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
383 28 2 12 24 0 1 35

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 2 1 0 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 0 1 0 19 7
likely benign 0 0 19 0 11
benign 0 0 7 11 0

All variants with conflicting interpretations #

Total variants: 35
Download table as spreadsheet
HGVS dbSNP
NM_002529.3(NTRK1):c.1068C>T (p.Asn356=) rs145823996
NM_002529.3(NTRK1):c.1236C>T (p.Asp412=) rs147438950
NM_002529.3(NTRK1):c.1522C>A (p.Arg508=) rs200575096
NM_002529.3(NTRK1):c.157G>C (p.Asp53His) rs200815412
NM_002529.3(NTRK1):c.1660del (p.Arg554fs) rs80356675
NM_002529.3(NTRK1):c.16C>T (p.Arg6Trp) rs201472270
NM_002529.3(NTRK1):c.1810C>T (p.His604Tyr) rs6336
NM_002529.3(NTRK1):c.1838G>T (p.Gly613Val) rs6339
NM_002529.3(NTRK1):c.1887C>T (p.Ala629=) rs6337
NM_002529.3(NTRK1):c.1908G>A (p.Ala636=) rs17838192
NM_002529.3(NTRK1):c.1995G>A (p.Lys665=) rs553270591
NM_002529.3(NTRK1):c.2047-8C>T rs769308621
NM_002529.3(NTRK1):c.2084C>T (p.Pro695Leu) rs121964868
NM_002529.3(NTRK1):c.212+10C>T rs183517027
NM_002529.3(NTRK1):c.2169C>T (p.Tyr723=) rs140852621
NM_002529.3(NTRK1):c.2272G>A (p.Ala758Thr) rs62640939
NM_002529.3(NTRK1):c.2281C>T (p.Arg761Trp) rs759637817
NM_002529.3(NTRK1):c.2339G>A (p.Arg780Gln) rs35669708
NM_002529.3(NTRK1):c.2355C>T (p.Ala785=) rs772156529
NM_002529.3(NTRK1):c.254G>A (p.Arg85His) rs79678945
NM_002529.3(NTRK1):c.279G>A (p.Leu93=) rs147983523
NM_002529.3(NTRK1):c.357C>T (p.Arg119=) rs149960336
NM_002529.3(NTRK1):c.375C>T (p.Asn125=) rs757803799
NM_002529.3(NTRK1):c.482G>A (p.Arg161His) rs150271893
NM_002529.3(NTRK1):c.509T>C (p.Val170Ala) rs201503610
NM_002529.3(NTRK1):c.53G>A (p.Gly18Glu) rs1007211
NM_002529.3(NTRK1):c.570C>G (p.Ser190Arg) rs138608619
NM_002529.3(NTRK1):c.575G>C (p.Gly192Ala) rs201185829
NM_002529.3(NTRK1):c.585G>A (p.Thr195=) rs182531655
NM_002529.3(NTRK1):c.612G>A (p.Ser204=) rs114320051
NM_002529.3(NTRK1):c.630C>T (p.Asp210=) rs147882947
NM_002529.3(NTRK1):c.658C>T (p.Arg220Trp) rs202030811
NM_002529.3(NTRK1):c.711G>A (p.Thr237=) rs537430475
NM_002529.3(NTRK1):c.851-33T>A rs80356674
NM_002529.3(NTRK1):c.865C>A (p.Gln289Lys) rs137979116

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