ClinVar Miner

List of variants in gene BRIP1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 141
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HGVS dbSNP gnomAD frequency
NM_032043.3(BRIP1):c.627+271A>G rs36015135 0.02249
NM_032043.3(BRIP1):c.93+286T>C rs115322434 0.01623
NM_032043.3(BRIP1):c.*172G>C rs111898257 0.01099
NM_032043.3(BRIP1):c.2492+309G>T rs72842963 0.00942
NM_032043.3(BRIP1):c.2379+218G>A rs72842977 0.00941
NM_032043.3(BRIP1):c.205+162T>C rs191637671 0.00751
NM_032043.3(BRIP1):c.627+246C>A rs114365025 0.00720
NM_032043.3(BRIP1):c.1341-179A>G rs114198716 0.00594
NM_032043.3(BRIP1):c.206-21T>C rs2048717 0.00589
NM_032043.3(BRIP1):c.1141-94G>T rs114901675 0.00573
NM_032043.3(BRIP1):c.*3489T>C rs140891191 0.00554
NM_032043.3(BRIP1):c.1473+142T>C rs111842788 0.00532
NM_032043.3(BRIP1):c.2493-171C>T rs116794449 0.00523
NM_032043.3(BRIP1):c.-197C>A rs180948389 0.00518
NM_032043.3(BRIP1):c.-30-195C>G rs73332552 0.00403
NM_032043.3(BRIP1):c.-127C>T rs148498140 0.00393
NM_032043.3(BRIP1):c.517C>T (p.Arg173Cys) rs4988345 0.00363
NM_032043.3(BRIP1):c.*4040T>A rs111580456 0.00356
NM_032043.3(BRIP1):c.577G>A (p.Val193Ile) rs4988346 0.00305
NM_032043.3(BRIP1):c.2097+7G>A rs4988352 0.00271
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro) rs4988347 0.00197
NM_032043.3(BRIP1):c.2937A>G (p.Lys979=) rs75091137 0.00194
NM_032043.3(BRIP1):c.2286T>C (p.Arg762=) rs61754141 0.00173
NM_032043.3(BRIP1):c.890A>G (p.Lys297Arg) rs28997570 0.00113
NM_032043.3(BRIP1):c.790C>T (p.Arg264Trp) rs28997569 0.00104
NM_032043.3(BRIP1):c.918+15T>A rs117820198 0.00078
NM_032043.3(BRIP1):c.195A>G (p.Gln65=) rs141436143 0.00076
NM_032043.3(BRIP1):c.3459T>C (p.Asp1153=) rs4987050 0.00069
NM_032043.3(BRIP1):c.430G>A (p.Ala144Thr) rs116952709 0.00055
NM_032043.3(BRIP1):c.1935+11G>A rs79121306 0.00051
NM_032043.3(BRIP1):c.317G>A (p.Arg106His) rs143615668 0.00048
NM_032043.3(BRIP1):c.2220G>T (p.Gln740His) rs45589637 0.00041
NM_032043.3(BRIP1):c.380-17T>A rs200050729 0.00034
NM_032043.3(BRIP1):c.852C>T (p.Val284=) rs144940449 0.00021
NM_032043.3(BRIP1):c.36G>T (p.Gly12=) rs45566938 0.00019
NM_032043.3(BRIP1):c.628C>T (p.Pro210Ser) rs150313156 0.00019
NM_032043.3(BRIP1):c.1890A>G (p.Thr630=) rs145796331 0.00017
NM_032043.3(BRIP1):c.587A>G (p.Asn196Ser) rs550707862 0.00017
NM_032043.3(BRIP1):c.2440C>T (p.Arg814Cys) rs201869624 0.00016
NM_032043.3(BRIP1):c.-30-3T>C rs370728413 0.00014
NM_032043.3(BRIP1):c.595C>T (p.Leu199=) rs144969738 0.00014
NM_032043.3(BRIP1):c.1089C>T (p.Asp363=) rs139701369 0.00011
NM_032043.3(BRIP1):c.249A>G (p.Gln83=) rs45528833 0.00011
NM_032043.3(BRIP1):c.3444C>A (p.Asp1148Glu) rs28997573 0.00011
NM_032043.3(BRIP1):c.316C>T (p.Arg106Cys) rs587780247 0.00009
NM_032043.3(BRIP1):c.3336T>C (p.Asp1112=) rs369843642 0.00007
NM_032043.3(BRIP1):c.1053A>G (p.Pro351=) rs544977115 0.00006
NM_032043.3(BRIP1):c.1176A>G (p.Leu392=) rs550092661 0.00006
NM_032043.3(BRIP1):c.2232C>T (p.Asp744=) rs374362388 0.00006
NM_032043.3(BRIP1):c.2233G>A (p.Ala745Thr) rs587780235 0.00006
NM_032043.3(BRIP1):c.3103C>T (p.Arg1035Cys) rs45437094 0.00006
NM_032043.3(BRIP1):c.3567T>C (p.Asp1189=) rs764848326 0.00005
NM_032043.3(BRIP1):c.1443T>C (p.Gly481=) rs775431508 0.00004
NM_032043.3(BRIP1):c.1935+7T>C rs201024366 0.00004
NM_032043.3(BRIP1):c.297C>T (p.Asp99=) rs201617644 0.00004
NM_032043.3(BRIP1):c.3051G>A (p.Pro1017=) rs776990704 0.00004
NM_032043.3(BRIP1):c.69G>A (p.Pro23=) rs45458996 0.00004
NM_032043.3(BRIP1):c.3042T>C (p.Gly1014=) rs188258913 0.00003
NM_032043.3(BRIP1):c.312T>G (p.Thr104=) rs769190318 0.00003
NM_032043.3(BRIP1):c.672A>G (p.Gly224=) rs752356873 0.00003
NM_032043.3(BRIP1):c.702G>A (p.Lys234=) rs45512798 0.00003
NM_032043.3(BRIP1):c.1433A>G (p.His478Arg) rs45501097 0.00002
NM_032043.3(BRIP1):c.159C>T (p.Ser53=) rs779686432 0.00002
NM_032043.3(BRIP1):c.1644T>C (p.Tyr548=) rs372760869 0.00002
NM_032043.3(BRIP1):c.2406C>T (p.Asp802=) rs748981650 0.00002
NM_032043.3(BRIP1):c.736A>G (p.Ile246Val) rs376893571 0.00002
NM_032043.3(BRIP1):c.778A>G (p.Thr260Ala) rs138743097 0.00002
NM_032043.3(BRIP1):c.924A>G (p.Lys308=) rs374974885 0.00002
NM_032043.3(BRIP1):c.-30-7G>A rs758477620 0.00001
NM_032043.3(BRIP1):c.1074A>C (p.Leu358=) rs771682192 0.00001
NM_032043.3(BRIP1):c.1194C>T (p.Ile398=) rs757427498 0.00001
NM_032043.3(BRIP1):c.1455T>C (p.Ala485=) rs773489367 0.00001
NM_032043.3(BRIP1):c.1731G>A (p.Lys577=) rs587780829 0.00001
NM_032043.3(BRIP1):c.1752T>G (p.Thr584=) rs778774207 0.00001
NM_032043.3(BRIP1):c.2031A>T (p.Gly677=) rs1288620174 0.00001
NM_032043.3(BRIP1):c.2098-3T>C rs1057520463 0.00001
NM_032043.3(BRIP1):c.2257+17T>C rs730881639 0.00001
NM_032043.3(BRIP1):c.225C>T (p.Gly75=) rs186802750 0.00001
NM_032043.3(BRIP1):c.2304T>C (p.Gly768=) rs1603303843 0.00001
NM_032043.3(BRIP1):c.2419T>C (p.Leu807=) rs786201708 0.00001
NM_032043.3(BRIP1):c.2493-11A>G rs890923836 0.00001
NM_032043.3(BRIP1):c.2598G>A (p.Gln866=) rs769021796 0.00001
NM_032043.3(BRIP1):c.2820G>A (p.Lys940=) rs786201396 0.00001
NM_032043.3(BRIP1):c.3093T>C (p.Ser1031=) rs937490699 0.00001
NM_032043.3(BRIP1):c.3243C>T (p.Ala1081=) rs754003636 0.00001
NM_032043.3(BRIP1):c.3252T>C (p.Thr1084=) rs1555572745 0.00001
NM_032043.3(BRIP1):c.3354T>C (p.Asn1118=) rs757427210 0.00001
NM_032043.3(BRIP1):c.3681T>C (p.His1227=) rs370581038 0.00001
NM_032043.3(BRIP1):c.3717C>T (p.Ser1239=) rs758809865 0.00001
NM_032043.3(BRIP1):c.412T>C (p.Leu138=) rs786201292 0.00001
NM_032043.3(BRIP1):c.426A>G (p.Lys142=) rs768008017 0.00001
NM_032043.3(BRIP1):c.628-11C>G rs762672738 0.00001
NM_032043.3(BRIP1):c.684G>A (p.Glu228=) rs876659909 0.00001
NM_032043.3(BRIP1):c.732C>A (p.Pro244=) rs786202300 0.00001
NM_032043.3(BRIP1):c.750A>G (p.Thr250=) rs1057522393 0.00001
NM_032043.3(BRIP1):c.753C>T (p.Arg251=) rs876659416 0.00001
NM_032043.3(BRIP1):c.984C>T (p.Phe328=) rs745379285 0.00001
NM_032043.3(BRIP1):c.*2809_*2815dup
NM_032043.3(BRIP1):c.1008T>C (p.Asp336=) rs876660706
NM_032043.3(BRIP1):c.1170C>T (p.Val390=) rs754755989
NM_032043.3(BRIP1):c.1287T>C (p.Asn429=) rs863224431
NM_032043.3(BRIP1):c.1362A>G (p.Glu454=) rs786202553
NM_032043.3(BRIP1):c.1474-196_1474-194del rs140395804
NM_032043.3(BRIP1):c.1485T>G (p.Ser495=) rs370658123
NM_032043.3(BRIP1):c.1552G>A (p.Val518Ile) rs786201701
NM_032043.3(BRIP1):c.1566A>G (p.Ser522=) rs985465808
NM_032043.3(BRIP1):c.1629-295G>A rs147269748
NM_032043.3(BRIP1):c.1773T>C (p.Phe591=) rs1057523507
NM_032043.3(BRIP1):c.1795-12_1795-10del rs1475317357
NM_032043.3(BRIP1):c.1806T>C (p.Asp602=) rs878855142
NM_032043.3(BRIP1):c.186A>G (p.Ala62=) rs764252214
NM_032043.3(BRIP1):c.1983T>C (p.Cys661=) rs1603328829
NM_032043.3(BRIP1):c.2052C>T (p.Cys684=)
NM_032043.3(BRIP1):c.2154G>A (p.Glu718=) rs1057523978
NM_032043.3(BRIP1):c.2258-6dup rs1254598966
NM_032043.3(BRIP1):c.2379+3737A>C
NM_032043.3(BRIP1):c.2397A>G (p.Gln799=) rs1567755971
NM_032043.3(BRIP1):c.2400C>T (p.Tyr800=) rs574552037
NM_032043.3(BRIP1):c.2409C>T (p.His803=) rs762039913
NM_032043.3(BRIP1):c.2592A>G (p.Val864=) rs2061361778
NM_032043.3(BRIP1):c.2835A>G (p.Glu945=) rs786203633
NM_032043.3(BRIP1):c.288A>G (p.Thr96=) rs1278121295
NM_032043.3(BRIP1):c.3039T>A (p.Thr1013=) rs863224803
NM_032043.3(BRIP1):c.3039T>C (p.Thr1013=) rs863224803
NM_032043.3(BRIP1):c.3069C>G (p.Leu1023=) rs61754142
NM_032043.3(BRIP1):c.3087T>C (p.Ser1029=) rs1555572848
NM_032043.3(BRIP1):c.3117G>A (p.Glu1039=) rs769310105
NM_032043.3(BRIP1):c.33T>C (p.Gly11=) rs759187663
NM_032043.3(BRIP1):c.342A>G (p.Pro114=) rs756764576
NM_032043.3(BRIP1):c.380-28G>A rs4988343
NM_032043.3(BRIP1):c.432A>T (p.Ala144=) rs1342776835
NM_032043.3(BRIP1):c.507+9_507+10del rs747185394
NM_032043.3(BRIP1):c.576T>C (p.Thr192=) rs781282996
NM_032043.3(BRIP1):c.618G>A (p.Ser206=) rs367614726
NM_032043.3(BRIP1):c.618G>T (p.Ser206=) rs367614726
NM_032043.3(BRIP1):c.627+1284G>T
NM_032043.3(BRIP1):c.630C>T (p.Pro210=) rs864622510
NM_032043.3(BRIP1):c.690G>C (p.Ser230=) rs751460179
NM_032043.3(BRIP1):c.789C>G (p.Leu263=) rs1603346789
NM_032043.3(BRIP1):c.864A>G (p.Val288=) rs748545827
NM_032043.3(BRIP1):c.918C>T (p.Asn306=) rs876660724

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