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WormBase Tree Display for Variation: WBVar01987604

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Name Class

WBVar01987604NamePublic_nameWBVar01987604
Other_namecewivar00714158
T06H11.1f.1:c.413-7951_413-7950dup
T06H11.1b.1:c.262+7737_262+7738dup
T06H11.1d.1:c.292+5424_292+5425dup
T06H11.1c.1:c.148+56_148+57dup
HGVSgCHROMOSOME_X:g.10117280_10117281insAA
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesATCAAAAACCAGAATCCGTAGTTAAACAACAAAAAAAAATAAAAAGAAGAAGAAAGATAA
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011722110117222From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.262+7737_262+7738dup
Intron_number3/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-7951_413-7950dup
Intron_number4/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.292+5424_292+5425dup
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.148+56_148+57dup
Intron_number2/13
MethodWGS_Flibotte