ClinVar Miner

List of variants in gene TERT reported as benign for Idiopathic fibrosing alveolitis, chronic form; Dyskeratosis congenita, autosomal dominant, 2

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Total variants: 30
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HGVS dbSNP
NM_198253.2(TERT):c.1138C>T (p.Pro380Ser) rs144756946
NM_198253.2(TERT):c.1234C>T (p.His412Tyr) rs34094720
NM_198253.2(TERT):c.1392C>T (p.Phe464=) rs186596886
NM_198253.2(TERT):c.1574-3235G>T rs7705526
NM_198253.2(TERT):c.1574-7G>A rs34846301
NM_198253.2(TERT):c.1659C>T (p.Val553=) rs35809415
NM_198253.2(TERT):c.1785G>A (p.Arg595=) rs765708956
NM_198253.2(TERT):c.1812A>G (p.Ala604=) rs33959226
NM_198253.2(TERT):c.1849C>T (p.Leu617=) rs140951453
NM_198253.2(TERT):c.1884C>T (p.Asp628=) rs143992655
NM_198253.2(TERT):c.1950+10C>T rs33948291
NM_198253.2(TERT):c.1950+245C>T rs2242652
NM_198253.2(TERT):c.1951-205G>A rs10069690
NM_198253.2(TERT):c.2031C>T (p.Gly677=) rs33956095
NM_198253.2(TERT):c.2097C>T (p.Ala699=) rs33963617
NM_198253.2(TERT):c.2139G>A (p.Val713=) rs775722062
NM_198253.2(TERT):c.2383-15C>T rs574645600
NM_198253.2(TERT):c.2391C>G (p.Ser797=) rs377216965
NM_198253.2(TERT):c.2517G>A (p.Thr839=) rs140124989
NM_198253.2(TERT):c.2520G>A (p.Leu840=) rs144310369
NM_198253.2(TERT):c.2654+269T>C rs2075786
NM_198253.2(TERT):c.2658C>A (p.Thr886=) rs371744235
NM_198253.2(TERT):c.2769G>A (p.Pro923=) rs200174990
NM_198253.2(TERT):c.2775C>T (p.His925=) rs34528119
NM_198253.2(TERT):c.3105C>T (p.Val1035=) rs181612536
NM_198253.2(TERT):c.3184G>A (p.Ala1062Thr) rs35719940
NM_198253.2(TERT):c.3324G>A (p.Pro1108=) rs35033501
NM_198253.2(TERT):c.534C>T (p.Leu178=) rs370420108
NM_198253.2(TERT):c.835G>A (p.Ala279Thr) rs61748181
NM_198253.2(TERT):c.969G>A (p.Pro323=) rs148549782

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