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WormBase Tree Display for Variation: WBVar01587132

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Name Class

WBVar01587132NamePublic_nameWBVar01587132
Other_namecewivar00229521
T27C4.4b.2:c.2526+450C>A
T27C4.4d.1:c.2526+450C>A
T27C4.4e.1:c.2121+450C>A
T27C4.4b.1:c.2526+450C>A
T27C4.4a.1:c.2526+450C>A
HGVSgCHROMOSOME_V:g.3709463C>A
Sequence_detailsSMapS_parentSequenceT27C4
Flanking_sequencesCAACATATTTGACGCGCAAAATATCTTGTAGCGAAAACTAAGTAATTCTTTACATGACTACTGTAGCGCTAGTCGATTTA
Mapping_targetT27C4
Source_location225CHROMOSOME_V37094503709450From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003025
TranscriptT27C4.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4d.1:c.2526+450C>A
Intron_number6/8
T27C4.4b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.2:c.2526+450C>A
Intron_number6/8
T27C4.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4a.1:c.2526+450C>A
Intron_number6/9
T27C4.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4e.1:c.2121+450C>A
Intron_number3/4
T27C4.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT27C4.4b.1:c.2526+450C>A
Intron_number6/8
MethodWGS_Flibotte