List of variants in gene TERT reported as benign by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.915G>A (p.Ala305=)	rs2736098	0.21206
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.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.2517G>A (p.Thr839=)	rs140124989	0.00178
NM_198253.3(TERT):c.1849C>T (p.Leu617=)	rs140951453	0.00083
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.838G>A (p.Glu280Lys)	rs199701877	0.00018

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