ClinVar Miner

List of variants in gene BRIP1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP gnomAD frequency
NM_032043.3(BRIP1):c.1474-314C>T rs8078977 0.78407
NM_032043.3(BRIP1):c.1795-47G>C rs4988351 0.77857
NM_032043.3(BRIP1):c.2379+204G>T rs12937232 0.77268
NM_032043.3(BRIP1):c.2637A>G (p.Glu879=) rs4986765 0.74166
NM_032043.3(BRIP1):c.2379+306C>T rs9904294 0.72533
NM_032043.3(BRIP1):c.2755T>C (p.Ser919Pro) rs4986764 0.61453
NM_032043.3(BRIP1):c.*483C>T rs7213430 0.61289
NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=) rs4986763 0.60694
NM_032043.3(BRIP1):c.-205G>A rs2048718 0.42481
NM_032043.3(BRIP1):c.508-281A>G rs9908659 0.40613
NM_032043.3(BRIP1):c.2905+83T>A rs4988357 0.33913
NM_032043.3(BRIP1):c.2906-205T>C rs11871785 0.33884
NM_032043.3(BRIP1):c.1340+109G>A rs2191248 0.25912
NM_032043.3(BRIP1):c.-31+12G>A rs4988340 0.23980
NM_032043.3(BRIP1):c.206-270T>C rs72843735 0.16721
NM_032043.3(BRIP1):c.206-287C>G rs4968452 0.15338
NM_032043.3(BRIP1):c.508-31C>G rs4988344 0.15259
NM_032043.3(BRIP1):c.1474-297C>T rs72842992 0.11933
NM_032043.3(BRIP1):c.93+72T>G rs4988342 0.07661
NM_032043.3(BRIP1):c.-30-71C>T rs7226248 0.07556
NM_032043.3(BRIP1):c.-30-88C>T rs76477362 0.07549
NM_032043.3(BRIP1):c.628-192A>G rs16945638 0.06239
NM_032043.3(BRIP1):c.2098-84C>T rs9892156 0.03663
NM_032043.3(BRIP1):c.2379+230C>G rs76111733 0.03569
NM_032043.3(BRIP1):c.507+67T>C rs73991950 0.03383
NM_032043.3(BRIP1):c.94-18T>G rs2138005 0.03086
NM_032043.3(BRIP1):c.1141-237C>T rs115556864 0.01711
NM_032043.3(BRIP1):c.2098-22T>C rs114505031 0.00684
NM_032043.3(BRIP1):c.1936-44C>A rs139659736 0.00526
NM_032043.3(BRIP1):c.2236A>G (p.Ile746Val) rs111536363 0.00480
NM_032043.3(BRIP1):c.517C>T (p.Arg173Cys) rs4988345 0.00363
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.2061G>C (p.Val687=) rs112414873 0.00153
NM_032043.3(BRIP1):c.2257+19A>C rs77851913 0.00079
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.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.-30-3T>C rs370728413 0.00014
NM_032043.3(BRIP1):c.3099T>C (p.Pro1033=) rs202228407 0.00013
NM_032043.3(BRIP1):c.3069C>T (p.Leu1023=) rs61754142 0.00012
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.93+15G>A rs113052745 0.00009
NM_032043.3(BRIP1):c.1629-11T>C rs375710640 0.00007
NM_032043.3(BRIP1):c.3336T>C (p.Asp1112=) rs369843642 0.00007
NM_032043.3(BRIP1):c.1356C>T (p.Asn452=) rs730881640 0.00006
NM_032043.3(BRIP1):c.1629-3T>C rs587780828 0.00006
NM_032043.3(BRIP1):c.2232C>T (p.Asp744=) rs374362388 0.00006
NM_032043.3(BRIP1):c.-5G>A rs754270436 0.00004
NM_032043.3(BRIP1):c.1626C>T (p.Ser542=) rs373709958 0.00004
NM_032043.3(BRIP1):c.1935+7T>C rs201024366 0.00004
NM_032043.3(BRIP1):c.-30-9C>T rs537183380 0.00003
NM_032043.3(BRIP1):c.1257G>A (p.Arg419=) rs148429663 0.00003
NM_032043.3(BRIP1):c.2100A>G (p.Leu700=) rs766047812 0.00003
NM_032043.3(BRIP1):c.3042T>C (p.Gly1014=) rs188258913 0.00003
NM_032043.3(BRIP1):c.702G>A (p.Lys234=) rs45512798 0.00003
NM_032043.3(BRIP1):c.-31+3A>G rs930831946 0.00002
NM_032043.3(BRIP1):c.1433A>G (p.His478Arg) rs45501097 0.00002
NM_032043.2(BRIP1):c.2097+8A>C rs730881642 0.00001
NM_032043.3(BRIP1):c.-41C>T rs1431387778 0.00001
NM_032043.3(BRIP1):c.1071A>G (p.Glu357=) rs761017296 0.00001
NM_032043.3(BRIP1):c.1455T>C (p.Ala485=) rs773489367 0.00001
NM_032043.3(BRIP1):c.1473+6A>G rs587780827 0.00001
NM_032043.3(BRIP1):c.1474-3T>C rs552752779 0.00001
NM_032043.3(BRIP1):c.2257+17T>C rs730881639 0.00001
NM_032043.3(BRIP1):c.2310T>C (p.Asp770=) rs148752066 0.00001
NC_000017.11:g.61863673dup rs3840867
NM_032043.3(BRIP1):c.*158T>C rs1978111
NM_032043.3(BRIP1):c.-38C>G rs371225829
NM_032043.3(BRIP1):c.-38C>T rs371225829
NM_032043.3(BRIP1):c.1140+198C>G rs62068834
NM_032043.3(BRIP1):c.1140+84dup rs11390869
NM_032043.3(BRIP1):c.1140+92_1140+93insT rs2077983610
NM_032043.3(BRIP1):c.1141-126_1141-125del rs5821340
NM_032043.3(BRIP1):c.1383T>C (p.Tyr461=) rs587780875
NM_032043.3(BRIP1):c.1628+5G>A rs754929230
NM_032043.3(BRIP1):c.1935+5GTT[2] rs730881641
NM_032043.3(BRIP1):c.2492+80A>G rs9901948
NM_032043.3(BRIP1):c.2576-8T>C rs587780874
NM_032043.3(BRIP1):c.2755T>A (p.Ser919Thr) rs4986764
NM_032043.3(BRIP1):c.380-17dup rs545021924
NM_032043.3(BRIP1):c.380-226dup rs141367697
NM_032043.3(BRIP1):c.380-28G>A rs4988343
NM_032043.3(BRIP1):c.508-8G>A rs202074040

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