.3(BBS9):c.1760G>A (p.Arg587Gln) rs149042169 0.00014
NM_198428.3(BBS9):c.2309A>G (p.Glu770Gly) rs149668719 0.00013
NM_198428.3(BBS9):c.1112T>C (p.Val371Ala) rs138436479 0.00012
NM_198428.3(BBS9):c.1487C>T (p.Thr496Ile) rs139303948 0.00011
NM_198428.3(BBS9):c.2403A>G (p.Ile801Met) rs137993290 0.00011
NM_198428.3(BBS9):c.862A>G (p.Ser288Gly) rs146770174 0.00011
NM_198428.3(BBS9):c.928A>G (p.Asn310Asp) rs369647403 0.00011
NM_198428.3(BBS9):c.436G>A (p.Val146Ile) rs372412756 0.00010
NM_198428.3(BBS9):c.1610C>T (p.Pro537Leu) rs1486252113 0.00009
NM_198428.3(BBS9):c.2509A>G (p.Met837Val) rs771310981 0.00008
NM_198428.3(BBS9):c.1768G>A (p.Val590Ile) rs143016114 0.00007
NM_198428.3(BBS9):c.2033G>A (p.Arg678His) rs200654248 0.00007
NM_198428.3(BBS9):c.138G>A (p.Met46Ile) rs145241295 0.00006
NM_198428.3(BBS9):c.833G>A (p.Arg278Gln) rs754343745 0.00006
NM_198428.3(BBS9):c.2358G>C (p.Lys786Asn) rs377403564 0.00005
NM_198428.3(BBS9):c.2449G>A (p.Asp817Asn) rs781476538 0.00005
NM_198428.3(BBS9):c.663G>T (p.Glu221Asp) rs767766656 0.00005
NM_198428.3(BBS9):c.1199G>A (p.Gly400Asp) rs1312526837 0.00004
NM_198428.3(BBS9):c.1293G>C (p.Glu431Asp) rs767170924 0.00004
NM_198428.3(BBS9):c.1322C>T (p.Thr441Met) rs140675013 0.00004
NM_198428.3(BBS9):c.1468T>C (p.Tyr490His) rs760084192 0.00004
NM_198428.3(BBS9):c.2020C>T (p.Arg674Trp) rs368526968 0.00004
NM_198428.3(BBS9):c.2632G>T (p.Glu878Ter) rs150826095 0.00004
NM_198428.3(BBS9):c.559A>G (p.Ser187Gly) rs771447042 0.00004
NM_198428.3(BBS9):c.58T>G (p.Phe20Val) rs779638896 0.00004
NM_198428.3(BBS9):c.1264G>T (p.Asp422Tyr) rs140198337 0.00003
NM_198428.3(BBS9):c.1480A>T (p.Ser494Cys) rs765846163 0.00003
NM_198428.3(BBS9):c.1486A>G (p.Thr496Ala) rs369146555 0.00003
NM_198428.3(BBS9):c.1741C>T (p.His581Tyr) rs537110423 0.00003
NM_198428.3(BBS9):c.1801A>G (p.Ile601Val) rs377588119 0.00003
NM_198428.3(BBS9):c.2174C>T (p.Thr725Ile) rs749948775 0.00003
NM_198428.3(BBS9):c.2273C>T (p.Pro758Leu) rs757754301 0.00003
NM_198428.3(BBS9):c.2312C>T (p.Thr771Met) rs370662412 0.00003
NM_198428.3(BBS9):c.2434A>T (p.Ile812Phe) rs779871496 0.00003
NM_198428.3(BBS9):c.2488G>A (p.Asp830Asn) rs368704638 0.00003
NM_198428.3(BBS9):c.2605C>T (p.His869Tyr) rs938197989 0.00003
NM_198428.3(BBS9):c.2657C>T (p.Ser886Leu) rs779169794 0.00003
NM_198428.3(BBS9):c.566G>A (p.Arg189His) rs547643751 0.00003
NM_198428.3(BBS9):c.702+6G>A rs777329822 0.00003
NM_198428.3(BBS9):c.1431G>A (p.Met477Ile) rs1443035026 0.00002
NM_198428.3(BBS9):c.1798C>T (p.Arg600Cys) rs775703296 0.00002
NM_198428.3(BBS9):c.1966C>T (p.Arg656Trp) rs762045410 0.00002
NM_198428.3(BBS9):c.2044G>A (p.Ala682Thr) rs772347593 0.00002
NM_198428.3(BBS9):c.2059A>G (p.Lys687Glu) rs760800602 0.00002
NM_198428.3(BBS9):c.2468G>A (p.Gly823Asp) rs1176589347 0.00002
NM_198428.3(BBS9):c.2653G>T (p.Val885Phe) rs950624105 0.00002
NM_198428.3(BBS9):c.335T>C (p.Leu112Ser) rs904098347 0.00002
NM_198428.3(BBS9):c.529G>T (p.Gly177Cys) rs750278720 0.00002
NM_198428.3(BBS9):c.818A>G (p.Asp273Gly) rs1264926096 0.00002
NM_198428.3(BBS9):c.1033A>G (p.Ile345Val) rs1426530664 0.00001
NM_198428.3(BBS9):c.1111G>A (p.Val371Ile) rs1366355966 0.00001
NM_198428.3(BBS9):c.1147G>A (p.Val383Ile) rs1030973947 0.00001
NM_198428.3(BBS9):c.1183G>A (p.Val395Ile) rs1300725879 0.00001
NM_198428.3(BBS9):c.122T>G (p.Ile41Ser) rs1381039813 0.00001
NM_198428.3(BBS9):c.1323G>A (p.Thr441=) rs1044033927 0.00001
NM_198428.3(BBS9):c.1329+5T>C rs200033003 0.00001
NM_198428.3(BBS9):c.1330-10G>T rs779072984 0.00001
NM_198428.3(BBS9):c.1352T>C (p.Ile451Thr) rs773192233 0.00001
NM_198428.3(BBS9):c.1379A>G (p.Tyr460Cys) rs377149733 0.00001
NM_198428.3(BBS9):c.1481G>A (p.Ser494Asn) rs775868685 0.00001
NM_198428.3(BBS9):c.1537+14C>T rs754694089 0.00001
NM_198428.3(BBS9):c.1538-7T>G rs375661214 0.00001
NM_198428.3(BBS9):c.1836A>G (p.Ile612Met) rs752845007 0.00001
NM_198428.3(BBS9):c.1844A>G (p.Glu615Gly) rs370925964 0.00001
NM_198428.3(BBS9):c.1855C>T (p.Arg619Cys) rs543113169 0.00001
NM_198428.3(BBS9):c.1897G>A (p.Ala633Thr) rs778505224 0.00001
NM_198428.3(BBS9):c.1911G>A (p.Ser637=) rs138454676 0.00001
NM_198428.3(BBS9):c.1928A>G (p.Gln643Arg) rs1048014676 0.00001
NM_198428.3(BBS9):c.2032C>T (p.Arg678Cys) rs746543061 0.00001
NM_198428.3(BBS9):c.2036G>A (p.Arg679Gln) rs768958916 0.00001
NM_198428.3(BBS9):c.2134G>A (p.Ala712Thr) rs751173437 0.00001
NM_198428.3(BBS9):c.2294_2296del (p.Glu765_Leu766delinsVal) rs752782918 0.00001
NM_198428.3(BBS9):c.2365A>G (p.Lys789Glu) rs1402083567 0.00001
NM_198428.3(BBS9):c.2381A>G (p.Asn794Ser) rs774701632 0.00001
NM_198428.3(BBS9):c.2533A>G (p.Thr845Ala) rs545725547 0.00001
NM_198428.3(BBS9):c.2566G>T (p.Val856Leu) rs764122627 0.00001
NM_198428.3(BBS9):c.2623C>T (p.Pro875Ser) rs755911247 0.00001
NM_198428.3(BBS9):c.263C>T (p.Ser88Leu) rs749974697 0.00001
NM_198428.3(BBS9):c.349C>T (p.His117Tyr) rs780063415 0.00001
NM_198428.3(BBS9):c.397A>G (p.Arg133Gly) rs759120113 0.00001
NM_198428.3(BBS9):c.469A>G (p.Met157Val) rs148763093 0.00001
NM_198428.3(BBS9):c.761A>G (p.Asn254Ser) rs1279852557 0.00001
NM_198428.3(BBS9):c.894A>C (p.Glu298Asp) rs757469936 0.00001
NM_198428.3(BBS9):c.929A>T (p.Asn310Ile) rs1341125124 0.00001
NM_198428.3(BBS9):c.938A>G (p.His313Arg) rs533714503 0.00001
NM_198428.3(BBS9):c.940A>G (p.Ile314Val) rs372698195 0.00001
NM_198428.3(BBS9):c.979C>T (p.Pro327Ser) rs760272596 0.00001
NM_198428.3(BBS9):c.1065G>T (p.Gln355His)
NM_198428.3(BBS9):c.1133A>G (p.Tyr378Cys)
NM_198428.3(BBS9):c.11T>A (p.Phe4Tyr) rs746345067
NM_198428.3(BBS9):c.1245C>A (p.Val415=) rs61764066
NM_198428.3(BBS9):c.1249G>T (p.Val417Phe) rs751604593
NM_198428.3(BBS9):c.1255C>G (p.Pro419Ala)
NM_198428.3(BBS9):c.1279G>T (p.Ala427Ser)
NM_198428.3(BBS9):c.1285G>A (p.Asp429Asn)
NM_198428.3(BBS9):c.128G>A (p.Gly43Asp)
NM_198428.3(BBS9):c.1307T>C (p.Leu436Pro)
NM_198428.3(BBS9):c.1344C>G (p.Asn448Lys)
NM_198428.3(BBS9):c.1370T>C (p.Leu457Ser) rs762511626
NM_198428.3(BBS9):c.1391C>T (p.Pro464Leu)
NM_198428.3(BBS9):c.1472T>G (p.Leu491Arg)
NM_198428.3(BBS9):c.1489C>A (p.Pro497Thr)
NM_198428.3(BBS9):c.1525T>G (p.Ser509Ala)
NM_198428.3(BBS9):c.1537+3A>G
NM_198428.3(BBS9):c.1552+5G>T rs1818927271
NM_198428.3(BBS9):c.1646C>G (p.Thr549Ser) rs59252892
NM_198428.3(BBS9):c.1658A>C (p.Asn553Thr)
NM_198428.3(BBS9):c.1668A>G (p.Pro556=)
NM_198428.3(BBS9):c.1673G>A (p.Ser558Asn)
NM_198428.3(BBS9):c.1679T>C (p.Leu560Pro)
NM_198428.3(BBS9):c.1759C>G (p.Arg587Gly)
NM_198428.3(BBS9):c.176C>T (p.Thr59Ile)
NM_198428.3(BBS9):c.1799G>A (p.Arg600His) rs749018243
NM_198428.3(BBS9):c.1805A>G (p.Gln602Arg)
NM_198428.3(BBS9):c.187G>A (p.Ala63Thr)
NM_198428.3(BBS9):c.1967G>A (p.Arg656Gln)
NM_198428.3(BBS9):c.1987GAA[1] (p.Glu664del)
NM_198428.3(BBS9):c.19C>A (p.Arg7Ser) rs184994140
NM_198428.3(BBS9):c.19C>T (p.Arg7Cys) rs184994140
NM_198428.3(BBS9):c.2055A>T (p.Lys685Asn)
NM_198428.3(BBS9):c.2080C>T (p.His694Tyr) rs2128756856
NM_198428.3(BBS9):c.2098G>A (p.Asp700Asn) rs1274816953
NM_198428.3(BBS9):c.20G>A (p.Arg7His) rs746340993
NM_198428.3(BBS9):c.20G>T (p.Arg7Leu) rs746340993
NM_198428.3(BBS9):c.2101G>A (p.Gly701Arg) rs2536370644
NM_198428.3(BBS9):c.2116-10A>G
NM_198428.3(BBS9):c.2120T>C (p.Ile707Thr) rs2537394608
NM_198428.3(BBS9):c.2128G>A (p.Ala710Thr)
NM_198428.3(BBS9):c.214G>A (p.Val72Met) rs765240871
NM_198428.3(BBS9):c.2150A>G (p.Gln717Arg)
NM_198428.3(BBS9):c.2186G>A (p.Ser729Asn) rs1393453305
NM_198428.3(BBS9):c.2217G>T (p.Ala739=) rs749322793
NM_198428.3(BBS9):c.2245G>T (p.Val749Phe)
NM_198428.3(BBS9):c.2305G>A (p.Glu769Lys)
NM_198428.3(BBS9):c.2318A>C (p.Asp773Ala)
NM_198428.3(BBS9):c.2340G>C (p.Leu780Phe)
NM_198428.3(BBS9):c.2344A>G (p.Thr782Ala)
NM_198428.3(BBS9):c.2374G>T (p.Ala792Ser)
NM_198428.3(BBS9):c.2438C>T (p.Thr813Ile)
NM_198428.3(BBS9):c.2453G>C (p.Arg818Thr)
NM_198428.3(BBS9):c.2464G>C (p.Gly822Arg)
NM_198428.3(BBS9):c.2477G>A (p.Cys826Tyr)
NM_198428.3(BBS9):c.2518C>G (p.Pro840Ala)
NM_198428.3(BBS9):c.2522-3T>C rs750216247
NM_198428.3(BBS9):c.2530A>G (p.Thr844Ala)
NM_198428.3(BBS9):c.2595_2598delinsGTTGGTAAA (p.Asn866fs)
NM_198428.3(BBS9):c.2633-2A>G rs1864417554
NM_198428.3(BBS9):c.2642C>A (p.Pro881His)
NM_198428.3(BBS9):c.2659G>A (p.Glu887Lys)
NM_198428.3(BBS9):c.327A>G (p.Ser109=)
NM_198428.3(BBS9):c.328+20A>G rs761676028
NM_198428.3(BBS9):c.396G>C (p.Gln132His) rs10255104
NM_198428.3(BBS9):c.467C>A (p.Ser156Tyr)
NM_198428.3(BBS9):c.541C>T (p.Pro181Ser)
NM_198428.3(BBS9):c.563C>T (p.Ser188Phe) rs2128312652
NM_198428.3(BBS9):c.580C>T (p.Leu194Phe) rs1797251379
NM_198428.3(BBS9):c.620A>T (p.Tyr207Phe)
NM_198428.3(BBS9):c.660_677delinsAAC (p.Glu221_Lys226delinsThr)
NM_198428.3(BBS9):c.672G>C (p.Gln224His)
NM_198428.3(BBS9):c.682G>C (p.Gly228Arg)
NM_198428.3(BBS9):c.688G>A (p.Gly230Arg) rs1798450904
NM_198428.3(BBS9):c.694A>G (p.Arg232Gly)
NM_198428.3(BBS9):c.700G>A (p.Val234Ile)
NM_198428.3(BBS9):c.748A>G (p.Ile250Val)
NM_198428.3(BBS9):c.898A>T (p.Thr300Ser)
NM_198428.3(BBS9):c.955A>G (p.Thr319Ala)

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