ClinVar Miner

List of variants in gene NTRK1 reported by Illumina Clinical Services Laboratory,Illumina

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Total variants: 78
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HGVS dbSNP
NM_001007792.1(NTRK1):c.*6C>T rs370807813
NM_001007792.1(NTRK1):c.1128C>T (p.Asp376=) rs147438950
NM_001007792.1(NTRK1):c.1144-15C>G rs186649954
NM_001007792.1(NTRK1):c.1144-6C>G
NM_001007792.1(NTRK1):c.1223G>A (p.Arg408Gln) rs56320207
NM_001007792.1(NTRK1):c.123-3198C>T rs183517027
NM_001007792.1(NTRK1):c.123-3263G>C rs200815412
NM_001007792.1(NTRK1):c.123-3367G>A rs1007211
NM_001007792.1(NTRK1):c.123-3404C>T rs201472270
NM_001007792.1(NTRK1):c.123-5C>G
NM_001007792.1(NTRK1):c.1340G>A (p.Gly447Asp)
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.1538C>T (p.Ala513Val)
NM_001007792.1(NTRK1):c.1566G>A (p.Gln522=) rs6334
NM_001007792.1(NTRK1):c.1609G>A (p.Val537Met)
NM_001007792.1(NTRK1):c.1620C>T (p.Phe540=) rs6335
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.175G>A (p.Gly59Ser)
NM_001007792.1(NTRK1):c.1779C>T (p.Ala593=) rs6337
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.1809G>A (p.Val603=)
NM_001007792.1(NTRK1):c.1887G>A (p.Lys629=) rs553270591
NM_001007792.1(NTRK1):c.189G>A (p.Leu63=) rs147983523
NM_001007792.1(NTRK1):c.1907G>A (p.Ser636Asn) rs1558108205
NM_001007792.1(NTRK1):c.1927G>C (p.Asp643His)
NM_001007792.1(NTRK1):c.1939-8C>T rs769308621
NM_001007792.1(NTRK1):c.1944A>G (p.Gly648=) rs34271945
NM_001007792.1(NTRK1):c.1949G>A (p.Arg650His) rs754452975
NM_001007792.1(NTRK1):c.198-5C>T
NM_001007792.1(NTRK1):c.198-8C>T rs80026148
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.2106C>T (p.Asp702=)
NM_001007792.1(NTRK1):c.2140C>T (p.Arg714Cys)
NM_001007792.1(NTRK1):c.2164G>A (p.Ala722Thr) rs62640939
NM_001007792.1(NTRK1):c.2191G>C (p.Glu731Gln) rs886045373
NM_001007792.1(NTRK1):c.2231G>A (p.Arg744Gln) rs35669708
NM_001007792.1(NTRK1):c.2247C>T (p.Ala749=) rs772156529
NM_001007792.1(NTRK1):c.2263T>C (p.Tyr755His)
NM_001007792.1(NTRK1):c.236A>G (p.Asp79Gly)
NM_001007792.1(NTRK1):c.267C>T (p.Arg89=) rs149960336
NM_001007792.1(NTRK1):c.285C>T (p.Asn95=) rs757803799
NM_001007792.1(NTRK1):c.338+12C>A rs41267425
NM_001007792.1(NTRK1):c.378G>C (p.Leu126=)
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.419T>C (p.Val140Ala) rs201503610
NM_001007792.1(NTRK1):c.480C>G (p.Ser160Arg) rs138608619
NM_001007792.1(NTRK1):c.485G>C (p.Gly162Ala) rs201185829
NM_001007792.1(NTRK1):c.495G>A (p.Thr165=) rs182531655
NM_001007792.1(NTRK1):c.522G>A (p.Ser174=) rs114320051
NM_001007792.1(NTRK1):c.538G>A (p.Asp180Asn)
NM_001007792.1(NTRK1):c.540C>T (p.Asp180=) rs147882947
NM_001007792.1(NTRK1):c.541G>A (p.Val181Met) rs201192875
NM_001007792.1(NTRK1):c.550C>T (p.Arg184Trp) rs372041586
NM_001007792.1(NTRK1):c.551G>A (p.Arg184Gln) rs200132482
NM_001007792.1(NTRK1):c.568C>T (p.Arg190Trp) rs202030811
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.775C>A (p.Gln259Lys) rs137979116
NM_001007792.1(NTRK1):c.915G>A (p.Pro305=)
NM_001007792.1(NTRK1):c.978C>T (p.Asn326=) rs145823996
NM_001007792.1(NTRK1):c.990G>A (p.Thr330=) rs2274498
NM_002529.3(NTRK1):c.*39C>T
NM_002529.3(NTRK1):c.*56C>G rs773036874
NM_002529.3(NTRK1):c.*96G>A rs886045374
NM_002529.3(NTRK1):c.1196-11T>C
NM_002529.3(NTRK1):c.1632+4A>G rs886045372
NM_002529.3(NTRK1):c.2047-11G>A rs79173278
NM_002529.3(NTRK1):c.2205+13C>A
NM_002529.3(NTRK1):c.287+12G>A rs202238126
NM_002529.3(NTRK1):c.575-15G>A
NM_002529.3(NTRK1):c.850+11G>A

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