ClinVar Miner

List of variants in gene BRD4 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001379291.1(BRD4):c.285+44G>T rs34855805 0.19620
NM_001379291.1(BRD4):c.285+110G>A rs2240304 0.16363
NM_001379291.1(BRD4):c.2865A>C (p.Pro955=) rs775889378 0.05892
NM_001379291.1(BRD4):c.1342-108C>T rs73508410 0.03480
NM_001379291.1(BRD4):c.1950C>T (p.Asp650=) rs17707730 0.02727
NM_001379291.1(BRD4):c.1342-144C>T rs80227750 0.01865
NM_001379291.1(BRD4):c.3446-34G>A rs60057301 0.01559
NM_001379291.1(BRD4):c.3290G>A (p.Arg1097His) rs35676845 0.01226
NM_001379291.1(BRD4):c.1982C>T (p.Pro661Leu) rs2047396651 0.00001
NM_001379291.1(BRD4):c.706A>G (p.Thr236Ala) rs2047523525 0.00001
NM_001379291.1(BRD4):c.1009G>A (p.Asp337Asn) rs1471575560
NM_001379291.1(BRD4):c.1015C>G (p.Gln339Glu)
NM_001379291.1(BRD4):c.1084A>C (p.Lys362Gln)
NM_001379291.1(BRD4):c.137dup (p.Pro47fs)
NM_001379291.1(BRD4):c.1400C>T (p.Ala467Val) rs929177624
NM_001379291.1(BRD4):c.1420_1440del (p.Pro474_Val480del) rs1406509488
NM_001379291.1(BRD4):c.1448C>T (p.Pro483Leu)
NM_001379291.1(BRD4):c.1504G>A (p.Asp502Asn) rs2512562116
NM_001379291.1(BRD4):c.1510GAG[2] (p.Glu506del) rs2512562053
NM_001379291.1(BRD4):c.1526_1527delinsTA (p.Gln509Leu) rs2145575627
NM_001379291.1(BRD4):c.1574T>C (p.Leu525Pro)
NM_001379291.1(BRD4):c.1774A>G (p.Lys592Glu)
NM_001379291.1(BRD4):c.182A>G (p.Asn61Ser)
NM_001379291.1(BRD4):c.1917_1923delinsCCTGAAGAATTCCAA (p.Arg640fs) rs2145570218
NM_001379291.1(BRD4):c.2047+89_2047+90dup rs71333363
NM_001379291.1(BRD4):c.2047+89dup rs71333363
NM_001379291.1(BRD4):c.2078C>G (p.Ser693Cys) rs2145566066
NM_001379291.1(BRD4):c.2104G>C (p.Glu702Gln)
NM_001379291.1(BRD4):c.220C>G (p.Leu74Val)
NM_001379291.1(BRD4):c.251A>G (p.Gln84Arg)
NM_001379291.1(BRD4):c.2579C>G (p.Pro860Arg)
NM_001379291.1(BRD4):c.263A>T (p.Asp88Val) rs2145624320
NM_001379291.1(BRD4):c.2713A>G (p.Met905Val)
NM_001379291.1(BRD4):c.2833C>G (p.Leu945Val)
NM_001379291.1(BRD4):c.286-206dup rs112184222
NM_001379291.1(BRD4):c.3088C>G (p.Pro1030Ala) rs142887410
NM_001379291.1(BRD4):c.3517G>C (p.Gly1173Arg)
NM_001379291.1(BRD4):c.3694C>T (p.Arg1232Trp)
NM_001379291.1(BRD4):c.424-76_424-73del rs139141985
NM_001379291.1(BRD4):c.538G>A (p.Gly180Arg)
NM_001379291.1(BRD4):c.599C>G (p.Thr200Ser)
NM_001379291.1(BRD4):c.766dup (p.Gln256fs) rs780128218
NM_001379291.1(BRD4):c.800C>G (p.Pro267Arg) rs2512587250
NM_001379291.1(BRD4):c.875C>G (p.Ala292Gly)
NM_001379291.1(BRD4):c.884C>T (p.Thr295Ile)
NM_001379291.1(BRD4):c.967del (p.Glu323fs) rs2145599923

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.