ClinVar Miner

Variants in gene CUL7 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 11
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NM_014780.4(CUL7):c.1067G>A (p.Arg356His) rs146227929
NM_014780.4(CUL7):c.136C>T (p.Arg46Trp) rs141692693
NM_014780.4(CUL7):c.1859C>T (p.Pro620Leu) rs147326417
NM_014780.4(CUL7):c.2115C>T (p.His705=) rs143128153
NM_014780.4(CUL7):c.2163T>C (p.Asp721=) rs145572983
NM_014780.4(CUL7):c.2645G>A (p.Arg882Gln) rs45574335
NM_014780.4(CUL7):c.2754G>A (p.Thr918=) rs138777262
NM_014780.4(CUL7):c.2802C>A (p.Leu934=) rs144926293
NM_014780.4(CUL7):c.3432G>A (p.Thr1144=) rs144556973
NM_014780.4(CUL7):c.3747G>A (p.Leu1249=) rs141211365
NM_014780.4(CUL7):c.981C>T (p.Pro327=) rs144880219

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