ClinVar Miner

List of variants in gene TERT reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_198253.2(TERT):c.2383-15C>T rs574645600
NM_198253.2(TERT):c.2775C>T (p.His925=) rs34528119
NM_198253.3(TERT):c.1234C>T (p.His412Tyr) rs34094720
NM_198253.3(TERT):c.1317_1319GGA[2] (p.Glu441del) rs377639087
NM_198253.3(TERT):c.1392C>T (p.Phe464=) rs186596886
NM_198253.3(TERT):c.1574-7G>A rs34846301
NM_198253.3(TERT):c.1659C>T (p.Val553=) rs35809415
NM_198253.3(TERT):c.1812A>G (p.Ala604=) rs33959226
NM_198253.3(TERT):c.1849C>T (p.Leu617=) rs140951453
NM_198253.3(TERT):c.1939A>C (p.Arg647=) rs144821759
NM_198253.3(TERT):c.2517G>A (p.Thr839=) rs140124989
NM_198253.3(TERT):c.2580C>T (p.Asp860=) rs751752830
NM_198253.3(TERT):c.2946T>C (p.Cys982=) rs201689770
NM_198253.3(TERT):c.3105C>T (p.Val1035=) rs181612536
NM_198253.3(TERT):c.3184G>A (p.Ala1062Thr) rs35719940
NM_198253.3(TERT):c.3323C>T (p.Pro1108Leu) rs376255453
NM_198253.3(TERT):c.3333G>A (p.Thr1111=) rs200102606
NM_198253.3(TERT):c.534C>T (p.Leu178=) rs370420108
NM_198253.3(TERT):c.572G>C (p.Ser191Thr) rs11952056

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