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WormBase Tree Display for Variation: WBVar01894562

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Name Class

WBVar01894562NamePublic_nameWBVar01894562
Other_namecewivar00609835
F25C8.3c.1:c.2771+416A>T
F25C8.3b.1:c.2825+416A>T
F25C8.3a.1:c.2825+416A>T
F25C8.3d.1:c.2825+416A>T
F25C8.3e.1:c.2825+416A>T
HGVSgCHROMOSOME_V:g.20887117A>T
Sequence_detailsSMapS_parentSequenceF25C8
Flanking_sequencesGTCATTTTGGCACCTTAAGAGTAGTTTTTACACTTTCCTCACTGGCGCTATTTCACCTTT
Mapping_targetF25C8
Source_location225CHROMOSOME_V2088708620887086From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006812
TranscriptF25C8.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3d.1:c.2825+416A>T
Intron_number13/36
F25C8.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3b.1:c.2825+416A>T
Intron_number14/35
F25C8.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3e.1:c.2825+416A>T
Intron_number13/33
F25C8.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3c.1:c.2771+416A>T
Intron_number13/34
F25C8.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3a.1:c.2825+416A>T
Intron_number13/36
MethodWGS_Flibotte