ClinVar Miner

Variants in gene TERT 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: 5
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HGVS dbSNP
NM_198253.2(TERT):c.2769G>A (p.Pro923=) rs200174990
NM_198253.3(TERT):c.1317GGA[2] (p.Glu441del) rs377639087
NM_198253.3(TERT):c.1590G>C (p.Pro530=) rs1396912668
NM_198253.3(TERT):c.3184G>A (p.Ala1062Thr) rs35719940
NM_198253.3(TERT):c.604G>A (p.Ala202Thr) rs121918661

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