ClinVar Miner

List of variants in gene BCOR reported as benign for X-linked syndromic intellectual disability

Included ClinVar conditions (168):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_001123383.1(BCOR):c.1260T>C (p.Asp420=) rs5917933
NM_001123383.1(BCOR):c.1448C>T (p.Pro483Leu) rs587778096
NM_001123383.1(BCOR):c.1650C>T (p.Thr550=) rs17145653
NM_001123383.1(BCOR):c.1692A>G (p.Ala564=) rs6520618
NM_001123383.1(BCOR):c.1779C>A (p.Ser593=) rs17145652
NM_001123383.1(BCOR):c.1791C>T (p.His597=) rs144606152
NM_001123383.1(BCOR):c.1848C>T (p.Gly616=) rs758579970
NM_001123383.1(BCOR):c.2035G>A (p.Val679Ile) rs144722432
NM_001123383.1(BCOR):c.2129G>A (p.Arg710His) rs200732803
NM_001123383.1(BCOR):c.2199G>T (p.Thr733=) rs140693978
NM_001123383.1(BCOR):c.2633T>C (p.Val878Ala) rs759983308
NM_001123383.1(BCOR):c.2691G>C (p.Ser897=) rs3810693
NM_001123383.1(BCOR):c.3036C>T (p.Pro1012=) rs190344757
NM_001123383.1(BCOR):c.3413T>C (p.Val1138Ala) rs145327925
NM_001123383.1(BCOR):c.3491G>A (p.Arg1164Gln) rs769057299
NM_001123383.1(BCOR):c.3745+7G>C rs142686469
NM_001123383.1(BCOR):c.3848C>T (p.Pro1283Leu) rs780412607
NM_001123383.1(BCOR):c.3872A>G (p.Lys1291Arg) rs187172641
NM_001123383.1(BCOR):c.408C>T (p.Ala136=) rs139802143
NM_001123383.1(BCOR):c.4578G>A (p.Thr1526=) rs146007249
NM_001123383.1(BCOR):c.4722A>C (p.Pro1574=) rs760093247
NM_001123383.1(BCOR):c.4875-4G>T rs5963725
NM_001123383.1(BCOR):c.4935A>T (p.Ile1645=) rs113588421
NM_001123383.1(BCOR):c.711C>T (p.Val237=) rs727503827

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