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WormBase Tree Display for Variation: WBVar01987603

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Name Class

WBVar01987603NamePublic_nameWBVar01987603
Other_namecewivar00714157
T06H11.1d.1:c.292+5740_292+5790del
T06H11.1c.1:c.148+372_148+422del
T06H11.1f.1:c.413-7635_413-7585del
T06H11.1b.1:c.263-7635_263-7585del
HGVSgCHROMOSOME_X:g.10116916_10116966del
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesAGGTGCAAAACTAAACATGTCAAAGTCGAGTCCCAAAAAACTTTTTTTCAGTTCTTCACA
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011685710116907From_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
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.263-7635_263-7585del
Intron_number3/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-7635_413-7585del
Intron_number4/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.292+5740_292+5790del
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.148+372_148+422del
Intron_number2/13
MethodWGS_Flibotte