ClinVar Miner

List of variants in gene BCOR reported as benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NM_001123385.2(BCOR):c.1257A>G (p.Lys419=) rs531585800
NM_001123385.2(BCOR):c.1260T>C (p.Asp420=) rs5917933
NM_001123385.2(BCOR):c.1650C>T (p.Thr550=) rs17145653
NM_001123385.2(BCOR):c.1692A>G (p.Ala564=) rs6520618
NM_001123385.2(BCOR):c.1779C>A (p.Ser593=) rs17145652
NM_001123385.2(BCOR):c.1791C>T (p.His597=) rs144606152
NM_001123385.2(BCOR):c.1848C>T (p.Gly616=) rs758579970
NM_001123385.2(BCOR):c.2035G>A (p.Val679Ile) rs144722432
NM_001123385.2(BCOR):c.2129G>A (p.Arg710His) rs200732803
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.2514C>A (p.Pro838=) rs147497014
NM_001123385.2(BCOR):c.2525T>C (p.Val842Ala) rs143119333
NM_001123385.2(BCOR):c.2691G>C (p.Ser897=) rs3810693
NM_001123385.2(BCOR):c.3036C>T (p.Pro1012=) rs190344757
NM_001123385.2(BCOR):c.3226G>A (p.Glu1076Lys) rs202065982
NM_001123385.2(BCOR):c.3277G>A (p.Glu1093Lys) rs144736705
NM_001123385.2(BCOR):c.3366G>A (p.Ser1122=) rs374359497
NM_001123385.2(BCOR):c.3378C>T (p.His1126=) rs137923016
NM_001123385.2(BCOR):c.3491G>A (p.Arg1164Gln) rs769057299
NM_001123385.2(BCOR):c.3669G>A (p.Ser1223=) rs372032523
NM_001123385.2(BCOR):c.3802A>G (p.Arg1268Gly) rs140897453
NM_001123385.2(BCOR):c.3847+7G>A rs142686469
NM_001123385.2(BCOR):c.3847+7G>C rs142686469
NM_001123385.2(BCOR):c.3950C>T (p.Pro1317Leu) rs780412607
NM_001123385.2(BCOR):c.3974A>G (p.Lys1325Arg) rs187172641
NM_001123385.2(BCOR):c.408C>T (p.Ala136=) rs139802143
NM_001123385.2(BCOR):c.4620C>T (p.Asn1540=) rs370429826
NM_001123385.2(BCOR):c.4680G>A (p.Thr1560=) rs146007249
NM_001123385.2(BCOR):c.4724T>C (p.Met1575Thr) rs142595337
NM_001123385.2(BCOR):c.4824A>C (p.Pro1608=) rs760093247
NM_001123385.2(BCOR):c.482C>T (p.Ala161Val) rs142236686
NM_001123385.2(BCOR):c.4931C>T (p.Thr1644Ile) rs780610123
NM_001123385.2(BCOR):c.4977-4G>T rs5963725
NM_001123385.2(BCOR):c.5037A>T (p.Ile1679=) rs113588421
NM_001123385.2(BCOR):c.5190G>A (p.Thr1730=) rs375139386
NM_001123385.2(BCOR):c.626C>T (p.Ser209Leu) rs143697110
NM_001123385.2(BCOR):c.711C>T (p.Val237=) rs727503827
NM_001123385.2(BCOR):c.946C>T (p.Pro316Ser) rs200052076

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