ClinVar Miner

List of variants in gene BRIP1 reported as likely pathogenic for Hereditary cancer-predisposing syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
Download table as spreadsheet
HGVS dbSNP
NM_032043.2(BRIP1):c.1045G>C (p.Ala349Pro) rs149364097
NM_032043.2(BRIP1):c.1140+1G>A rs1555607628
NM_032043.2(BRIP1):c.1340+1G>A rs1555607022
NM_032043.2(BRIP1):c.1473+1G>A rs748274524
NM_032043.2(BRIP1):c.1474-1G>A rs1555603638
NM_032043.2(BRIP1):c.1475del rs869312762
NM_032043.2(BRIP1):c.14G>A (p.Trp5Ter) rs1555618738
NM_032043.2(BRIP1):c.1936-1G>A rs1555601204
NM_032043.2(BRIP1):c.205+1del rs1057517648
NM_032043.2(BRIP1):c.206-1G>T rs1555617934
NM_032043.2(BRIP1):c.206-2A>G rs786203700
NM_032043.2(BRIP1):c.2097+1G>C rs786202941
NM_032043.2(BRIP1):c.2379+1G>A rs1555590286
NM_032043.2(BRIP1):c.2380-1G>A rs1567756032
NM_032043.2(BRIP1):c.2492+1G>C rs1567755539
NM_032043.2(BRIP1):c.2492+2dup rs587780240
NM_032043.2(BRIP1):c.2493-1G>C rs786203451
NM_032043.2(BRIP1):c.2575+2dup rs1555574711
NM_032043.2(BRIP1):c.2576-2A>G rs869312763
NM_032043.2(BRIP1):c.2905+1G>A rs876660203
NM_032043.2(BRIP1):c.2947del (p.Ile983fs) rs774684620
NM_032043.2(BRIP1):c.2999_3002del (p.Val1000fs) rs1567729445
NM_032043.2(BRIP1):c.3173_3179delinsCTC (p.Leu1058fs) rs1555572799
NM_032043.2(BRIP1):c.3196del (p.Ser1066fs) rs730881645
NM_032043.2(BRIP1):c.3232A>T (p.Lys1078Ter) rs786202927
NM_032043.2(BRIP1):c.3260dup (p.Asn1087fs) rs771654971
NM_032043.2(BRIP1):c.3390_3393delCTAT rs778664039
NM_032043.2(BRIP1):c.3411_3420del (p.Leu1136_Tyr1137insTer) rs876660100
NM_032043.2(BRIP1):c.3440dup (p.Asn1147fs) rs753683450
NM_032043.2(BRIP1):c.3525dup (p.Ile1176fs) rs777367075
NM_032043.2(BRIP1):c.379+1G>A rs1437158047
NM_032043.2(BRIP1):c.380-2A>G rs1567868785
NM_032043.2(BRIP1):c.507G>A (p.Gln169=) rs876660937
NM_032043.2(BRIP1):c.508-1G>C rs864622277
NM_032043.2(BRIP1):c.508-2A>T rs876659707
NM_032043.2(BRIP1):c.627+1G>A rs587780833
NM_032043.2(BRIP1):c.628-5_629del rs1555609402
NM_032043.2(BRIP1):c.751C>T (p.Arg251Cys) rs752309409
NM_032043.2(BRIP1):c.918+1G>A rs587781655
NM_032043.2(BRIP1):c.93+1G>T rs587782047

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.