ClinVar Miner

Variants in gene CBL 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: 6
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NM_005188.3(CBL):c.1942A>C (p.Ser648Arg) rs143264567
NM_005188.3(CBL):c.2190G>A (p.Thr730=) rs143840974
NM_005188.4(CBL):c.2206A>G (p.Asn736Asp) rs397507497
NM_005188.4(CBL):c.2312A>T (p.Asp771Val) rs199788586
NM_005188.4(CBL):c.2345C>T (p.Pro782Leu) rs2229073
NM_005188.4(CBL):c.2588A>G (p.Asn863Ser) rs146250423

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