case class RawClinvar(contigName: String = "2", start: Long = 69359260, end: Long = 69359261, names: List[String] = List("257668"), referenceAllele: String = "T", alternateAlleles: List[String] = List("A"), qual: Option[Double] = None, filters: List[String] = List(""), splitFromMultiAllelic: Boolean = false, INFO_AF_EXAC: Double = 0.00394, INFO_CLNVCSO: String = "SO:0001483", INFO_GENEINFO: String = "GFPT1:2673", INFO_CLNSIGINCL: Option[List[String]] = None, INFO_CLNVI: List[String] = ..., INFO_CLNDISDB: List[String] = ..., INFO_CLNREVSTAT: List[String] = ..., INFO_CLNDN: List[String] = ..., INFO_ALLELEID: Int = 250763, INFO_ORIGIN: List[String] = List("1"), INFO_SSR: Option[Int] = None, INFO_CLNDNINCL: Option[List[String]] = None, INFO_CLNSIG: List[String] = List("Benign"), INFO_RS: List[String] = List("112682152"), INFO_DBVARID: Option[List[String]] = None, INFO_AF_TGP: Double = 0.01118, INFO_CLNVC: String = "single_nucleotide_variant", INFO_CLNHGVS: List[String] = List("NC_000002.12:g.69359261T>A"), INFO_MC: List[String] = List("SO:0001627|intron_variant"), INFO_CLNSIGCONF: Option[List[String]] = None, INFO_AF_ESP: Double = 0.01415, INFO_CLNDISDBINCL: Option[List[String]] = None, genotypes: List[GENOTYPES] = List(GENOTYPES())) extends Product with Serializable
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- new RawClinvar(contigName: String = "2", start: Long = 69359260, end: Long = 69359261, names: List[String] = List("257668"), referenceAllele: String = "T", alternateAlleles: List[String] = List("A"), qual: Option[Double] = None, filters: List[String] = List(""), splitFromMultiAllelic: Boolean = false, INFO_AF_EXAC: Double = 0.00394, INFO_CLNVCSO: String = "SO:0001483", INFO_GENEINFO: String = "GFPT1:2673", INFO_CLNSIGINCL: Option[List[String]] = None, INFO_CLNVI: List[String] = ..., INFO_CLNDISDB: List[String] = ..., INFO_CLNREVSTAT: List[String] = ..., INFO_CLNDN: List[String] = ..., INFO_ALLELEID: Int = 250763, INFO_ORIGIN: List[String] = List("1"), INFO_SSR: Option[Int] = None, INFO_CLNDNINCL: Option[List[String]] = None, INFO_CLNSIG: List[String] = List("Benign"), INFO_RS: List[String] = List("112682152"), INFO_DBVARID: Option[List[String]] = None, INFO_AF_TGP: Double = 0.01118, INFO_CLNVC: String = "single_nucleotide_variant", INFO_CLNHGVS: List[String] = List("NC_000002.12:g.69359261T>A"), INFO_MC: List[String] = List("SO:0001627|intron_variant"), INFO_CLNSIGCONF: Option[List[String]] = None, INFO_AF_ESP: Double = 0.01415, INFO_CLNDISDBINCL: Option[List[String]] = None, genotypes: List[GENOTYPES] = List(GENOTYPES()))
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- val INFO_AF_ESP: Double
- val INFO_AF_EXAC: Double
- val INFO_AF_TGP: Double
- val INFO_ALLELEID: Int
- val INFO_CLNDISDB: List[String]
- val INFO_CLNDISDBINCL: Option[List[String]]
- val INFO_CLNDN: List[String]
- val INFO_CLNDNINCL: Option[List[String]]
- val INFO_CLNHGVS: List[String]
- val INFO_CLNREVSTAT: List[String]
- val INFO_CLNSIG: List[String]
- val INFO_CLNSIGCONF: Option[List[String]]
- val INFO_CLNSIGINCL: Option[List[String]]
- val INFO_CLNVC: String
- val INFO_CLNVCSO: String
- val INFO_CLNVI: List[String]
- val INFO_DBVARID: Option[List[String]]
- val INFO_GENEINFO: String
- val INFO_MC: List[String]
- val INFO_ORIGIN: List[String]
- val INFO_RS: List[String]
- val INFO_SSR: Option[Int]
- val alternateAlleles: List[String]
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- val contigName: String
- val end: Long
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eq(arg0: AnyRef): Boolean
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- val filters: List[String]
- val genotypes: List[GENOTYPES]
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- val qual: Option[Double]
- val referenceAllele: String
- val splitFromMultiAllelic: Boolean
- val start: Long
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