Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01678827

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01678827NamePublic_nameWBVar01678827
Other_namecewivar00369079
F25C8.3c.1:c.4324+218A>G
F25C8.3a.1:c.4378+218A>G
F25C8.3e.1:c.4246+218A>G
F25C8.3d.1:c.4492+13A>G
F25C8.3b.1:c.4378+218A>G
HGVSgCHROMOSOME_V:g.20890631A>G
Sequence_detailsSMapS_parentSequenceF25C8
Flanking_sequencesTTCCAGAGTTTTTAGATGGTAAAAATGAATAAAATAGTCATGTGATCCCTTGTTAAAGTA
Mapping_targetF25C8
Source_location225CHROMOSOME_V2089060020890600From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006637From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006812
TranscriptF25C8.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3d.1:c.4492+13A>G
Intron_number20/36
F25C8.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3b.1:c.4378+218A>G
Intron_number20/35
F25C8.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3e.1:c.4246+218A>G
Intron_number18/33
F25C8.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3c.1:c.4324+218A>G
Intron_number19/34
F25C8.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3a.1:c.4378+218A>G
Intron_number19/36
MethodWGS_Flibotte