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WormBase Tree Display for Variation: WBVar01987691

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Name Class

WBVar01987691NamePublic_nameWBVar01987691
Other_namecewivar00714246
F13D2.1a.1:c.814-1657dup
F13D2.1b.1:c.814-1657dup
HGVSgCHROMOSOME_X:g.11177671_11177672insA
Sequence_detailsSMapS_parentSequenceF13D2
Flanking_sequencesAAGAAAAGGTTTATAGTGCTAAACCGTGCTAAAAAATAATTGAAAACCTCTTTAAAACAA
Mapping_targetF13D2
Source_location225CHROMOSOME_X1117760611177607From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008735
TranscriptF13D2.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF13D2.1b.1:c.814-1657dup
Intron_number9/38
F13D2.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF13D2.1a.1:c.814-1657dup
Intron_number8/37
MethodWGS_Flibotte