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WormBase Tree Display for Variation: WBVar01616284

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Name Class

WBVar01616284NamePublic_nameWBVar01616284
Other_namecewivar00295771
W08A12.1b.1:c.142-1751T>C
W08A12.1c.1:c.124-1751T>C
W08A12.1b.2:c.142-1751T>C
W08A12.1a.1:c.48-270T>C
W08A12.1b.3:c.142-1751T>C
W08A12.1e.1:c.67-1751T>C
HGVSgCHROMOSOME_V:g.3695701T>C
Sequence_detailsSMapS_parentSequenceW08A12
Flanking_sequencesGCCTAGAGGGCTTTTCTTTGATTAATAAGAAAGCGCATTTTCGGAAATTGAATTAGTCGG
Mapping_targetW08A12
Source_location225CHROMOSOME_V36956883695688From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021078
TranscriptW08A12.1b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.3:c.142-1751T>C
Intron_number3/7
W08A12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1a.1:c.48-270T>C
Intron_number2/7
W08A12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1c.1:c.124-1751T>C
Intron_number3/7
W08A12.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.2:c.142-1751T>C
Intron_number4/8
W08A12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.1:c.142-1751T>C
Intron_number4/8
W08A12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1e.1:c.67-1751T>C
Intron_number1/4
MethodWGS_Flibotte