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WormBase Tree Display for Variation: WBVar01982078

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Name Class

WBVar01982078NamePublic_nameWBVar01982078
Other_namecewivar00708209
C45E1.1a.1:c.861+147_861+157del
C45E1.1b.1:c.786+147_786+157del
C45E1.1a.2:c.861+147_861+157del
C45E1.1c.1:c.879+147_879+157del
HGVSgCHROMOSOME_I:g.3108870_3108880del
Sequence_detailsSMapS_parentSequenceC45E1
Flanking_sequencesTGTATTAATAAAATCATACGAATCAAGGGTGATTTTTTCTGGCAAATTGAAAAATCGGCA
Mapping_targetC45E1
Source_location225CHROMOSOME_I31088723108882From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003654
TranscriptC45E1.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1b.1:c.786+147_786+157del
Intron_number6/6
C45E1.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1c.1:c.879+147_879+157del
Intron_number8/8
C45E1.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1a.2:c.861+147_861+157del
Intron_number9/10
C45E1.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1a.1:c.861+147_861+157del
Intron_number8/9
MethodWGS_Flibotte