ClinVar Miner

List of variants in gene BRIP1 reported as likely benign by University of Washington Department of Laboratory Medicine,University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_032043.2(BRIP1):c.1140+181A>G rs181682617
NM_032043.2(BRIP1):c.1140+721T>G rs760193728
NM_032043.2(BRIP1):c.1141-94G>T rs114901675
NM_032043.2(BRIP1):c.1340+426T>A rs145491062
NM_032043.2(BRIP1):c.1935+164T>G rs188084183
NM_032043.2(BRIP1):c.1936-429A>G rs869312538
NM_032043.2(BRIP1):c.1936-84C>A rs869312543
NM_032043.2(BRIP1):c.205+1013A>C rs140250366
NM_032043.2(BRIP1):c.2097+7948C>T rs567188409
NM_032043.2(BRIP1):c.2097+8116A>G rs868271534
NM_032043.2(BRIP1):c.2098-12300T>C rs148923786
NM_032043.2(BRIP1):c.2379+11656A>G rs113789760
NM_032043.2(BRIP1):c.2379+12823C>T rs114965923
NM_032043.2(BRIP1):c.2379+8266G>C rs869312537
NM_032043.2(BRIP1):c.2379+8422T>C rs869312531
NM_032043.2(BRIP1):c.2379+8473G>T rs869312532
NM_032043.2(BRIP1):c.2379+9531G>A rs869312534
NM_032043.2(BRIP1):c.2380-10318C>A rs869312540
NM_032043.2(BRIP1):c.2380-10425T>C rs116498010
NM_032043.2(BRIP1):c.2380-10657A>T rs192416342
NM_032043.2(BRIP1):c.2380-7505T>C rs371550316
NM_032043.2(BRIP1):c.2380-7638A>G rs17612238
NM_032043.2(BRIP1):c.2380-8850G>T rs114192527
NM_032043.2(BRIP1):c.2492+4475C>T rs138708470
NM_032043.2(BRIP1):c.2492+5316A>G rs745912247
NM_032043.2(BRIP1):c.2492+6009G>A rs869312536
NM_032043.2(BRIP1):c.2492+6114A>G rs762606772
NM_032043.2(BRIP1):c.2492+693G>T rs869312539
NM_032043.2(BRIP1):c.2493-163T>C rs192441895
NM_032043.2(BRIP1):c.507+584T>G rs530763001
NM_032043.2(BRIP1):c.508-175T>A rs573624932
NM_032043.2(BRIP1):c.508-407A>G rs544936287
NM_032043.2(BRIP1):c.627+12089T>A rs869312541
NM_032043.2(BRIP1):c.627+1905G>A rs116444001
NM_032043.2(BRIP1):c.627+2406A>G rs869312544
NM_032043.2(BRIP1):c.627+7958A>G rs145385282
NM_032043.2(BRIP1):c.627+8090C>A rs868675107
NM_032043.2(BRIP1):c.628-1085C>T rs869312535
NM_032043.2(BRIP1):c.628-1309G>A rs866215451
NM_032043.2(BRIP1):c.628-1326G>C rs869312545
NM_032043.2(BRIP1):c.628-14164G>A rs869312542
NM_032043.2(BRIP1):c.628-1855G>A rs183242889
NM_032043.2(BRIP1):c.628-3799T>A rs575725103
NM_032043.2(BRIP1):c.628-9955A>T rs187029209
NM_032043.2(BRIP1):c.689C>T (p.Ser230Leu) rs759031349
NM_032043.2(BRIP1):c.790C>T (p.Arg264Trp) rs28997569
NM_032043.2(BRIP1):c.918+15T>A rs117820198
NM_032043.2(BRIP1):c.918+2262A>G rs540914851
NM_032043.2(BRIP1):c.918+2479T>G rs573489745
NM_032043.2(BRIP1):c.918+42A>C rs766569933

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