ClinVar Miner

List of variants in gene BRIP1 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_032043.3(BRIP1):c.*3489T>C rs140891191 0.00554
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.*128A>G rs150444311 0.00277
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.*2337A>T rs373664066 0.00093
NM_032043.3(BRIP1):c.*3188G>A rs369850537 0.00090
NM_032043.3(BRIP1):c.*132G>A rs143361598 0.00089
NM_032043.3(BRIP1):c.3459T>C (p.Asp1153=) rs4987050 0.00069
NM_032043.3(BRIP1):c.*2070G>A rs764258526 0.00056
NM_032043.3(BRIP1):c.*2667C>T rs373156872 0.00053
NM_032043.3(BRIP1):c.2220G>T (p.Gln740His) rs45589637 0.00041
NM_032043.3(BRIP1):c.*380C>T rs556729826 0.00034
NM_032043.3(BRIP1):c.1735C>T (p.Arg579Cys) rs28997571 0.00034
NM_032043.3(BRIP1):c.-237dup rs112243287 0.00029
NM_032043.3(BRIP1):c.*1868G>T rs184666432 0.00028
NM_032043.3(BRIP1):c.1255C>T (p.Arg419Trp) rs150624408 0.00026
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala) rs28903098 0.00024
NM_032043.3(BRIP1):c.*3465A>T rs539412199 0.00023
NM_032043.3(BRIP1):c.*2812A>G rs112375062 0.00020
NM_032043.3(BRIP1):c.36G>T (p.Gly12=) rs45566938 0.00019
NM_032043.3(BRIP1):c.*3827T>C rs1377513104 0.00015
NM_032043.3(BRIP1):c.-30-3T>C rs370728413 0.00014
NM_032043.3(BRIP1):c.*2656A>G rs1052477488 0.00012
NM_032043.3(BRIP1):c.*4053T>C rs191840743 0.00012
NM_032043.3(BRIP1):c.*1792G>A rs746869920 0.00009
NM_032043.3(BRIP1):c.316C>T (p.Arg106Cys) rs587780247 0.00009
NM_032043.3(BRIP1):c.93+15G>A rs113052745 0.00009
NM_032043.3(BRIP1):c.*477A>G rs1030551071 0.00007
NM_032043.3(BRIP1):c.1629-11T>C rs375710640 0.00007
NM_032043.3(BRIP1):c.1140+11G>A rs369153270 0.00006
NM_032043.3(BRIP1):c.3103C>T (p.Arg1035Cys) rs45437094 0.00006
NM_032043.3(BRIP1):c.*2692A>G rs886053204 0.00005
NM_032043.3(BRIP1):c.*659G>A rs769375960 0.00005
NM_032043.3(BRIP1):c.3567T>C (p.Asp1189=) rs764848326 0.00005
NM_032043.3(BRIP1):c.*524A>G rs371689236 0.00004
NM_032043.3(BRIP1):c.1000G>A (p.Ala334Thr) rs535414791 0.00004
NM_032043.3(BRIP1):c.415T>G (p.Ser139Ala) rs202072866 0.00004
NM_032043.2(BRIP1):c.-307G>A rs936277521 0.00003
NM_032043.3(BRIP1):c.*1393G>T rs754698039 0.00003
NM_032043.3(BRIP1):c.*2668G>A rs886053206 0.00003
NM_032043.3(BRIP1):c.*2691C>G rs886053205 0.00003
NM_032043.3(BRIP1):c.*2999T>C rs1357312726 0.00003
NM_032043.3(BRIP1):c.*3635T>C rs548812634 0.00003
NM_032043.3(BRIP1):c.*3924T>G rs886053195 0.00003
NM_032043.3(BRIP1):c.*900C>A rs886053210 0.00003
NM_032043.3(BRIP1):c.-229C>G rs886053217 0.00003
NM_032043.3(BRIP1):c.2285G>A (p.Arg762His) rs200960251 0.00003
NM_032043.3(BRIP1):c.2830C>G (p.Gln944Glu) rs140233356 0.00003
NM_032043.3(BRIP1):c.2854A>G (p.Ile952Val) rs200239986 0.00003
NM_032043.3(BRIP1):c.*1330C>T rs933049932 0.00002
NM_032043.3(BRIP1):c.*3000C>G rs1373033399 0.00002
NM_032043.3(BRIP1):c.*3307T>C rs886053199 0.00002
NM_032043.3(BRIP1):c.736A>G (p.Ile246Val) rs376893571 0.00002
NM_032043.3(BRIP1):c.820A>G (p.Thr274Ala) rs62620988 0.00002
NM_032043.3(BRIP1):c.*1239C>A rs1042958451 0.00001
NM_032043.3(BRIP1):c.*1908T>C rs1264916802 0.00001
NM_032043.3(BRIP1):c.*2522A>G rs886053207 0.00001
NM_032043.3(BRIP1):c.*339G>C rs886053212 0.00001
NM_032043.3(BRIP1):c.*3580T>A rs372023591 0.00001
NM_032043.3(BRIP1):c.*3617T>C rs886053198 0.00001
NM_032043.3(BRIP1):c.1018C>T (p.Leu340Phe) rs755796609 0.00001
NM_032043.3(BRIP1):c.1109A>G (p.Asn370Ser) rs777511615 0.00001
NM_032043.3(BRIP1):c.1442G>A (p.Gly481Asp) rs200062099 0.00001
NM_032043.3(BRIP1):c.1474-3T>C rs552752779 0.00001
NM_032043.3(BRIP1):c.1641T>G (p.Asp547Glu) rs754414731 0.00001
NM_032043.3(BRIP1):c.2594G>A (p.Arg865Gln) rs781609846 0.00001
NM_032043.3(BRIP1):c.2776G>A (p.Ala926Thr) rs1003917080 0.00001
NM_032043.3(BRIP1):c.2801T>C (p.Phe934Ser) rs778916092 0.00001
NM_032043.3(BRIP1):c.2811T>C (p.Asp937=) rs374335608 0.00001
NM_032043.3(BRIP1):c.3093T>C (p.Ser1031=) rs937490699 0.00001
NM_032043.3(BRIP1):c.612C>G (p.Ser204=) rs587780832 0.00001
NM_032043.3(BRIP1):c.*1048_*1050del rs564290244
NM_032043.3(BRIP1):c.*1255AG[1] rs886053209
NM_032043.3(BRIP1):c.*1381G>T rs886053208
NM_032043.3(BRIP1):c.*1409T>A rs554933640
NM_032043.3(BRIP1):c.*1801T>G rs1479468180
NM_032043.3(BRIP1):c.*1930G>C rs2061267341
NM_032043.3(BRIP1):c.*2672G>A rs924486012
NM_032043.3(BRIP1):c.*2715C>T rs886053203
NM_032043.3(BRIP1):c.*2744A>G rs1311178838
NM_032043.3(BRIP1):c.*2756G>A rs182264505
NM_032043.3(BRIP1):c.*2811_*2815dup rs768910110
NM_032043.3(BRIP1):c.*2812_*2815dup rs768910110
NM_032043.3(BRIP1):c.*2813_*2815A[4]GAAA[1] rs1555571892
NM_032043.3(BRIP1):c.*2813_*2815A[5]GAAA[1] rs1555571892
NM_032043.3(BRIP1):c.*2813_*2815A[6]GAAA[1] rs1555571892
NM_032043.3(BRIP1):c.*2817_*2818insGAAAGA rs886053202
NM_032043.3(BRIP1):c.*2819_*2820insAAAA rs551338531
NM_032043.3(BRIP1):c.*2819_*2820insAAAAAA rs551338531
NM_032043.3(BRIP1):c.*2819_*2820insAAAAAAA rs551338531
NM_032043.3(BRIP1):c.*2868A>G rs1044791743
NM_032043.3(BRIP1):c.*288A>G rs886053213
NM_032043.3(BRIP1):c.*2926T>A rs886053201
NM_032043.3(BRIP1):c.*3093A>T rs944576811
NM_032043.3(BRIP1):c.*3145A>G rs886053200
NM_032043.3(BRIP1):c.*3821A>G rs886053197
NM_032043.3(BRIP1):c.*3918C>T rs886053196
NM_032043.3(BRIP1):c.*394CT[1] rs546666211
NM_032043.3(BRIP1):c.*421C>T rs886053211
NM_032043.3(BRIP1):c.*612A>G rs2061285626
NM_032043.3(BRIP1):c.*684C>A rs2061284724
NM_032043.3(BRIP1):c.-232G>A rs2078998991
NM_032043.3(BRIP1):c.-38C>T rs371225829
NM_032043.3(BRIP1):c.1652C>T (p.Ala551Val) rs375246789
NM_032043.3(BRIP1):c.1774T>G (p.Trp592Gly) rs587780231
NM_032043.3(BRIP1):c.1935+5GTT[2] rs730881641
NM_032043.3(BRIP1):c.2301G>C (p.Glu767Asp) rs369434185
NM_032043.3(BRIP1):c.2741T>C (p.Leu914Ser) rs886053215
NM_032043.3(BRIP1):c.2829C>A (p.Val943=) rs767164240
NM_032043.3(BRIP1):c.3020C>A (p.Ser1007Tyr) rs886053214
NM_032043.3(BRIP1):c.3203C>T (p.Pro1068Leu) rs2061316462
NM_032043.3(BRIP1):c.3240dup (p.Ala1081fs) rs779741278
NM_032043.3(BRIP1):c.3251C>G (p.Thr1084Ser) rs876660768
NM_032043.3(BRIP1):c.3390_3393del (p.Tyr1131fs) rs778664039
NM_032043.3(BRIP1):c.54T>C (p.Pro18=) rs886053216
NM_032043.3(BRIP1):c.82A>G (p.Met28Val) rs1330147176

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