ClinVar Miner

Variants in gene NTRK1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 43
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HGVS dbSNP
NM_001007792.1(NTRK1):c.1129G>C (p.Glu377Gln) rs199826686
NM_001007792.1(NTRK1):c.1144-6C>G
NM_001007792.1(NTRK1):c.123-3263G>C rs200815412
NM_001007792.1(NTRK1):c.123-3404C>T rs201472270
NM_001007792.1(NTRK1):c.123-5C>G
NM_001007792.1(NTRK1):c.129C>T (p.Ile43=) rs563296138
NM_001007792.1(NTRK1):c.1365C>T (p.Ile455=) rs373181158
NM_001007792.1(NTRK1):c.1414C>A (p.Arg472=) rs200575096
NM_001007792.1(NTRK1):c.1539G>A (p.Ala513=) rs771010259
NM_001007792.1(NTRK1):c.1670G>A (p.Arg557Gln) rs748133401
NM_001007792.1(NTRK1):c.1697+8C>A rs780424308
NM_001007792.1(NTRK1):c.1809G>A (p.Val603=)
NM_001007792.1(NTRK1):c.189G>A (p.Leu63=) rs147983523
NM_001007792.1(NTRK1):c.1939-8C>T rs769308621
NM_001007792.1(NTRK1):c.198-5C>T
NM_001007792.1(NTRK1):c.2005A>T (p.Thr669Ser) rs200935209
NM_001007792.1(NTRK1):c.2061C>T (p.Tyr687=) rs140852621
NM_001007792.1(NTRK1):c.2106C>T (p.Asp702=)
NM_001007792.1(NTRK1):c.2231G>A (p.Arg744Gln) rs35669708
NM_001007792.1(NTRK1):c.2247C>T (p.Ala749=) rs772156529
NM_001007792.1(NTRK1):c.236A>G (p.Asp79Gly)
NM_001007792.1(NTRK1):c.267C>T (p.Arg89=) rs149960336
NM_001007792.1(NTRK1):c.285C>T (p.Asn95=) rs757803799
NM_001007792.1(NTRK1):c.392G>A (p.Arg131His) rs150271893
NM_001007792.1(NTRK1):c.414C>T (p.Gly138=) rs144594313
NM_001007792.1(NTRK1):c.415G>A (p.Gly139Arg) rs367836863
NM_001007792.1(NTRK1):c.419T>C (p.Val140Ala) rs201503610
NM_001007792.1(NTRK1):c.480C>G (p.Ser160Arg) rs138608619
NM_001007792.1(NTRK1):c.485G>C (p.Gly162Ala) rs201185829
NM_001007792.1(NTRK1):c.495G>A (p.Thr165=) rs182531655
NM_001007792.1(NTRK1):c.540C>T (p.Asp180=) rs147882947
NM_001007792.1(NTRK1):c.568C>T (p.Arg190Trp) rs202030811
NM_001007792.1(NTRK1):c.621G>A (p.Thr207=) rs537430475
NM_001007792.1(NTRK1):c.734A>C (p.Glu245Ala) rs138533001
NM_001007792.1(NTRK1):c.775C>A (p.Gln259Lys) rs137979116
NM_001007792.1(NTRK1):c.864T>C (p.Asn288=) rs769539870
NM_001007792.1(NTRK1):c.915G>A (p.Pro305=)
NM_001007792.1(NTRK1):c.978C>T (p.Asn326=) rs145823996
NM_002529.4(NTRK1):c.1569G>A (p.Lys523=)
NM_002529.4(NTRK1):c.1650C>T (p.Ser550=)
NM_002529.4(NTRK1):c.2124C>T (p.Ser708=)
NM_002529.4(NTRK1):c.2205+10G>A
NM_002529.4(NTRK1):c.2301G>A (p.Glu767=)

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