ClinVar Miner

Variants in gene BCOR with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP
NM_001123385.2(BCOR):c.3446C>T (p.Ala1149Val) rs368780561
NM_001123385.2(BCOR):c.4320T>C (p.Pro1440=) rs753786462
NM_001123385.2(BCOR):c.4488A>C (p.Ala1496=) rs138741225
NM_001123385.2(BCOR):c.837C>T (p.Leu279=) rs753531268

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