ClinVar Miner

List of variants in gene NTRK1 reported by Natera, Inc.

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 99
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HGVS dbSNP
NM_001007792.1(NTRK1):c.1024G>A (p.Ala342Thr) rs754611476
NM_001007792.1(NTRK1):c.1128C>T (p.Asp376=) rs147438950
NM_001007792.1(NTRK1):c.1129G>C (p.Glu377Gln) rs199826686
NM_001007792.1(NTRK1):c.1148C>T (p.Ser383Leu) rs765681685
NM_001007792.1(NTRK1):c.1193C>T (p.Thr398Met) rs771342578
NM_001007792.1(NTRK1):c.123-3198C>T rs183517027
NM_001007792.1(NTRK1):c.123-3263G>C rs200815412
NM_001007792.1(NTRK1):c.123-3317C>T
NM_001007792.1(NTRK1):c.123-3332T>C rs1350547406
NM_001007792.1(NTRK1):c.123-3355T>A rs748402400
NM_001007792.1(NTRK1):c.123-3404C>T rs201472270
NM_001007792.1(NTRK1):c.1246C>G (p.Arg416Gly) rs34900547
NM_001007792.1(NTRK1):c.1246C>T (p.Arg416Cys) rs34900547
NM_001007792.1(NTRK1):c.1273G>A (p.Gly425Arg) rs761247634
NM_001007792.1(NTRK1):c.129C>T (p.Ile43=) rs563296138
NM_001007792.1(NTRK1):c.1365C>T (p.Ile455=) rs373181158
NM_001007792.1(NTRK1):c.1366G>A (p.Glu456Lys) rs144901788
NM_001007792.1(NTRK1):c.1372C>A (p.Pro458Thr) rs764737760
NM_001007792.1(NTRK1):c.1417G>A (p.Asp473Asn) rs1035934237
NM_001007792.1(NTRK1):c.1417G>C (p.Asp473His) rs1035934237
NM_001007792.1(NTRK1):c.1489C>T (p.Leu497=) rs760564817
NM_001007792.1(NTRK1):c.149A>G (p.Gln50Arg) rs55891455
NM_001007792.1(NTRK1):c.1539G>A (p.Ala513=) rs771010259
NM_001007792.1(NTRK1):c.1553G>A (p.Arg518Gln) rs764417252
NM_001007792.1(NTRK1):c.1566G>A (p.Gln522=) rs6334
NM_001007792.1(NTRK1):c.1620C>T (p.Phe540=) rs6335
NM_001007792.1(NTRK1):c.1626C>G (p.Val542=) rs953974597
NM_001007792.1(NTRK1):c.1670G>A (p.Arg557Gln) rs748133401
NM_001007792.1(NTRK1):c.1697+8C>A rs780424308
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.1752C>T (p.Gly584=) rs6338
NM_001007792.1(NTRK1):c.1779C>T (p.Ala593=) rs6337
NM_001007792.1(NTRK1):c.1831G>T (p.Val611Leu) rs142870382
NM_001007792.1(NTRK1):c.1887G>A (p.Lys629=) rs553270591
NM_001007792.1(NTRK1):c.1939-6T>C rs762866535
NM_001007792.1(NTRK1):c.1949G>A (p.Arg650His) rs754452975
NM_001007792.1(NTRK1):c.197+2dup
NM_001007792.1(NTRK1):c.198-5C>T
NM_001007792.1(NTRK1):c.198-8C>T rs80026148
NM_001007792.1(NTRK1):c.2005A>T (p.Thr669Ser) rs200935209
NM_001007792.1(NTRK1):c.2011G>A (p.Glu671Lys) rs747855434
NM_001007792.1(NTRK1):c.2035G>A (p.Val679Met) rs759190964
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.2189G>A (p.Arg730Gln) rs764581997
NM_001007792.1(NTRK1):c.2204G>A (p.Arg735His)
NM_001007792.1(NTRK1):c.2254C>T (p.Pro752Ser) rs768876280
NM_001007792.1(NTRK1):c.225C>T (p.Phe75=) rs6340
NM_001007792.1(NTRK1):c.2260G>A (p.Val754Ile) rs55948542
NM_001007792.1(NTRK1):c.265C>T (p.Arg89Cys) rs757031354
NM_001007792.1(NTRK1):c.266G>A (p.Arg89His) rs778566154
NM_001007792.1(NTRK1):c.267C>T (p.Arg89=) rs149960336
NM_001007792.1(NTRK1):c.286G>A (p.Ala96Thr) rs922936206
NM_001007792.1(NTRK1):c.380G>A (p.Arg127His) rs141021604
NM_001007792.1(NTRK1):c.410T>G (p.Leu137Arg)
NM_001007792.1(NTRK1):c.414C>T (p.Gly138=) rs144594313
NM_001007792.1(NTRK1):c.453del (p.Leu153fs) rs1485714154
NM_001007792.1(NTRK1):c.500A>G (p.Lys167Arg)
NM_001007792.1(NTRK1):c.512C>A (p.Pro171His) rs146201511
NM_001007792.1(NTRK1):c.515A>G (p.Asn172Ser) rs1475036463
NM_001007792.1(NTRK1):c.569G>A (p.Arg190Gln) rs540751200
NM_001007792.1(NTRK1):c.585C>T (p.Ala195=) rs1407589933
NM_001007792.1(NTRK1):c.586G>A (p.Gly196Ser)
NM_001007792.1(NTRK1):c.620C>T (p.Thr207Met) rs55909005
NM_001007792.1(NTRK1):c.702G>A (p.Thr234=) rs201110800
NM_001007792.1(NTRK1):c.734A>C (p.Glu245Ala) rs138533001
NM_001007792.1(NTRK1):c.752A>G (p.Asn251Ser) rs547972574
NM_001007792.1(NTRK1):c.754G>A (p.Val252Ile) rs774654606
NM_001007792.1(NTRK1):c.761-33T>A rs80356674
NM_001007792.1(NTRK1):c.775C>A (p.Gln259Lys) rs137979116
NM_001007792.1(NTRK1):c.785C>T (p.Thr262Met) rs764645590
NM_001007792.1(NTRK1):c.788C>T (p.Ala263Val) rs567093941
NM_001007792.1(NTRK1):c.809G>A (p.Cys270Tyr)
NM_001007792.1(NTRK1):c.851G>A (p.Arg284His) rs368769883
NM_001007792.1(NTRK1):c.864T>C (p.Asn288=) rs769539870
NM_001007792.1(NTRK1):c.939C>T (p.His313=) rs772855825
NM_001007792.1(NTRK1):c.989C>T (p.Thr330Met)
NM_001007792.1(NTRK1):c.990G>A (p.Thr330=) rs2274498
NM_002529.4(NTRK1):c.1021G>A (p.Val341Met)
NM_002529.4(NTRK1):c.1114G>T (p.Ala372Ser)
NM_002529.4(NTRK1):c.116C>A (p.Ala39Asp)
NM_002529.4(NTRK1):c.1177+4C>T
NM_002529.4(NTRK1):c.1196-9T>C
NM_002529.4(NTRK1):c.1521C>T (p.Arg507=)
NM_002529.4(NTRK1):c.1569G>A (p.Lys523=)
NM_002529.4(NTRK1):c.1650C>T (p.Ser550=)
NM_002529.4(NTRK1):c.2124C>T (p.Ser708=)
NM_002529.4(NTRK1):c.2205+10G>A
NM_002529.4(NTRK1):c.2301G>A (p.Glu767=)
NM_002529.4(NTRK1):c.254G>T (p.Arg85Leu)
NM_002529.4(NTRK1):c.435G>C (p.Leu145=)
NM_002529.4(NTRK1):c.520A>G (p.Lys174Glu)
NM_002529.4(NTRK1):c.787G>A (p.Val263Met)
NM_002529.4(NTRK1):c.7C>G (p.Arg3Gly)
NM_002529.4(NTRK1):c.956G>A (p.Gly319Asp)

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