ClinVar Miner

List of variants in gene NTRK2 reported as benign for not provided

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_006180.6(NTRK2):c.1765-125T>C rs1078947 0.81376
NM_006180.6(NTRK2):c.212+117G>A rs1211166 0.77023
NM_006180.6(NTRK2):c.1296+119_1296+123del rs144586764 0.76269
NM_006180.6(NTRK2):c.212+40C>T rs1187326 0.72197
NM_006180.6(NTRK2):c.584-221T>A rs1187362 0.65987
NM_006180.6(NTRK2):c.583+288A>G rs1659400 0.59597
NM_006180.6(NTRK2):c.1296+165G>A rs7048278 0.59050
NM_006180.6(NTRK2):c.*267_*268insC rs35903164 0.53739
NM_006180.6(NTRK2):c.360-219T>C rs1778929 0.50181
NM_006180.6(NTRK2):c.2331+261C>T rs12378021 0.20353
NM_006180.6(NTRK2):c.1937+13G>A rs2289656 0.15606
NM_006180.6(NTRK2):c.1445-306G>A rs10868233 0.11267
NM_006180.6(NTRK2):c.2172+273C>T rs7046509 0.09333
NM_006180.6(NTRK2):c.1938-55C>T rs3739807 0.09328
NM_006180.6(NTRK2):c.1938-194C>T rs3824519 0.09152
NM_006180.6(NTRK2):c.1765-235T>C rs12006041 0.07589
NM_006180.6(NTRK2):c.721-140G>A rs13284421 0.07526
NM_006180.6(NTRK2):c.-372-55A>G rs45554739 0.07238
NM_006180.6(NTRK2):c.1296+114G>A rs41318035 0.06690
NM_006180.6(NTRK2):c.2172+169G>A rs7046578 0.06033
NM_006180.6(NTRK2):c.1765-7T>C rs2289658 0.05083
NM_006180.6(NTRK2):c.1196-318G>A rs113722236 0.02081
NM_006180.6(NTRK2):c.1195+271A>G rs78687658 0.01807
NM_006180.6(NTRK2):c.933C>A (p.Pro311=) rs75615014 0.01035
NM_006180.6(NTRK2):c.2361C>A (p.Val787=) rs144491317 0.00677
NM_006180.6(NTRK2):c.2113C>T (p.Leu705=) rs75380746 0.00617
NM_006180.6(NTRK2):c.288-15T>C rs79043758 0.00366
NM_006180.6(NTRK2):c.2430C>T (p.Pro810=) rs56142442 0.00225
NM_006180.6(NTRK2):c.2478G>A (p.Leu826=) rs138503321 0.00107
NM_006180.6(NTRK2):c.611C>A (p.Pro204His) rs139913267 0.00106
NM_006180.6(NTRK2):c.1941A>T (p.Ala647=) rs61731264 0.00101
NM_006180.6(NTRK2):c.1029C>T (p.His343=) rs147059990 0.00018
NM_006180.6(NTRK2):c.330A>G (p.Ala110=) rs201225877 0.00014
NM_006180.6(NTRK2):c.1071G>C (p.Gly357=) rs138437877 0.00012
NM_006180.6(NTRK2):c.1288C>T (p.His430Tyr) rs145968424 0.00010
NM_006180.6(NTRK2):c.1260A>G (p.Thr420=) rs55939150 0.00009
NM_006180.6(NTRK2):c.746C>A (p.Ser249Tyr) rs772111782 0.00006
NM_006180.6(NTRK2):c.1160-9G>A rs201490399 0.00001
NM_006180.6(NTRK2):c.-69C>G rs1187325
NM_006180.6(NTRK2):c.1396+10del rs781678424
NM_006180.6(NTRK2):c.1397-148TTTA[8] rs143811359
NM_006180.6(NTRK2):c.1397-49532A>G
NM_006180.6(NTRK2):c.1765-4C>A rs200663989
NM_006180.6(NTRK2):c.1848C>A (p.Ile616=) rs2289657
NM_006180.6(NTRK2):c.1979C>T (p.Pro660Leu)
NM_006180.6(NTRK2):c.213-206A>T rs1187336
NM_006180.6(NTRK2):c.2173-2799T>C
NM_006180.6(NTRK2):c.2173-3del rs1442849861

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