ClinVar Miner

List of variants in gene NTRK1 reported as likely benign for not provided

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Total variants: 64
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HGVS dbSNP gnomAD frequency
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.1354+179A>C rs151240002 0.01915
NM_002529.4(NTRK1):c.2047-91A>G rs151288310 0.01350
NM_002529.4(NTRK1):c.850+323C>T rs141434673 0.01257
NM_002529.4(NTRK1):c.1178-108C>T rs142804759 0.01022
NM_002529.4(NTRK1):c.575-65A>G rs111622617 0.00987
NM_002529.4(NTRK1):c.53G>A (p.Gly18Glu) rs1007211 0.00957
NM_002529.4(NTRK1):c.1633-40C>T rs141373787 0.00795
NM_002529.4(NTRK1):c.718-79G>A rs145816660 0.00688
NM_002529.4(NTRK1):c.212+107C>T rs73004743 0.00667
NM_002529.4(NTRK1):c.851-37G>A rs74118786 0.00616
NM_002529.4(NTRK1):c.851-91C>T rs79700551 0.00603
NM_002529.4(NTRK1):c.1177+69A>G rs112966253 0.00595
NM_002529.4(NTRK1):c.2272G>A (p.Ala758Thr) rs62640939 0.00591
NM_002529.4(NTRK1):c.429-189C>T rs57172000 0.00582
NM_002529.4(NTRK1):c.2046+170C>T rs146585187 0.00566
NM_002529.4(NTRK1):c.1502-106C>T rs76886455 0.00544
NM_002529.4(NTRK1):c.1632+64A>G rs75311154 0.00540
NM_002529.4(NTRK1):c.1502-96G>A rs74417893 0.00496
NM_002529.4(NTRK1):c.1178-155A>G rs140550074 0.00451
NM_002529.4(NTRK1):c.2339G>A (p.Arg780Gln) rs35669708 0.00406
NM_002529.4(NTRK1):c.717+86G>C rs150452564 0.00397
NM_002529.4(NTRK1):c.212+237G>C rs570187831 0.00266
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.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.865C>A (p.Gln289Lys) rs137979116 0.00118
NM_002529.4(NTRK1):c.212+10C>T rs183517027 0.00108
NM_002529.4(NTRK1):c.1502-24G>A rs184260214 0.00066
NM_002529.4(NTRK1):c.1803C>G (p.Leu601=) rs146129485 0.00042
NM_002529.4(NTRK1):c.*6C>T rs370807813 0.00037
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.851-30C>A rs552893549 0.00028
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.711G>A (p.Thr237=) rs537430475 0.00010
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.117C>T (p.Ala39=) rs746293720 0.00003
NM_002529.4(NTRK1):c.1638G>C (p.Leu546=) rs747000102 0.00003
NM_002529.4(NTRK1):c.2169C>T (p.Tyr723=) rs140852621 0.00002
NM_002529.4(NTRK1):c.549G>T (p.Leu183=) rs756232321 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.2383C>T (p.Leu795=) rs749041981 0.00001
NM_002529.4(NTRK1):c.810T>C (p.Asp270=) rs755895954 0.00001
NM_001007792.1(NTRK1):c.123-3611G>T rs1007210
NM_002529.4(NTRK1):c.1177+31C>T
NM_002529.4(NTRK1):c.1501+32C>G rs191705000
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.718-206dup rs547351773
NM_002529.4(NTRK1):c.851-614GT[17]

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