List of variants in gene TERT reported as likely benign for cancer

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.3184G>A (p.Ala1062Thr)	rs35719940	0.01370
NM_198253.3(TERT):c.1234C>T (p.His412Tyr)	rs34094720	0.00316
NM_198253.3(TERT):c.1574-7G>A	rs34846301	0.00220
NM_198253.3(TERT):c.572G>C (p.Ser191Thr)	rs11952056	0.00100
NM_198253.3(TERT):c.1836C>G (p.Ala612=)	rs34170122	0.00056
NM_198253.3(TERT):c.2582+11C>T	rs180675821	0.00036
NM_198253.3(TERT):c.1932G>A (p.Thr644=)	rs148582238	0.00031
NM_198253.3(TERT):c.2991G>A (p.Val997=)	rs376266401	0.00030
NM_198253.3(TERT):c.838G>A (p.Glu280Lys)	rs199701877	0.00018
NM_198253.3(TERT):c.2079C>T (p.Phe693=)	rs371759577	0.00011
NM_198253.3(TERT):c.2190C>T (p.Ala730=)	rs138128892	0.00003
NM_198253.3(TERT):c.2262C>T (p.His754=)	rs778622091	0.00003
NM_198253.3(TERT):c.3303G>A (p.Thr1101=)	rs551516320	0.00001
NM_198253.3(TERT):c.375C>T (p.Asn125=)	rs1751256209	0.00001
NM_198253.3(TERT):c.729C>T (p.Ala243=)	rs762491880	0.00001
NM_198253.3(TERT):c.1110C>G (p.Pro370=)	rs1579597009
NM_198253.3(TERT):c.1662C>T (p.Val554=)	rs200539091
NM_198253.3(TERT):c.2007G>A (p.Arg669=)	rs1060504788

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