ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP
NM_014780.4(CUL7):c.1846A>G (p.Ser616Gly) rs7774330
NM_014780.4(CUL7):c.3432G>A (p.Thr1144=) rs144556973
NM_014780.4(CUL7):c.3876C>T (p.Ile1292=) rs147056081
NM_014780.4(CUL7):c.4914C>T (p.Asp1638=) rs61731584
NM_014780.4(CUL7):c.861G>A (p.Gly287=) rs61750322

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