ClinVar Miner

List of variants in gene TERT studied for not specified

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Gene type:
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Total variants: 62
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HGVS dbSNP
NM_001193376.2(TERT):c.1317_1319GGA[2] (p.Glu441del) rs377639087
NM_001193376.2(TERT):c.2654+1925C>T rs727505125
NM_198253.2(TERT):c.1234C>T (p.His412Tyr) rs34094720
NM_198253.2(TERT):c.1269C>A (p.Ala423=) rs190411812
NM_198253.2(TERT):c.1449C>T (p.Asn483=) rs761174773
NM_198253.2(TERT):c.1462C>T (p.Leu488Phe) rs746216837
NM_198253.2(TERT):c.1574-7G>A rs34846301
NM_198253.2(TERT):c.1590G>C
NM_198253.2(TERT):c.1609C>T (p.Arg537Cys) rs760352197
NM_198253.2(TERT):c.1659C>T (p.Val553=) rs35809415
NM_198253.2(TERT):c.1769+16G>A rs202108457
NM_198253.2(TERT):c.1793T>C
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.2031C>T (p.Gly677=) rs33956095
NM_198253.2(TERT):c.2097C>T (p.Ala699=) rs33963617
NM_198253.2(TERT):c.2106G>A (p.Pro702=) rs151055240
NM_198253.2(TERT):c.2127C>G (p.Val709=) rs765264494
NM_198253.2(TERT):c.2130+10G>A rs373879259
NM_198253.2(TERT):c.2225G>A (p.Arg742His) rs727503468
NM_198253.2(TERT):c.2255A>G (p.His752Arg) rs375699185
NM_198253.2(TERT):c.2256T>C (p.His752=) rs745650751
NM_198253.2(TERT):c.2301A>G (p.Thr767=) rs374592280
NM_198253.2(TERT):c.2329G>A (p.Val777Met) rs1554040129
NM_198253.2(TERT):c.2382+20G>C rs886038759
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.2575C>T (p.Arg859Trp) rs876658018
NM_198253.2(TERT):c.2582+7C>A rs766415474
NM_198253.2(TERT):c.264G>C (p.Leu88=) rs768398792
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.2793C>T (p.Cys931=) rs764925909
NM_198253.2(TERT):c.2844-11_2844-10del rs773793700
NM_198253.2(TERT):c.2936G>A (p.Arg979Gln) rs765566930
NM_198253.2(TERT):c.2946T>C (p.Cys982=) rs201689770
NM_198253.2(TERT):c.3032+69G>A rs186849858
NM_198253.2(TERT):c.3032+7C>T rs371500615
NM_198253.2(TERT):c.3039C>T (p.His1013=) rs33954691
NM_198253.2(TERT):c.3100C>T (p.Arg1034Cys) rs777672180
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.320_328del (p.Ala107_Gly109del) rs1554043095
NM_198253.2(TERT):c.327G>A (p.Gly109=) rs1060504786
NM_198253.2(TERT):c.3281G>T (p.Gly1094Val) rs1554038180
NM_198253.2(TERT):c.3324G>A (p.Pro1108=) rs35033501
NM_198253.2(TERT):c.3333G>A (p.Thr1111=) rs200102606
NM_198253.2(TERT):c.343T>A (p.Phe115Ile) rs1554043085
NM_198253.2(TERT):c.359G>C (p.Arg120Pro) rs1554043083
NM_198253.2(TERT):c.404G>C (p.Gly135Ala) rs1414898591
NM_198253.2(TERT):c.534C>T (p.Leu178=) rs370420108
NM_198253.2(TERT):c.604G>A (p.Ala202Thr) rs121918661
NM_198253.2(TERT):c.834C>A (p.Pro278=) rs375423906
NM_198253.2(TERT):c.835G>A (p.Ala279Thr) rs61748181
NM_198253.2(TERT):c.900C>T (p.Gly300=) rs987435263
NM_198253.2(TERT):c.915G>A (p.Ala305=) rs2736098
NM_198253.2(TERT):c.931T>A (p.Ser311Thr) rs1060502998
NM_198253.2(TERT):c.943C>A (p.Arg315Ser) rs1554042911
NM_198253.2(TERT):c.969G>A (p.Pro323=) rs148549782

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