ClinVar Miner

List of variants in gene NTRK1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_002529.4(NTRK1):c.1178-155A>G rs140550074 0.00451
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.1803C>G (p.Leu601=) rs146129485 0.00042
NM_002529.4(NTRK1):c.505G>A (p.Gly169Arg) rs367836863 0.00030
NM_002529.4(NTRK1):c.1068C>T (p.Asn356=) rs145823996 0.00029
NM_002529.4(NTRK1):c.575G>C (p.Gly192Ala) rs201185829 0.00027
NM_002529.4(NTRK1):c.630C>T (p.Asp210=) rs147882947 0.00021
NM_002529.4(NTRK1):c.279G>A (p.Leu93=) rs147983523 0.00011
NM_002529.4(NTRK1):c.1101C>T (p.Phe367=) rs534972681 0.00009
NM_002529.4(NTRK1):c.659G>A (p.Arg220Gln) rs540751200 0.00009
NM_002529.4(NTRK1):c.2229A>C (p.Gly743=) rs756505247 0.00007
NM_002529.4(NTRK1):c.585G>A (p.Thr195=) rs182531655 0.00007
NM_002529.4(NTRK1):c.1557C>T (p.Gly519=) rs564775946 0.00005
NM_002529.4(NTRK1):c.2169C>T (p.Tyr723=) rs140852621 0.00002
NM_002529.4(NTRK1):c.1005G>A (p.Pro335=) rs780334454 0.00001
NM_002529.4(NTRK1):c.1302G>A (p.Thr434=) rs767104704 0.00001
NM_002529.4(NTRK1):c.810T>C (p.Asp270=) rs755895954 0.00001
NM_002529.4(NTRK1):c.1177+31C>T
NM_002529.4(NTRK1):c.2232T>G (p.Arg744=)
NM_002529.4(NTRK1):c.429-452C>A
NM_002529.4(NTRK1):c.435G>A (p.Leu145=)
NM_002529.4(NTRK1):c.588G>A (p.Leu196=) rs971243513
NM_002529.4(NTRK1):c.717+373_717+397del
NM_002529.4(NTRK1):c.851-614GT[17]

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