ClinVar Miner

List of variants in gene BRWD3 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_153252.5(BRWD3):c.*6439G>A rs375704347 0.00132
NM_153252.5(BRWD3):c.*2154A>G rs184067970 0.00131
NM_153252.5(BRWD3):c.-267C>T rs1306232684 0.00130
NM_153252.5(BRWD3):c.*4139T>C rs765392888 0.00091
NM_153252.5(BRWD3):c.*5790G>A rs759779733 0.00085
NM_153252.5(BRWD3):c.*3293C>A rs765169545 0.00043
NM_153252.5(BRWD3):c.*847G>A rs897278146 0.00034
NM_153252.5(BRWD3):c.*5142A>G rs41300244 0.00032
NM_153252.5(BRWD3):c.*1473T>A rs756025042 0.00012
NM_153252.5(BRWD3):c.*3083G>T rs987452216 0.00012
NM_153252.5(BRWD3):c.*3594T>C rs879201626 0.00009
NM_153252.5(BRWD3):c.2326-14C>A rs765268982 0.00009
NM_153252.5(BRWD3):c.*3377T>G rs769363805 0.00006
NM_153252.5(BRWD3):c.*121C>G rs760166411 0.00005
NM_153252.5(BRWD3):c.*1820G>C rs960827578 0.00005
NM_153252.5(BRWD3):c.*2626C>T rs1028184110 0.00005
NM_153252.5(BRWD3):c.*5773A>C rs765604641 0.00004
NM_153252.5(BRWD3):c.*2413T>A rs1009993995 0.00003
NM_153252.5(BRWD3):c.*1394G>C rs1314935865 0.00002
NM_153252.5(BRWD3):c.*248C>T rs538786513 0.00002
NM_153252.5(BRWD3):c.*4661A>G rs1439226627 0.00002
NM_153252.5(BRWD3):c.*799C>A rs985109628 0.00002
NM_153252.5(BRWD3):c.96A>G (p.Leu32=) rs1034284582 0.00002
NM_153252.5(BRWD3):c.*2877G>A rs187241080 0.00001
NM_153252.5(BRWD3):c.*6197T>C rs1057515994 0.00001
NM_153252.5(BRWD3):c.*6248A>G rs1057515993 0.00001
NM_153252.5(BRWD3):c.1118A>G (p.Asn373Ser) rs1344040839 0.00001
NM_153252.5(BRWD3):c.2943+13A>G rs760769986 0.00001
NM_153252.5(BRWD3):c.3965C>T (p.Ser1322Leu) rs372993559 0.00001
NM_153252.5(BRWD3):c.4263C>T (p.Ala1421=) rs749607717 0.00001
NM_153252.5(BRWD3):c.4328G>C (p.Arg1443Thr) rs1569244634 0.00001
NM_153252.5(BRWD3):c.637C>T (p.Arg213Cys) rs777162950 0.00001
NM_153252.5(BRWD3):c.814-8T>A rs1057516005 0.00001
NM_153252.5(BRWD3):c.*1703T>C rs1057516003
NM_153252.5(BRWD3):c.*1895C>G rs1057516002
NM_153252.5(BRWD3):c.*2329A>T rs1057516001
NM_153252.5(BRWD3):c.*244CA[2] rs1057516004
NM_153252.5(BRWD3):c.*2594T>C rs1057516000
NM_153252.5(BRWD3):c.*2710G>A rs898420202
NM_153252.5(BRWD3):c.*2875A>G rs926354680
NM_153252.5(BRWD3):c.*3252T>C rs2072338016
NM_153252.5(BRWD3):c.*3738A>G rs2072334243
NM_153252.5(BRWD3):c.*4581C>T rs1057515996
NM_153252.5(BRWD3):c.*5514T>C rs1057515995
NM_153252.5(BRWD3):c.*6451T>C rs1166674482
NM_153252.5(BRWD3):c.*6692A>G rs2072310229
NM_153252.5(BRWD3):c.*6871G>T rs567910666
NM_153252.5(BRWD3):c.*6957C>G rs1057515992
NM_153252.5(BRWD3):c.*802A>G rs2072359014
NM_153252.5(BRWD3):c.-229_-228dup rs1057516006
NM_153252.5(BRWD3):c.-265TC[7] rs1057516007
NM_153252.5(BRWD3):c.1384T>C (p.Ser462Pro) rs202197853
NM_153252.5(BRWD3):c.2026G>A (p.Ala676Thr) rs2073115463
NM_153252.5(BRWD3):c.3326-14del rs765175433
NM_153252.5(BRWD3):c.3326-26dup rs765175433
NM_153252.5(BRWD3):c.3730G>C (p.Asp1244His) rs2147690102
NM_153252.5(BRWD3):c.4384A>G (p.Ser1462Gly)

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