ClinVar Miner

List of variants in gene NTRK1 reported as uncertain significance for not provided

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_002529.4(NTRK1):c.157G>C (p.Asp53His) rs200815412 0.00187
NM_002529.4(NTRK1):c.865C>A (p.Gln289Lys) rs137979116 0.00118
NM_002529.4(NTRK1):c.1320C>G (p.Asn440Lys) rs147443162 0.00050
NM_002529.4(NTRK1):c.1803C>G (p.Leu601=) rs146129485 0.00042
NM_002529.4(NTRK1):c.1474G>A (p.Glu492Lys) rs144901788 0.00040
NM_002529.4(NTRK1):c.*6C>T rs370807813 0.00037
NM_002529.4(NTRK1):c.482G>A (p.Arg161His) rs150271893 0.00031
NM_002529.4(NTRK1):c.295G>A (p.Val99Met) rs201509045 0.00029
NM_002529.4(NTRK1):c.940C>T (p.Arg314Cys) rs137994522 0.00027
NM_002529.4(NTRK1):c.641G>A (p.Arg214Gln) rs200132482 0.00023
NM_002529.4(NTRK1):c.631G>A (p.Val211Met) rs201192875 0.00017
NM_002529.4(NTRK1):c.1661G>A (p.Arg554Gln) rs764417252 0.00013
NM_002529.4(NTRK1):c.1747C>T (p.Arg583Cys) rs371344688 0.00013
NM_002529.4(NTRK1):c.570C>G (p.Ser190Arg) rs138608619 0.00013
NM_002529.4(NTRK1):c.1808C>G (p.Ser603Cys) rs188270548 0.00011
NM_002529.4(NTRK1):c.1354C>T (p.Arg452Cys) rs34900547 0.00010
NM_002529.4(NTRK1):c.1741G>A (p.Glu581Lys) rs150579345 0.00010
NM_002529.4(NTRK1):c.185T>C (p.Leu62Pro) rs766307207 0.00010
NM_002529.4(NTRK1):c.1187C>T (p.Ser396Leu) rs199646180 0.00009
NM_002529.4(NTRK1):c.2057G>A (p.Arg686His) rs754452975 0.00008
NM_002529.4(NTRK1):c.509T>C (p.Val170Ala) rs201503610 0.00008
NM_002529.4(NTRK1):c.2231G>A (p.Arg744His) rs751281792 0.00006
NM_002529.4(NTRK1):c.470G>A (p.Arg157His) rs141021604 0.00006
NM_002529.4(NTRK1):c.1939G>T (p.Val647Leu) rs142870382 0.00005
NM_002529.4(NTRK1):c.2222C>T (p.Thr741Met) rs145081333 0.00004
NM_002529.4(NTRK1):c.2282G>A (p.Arg761Gln) rs201891311 0.00004
NM_002529.4(NTRK1):c.2242C>T (p.Arg748Trp) rs778520978 0.00003
NM_002529.4(NTRK1):c.808G>A (p.Asp270Asn) rs145222195 0.00003
NM_002529.4(NTRK1):c.1037T>C (p.Leu346Pro) rs150651692 0.00002
NM_002529.4(NTRK1):c.1888G>A (p.Val630Met) rs1405634315 0.00002
NM_002529.4(NTRK1):c.941G>A (p.Arg314His) rs368769883 0.00002
NM_002529.4(NTRK1):c.1276G>A (p.Val426Ile) rs986498490 0.00001
NM_002529.4(NTRK1):c.1424C>G (p.Ser475Cys) rs756402401 0.00001
NM_002529.4(NTRK1):c.1528A>T (p.Ile510Phe) rs781478411 0.00001
NM_002529.4(NTRK1):c.1717G>A (p.Val573Met) rs755016431 0.00001
NM_002529.4(NTRK1):c.1925C>T (p.Ala642Val) rs920692665 0.00001
NM_002529.4(NTRK1):c.2013G>A (p.Met671Ile) rs1236732726 0.00001
NM_002529.4(NTRK1):c.215A>G (p.Tyr72Cys) rs758965412 0.00001
NM_002529.4(NTRK1):c.2296C>T (p.Arg766Trp) rs760974854 0.00001
NM_002529.4(NTRK1):c.311G>A (p.Arg104His) rs578095133 0.00001
NM_002529.4(NTRK1):c.817C>T (p.Arg273Trp) rs151334385 0.00001
NM_002529.4(NTRK1):c.842A>G (p.Asn281Ser) rs547972574 0.00001
NM_002529.4(NTRK1):c.878C>T (p.Ala293Val) rs567093941 0.00001
NM_002529.4(NTRK1):c.97G>T (p.Ala33Ser) rs777913530 0.00001
NM_002529.4(NTRK1):c.1040_1041delinsCT (p.Arg347Pro)
NM_002529.4(NTRK1):c.1203C>A (p.Asn401Lys)
NM_002529.4(NTRK1):c.130G>A (p.Gly44Ser)
NM_002529.4(NTRK1):c.1593C>A (p.Asn531Lys)
NM_002529.4(NTRK1):c.1714A>G (p.Ile572Val)
NM_002529.4(NTRK1):c.1721G>A (p.Arg574His)
NM_002529.4(NTRK1):c.1748G>A (p.Arg583His) rs762542314
NM_002529.4(NTRK1):c.2023A>G (p.Ile675Val)
NM_002529.4(NTRK1):c.2141G>A (p.Gly714Asp) rs944740609
NM_002529.4(NTRK1):c.2243G>T (p.Arg748Leu)
NM_002529.4(NTRK1):c.2319C>T (p.Ser773=)
NM_002529.4(NTRK1):c.410G>A (p.Gly137Asp)
NM_002529.4(NTRK1):c.429-3del rs766806139
NM_002529.4(NTRK1):c.496G>A (p.Gly166Arg)
NM_002529.4(NTRK1):c.514G>A (p.Glu172Lys) rs267598081
NM_002529.4(NTRK1):c.560C>T (p.Pro187Leu) rs879253918
NM_002529.4(NTRK1):c.662G>A (p.Gly221Asp) rs369478563
NM_002529.4(NTRK1):c.787G>C (p.Val263Leu) rs201509717
NM_002529.4(NTRK1):c.92C>T (p.Ala31Val) rs756222046
NM_002529.4(NTRK1):c.961G>A (p.Val321Met)

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