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Gene: TERT & Disease: AML, 114 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
39121	TERT	c.3184G>A	p.Ala1062Thr (p.A1062T)	NM_198253.3 M	SNV	LB	6 +	17
39121	TERT	c.2995G>A	p.Ala999Thr (p.A999T)	NM_001193376.3	SNV	LB	6 +	17
212398	TERT	c.1317_1319GGA[2]	p.Glu441Del (p.E441del)	NM_198253.3 M	MS	P	8 +	8
	TERT	c.1317GGA[2]	p.Glu441Del (p.E441del)	NM_198253.3 M	MS	P	8 +	8
	TERT	c.1317GGA[2]	p.Glu441Del (p.E441del)	NM_001193376.3	MS	P	8 +	8
12730	TERT	c.1234C>T	p.His412Tyr (p.H412Y)	NM_198253.3 M	SNV	P	7 +	7
12733	TERT	c.3268G>A	p.Val1090Met (p.V1090M)	NM_198253.3 M	SNV	P	7 +	7
12730	TERT	c.1234C>T	p.His412Tyr (p.H412Y)	NM_001193376.3	SNV	P	7 +	7
12733	TERT	c.3079G>A	p.Val1027Met (p.V1027M)	NM_001193376.3	SNV	P	7 +	7
916675	TERT	c.1891C>T	p.Arg631Trp (p.R631W)	NM_198253.3 M	SNV	P	5 +	5
916675	TERT	c.1891C>T	p.Arg631Trp (p.R631W)	NM_001193376.3	SNV	P	5 +	5
410651	TERT	c.336dup	p.Glu113fs (p.E113fs)	NM_198253.3 M	Dup	P	8 +	3
410651	TERT	c.336dupC	--	NM_198253.3 M	Dup	P	8 +	3
36947	TERT	c.508G>A	p.Val170Met (p.V170M)	NM_198253.3 M	SNV	P	7 +	3
39122	TERT	c.3329C>T	p.Thr1110Met (p.T1110M)	NM_198253.3 M	SNV	VUS	8 +	3
410651	TERT	c.336dup	p.Glu113fs (p.E113fs)	NM_001193376.3	Dup	P	8 +	3
36947	TERT	c.508G>A	p.Val170Met (p.V170M)	NM_001193376.3	SNV	P	7 +	3
39122	TERT	c.3140C>T	p.Thr1047Met (p.T1047M)	NM_001193376.3	SNV	VUS	8 +	3
165380	TERT	c.969G>A	p.Pro323= (p.P323=)	NM_198253.3 M	SNV	LB	4 +	2
350804	TERT	c.572G>C	p.Ser191Thr (p.S191T)	NM_198253.3 M	SNV	LB	6 +	2

114 Results, 20 per Page

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