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WormBase Tree Display for Variation: WBVar01739304

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Name Class

WBVar01739304NamePublic_nameWBVar01739304
Other_namecewivar00438286
W08A12.1e.1:c.66+1598A>T
W08A12.1b.1:c.141+1598A>T
W08A12.1b.3:c.141+1598A>T
W08A12.1b.2:c.141+1598A>T
W08A12.1a.1:c.47+1598A>T
W08A12.1c.1:c.123+1598A>T
HGVSgCHROMOSOME_V:g.3693656A>T
Sequence_detailsSMapS_parentSequenceW08A12
Flanking_sequencesATCTACAAAAAAATGCGGGAATTTTTTACTGAAAAAATGTGACGTCAGCACGCTATTAAC
Mapping_targetW08A12
Source_location225CHROMOSOME_V36936433693643From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021078
TranscriptW08A12.1b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.3:c.141+1598A>T
Intron_number3/7
W08A12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1a.1:c.47+1598A>T
Intron_number2/7
W08A12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1c.1:c.123+1598A>T
Intron_number3/7
W08A12.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.2:c.141+1598A>T
Intron_number4/8
W08A12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.1:c.141+1598A>T
Intron_number4/8
W08A12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1e.1:c.66+1598A>T
Intron_number1/4
MethodWGS_Flibotte