ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP
NM_014780.4(CUL7):c.2229C>G (p.Ala743=) rs188565648
NM_014780.4(CUL7):c.3432G>A (p.Thr1144=) rs144556973
NM_014780.4(CUL7):c.3490C>T (p.Arg1164Trp) rs201135654
NM_014780.4(CUL7):c.4659G>A (p.Glu1553=) rs139243761

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