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WormBase Tree Display for Variation: WBVar01740718

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Name Class

WBVar01740718NamePublic_nameWBVar01740718
Other_namecewivar00439768
W01A11.3b.2:c.867-460G>A
W01A11.3b.1:c.867-460G>A
W01A11.3c.2:c.162-460G>A
W01A11.3a.1:c.1065-460G>A
W01A11.3c.1:c.162-460G>A
HGVSgCHROMOSOME_V:g.6482303G>A
Sequence_detailsSMapS_parentSequenceW01A11
Flanking_sequencesGGACAAGTGATACGTGATATCCTACTCCCGGGAGTCCACACCGCATACTTATTGGCCTCC
Mapping_targetW01A11
Source_location225CHROMOSOME_V64822866482286From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006815
TranscriptW01A11.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW01A11.3a.1:c.1065-460G>A
Intron_number10/17
W01A11.3c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW01A11.3c.2:c.162-460G>A
Intron_number3/10
W01A11.3b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW01A11.3b.2:c.867-460G>A
Intron_number9/16
W01A11.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW01A11.3b.1:c.867-460G>A
Intron_number8/15
W01A11.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW01A11.3c.1:c.162-460G>A
Intron_number5/12
MethodWGS_Flibotte