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Mutation Direct

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Gene: NTRK1 & Disease: MTC, 70 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
12308	NTRK1	c.1838G>T	p.Gly613Val (p.G613V)	NM_002529.4 M	SNV	P	2 +	7
37077	NTRK1	c.1810C>T	p.His604Tyr (p.H604Y)	NM_002529.4 M	SNV	P	2 +	7
12308	NTRK1	c.1730G>T	p.Gly577Val (p.G577V)	NM_001007792.1	SNV	P	2 +	7
12308	NTRK1	c.1820G>T	p.Gly607Val (p.G607V)	NM_001012331.2	SNV	P	2 +	7
37077	NTRK1	c.1702C>T	p.His568Tyr (p.H568Y)	NM_001007792.1	SNV	P	2 +	7
37077	NTRK1	c.1792C>T	p.His598Tyr (p.H598Y)	NM_001012331.2	SNV	P	2 +	7
584603	NTRK1	c.2105G>A	p.Arg702His (p.R702H)	NM_002529.4 M	SNV	VUS	2 +	1
245652	NTRK1	c.865C>A	p.Gln289Lys (p.Q289K)	NM_002529.4 M	SNV	LB	2 +	1
584603	NTRK1	c.1997G>A	p.Arg666His (p.R666H)	NM_001007792.1	SNV	VUS	2 +	1
584603	NTRK1	c.2087G>A	p.Arg696His (p.R696H)	NM_001012331.2	SNV	VUS	2 +	1
245652	NTRK1	c.775C>A	p.Gln259Lys (p.Q259K)	NM_001007792.1	SNV	LB	2 +	1
245652	NTRK1	c.865C>A	p.Gln289Lys (p.Q289K)	NM_001012331.2	SNV	LB	2 +	1
245994	NTRK1	c.940C>T	p.Arg314Cys (p.R314C)	NM_002529.4 M	SNV	LB	2 +	0
452208	NTRK1	c.2222C>T	p.Thr741Met (p.T741M)	NM_002529.4 M	SNV	VUS	2 +	0
584594	NTRK1	c.341C>G	p.Thr114Ser (p.T114S)	NM_002529.4 M	SNV	VUS	2 +	0
584595	NTRK1	c.355C>T	p.Arg119Cys (p.R119C)	NM_002529.4 M	SNV	VUS	2 +	0
584596	NTRK1	c.422A>C	p.Gln141Pro (p.Q141P)	NM_002529.4 M	SNV	VUS	2 +	0
584597	NTRK1	c.584C>T	p.Thr195Met (p.T195M)	NM_002529.4 M	SNV	LB	2 +	0
584598	NTRK1	c.842A>G	p.Asn281Ser (p.N281S)	NM_002529.4 M	SNV	VUS	2 +	0
584599	NTRK1	c.1120A>G	p.Ile374Val (p.I374V)	NM_002529.4 M	SNV	VUS	2 +	0

70 Results, 20 per Page

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