ClinVar Miner

List of variants in gene BCOR reported as benign

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Gene type:
ClinVar version:
Total variants: 102
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HGVS dbSNP gnomAD frequency
NM_001123385.2(BCOR):c.1692A>G (p.Ala564=) rs6520618 0.34271
NM_001123385.2(BCOR):c.166-55G>A rs6610384 0.22165
NM_001123385.2(BCOR):c.4977-4G>T rs5963725 0.16998
NM_001123385.2(BCOR):c.4741+317T>C rs6609049 0.15390
NM_001123385.2(BCOR):c.3503-158C>A rs5963155 0.13952
NM_001123385.2(BCOR):c.3502+127G>T rs5963731 0.09813
NM_001123385.2(BCOR):c.4173+139G>T rs55700604 0.09430
NM_001123385.2(BCOR):c.4742-69G>A rs112054628 0.07508
NM_001123385.2(BCOR):c.1791C>T (p.His597=) rs144606152 0.03194
NM_001123385.2(BCOR):c.87-202C>T rs111448219 0.02845
NM_001123385.2(BCOR):c.4976+69G>A rs148923231 0.02072
NM_001123385.2(BCOR):c.1650C>T (p.Thr550=) rs17145653 0.00806
NM_001123385.2(BCOR):c.4680G>A (p.Thr1560=) rs146007249 0.00140
NM_001123385.2(BCOR):c.3413T>C (p.Val1138Ala) rs145327925 0.00090
NM_001123385.2(BCOR):c.2424T>C (p.Leu808=) rs142968718 0.00085
NM_001123385.2(BCOR):c.2423T>A (p.Leu808His) rs151125150 0.00083
NM_001123385.2(BCOR):c.2514C>A (p.Pro838=) rs147497014 0.00082
NM_001123385.2(BCOR):c.4488A>C (p.Ala1496=) rs138741225 0.00076
NM_001123385.2(BCOR):c.5037A>T (p.Ile1679=) rs113588421 0.00064
NM_001123385.2(BCOR):c.3802A>G (p.Arg1268Gly) rs140897453 0.00058
NM_001123385.2(BCOR):c.2035G>A (p.Val679Ile) rs144722432 0.00053
NM_001123385.2(BCOR):c.4724T>C (p.Met1575Thr) rs142595337 0.00043
NM_001123385.2(BCOR):c.242G>A (p.Gly81Glu) rs144450053 0.00037
NM_001123385.2(BCOR):c.2525T>C (p.Val842Ala) rs143119333 0.00032
NM_001123385.2(BCOR):c.5190G>A (p.Thr1730=) rs375139386 0.00032
NM_001123385.2(BCOR):c.3378C>T (p.His1126=) rs137923016 0.00030
NM_001123385.2(BCOR):c.3974A>G (p.Lys1325Arg) rs187172641 0.00027
NM_001123385.2(BCOR):c.4383C>T (p.Asn1461=) rs189731022 0.00023
NM_001123385.2(BCOR):c.3669G>A (p.Ser1223=) rs372032523 0.00016
NM_001123385.2(BCOR):c.3226G>A (p.Glu1076Lys) rs202065982 0.00015
NM_001123385.2(BCOR):c.4765C>T (p.Arg1589Cys) rs754643148 0.00015
NM_001123385.2(BCOR):c.2124C>T (p.Thr708=) rs749386912 0.00014
NM_001123385.2(BCOR):c.3277G>A (p.Glu1093Lys) rs144736705 0.00013
NM_001123385.2(BCOR):c.5001G>A (p.Ser1667=) rs375878497 0.00012
NM_001123385.2(BCOR):c.5058C>T (p.Asn1686=) rs369322807 0.00012
NM_001123385.2(BCOR):c.3446C>T (p.Ala1149Val) rs368780561 0.00011
NM_001123385.2(BCOR):c.4320T>C (p.Pro1440=) rs753786462 0.00011
NM_001123385.2(BCOR):c.1669G>A (p.Val557Ile) rs201939220 0.00010
NM_001123385.2(BCOR):c.2032C>T (p.Pro678Ser) rs145560179 0.00009
NM_001123385.2(BCOR):c.3366G>A (p.Ser1122=) rs374359497 0.00009
NM_001123385.2(BCOR):c.4203G>A (p.Pro1401=) rs376940750 0.00009
NM_001123385.2(BCOR):c.4305A>G (p.Pro1435=) rs144653977 0.00009
NM_001123385.2(BCOR):c.4931C>T (p.Thr1644Ile) rs780610123 0.00009
NM_001123385.2(BCOR):c.2633T>C (p.Val878Ala) rs759983308 0.00008
NM_001123385.2(BCOR):c.4174-20G>A rs374547123 0.00008
NM_001123385.2(BCOR):c.4779C>T (p.Asp1593=) rs776232139 0.00008
NM_001123385.2(BCOR):c.5193C>T (p.Asn1731=) rs766578072 0.00008
NM_001123385.2(BCOR):c.188G>A (p.Arg63Lys) rs751977474 0.00007
NM_001123385.2(BCOR):c.2129G>A (p.Arg710His) rs200732803 0.00007
NM_001123385.2(BCOR):c.3036C>T (p.Pro1012=) rs190344757 0.00006
NM_001123385.2(BCOR):c.3491G>A (p.Arg1164Gln) rs769057299 0.00006
NM_001123385.2(BCOR):c.3848-10C>T rs765267478 0.00006
NM_001123385.2(BCOR):c.4890C>T (p.Asp1630=) rs750330961 0.00006
NM_001123385.2(BCOR):c.4960G>C (p.Val1654Leu) rs138012019 0.00006
NM_001123385.2(BCOR):c.1620G>A (p.Arg540=) rs144347073 0.00005
NM_001123385.2(BCOR):c.1645G>A (p.Gly549Ser) rs183680206 0.00005
NM_001123385.2(BCOR):c.4008C>T (p.Asp1336=) rs373762694 0.00005
NM_001123385.2(BCOR):c.179C>T (p.Thr60Met) rs202121665 0.00004
NM_001123385.2(BCOR):c.2598C>T (p.His866=) rs778532489 0.00004
NM_001123385.2(BCOR):c.3813G>A (p.Ser1271=) rs746505412 0.00004
NM_001123385.2(BCOR):c.4581C>T (p.Ala1527=) rs758631631 0.00004
NM_001123385.2(BCOR):c.1651G>A (p.Asp551Asn) rs372463512 0.00003
NM_001123385.2(BCOR):c.2512C>T (p.Pro838Ser) rs148571491 0.00003
NM_001123385.2(BCOR):c.2769A>G (p.Pro923=) rs371210264 0.00003
NM_001123385.2(BCOR):c.3138C>T (p.Phe1046=) rs201819559 0.00003
NM_001123385.2(BCOR):c.3831C>T (p.Pro1277=) rs775358295 0.00003
NM_001123385.2(BCOR):c.4062C>T (p.Ser1354=) rs747055096 0.00003
NM_001123385.2(BCOR):c.2898C>T (p.Ile966=) rs775251964 0.00002
NM_001123385.2(BCOR):c.3950C>T (p.Pro1317Leu) rs780412607 0.00002
NM_001123385.2(BCOR):c.4620C>T (p.Asn1540=) rs370429826 0.00002
NM_001123385.2(BCOR):c.1848C>T (p.Gly616=) rs758579970 0.00001
NM_001123385.2(BCOR):c.3349G>A (p.Ala1117Thr) rs374493655 0.00001
NM_001123385.2(BCOR):c.3410A>G (p.Lys1137Arg) rs758078994 0.00001
NM_001123385.2(BCOR):c.4824A>C (p.Pro1608=) rs760093247 0.00001
NM_001123385.2(BCOR):c.*299_*300dup rs35289701
NM_001123385.2(BCOR):c.111C>T (p.Asp37=)
NM_001123385.2(BCOR):c.1779C>A (p.Ser593=) rs17145652
NM_001123385.2(BCOR):c.2199G>T (p.Thr733=) rs140693978
NM_001123385.2(BCOR):c.2288G>T (p.Arg763Leu) rs139011455
NM_001123385.2(BCOR):c.2423_2424delinsAC (p.Leu808His) rs1569155643
NM_001123385.2(BCOR):c.2691G>C (p.Ser897=) rs3810693
NM_001123385.2(BCOR):c.2691G>T (p.Ser897=)
NM_001123385.2(BCOR):c.2997+12del
NM_001123385.2(BCOR):c.2997+12dup
NM_001123385.2(BCOR):c.3052-13G>A
NM_001123385.2(BCOR):c.3052-22del rs374448325
NM_001123385.2(BCOR):c.3052-34dup rs374448325
NM_001123385.2(BCOR):c.3225C>T (p.Asn1075=)
NM_001123385.2(BCOR):c.3305T>G (p.Val1102Gly) rs111622737
NM_001123385.2(BCOR):c.3392G>T (p.Arg1131Leu) rs758883383
NM_001123385.2(BCOR):c.3633G>A (p.Leu1211=)
NM_001123385.2(BCOR):c.3847+7G>A rs142686469
NM_001123385.2(BCOR):c.3847+7G>C rs142686469
NM_001123385.2(BCOR):c.3848-35T>C rs3810694
NM_001123385.2(BCOR):c.3893C>T (p.Ser1298Phe)
NM_001123385.2(BCOR):c.4173+127T>G rs2147025624
NM_001123385.2(BCOR):c.4281A>T (p.Pro1427=)
NM_001123385.2(BCOR):c.4429-35T>C rs2146925614
NM_001123385.2(BCOR):c.4560C>G (p.Gly1520=) rs375830184
NM_001123385.2(BCOR):c.4560C>T (p.Gly1520=)
NM_001123385.2(BCOR):c.4742-167del rs147324206
NM_001123385.2(BCOR):c.4977-182C>A rs5917929

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