WormBase Tree Display for Variation: WBVar00248983

WBVar00248983 Name: Public_name: sy424
    Other_name: C09E10.2a.1:c.2300G>A
      C09E10.2c.1:c.1832G>A
      CE38270:p.Trp736Ter
      C09E10.2d.1:c.1838G>A
      CE38269:p.Trp613Ter
      C09E10.2b.1:c.2306G>A
      CE38268:p.Trp611Ter
      C09E10.2e.1:c.2207G>A
      CE08038:p.Trp767Ter
      CE08039:p.Trp769Ter
    HGVSg: CHROMOSOME_X:g.986039C>T
  Sequence_details: SMap: S_parent: Sequence: C09E10
    Flanking_sequences: tgttcttcgaaaggacatgtaaagatttat gaaacgtatcgaattagaggtatgatctac
    Mapping_target: C09E10
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00024616
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: PS
    Status: Live
  Affects: Gene: WBGene00000958
    Transcript: C09E10.2d.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: C09E10.2d.1:c.1838G>A
        HGVSp: CE38269:p.Trp613Ter
        cDNA_position: 1838
        CDS_position: 1838
        Protein_position: 613
        Exon_number: 10/14
        Codon_change: tGg/tAg
        Amino_acid_change: W/*
      C09E10.2c.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: C09E10.2c.1:c.1832G>A
        HGVSp: CE38268:p.Trp611Ter
        cDNA_position: 1832
        CDS_position: 1832
        Protein_position: 611
        Exon_number: 10/14
        Codon_change: tGg/tAg
        Amino_acid_change: W/*
      C09E10.2a.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: C09E10.2a.1:c.2300G>A
        HGVSp: CE08038:p.Trp767Ter
        cDNA_position: 2443
        CDS_position: 2300
        Protein_position: 767
        Exon_number: 13/18
        Codon_change: tGg/tAg
        Amino_acid_change: W/*
      C09E10.2e.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: C09E10.2e.1:c.2207G>A
        HGVSp: CE38270:p.Trp736Ter
        cDNA_position: 2207
        CDS_position: 2207
        Protein_position: 736
        Exon_number: 11/15
        Codon_change: tGg/tAg
        Amino_acid_change: W/*
      C09E10.2b.1 VEP_consequence: stop_gained
        VEP_impact: HIGH
        HGVSc: C09E10.2b.1:c.2306G>A
        HGVSp: CE08039:p.Trp769Ter
        cDNA_position: 2449
        CDS_position: 2306
        Protein_position: 769
        Exon_number: 13/18
        Codon_change: tGg/tAg
        Amino_acid_change: W/*
  Genetics: Interpolated_map_position: X -18.8717
  Method: Substitution_allele