ClinVar Miner

List of variants in gene NTRK1 reported as benign by Invitae

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Total variants: 38
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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.1806-4del rs1799770 0.06316
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.2047-11G>A rs79173278 0.01269
NM_002529.4(NTRK1):c.1331G>A (p.Arg444Gln) rs56320207 0.01010
NM_002529.4(NTRK1):c.288-8C>T rs80026148 0.00947
NM_002529.4(NTRK1):c.2272G>A (p.Ala758Thr) rs62640939 0.00591
NM_002529.4(NTRK1):c.1728C>T (p.Phe576=) rs6335 0.00563
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.1908G>A (p.Ala636=) rs17838192 0.00198
NM_002529.4(NTRK1):c.157G>C (p.Asp53His) rs200815412 0.00187
NM_002529.4(NTRK1):c.1354+18A>T rs73004759 0.00164
NM_002529.4(NTRK1):c.287+12G>A rs202238126 0.00138
NM_002529.4(NTRK1):c.212+10C>T rs183517027 0.00108
NM_002529.4(NTRK1):c.1080G>A (p.Thr360=) rs2274498 0.00095
NM_002529.4(NTRK1):c.1252-15C>G rs186649954 0.00049
NM_002529.4(NTRK1):c.1803C>G (p.Leu601=) rs146129485 0.00042
NM_002529.4(NTRK1):c.428+19A>G rs192153341 0.00024
NM_002529.4(NTRK1):c.1257G>A (p.Ser419=) rs750968694 0.00012
NM_002529.4(NTRK1):c.1149C>T (p.Phe383=) rs776605207 0.00005
NM_002529.4(NTRK1):c.1597C>T (p.Leu533=) rs760564817 0.00001
NM_002529.4(NTRK1):c.1632+21dup
NM_002529.4(NTRK1):c.1806-11C>G
NM_002529.4(NTRK1):c.1806-12dup
NM_002529.4(NTRK1):c.1995G>A (p.Lys665=) rs553270591
NM_002529.4(NTRK1):c.428+11dup
NM_002529.4(NTRK1):c.429-16C>T
NM_002529.4(NTRK1):c.429-3dup rs766806139

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