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WormBase Tree Display for Variation: WBVar01602566

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Name Class

WBVar01602566NamePublic_nameWBVar01602566
Other_name (11)
HGVSgCHROMOSOME_X:g.15131152T>C
Sequence_detailsSMapS_parentSequenceR07D5
Flanking_sequencesATATTTTTGTTGTCTCTTCATCTCCTTTTTGGGAGAGCTCAGGGGCCTCCACAAAGAAAT
Mapping_targetR07D5
Source_location225CHROMOSOME_X1513108215131082From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00199254
WBGene00006747
WBGene00196247
TranscriptR07D5.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1i.1:c.57+601A>G
Intron_number2/11
R07D5.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1f.1:c.18+3426A>G
Intron_number1/9
R07D5.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1h.1:c.57+601A>G
Intron_number1/9
R07D5.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1c.1:c.-165-3977A>G
Intron_number1/11
R07D5.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1a.1:c.-8-3570A>G
Intron_number1/12
R07D5.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1g.1:c.18+3426A>G
Intron_number2/11
R07D5.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1d.1:c.268-3977A>G
Intron_number1/9
R07D5.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR07D5.1e.1:c.268-3977A>G
Intron_number1/10
R07D5.4VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScR07D5.4:n.69T>C
cDNA_position69
Exon_number1/1
R07D5.6VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScR07D5.6:n.64A>G
cDNA_position64
Exon_number1/1
MethodWGS_Flibotte