ClinVar Miner

Variants in gene NTRK1 with conflicting interpretations

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Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
434 74 3 14 46 0 2 60

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 3 1 0 0 0
likely pathogenic 1 0 2 0 0
uncertain significance 0 2 0 40 9
likely benign 0 0 40 0 13
benign 0 0 9 13 0

All variants with conflicting interpretations #

Total variants: 60
Download table as spreadsheet
HGVS dbSNP
NM_001007792.1(NTRK1):c.1128C>T (p.Asp376=) rs147438950
NM_001007792.1(NTRK1):c.1129G>C (p.Glu377Gln) rs199826686
NM_001007792.1(NTRK1):c.1144-6C>G
NM_001007792.1(NTRK1):c.123-3198C>T rs183517027
NM_001007792.1(NTRK1):c.123-3263G>C rs200815412
NM_001007792.1(NTRK1):c.123-3367G>A rs1007211
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.1489C>T (p.Leu497=) rs760564817
NM_001007792.1(NTRK1):c.1539G>A (p.Ala513=) rs771010259
NM_001007792.1(NTRK1):c.1552del (p.Arg518fs) rs80356675
NM_001007792.1(NTRK1):c.163C>A (p.Arg55Ser) rs543320028
NM_001007792.1(NTRK1):c.164G>A (p.Arg55His) rs79678945
NM_001007792.1(NTRK1):c.1670G>A (p.Arg557Gln) rs748133401
NM_001007792.1(NTRK1):c.1697+8C>A rs780424308
NM_001007792.1(NTRK1):c.1698-4del rs1799770
NM_001007792.1(NTRK1):c.1702C>T (p.His568Tyr) rs6336
NM_001007792.1(NTRK1):c.1730G>T (p.Gly577Val) rs6339
NM_001007792.1(NTRK1):c.1752_1753insT (p.Pro585fs) rs80356676
NM_001007792.1(NTRK1):c.1779C>T (p.Ala593=) rs6337
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.1809G>A (p.Val603=)
NM_001007792.1(NTRK1):c.1887G>A (p.Lys629=) rs553270591
NM_001007792.1(NTRK1):c.189G>A (p.Leu63=) rs147983523
NM_001007792.1(NTRK1):c.1939-8C>T rs769308621
NM_001007792.1(NTRK1):c.1976C>T (p.Pro659Leu) rs121964868
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.2164G>A (p.Ala722Thr) rs62640939
NM_001007792.1(NTRK1):c.2173C>T (p.Arg725Trp) rs759637817
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.267C>T (p.Arg89=) rs149960336
NM_001007792.1(NTRK1):c.285C>T (p.Asn95=) rs757803799
NM_001007792.1(NTRK1):c.338+12C>A rs41267425
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.522G>A (p.Ser174=) rs114320051
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.761-33T>A rs80356674
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

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