List of variants in gene TERT studied for Acute myeloid leukemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 25

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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.2031C>T (p.Gly677=)	rs33956095	0.02136
NM_198253.3(TERT):c.1950+10C>T	rs33948291	0.01758
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.969G>A (p.Pro323=)	rs148549782	0.00224
NM_198253.3(TERT):c.1574-7G>A	rs34846301	0.00220
NM_198253.3(TERT):c.2517G>A (p.Thr839=)	rs140124989	0.00178
NM_198253.3(TERT):c.2769G>A (p.Pro923=)	rs200174990	0.00118
NM_198253.3(TERT):c.572G>C (p.Ser191Thr)	rs11952056	0.00100
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.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.1392C>T (p.Phe464=)	rs186596886	0.00008
NM_198253.3(TERT):c.2262C>T (p.His754=)	rs778622091	0.00003
NM_198253.3(TERT):c.1331A>G (p.Asp444Gly)	rs878855299	0.00001
NM_198253.3(TERT):c.729C>T (p.Ala243=)	rs762491880	0.00001
NM_198253.3(TERT):c.1620C>G (p.Ile540Met)	rs797046041
NM_198253.3(TERT):c.1662C>T (p.Val554=)	rs200539091
NM_198253.3(TERT):c.1891C>T (p.Arg631Trp)	rs1194223999

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