ClinVar Miner

Variants in gene DEPDC5 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
281 70 0 8 7 0 8 22

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 0 1 5 2 2
likely pathogenic 1 0 0 0 0
uncertain significance 5 0 0 4 3
likely benign 2 0 4 0 7
benign 2 0 3 7 0

All variants with conflicting interpretations #

Total variants: 22
Download table as spreadsheet
NM_001242896.1(DEPDC5):c.1290C>T (p.Pro430=) rs201202102
NM_001242896.1(DEPDC5):c.1389C>T (p.Asp463=) rs188147862
NM_001242896.1(DEPDC5):c.146+5G>A rs748264035
NM_001242896.1(DEPDC5):c.1909C>T (p.Arg637Ter) rs780960812
NM_001242896.1(DEPDC5):c.2020C>T (p.Arg674Cys) rs181347577
NM_001242896.1(DEPDC5):c.2135C>T (p.Ser712Phe) rs16989535
NM_001242896.1(DEPDC5):c.262A>G (p.Asn88Asp) rs144712084
NM_001242896.1(DEPDC5):c.2672G>C (p.Ser891Thr) rs185576553
NM_001242896.1(DEPDC5):c.3265-3C>T rs371377906
NM_001242896.1(DEPDC5):c.3331-10del rs377356885
NM_001242896.1(DEPDC5):c.3567A>G (p.Thr1189=) rs142197878
NM_001242896.1(DEPDC5):c.3643G>A (p.Val1215Met) rs201603222
NM_001242896.1(DEPDC5):c.3810C>T (p.Ala1270=) rs200033252
NM_001242896.2(DEPDC5):c.1355C>T (p.Ala452Val) rs202226316
NM_001242896.2(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113
NM_001242896.2(DEPDC5):c.2286C>T (p.Asp762=) rs200465447
NM_001242896.2(DEPDC5):c.2591C>T (p.Thr864Met) rs564667614
NM_001242896.2(DEPDC5):c.268G>A (p.Val90Ile) rs768456731
NM_001242896.2(DEPDC5):c.3241A>C (p.Thr1081Pro) rs142540948
NM_001242896.2(DEPDC5):c.3484A>G (p.Ser1162Gly) rs886039280
NM_001242896.2(DEPDC5):c.814G>A (p.Val272Ile) rs187334123
NM_001242896.2(DEPDC5):c.814G>T (p.Val272Leu) rs187334123

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