ClinVar Miner

Variants in gene DOK7 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: 3
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HGVS dbSNP
NM_173660.5(DOK7):c.1029C>T (p.Gly343=) rs375877997
NM_173660.5(DOK7):c.1278C>T (p.Pro426=) rs139468087
NM_173660.5(DOK7):c.781C>T (p.Arg261Cys) rs142821143

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