ClinVar Miner

List of variants in gene NTRK1 reported as uncertain significance for Familial medullary thyroid carcinoma

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Total variants: 17
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NM_001007792.1(NTRK1):c.1030A>G (p.Ile344Val) rs1347421266
NM_001007792.1(NTRK1):c.1088-179C>T rs199646180
NM_001007792.1(NTRK1):c.1273G>A (p.Gly425Arg) rs761247634
NM_001007792.1(NTRK1):c.1355G>A (p.Gly452Asp) rs760222071
NM_001007792.1(NTRK1):c.1417G>C (p.Asp473His) rs1035934237
NM_001007792.1(NTRK1):c.1553G>A (p.Arg518Gln) rs764417252
NM_001007792.1(NTRK1):c.1700C>G (p.Ser567Cys) rs188270548
NM_001007792.1(NTRK1):c.1997G>A (p.Arg666His) rs200022271
NM_001007792.1(NTRK1):c.251C>G (p.Thr84Ser) rs202161010
NM_001007792.1(NTRK1):c.265C>T (p.Arg89Cys) rs757031354
NM_001007792.1(NTRK1):c.332A>C (p.Gln111Pro) rs1306924167
NM_001007792.1(NTRK1):c.419T>C (p.Val140Ala) rs201503610
NM_001007792.1(NTRK1):c.480C>G (p.Ser160Arg) rs138608619
NM_001007792.1(NTRK1):c.494C>T (p.Thr165Met) rs552776147
NM_001007792.1(NTRK1):c.752A>G (p.Asn251Ser) rs547972574
NM_001007792.1(NTRK1):c.775C>A (p.Gln259Lys) rs137979116
NM_001007792.1(NTRK1):c.850C>T (p.Arg284Cys) rs137994522

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