ClinVar Miner

Variants in gene DCTN1 with conflicting interpretations

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
175 49 5 13 7 2 2 24

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 uncertain significance likely benign benign risk factor
pathogenic 4 2 0 0 0
uncertain significance 2 0 7 2 2
likely benign 0 7 0 13 1
benign 0 2 13 1 1
risk factor 0 2 1 1 0

All variants with conflicting interpretations #

Total variants: 24
Download table as spreadsheet
HGVS dbSNP
NM_004082.4(DCTN1):c.1288-3C>T rs72466490
NM_004082.4(DCTN1):c.1484G>A (p.Arg495Gln) rs17721059
NM_004082.4(DCTN1):c.167A>G (p.Lys56Arg) rs566433112
NM_004082.4(DCTN1):c.175G>A (p.Gly59Ser) rs121909342
NM_004082.4(DCTN1):c.211G>A (p.Gly71Arg) rs72466485
NM_004082.4(DCTN1):c.212G>A (p.Gly71Glu) rs67586389
NM_004082.4(DCTN1):c.2213A>G (p.Gln738Arg) rs143800457
NM_004082.4(DCTN1):c.221A>C (p.Gln74Pro) rs72466487
NM_004082.4(DCTN1):c.2278A>G (p.Met760Val) rs754780894
NM_004082.4(DCTN1):c.2353C>T (p.Arg785Trp) rs121909344
NM_004082.4(DCTN1):c.2448A>G (p.Ala816=) rs1130484
NM_004082.4(DCTN1):c.34-11G>T rs73948789
NM_004082.4(DCTN1):c.3490A>G (p.Thr1164Ala) rs72466493
NM_004082.4(DCTN1):c.3498G>A (p.Thr1166=) rs142030960
NM_004082.4(DCTN1):c.3519C>T (p.Arg1173=) rs146094433
NM_004082.4(DCTN1):c.3529+5G>A rs72466494
NM_004082.4(DCTN1):c.3594C>T (p.Thr1198=) rs115689748
NM_004082.4(DCTN1):c.3746C>T (p.Thr1249Ile) rs72466496
NM_004082.4(DCTN1):c.3782G>A (p.Arg1261Gln) rs553822174
NM_004082.4(DCTN1):c.442C>T (p.Arg148Trp) rs148810193
NM_004082.4(DCTN1):c.586A>G (p.Ile196Val) rs55862001
NM_004082.4(DCTN1):c.60G>A (p.Ala20=) rs150204862
NM_004082.4(DCTN1):c.837G>A (p.Ala279=) rs72466489
NM_004082.4(DCTN1):c.999C>G (p.Asp333Glu) rs200952455

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