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WormBase Tree Display for Variation: WBVar01889557

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Name Class

WBVar01889557NamePublic_nameWBVar01889557
Other_namecewivar00604604
Y71G12B.11b.1:c.*286+229A>T
Y71G12B.11e.1:c.1886+229A>T
Y71G12B.11d.1:c.-146+229A>T
Y71G12B.11c.1:c.992+229A>T
Y71G12B.11a.1:c.2981+229A>T
HGVSgCHROMOSOME_I:g.1733599A>T
Sequence_detailsSMapS_parentSequenceY71G12B
Flanking_sequencesAGTTTGAAACGAAACAAAAAGTTTGGGCCAAGTTTGGCAAGAGTTGGGTGAAACTTGGCT
Mapping_targetY71G12B
Source_location225CHROMOSOME_I17336011733601From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006771
TranscriptY71G12B.11c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11c.1:c.992+229A>T
Intron_number4/6
Y71G12B.11e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11e.1:c.1886+229A>T
Intron_number4/6
Y71G12B.11a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11a.1:c.2981+229A>T
Intron_number8/11
Y71G12B.11d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11d.1:c.-146+229A>T
Intron_number1/5
Y71G12B.11b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY71G12B.11b.1:c.*286+229A>T
Intron_number10/12
MethodWGS_Flibotte