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WormBase Tree Display for Variation: WBVar01878006

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Name Class

WBVar01878006NamePublic_nameWBVar01878006
Other_namecewivar00592447
F25C8.3c.1:c.7317+42A>T
F25C8.3b.1:c.7344+42A>T
F25C8.3d.1:c.7521+42A>T
F25C8.3a.1:c.7407+42A>T
F25C8.3e.1:c.7212+42A>T
HGVSgCHROMOSOME_V:g.20895631A>T
Sequence_detailsSMapS_parentSequenceF25C8
Flanking_sequencesGATAGTTCCTGGAGGAGCTAAATAACCCATATAAAATAGATAATCAATGAGAAATAATTT
Mapping_targetF25C8
Source_location225CHROMOSOME_V2089560020895600From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006812
TranscriptF25C8.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3d.1:c.7521+42A>T
Intron_number30/36
F25C8.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3b.1:c.7344+42A>T
Intron_number28/35
F25C8.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3e.1:c.7212+42A>T
Intron_number26/33
F25C8.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3c.1:c.7317+42A>T
Intron_number28/34
F25C8.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3a.1:c.7407+42A>T
Intron_number29/36
MethodWGS_Flibotte