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Merge pull request #1599 from griffithlab/Add-Evidence-Tooltips
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Add Evidence Form tool tip modifications
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kkrysiak authored Mar 5, 2021
2 parents 3dc9934 + 5ec25a6 commit 4868188
Showing 1 changed file with 5 additions and 5 deletions.
10 changes: 5 additions & 5 deletions src/components/services/ConfigService.js
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'Does Not Support': 'The experiment or study does not support a prognostic association between variant and outcome'
},
'Predisposing': {
'N/A': 'Evidence Direction is Not Applicable for Predisposing Evidence Type.'
'N/A': 'Evidence Direction is Not Applicable.'
},
'Functional': {
'Supports': 'The experiment or study supports this variant causing alteration or non-alteration of the gene product function',
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'N/A': 'Clinical Significance is Not Applicable for Predisposing Evidence Type'
},
'Functional': {
'Gain of Function': 'Sequence variant conferrs a new or enhanced function',
'Loss of Function': 'Sequence variant conferrs a diminished or abolished function',
'Gain of Function': 'Sequence variant confers an increase in normal gene function',
'Loss of Function': 'Sequence variant confers a diminished or abolished function',
'Unaltered Function': 'Gene product of sequence variant is unchanged',
'Neomorphic': 'Sequence variant creates a novel function',
'Dominant Negative': 'Seuqnce variant abolishes wild type allele function',
'Unknown': 'Sequence variant that cannot be precisely defined the other listed categories',
'Dominant Negative': 'Sequence variant abrogates function of wildtype allele gene product',
'Unknown': 'Sequence variant that cannot be precisely defined by the other listed categories',
},
'Oncogenic': {
'N/A': 'Clinical Significance is Not Applicable for Oncogenic Evidence Type'
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