ClinVar Miner

Variants in gene combination ASTN2, TRIM32 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
110 65 0 6 10 1 3 15

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 association
pathogenic 0 2 1 0 0 0
likely pathogenic 3 0 2 2 1 1
uncertain significance 1 1 0 10 2 0
likely benign 0 1 10 0 3 0
benign 0 0 2 3 0 0

All variants with conflicting interpretations #

Total variants: 15
Download table as spreadsheet
NM_012210.3(TRIM32):c.1108del (p.Met370fs) rs759376012
NM_012210.3(TRIM32):c.1134C>T (p.Tyr378=) rs776448126
NM_012210.3(TRIM32):c.1140C>T (p.Thr380=) rs142715198
NM_012210.3(TRIM32):c.1181G>A (p.Arg394His) rs121434447
NM_012210.3(TRIM32):c.1222C>T (p.Arg408Cys) rs3747835
NM_012210.3(TRIM32):c.1254G>A (p.Val418=) rs1661300
NM_012210.3(TRIM32):c.1326T>A (p.Ile442=) rs1372713940
NM_012210.3(TRIM32):c.1710G>A (p.Ser570=) rs555217187
NM_012210.3(TRIM32):c.201T>C (p.Ile67=) rs780799984
NM_012210.3(TRIM32):c.501G>A (p.Lys167=) rs200085883
NM_012210.3(TRIM32):c.691del (p.Ala231fs) rs747685252
NM_012210.3(TRIM32):c.693A>C (p.Ala231=) rs368455215
NM_012210.3(TRIM32):c.6T>G (p.Ala2=) rs141352486
NM_012210.3(TRIM32):c.770C>G (p.Thr257Arg) rs3747834
Single allele

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