List of variants in gene TERT reported as benign by Invitae

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.2654+269T>C	rs2075786	0.54966
NM_198253.3(TERT):c.1574-3777G>T	rs2736100	0.52208
NM_198253.3(TERT):c.1951-205G>A	rs10069690	0.35840
NM_198253.3(TERT):c.1574-3235G>T	rs7705526	0.28965
NM_198253.3(TERT):c.1769+225G>T	rs7726159	0.28907
NM_198253.3(TERT):c.915G>A (p.Ala305=)	rs2736098	0.21206
NM_198253.3(TERT):c.1950+245C>T	rs2242652	0.17562
NM_198253.3(TERT):c.3039C>T (p.His1013=)	rs33954691	0.08834
NM_198253.3(TERT):c.835G>A (p.Ala279Thr)	rs61748181	0.02258
NM_198253.3(TERT):c.2031C>T (p.Gly677=)	rs33956095	0.02136
NM_198253.3(TERT):c.3324G>A (p.Pro1108=)	rs35033501	0.01868
NM_198253.3(TERT):c.1950+10C>T	rs33948291	0.01758
NM_198253.3(TERT):c.3184G>A (p.Ala1062Thr)	rs35719940	0.01370
NM_198253.3(TERT):c.1659C>T (p.Val553=)	rs35809415	0.00838
NM_198253.3(TERT):c.2097C>T (p.Ala699=)	rs33963617	0.00739
NM_198253.3(TERT):c.1950+15G>A	rs35695689	0.00326
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.2769G>A (p.Pro923=)	rs200174990	0.00118
NM_198253.3(TERT):c.1884C>T (p.Asp628=)	rs143992655	0.00088
NM_198253.3(TERT):c.1849C>T (p.Leu617=)	rs140951453	0.00083
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.2520G>A (p.Leu840=)	rs144310369	0.00029
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.2884C>T (p.Arg962Cys)	rs144697790	0.00019
NM_198253.3(TERT):c.642G>A (p.Leu214=)	rs549656839	0.00015
NM_198253.3(TERT):c.2383-15C>T	rs574645600	0.00013
NM_198253.3(TERT):c.2573G>A (p.Arg858Gln)	rs144779807	0.00011
NM_198253.3(TERT):c.1785G>A (p.Arg595=)	rs765708956	0.00010
NM_198253.3(TERT):c.779G>A (p.Gly260Asp)	rs148798048	0.00009
NM_198253.3(TERT):c.1392C>T (p.Phe464=)	rs186596886	0.00008
NM_198253.3(TERT):c.2139G>A (p.Val713=)	rs775722062	0.00008
NM_198253.3(TERT):c.1025G>A (p.Arg342Gln)	rs773366454	0.00006
NM_198253.3(TERT):c.737C>T (p.Pro246Leu)	rs377315722	0.00006
NM_198253.3(TERT):c.1769+13del	rs1301313710
NM_198253.3(TERT):c.1770-14dup
NM_198253.3(TERT):c.1951-6del	rs2126642447
NM_198253.3(TERT):c.2658C>A (p.Thr886=)	rs371744235
NM_198253.3(TERT):c.2844-11dup	rs1491484726
NM_198253.3(TERT):c.3158-3del	rs748986490

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