List of variants in gene TERT reported as likely benign for hematologic disorder

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: 31

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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.1812A>G (p.Ala604=)	rs33959226	0.00255
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.534C>T (p.Leu178=)	rs370420108	0.00124
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.2775C>T (p.His925=)	rs34528119	0.00035
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.3333G>A (p.Thr1111=)	rs200102606	0.00030
NM_198253.3(TERT):c.838G>A (p.Glu280Lys)	rs199701877	0.00018
NM_198253.3(TERT):c.2383-15C>T	rs574645600	0.00013
NM_198253.3(TERT):c.2079C>T (p.Phe693=)	rs371759577	0.00011
NM_198253.3(TERT):c.1392C>T (p.Phe464=)	rs186596886	0.00008
NM_198253.3(TERT):c.2580C>T (p.Asp860=)	rs751752830	0.00004
NM_198253.3(TERT):c.2946T>C (p.Cys982=)	rs201689770	0.00004
NM_198253.3(TERT):c.3323C>T (p.Pro1108Leu)	rs376255453	0.00004
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.1939A>C (p.Arg647=)	rs144821759	0.00001
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.1317GGA[2] (p.Glu441del)	rs377639087
NM_198253.3(TERT):c.1662C>T (p.Val554=)	rs200539091
NM_198253.3(TERT):c.2007G>A (p.Arg669=)	rs1060504788

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