ClinVar Miner

List of variants in gene NTRK1 reported as likely benign for not provided

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Total variants: 41
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HGVS dbSNP
NM_001007792.1(NTRK1):c.1053C>T (p.Asn351=) rs374700842
NM_001007792.1(NTRK1):c.1088-173T>C rs764543935
NM_001007792.1(NTRK1):c.1088-177C>A rs767630555
NM_001007792.1(NTRK1):c.1144-8C>G rs372743293
NM_001007792.1(NTRK1):c.1194G>A (p.Thr398=)
NM_001007792.1(NTRK1):c.123-3237C>T rs1571681483
NM_001007792.1(NTRK1):c.123-3404C>T rs201472270
NM_001007792.1(NTRK1):c.123-9T>C rs1571685066
NM_001007792.1(NTRK1):c.1239G>T (p.Gly413=) rs1571697785
NM_001007792.1(NTRK1):c.1287C>T (p.Ser429=) rs1311708647
NM_001007792.1(NTRK1):c.1290G>T (p.Leu430=) rs750362227
NM_001007792.1(NTRK1):c.1329C>T (p.Thr443=) rs770948722
NM_001007792.1(NTRK1):c.1344T>C (p.Ser448=) rs1571698553
NM_001007792.1(NTRK1):c.1394-5dup rs750026012
NM_001007792.1(NTRK1):c.1530G>C (p.Leu510=) rs747000102
NM_001007792.1(NTRK1):c.1626C>G (p.Val542=) rs953974597
NM_001007792.1(NTRK1):c.1644C>G (p.Pro548=) rs754567573
NM_001007792.1(NTRK1):c.1671G>A (p.Arg557=) rs1571699995
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.189G>A (p.Leu63=) rs147983523
NM_001007792.1(NTRK1):c.1908C>T (p.Ser636=) rs757891009
NM_001007792.1(NTRK1):c.1920C>T (p.Tyr640=) rs1052882544
NM_001007792.1(NTRK1):c.2097+9C>G rs748710832
NM_001007792.1(NTRK1):c.2115G>A (p.Thr705=) rs753013914
NM_001007792.1(NTRK1):c.2151A>C (p.Pro717=) rs746732506
NM_001007792.1(NTRK1):c.216T>A (p.Gly72=) rs1366600162
NM_001007792.1(NTRK1):c.2231G>A (p.Arg744Gln) rs35669708
NM_001007792.1(NTRK1):c.2274C>T (p.Val758=) rs1570912582
NM_001007792.1(NTRK1):c.2275C>T (p.Leu759=) rs749041981
NM_001007792.1(NTRK1):c.414C>A (p.Gly138=) rs144594313
NM_001007792.1(NTRK1):c.415G>A (p.Gly139Arg) rs367836863
NM_001007792.1(NTRK1):c.484+9C>T rs771749558
NM_001007792.1(NTRK1):c.528T>C (p.Asp176=) rs1571690231
NM_001007792.1(NTRK1):c.549G>T (p.Leu183=) rs890893982
NM_001007792.1(NTRK1):c.621G>C (p.Thr207=) rs537430475
NM_001007792.1(NTRK1):c.627+86G>C rs150452564
NM_001007792.1(NTRK1):c.702G>A (p.Thr234=) rs201110800
NM_001007792.1(NTRK1):c.756C>G (p.Val252=) rs768096430
NM_001007792.1(NTRK1):c.789G>A (p.Ala263=) rs766259168
NM_001007792.1(NTRK1):c.978C>T (p.Asn326=) rs145823996
NM_001007792.1(NTRK1):c.996G>A (p.Leu332=) rs1571696163

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