ClinVar Miner

List of variants in gene NTRK1 studied for not specified

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_002529.4(NTRK1):c.1887C>T (p.Ala629=) rs6337 0.53946
NM_002529.4(NTRK1):c.1674G>A (p.Gln558=) rs6334 0.19892
NM_002529.4(NTRK1):c.2047-16T>C rs12076232 0.10434
NM_002529.4(NTRK1):c.1838G>T (p.Gly613Val) rs6339 0.03698
NM_002529.4(NTRK1):c.1810C>T (p.His604Tyr) rs6336 0.03696
NM_002529.4(NTRK1):c.1860C>T (p.Gly620=) rs6338 0.03397
NM_002529.4(NTRK1):c.2052A>G (p.Gly684=) rs34271945 0.03311
NM_002529.4(NTRK1):c.710C>T (p.Thr237Met) rs55909005 0.01791
NM_002529.4(NTRK1):c.1331G>A (p.Arg444Gln) rs56320207 0.01010
NM_002529.4(NTRK1):c.53G>A (p.Gly18Glu) rs1007211 0.00957
NM_002529.4(NTRK1):c.288-8C>T rs80026148 0.00947
NM_002529.4(NTRK1):c.2202G>A (p.Thr734=) rs55668752 0.00562
NM_002529.4(NTRK1):c.2339G>A (p.Arg780Gln) rs35669708 0.00406
NM_002529.4(NTRK1):c.428+12C>A rs41267425 0.00357
NM_002529.4(NTRK1):c.1236C>T (p.Asp412=) rs147438950 0.00289
NM_002529.4(NTRK1):c.612G>A (p.Ser204=) rs114320051 0.00251
NM_002529.4(NTRK1):c.254G>A (p.Arg85His) rs79678945 0.00220
NM_002529.4(NTRK1):c.*7G>T rs145060242 0.00210
NM_002529.4(NTRK1):c.865C>A (p.Gln289Lys) rs137979116 0.00118
NM_002529.4(NTRK1):c.212+10C>T rs183517027 0.00108
NM_002529.4(NTRK1):c.1252-15C>G rs186649954 0.00049
NM_002529.4(NTRK1):c.1474G>A (p.Glu492Lys) rs144901788 0.00040
NM_002529.4(NTRK1):c.1068C>T (p.Asn356=) rs145823996 0.00029
NM_002529.4(NTRK1):c.574+10G>A rs201336491 0.00026
NM_002529.4(NTRK1):c.927G>A (p.Pro309=) rs144015813 0.00018
NM_002529.4(NTRK1):c.1747C>T (p.Arg583Cys) rs371344688 0.00013
NM_002529.4(NTRK1):c.1257G>A (p.Ser419=) rs750968694 0.00012
NM_002529.4(NTRK1):c.279G>A (p.Leu93=) rs147983523 0.00011
NM_002529.4(NTRK1):c.575-16C>T rs143312136 0.00009
NM_002529.4(NTRK1):c.2057G>A (p.Arg686His) rs754452975 0.00008
NM_002529.4(NTRK1):c.1522C>A (p.Arg508=) rs200575096 0.00006
NM_001007792.1(NTRK1):c.163C>A (p.Arg55Ser) rs543320028 0.00004
NM_002529.4(NTRK1):c.117C>T (p.Ala39=) rs746293720 0.00003
NM_002529.4(NTRK1):c.1354+8G>A rs763576316 0.00003
NM_002529.4(NTRK1):c.2169C>T (p.Tyr723=) rs140852621 0.00002
NM_002529.4(NTRK1):c.2368G>A (p.Val790Ile) rs55948542 0.00002
NM_002529.4(NTRK1):c.531T>C (p.Cys177=) rs1057523619 0.00002
NM_002529.4(NTRK1):c.2047-6T>C rs762866535 0.00001
NM_002529.4(NTRK1):c.2067G>A (p.Leu689=) rs1057521447 0.00001
NM_002529.4(NTRK1):c.647A>G (p.Gln216Arg) rs1471711796 0.00001
NM_002529.4(NTRK1):c.718-15T>C rs778745696 0.00001
NM_002529.4(NTRK1):c.1077C>T (p.Tyr359=) rs1057521034
NM_002529.4(NTRK1):c.1579G>C (p.Ala527Pro)
NM_002529.4(NTRK1):c.291C>T (p.Thr97=) rs1057522997
NM_002529.4(NTRK1):c.321G>T (p.Ala107=) rs774351278
NM_002529.4(NTRK1):c.428+12C>T rs41267425
NM_002529.4(NTRK1):c.571T>C (p.Cys191Arg) rs1026300967

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