ClinVar Miner

List of variants in gene VPS33B reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_018668.5(VPS33B):c.944G>A (p.Arg315Gln) rs145303578 0.00116
NM_018668.5(VPS33B):c.1148T>C (p.Ile383Thr) rs149121639 0.00114
NM_018668.5(VPS33B):c.1274G>A (p.Ser425Asn) rs139709507 0.00094
NM_018668.5(VPS33B):c.1714T>G (p.Phe572Val) rs145092724 0.00079
NM_018668.5(VPS33B):c.1170+4C>T rs201991604 0.00052
NM_018668.5(VPS33B):c.1362C>T (p.Ala454=) rs142964161 0.00049
NM_018668.5(VPS33B):c.1207T>C (p.Leu403=) rs139655526 0.00039
NM_018668.5(VPS33B):c.136A>T (p.Met46Leu) rs202141764 0.00029
NM_018668.5(VPS33B):c.1351A>G (p.Thr451Ala) rs148809175 0.00024
NM_018668.5(VPS33B):c.1658-7C>T rs375376103 0.00023
NM_018668.5(VPS33B):c.240-9C>T rs781107857 0.00023
NM_018668.5(VPS33B):c.133C>A (p.Leu45Ile) rs199874738 0.00021
NM_018668.5(VPS33B):c.1198A>G (p.Met400Val) rs149943529 0.00016
NM_018668.5(VPS33B):c.637G>A (p.Glu213Lys) rs951699405 0.00013
NM_018668.5(VPS33B):c.1015C>G (p.Arg339Gly) rs140237411 0.00010
NM_018668.5(VPS33B):c.1105+10G>A rs370555380 0.00010
NM_018668.5(VPS33B):c.499-3C>G rs201919090 0.00009
NM_018668.5(VPS33B):c.512G>A (p.Arg171His) rs748029830 0.00009
NM_018668.5(VPS33B):c.787G>A (p.Asp263Asn) rs749811246 0.00009
NM_018668.5(VPS33B):c.177+5T>A rs747146575 0.00008
NM_018668.5(VPS33B):c.1851C>T (p.Ala617=) rs145759754 0.00008
NM_018668.5(VPS33B):c.869G>A (p.Arg290Gln) rs767353387 0.00008
NM_018668.5(VPS33B):c.403G>A (p.Asp135Asn) rs369726600 0.00007
NM_018668.5(VPS33B):c.662G>A (p.Arg221Gln) rs377754864 0.00006
NM_018668.5(VPS33B):c.1749C>T (p.Ala583=) rs201436915 0.00005
NM_018668.5(VPS33B):c.299A>G (p.Asn100Ser) rs750764857 0.00005
NM_018668.5(VPS33B):c.1170+5G>A rs201431055 0.00004
NM_018668.5(VPS33B):c.1193G>A (p.Arg398His) rs762843831 0.00004
NM_018668.5(VPS33B):c.1780A>G (p.Arg594Gly) rs868354713 0.00004
NM_018668.5(VPS33B):c.565C>T (p.Pro189Ser) rs763334651 0.00004
NM_018668.5(VPS33B):c.941G>A (p.Arg314His) rs201698361 0.00004
NM_018668.5(VPS33B):c.122T>C (p.Ile41Thr) rs757313661 0.00003
NM_018668.5(VPS33B):c.1393G>A (p.Asp465Asn) rs756974736 0.00003
NM_018668.5(VPS33B):c.598G>A (p.Ala200Thr) rs142610315 0.00003
NM_018668.5(VPS33B):c.767G>A (p.Arg256His) rs375557658 0.00003
NM_018668.5(VPS33B):c.1014C>T (p.His338=) rs765002211 0.00002
NM_018668.5(VPS33B):c.1259C>T (p.Thr420Ile) rs963559069 0.00002
NM_018668.5(VPS33B):c.1534G>A (p.Val512Ile) rs768250541 0.00002
NM_018668.5(VPS33B):c.198A>G (p.Leu66=) rs1416595652 0.00002
NM_018668.5(VPS33B):c.766C>T (p.Arg256Cys) rs369458612 0.00002
NM_018668.5(VPS33B):c.978C>T (p.Phe326=) rs565539191 0.00002
NM_018668.5(VPS33B):c.1165C>T (p.Arg389Trp) rs778274271 0.00001
NM_018668.5(VPS33B):c.1192C>T (p.Arg398Cys) rs943813904 0.00001
NM_018668.5(VPS33B):c.1454G>A (p.Arg485His) rs141601851 0.00001
NM_018668.5(VPS33B):c.152G>A (p.Arg51Gln) rs376401320 0.00001
NM_018668.5(VPS33B):c.1685G>A (p.Ser562Asn) rs566630364 0.00001
NM_018668.5(VPS33B):c.434T>C (p.Leu145Ser) rs778351669 0.00001
NM_018668.5(VPS33B):c.456G>T (p.Leu152=) rs997425993 0.00001
NM_018668.5(VPS33B):c.646G>A (p.Gly216Ser) rs756881578 0.00001
NM_018668.5(VPS33B):c.75G>A (p.Gln25=) rs1289650070 0.00001
NM_018668.5(VPS33B):c.761C>G (p.Thr254Ser) rs144850957 0.00001
NM_018668.5(VPS33B):c.874G>A (p.Glu292Lys) rs150252392 0.00001
NM_018668.5(VPS33B):c.917G>A (p.Arg306Gln) rs200733204 0.00001
NM_018668.5(VPS33B):c.96+1G>T rs1567232168 0.00001
NM_018668.5(VPS33B):c.1015C>T (p.Arg339Cys)
NM_018668.5(VPS33B):c.1030C>A (p.His344Asn) rs368931670
NM_018668.5(VPS33B):c.1033A>T (p.Ile345Phe) rs1567221734
NM_018668.5(VPS33B):c.1129C>T (p.Arg377Trp)
NM_018668.5(VPS33B):c.1130G>A (p.Arg377Gln) rs864622006
NM_018668.5(VPS33B):c.1133A>G (p.Glu378Gly)
NM_018668.5(VPS33B):c.1144T>A (p.Tyr382Asn) rs1209255671
NM_018668.5(VPS33B):c.1157A>C (p.His386Pro) rs1567221376
NM_018668.5(VPS33B):c.1170+2T>C rs753008447
NM_018668.5(VPS33B):c.1201T>C (p.Cys401Arg)
NM_018668.5(VPS33B):c.1294C>A (p.Leu432Ile)
NM_018668.5(VPS33B):c.1368G>C (p.Glu456Asp)
NM_018668.5(VPS33B):c.1520G>A (p.Arg507Gln)
NM_018668.5(VPS33B):c.1529C>T (p.Ala510Val)
NM_018668.5(VPS33B):c.153A>G (p.Arg51=) rs538445830
NM_018668.5(VPS33B):c.1540G>C (p.Gly514Arg)
NM_018668.5(VPS33B):c.1559T>C (p.Leu520Pro)
NM_018668.5(VPS33B):c.1567C>G (p.Arg523Gly) rs751982861
NM_018668.5(VPS33B):c.1568G>A (p.Arg523Gln)
NM_018668.5(VPS33B):c.1588G>C (p.Glu530Gln) rs376948701
NM_018668.5(VPS33B):c.1595G>A (p.Arg532Gln)
NM_018668.5(VPS33B):c.161A>G (p.Asn54Ser)
NM_018668.5(VPS33B):c.1625G>A (p.Arg542Gln)
NM_018668.5(VPS33B):c.1654A>C (p.Thr552Pro)
NM_018668.5(VPS33B):c.1657+4T>G
NM_018668.5(VPS33B):c.1672G>C (p.Asp558His)
NM_018668.5(VPS33B):c.1685G>T (p.Ser562Ile) rs566630364
NM_018668.5(VPS33B):c.1754G>A (p.Arg585Gln)
NM_018668.5(VPS33B):c.177+3A>G rs2151684530
NM_018668.5(VPS33B):c.177G>C (p.Lys59Asn)
NM_018668.5(VPS33B):c.1796C>T (p.Thr599Met)
NM_018668.5(VPS33B):c.1840_1841delinsCT (p.Glu614Leu)
NM_018668.5(VPS33B):c.217C>A (p.Pro73Thr)
NM_018668.5(VPS33B):c.232A>G (p.Asn78Asp)
NM_018668.5(VPS33B):c.290G>A (p.Ser97Asn)
NM_018668.5(VPS33B):c.313G>T (p.Ala105Ser)
NM_018668.5(VPS33B):c.320G>A (p.Arg107Gln)
NM_018668.5(VPS33B):c.346A>G (p.Ser116Gly)
NM_018668.5(VPS33B):c.365C>T (p.Ala122Val)
NM_018668.5(VPS33B):c.39T>A (p.Pro13=) rs1567232246
NM_018668.5(VPS33B):c.403+3G>A
NM_018668.5(VPS33B):c.50T>A (p.Met17Lys) rs1555461182
NM_018668.5(VPS33B):c.544C>G (p.Leu182Val) rs2040647887
NM_018668.5(VPS33B):c.571C>T (p.Pro191Ser)
NM_018668.5(VPS33B):c.590G>A (p.Gly197Asp)
NM_018668.5(VPS33B):c.5C>T (p.Ala2Val)
NM_018668.5(VPS33B):c.604-3C>A rs1166642596
NM_018668.5(VPS33B):c.638A>T (p.Glu213Val)
NM_018668.5(VPS33B):c.658G>C (p.Gly220Arg) rs2151671309
NM_018668.5(VPS33B):c.680A>C (p.His227Pro)
NM_018668.5(VPS33B):c.697A>G (p.Arg233Gly)
NM_018668.5(VPS33B):c.701-8_701-5delinsGA rs1555459036
NM_018668.5(VPS33B):c.800A>T (p.Glu267Val)
NM_018668.5(VPS33B):c.96+18_96+19delinsAT
NM_018668.5(VPS33B):c.966G>A (p.Gln322=) rs201383365
NM_018668.5(VPS33B):c.983C>T (p.Ser328Phe)

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