ClinVar Miner

List of variants in gene NTRK1 reported as uncertain significance for not provided

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Total variants: 26
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HGVS dbSNP
NM_001007792.1(NTRK1):c.*6C>T rs370807813
NM_001007792.1(NTRK1):c.123-3367G>A rs1007211
NM_001007792.1(NTRK1):c.123-3410G>A rs556840308
NM_001007792.1(NTRK1):c.1366G>A (p.Glu456Lys) rs144901788
NM_001007792.1(NTRK1):c.1420A>T (p.Ile474Phe) rs781478411
NM_001007792.1(NTRK1):c.1553G>A (p.Arg518Gln) rs764417252
NM_001007792.1(NTRK1):c.1639C>T (p.Arg547Cys) rs371344688
NM_001007792.1(NTRK1):c.1700C>G (p.Ser567Cys) rs188270548
NM_001007792.1(NTRK1):c.1949G>A (p.Arg650His) rs754452975
NM_001007792.1(NTRK1):c.2033G>A (p.Gly678Asp) rs944740609
NM_001007792.1(NTRK1):c.2114C>T (p.Thr705Met) rs145081333
NM_001007792.1(NTRK1):c.2123G>A (p.Arg708His)
NM_001007792.1(NTRK1):c.2134C>T (p.Arg712Trp) rs778520978
NM_001007792.1(NTRK1):c.380G>A (p.Arg127His) rs141021604
NM_001007792.1(NTRK1):c.392G>A (p.Arg131His) rs150271893
NM_001007792.1(NTRK1):c.419T>C (p.Val140Ala) rs201503610
NM_001007792.1(NTRK1):c.424G>A (p.Glu142Lys) rs267598081
NM_001007792.1(NTRK1):c.470C>T (p.Pro157Leu) rs879253918
NM_001007792.1(NTRK1):c.480C>G (p.Ser160Arg) rs138608619
NM_001007792.1(NTRK1):c.541G>A (p.Val181Met) rs201192875
NM_001007792.1(NTRK1):c.551G>A (p.Arg184Gln) rs200132482
NM_001007792.1(NTRK1):c.697G>C (p.Val233Leu) rs201509717
NM_001007792.1(NTRK1):c.775C>A (p.Gln259Lys) rs137979116
NM_001007792.1(NTRK1):c.850C>T (p.Arg284Cys) rs137994522
NM_001007792.1(NTRK1):c.851G>A (p.Arg284His) rs368769883
NM_001007792.1(NTRK1):c.947T>C (p.Leu316Pro) rs150651692

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