ClinVar Miner

List of variants in gene TERT studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP
NM_198253.2(TERT):c.1574-3235G>T rs7705526
NM_198253.2(TERT):c.2354C>A (p.Pro785Gln) rs483352771
NM_198253.2(TERT):c.2455C>T (p.Arg819Cys) rs746621306
NM_198253.2(TERT):c.2468+10G>T rs878855301
NM_198253.2(TERT):c.2654+9C>T rs1060504793
NM_198253.2(TERT):c.2769G>A (p.Pro923=) rs200174990
NM_198253.3(TERT):c.1050G>A (p.Leu350=) rs1440641613
NM_198253.3(TERT):c.1144C>T (p.Leu382=) rs994804257
NM_198253.3(TERT):c.1234C>T (p.His412Tyr) rs34094720
NM_198253.3(TERT):c.1242G>A (p.Pro414=) rs775795705
NM_198253.3(TERT):c.1293C>T (p.Pro431=) rs1579596653
NM_198253.3(TERT):c.1317_1319GGA[2] (p.Glu441del) rs377639087
NM_198253.3(TERT):c.1335C>T (p.Pro445=) rs1579596558
NM_198253.3(TERT):c.1374C>T (p.Pro458=) rs1173874085
NM_198253.3(TERT):c.1398G>T (p.Arg466=) rs1579596423
NM_198253.3(TERT):c.1425A>C (p.Pro475=) rs1579596372
NM_198253.3(TERT):c.1485C>T (p.Ile495=) rs1352932374
NM_198253.3(TERT):c.1489C>T (p.Leu497=) rs747756167
NM_198253.3(TERT):c.1563C>T (p.Arg521=) rs764171875
NM_198253.3(TERT):c.1590G>C (p.Pro530=) rs1396912668
NM_198253.3(TERT):c.1676C>G (p.Ser559Cys) rs1579580077
NM_198253.3(TERT):c.1700C>T (p.Thr567Met) rs886039438
NM_198253.3(TERT):c.1731G>A (p.Arg577=) rs143585580
NM_198253.3(TERT):c.1731G>C (p.Arg577=) rs143585580
NM_198253.3(TERT):c.1818C>T (p.Val606=) rs1579577325
NM_198253.3(TERT):c.1843G>A (p.Ala615Thr) rs112614087
NM_198253.3(TERT):c.1854G>T (p.Thr618=) rs746040728
NM_198253.3(TERT):c.1888C>T (p.Leu630=) rs1579577146
NM_198253.3(TERT):c.1951-4C>G rs1023830541
NM_198253.3(TERT):c.1951-8C>T rs1378410963
NM_198253.3(TERT):c.1990G>A (p.Val664Met) rs797046042
NM_198253.3(TERT):c.1990G>C (p.Val664Leu) rs797046042
NM_198253.3(TERT):c.2007G>C (p.Arg669=) rs1060504788
NM_198253.3(TERT):c.2072G>A (p.Arg691His) rs202123213
NM_198253.3(TERT):c.2109G>T (p.Pro703=) rs763147123
NM_198253.3(TERT):c.2110C>T (p.Pro704Ser) rs199422297
NM_198253.3(TERT):c.2154C>T (p.Asp718=) rs377437136
NM_198253.3(TERT):c.2337C>T (p.His779=) rs747564177
NM_198253.3(TERT):c.2388C>T (p.Ser796=) rs950145141
NM_198253.3(TERT):c.2451C>T (p.Ala817=) rs752794198
NM_198253.3(TERT):c.2523C>G (p.Leu841=) rs1554039733
NM_198253.3(TERT):c.2594G>A (p.Arg865His) rs121918666
NM_198253.3(TERT):c.2596T>C (p.Leu866=) rs1060504798
NM_198253.3(TERT):c.2603A>G (p.Asp868Gly)
NM_198253.3(TERT):c.2604T>C (p.Asp868=) rs1579558147
NM_198253.3(TERT):c.2619G>A (p.Val873=) rs1579558137
NM_198253.3(TERT):c.2637C>T (p.His879=) rs1307380469
NM_198253.3(TERT):c.2639C>T (p.Ala880Val)
NM_198253.3(TERT):c.2655-10T>C rs1579556032
NM_198253.3(TERT):c.2698T>C (p.Leu900=) rs1579555964
NM_198253.3(TERT):c.2796C>A (p.Gly932=) rs375675196
NM_198253.3(TERT):c.2835C>T (p.Asp945=) rs1269153908
NM_198253.3(TERT):c.2895G>A (p.Lys965=) rs878855302
NM_198253.3(TERT):c.2947C>T (p.His983Tyr) rs1554038803
NM_198253.3(TERT):c.2971-10G>C rs878855303
NM_198253.3(TERT):c.2971-6C>T rs1579548036
NM_198253.3(TERT):c.2982C>T (p.Leu994=) rs762178169
NM_198253.3(TERT):c.2991del (p.Cys998fs) rs1554038539
NM_198253.3(TERT):c.3000C>T (p.Asn1000=) rs1579547985
NM_198253.3(TERT):c.3012C>T (p.Ile1004=) rs1308544817
NM_198253.3(TERT):c.3042A>T (p.Ala1014=) rs1337149388
NM_198253.3(TERT):c.312G>C (p.Leu104=) rs757915567
NM_198253.3(TERT):c.3132C>T (p.Tyr1044=) rs771543669
NM_198253.3(TERT):c.3158-7C>T rs1191106139
NM_198253.3(TERT):c.3189C>A (p.Gly1063=) rs1330114272
NM_198253.3(TERT):c.3201C>T (p.Ser1067=) rs755223754
NM_198253.3(TERT):c.327G>A (p.Gly109=) rs1060504786
NM_198253.3(TERT):c.3296-7C>T rs1579541812
NM_198253.3(TERT):c.3309G>A (p.Leu1103=) rs1311028871
NM_198253.3(TERT):c.3321C>G (p.Leu1107=) rs1382097700
NM_198253.3(TERT):c.3324G>C (p.Pro1108=) rs35033501
NM_198253.3(TERT):c.3362C>T (p.Pro1121Leu) rs1554038054
NM_198253.3(TERT):c.411G>T (p.Trp137Cys) rs1554043076
NM_198253.3(TERT):c.426C>T (p.Arg142=) rs1579598521
NM_198253.3(TERT):c.430G>A (p.Val144Met) rs199422291
NM_198253.3(TERT):c.438C>T (p.Asp146=) rs1579598506
NM_198253.3(TERT):c.462A>G (p.Ala154=) rs558025297
NM_198253.3(TERT):c.462A>T (p.Ala154=) rs558025297
NM_198253.3(TERT):c.474C>A (p.Leu158=) rs752933900
NM_198253.3(TERT):c.544A>T (p.Thr182Ser) rs878855305
NM_198253.3(TERT):c.604G>A (p.Ala202Thr) rs121918661
NM_198253.3(TERT):c.672C>T (p.Arg224=) rs996032219
NM_198253.3(TERT):c.684C>T (p.Ala228=) rs1403152390
NM_198253.3(TERT):c.699G>T (p.Pro233=) rs757862712
NM_198253.3(TERT):c.702G>A (p.Leu234=) rs754359147
NM_198253.3(TERT):c.750C>G (p.Pro250=) rs761741087
NM_198253.3(TERT):c.837C>T (p.Ala279=) rs1448995569
NM_198253.3(TERT):c.921C>T (p.Pro307=) rs1352359181
NM_198253.3(TERT):c.942A>G (p.Pro314=) rs1060504784
NM_198253.3(TERT):c.984C>G (p.Thr328=) rs762993766
NM_198253.3(TERT):c.999C>T (p.Tyr333=) rs1579597129

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.