case class InfoCSQ(Allele: String = "C", Consequence: List[String] = List("synonymous_variant"), IMPACT: String = "LOW", SYMBOL: String = "OR4F5", Gene: String = "ENSG00000186092", Feature_type: String = "Transcript", Feature: String = "ENST00000335137", BIOTYPE: String = "protein_coding", EXON: Exon = Exon("1", 1), INTRON: Intron = Intron(None, None), HGVSc: String = "ENST00000335137.4:c.807T>C", HGVSp: String = "ENSP00000334393.3:p.Ser269%3D", cDNA_position: Int = 843, CDS_position: Int = 807, Protein_position: Int = 269, Amino_acids: AminoAcids = AminoAcids("S", None), Codons: CODONS = CODONS("tcT", "tcC"), Existing_variation: List[String] = List("rs200676709"), DISTANCE: Option[Int] = None, STRAND: Int = 1, FLAGS: Option[List[String]] = None, PICK: String = "1", VARIANT_CLASS: String = "SNV", SYMBOL_SOURCE: String = "HGNC", HGNC_ID: String = "HGNC:14825", CANONICAL: String = "YES", RefSeq: String = ..., HGVS_OFFSET: Option[String] = None, HGVSg: String = "chr1:g.69897T>C", CLIN_SIG: Option[String] = None, SOMATIC: Option[String] = None, PHENO: Option[String] = None, PUBMED: Option[String] = Some("29135816"), CADD_raw_rankscore: Option[String] = None, DANN_rankscore: Option[String] = None, Ensembl_geneid: Option[String] = None, Ensembl_transcriptid: Option[String] = None, ExAC_AC: Option[String] = None, ExAC_AF: Option[String] = None, FATHMM_converted_rankscore: Option[String] = None, FATHMM_pred: Option[String] = None, GTEx_V7_tissue: Option[String] = None, Interpro_domain: Option[String] = None, LRT_converted_rankscore: Option[String] = None, LRT_pred: Option[String] = None, Polyphen2_HVAR_pred: Option[String] = None, Polyphen2_HVAR_rankscore: Option[String] = None, REVEL_rankscore: Option[String] = None, SIFT_converted_rankscore: Option[String] = None, SIFT_pred: Option[String] = None, UK10K_AC: Option[String] = None, UK10K_AF: Option[String] = None, clinvar_MedGen_id: Option[String] = None, clinvar_OMIM_id: Option[String] = None, clinvar_Orphanet_id: Option[String] = None, clinvar_clnsig: Option[String] = None, clinvar_id: Option[String] = None, clinvar_trait: Option[String] = None, gnomAD_exomes_AC: Option[String] = None, gnomAD_exomes_AF: Option[String] = None, gnomAD_genomes_AC: Option[String] = None, gnomAD_genomes_AF: Option[String] = None, phyloP17way_primate_rankscore: Option[String] = None, rs_dbSNP151: Option[String] = None) extends Product with Serializable
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Instance Constructors
- new InfoCSQ(Allele: String = "C", Consequence: List[String] = List("synonymous_variant"), IMPACT: String = "LOW", SYMBOL: String = "OR4F5", Gene: String = "ENSG00000186092", Feature_type: String = "Transcript", Feature: String = "ENST00000335137", BIOTYPE: String = "protein_coding", EXON: Exon = Exon("1", 1), INTRON: Intron = Intron(None, None), HGVSc: String = "ENST00000335137.4:c.807T>C", HGVSp: String = "ENSP00000334393.3:p.Ser269%3D", cDNA_position: Int = 843, CDS_position: Int = 807, Protein_position: Int = 269, Amino_acids: AminoAcids = AminoAcids("S", None), Codons: CODONS = CODONS("tcT", "tcC"), Existing_variation: List[String] = List("rs200676709"), DISTANCE: Option[Int] = None, STRAND: Int = 1, FLAGS: Option[List[String]] = None, PICK: String = "1", VARIANT_CLASS: String = "SNV", SYMBOL_SOURCE: String = "HGNC", HGNC_ID: String = "HGNC:14825", CANONICAL: String = "YES", RefSeq: String = ..., HGVS_OFFSET: Option[String] = None, HGVSg: String = "chr1:g.69897T>C", CLIN_SIG: Option[String] = None, SOMATIC: Option[String] = None, PHENO: Option[String] = None, PUBMED: Option[String] = Some("29135816"), CADD_raw_rankscore: Option[String] = None, DANN_rankscore: Option[String] = None, Ensembl_geneid: Option[String] = None, Ensembl_transcriptid: Option[String] = None, ExAC_AC: Option[String] = None, ExAC_AF: Option[String] = None, FATHMM_converted_rankscore: Option[String] = None, FATHMM_pred: Option[String] = None, GTEx_V7_tissue: Option[String] = None, Interpro_domain: Option[String] = None, LRT_converted_rankscore: Option[String] = None, LRT_pred: Option[String] = None, Polyphen2_HVAR_pred: Option[String] = None, Polyphen2_HVAR_rankscore: Option[String] = None, REVEL_rankscore: Option[String] = None, SIFT_converted_rankscore: Option[String] = None, SIFT_pred: Option[String] = None, UK10K_AC: Option[String] = None, UK10K_AF: Option[String] = None, clinvar_MedGen_id: Option[String] = None, clinvar_OMIM_id: Option[String] = None, clinvar_Orphanet_id: Option[String] = None, clinvar_clnsig: Option[String] = None, clinvar_id: Option[String] = None, clinvar_trait: Option[String] = None, gnomAD_exomes_AC: Option[String] = None, gnomAD_exomes_AF: Option[String] = None, gnomAD_genomes_AC: Option[String] = None, gnomAD_genomes_AF: Option[String] = None, phyloP17way_primate_rankscore: Option[String] = None, rs_dbSNP151: Option[String] = None)
Value Members
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final
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!=(arg0: Any): Boolean
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final
def
##(): Int
- Definition Classes
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final
def
==(arg0: Any): Boolean
- Definition Classes
- AnyRef → Any
- val Allele: String
- val Amino_acids: AminoAcids
- val BIOTYPE: String
- val CADD_raw_rankscore: Option[String]
- val CANONICAL: String
- val CDS_position: Int
- val CLIN_SIG: Option[String]
- val Codons: CODONS
- val Consequence: List[String]
- val DANN_rankscore: Option[String]
- val DISTANCE: Option[Int]
- val EXON: Exon
- val Ensembl_geneid: Option[String]
- val Ensembl_transcriptid: Option[String]
- val ExAC_AC: Option[String]
- val ExAC_AF: Option[String]
- val Existing_variation: List[String]
- val FATHMM_converted_rankscore: Option[String]
- val FATHMM_pred: Option[String]
- val FLAGS: Option[List[String]]
- val Feature: String
- val Feature_type: String
- val GTEx_V7_tissue: Option[String]
- val Gene: String
- val HGNC_ID: String
- val HGVS_OFFSET: Option[String]
- val HGVSc: String
- val HGVSg: String
- val HGVSp: String
- val IMPACT: String
- val INTRON: Intron
- val Interpro_domain: Option[String]
- val LRT_converted_rankscore: Option[String]
- val LRT_pred: Option[String]
- val PHENO: Option[String]
- val PICK: String
- val PUBMED: Option[String]
- val Polyphen2_HVAR_pred: Option[String]
- val Polyphen2_HVAR_rankscore: Option[String]
- val Protein_position: Int
- val REVEL_rankscore: Option[String]
- val RefSeq: String
- val SIFT_converted_rankscore: Option[String]
- val SIFT_pred: Option[String]
- val SOMATIC: Option[String]
- val STRAND: Int
- val SYMBOL: String
- val SYMBOL_SOURCE: String
- val UK10K_AC: Option[String]
- val UK10K_AF: Option[String]
- val VARIANT_CLASS: String
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final
def
asInstanceOf[T0]: T0
- Definition Classes
- Any
- val cDNA_position: Int
- val clinvar_MedGen_id: Option[String]
- val clinvar_OMIM_id: Option[String]
- val clinvar_Orphanet_id: Option[String]
- val clinvar_clnsig: Option[String]
- val clinvar_id: Option[String]
- val clinvar_trait: Option[String]
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getClass(): Class[_]
- Definition Classes
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- val gnomAD_exomes_AC: Option[String]
- val gnomAD_exomes_AF: Option[String]
- val gnomAD_genomes_AC: Option[String]
- val gnomAD_genomes_AF: Option[String]
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- val phyloP17way_primate_rankscore: Option[String]
- val rs_dbSNP151: Option[String]
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