case class NormalizedConsequences(chromosome: String = "1", start: Long = 69897, end: Long = 69898, reference: String = "T", alternate: String = "C", name: String = "rs200676709", consequences: List[String] = List("synonymous_variant"), impact: String = "LOW", symbol: String = "OR4F5", ensembl_gene_id: String = "ENSG00000186092", ensembl_feature_id: String = "ENST00000335137", ensembl_transcript_id: String = "ENST00000335137", ensembl_regulatory_id: Option[String] = None, feature_type: String = "Transcript", strand: Int = 1, biotype: String = "protein_coding", variant_class: String = "SNV", exon: Exon = Exon(), intron: Intron = Intron(), hgvsc: String = "ENST00000335137.4:c.807T>C", hgvsp: String = "ENSP00000334393.3:p.Ser269=", hgvsg: String = "chr1:g.69897T>C", cds_position: Int = 807, cdna_position: Int = 843, protein_position: Int = 269, amino_acids: AminoAcids = AminoAcids(), codons: CODONS = CODONS(), original_canonical: Boolean = true, refseq_mrna_id: List[String] = ..., aa_change: String = "p.Ser269=", coding_dna_change: String = "c.807T>C", impact_score: Int = 2, created_on: Timestamp = ..., updated_on: Timestamp = ..., normalized_consequences_oid: Timestamp = ...) extends Product with Serializable
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- new NormalizedConsequences(chromosome: String = "1", start: Long = 69897, end: Long = 69898, reference: String = "T", alternate: String = "C", name: String = "rs200676709", consequences: List[String] = List("synonymous_variant"), impact: String = "LOW", symbol: String = "OR4F5", ensembl_gene_id: String = "ENSG00000186092", ensembl_feature_id: String = "ENST00000335137", ensembl_transcript_id: String = "ENST00000335137", ensembl_regulatory_id: Option[String] = None, feature_type: String = "Transcript", strand: Int = 1, biotype: String = "protein_coding", variant_class: String = "SNV", exon: Exon = Exon(), intron: Intron = Intron(), hgvsc: String = "ENST00000335137.4:c.807T>C", hgvsp: String = "ENSP00000334393.3:p.Ser269=", hgvsg: String = "chr1:g.69897T>C", cds_position: Int = 807, cdna_position: Int = 843, protein_position: Int = 269, amino_acids: AminoAcids = AminoAcids(), codons: CODONS = CODONS(), original_canonical: Boolean = true, refseq_mrna_id: List[String] = ..., aa_change: String = "p.Ser269=", coding_dna_change: String = "c.807T>C", impact_score: Int = 2, created_on: Timestamp = ..., updated_on: Timestamp = ..., normalized_consequences_oid: Timestamp = ...)
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- val aa_change: String
- val alternate: String
- val amino_acids: AminoAcids
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- val biotype: String
- val cdna_position: Int
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- val coding_dna_change: String
- val codons: CODONS
- val consequences: List[String]
- val created_on: Timestamp
- val end: Long
- val ensembl_feature_id: String
- val ensembl_gene_id: String
- val ensembl_regulatory_id: Option[String]
- val ensembl_transcript_id: String
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- val exon: Exon
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- val hgvsc: String
- val hgvsg: String
- val hgvsp: String
- val impact: String
- val impact_score: Int
- val intron: Intron
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- val normalized_consequences_oid: Timestamp
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- val original_canonical: Boolean
- val protein_position: Int
- val reference: String
- val refseq_mrna_id: List[String]
- val start: Long
- val strand: Int
- val symbol: String
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- val updated_on: Timestamp
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