import React from 'react' import { vi, describe, it, expect } from 'vitest' import { render } from '@testing-library/react' import { ThemeProvider } from '@mui/material' import { createJBrowseTheme } from '@jbrowse/core/ui/theme' import { GDCExtraPanel } from './GDCFeatureWidget' describe('GDCTrack widget', () => { it('renders mutation extra panel', () => { console.warn = vi.fn() const feature = { uniqueId: '0208efeb-f1e8-57e4-8447-299c5f050380', refName: 'chr3', type: 'Simple Somatic Mutation', start: 377917, end: 377918, chromosome: 'chr3', ssmId: '0208efeb-f1e8-57e4-8447-299c5f050380', consequence: { hits: { edges: [ { node: { id: 'U1NNQ29uc2VxdWVuY2U6MDIwOGVmZWItZjFlOC01N2U0LTg0NDctMjk5YzVmMDUwMzgwOjZkYmQ5M2M2LWYwZWYtNTdhZS1iZmQxLWYxM2RlNmM5ZWI0Ng==', transcript: { aa_change: 'D618N', annotation: { hgvsc: 'c.1852G>A', polyphen_impact: 'benign', polyphen_score: 0.008, sift_impact: 'tolerated', sift_score: 0.08, vep_impact: 'MODERATE', }, consequence_type: 'missense_variant', gene: { gene_id: 'ENSG00000134121', gene_strand: 1, symbol: 'CHL1', }, is_canonical: false, transcript_id: 'ENST00000620033', }, }, }, ], }, }, cosmicId: ['COSM1044638'], genomicDnaChange: 'chr3:g.377918G>A', } const { container } = render( , ) expect(container.firstChild).toMatchSnapshot() }) it('renders gene extra panel', () => { console.warn = vi.fn() const feature = { uniqueId: 'ENSG00000134121', refName: '3', type: 'protein_coding', start: 196595, end: 409417, geneId: 'ENSG00000134121', canonicalTranscriptId: 'ENST00000256509', externalDbIds: { entrezGene: ['10752'], hgnc: ['HGNC:1939'], omimGene: ['607416'], uniprotkbSwissprot: ['O00533'], }, symbol: 'CHL1', } const { container } = render( , ) expect(container.firstChild).toMatchSnapshot() }) })