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WormBase Tree Display for Variation: WBVar01711979

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Name Class

WBVar01711979NamePublic_nameWBVar01711979
Other_namecewivar00409692
Y71G12B.11e.1:c.1813-833A>C
Y71G12B.11a.1:c.2908-833A>C
Y71G12B.11c.1:c.919-833A>C
Y71G12B.11b.1:c.2908-328A>C
Y71G12B.11f.1:c.1813-328A>C
HGVSgCHROMOSOME_I:g.1732464A>C
Sequence_detailsSMapS_parentSequenceY71G12B
Flanking_sequencesCAAACAATGTGACGTCCGTTGAGAACTCTGGTCTCTTTTCCCGCATTTTTTGTAGATCCA
Mapping_targetY71G12B
Source_location225CHROMOSOME_I17324661732466From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAC
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
AffectsGeneWBGene00006771
TranscriptY71G12B.11f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11f.1:c.1813-328A>C
Intron_number3/3
Y71G12B.11c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11c.1:c.919-833A>C
Intron_number3/6
Y71G12B.11e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11e.1:c.1813-833A>C
Intron_number3/6
Y71G12B.11a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11a.1:c.2908-833A>C
Intron_number7/11
Y71G12B.11b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11b.1:c.2908-328A>C
Intron_number7/12
MethodWGS_Flibotte