List of variants in gene NTRK1 reported as uncertain significance for cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.940C>T (p.Arg314Cys)	rs137994522	0.00027
NM_002529.4(NTRK1):c.584C>T (p.Thr195Met)	rs552776147	0.00014
NM_002529.4(NTRK1):c.1661G>A (p.Arg554Gln)	rs764417252	0.00013
NM_002529.4(NTRK1):c.570C>G (p.Ser190Arg)	rs138608619	0.00013
NM_002529.4(NTRK1):c.1808C>G (p.Ser603Cys)	rs188270548	0.00011
NM_002529.4(NTRK1):c.1187C>T (p.Ser396Leu)	rs199646180	0.00009
NM_002529.4(NTRK1):c.509T>C (p.Val170Ala)	rs201503610	0.00008
NM_002529.4(NTRK1):c.2222C>T (p.Thr741Met)	rs145081333	0.00004
NM_002529.4(NTRK1):c.355C>T (p.Arg119Cys)	rs757031354	0.00004
NM_002529.4(NTRK1):c.1463G>A (p.Gly488Asp)	rs760222071	0.00003
NM_002529.4(NTRK1):c.1480C>A (p.Pro494Thr)	rs764737760	0.00003
NM_002529.4(NTRK1):c.2105G>A (p.Arg702His)	rs200022271	0.00003
NM_002529.4(NTRK1):c.1381G>A (p.Gly461Arg)	rs761247634	0.00001
NM_002529.4(NTRK1):c.422A>C (p.Gln141Pro)	rs1306924167	0.00001
NM_002529.4(NTRK1):c.842A>G (p.Asn281Ser)	rs547972574	0.00001
NM_002529.4(NTRK1):c.1120A>G (p.Ile374Val)	rs1347421266
NM_002529.4(NTRK1):c.1525G>C (p.Asp509His)	rs1035934237
NM_002529.4(NTRK1):c.341C>G (p.Thr114Ser)	rs202161010

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