ClinVar Miner

List of variants in gene NTRK1 studied for not provided

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Gene type:
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Total variants: 89
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HGVS dbSNP
NM_001007792.1(NTRK1):c.*6C>T rs370807813
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.123-233A>G rs74118782
NM_001007792.1(NTRK1):c.123-3237C>T rs1571681483
NM_001007792.1(NTRK1):c.123-3301_123-3300insT rs1131691595
NM_001007792.1(NTRK1):c.123-3367G>A rs1007211
NM_001007792.1(NTRK1):c.123-3404C>T rs201472270
NM_001007792.1(NTRK1):c.123-3410G>A rs556840308
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.1336A>T (p.Lys446Ter) rs879253890
NM_001007792.1(NTRK1):c.1344T>C (p.Ser448=) rs1571698553
NM_001007792.1(NTRK1):c.1366G>A (p.Glu456Lys) rs144901788
NM_001007792.1(NTRK1):c.1394-5dup rs750026012
NM_001007792.1(NTRK1):c.1420A>T (p.Ile474Phe) rs781478411
NM_001007792.1(NTRK1):c.1530G>C (p.Leu510=) rs747000102
NM_001007792.1(NTRK1):c.1553G>A (p.Arg518Gln) rs764417252
NM_001007792.1(NTRK1):c.1626C>G (p.Val542=) rs953974597
NM_001007792.1(NTRK1):c.1639C>T (p.Arg547Cys) rs371344688
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.1696C>T (p.Arg566Ter) rs763758904
NM_001007792.1(NTRK1):c.1698-106T>C rs2768757
NM_001007792.1(NTRK1):c.1698-120C>T rs2768756
NM_001007792.1(NTRK1):c.1698-4del rs1799770
NM_001007792.1(NTRK1):c.1700C>G (p.Ser567Cys) rs188270548
NM_001007792.1(NTRK1):c.1702C>T (p.His568Tyr) rs6336
NM_001007792.1(NTRK1):c.1730G>T (p.Gly577Val) rs6339
NM_001007792.1(NTRK1):c.1752_1753insT (p.Pro585fs) rs80356676
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.1838G>A (p.Arg613Gln) rs786205449
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.1949G>A (p.Arg650His) rs754452975
NM_001007792.1(NTRK1):c.2033G>A (p.Gly678Asp) rs944740609
NM_001007792.1(NTRK1):c.2094G>A (p.Thr698=) rs55668752
NM_001007792.1(NTRK1):c.2097+155G>C rs2274499
NM_001007792.1(NTRK1):c.2097+163T>G rs2274500
NM_001007792.1(NTRK1):c.2097+9C>G rs748710832
NM_001007792.1(NTRK1):c.2098-208T>G rs2768758
NM_001007792.1(NTRK1):c.2114C>T (p.Thr705Met) rs145081333
NM_001007792.1(NTRK1):c.2115G>A (p.Thr705=) rs753013914
NM_001007792.1(NTRK1):c.2123G>A (p.Arg708His)
NM_001007792.1(NTRK1):c.2134C>T (p.Arg712Trp) rs778520978
NM_001007792.1(NTRK1):c.2151A>C (p.Pro717=) rs746732506
NM_001007792.1(NTRK1):c.2164G>A (p.Ala722Thr) rs62640939
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.380G>A (p.Arg127His) rs141021604
NM_001007792.1(NTRK1):c.392G>A (p.Arg131His) rs150271893
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.419T>C (p.Val140Ala) rs201503610
NM_001007792.1(NTRK1):c.424G>A (p.Glu142Lys) rs267598081
NM_001007792.1(NTRK1):c.436C>T (p.Gln146Ter) rs879253889
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.484+100T>C rs1800879
NM_001007792.1(NTRK1):c.484+9C>T rs771749558
NM_001007792.1(NTRK1):c.528T>C (p.Asp176=) rs1571690231
NM_001007792.1(NTRK1):c.541G>A (p.Val181Met) rs201192875
NM_001007792.1(NTRK1):c.542T>A (p.Val181Glu) rs1064793219
NM_001007792.1(NTRK1):c.549G>T (p.Leu183=) rs890893982
NM_001007792.1(NTRK1):c.551G>A (p.Arg184Gln) rs200132482
NM_001007792.1(NTRK1):c.620C>T (p.Thr207Met) rs55909005
NM_001007792.1(NTRK1):c.621G>C (p.Thr207=) rs537430475
NM_001007792.1(NTRK1):c.627+86G>C rs150452564
NM_001007792.1(NTRK1):c.628-156A>C rs2644614
NM_001007792.1(NTRK1):c.697G>C (p.Val233Leu) rs201509717
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.760+127G>A rs1410082
NM_001007792.1(NTRK1):c.775C>A (p.Gln259Lys) rs137979116
NM_001007792.1(NTRK1):c.789G>A (p.Ala263=) rs766259168
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
NM_001007792.1(NTRK1):c.978C>T (p.Asn326=) rs145823996
NM_001007792.1(NTRK1):c.996G>A (p.Leu332=) rs1571696163

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