ClinVar Miner

List of variants in gene NTRK1 reported by GeneDx

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Gene type:
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Total variants: 70
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HGVS dbSNP
NM_001007792.1(NTRK1):c.*7G>T rs145060242
NM_001007792.1(NTRK1):c.1128C>T (p.Asp376=) rs147438950
NM_001007792.1(NTRK1):c.1144-15C>G rs186649954
NM_001007792.1(NTRK1):c.1149G>A (p.Ser383=) rs750968694
NM_001007792.1(NTRK1):c.1223G>A (p.Arg408Gln) rs56320207
NM_001007792.1(NTRK1):c.123-233A>G rs74118782
NM_001007792.1(NTRK1):c.123-3198C>T rs183517027
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.123-3447C>A rs753655855
NM_001007792.1(NTRK1):c.123-3458A>G rs570123832
NM_001007792.1(NTRK1):c.123-3463C>T rs1057522593
NM_001007792.1(NTRK1):c.1246+18A>T rs73004759
NM_001007792.1(NTRK1):c.1246+8G>A rs763576316
NM_001007792.1(NTRK1):c.1336A>T (p.Lys446Ter) rs879253890
NM_001007792.1(NTRK1):c.1366G>A (p.Glu456Lys) rs144901788
NM_001007792.1(NTRK1):c.1414C>A (p.Arg472=) rs200575096
NM_001007792.1(NTRK1):c.1420A>T (p.Ile474Phe) rs781478411
NM_001007792.1(NTRK1):c.1449C>T (p.Gly483=) rs564775946
NM_001007792.1(NTRK1):c.1553G>A (p.Arg518Gln) rs764417252
NM_001007792.1(NTRK1):c.164G>A (p.Arg55His) rs79678945
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.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.189G>A (p.Leu63=) rs147983523
NM_001007792.1(NTRK1):c.1939-16T>C rs12076232
NM_001007792.1(NTRK1):c.1939-6T>C rs762866535
NM_001007792.1(NTRK1):c.1959G>A (p.Leu653=) rs1057521447
NM_001007792.1(NTRK1):c.198-8C>T rs80026148
NM_001007792.1(NTRK1):c.201C>T (p.Thr67=) rs1057522997
NM_001007792.1(NTRK1):c.2061C>T (p.Tyr687=) rs140852621
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.2098-208T>G rs2768758
NM_001007792.1(NTRK1):c.2114C>T (p.Thr705Met) rs145081333
NM_001007792.1(NTRK1):c.2134C>T (p.Arg712Trp) rs778520978
NM_001007792.1(NTRK1):c.2164G>A (p.Ala722Thr) rs62640939
NM_001007792.1(NTRK1):c.2231G>A (p.Arg744Gln) rs35669708
NM_001007792.1(NTRK1):c.231G>T (p.Ala77=) rs774351278
NM_001007792.1(NTRK1):c.338+12C>A rs41267425
NM_001007792.1(NTRK1):c.338+12C>T rs41267425
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.415G>A (p.Gly139Arg) rs367836863
NM_001007792.1(NTRK1):c.436C>T (p.Gln146Ter) rs879253889
NM_001007792.1(NTRK1):c.441T>C (p.Cys147=) rs1057523619
NM_001007792.1(NTRK1):c.470C>T (p.Pro157Leu) rs879253918
NM_001007792.1(NTRK1):c.484+100T>C rs1800879
NM_001007792.1(NTRK1):c.484+10G>A rs201336491
NM_001007792.1(NTRK1):c.522G>A (p.Ser174=) rs114320051
NM_001007792.1(NTRK1):c.540C>T (p.Asp180=) rs147882947
NM_001007792.1(NTRK1):c.542T>A (p.Val181Glu) rs1064793219
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>A (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.628-15T>C rs778745696
NM_001007792.1(NTRK1):c.697G>C (p.Val233Leu) rs201509717
NM_001007792.1(NTRK1):c.760+127G>A rs1410082
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.978C>T (p.Asn326=) rs145823996
NM_001007792.1(NTRK1):c.987C>T (p.Tyr329=) rs1057521034

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