List of variants in gene TERT reported as not provided 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: 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.835G>A (p.Ala279Thr)	rs61748181	0.02258
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.604G>A (p.Ala202Thr)	rs121918661	0.00018
NM_198253.3(TERT):c.3268G>A (p.Val1090Met)	rs121918664	0.00009
NM_198253.3(TERT):c.2080G>A (p.Val694Met)	rs121918662	0.00001
NM_198253.3(TERT):c.2147C>T (p.Ala716Val)	rs199422298
NM_198253.3(TERT):c.2315A>G (p.Tyr772Cys)	rs121918663
NM_198253.3(TERT):c.2537A>G (p.Tyr846Cys)	rs199422302
NM_198253.3(TERT):c.2628C>G (p.His876Gln)	rs199422303
NM_198253.3(TERT):c.2935C>T (p.Arg979Trp)	rs199422305
NM_198253.3(TERT):c.3043T>C (p.Cys1015Arg)	rs199422307

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