ClinVar Miner

List of variants in gene BRIP1 reported as likely benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
Download table as spreadsheet
HGVS dbSNP
NM_032043.2(BRIP1):c.1053A>G (p.Pro351=) rs544977115
NM_032043.2(BRIP1):c.1149A>G (p.Leu383=) rs1567829755
NM_032043.2(BRIP1):c.1315C>A (p.Arg439=) rs587780226
NM_032043.2(BRIP1):c.1383T>C (p.Tyr461=) rs587780875
NM_032043.2(BRIP1):c.1442G>A (p.Gly481Asp) rs200062099
NM_032043.2(BRIP1):c.1455T>C (p.Ala485=) rs773489367
NM_032043.2(BRIP1):c.1659A>G (p.Gln553=) rs876660693
NM_032043.2(BRIP1):c.1890A>G (p.Thr630=) rs145796331
NM_032043.2(BRIP1):c.1953T>C (p.Ile651=) rs754400631
NM_032043.2(BRIP1):c.1989C>A (p.Thr663=) rs376628979
NM_032043.2(BRIP1):c.2223G>T (p.Val741=) rs1057522996
NM_032043.2(BRIP1):c.2322C>T (p.Asp774=) rs1057520434
NM_032043.2(BRIP1):c.2370A>G (p.Lys790=) rs372122365
NM_032043.2(BRIP1):c.2433A>G (p.Leu811=) rs751455420
NM_032043.2(BRIP1):c.2751T>C (p.Ser917=) rs150780318
NM_032043.2(BRIP1):c.2811T>C (p.Asp937=) rs374335608
NM_032043.2(BRIP1):c.2907T>C (p.Asn969=) rs1555572999
NM_032043.2(BRIP1):c.3009A>G (p.Ser1003=) rs751823379
NM_032043.2(BRIP1):c.312T>G (p.Thr104=) rs769190318
NM_032043.2(BRIP1):c.3336T>C (p.Asp1112=) rs369843642
NM_032043.2(BRIP1):c.342A>G (p.Pro114=) rs756764576
NM_032043.2(BRIP1):c.357T>C (p.Asn119=) rs786202477
NM_032043.2(BRIP1):c.387T>C (p.Pro129=) rs779324498
NM_032043.2(BRIP1):c.587A>G (p.Asn196Ser) rs550707862
NM_032043.2(BRIP1):c.595C>T (p.Leu199=) rs144969738
NM_032043.2(BRIP1):c.618G>T (p.Ser206=) rs367614726
NM_032043.2(BRIP1):c.628C>T (p.Pro210Ser) rs150313156
NM_032043.2(BRIP1):c.672A>G (p.Gly224=) rs752356873
NM_032043.2(BRIP1):c.820A>G (p.Thr274Ala) rs62620988
NM_032043.2(BRIP1):c.867C>T (p.Val289=) rs147739458
NM_032043.3(BRIP1):c.1255C>T (p.Arg419Trp) rs150624408
NM_032043.3(BRIP1):c.1735C>T (p.Arg579Cys) rs28997571
NM_032043.3(BRIP1):c.2220G>T (p.Gln740His) rs45589637
NM_032043.3(BRIP1):c.2440C>T (p.Arg814Cys) rs201869624
NM_032043.3(BRIP1):c.316C>T (p.Arg106Cys) rs587780247
NM_032043.3(BRIP1):c.3559G>A (p.Ala1187Thr) rs367610893
NM_032043.3(BRIP1):c.854A>G (p.His285Arg) rs141055990

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.