WormBase Tree Display for Variation: WBVar00296666

WBVar00296666 Name: Public_name: ok3664
    Other_name: B0285.1c.2:c.854+13_1093delinsT
      B0285.1b.2:c.854+13_1093delinsT
      B0285.1a.2:c.854+13_1093delinsT
      B0285.1c.1:c.854+13_1093delinsT
      B0285.1b.1:c.854+13_1093delinsT
      B0285.1a.1:c.854+13_1093delinsT
    HGVSg: CHROMOSOME_III:g.4337192_4337823delinsT
  Sequence_details: SMap: S_parent: Sequence: B0285
    Flanking_sequences: gatagccactcggcctgtgtaagttatttg ttcatcataagaatatcgtccgtcttatgg
    Mapping_target: B0285
    Type_of_mutation: Insertion: T
      Deletion
    PCR_product: ok3664_external
      ok3664_internal
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00024069
      WBStrain00024070
      WBStrain00037602
    Laboratory: RB
    Person: WBPerson46
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00007135
    Transcript: B0285.1c.2 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: B0285.1c.2:c.854+13_1093delinsT
        cDNA_position: ?-1102
        CDS_position: ?-1093
        Protein_position: ?-365
        Intron_number: 6-7/14
        Exon_number: 7-8/15
      B0285.1b.2 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: B0285.1b.2:c.854+13_1093delinsT
        cDNA_position: ?-1097
        CDS_position: ?-1093
        Protein_position: ?-365
        Intron_number: 6-7/14
        Exon_number: 7-8/15
      B0285.1c.1 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: B0285.1c.1:c.854+13_1093delinsT
        cDNA_position: ?-1253
        CDS_position: ?-1093
        Protein_position: ?-365
        Intron_number: 8-9/16
        Exon_number: 9-10/17
      B0285.1a.2 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: B0285.1a.2:c.854+13_1093delinsT
        cDNA_position: ?-1101
        CDS_position: ?-1093
        Protein_position: ?-365
        Intron_number: 6-7/14
        Exon_number: 7-8/15
      B0285.1b.1 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: B0285.1b.1:c.854+13_1093delinsT
        cDNA_position: ?-1256
        CDS_position: ?-1093
        Protein_position: ?-365
        Intron_number: 8-9/16
        Exon_number: 9-10/17
      B0285.1a.1 VEP_consequence: splice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
        VEP_impact: HIGH
        HGVSc: B0285.1a.1:c.854+13_1093delinsT
        cDNA_position: ?-1229
        CDS_position: ?-1093
        Protein_position: ?-365
        Intron_number: 8-9/16
        Exon_number: 9-10/17
  Isolation: Mutagen: EMS
  Remark: Sequenced by the C. elegans Gene Knockout Consortium Paper_evidence: WBPaper00041807
  Method: KO_consortium_allele