List of variants in gene TERT reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 87

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.2844-336G>A	rs34041736	0.02409
NM_198253.3(TERT):c.3184G>A (p.Ala1062Thr)	rs35719940	0.01370
NM_198253.3(TERT):c.2287-103G>A	rs192999400	0.01168
NM_198253.3(TERT):c.*63C>T	rs5031049	0.01135
NM_198253.3(TERT):c.1950+21C>T	rs34471035	0.00980
NM_198253.3(TERT):c.3033-318G>A	rs35387865	0.00938
NM_198253.3(TERT):c.2130+100C>T	rs33951489	0.00808
NM_198253.3(TERT):c.3158-133C>T	rs35080081	0.00772
NM_198253.3(TERT):c.2287-236A>C	rs1351343356	0.00761
NM_198253.3(TERT):c.2970+128C>T	rs35703455	0.00612
NM_198253.3(TERT):c.2844-122C>T	rs35605907	0.00608
NM_198253.3(TERT):c.2971-200T>C	rs35300412	0.00607
NM_198253.3(TERT):c.2844-162G>T	rs35550096	0.00606
NM_198253.3(TERT):c.2970+258A>G	rs34018970	0.00606
NM_198253.3(TERT):c.2844-246G>A	rs36049021	0.00531
NM_198253.3(TERT):c.2655-192C>T	rs113192843	0.00529
NM_198253.3(TERT):c.2970+140T>C	rs34238050	0.00525
NM_198253.3(TERT):c.2287-243A>G	rs1216918433	0.00503
NM_198253.3(TERT):c.2287-245T>C	rs113488319	0.00503
NM_198253.3(TERT):c.2382+109G>T	rs35929262	0.00502
NM_198253.3(TERT):c.2287-241C>T	rs1003715343	0.00496
NM_198253.3(TERT):c.1234C>T (p.His412Tyr)	rs34094720	0.00316
NM_198253.3(TERT):c.1812A>G (p.Ala604=)	rs33959226	0.00255
NM_198253.3(TERT):c.969G>A (p.Pro323=)	rs148549782	0.00224
NM_198253.3(TERT):c.1574-7G>A	rs34846301	0.00220
NM_198253.3(TERT):c.3105C>T (p.Val1035=)	rs181612536	0.00207
NM_198253.3(TERT):c.2517G>A (p.Thr839=)	rs140124989	0.00178
NM_198253.3(TERT):c.1574-16G>C	rs79698601	0.00144
NM_198253.3(TERT):c.534C>T (p.Leu178=)	rs370420108	0.00124
NM_198253.3(TERT):c.1849C>T (p.Leu617=)	rs140951453	0.00083
NM_198253.3(TERT):c.2106G>A (p.Pro702=)	rs151055240	0.00050
NM_198253.3(TERT):c.2130+10G>A	rs373879259	0.00048
NM_198253.3(TERT):c.2582+11C>T	rs180675821	0.00036
NM_198253.3(TERT):c.2775C>T (p.His925=)	rs34528119	0.00035
NM_198253.3(TERT):c.3333G>A (p.Thr1111=)	rs200102606	0.00030
NM_198253.3(TERT):c.1138C>T (p.Pro380Ser)	rs144756946	0.00024
NM_198253.3(TERT):c.2391C>G (p.Ser797=)	rs377216965	0.00020
NM_198253.3(TERT):c.604G>A (p.Ala202Thr)	rs121918661	0.00018
NM_198253.3(TERT):c.838G>A (p.Glu280Lys)	rs199701877	0.00018
NM_198253.3(TERT):c.645C>T (p.Gly215=)	rs768426236	0.00014
NM_198253.3(TERT):c.2383-15C>T	rs574645600	0.00013
NM_198253.3(TERT):c.1974G>A (p.Val658=)	rs778496417	0.00009
NM_198253.3(TERT):c.1392C>T (p.Phe464=)	rs186596886	0.00008
NM_198253.3(TERT):c.2127C>G (p.Val709=)	rs765264494	0.00008
NM_198253.3(TERT):c.2139G>A (p.Val713=)	rs775722062	0.00008
NM_198253.3(TERT):c.2256T>C (p.His752=)	rs745650751	0.00007
NM_198253.3(TERT):c.2328C>T (p.Phe776=)	rs748248614	0.00004
NM_198253.3(TERT):c.2301A>G (p.Thr767=)	rs374592280	0.00003
NM_198253.3(TERT):c.2751G>A (p.Thr917=)	rs375200599	0.00003
NM_198253.3(TERT):c.2061C>T (p.His687=)	rs370486790	0.00002
NM_198253.3(TERT):c.3126C>T (p.Leu1042=)	rs377570406	0.00002
NM_198253.3(TERT):c.1215C>T (p.Tyr405=)	rs1416285081	0.00001
NM_198253.3(TERT):c.1443G>A (p.Arg481=)	rs1373208248	0.00001
NM_198253.3(TERT):c.1692G>A (p.Thr564=)	rs377217777	0.00001
NM_198253.3(TERT):c.1896G>A (p.Pro632=)	rs140056333	0.00001
NM_198253.3(TERT):c.2367C>T (p.Ala789=)	rs759014638	0.00001
NM_198253.3(TERT):c.2850C>G (p.Ala950=)	rs758664162	0.00001
NM_198253.3(TERT):c.315C>T (p.Asp105=)	rs970934345	0.00001
NM_198253.3(TERT):c.3165G>A (p.Ser1055=)	rs554739019	0.00001
NM_198253.3(TERT):c.3303G>A (p.Thr1101=)	rs551516320	0.00001
NM_198253.3(TERT):c.567C>T (p.His189=)	rs747935528	0.00001
NM_198253.3(TERT):c.1269C>A (p.Ala423=)	rs190411812
NM_198253.3(TERT):c.1317GGA[2] (p.Glu441del)	rs377639087
NM_198253.3(TERT):c.1545G>T (p.Arg515=)
NM_198253.3(TERT):c.1574-298T>G	rs1171291378
NM_198253.3(TERT):c.1713C>T (p.Asn571=)	rs1750089799
NM_198253.3(TERT):c.1951-228T>G	rs34227159
NM_198253.3(TERT):c.1951-230_1951-229del	rs35278664
NM_198253.3(TERT):c.2286+309G>T	rs144020096
NM_198253.3(TERT):c.2287-234A>G	rs1016273541
NM_198253.3(TERT):c.2287-263TG[3]	rs10700998
NM_198253.3(TERT):c.2565G>A (p.Ala855=)	rs769077049
NM_198253.3(TERT):c.2655-10T>C	rs1579556032
NM_198253.3(TERT):c.2655G>A (p.Arg885=)	rs754372863
NM_198253.3(TERT):c.2658C>A (p.Thr886=)	rs371744235
NM_198253.3(TERT):c.2698T>C (p.Leu900=)	rs1579555964
NM_198253.3(TERT):c.2841C>T (p.Ser947=)
NM_198253.3(TERT):c.2843+229G>A	rs34656059
NM_198253.3(TERT):c.2970+7A>G	rs530914674
NM_198253.3(TERT):c.2971-6C>T	rs1579548036
NM_198253.3(TERT):c.3132C>T (p.Tyr1044=)	rs771543669
NM_198253.3(TERT):c.3158-253G>A	rs34321948
NM_198253.3(TERT):c.3309G>A (p.Leu1103=)	rs1311028871
NM_198253.3(TERT):c.750C>T (p.Pro250=)	rs761741087
NM_198253.3(TERT):c.780C>A (p.Gly260=)	rs2126687848
NM_198253.3(TERT):c.930A>G (p.Thr310=)
NM_198253.3(TERT):c.999C>T (p.Tyr333=)	rs1579597129

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