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 Variants with at least 2 submissions 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 kind of conflict
163 22 3 18 17 0 7 42

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 4 2 2
likely pathogenic 1 0 1 0 0
uncertain significance 4 1 0 12 6
likely benign 2 0 12 0 17
benign 2 0 6 17 0

All variants with conflicting interpretations #

Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_001007792.1(NTRK1):c.1730G>T (p.Gly577Val) rs6339
NM_001012331.1(NTRK1):c.1076A>G (p.Tyr359Cys) rs121964869
NM_001012331.1(NTRK1):c.1080G>A (p.Thr360=) rs2274498
NM_001012331.1(NTRK1):c.10G>A (p.Gly4Ser) rs556840308
NM_001012331.1(NTRK1):c.1178-179C>T rs199646180
NM_001012331.1(NTRK1):c.1218C>T (p.Asp406=) rs147438950
NM_001012331.1(NTRK1):c.1234-15C>G rs186649954
NM_001012331.1(NTRK1):c.1313G>A (p.Arg438Gln) rs56320207
NM_001012331.1(NTRK1):c.1504C>A (p.Arg502=) rs200575096
NM_001012331.1(NTRK1):c.157G>C (p.Asp53His) rs200815412
NM_001012331.1(NTRK1):c.16C>T (p.Arg6Trp) rs201472270
NM_001012331.1(NTRK1):c.1710C>T (p.Phe570=) rs6335
NM_001012331.1(NTRK1):c.1786C>T (p.Arg596Ter)
NM_001012331.1(NTRK1):c.1788-4delA rs1799770
NM_001012331.1(NTRK1):c.1842C>T (p.Gly614=) rs6338
NM_001012331.1(NTRK1):c.1869C>T (p.Ala623=) rs6337
NM_001012331.1(NTRK1):c.1890G>A (p.Ala630=) rs17838192
NM_001012331.1(NTRK1):c.2028+3A>C
NM_001012331.1(NTRK1):c.2029-6T>C rs762866535
NM_001012331.1(NTRK1):c.2034A>G (p.Gly678=) rs34271945
NM_001012331.1(NTRK1):c.212+10C>T rs183517027
NM_001012331.1(NTRK1):c.2151C>T (p.Tyr717=) rs140852621
NM_001012331.1(NTRK1):c.2184G>A (p.Thr728=) rs55668752
NM_001012331.1(NTRK1):c.2254G>A (p.Ala752Thr) rs62640939
NM_001012331.1(NTRK1):c.2321G>A (p.Arg774Gln) rs35669708
NM_001012331.1(NTRK1):c.253C>A (p.Arg85Ser)
NM_001012331.1(NTRK1):c.254G>A (p.Arg85His) rs79678945
NM_001012331.1(NTRK1):c.288-8C>T rs80026148
NM_001012331.1(NTRK1):c.428+12C>A rs41267425
NM_001012331.1(NTRK1):c.505G>A (p.Gly169Arg) rs367836863
NM_001012331.1(NTRK1):c.53G>A (p.Gly18Glu) rs1007211
NM_001012331.1(NTRK1):c.570C>G (p.Ser190Arg) rs138608619
NM_001012331.1(NTRK1):c.612G>A (p.Ser204=) rs114320051
NM_001012331.1(NTRK1):c.638T>C (p.Leu213Pro) rs747711259
NM_001012331.1(NTRK1):c.710C>T (p.Thr237Met) rs55909005
NM_001012331.1(NTRK1):c.865C>A (p.Gln289Lys) rs137979116
NM_001012331.1(NTRK1):c.940C>T (p.Arg314Cys) rs137994522
NM_002529.3(NTRK1):c.1660delC (p.Arg554Glyfs) rs80356675
NM_002529.3(NTRK1):c.1810C>T (p.His604Tyr) rs6336
NM_002529.3(NTRK1):c.1860_1861insT (p.Pro621Serfs) rs80356676
NM_002529.3(NTRK1):c.2281C>T (p.Arg761Trp) rs759637817
NM_002529.3(NTRK1):c.851-33T>A rs80356674

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