ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 8
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HGVS dbSNP
NM_001918.4(DBT):c.1150= (p.Gly384=) rs12021720
NM_001918.4(DBT):c.1210-8A>T rs535837017
NM_001918.4(DBT):c.1281+31T>G rs115696850
NM_001918.4(DBT):c.251+14dup rs201469612
NM_001918.4(DBT):c.724T>C (p.Ser242Pro) rs146249007
NM_001918.4(DBT):c.747C>A (p.Gly249=) rs200612682
NM_001918.4(DBT):c.753C>T (p.Asp251=) rs79292123
NM_001918.4(DBT):c.76T>C (p.Cys26Arg) rs145674833

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